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As filed with the Securities and Exchange Commission on January 23, 2009

Registration Statement No. 333-156035

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549

Amendment No. 1
to

FORM S-4
REGISTRATION STATEMENT
Under
THE SECURITIES ACT OF 1933



INOVIO BIOMEDICAL CORPORATION
(Exact name of registrant as specified in its charter)



Delaware
(State or other jurisdiction of
incorporation or organization)
  3841
(Primary Standard Industrial
Classification Code Number)
  33-0969592
(I.R.S. Employer
Identification No.)



11494 Sorrento Valley Road
San Diego, California 92121
(858) 597-6006
(Address and telephone number of registrant's principal executive offices)



Avtar Dhillon, M.D.
Chief Executive Officer and President
Inovio Biomedical Corporation
11494 Sorrento Valley Road
San Diego, California 92121
(858) 597-6006
(Name, address and telephone number, of agent for service)



Copies of all communications to be sent to:

Shoshannah D. Katz, Esq.
Thomas J. Poletti, Esq.
K&L Gates LLP
10100 Santa Monica Blvd.
Suite 700
Los Angeles, CA 90067
Tel.: (310) 552-5000
Fax: (310) 552-5001

 

J. Joseph Kim, Ph.D.
VGX Pharmaceuticals, Inc.
450 Sentry Parkway
Blue Bell, PA 19422
Tel.: (267) 440-4200
Fax: (267) 440-4242

 

Kathleen M. Shay, Esq.
John W. Kauffman, Esq.
Duane Morris LLP
30 South 17 th  Street
Philadelphia, PA 19103
Tel.: (215) 979-1000
Fax: (215) 979-1020



         Approximate date of commencement of proposed sale to the public: As soon as practicable after the effectiveness of this registration statement and the satisfaction or waiver of all other terms and conditions to the merger described in the joint proxy statement/prospectus contained herein.



        If the securities being registered on this Form are being offered in connection with the formation of a holding company and there is compliance with General Instruction G, check the following box. o

        If this Form is filed to register additional securities for an offering pursuant to Rule 462(b) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. o

        If this Form is a post-effective amendment filed pursuant to Rule 462(d) under the Securities Act, check the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same offering. o

        Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of "large accelerated filer," "accelerated filer" and "smaller reporting company" in Rule 12b-2 of the Exchange Act.

Large accelerated filer  o   Accelerated filer  o   Non-accelerated filer  o
(Do not check if a smaller reporting company)
  Smaller reporting company  ý


If applicable, place an X in the box to designate the appropriate rule provision relied upon in conducting this transaction:

Exchange Act Rule 13e-4(i) (Cross-Border Issuer Tender Offer) o

Exchange Act Rule 14d-1(d) (Cross-Border Third-Party Tender Offer) o


CALCULATION OF REGISTRATION FEE

 
Title of Each Class of
Securities to be Registered

  Amount to
be Registered(15)

  Proposed Maximum
Offering Price
Per Unit

  Proposed Maximum
Aggregate Offering
Price

  Amount of
Registration Fee(14)

 

Common Stock, par value $0.001 per share

  42,506,544(1)   N/A   $1,417(2)   $1
 

Options to purchase Common Stock

  8,421,552(3)   N/A   N/A   N/A(4)
 

Common Stock, par value $0.001 per share underlying Options

  8,421,552(5)   N/A   $9,263,708(6)   $364
 

Warrants to purchase Common Stock

  4,973,327(7)   N/A   N/A   N/A(4)
 

Common Stock, par value $0.001 per share underlying Warrants

  4,973,327(8)   N/A   $5,420,927(9)   $213
 

Debt convertible into Common Stock

  $4,400,000(10)   N/A   $1,466,667(11)   $57
 

Common Stock, par value $0.001 per share underlying Convertible Debt

  4,788,100(12)   N/A   N/A   N/A(13)

 

(1)
Represents the maximum number of shares of common stock, par value $0.001 per share ("Common Stock"), of the registrant, Inovio Biomedical Corporation, or "Inovio," to be issued upon completion of the merger of VGX Pharmaceuticals, Inc., or "VGX," with and into a wholly-owned subsidiary of Inovio, to be issued in exchange for all of the outstanding shares of the common stock of VGX, estimated based on the anticipated exchange ratio of 0.9911488 (the "Merger Exchange Ratio") based on the total capital stock, options and warrants of Inovio outstanding and the total capital stock, options and warrants outstanding of VGX as of January 16, 2009.

(2)
Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(f)(2) under the Securities Act of 1933, as amended (the "Securities Act"). As VGX, the issuer of the securities to be acquired and cancelled in the proposed transaction, has an accumulated capital deficit of approximately $63 million as of September 30, 2008, the offering price shown is calculated based on one-third of the $0.0001 per share par value of VGX common stock.

(3)
Represents the maximum number of options to purchase Inovio Common Stock to be issued upon assumption of VGX options, based upon the Merger Exchange Ratio.

(4)
In accordance with Rule 457(g) under the Securities Act, because the shares of Inovio Common Stock underlying the options and warrants are registered hereby, no separate registration fee is required with respect to the options and warrants registered hereby.

(5)
Represents the maximum number of shares of Inovio Common Stock to be issued upon exercise of the assumed VGX options, based upon the Merger Exchange Ratio.

(6)
Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(g) under the Securities Act, based on an anticipated weighted average exercise price of $1.10 per share (reflecting anticipated adjusted prices ranging from $0.03 to $2.28 per share), based upon the Merger Exchange Ratio.

(7)
Represents the maximum number of Inovio warrants to purchase Inovio Common Stock to be issued upon assumption of VGX warrants, based upon the Merger Exchange Ratio.

(8)
Represents the maximum number of shares of Inovio Common Stock to be issued upon exercise of the assumed VGX warrants, based upon the Merger Exchange Ratio.

(9)
Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(g) under the Securities Act, based on an anticipated weighted average exercise price of $1.09 per share (reflecting anticipated adjusted prices ranging from $0.26 to $1.27 per share), based upon the Merger Exchange Ratio.

(10)
Represents the maximum principal amount of convertible debt to be assumed in connection with the Merger based on the amount of VGX convertible debt outstanding as of September 30, 2008. In addition, Inovio, on a consolidated basis via the Merger, shall assume the interest accrued or accruable on such principal amount, which may total up to an additional $627,500 upon maturity.

(11)
Estimated solely for the purpose of calculating the registration fee pursuant to Rule 457(f)(2) under the Securities Act. As VGX, the issuer of the convertible debt securities to be acquired and cancelled in the proposed transaction, has an accumulated capital deficit of approximately $63 million as of September 30, 3008, the offering price shown is calculated based on one-third of $4.4 million, the principal amount of such convertible debt securities.

(12)
Represents the maximum number of shares of Inovio Common Stock to be issued upon conversion of the assumed and adjusted VGX convertible debt on its negotiated terms at a conversion price of $1.05 per share, including the maximum number of shares issuable upon conversion of accrued interest, where allowable pursuant to the terms of such convertible debt.

(13)
In accordance with Rule 457(i) under the Securities Act, where convertible debt and the securities into which the debt is convertible are registered concurrently, the registration fee is to be calculated on the basis of the proposed offering price of the convertible securities alone and no separate registration fee is required for the underlying securities where no additional consideration is to be received by the issuer upon conversion.

(14)
A filing fee of $642 was paid with the filing of the registrant's Registration Statement on December 10, 2008.

(15)
In accordance with Rule 416, the registrant is also registering hereunder an indeterminate number of shares that may be issued and/or become issuable as a result of any stock splits or anti-dilution provisions of the securities registered hereby.

           The registrant hereby amends this registration statement on such date or dates as may be necessary to delay its effective date until the registrant shall file a further amendment which specifically states that this joint proxy statement/prospectus shall thereafter become effective in accordance with section 8(a) of the Securities Act of 1933 or until the registration statement shall become effective on such date as the Commission, acting pursuant to said section 8(a), may determine.


The information in the accompanying joint proxy statement/prospectus is not complete and may be changed. Inovio Biomedical Corporation may not complete the offer and sell its securities until the registration statement filed with the U.S. Securities and Exchange Commission is effective. The accompanying joint proxy statement/prospectus is not an offer to sell these securities and it is not soliciting an offer to buy these securities in any jurisdiction where the offer or sale is not permitted.

SUBJECT TO COMPLETION, DATED JANUARY 23, 2009

GRAPHIC   GRAPHIC


PROPOSED MERGER—YOUR VOTE IS VERY IMPORTANT

To the Stockholders of Inovio Biomedical Corporation and the Stockholders of VGX Pharmaceuticals, Inc.:

         As previously announced, Inovio Biomedical Corporation, or Inovio, and VGX Pharmaceuticals, Inc., or VGX, have agreed to combine under the terms of an acquisition agreement. If the merger is consummated, among other things, based on an exchange ratio and on the terms and conditions of which are described in the accompanying joint proxy statement/prospectus:

         If the merger is consummated, based on the fully-diluted share capital outstanding of each of Inovio and VGX as of the record date, current holders of Inovio capital stock will own approximately [        ]% and current holders of VGX common stock will own approximately [        ]% of the outstanding capital stock of the combined company, and current holders of Inovio securities will own approximately [        ]% and holders of VGX securities will own approximately [        ]% of the fully-diluted share capital of the combined company. Inovio's common stock is listed on the NYSE Alternext under the trading symbol "INO."

         Inovio and VGX cannot complete the proposed merger unless the stockholders of both Inovio and VGX approve proposals relating to the merger. After careful consideration, each of the boards of directors of Inovio and VGX have determined that the merger is fair and in the best interests of the stockholders of their respective companies and recommend that the stockholders of their respective companies vote FOR the proposals submitted to them in connection with the proposed merger. This joint proxy statement/prospectus provides you with detailed information about the merger and the other matters to be voted on at the respective stockholders' meetings.

         Inovio is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because Inovio's board of directors is soliciting their proxy to vote on the Inovio matters set forth in the joint proxy statement/prospectus at the announced special meeting of Inovio's stockholders to be held [                        ], 2009, which we refer to as the "Inovio special meeting." VGX is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because VGX's board of directors is soliciting their proxy to vote on the VGX matters set forth in the joint proxy statement/prospectus at the announced special meeting of VGX's stockholders to be held [                        ], 2009, which we refer to as the "VGX special meeting." Before voting, whether you are an Inovio stockholder or a VGX stockholder, you should carefully review all the information contained in the attached joint proxy statement/prospectus, including its annexes and information incorporated by references. IN PARTICULAR, YOU SHOULD CAREFULLY CONSIDER THE MATTERS DISCUSSED UNDER "RISK FACTORS" BEGINNING ON PAGE 28.

         In considering the recommendation of each company's board of directors, you should be aware that directors and officers of Inovio and VGX may have interests in the merger that are different from, or are in addition to, the interests of Inovio and VGX stockholders generally, and that these directors and officers may directly benefit if the merger is consummated. These interests and benefits are described in the joint proxy statement/prospectus. Whether or not you expect to attend the Inovio or VGX special meeting, the details of which are described on the respective Notices of Special Meeting of Stockholders enclosed, please complete, date, sign and promptly return the accompanying proxy in the enclosed envelope.

         We strongly support the combination of Inovio and VGX and join our respective boards of directors in recommending that Inovio's stockholders and VGX's stockholders vote FOR the proposals presented for their approval at the Inovio special meeting and the VGX special meeting, respectively.

INOVIO BIOMEDICAL CORPORATION   VGX PHARMACEUTICALS, INC.

Avtar Dhillon, M.D.
President and Chief Executive Officer

 

J. Joseph Kim, Ph.D.
President and Chief Executive Officer

          Neither the Securities and Exchange Commission nor any state securities commission has approved or disapproved of the securities to be issued in connection with the transaction described in this joint proxy statement/prospectus or determined whether this joint proxy statement/prospectus is truthful or complete. Any representation to the contrary is a criminal offense.

         This joint proxy statement/prospectus is dated [                        ], 2009 and is first being mailed to the Inovio stockholders and the VGX stockholders on or about [                        ], 2009.


INOVIO BIOMEDICAL CORPORATION



11494 Sorrento Valley Road
San Diego, California 92121
(858) 597-6006

NOTICE OF SPECIAL MEETING OF STOCKHOLDERS
To Be Held on [                                    ], 2009

To the Stockholders of Inovio Biomedical Corporation:

        You are cordially invited to attend a Special Meeting of Stockholders of Inovio Biomedical Corporation, a Delaware corporation ("Inovio"). The meeting will be held on [                                    ], 2009 at [            ] p.m., Pacific Standard Time (local time), at Inovio's principal executive offices, located 11494 Sorrento Valley Road, San Diego, California 92121, for the following purposes:

        These items of business are more fully described in the joint proxy statement/prospectus accompanying this notice. Inovio encourages you to read the joint proxy statement/prospectus in its entirety before voting.

        The record date for the Inovio special meeting is [                        ], 2009. Only Inovio stockholders of record at the close of business on that date may vote at the Inovio special meeting or any adjournments thereof.

        All Inovio stockholders of record are cordially invited to attend the meeting in person. Whether or not you expect to attend the meeting, please complete, date, sign and return the enclosed proxy card as promptly as possible in order to ensure your representation at the meeting. A return envelope (with postage prepaid if mailed in the United States) is enclosed for your convenience. Even if you have voted by proxy, you may still vote in person if you attend the meeting. Please note, however, that if your shares are held of record by a broker, bank or other nominee and you wish to vote at the meeting, you must obtain a proxy issued in your name from that record holder.

         Your vote is important regardless of the number of shares you own. Inovio and VGX cannot complete the Merger described above unless holders of a majority of the shares of Inovio common stock entitled to vote at the Inovio special meeting are present, either in person or by proxy, and vote in favor of the proposals.

San Diego, California
[                        ], 2009


VGX PHARMACEUTICALS, INC.



450 Sentry Parkway
Blue Bell, Pennsylvania 19422
(267) 440-4200

NOTICE OF SPECIAL MEETING OF STOCKHOLDERS
To Be Held on [                                    ], 2009

To the Stockholders of VGX Pharmaceuticals, Inc.:

        You are cordially invited to attend a Special Meeting of Stockholders of VGX Pharmaceuticals, Inc., a Delaware corporation ("VGX"). The meeting will be held on [                                    ], 2009 at [            ] p.m., Eastern Standard Time (local time), at VGX's principal executive offices, located 450 Sentry Parkway, Blue Bell, Pennsylvania 19422, for the following purposes:

        The Merger is more fully described in the joint proxy statement/prospectus accompanying this notice. VGX encourages you to read the joint proxy statement/prospectus in its entirety before voting.

        The record date for the VGX special meeting is [                        ], 2009. Only VGX stockholders of record at the close of business on that date may vote at the VGX special meeting or any adjournments thereof.

        All VGX stockholders of record are cordially invited to attend the meeting in person. Whether or not you expect to attend the meeting, please complete, date, sign and return the enclosed proxy card as promptly as possible in order to ensure your representation at the meeting. A return envelope (with postage prepaid if mailed in the United States) is enclosed for your convenience. Even if you have voted by proxy, you may still vote in person if you attend the meeting. Please note, however, that if your shares are held of record by a broker, bank or other nominee and you wish to vote at the meeting, you must obtain a proxy issued in your name from that record holder.

         Your vote is important regardless of the number of shares you own. Inovio and VGX cannot complete the Merger described above unless holders of a majority of the shares of VGX common stock entitled to vote at the VGX special meeting are present, either in person or by proxy, and vote in favor of the Merger proposal.

Blue Bell, Pennsylvania
[                        ], 2009



Table of Contents

 
  Page  

       

ADDITIONAL INFORMATION

    1  

ABOUT THIS JOINT PROXY STATEMENT/PROSPECTUS

    1  

QUESTIONS AND ANSWERS ABOUT THE TRANSACTION AND THE MEETINGS

    3  

SUMMARY OF THE JOINT PROXY STATEMENT/PROSPECTUS

    10  
 

The Companies

    10  
 

The Combined Group

    11  
 

Summary of the Transaction

    11  
 

Conditions to the Transaction

    12  
 

Termination of the Acquisition Agreement

    14  
 

No Solicitation

    15  
 

Vote of Stockholders Required

    15  
 

Appraisal and Dissenters Rights

    16  
 

Directors and Management of Inovio Following the Transaction

    16  
 

Opinion of Inovio's Financial Advisor

    17  
 

Interests of Directors, Officers and Affiliates

    18  
 

Accounting Treatment of the Merger

    18  
 

Certain Material U.S. Federal Income Tax Consequences of the Transaction

    19  
 

Listing of Inovio Common Stock on the NYSE Alternext

    19  
 

Matters To Be Considered At Special Meetings

       
 

Risk Factors

    19  
 

Comparative Market Price and Dividend Information

    19  

SELECTED SUMMARY HISTORICAL AND PRO FORMA COMBINED FINANCIAL DATA

    20  
 

Financial Information

    20  
 

Selected Summary Historical Financial Data of Inovio

    20  
 

Selected Summary Historical Financial Data of VGX

    23  
 

Selected Comparison of Historical and Pro Forma Per Share

    24  

COMPARATIVE STOCK PRICE AND DIVIDEND INFORMATION

    25  

CAUTIONARY NOTE REGARDING FORWARD LOOKING STATEMENTS

    26  

RISK FACTORS

    28  
 

Risks Relating to the Transaction

    28  
 

Risks Relating to the Business of the Combined Group

    38  

THE TRANSACTION

    62  
 

General Description of the Merger

    62  
 

Background to the Transaction

    63  
 

Inovio's Reasons for the Transaction

    66  
 

Recommendation of Inovio's Board of Directors

    69  
 

VGX's Reasons for the Transaction

    69  
 

Recommendation of VGX's Board of Directors

    73  
 

Resulting Ownership of Inovio; Change of Control

    73  
 

Opinion of Inovio's Financial Advisor

    74  
 

Appraisal Rights

    81  
 

Accounting Treatment

    84  
 

Listing or Quotation of Inovio Common Stock

    85  
 

Restrictions on Ability to Sell Inovio Common Stock

    85  
 

Interests of Directors, Officers And Affiliates

    86  
 

Directors And Management of Inovio Following The Transaction

    87  
 

Material Contracts and Relationships Between Inovio and VGX

    95  

i


 
  Page  

       

CERTAIN MATERIAL U.S. FEDERAL INCOME TAX CONSEQUENCES OF THE MERGER

    96  

THE ACQUISITION AGREEMENT

    99  
 

Structure of and Consideration for the Transaction

    99  
 

Merger Exchange Ratio

    102  
 

Effective Time of the Transaction

    102  
 

Exchange of Securities

    102  
 

Representations and Warranties

    103  
 

Conduct of Business Prior to Completion of the Transaction

    105  
 

Regulatory Matters

    110  
 

No Solicitation

    110  
 

Other Covenants

    112  
 

Conditions to the Transaction

    113  
 

Termination of the Acquisition Agreement

    115  
 

Termination Payment

    116  
 

Transaction Expenses

    116  
 

Indemnification

    116  
 

Amendment and Waiver

    117  
 

Governing Law

    117  

OTHER AGREEMENTS RELATED TO THE TRANSACTION

    117  
 

VGX Support Stockholders Voting Agreements

    117  
 

Voting Trust Agreement

    118  
 

Lock-Up Agreements

    118  
 

Employment Agreements

    118  

INFORMATION ABOUT THE COMPANIES

    124  
 

Inovio Biomedical Corporation

    124  
 

VGX Pharmaceuticals, Inc. 

    165  

SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT

    191  
 

Security Ownership of Certain Beneficial Owners and Management of Inovio Prior to the Transaction

    191  
 

Security Ownership of Certain Beneficial Owners and Management of VGX Prior to the Transaction

    192  
 

Security Ownership of Certain Beneficial Owners and Management of Inovio Following the Completion of the Transaction

    194  

QUANTITATIVE AND QUALITATIVE DISCLOSURE ABOUT MARKET RISKS

    197  

CAPITAL STRUCTURE OF INOVIO

    199  

COMPARISON OF RIGHTS OF HOLDERS OF INOVIO COMMON STOCK AND VGX COMMON STOCK

    200  

SPECIAL MEETING OF INOVIO STOCKHOLDERS

    209  
 

Questions and Answers About The Inovio Special Meeting

    209  
 

Proposal 1—Approval of Merger and Acquisition Agreement, Including Issuance of Inovio Securities

    213  
 

Proposal 2—Approval of Amendment to the Inovio 2000 Plan

    214  
 

Other Matters

    217  
 

Householding of Proxy Materials

    217  

SPECIAL MEETING OF VGX STOCKHOLDERS

    219  
 

Questions and Answers About The VGX Special Meeting

    219  
 

Proposal 1—Approval of Merger and Acquisition Agreement

    221  
 

Other Matters

    222  

LEGAL MATTERS

    222  

ii


 
  Page  

       

EXPERTS

    223  

WHERE YOU CAN FIND MORE INFORMATION ABOUT INOVIO

    223  

INFORMATION ON INOVIO'S WEBSITE

    223  

INFORMATION ON VGX'S WEBSITE

    224  

INDEX TO INOVIO FINANCIAL STATEMENTS

    F-1  

INDEX TO VGX FINANCIAL STATEMENTS

    F-74  

UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS

    I-1  

ANNEX A: ACQUISITION AGREEMENT

   
A-1
 

ANNEX B: OPINION OF OPPENHEIMER & CO. INC. 

   
B-1
 

ANNEX C: FORM OF PROPOSED CERTIFICATE OF MERGER

   
C-1
 

ANNEX D: PROPOSED AMENDED AND RESTATED INOVIO 2000 PLAN

   
D-1
 

ANNEX E: SECTION 262 OF THE GENERAL CORPORATION LAW OF THE STATE OF DELAWARE

   
E-1
 

iii



ADDITIONAL INFORMATION

        This joint proxy statement/prospectus incorporates by reference certain business and financial information about Inovio Biomedical Corporation, or Inovio, that is not included in or delivered with this joint proxy statement/prospectus. Such information is included in documents filed by Inovio with the U.S. Securities and Exchange Commission, which we refer to as the "SEC," which are available to the stockholders of Inovio and VGX Pharmaceuticals, Inc., or VGX, without charge from the SEC's website at www.sec.gov , or upon written or oral request, excluding any exhibits to those documents, unless the exhibit is specifically incorporated by reference as an exhibit in this joint proxy statement/prospectus. You can obtain any of these documents by requesting them in writing or by telephone from:

Inovio Biomedical Corporation
11494 Sorrento Valley Road
San Diego, California 92121
(858) 597-6006

        See " Where You Can Find More Information About Inovio " beginning on page 223 for a detailed description of the documents of Inovio incorporated by reference into this joint proxy statement/prospectus.

         In order for you to receive timely delivery of the documents in advance of the Inovio or VGX special meetings, as applicable, you should make your request by no later than [                        ].

        Information contained on the Inovio and VGX websites is expressly not incorporated by reference into this joint proxy statement/prospectus.

        All information in this joint proxy statement/prospectus concerning Inovio has been furnished by Inovio. All information in this document concerning VGX has been furnished by VGX. VGX has represented to Inovio, and Inovio has represented to VGX, that the information furnished by and concerning it is true and complete in all material respects.


ABOUT THIS JOINT PROXY STATEMENT/PROSPECTUS

        This document, which forms part of a registration statement on Form S-4 filed with the SEC by Inovio (File No. 333-156035), constitutes a prospectus of Inovio under Section 5 of the Securities Act of 1933, as amended, which we refer to as the "Securities Act," with respect to the securities of Inovio to be issued to holders of VGX securities in the proposed merger pursuant to the acquisition agreement described in this joint proxy statement/prospectus. This document also constitutes a notice of meeting and a proxy statement under Section 14(a) of the Securities Exchange Act of 1934, as amended, which we refer to as the "Exchange Act," with respect to the Inovio special meeting, at which Inovio stockholders will be asked to consider and vote upon certain proposals, including a proposal to approve the issuance of Inovio securities to holders of VGX securities in the merger pursuant to the acquisition agreement. This joint proxy statement/prospectus will also be utilized by VGX as a notice of meeting and proxy statement with respect to the VGX special meeting, at which VGX stockholders will be asked to consider and vote upon a proposal to approve and adopt the acquisition agreement and approve the merger.

        Throughout this joint proxy statement/prospectus, when we use the term "Inovio," we are referring to Inovio Biomedical Corporation, and when we use the term "VGX," we are referring to VGX Pharmaceuticals, Inc. When we use the term "combined company" or "combined group" we are referring to these entities as they will exist and operate if the proposed transaction closes, as described in this joint proxy statement/prospectus. When we use the term "Acquisition Agreement," we are referring to the Amended and Restated Agreement and Plan of Merger, dated December 5, 2008, by and among Inovio, Inovio Acquisition, LLC, a Delaware limited liability company (which we refer to as "Submerger"), and VGX, which is attached to this joint proxy statement/prospectus as Annex A , and

1



publicly filed by Inovio with the SEC as Exhibit 2.1 to the Inovio's Current Report on Form 8-K filed on December 8, 2008, and is incorporated by reference into this joint proxy statement/prospectus. Unless expressly specified otherwise, all of the numbers of Inovio common stock and share ownership numbers of Inovio common stock and all of the numbers of VGX common stock and share ownership numbers of VGX common stock referred to in this joint proxy statement/prospectus are calculated without giving effect to any issuance of such common stock upon the exercise of any outstanding options or conversion of any outstanding warrants or convertible debt after the record date. Further all references to percentages of the post-Merger fully-diluted share capital do not take into account potential conversion of any accrued interest on the assumed VGX convertible debt; however, references to the maximum shares to be issued or become issuable in relation to the Merger, includes the maximum number of shares potentially issuable upon conversion of accrued interest through maturity of the assumed VGX convertible debt.

        Additionally, sometimes when we use the terms "transaction" or the "transactions contemplated by the Acquisition Agreement," we are referring to:

2



QUESTIONS AND ANSWERS ABOUT THE TRANSACTION AND THE MEETINGS

Q:    Why am I receiving this joint proxy statement/prospectus?

A:     Inovio and VGX have agreed to a business combination pursuant to the terms of the Acquisition Agreement. In connection with the transaction, among other things, based on an exchange ratio and on the terms and conditions of which are described in this joint proxy statement/prospectus:

        In order to complete the transaction, Inovio stockholders must vote to approve the Merger, including the issuance of shares of Inovio common stock and other securities in exchange for all of the outstanding securities of VGX and the 2000 Plan Amendment, and VGX stockholders must vote to approve the Merger. Inovio is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because Inovio's board of directors is soliciting their proxy to vote on these matters and various other matters set forth in this joint proxy statement/prospectus at the announced special meeting of Inovio's stockholders to be held [                                    ], 2009, which we refer to as the "Inovio special meeting."

        VGX is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because VGX's board of directors is soliciting their proxy to vote on the VGX matters set forth in the joint proxy statement/prospectus at the announced special meeting of VGX's stockholders to be held [                                    ], 2009, which we refer to as the "VGX special meeting." This joint proxy statement/prospectus is also being sent to holders of VGX's outstanding options, warrants and convertible debt as a prospectus in relation to the assumption of such securities and the potential issuance of shares of Inovio common stock upon their respective exercise or conversion post-Merger, if the Merger is completed.

        This joint proxy statement/prospectus contains important information about the transaction and the other proposals to be presented at the special meetings. Inovio stockholders and all holders of VGX securities should read this joint proxy statement/prospectus carefully.

Q:    Why are Inovio and VGX proposing the transaction?

A:     Inovio and VGX believe that the proposed transaction will provide substantial benefits to both companies and their stockholders, including:

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        For details of the reasons for the transaction, see the sections entitled "Inovio's Reasons for the Transaction" and "VGX's Reasons for the Transaction" on pages 66 and 69, respectively.

Q:    What will happen in the transaction?

A:     Upon the terms and subject to the conditions of the Acquisition Agreement and in accordance with the Delaware General Corporation Law, or the "DGCL," Inovio, Submerger and VGX will enter into a business combination pursuant to which VGX will be merged with and into Submerger. Upon consummation of the Merger, VGX will cease to exist and Submerger will continue as the surviving entity and as a wholly-owned subsidiary of Inovio and change its name to VGX Pharmaceuticals, LLC, referenced sometimes as the "Surviving Entity."

        In consideration for the Merger, Inovio will issue and otherwise allocate for issuance under options and warrants to purchase common stock and debt convertible into common stock, a total of up to 60,689,523 shares of new Inovio common stock pursuant to the terms of the Acquisition Agreement.

        Following the completion of the Merger, holders of VGX common stock will become holders of Inovio common stock, and holders of options, warrants and debt exercisable or convertible for shares of VGX common stock will become holders of options, warrants and debt exercisable or convertible for shares of Inovio common stock, respectively.

Q:    What will VGX stockholders receive in the Merger?

A:     If the Merger is consummated, outstanding shares of VGX common stock will be cancelled and holders of VGX common stock will receive in exchange a number of shares of Inovio common stock calculated using an exchange ratio determined based on the ratio of the number of shares of Inovio common stock outstanding and issuable pursuant to outstanding exercisable or convertible securities as of the closing date, to the number of shares of VGX common stock outstanding and issuable pursuant to outstanding exercisable or convertible securities, as of such date, excluding VGX convertible debt, or the "Merger Exchange Ratio." Based on the respective fully-diluted share capitals of Inovio and VGX as of January 16, 2009 and certain forward election VGX option exercises anticipated prior to closing, we anticipate that the Merger Exchange Ratio will be approximately 0.9911488, meaning that each share of VGX common stock will be exchanged for 0.9911488 shares of Inovio common stock upon closing of the Merger. If you are a holder of VGX securities, see " Effect of Merger on VGX Securities" on page 100 for a detailed explanation of what you will receive upon completion of the Merger.

Q:    How will VGX's outstanding options, warrants and convertible debt be affected by the Merger?

A:     As a result of the Merger, Inovio will assume all outstanding options and warrants to purchase shares of VGX common stock and convert such securities into options and warrants, respectively, to purchase Inovio common stock, with the number of shares issuable and the exercise price of such securities adjusted based on the Merger Exchange Ratio. Inovio will also assume, on a consolidated basis, all outstanding debt of VGX convertible into shares of VGX common stock, which will become debt convertible into Inovio common stock, with a conversion price of $1.05 based on existing terms providing for such assumption and conversion. See " Effect of Merger on VGX Securities" on page 100 for a detailed explanation of the assumption and adjustment of the VGX options, warrants and convertible debt.

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Q:    Will I be able to freely trade the shares of Inovio common stock issued or issuable upon exercise or conversion of Inovio securities issued upon closing of the Merger?

A:     As Inovio has registered the shares of Inovio common stock to be issued upon closing of the Merger or subsequently issued upon exercise or conversion of the other securities assumed and converted at closing of the Merger, such shares should be freely tradable when issued, subject to the following restrictions:

        Inovio's shares of common stock are currently listed on the NYSE Alternext under the trading symbol "INO."

Q:    What are the material federal income tax consequences to holders of VGX common stock resulting from the Merger?

A:     Inovio and VGX each expect the Merger to qualify as a reorganization for U.S. federal income tax purposes. Accordingly, the parties expect that the Merger will be tax-free to holders of VGX common stock for U.S. federal income tax purposes.

        The tax consequences of the transaction are complex. VGX stockholders should consult with their own tax advisors as to the tax consequences to them of the Merger, as well as review the more detailed description of the tax consequences of the Merger in this joint proxy statement/prospectus entitled " Certain Material U.S. Federal Income Tax Consequences " beginning on page 96.

Q:    How will outstanding Inovio securities be affected by the Merger?

A:     The Merger will not affect the outstanding shares of Inovio common stock and Inovio's outstanding options and warrants to purchase shares of Inovio common stock, except:

        For more detailed information about the impact of the Merger on outstanding Inovio securities, see " Effect of Merger on Inovio Securities" on page 100 and " Resulting Ownership of Inovio; Change of Control" on page 73.

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Q:    Will there be changes to the Inovio board of directors if the Merger is consummated?

A:     The Acquisition Agreement provides that post-Merger Inovio's board of directors will consist of five individuals, comprised of three directors from Inovio's prior board of directors and two directors from VGX's prior board of directors. The parties anticipate that Dr. Avtar Dhillon, Dr. J. Joseph Kim, Mr. Simon Benito, Dr. Morton Collins and Mr. Chin-Cheong Chong will serve as directors of the post-Merger company. Dr. Avtar Dhillon, Inovio's current chief executive officer, will serve as chairman of the board of directors post-Merger. See " Directors and Management of Inovio Following the Transaction " on page 87 for biographies of the designated directors upon completion of the Merger.

Q:    Who will be the executive officers of Inovio if the Merger is consummated?

A:     The Acquisition Agreement also provides for an integrated management team, drawn from the senior management of Inovio and VGX, to lead the combined group upon completion of the Merger, including the following individuals:

Name
  Position in the Combined Company   Current Position

Dr. J. Joseph Kim

  Chief Executive Officer   President and Chief Executive Officer of VGX

Dr. Avtar Dhillon

 

President

 

President and Chief Executive Officer of Inovio

Peter Kies

 

Chief Financial Officer

 

Chief Financial Officer of Inovio

Dr. C. Jo White

 

Chief Medical Officer

 

Chief Medical Officer of VGX

Dr. Niranjan Sardesai

 

Senior Vice President, Research & Development

 

Senior Vice President, Research & Development of VGX

Kevin Rassas

 

Senior Vice President, Business Development

 

Senior Vice President, Business Development of VGX

Gene Kim

 

Vice President, Finance

 

Chief Financial Officer of VGX

Punit Dhillon

 

Vice President, Operations

 

Vice President, Finance & Operations of Inovio

Dr. Michael Fons

 

Vice President, Corporate Development

 

Vice President, Corporate Development of Inovio

Dr. Iacob Mathiesen

 

Vice President, Research & Development and Managing Director, Inovio AS

 

Managing Director, Inovio AS

Dr. Ruxandra Draghi-Akli

 

Vice President, Research

 

Vice President, Research of VGX

Q:    Does Inovio's board of directors recommend voting in favor of the Merger, including the issuance of Inovio securities to the holders of VGX securities pursuant to the terms of the Acquisition Agreement?

A:     Yes. After careful consideration, Inovio's board of directors determined that the transaction is fair to, and in the best interests of, Inovio and its stockholders. Inovio's board of directors recommends that Inovio stockholders vote FOR the Merger, including the issuance of Inovio securities pursuant to the Acquisition Agreement.

For a description of the factors considered by Inovio's board of directors in making its determination, Inovio stockholders should read the section entitled " Inovio's Reasons for the Transaction " on page 66.

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Q:    Does Inovio's board of directors recommend voting in favor of the proposed amendment and restatement of the Inovio 2000 Plan?

A:     Yes. Inovio's board of directors determined that an amendment and restatement of the Inovio 2000 Plan to clarify the acceleration of vesting of Inovio options issued and outstanding under the Inovio 2000 Plan at the Effective Time and to remove the termination of unexercised Inovio options issued and outstanding under the Inovio 2000 Plan at the Effective Time is vital to the success of the transaction. Inovio's board of directors recommends that Inovio stockholders vote FOR the proposed amendment and restatement of the Inovio 2000 Plan.

Q:    Does VGX's board of directors recommend voting in favor of the Merger and the Acquisition Agreement?

A:     Yes. After careful consideration, VGX's board of directors consider the terms of the Merger, including the Acquisition Agreement, to be fair and reasonable and to be in the best interests of VGX and its stockholders. VGX's board of directors unanimously recommends that VGX's stockholders vote FOR the Merger and the Acquisition Agreement.

For a description of the factors considered by VGX's board of directors in making its determination, see the section entitled "VGX's Reasons for the Transaction" on page 69.

Q:    When do you expect to complete the Merger?

A:     Inovio and VGX are working to complete the Merger as quickly as possible. Inovio and VGX hope to complete the Merger shortly after obtaining the requisite stockholder approvals at the Inovio special meeting and the VGX special meeting, and they believe the closing will occur within the first quarter of the 2009 fiscal year. However, Inovio and VGX cannot predict the exact timing of the completion of the Merger because the Merger is subject to several conditions. There may be a substantial period of time between the Inovio and VGX special meetings and the completion of the Merger, and Inovio and VGX may not complete the Merger within the first quarter of the 2009 fiscal year, if at all. For a detailed description of the conditions to the transaction, see the section entitled "Conditions to the Transaction" on page 113.

Q:    What do I need to do now?

A:     You should carefully read and consider the information contained in this joint proxy statement/prospectus, including the Annexes, and consider how the transaction will affect you as an Inovio stockholder or VGX stockholder. You also may want to review the documents referenced under the section entitled "Where You Can Find More Information About Inovio" on page 223.

If you are an Inovio or VGX stockholder, whether or not you intend to attend the Inovio or VGX special meeting, you should complete and return the enclosed proxy card as soon as possible in accordance with the instructions provided in this joint proxy statement/prospectus and on the enclosed proxy card.

Q:    When and where are the Inovio and VGX special meetings?

A:     The Inovio special meeting will be held on [                                    ], 2009 at [    ] p.m., Pacific Standard Time (local time), at Inovio's principal executive offices, located 11494 Sorrento Valley Road, San Diego, California 92121. See " Special Meeting of Inovio Stockholders " beginning on page 209 for more information about the Inovio special meeting and the proposals to be presented for the approval of the Inovio stockholders.

The VGX meeting will be held on [                                    ], 2009 at [      ] p.m., Eastern Standard Time (local time), at VGX's principal executive offices, located 450 Sentry Parkway, Blue Bell, Pennsylvania

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19422. See " Special Meeting of VGX Stockholders " beginning on page 219 for more information about the VGX special meeting and the proposals to be presented for the approval of the VGX stockholders.

Q:    Have any VGX stockholders committed to vote in favor of the Merger and the resulting change of control of VGX?

A:     Yes. Subsequent to the execution of the Acquisition Agreement and consistent with the terms thereof, four VGX stockholders, who hold approximately 41% of the issued and outstanding VGX common stock as of the date of this joint proxy statement/prospectus, have each executed voting agreements with Inovio in which such stockholders agreed to vote their shares of VGX common stock for the adoption of the Acquisition Agreement and consummation of the Merger. The form of voting agreement is provided as an exhibit to the Acquisition Agreement included with this joint proxy statement/prospectus as Annex A ; for further details of the vote required from the VGX stockholders and the voting agreement see "VGX Support Stockholders' Voting Agreement" beginning on page 117.

Q:    As a VGX stockholder, do I have appraisal or dissenter's rights?

A:     Under the DGCL, holders of VGX common stock who do not vote for the adoption of the Acquisition Agreement and the Merger have the right to seek appraisal and receive cash for the fair value of their shares as determined by the Delaware Court of Chancery if the Merger is completed, but only if they comply with all requirements of Delaware law, which are summarized in this joint proxy statement/prospectus. This appraisal amount could be more than, the same as, or less than the fair value of the Inovio common stock that a VGX stockholder would be entitled to receive under the terms of the Acquisition Agreement. Any holder of VGX common stock intending to exercise its appraisal rights, among other things, must submit a written demand for appraisal to VGX prior to the vote on the adoption of the Acquisition Agreement and must not vote or otherwise submit a proxy in favor of adoption of the Acquisition Agreement. Failure to follow exactly the procedures specified under Delaware law will result in the loss of appraisal rights. Because of the complexity of the Delaware law relating to appraisal rights, if you are considering exercising your appraisal right, we encourage you to seek the advice of your own legal counsel. For a full description of the appraisal rights, see " Appraisal Rights " beginning on page 81 of this joint proxy statement/prospectus.

Q:    As an Inovio stockholder, how do I vote?

A:     If you are an Inovio stockholder of record, you may vote in person at the Inovio special meeting or by submitting a proxy for the meeting. You can submit your proxy by completing, signing, dating and returning the enclosed proxy card in the accompanying pre-addressed postage paid envelope.

If you are an Inovio stockholder and you hold your shares in "street name," which means your shares are held of record by a broker, bank or nominee, you must provide the record holder of your shares with instructions on how to vote your shares with regard to the proposals described in this joint proxy statement/prospectus or obtain a proxy issued in your name from that record holder.

For a more complete description of voting shares of Inovio common stock, see " Special Meeting of Inovio Stockholders" on page 209.

Q:    As a VGX stockholder, how do I vote?

A:     If you are a VGX stockholder of record, you may vote in person at the VGX special meeting or by submitting a proxy for the meeting. You can submit your proxy by completing, signing, dating and returning the enclosed proxy card in the accompanying pre-addressed postage paid envelope.

For a more complete description of voting shares of VGX common stock, see " Special Meeting of VGX Stockholders" on page 219.

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Q:    As a VGX stockholder, should I send in my VGX share certificates now?

A:     No. If the Merger is completed, we will send the former stockholders of VGX written instructions for exchanging their share certificates. Additional information on the anticipated procedures for exchanging certificates representing shares of VGX common stock for shares of Inovio common stock is set forth in " Exchange of Securities " beginning on page 102.

Q:    As a holder of VGX options, warrants or convertible debt, what do I do?

A:     Holders of other VGX securities do not need to take any action at this time. If the Merger is completed, any exercise or conversion of such securities will be completed on their existing terms and conditions, as adjusted according to the Merger Exchange Ratio as applicable, for shares of Inovio common stock. You will not be sent a replacement form of option, warrant or note, unless requested subsequent to the consummation of the Merger.

Q:    Whom should I call with questions?

A:     If you have any questions about the transaction or if you need additional copies of this joint proxy statement/prospectus or the enclosed proxy card, you should contact:

Inovio Stockholders:   VGX Stockholders:
Inovio Biomedical Corporation   VGX Pharmaceuticals, Inc.
114994 Sorrento Valley Road   450 Sentry Parkway
San Diego, California 92121   Blue Bell, Pennsylvania 19422
(858) 597-6006   (267) 440-4200
Attention: Investor Relations   Attention: Investor Relations

You may also obtain additional information about Inovio from documents filed with the U.S. Securities and Exchange Commission, which we refer to as the "SEC," by following the instructions in the section entitled "Where You Can Find More Information About Inovio" on page 223.

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SUMMARY OF THE JOINT PROXY STATEMENT/PROSPECTUS

        This summary highlights selected information from this joint proxy statement/prospectus and does not contain all of the information that is important to you. To better understand the proposed transaction and the proposals on which your vote is being solicited, you should read this entire document carefully, including the annexes, and in particular, the Acquisition Agreement attached as Annex A. The page references provided parenthetically in this summary indicate where you can find a more complete description of the topics presented in this summary.

The Companies

        Inovio Biomedical Corporation, a Delaware corporation, organized in 2001, is a San Diego-based biomedical company focused on the development of next-generation vaccines to prevent or treat cancers and chronic infectious diseases. Inovio is a leader in developing DNA delivery solutions based on electroporation, which uses brief, controlled electrical pulses to create temporary pores in cell membranes and enable increased cellular uptake of a useful biopharmaceutical. Inovio has licensing and collaborative arrangements for use of its patented technologies with research-driven biopharmaceutical companies and government and non-government agencies. Inovio licenses the use of its electroporation-based DNA delivery systems, and contracts to manufacture and supply such systems, for partners to use in conjunction with their proprietary DNA vaccines or DNA-based immunotherapies. These arrangements provide Inovio with some combination of upfront payments, development fees, milestone payments, royalties and a supply agreement, while the partners pursue development of proprietary agents or conduct research using Inovio's electroporation technology. Inovio has also been pursuing proprietary vaccine development or co-development, resulting in whole or partial ownership in promising vaccines to prevent or treat cancers and chronic infectious diseases. Inovio's technology is protected by an extensive patent portfolio covering in vivo electroporation, encompassing a range of apparatuses, methodologies, conditions and applications including oncology, gene delivery, vascular, and transdermal as well as ex vivo electroporation.

        Inovio's common stock is currently traded on the NYSE Alternext under the trading symbol "INO."

        Inovio's website address is www.inovio.com ; however, information on Inovio's website is not a part of, or incorporated by reference in, this joint proxy statement/prospectus, and should not be relied upon in evaluating the proposals set forth for approval by the Inovio or VGX stockholders.

        Inovio Acquisition, LLC, or Submerger, is a wholly-owned direct subsidiary of Inovio that was originally incorporated in Delaware as Inovio Acquisition Corporation in June 2008 and converted into a limited liability company in October 2008. Submerger does not engage in any operations and exists solely to facilitate the Merger.

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        VGX Pharmaceuticals, Inc., a Delaware corporation organized in December 2000, is a biopharmaceutical company with DNA Vaccines and small molecule product candidates for the treatment of infectious diseases, cancer and inflammatory diseases. VGX's clinical development programs include programs focused on HIV infection, inflammatory diseases and a DNA-based therapeutic for cervical cancer. In addition, VGX has filed investigational new drug, or IND, applications with the U.S. Food and Drug Administration, or FDA, for a novel DNA therapy that utilizes growth hormone releasing hormone, or GHRH, for the treatment of cancer cachexia and anemia and a DNA preventative vaccine for avian influenza. VGX has established a vertically-integrated DNA vaccines and therapies platform, which includes a patented DNA delivery system (CELLECTRA® electroporation), and access to advanced cGMP plasmid manufacturing capabilities through its affiliate, VGX International. VGX is also a majority shareholder of VGX Animal Health, whose lead product candidate, LifeTide™ SW 5, received regulatory approval in Australia in January 2008 and became the world's first approved DNA therapy for food animals. VGX's product candidates and technology programs are protected by the VGX's extensive intellectual property portfolio.

        VGX's website address is www.vgxp.com ; however, information on VGX's website is not part of, or incorporated by reference in, this joint proxy statement/prospectus, and should not be relied upon in evaluating the proposals set forth for approval by Inovio or VGX stockholders.

The Combined Group

        Inovio and VGX both operate in the biotechnology industry, focused primarily on the development of DNA-based vaccines and therapies. The combined group intends to remain focused on this goal utilizing Inovio's proprietary electroporation technology to continue development of Inovio's pipeline of pre-clinical and clinical candidates and maintaining a substantial number of Inovio's ongoing collaborations and partnerships with pharmaceutical industry leaders and academic institutions, while adding existing VGX pre-clinical and clinical programs and VGX's ongoing collaborations with other pharmaceutical industry leaders and academic institutions. The combined group anticipates integrating and maintaining a balanced portfolio of programs drawn from Inovio's and VGX's current pre-clinical and clinical efforts that are most likely to benefit from and extend the strength of the combined group's intellectual property related to use of Inovio's electroporation technology for DNA delivery and VGX's DNA therapeutics platform. The combined group expects that its initial product pipeline will include DNA-based therapeutics for delivery via electroporation targeted to HIV, hepatitis C virus, human papilloma virus, and influenza. Management of the combined group will be primarily located in San Diego, California, with additional research and development facilities in Blue Bell, Pennsylvania, The Woodlands, Texas and Oslo, Norway.

Summary of the Transaction (see Page 62)

        Upon the terms and subject to the conditions of the Acquisition Agreement and in accordance with the DGCL, Inovio, Submerger and VGX will enter into a business combination pursuant to which VGX will be merged with and into Submerger. Upon consummation of the Merger, VGX will cease to exist and Submerger will continue as the surviving entity and as a wholly-owned subsidiary of Inovio and change its name to VGX Pharmaceuticals, LLC. Thus, Inovio will remain the parent, publicly reporting and listed entity, retain its current subsidiaries, and hold VGX Pharmaceuticals, LLC and the current VGX subsidiaries as its direct and indirect subsidiaries upon completion of the transaction.

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        In consideration for the Merger, based on an exchange ratio and on the terms and conditions described in this joint proxy statement/prospectus:

        As a result, Inovio will issue and otherwise allocate for issuance under options and warrants to purchase common stock and debt convertible into common stock, a total of up to 60,689,523 shares of new Inovio common stock pursuant to the terms of the Acquisition Agreement. Following the completion of the Merger, holders of VGX common stock will become holders of Inovio common stock, and holders of options, warrants and debt exercisable or convertible for shares of VGX common stock will become holders of options, warrants, and debt exercisable or convertible for shares of Inovio common stock, respectively. In addition, Inovio and VGX have agreed that any other contractual rights to receive shares of VGX common stock, other than the VGX options, warrants and convertible debt to be assumed and converted as described above, shall be converted into rights to receive shares of Inovio common stock in accordance with the terms and conditions of the contract(s) providing such rights.

        In order to complete the transaction, Inovio stockholders must vote to approve the Merger, including the issuance of shares of Inovio common stock and other securities in exchange for all of the outstanding securities of VGX, and the 2000 Plan Amendment, and VGX stockholders must vote to approve the Merger. Pursuant to the Acquisition Agreement, upon the closing date, three members of Inovio's current board of directors and two members of the VGX board of directors will be appointed to the Inovio board of directors, and the senior management team of the combined group will be composed of executives from both Inovio and VGX will take over management of the Surviving Entity. Further terms, conditions and results of the transaction are described in the sections entitled "The Transaction" on page 62 and "The Acquisition Agreement" on page 99.

Conditions to the Transaction (see Page 112)

        Inovio's obligation to consummate the Merger and issue its securities pursuant to the Acquisition Agreement, which we refer to as the "closing," will not take place until the parties satisfy, or waive where allowable, the conditions listed in the Acquisition Agreement. These closing conditions include, but are not limited to, the following:

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Termination of the Acquisition Agreement (see Page 115)

        The Acquisition Agreement may be terminated prior to the date the registration statement, of which this joint proxy statement/prospectus is a part, becomes effective, or the subsequent closing of the Merger, under several circumstances, including:

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        In the event that the Acquisition Agreement is terminated by either Inovio or VGX pursuant to the provisions related to recommendation of a competing superior offer, the terminating party shall pay the other party a fee equal to $3,500,000 in immediately available funds and such payment shall be the sole and exclusive remedy relating to such termination.

No Solicitation (see Page 110)

        The Acquisition Agreement contains detailed provisions prohibiting Inovio and VGX, as well as their respective officers, directors, employees, agents and representatives, from taking any action to solicit a competing acquisition proposal. Notwithstanding these restrictions, the Acquisition Agreement provides that under limited circumstances prior to the approval of the Acquisition Agreement by their respective stockholders, Inovio or VGX, upon receipt of an acquisition proposal from a third party, may furnish non-public information to that third party and/or enter into discussions or negotiations with that third party. We refer to an acquisition proposal from a third party which meets the specified criteria and is recognized as such by the relevant board of directors as a "superior offer." If either Inovio or VGX receives a superior offer, then the board of directors of the receiving party may change its recommendation relating to the transaction.

Vote of Stockholders Required (see Pages 214 and 222)

        In order to transact business at the Inovio special meeting, holders of a majority of the shares of Inovio common stock entitled to vote as of the record date for the Inovio special meeting must be present, either in person or by proxy. The approval of a business combination between Inovio and VGX, whereby Inovio will issue shares of common stock to outstanding stockholders of VGX in the Merger and upon exercise of assumed VGX options and warrants and upon conversion of VGX convertible debt assumed by Inovio on a consolidated basis, on the terms and conditions set forth in the joint proxy statement/prospectus, requires the approval of the holders of a majority of the shares of Inovio common stock entitled to vote and present at the Inovio special meeting, either in person or by proxy duly authorized. The approval of the proposed changes to the Inovio 2000 Plan requires approval of the holders of a majority of the shares of Inovio common stock entitled to vote and present at the Inovio special meeting, either in person or by proxy duly authorized. As of the close of business on the record date for the Inovio special meeting, [                ] 2009, Inovio directors, executive officers and affiliates beneficially owned and were entitled to vote [                ] shares of Inovio common stock, which represented [        ]% of the [                ] shares of Inovio common stock outstanding and entitled to vote on that date.

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        In order to transact business at the VGX special meeting, holders of the majority of the shares of VGX common stock entitled to vote as of the record date for the VGX special meeting must be present, either in person or by proxy. The approval of the business combination between Inovio and VGX, whereby Inovio will issue shares of common stock to outstanding stockholders of VGX in the Merger and upon exercise of assumed VGX options and warrants and upon conversion of VGX convertible debt assumed by Inovio on a consolidated basis, on the terms and conditions set forth in the joint proxy statement/prospectus, requires the approval of the holders of a majority of the outstanding shares of VGX common stock entitled to vote at the VGX special meeting.

        As of the close of business on the record date for the VGX special meeting, [                ] 2009, VGX directors, executive officers and affiliates beneficially owned and were entitled to vote [    ] shares of VGX common stock, which represented [    ]% of the [                ] shares of VGX common stock outstanding and entitled to vote on that date. Of such shares, shares representing        % of the shares of VGX common stock outstanding and entitled to vote are already committed to voting in favor of the Merger pursuant to certain voting agreements, as described in "Support Stockholders' Voting Agreements " beginning on page 117.

Appraisal and Dissenters Rights (see Page 81)

        If any VGX stockholder entitled to appraisal rights under DGCL with respect to the Merger has properly exercised and perfected such appraisal rights pursuant to and in accordance with Section 262 of the DGCL, and the Merger is consummated, such holder shall, to the extent allowed under applicable laws, be entitled to an appraisal by the Delaware Court of Chancery of the fair value of such shares of VGX common stock as provided in Section 262 of the DGCL, provided that such VGX stockholder acts in accordance with and meets all the requirements of Section 262 of the DGCL. Prior to the closing, Inovio, Submerger and VGX shall comply, and after the closing, Inovio and the Surviving Entity shall comply, with the information delivery and other requirements pursuant to Section 262 of the DGCL and applicable Delaware law. See Annex E for a copy of Section 262 of the DGCL.

        Notwithstanding any other provision in the Acquisition Agreement to the contrary, shares of VGX common stock that have not consented to or been voted for approval of, as applicable, the Merger and with respect to which such VGX stockholders become entitled to, and do properly exercise dissenters' rights in accordance with Section 262 of DGCL, or the "dissenting shares," will not be converted into or represent a right to receive consideration in connection with the Merger, but will instead be converted into the right to receive such consideration as may be determined to be due with respect to such dissenting shares pursuant to the DGCL. If a holder of dissenting shares, or a "dissenting stockholder," withdraws such dissenting stockholder's demand for such payment and appraisal or becomes ineligible for such payment and appraisal, then, as of the Effective Time or the occurrence of such event of withdrawal or ineligibility, whichever last occurs, such dissenting stockholder's dissenting shares will cease to be dissenting shares and will be converted into the right to receive, and will be exchangeable for the merger consideration. However, if the number of dissenting shares exceeds 10% of the number of shares of outstanding VGX common stock outstanding just prior to closing, a condition to consummation of the Merger will not be satisfied and the Merger will not close unless Inovio waives the condition.

Directors and Management of Inovio Following the Transaction (see Page 87)

        The Acquisition Agreement provides that Inovio's board of directors will take all actions necessary such that, on the closing date of the transaction, three directors who shall be acceptable to Inovio's board of directors shall be nominated and appointed to the Inovio board, including Dr. Avtar Dhillon, who shall serve as chairman of the board of the post-Merger board of directors. Further, the Acquisition Agreement provides that VGX's board of directors will take all actions necessary such that,

16



on the closing date of the transaction, two directors who shall be acceptable to VGX's board of directors shall be nominated and appointed to the Inovio board. The parties shall ensure that the composition of the Inovio board upon such appointments shall comply with the rules and regulations of the NYSE Alternext, or other applicable securities exchange or quotation system, and the SEC. Consistent with these requirements, the parties have identified and anticipate that Dr. Avtar Dhillon, Dr. J. Joseph Kim, Mr. Simon Benito, Mr. Chin-Cheong Chong and Dr. Morton Collins will serve on the post-Merger board of directors.

        The post-Merger management team of the combined group shall consist of the following persons as of closing:

Opinion of Inovio's Financial Advisor (see Page 74)

        In connection with the Merger, Inovio's board of directors received a written opinion, dated July 2, 2008, of Inovio's financial advisor, Oppenheimer & Co. Inc., referred to as Oppenheimer, as to the fairness, from a financial point of view and as of the date of the opinion, to Inovio of the Merger Exchange Ratio provided for in the original agreement and plan of merger (prior to its amendment). Oppenheimer's opinion, dated July 2, 2008, relates only to the Merger Exchange Ratio provided for in the original merger agreement and does not take into account any events or developments after the date of such opinion, including any modification to the proposed Merger or the Merger Exchange Ratio provided for in the Acquisition Agreement, dated as of December 5, 2008.

        The full text of Oppenheimer's written opinion, dated July 2, 2008, which describes the assumptions made, procedures followed, matters considered and limitations on the review undertaken, is attached to this joint proxy statement/prospectus as Annex B . Oppenheimer's opinion was provided to Inovio's board of directors in connection with its evaluation of the Merger Exchange Ratio from a financial point of view to Inovio and does not address any other aspect of the Merger. Oppenheimer's opinion does not address the underlying business decision of Inovio to effect the Merger, the relative merits of the Merger as compared to any alternative business strategies that might exist for Inovio or the effect of any other transaction in which Inovio might engage and does not constitute a recommendation to any stockholder as to how such stockholder should vote or act with respect to any matters relating to the Merger.

17


Interests of Directors, Officers and Affiliates (see Page 86)

        In considering the recommendation of Inovio's board of directors that Inovio stockholders vote in favor of the issuance of Inovio's securities in conjunction with the Merger and the resulting change of control of Inovio, Inovio stockholders should be aware that some Inovio executive officers and directors have interests in the transaction that may be different from, or in addition to, their interests as stockholders of Inovio. These interests include the execution of new employment agreements, to be effective upon closing of the Merger, between Inovio and its current executive officers, which provide for certain payments upon closing of the Merger and eligibility for future severance payments under certain terms and conditions.

        Inovio's board of directors was aware of these interests and considered them, among other matters, in making its recommendation to Inovio's stockholders that they approve the transaction and other related proposals. In addition, subsequent to such recommendation, Dr. Avtar Dhillon, Mr. Simon Benito and Mr. Chin-Cheong Chong were selected to continue service on the Inovio board as directors post-Merger, for which Mr. Benito and Mr. Chong will continue to receive customary director compensation, and Dr. Dhillon will also serve as chairman of the board of directors and president of Inovio post-Merger.

        In considering the recommendation of VGX's board of directors to VGX's stockholders that they approve the transaction, VGX stockholders should be aware that some officers and directors of VGX have interests in the transaction that are different from, or in addition to, the other VGX stockholders. These interests include:

        As of September 30, 2008, all current directors and executive officers of VGX as a group beneficially owned approximately 33.6% of the shares of VGX common stock. Under the terms of the Acquisition Agreement, at the effective time of the Merger, each outstanding and unexercised option to purchase shares of VGX common stock, whether vested or unvested, will be assumed by Inovio and will become an option to acquire, on the same terms and conditions as were applicable under the stock option agreement by which such option is evidenced and the stock option plan under which such option was issued, an option to purchase shares of Inovio common stock. VGX's current executive officers and directors, as of September 30, 2008, own vested and unvested options and warrants to purchase an aggregate of 8,181,800 shares VGX common stock.

        VGX's board of directors was aware of these interests and considered them, among other matters, in making its recommendation to VGX's stockholders that they approve the transaction. In addition, subsequent to such recommendation, Dr. J. Joseph Kim and Dr. Morton Collins were selected to serve as directors of Inovio post-Merger, for which Dr. Collins will receive customary director compensation.

Accounting Treatment of the Merger (see Page 84)

        The Merger will be accounted for using the purchase method of accounting for business combinations under United States generally accepted accounting principles, which is referred to as GAAP. Although the parties view the business combination of Inovio and VGX as a "merger of equals," Inovio has been determined to be the acquirer for purposes of generally accepted accounting principles, in accordance with the provisions of Statement of Financial Accounting Standards No. 141, Business Combinations (SFAS 141). Accordingly, the historical consolidated financial statements of Inovio will be carried forward at their historical cost, the assets and liabilities of VGX will be recorded at their fair value and the results of operations of VGX will be included in the consolidated financial statements from the date of the closing of the Merger. In evaluating the appropriate accounting

18



treatment under SFAS 141, the parties and their accountants considered all relevant facts and circumstances, including, without limitation, the relative operational size and revenue production of the legacy entities, the relative voting rights of the legacy holders in the combined group, the composition of the post-Merger company's board of directors and its committees, and the composition and relevant experience of senior management.

Certain Material U.S. Federal Income Tax Consequences of the Transaction (see Page 96)

        The Merger is intended to qualify as a "reorganization" under Section 368(a) of the Code. It is a condition to the completion of the Merger that each of Inovio and VGX receives a legal opinion from their respective tax counsel to the effect that the Merger will be treated as a "reorganization" under the Code. Accordingly, VGX stockholders will generally not recognize any gain or loss for U.S. federal income tax purposes of their exchange of their VGX common stock for Inovio common stock in the Merger. The companies themselves will not recognize gain or loss for U.S. federal income tax purposes as a result of the Merger.

         The U.S. federal income tax consequences described above may not apply to all holders of VGX common stock. Your tax consequences will depend on your individual situation. Accordingly, you should consult your own tax advisor concerning all federal, state, local, gift, and foreign tax consequences of the Merger that may apply to you.

Listing of Inovio Common Stock on the NYSE Alternext (see Page 85)

        Inovio has notified the NYSE Alternext of the Acquisition Agreement, the anticipated Merger and the other transactions contemplated by the Acquisition Agreement, and has submitted an additional listing application for the shares of Inovio common stock to be issued or to become issuable pursuant to assume securities in the Merger. In the Acquisition Agreement, Inovio agrees to use all commercially reasonable efforts to cause the shares of Inovio common stock issuable in connection with the Acquisition Agreement to be approved for listing on the NYSE Alternext, or if applicable under certain circumstances described in the Acquisition Agreement, to be approved for listing or quotation on another securities exchange or quotation system.

Risk Factors (see Page 28)

        There are material risks to the transaction and to the parties' separate and proposed combined businesses, which may impact the parties' ability to complete the transaction and its results if consummated, the business prospects of the parties to the transaction and the anticipated operations and financial condition of the proposed combined group. In evaluating the Acquisition Agreement, the principal terms of the transaction or the issuance of Inovio securities in the transaction, you should carefully read this joint proxy statement/prospectus and especially consider the factors discussed in the section entitled "Risk Factors" beginning on page 28 as well as the risk factors listed in the annual report on Form 10-K of Inovio for the year ended December 31, 2007, and the quarterly report on Form 10-Q of Inovio for the quarter ended September 30, 2008.

Comparative Market Price and Dividend Information (see Page 25)

        Inovio common stock is currently listed on the NYSE Alternext, the successor to the American Stock Exchange, under the trading symbol "INO." On July 7, 2008, the last full trading day prior to the initial public announcement of the transaction, Inovio common stock closed at $1.08 per share on the American Stock Exchange. On December 5, 2008, the last full trading day prior to the public announcement of the Acquisition Agreement, Inovio common stock closed at $0.39 per share on the NYSE Alternext. On                         , 2009, the most recent practicable date prior to mailing of this joint proxy statement/prospectus, Inovio common stock closed at $         per share on the NYSE Alternext.

        Shares of VGX common stock are not currently listed on an exchange.

19



SELECTED SUMMARY HISTORICAL AND PRO FORMA COMBINED FINANCIAL DATA

        The following tables present summary historical financial data, comparative per share historical and pro forma data as well as market price and dividend data of Inovio and VGX.

Financial Information

        The extracts from the financial statements of, and other information about, Inovio and VGX appearing in this joint proxy statement/prospectus are presented in U.S. dollars ($) and have been prepared in accordance with U.S. GAAP.

Selected Summary Historical Financial Data of Inovio

        The following table sets forth selected summary historical financial data of Inovio. The information presented below was derived from Inovio's audited annual consolidated financial statements as of December 31, 2007, for the five years ended December 31, 2007, and from Inovio's unaudited consolidated financial statements for the nine months ended September 30, 2008 and 2007 which, in the opinion of Inovio's management, include all adjustments, consisting of normal recurring adjustments, necessary for a fair statement of the results of the unaudited interim periods. This information is only a summary. This information should be read together with Inovio's historical financial statements and accompanying notes and Inovio's " Management's Discussion and Analysis of Financial Condition and Results of Operations " included elsewhere into this joint proxy statement/prospectus. Historical results are not necessarily indicative of future results.

20


Consolidated Statement of Operations Data:

 
  Nine Months Ended    
   
   
   
   
 
 
  Years Ended December 31,  
 
  September 30, 2008   September 30, 2007  
 
  2007   2006   2005   2004   2003  

Revenue:

                                           

License fee and milestone payments

  $ 611,578   $ 580,624   $ 2,793,478   $ 1,337,105   $ 2,563,283   $ 214,351   $ 5,882  

Revenue under collaborative research and development arrangements

    1,159,207     800,272     1,854,303     962,207     1,492,145     945,591     74,647  

Grants and miscellaneous revenue

        105,094     159,948     1,168,866     1,411,825     7,157      
                               

Total revenue

    1,770,785     1,485,990     4,807,729     3,468,178     5,467,253     1,167,099     80,529  
                               

Operating Expenses:

                                           

Research and development

    4,551,039     7,759,625     9,625,947     8,509,785     11,454,773     6,548,599     2,146,909  

General and administrative

    7,416,613     7,813,435     11,080,202     8,304,587     6,187,450     6,129,195     4,566,882  

Charge for acquired in-process research and development

                    3,332,000          
                               

Total operating expenses

   
11,967,652
   
15,573,060
   
20,706,149
   
16,814,372
   
20,974,223
   
12,677,794
   
6,713,791
 
                               

Loss from operations

   
(10,196,867

)
 
(14,087,070

)
 
(15,898,420

)
 
(13,346,194

)
 
(15,506,970

)
 
(11,510,695

)
 
(6,633,262

)
                               

Interest income (expense)

    587,128     914,883     1,272,397     681,546     207,675     247,555     45,017  

Other income (expense)

    219,850     2,993,674     3,421,580     320,706     2,443          
                               

Loss from continuing operations

    (9,389,889 )   (10,178,513 )   (11,204,443 )   (12,343,942 )   (15,296,852 )   (11,263,140 )   (6,588,245 )

Discontinued operations:

                                           

Gain on disposal of assets

                        290,209     2,034,078  

Loss from discontinued operations

                            (110,740 )
                               

Net loss

   
(9,389,889

)
 
(10,178,513

)
 
(11,204,443

)
 
(12,343,942

)
 
(15,296,852

)
 
(10,972,931

)
 
(4,664,907

)

Imputed and declared dividends on common stock

                    (8,329,112 )        

Imputed and declared dividends on preferred stock

        (23,335 )   (23,335 )   (2,005,664 )   (2,736,658 )   (732,405 )   (18,210,530 )
                               

Net loss attributable to common stockholders

  $ (9,389,889 ) $ (10,201,848 ) $ (11,227,778 ) $ (14,349,606 ) $ (26,362,622 ) $ (11,705,336 ) $ (22,875,437 )
                               

Amounts per common share—basic and diluted:

                                           

Loss from continuing operations

  $ (0.21 ) $ (0.25 ) $ (0.27 ) $ (0.40 ) $ (0.81 ) $ (0.64 ) $ (0.49 )

Income (loss) from discontinued operations, net

                        0.02     0.14  

Net loss

 
$

(0.21

)

$

(0.25

)

$

(0.27

)

$

(0.40

)

$

(0.81

)

$

(0.62

)

$

(0.35

)

Imputed and declared dividends on common stock

                    (0.44 )        

Imputed and declared dividends on preferred stock

                (0.06 )   (0.14 )   (0.04 )   (1.37 )
                               

Net loss attributable to common stockholders

  $ (0.21 ) $ (0.25 ) $ (0.27 ) $ (0.46 ) $ (1.39 ) $ (0.66 ) $ (1.72 )
                               

Weighted average number of common shares—basic and diluted

    43,881,047     40,711,751     41,493,412     31,511,683     19,009,189     17,623,559     13,316,624  
                               

21


Consolidated Balance Sheet Data:

 

 
  September 30,   December, 31  
 
  2008   2007   2007   2006   2005   2004   2003  

Working capital

  $ 3,444,588   $ 25,725,320   $ 25,649,652   $ 17,612,217   $ 14,185,032   $ 13,036,685   $ 12,593,153  

Cash and cash equivalents

    6,411,494     7,086,719     10,250,929     8,321,606     17,166,567     17,889,797     13,460,446  

Short-term investments

        21,362,700     16,999,600     14,700,000              

Total assets

    30,481,479     40,865,250     39,775,021     35,949,615     28,978,954     20,951,502     16,228,990  

Long-term investments

    12,057,775                          

Short-term liabilities

    4,455,245     3,895,659     3,354,499     6,859,722     4,002,280     5,401,992     1,158,819  

Accumulated deficit

    (149,237,215 )   (138,821,396 )   (139,847,326 )   (128,619,548 )   (114,269,942 )   (87,907,320 )   (76,201,984 )

Total stockholders' equity

    21,001,924     31,741,564     31,034,754     18,151,864     23,470,748     15,549,510     15,047,635  

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Selected Summary Historical Financial Data of VGX

        The following table sets forth selected summary historical financial data of VGX. The information presented below was derived from VGX's audited annual consolidated financial statements as of December 31, 2007, for the five years ended December 31, 2007, and from VGX's unaudited consolidated financial statements for the nine months ended September 30, 2008 and 2007 which, in the opinion of VGX's management, include all adjustments, consisting of normal recurring adjustments, necessary for a fair statement of the results of the unaudited interim periods. This information is only a summary. This information should be read together with VGX's historical financial statements and accompanying notes and VGX's " Management's Discussion and Analysis of Financial Condition and Results of Operations " included elsewhere into this joint proxy statement/prospectus. Historical results are not necessarily indicative of future results.

Consolidated Statement of Operations Data:
  Nine Months Ended   Years Ended December 31,  
 
  September 30,
2008
  September 30,
2007
  2007   2006   2005   2004   2003  

Revenue:

                                           

Revenue from Product Sales

  $ 40,000   $   $   $   $   $   $  

Government Contract Revenue

    1,962,305                          

Government Grant Revenue

    86,120     668,955     668,955     337,178     381,872     111,643     241,760  

License Fee Revenue

    100,000                         75,000  

Other Operating Revenue, net

    27,625     25,562     36,448                  
                               

Total revenue

    2,216,050     694,517     705,403     337,178     381,872     111,643     316,760  
                               

Operating Expenses:
                                           

Cost of Product Sales

    112,153                          

Research and development

    10,026,912     8,225,442     10,936,149     9,007,334     3,412,430     1,631,523     275,787  

General and administrative

    6,356,794     3,976,436     4,999,391     8,679,153     7,878,765     2,291,785     775,470  
                               

Total operating expenses

    16,495,859     12,201,878     15,935,540     17,686,487     11,291,195     3,923,308     1,051,257  
                               

Loss from operations

    (14,279,809 )   (11,507,361 )   (15,230,137 )   (17,349,309 )   (10,909,323 )   (3,811,665 )   (734,497 )
                               

Losses from Equity Investment

    (817,935 )   (562,638 )   (990,338 )   (700,451 )   (325,080 )        

Interest income (expense)

    (82,620 )   (136,484 )   (209,438 )   (110,934 )   (100,746 )   3,416     (14,048 )

Other Income

    97,497                          

Minority Interest

    253,662     5,853     43,503                  
                               

Loss from continuing operations

    (14,829,205 )   (12,200,630 )   (16,386,410 )   (18,160,694 )   (11,335,149 )   (3,808,249 )   (748,545 )

Discontinued operations:

                                           

Gain on Sale of Manufacturing Assets

    6,653,153                          

Loss from Manufacturing Operations

    (1,586,636 )   (1,044,779 )   (1,409,631 )                
                               

Total Gain/(Loss) from Discontinued Operations

    5,066,517     (1,044,779 )   (1,409,631 )                
                               

Net loss

  $ (9,762,688 ) $ (13,245,409 ) $ (17,796,041 ) $ (18,160,694 ) $ (11,335,149 ) $ (3,808,249 )) $ (748,545 )

Amounts per common share—basic and diluted:

                                           

Loss from continuing operations

  $ (0.34 ) $ (0.28 ) $ (0.37 ) $ (0.45 ) $ (0.34 ) $ (0.14 ) $ (0.04 )

Income (loss) from discontinued operations

    0.12     (0.02 )   (.03 )                
                               

Net loss

  $ (0.22 ) $ (0.30 ) $ (0.40 ) $ $(0.45 ) $ (0.34 ) $ (0.14 ) $ (0.04 )
                               

Weighted average number of common shares—basic and diluted

    43,959,706     43,641,329     43,915,950     40,535,848     33,795,625     26,314,113     21,170,454  
                               

23


Consolidated Balance Sheet Data:
  September 30,   December, 31  
 
  2008   2007   2007   2006   2005   2004   2003  
 
  (unaudited)
  (unaudited)
   
   
   
   
   
 

Current Assets—Continuing Operations

  $ 13,400,856   $ 22,216,002   $ 17,160,919   $ 21,948,415   $ 4,763,882   $ 1,505,395   $ 239,717  

Noncurrent assets—Continuing Operations

    7,236,197     13,755,105     13,121,067     9,108,878     5,751,481     9,517     4,867  

Assets—Discontinued Operations

        3,711,874     3,840,104                  

Current Liabilities—Continuing Operations

    10,723,907     13,628,019     13,728,362     12,444,467     1,944,959     776,934     330,425  

Noncurrent Liabilities—Continuing Operations

    100,000     4,300,000     2,940,000     4,000,000     5,000,000          

Liabilities—Discontinued Operations

        4,229,421     4,051,013                  

Minority Interest

    702,835     994,147     956,497                  

Accumulated deficit

    (63,048,018 )   (48,734,698 )   (53,285,330 )   (35,489,289 )   (17,328,595 )   (5,993,446 )   (2,185,197 )

Total stockholders' equity

    9,110,311     16,531,394     12,446,218     14,612,826     3,570,404     737,978     (85,840 )

        On June 10, 2008, VGX entered into an asset purchase agreement with VGXI, Inc., a wholly-owned subsidiary of VGX International, a publicly traded company in Korea of which VGX owns 30.37% of the outstanding shares. Under the agreement, VGX divested its assets related to the DNA plasmid manufacturing business; a business which it had acquired in February of 2007 under an asset purchase agreement with ADViSYS. The aggregate sale price was cash of $9,110,000 which is to be paid in installments. As a result, VGX recorded a one-time gain on the sale of manufacturing assets, net of tax, of $6,653,153, net of a $2,901,856 adjustment for VGX's 30.37% stake in VGX International. Consequently, the financial statements presented herein report the operating results of VGX's discontinued operations separately as a single line item. Likewise, the balance sheet has been recast to reflect the assets and liabilities related to the discontinued operations as a separate line item.

Selected Comparison of Historical and Pro Forma Per Share

        The following table sets forth selected historical per share information of Inovio and VGX and unaudited pro forma per share information after giving effect to the Merger between Inovio and VGX, assuming that 0.9911488 shares of Inovio common stock are issued in exchange for each outstanding share of VGX common stock. You should read this information in conjunction with the selected historical financial information, the unaudited pro forma condensed combined financial statements and the separate historical financial statements of Inovio and VGX and the notes thereto included elsewhere in this joint proxy statement/prospectus. The historical per share information is derived from unaudited consolidated financial statements of Inovio and VGX as of and for the nine months ended September 30, 2008 and the audited consolidated financial statements of Inovio and VGX as of the year ended December 31, 2007. The unaudited pro forma condensed combined financial statements are not necessarily indicative of the operating results or financial position that would have been achieved had the Merger been consummated at the beginning of the period presented and should not be construed as representative of future operations.

 
  Year Ended
December 31, 2007
 
  Inovio   VGX    
 
  Historical   Historical   Pro Forma

Basic and diluted net loss attributable to common stockholders per common share

  $ (0.27 ) $ (0.40)   $ (0.36)
             

Weighted average number of common shares—basic and diluted

    41,493,412     43,915,950     84,102,854
             

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  Nine Months Ended
September 30, 2008
 
  Inovio   VGX    
 
  Historical   Historical   Pro Forma

Basic and diluted net loss attributable to common stockholders per common share

  $ (0.21 ) $ (0.22)   $ (0.23)
             

Weighted average number of common shares—basic and diluted

    43,881,047     43,959,706     86,527,989
             


COMPARATIVE STOCK PRICE AND DIVIDEND INFORMATION

        Inovio's common stock is currently listed, and principally traded, on the NYSE Alternext under the symbol "INO." The following table sets forth the quarterly high and low per share closing prices of Inovio's common stock for the three years ending December 31, 2008.

 
  US$  
 
  High   Low  

Year ended December 31, 2008
             

Quarter ended December 31, 2008

    0.80     0.16  

Quarter ended September 30, 2008

    1.13     0.60  

Quarter ended June 30, 2008

    1.30     0.78  

Quarter ended March 31, 2008

    1.45     0.83  

Year ended December 31, 2007
             

Quarter ended December 31, 2007

    1.51     0.85  

Quarter ended September 30, 2007

    2.94     1.16  

Quarter ended June 30, 2007

    4.17     2.20  

Quarter ended March 31, 2007

    3.46     2.82  

Year ended December 31, 2006
             

Quarter ended December 31, 2006

    3.59     2.62  

Quarter ended September 30, 2006

    2.58     2.01  

Quarter ended June 30, 2006

    2.67     2.00  

Quarter ended March 31, 2006

    3.15     2.28  

        On July 7, 2008, the last full trading day prior to the initial public announcement date of the Merger, and on [            ], 2009, the most recent practicable date prior to the mailing of this joint proxy statement/prospectus, the last reported sales prices of Inovio's common stock as reported by the American Stock Exchange and NYSE Alternext, respectively, were $1.08 and $[            ], respectively. You are encouraged to obtain current trading prices for Inovio's common stock in considering whether to vote to approve the Merger or engage in any other transaction involving Inovio's securities. As of the record date for the Inovio special meeting, there were approximately [            ] holders of record of Inovio's common stock.

        No public market exists for VGX's common stock. As of the record date for the VGX special meeting, there were approximately [      ] holders of record of VGX's common stock

        Neither Inovio nor VGX have historically paid dividends on its common stock and neither has any intention to do so in the foreseeable future, whether as separate entities or as a combined group if the Merger is consummated.

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CAUTIONARY NOTE REGARDING FORWARD LOOKING STATEMENTS

        This joint proxy statement/prospectus and the documents that are incorporated into this joint proxy statement/prospectus by reference contain or incorporate by reference forward-looking statements, as defined by the Private Securities Litigation Reform Act of 1995, which are not purely historical. Forward-looking statements include, without limitation, statements regarding Inovio's, VGX's, the combined group's and the parties' management's expectations, hopes, beliefs, intentions or strategies regarding the future, including Inovio's and VGX's financial condition, results of operations, and the expected impact of the proposed transaction on the parties' financial performance, individually and as a combined group. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. The words "anticipate," "believe," "continue," "could," "estimate," "expect," "intend," "may," "might," "plan," "possible," "potential," "predict," "project," "seek," "shall," "should," "would," "will be," "will continue," "will result" and similar expressions or the negatives of such terms may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. Forward-looking statements include information concerning possible or assumed future results of the combined group's operations, including statements about the following subjects:

        These forward-looking statements are based on current expectations and beliefs concerning future developments and the potential effects on the parties and the transaction. There can be no assurance that future developments actually affecting Inovio, VGX and the proposed combined group will be those anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond the parties' control) or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. In addition to the risk factors described in this joint proxy statement/prospectus under the heading " Risk Factors ," beginning on page 28, as well as the risk factors described in the other documents Inovio files with the SEC and incorporate by reference in this joint proxy statement/prospectus, those factors include:

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        Should one or more of these risks or uncertainties materialize, or should any of the parties' assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Inovio and VGX undertake no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as may be required under applicable securities laws.

        The risks included in this joint proxy statement/prospectus are not exhaustive. Other sections of this joint proxy statement/prospectus may include additional factors that could adversely impact the parties' businesses and financial performance. Moreover, new risk factors emerge from time to time and neither Inovio nor VGX can predict all such risk factors, nor can either company assess the impact of all such risk factors on its current business or the combined group's anticipated business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forward looking statements. Given these risks and uncertainties, you should not place undue reliance on forward-looking statements as a prediction of actual results. You should also be aware that while Inovio does, and the combined group will, from time to time, communicate with securities analysts, Inovio does not, and the combined group does not, intend to disclose any material non-public information or other confidential commercial information to them. Accordingly, you should not assume that Inovio, VGX or the resulting combined group agrees with any statement or report issued by any analyst, regardless of the content of the analyst's report. Thus, to the extent that reports issued by securities analysts contain any projections, forecasts or opinions, such reports are not Inovio's, VGX's or the combined group's responsibility.

        All forward-looking statements attributable to Inovio or VGX or any person acting on their behalf are expressly qualified in their entirety by the cautionary statements contained or referred to in this section.

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RISK FACTORS

         Inovio stockholders should carefully consider the following factors in evaluating whether to approve the proposals to be voted on at the Inovio special meeting. VGX stockholders should carefully consider the following factors in evaluating whether to approve the proposals to be voted on at the VGX special meeting. Holders of VGX options, warrants and convertible debt should carefully consider the following factors in evaluating whether to exercise or convert such securities for Inovio common stock post-Merger. These factors should be considered in conjunction with the other information included in or incorporated by referenced into this proxy statement/ prospectus, including the risks discussed in Inovio's Form 10-K for the year ended December 31, 2007 and Inovio's Form 10-Q for the nine months ended September 30, 2008.

Risks Relating to the Transaction

The issuance of Inovio securities to VGX stockholders in the transaction will substantially reduce the percentage interests of Inovio stockholders.

        If the transaction is completed, Inovio will issue, or otherwise allocate for issuance under options, warrants and convertible debt to acquire Inovio common stock, a total of up to 60,689,523 shares of Inovio common stock pursuant to the terms of the Acquisition Agreement. The issuance and allocation of this substantial number of new shares of Inovio common stock, will cause a significant reduction in the relative percentage interests of current Inovio stockholders. Following the completion of the transaction and upon issuance of the new shares, subject to the approval of the Acquisition Agreement, Merger and the other transactions contemplated thereby, current VGX stockholders will own approximately 49.06% of Inovio's outstanding capital stock, and current Inovio stockholders will own approximately 50.94% of Inovio's outstanding capital stock. If the Merger is completed on the terms described in this joint proxy statement/prospectus, former holders of VGX securities will own approximately 51.82% of Inovio's share capital on a fully-diluted basis and current holders of Inovio securities will own approximately 48.18% of Inovio's common stock on a fully diluted basis.

The percentage ownership of Inovio's fully-diluted share capital post-Merger is not necessarily reflective of the anticipated voting power of the legacy Inovio and VGX stockholders post-Merger.

        The Acquisition Agreement anticipates the calculation of the Merger Exchange Ratio such that the legacy holders of Inovio's securities and VGX's securities will respectively hold 50 percent of the fully diluted share capital upon closing of the Merger, excluding the VGX convertible debt assumed in the Merger. Taking into account potential conversion of the assumed VGX convertible debt, the anticipated split in potential voting power between the legacy holders of the securities of Inovio and those of VGX, on a fully-diluted basis, would be 48.18% to 51.82%. However, under the terms of a voting trust agreement to be signed and become effective concurrent with the closing of the Merger, five significant stockholders of VGX will place 8,000,000 shares into a trust to be administered by an independent committee of the board of directors of Inovio post-Merger. The trustees would vote the shares in accordance with the percentage of votes cast by all stockholders on any particular matter. The trust will have a term of ten years and would terminate upon a change in control of the combined group. The effect of the voting trust reduces the voting power of the legacy holders of VGX securities on a fully-diluted basis to 44.92%, with the legacy holders of the Inovio's securities holding 48.18% voting power on a fully-diluted basis for the duration of the voting trust; the effect of the voting trust reduces the voting power of the legacy holders of VGX common stock to 39.83% and maintains the legacy holders of Inovio common stock at 50.94% based on the anticipated shares of Inovio common stock outstanding upon closing. The remaining voting power held in trust will reflect the pro rata vote of the stockholders overall. Thus, in the initial post-Merger period Inovio's legacy investors may control stockholder actions, presuming participation by all eligible common stockholders, until shares are transferred out of the voting trust pursuant to its terms or the voting trust is otherwise terminated.

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The Merger Exchange Ratio is not based on stock price or book value and the terms of the Merger will not be adjusted to reflect any increase or decrease in Inovio's stock price or either company's book value prior to the Effective Time.

        As noted above, the Acquisition Agreement anticipates the calculation of the Merger Exchange Ratio such that the legacy holders of Inovio's securities and VGX's securities will respectively hold 50 percent of the fully-diluted share capital of Inovio upon closing of the Merger, excluding any of the VGX convertible debt assumed in the Merger, an approach meant to reflect the parties' shared view of their integration as a "merger of equals." Although the Acquisition Agreement limits both parties' ability to issue additional securities in the interim period prior to closing, thereby limiting the amount of fluctuation possible in the Merger Exchange Ratio, the Acquisition Agreement does not provide for any value-based adjustment. Thus, any changes, whether an increase or decrease, in the perceived or actual value of Inovio or VGX will not be reflected in the Merger Exchange Ratio or in the final consideration received by the holders of VGX securities upon closing of the Merger.

Sales of substantial amounts of Inovio shares, or even the availability of Inovio shares for sale, in the open market could cause the market price of Inovio shares to decline.

        Under Inovio's "shelf registration statement" that the SEC declared effective on May 25, 2006, Inovio registered an aggregate of $75.0 million of Inovio's equity securities that it may issue from time to time, in one or more offerings at prices and on terms that it determines at the time of each offering. Under that registration statement, Inovio has registered multiple kinds of its equity securities, including common stock, preferred stock, warrants and a combination of these securities, or units.

        Through September 30, 2008, Inovio has "taken-down" from the shelf registration statement, and issued and sold, an aggregate of 9,035,378 shares of Inovio common stock valued at $26.9 million upon issuance and warrants to purchase up to 1,575,919 shares of Inovio common stock valued at $3.9 million upon issuance and, if those warrants are fully exercised, Inovio will have issued an additional 1,575,919 shares of Inovio common stock under that shelf registration statement. In other words, the shares of common stock sold in offerings from the shelf registration statement as of the date of this joint proxy statement/prospectus represent approximately 36% of the value of the aggregate equity securities from the shelf registration statement (41% if the warrants sold from the shelf registration statement are fully exercised). While that amount is only approximately 24% of Inovio's outstanding shares of common stock as of September 30, 2008, future issuances and sales of common stock or securities exercisable for or convertible into Inovio's common stock pursuant to the existing shelf registration statement, if in substantial numbers, and even the availability for issuance of the securities registered under the shelf registration statement, could adversely affect the market price of Inovio shares.

        In addition to the shares and warrants Inovio has issued under the shelf registration statement, during 2007 it also issued 2,201,644 shares of Inovio common stock and warrants to purchase up to 938,475 shares of Inovio common stock in other recent offerings, as well as other restricted shares pursuant to consulting arrangements and other registered securities pursuant to its stock incentive plan in 2007 and 2008. Further, effective February 15, 2008, the SEC revised Rule 144, which provides a safe harbor for the resale of restricted securities, shortening applicable holding periods and easing other restrictions and requirements for resales by Inovio's non-affiliates, thereby enabling an increased number of Inovio's outstanding restricted securities to be resold sooner in the public market.

        Further, in conjunction with the Merger, if completed, Inovio will issue a significant number of registered shares that will be freely tradable for non-affiliates of VGX or the combined group, limited only by the lock-up arrangements applicable to certain insiders and affiliates of VGX. Thus, approximately 32.99% of the shares issued or issuable in conjunction with the Merger, representing

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approximately 17.09% of Inovio's post-Merger share capital on a fully-diluted basis, will be freely tradable immediately post-closing.

        Sales of substantial amounts of shares of Inovio common stock at any one time or from time to time by the investors to whom Inovio has issued such shares, or even the availability of these shares for sale, could cause the market price of Inovio's common stock to decline. The significant amount of shares of Inovio common stock available for immediate sale pursuant to registration or Rule 144 could also serve to artificially limit the ability of Inovio's market price to increase in response to growth and improved financial condition of the combined group, if any.

Failure to complete the Merger could negatively impact the stock prices and the future business and financial results of Inovio and VGX because of, among other things, the disruption that would occur as a result of uncertainties relating to a failure to complete the Merger.

        The stockholders of Inovio and VGX may not approve the Merger. If the Merger is not completed for any reason, Inovio and VGX could be subject to several risks, including the following:

        In addition, Inovio and VGX would not realize any of the potential benefits of having completed the Merger.

        If the Merger is not completed, the price of Inovio common stock may decline to the extent that the current market price of that stock reflects a market assumption that the Merger will be completed and that the related benefits and synergies will be realized, or as a result of the market's perceptions that the Merger was not consummated due to an adverse change in Inovio's or VGX's business. In addition, each company's business may be harmed, to the extent that customers, suppliers and others believe that such company cannot compete in the marketplace as effectively without the Merger or otherwise remain uncertain about each company's future prospects in the absence of the Merger. Similarly, current and prospective employees of Inovio or VGX may experience uncertainty about their future roles with the combined group and choose to pursue other opportunities, which could adversely affect Inovio or VGX, as applicable, if the Merger is not completed. The realization of any of these risks may materially adversely affect the business, financial results, financial condition and stock price of each company.

Inovio and VGX will incur substantial costs whether or not the transaction is completed, and even if consummated, the costs associated with the transaction, being difficult to estimate, may be higher than expected and may harm the financial results of the post-Merger company.

        Inovio and VGX will incur substantial costs related to the transaction whether or not the transaction is completed. These costs include fees for attorneys, accountants and financial advisors, filing fees and financial printing costs. Inovio and VGX estimate that they will incur, in aggregate, direct transaction costs of approximately $3.3 million associated with the transaction prior to closing (approximately $1.8 million by Inovio and $1.5 million by VGX), and additional costs associated with the consolidation and integration of operations, which cannot be estimated accurately at this time. If

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the total costs of the transaction exceed the parties' estimates or the benefits of the Merger do not exceed the total costs of the Merger, the financial results of the combined company could be adversely affected. Unless the Acquisition Agreement is terminated under specific circumstances discussed below, the parties' will not recoup any of these costs if the Merger does not close, and will have diverted funds from other operational purposes, potentially to the detriment of each company's financial condition and ability to maintain or grow its respective operations.

        In addition, if the Acquisition Agreement is terminated by Inovio upon written notice to VGX setting forth (i) the Inovio board of directors' determination that an Inovio Acquisition Proposal (as defined in the Acquisition Agreement) constitutes an Inovio superior offer (as defined in the Acquisition Agreement), (ii) the Inovio board of directors' determination to withdraw its recommendation in favor of the adoption and approval of the Acquisition Agreement or the approval of the Merger in favor of recommending the Inovio superior offer to the Inovio stockholders, and (iii) Inovio's full and complete compliance with the terms of certain provisions in the Acquisition Agreement prior to such termination, Inovio will be required to pay VGX a termination fee equal to $3.5 million. On the other hand, if the Acquisition Agreement is terminated by VGX upon written to Inovio setting forth (i) the VGX board of directors' determination that a VGX Acquisition Proposal (as defined in the Acquisition Agreement) constitutes a VGX superior offer (as defined in the Acquisition Agreement), (ii) the VGX board of directors' determination to withdraw its recommendation in favor of the adoption and approval of the Acquisition Agreement or the approval of the Merger in favor of recommending the VGX superior offer to the VGX stockholders, and (iii) VGX's full and complete compliance with the terms of certain provisions in the Acquisition Agreement prior to such termination, VGX will be required to pay Inovio a termination fee equal to $3.5 million. See " The Acquisition Agreement—No Solicitation " beginning on page 110 of this joint proxy statement/prospectus, " The Acquisition Agreement—Termination of the Acquisition Agreement " beginning on page 115 of this joint proxy statement/prospectus, and " The Acquisition Agreement—Termination Payment " beginning on page 116 of this joint proxy statement/prospectus.

The Acquisition Agreement limits Inovio's and VGX's ability to pursue alternatives to the Merger.

        The Acquisition Agreement contains provisions that make it more difficult for Inovio and VGX to pursue alternative business combination transactions with a third party. These provisions include the general prohibition on both Inovio and VGX from soliciting any acquisition proposal or offer for a competing transaction except under limited circumstances and the requirement that the terminating party pay a termination fee of $3.5 million if the Acquisition Agreement is terminated under specified circumstances. Moreover, approximately 41% of the outstanding shares of VGX common stock as of the record date are subject to voting agreements pursuant to which such VGX stockholders agree to vote in favor of the Merger. See " The Acquisition Agreement—No Solicitation " beginning on page 110 of this joint proxy statement/prospectus, " The Acquisition Agreement—Termination of the Acquisition Agreement " beginning on page 115 of this joint proxy statement/prospectus, " The Acquisition Agreement—Termination Payment " beginning on page 116 of this joint proxy statement/prospectus, and " Other Agreements Related to the Transaction—VGX Support Stockholders Voting Agreement " beginning on page 117 of this joint proxy statement/prospectus.

        These provisions might discourage a third party that may have an interest in acquiring all of or a significant part of either Inovio or VGX from considering or proposing an acquisition, even if that party were prepared to pay consideration with a higher per share market price than the current proposed merger consideration. Furthermore, the termination fee may result in a potential competing acquirer proposing to pay a lower per share price to acquire Inovio or VGX than it might otherwise have proposed to pay. The payment of the termination fee could also have an adverse effect on the terminating company's financial condition and the ability of that company to fund its operations after the termination of the Acquisition Agreement.

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Inovio and VGX may not realize the benefits they expect from the transaction and if the benefits of the transaction, if any, do not exceed the costs of integrating the businesses of Inovio and VGX, the combined group's financial results may be adversely affected.

        Inovio and VGX have entered into the Acquisition Agreement with the expectation that the transaction will result in substantial benefits such as a potentially greater ability to mitigate overall development risk through creation of a broader, more balanced fully-integrated biopharmaceutical company with a deep product development pipeline, with anticipated significant market potential, synergies and efficiencies from the combination of experienced management and research and development teams, and a broader patent portfolio. The combination of Inovio and VGX will be complex, time consuming and expensive, and could disrupt Inovio's and VGX's businesses. The combined group will need to overcome significant integration and allocation of resources challenges in a timely and efficient manner in order to realize any benefits from the transaction and have a successful integration of the operations and personnel. In addition to the costs incurred thus far by each party in negotiating the Acquisition Agreement, planning for the special meetings and managing the pre-Merger process, the combined group will incur costs, which are not reasonably estimable, in the quarter in which the transaction is completed or following quarters, associated with integrating the two companies' operations and management. The combined group may incur additional material charges in subsequent quarters to reflect additional costs associated with the transaction. If the financial benefits of the transaction, if any, do not exceed the costs of planning for and completing the Merger and integrating the businesses of Inovio and VGX, the combined group's financial results may be adversely affected.

Management of the combined group will include numerous individuals that may not possess experience in a publicly traded corporate environment and may be unfamiliar with the reporting and compliance requirements applicable to publicly traded companies.

        The management of the combined group post-Merger, if completed, will draw from the current Inovio and VGX management. As VGX is a privately-held company, many of the legacy VGX members of the combined group's management may not possess experience in a publicly traded corporate environment and may be unfamiliar with the reporting and compliance requirements of a publicly traded company in general or of the post-Merger Inovio specifically. As a result, these individuals may have to rely on the legacy Inovio members of the combined group's management to gain the historical perspective with respect to Inovio that may be necessary to properly analyze the performance of the combined group for reporting purposes and to provide critical disclosures to the public. As a result, the combined group may be unable to fully or timely comply with applicable Exchange Act reporting requirements, or may incur greater costs in doing so due to inefficiencies in the reporting process and the need to provide relevant educational support regarding public company responsibilities and reporting requirements. Any noncompliance with the applicable reporting requirements could trigger, among other things, an investigation by the SEC, a stockholder lawsuit, an inability to utilize certain streamlined forms or processes or to rely on certain safe harbors under the federal securities laws, which may result in an unfavorable impact on the market price of the public company's stock post-Merger.

If Inovio and VGX lose key personnel prior to completion of the Merger, or the combined group loses key personnel shortly after the Merger, and are unable to attract and retain additional, highly skilled personnel required to develop products or obtain new collaborations, the business of Inovio, VGX and/or the combined group may suffer.

        Inovio and VGX depend, to a significant extent, on the efforts of their key employees, including senior management and senior scientific, clinical, regulatory and other personnel. The development of new therapeutic products requires expertise from a number of different disciplines, some of which is

32



not widely available. Both companies depend upon scientific staff to discover new product candidates and to develop and conduct pre-clinical studies of those new potential products, and rely on clinical and regulatory staff for the design and execution of clinical trials in accordance with FDA and foreign regulatory requirements and for the advancement of product candidates toward FDA and foreign regulatory approval. The manufacturing staffs are responsible for designing and conducting each company's manufacturing processes in accordance with the FDA's Quality System Regulations. The quality and reputation of the companies' scientific, clinical, regulatory and manufacturing staff, especially the senior staff, and their success in performing their responsibilities, have been and remain significant factors in attracting potential funding sources and collaborators. In addition, each company's executive officers are involved in a broad range of critical activities, including providing strategic and operational guidance. It is vital to each of Inovio and VGX to maintain its current management and senior staff in support of ongoing operations in case the Merger is not completed, and important to the combined group to retain such individuals so that they can be integrated post-Merger and provide the combined group the anticipated, continued benefit of their significant prior experience and their reputations for quality performance. Inovio and VGX each face, and the combined group will face, intense competition for personnel from other companies, universities, public and private research institutions, government entities and other organizations. The loss of these individuals, or an inability to retain or recruit other key management and scientific, clinical, regulatory, manufacturing and other personnel, may delay or prevent either company from achieving its current business objectives and, if the Merger is completed, could also substantially delay the integration process, undermine partner and investor confidence in the combined group and hamper the combined group's ability to complete in-process programs, all of which could adversely affect each of the companies' financial condition, operations and stock price.

Certain partners or collaborators of Inovio and VGX may have the right to terminate their existing license or collaboration agreements in conjunction with the Merger; such termination may have an adverse effect on the financial condition and operations of Inovio, VGX and/or, if the Merger is consummated, the combined group.

        Some of Inovio's and VGX's sponsored research, license and/or collaborative arrangements contain "Change of Control" or other protective provisions that may be triggered by the proposed transaction, if completed, which may enable premature termination of such arrangements or otherwise may impact the status of such arrangements for the combined group. For example, Inovio's agreement with Wyeth requires Inovio to provide Wyeth with certain notifications of a pending qualifying transaction and enables Wyeth to terminate the arrangement if such notice and certain other written assurances regarding the priority and commitment to the arrangement are not timely provided to Wyeth by Inovio prior to consummation of such transaction. Similarly, Inovio's arrangement with Merck requires certain notice of a Change of Control transaction and also enables termination under limited circumstances as a result. Other of Inovio's and VGX's arrangements, including certain of their patent licenses, require that the company seek and obtain prior written consent from the collaborative party ahead of the consummation of any Change of Control transaction. Although Inovio and VGX intend to comply with applicable notice and other documentation requirements, and to provide assurances and seek consent from the collaborator, pursuant to such "Change of Control" provisions in these and other collaborative arrangements, Inovio and VGX cannot assure you that, to the extent such rights exist, their partners will not seek to terminate or alter their arrangements with them in relation to the closing of the proposed transaction. If any of these arrangements are terminated and such arrangements, individually or in the aggregate, are material to Inovio, VGX and/or the combined group, such termination may have an adverse effect on the ability of the company/combined group to continue to conduct certain aspects of its business or fund its operations at historical levels or generate revenues, and thus may also adversely affect the company's and/or combined group's financial condition and Inovio's stock price.

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The holders of Inovio's Series C preferred stock and a limited number of Inovio's warrants may seek redemption of their shares or warrants for cash, which could result in litigation and if applicable to such securities, could impair the combined group's cash position.

        Inovio has reviewed the rights of the holders of its outstanding securities in conjunction with the Merger, which have a variety of provisions prescribing certain consequences upon a merger transaction, contingent upon the existence of specified shifts of ownership of Inovio's securities or voting power of Inovio stockholders. Although the holders of Inovio's equity securities prior to the closing of the Merger will hold less than 50% of the outstanding equity securities after closing of the Merger, the holders of outstanding Inovio capital stock prior to closing of the Merger will retain a majority of the voting power upon consummation of the Merger. As a result, the Merger does not appear to constitute a change of control or qualifying triggering event for shares of Inovio's Series C preferred stock and certain Inovio's warrants, which in the event of a change of control or qualifying triggering event as defined for such securities, would provide the holders of such securities the right to redeem such shares or warrants for cash. Although such redemption would not be mandatory, if triggered and sought by all holders of such Inovio securities, the costs of redemption would total approximately $853,000 in cash for the shares of Series C preferred stock and various warrants, which could impair the cash position of the combined group post-closing, and result in the combined group not having sufficient funds to support its operations initial post-combination. Although Inovio believes the Merger does not satisfy the applicable definitions of a change of control or qualifying triggering event applicable to the shares of Series C preferred stock and the certain warrants containing redemption rights, and thus the Merger does not trigger the redemption rights, if the holders of these securities believe otherwise, such holders could take legal action against Inovio, resulting in increased legal fees, which could also impair the cash position of the combined group post-closing.

If Inovio's due diligence investigation of VGX was inadequate, or VGX's due diligence of Inovio was inadequate, then stockholders of the combined group following the Merger could lose some or all of their investment. Additionally, if the representations and warranties made by Inovio and VGX in the Acquisition Agreement are inaccurate or breached, neither entity will be indemnified for any losses or damages incurred as a result of such breach.

        Even though Inovio conducted a due diligence investigation of VGX, and VGX conducted a due diligence investigation of Inovio, neither can be sure that this diligence surfaced all material issues that may be present inside either company's business, or that it would be possible to uncover all material issues through a customary amount of due diligence, or that factors outside of VGX, Inovio and their respective businesses and outside of their control will not later arise. Even if each party's due diligence successfully identified certain risks, unexpected risks may arise and previously known risks may materialize in a manner not consistent with the other party's preliminary risk analysis.

        In addition, Inovio and VGX are relying upon the representations and warranties made by the other party in the Acquisition Agreement, however the Acquisition Agreement does not include indemnification provisions allowing for clear procedures for recoupment of losses resulting from a breach of such representations or warranties. If either party breaches a representation or warranty made by such party and the other party suffers losses or damages as a result of such breach, the other party will not be indemnified for such loss or damage and would have to rely on potentially costly litigation to pursue and potentially recoup such costs.

Inovio and VGX may be unable to obtain the regulatory or exchange approvals required to complete the Merger.

        Inovio and VGX do not believe that the Merger is subject to review by any other governmental authorities under the antitrust laws of the other jurisdictions where Inovio and VGX conduct business. However, Inovio and VGX are continuing to review such requirements and there remains the

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possibility that the parties would be subject to a pre-Merger statutory filing under the HSR Act if the implied value of the transaction would change substantially prior to the consummation of the Merger. Also, even after completion of the Merger, U.S. or foreign governmental authorities could challenge or seek to block the Merger under the antitrust laws, as they deem necessary or desirable in the public interest. Moreover, in some jurisdictions, a competitor, customer or other third party could initiate a private action under the antitrust laws challenging or seeking to enjoin the Merger, before or after it is completed. Inovio and VGX cannot be sure that a challenge to the Merger will not be made or that, if a challenge is made, Inovio and VGX will prevail. For a full description of the regulatory clearances, consents and approvals required for the Merger, see " The Acquisition Agreement—Regulatory Matters " beginning on page 110 of this joint proxy statement/prospectus.

        The Acquisition Agreement conditions the closing of the Merger on the registration statement, of which this joint proxy statement/prospectus is a part, being declared effective by the SEC and the NYSE Alternext, or an alternate securities exchange or quotation system under certain circumstances, approving the Inovio common stock to be issued or to become issuable in the Merger for listing (or quotation, if applicable). While Inovio and VGX expect to obtain the required regulatory clearances, consents and approvals, Inovio and VGX cannot be certain that any required approvals will be obtained, nor can they be certain that the approvals will be obtained within the time contemplated by the Acquisition Agreement. A delay in obtaining any required clearances, consents and approvals might delay and may possibly prevent the completion of the Merger.

The NYSE Alternext may delist Inovio's securities from quotation on its exchange in the interim period of the pending Merger if Inovio is unable to maintain the required stock price, and if so, Inovio may be unable to relist its securities on the NYSE Alternext or another national securities exchange due to the level of the perceived market value of shares of its common stock.

        Inovio's securities are currently listed on the NYSE Alternext, a national securities exchange, and in recent months have traded at a low selling price. The NYSE Alternext may seek to delist Inovio's securities from trading on its exchange if Inovio continues to be unable to increase the per share price or otherwise fails to maintain compliance with other requirements of continued listing on the NYSE Alternext. If the NYSE Alternext delists Inovio's securities from trading on its exchange and Inovio is unable to relist its securities on the NYSE Alternext or to list its securities or another securities exchange or to have its securities quoted on a quotation system due to the level of the perceived market price of shares of its common stock, Inovio could face significant material adverse consequences, including:

        Further, the parties are in discussions with the NYSE Alternext regarding whether the transaction constitutes a "Reverse Merger" under Section 341 of the exchange's Company Guide, or "Section 341." If the transaction is ultimately determined to constitute a "Reverse Merger," Inovio must file an initial listing application and satisfy the initial listing requirements in order to remain listed on the NYSE Alternext and obtain listing approval for the shares issued and issuable upon closing of the Merger. If

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Inovio is not able to qualify for initial listing on the NYSE Alternext at such time, the Inovio common stock may transition to listing on an alternate securities exchange or quotation on a quotation system consistent with the terms of the Acquisition Agreement, which also could result in the significant material adverse consequences noted above.

The proposal to amend the Inovio 2000 Plan, the approval of which is a condition to the Merger pursuant to the Acquisition Agreement, may not receive the required stockholder approval.

        Pursuant to the Acquisition Agreement, the Merger is contingent upon, among other things, an amendment to the Inovio 2000 Plan. If the 2000 Plan Amendment is not approved by the stockholders of Inovio, and the parties do not waive the related closing condition in the Acquisition Agreement, the pending transaction may be delayed or terminated altogether, adversely affecting the financial condition of the parties. If the parties were to waive the related closing condition and consummate the Merger in absence of the 2000 Plan Amendment, legacy holders of Inovio securities will hold a smaller proportion of Inovio's fully-diluted share capital post-Merger.

VGX stockholders may exercise their dissenters' rights in connection with the Merger, which may impact the closing of the Merger and the availability of cash post-closing.

        VGX stockholders who exercise their dissenters' rights in connection with the Merger, including satisfying all statutory requirements for exercising such rights, will be entitled to cash payment for the fair value of their shares which will be determined in accordance with the DGCL. As the Acquisition Agreement includes a 10% cap on the percentage of VGX holders exercising such rights as a closing condition to the Merger, if the number of shares of VGX common stock held by dissenting stockholders exceeds this cap, the Merger may not close. Additionally, even if the Merger is consummated, the availability of cash to the company after the Merger may be significantly reduced and may adversely affect the financial condition and operations of the combined group.

If the taxation consequences of the transaction on the companies themselves and/or any participating VGX stockholders are significantly different than those anticipated by the parties and described in this joint proxy statement/prospectus, VGX and Inovio may be subject to expensive stockholder litigation, which could negatively impact the financial condition of the combined group.

        This joint proxy statement/prospectus contains a discussion of certain material U.S. federal income tax consequences to a VGX stockholder of the exchange of VGX common stock for Inovio common stock in the contemplated transaction. This discussion is based on current provisions of the Code, Treasury regulations promulgated under the Code, Internal Revenue Service, or IRS, rulings and pronouncements, and judicial decisions now in effect, all of which are subject to change at any time by legislative, judicial or administrative action. Any such changes may be applied retroactively. In addition, this discussion does not consider the effects of any applicable foreign, state, local or other tax laws, or estate or gift tax considerations, or the alternative minimum tax.

        Neither Inovio nor VGX has sought, and nor will either party seek, any rulings from the IRS with respect to the U.S. federal income tax consequences discussed in this joint proxy statement/prospectus. The provided discussion does not in any way bind the IRS or the courts or in any way constitute an assurance that the presentation of U.S. federal income tax consequences will be accepted by the IRS or the courts. Thus, there is a risk that the tax consequences described in this joint proxy statement/prospectus for Inovio stockholders and/or VGX stockholders may be incorrect. The provided discussion of tax consequences is not tax advice, and it is clearly stated that each holder of Inovio and VGX securities should consult his, her or its own tax advisor as to particular tax consequences to it of such events, including the applicability of any state, local or foreign tax laws and any proposed changes in applicable law.

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        As discussed, the parties intend that the proposed transaction and the exchange of Inovio common stock for VGX common stock, be tax-free to the entities' stockholders and tax-free to the entities themselves. However, should the tax consequences resulting from the issuance of common stock be different than as discussed in this joint proxy statement/prospectus, the combined group may face claims from individuals in connection with any unanticipated tax burden related to the transaction, which will result in increased legal costs to the combined group and negatively impact the combined group's financial condition.

The consummation of the Merger may limit the ability of Inovio and VGX to utilize existing net operating losses and certain other tax attributes.

        As disclosed in Inovio's annual report on Form 10-K for the 2007 fiscal year, as of December 31, 2007, Inovio had net operating losses, or "NOLs", of approximately $55.9 million for federal income tax purposes and approximately $50.8 million for state income tax purposes, plus federal research tax credit carry-forwards of approximately $714,000 as of December 31, 2007. As disclosed in VGX's audited financial statements for the year ended December 31, 2007, VGX had NOL carry-forwards of approximately $27.6 million for federal income tax purposes and approximately $23.3 million for state income tax purposes.

        Utilization of the NOLs and tax credit carryforwards may be subject to a substantial annual limitation under Section 382 of the Code, and similar state provisions due to ownership change limitations that have occurred previously or that could occur in the future. These ownership changes may limit the amount of NOL and tax credit carryforwards and other deferred tax assets that can be utilized to offset future taxable income and tax, respectively. In general, an ownership change, as defined by Section 382, results from transactions increasing ownership of certain stockholders or public groups in the stock of the corporation by more than 50 percentage points over a three-year period. Inovio previously performance an analysis which indicated that multiple ownership changes have occurred in previous years which created annual limitations on Inovio's ability to utilize NOL and tax credit carryovers prior to the Merger, including approximately $12.7 million of tax benefits related to NOL and tax credit carryforwards that would expire unused. VGX has not performed a detailed Section 382 analysis to determine whether there are any limitations with respect to the utilization of its NOLs.

        Inovio, VGX and their tax advisors are continuing to analyze the impact of the Merger, if consummated, on the parties' tax benefits related to NOL and tax credit carryforwards. Any limitation on the combined group's net operating loss carryforwards that could be used to offset post-ownership change in taxable income would adversely affect the combined group's liquidity and cash flow, if the combined group were to become profitable.

Some of Inovio's and VGX's officers and directors have conflicts of interest that may influence them to support or approve the Merger.

        Certain officers and directors of Inovio and VGX may participate in arrangements arising from the Merger that provide them with interests in the Merger that are different from those of other stockholders of Inovio and stockholders of VGX, including new employment agreements, closing payments due at the Effective Time and continuing indemnification pursuant to the terms of the Acquisition Agreement. These interests, among others, may influence the officers and directors of Inovio and VGX to support or approve the transaction. Inovio and VGX stockholders are encouraged to review the more detailed discussion entitled " Interests of Directors, Officers and Affiliates " on page 86, to evaluate the interests of such individuals and to weigh the impact such interests may have had on the support or recommendations of such individuals for the Merger.

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Inovio and VGX may be subject to the risks of litigation relating to the Merger.

        Any significant transaction generates some degree of litigation risk, and both Inovio and VGX may be subject to claims and actions incidental to the pending merger transaction, potentially from partners or collaborators of the parties' current programs, stockholders or other third parties who seek to disrupt the transaction to serve their own interests, or by each other if the parties' fail to consummate the transaction. Inovio and VGX are not currently aware of, nor do they presently anticipate, any such litigation, however the transaction may result in litigation prior to or upon closing of the transaction, if completed. If such litigation arises, the outcome of these proceedings cannot be predicted. If a plaintiff were successful in a claim against either or both companies, either or both of the companies, or the combined group if the Merger is closed, could be burdened with the required payment of a material sum of money. If this were to occur, it could have an adverse effect on either or both companies' financial condition and the financial condition of the combined group if the Merger is consummated.

The combined group may be required to file time-consuming and potentially costly subsequent registration statements or post-effective amendments to the registration statement, of which this joint proxy statement/prospectus is a part, related to the options, warrants and convertible debt assumed pursuant to the Merger.

        Pursuant to the Acquisition Agreement, Inovio is required to maintain a current prospectus covering the shares of common stock issuable upon the exercise or conversion of the warrants, options and convertible debt assumed from VGX by Inovio. Consequently, Inovio may be required to file subsequent registration statements or amend the registration statement of which this joint proxy statement/prospectus is a part in order to update and maintain the prospectus for the issuance of the shares underlying the options, warrants and convertible debt assumed in the Merger from VGX, until all such shares have been issued or such instruments have expired. The preparation and filing of such registration statements can be time-consuming and costly, and may divert management's attention from the combined group's business.

Risks Relating to the Business of the Combined Group

         For purposes of the following risk factors, the terms "we," "our," "our company" and "us" refer to the projected combined group, consisting of Inovio, VGX and their respective subsidiaries, unless otherwise explicitly stated.

The integration of the operations of Inovio and VGX may be difficult and may lead to adverse effects.

        The success of the Merger will depend, in part, on the ability of our company to realize the anticipated synergies, cost savings and growth opportunities from integrating VGX's business with our business. Our success in realizing these benefits and the timing of this realization depend upon the successful integration of the operations of VGX with those of Inovio. The integration of previously independent businesses is a complex, costly and time-consuming process, which requires coordination of different development, regulatory, manufacturing and business teams, and involves the integration of systems, applications, policies, procedures, business processes and operations. The difficulties of combining the operations of the businesses include, among others:

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        The combined group may not accomplish this integration smoothly or successfully. If cultural conflicts and different opinions on scientific and regulatory matters arise, the integration could become more difficult and unpredictable. The combined group may not succeed in addressing these risks and challenges, or any other problems encountered in connection with the transaction, which could have a material adverse effect on the combined group and its ability to realize any of the expected benefits of the Merger, which as a result may harm the market price of Inovio common stock.

Integrating Inovio and VGX may divert management's attention away from other operations.

        Successful integration of the operations, products and personnel may place a significant burden on the combined group's management and internal resources. The diversion of the attention of management from current programs to the integration effort and any difficulties encountered in combining operations could result in delays in the companies' clinical trial programs and could prevent the combined group from realizing the full benefits anticipated to result from the Merger, thus adversely affecting our business. In addition, the combined group may not be able to retain its senior management and other employees for the duration of the integration process or beyond. The failure to retain employees could result in higher operating expenses, disrupt the management of the combined group and have a materially adverse effect on the combined group's financial condition, results of operations and cash flow.

Inovio and VGX expect to incur significant costs integrating the companies into a single business.

        Inovio and VGX expect to incur significant costs integrating our operations, products and personnel. These costs may include costs for:

        Additionally, other costs associated with the integration of the combined group can be substantial. To the extent that the combined group incurs integration costs that were not anticipated, these unexpected costs could adversely impact the combined group's liquidity or force it to borrow or raise additional funds, further diverting management's attention from operations of the combined group and potentially further diluting the stockholders of the combined group.

The combined group will have a need for significant funds in the future and there is no guarantee that we will be able to obtain the funds needed timely or at all.

        Developing new medical devices and therapies and conducting clinical trials is expensive. The combined group's product development efforts may not lead to commercial products, either because our product candidates fail to be found safe or effective in clinical trials or because we lack the

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necessary financial or other resources or relationships to pursue its programs through advanced phases of clinical trials to commercialization. Our capital and future revenue may not be sufficient to support the expenses of our operations, the development of a commercial infrastructure and the conduct of our pre-clinical research and clinical trials, although based upon Inovio's and VGX's current budgeting and projected cash flow models, we believe that the combined group may be able to support its integrated operations for 12 months post-closing of the Merger.

        Our plans for conducting research, furthering development, continuing and integrating current and launching future pre-clinical and clinical trials and, eventually, marketing our human-use equipment and associated therapies will involve substantial costs. The extent of such costs will depend on many factors, including some of the following:

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        We plan to fund operations by several means. We will attempt to enter into contracts with partners that will fund either general operating expenses or specific programs or projects. Some funding also may be received through government grants. However, we may not be able to enter into any such contracts or may not receive such grants or, if we do, our partners and the grants may not provide enough funding to meet our needs.

        In the past, Inovio and VGX have both raised funds through the sale of their capital stock or issuing debt convertible into stock, and the combined group is likely to do this in the future. Sale of our stock to new investors post-Merger would result in dilution of the ownership interests of our existing stockholders, including the current Inovio stockholders and the former VGX stockholders. The greater the number of shares sold, the greater the dilution. A high degree of dilution, especially soon after completion of a highly dilutive event like the Merger, can make it difficult for the price of our stock to increase, among other things. Dilution also weakens existing stockholders' voting power; to the extent a planned issuance of shares of capital stock would require stockholder approval, there can be no assurance that our stockholders will support such an issuance, and thus we may not be able to raise funds in sufficient amounts or in a timely manner if such approvals would be needed.

        We cannot assure you that we will be able to raise additional capital to fund operations, or that we will be able to raise additional capital under terms that are favorable to us. Further, we cannot assure you that the Merger, if completed, will in any way negate or mitigate each of Inovio's and VGX's current need for future capital.

Negative conditions in the global credit markets may impair the liquidity of a portion of Inovio's investment portfolio and the combined group's ability to maintain overall liquidity, negatively impacting the combined group's operations and financial condition.

        The capital and credit markets have been experiencing extreme volatility and disruption for more than twelve months and in recent weeks, the volatility and disruption have reached unprecedented levels. In some cases, the markets have exerted downward pressure on availability of liquidity and credit capacity for certain issuers. We need liquidity to pay our operating expenses, make timely principal and interest payments on our debt and replace certain maturing liabilities.

        Inovio has historically invested in high-grade (AAA rated) auction rate securities, or ARS, issued primarily by municipalities. As of September 30, 2008, the estimated fair value of Inovio's ARS investments is $12.1 million, which reflects a $1.5 million adjustment to the principal value (cost) of $13.6 million as of September 30, 2008. The recent negative conditions in the global credit markets have prevented some investors from liquidating their holdings, including their holdings of ARS. In early March 2008, Inovio was informed that there was insufficient demand at auction for all six of its high-grade ARS. As a result, these affected securities are currently not liquid, and Inovio could be required to hold them until they are redeemed by the issuer or to maturity. In the event Inovio needs to access the funds that are in an illiquid state, Inovio will not be able to do so without a loss of principal, until a future auction on these investments is successful, the securities are redeemed by the issuer or they mature. At this time, Inovio's management has not obtained sufficient evidence to conclude that these investments are permanently impaired or that they will not be settled in the short term, although the market for these investments is presently uncertain. If the credit ratings of the security issuers deteriorate and any decline in market value is determined to be other-than-temporary,

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Inovio would be required to adjust the carrying value of the investment through a permanent impairment charge.

        On December 19, 2008, Inovio accepted an offer by UBS AG, or "UBS," of certain rights to cause UBS to purchase the ARS, at a future date. UBS offered the repurchase rights in connection with its obligations under settlement agreements with the SEC and other federal and state regulatory authorities, and as a result of accepting UBS's offer, Inovio, via its wholly-owned subsidiary Genetronics, Inc., or "Genetronics," which holds the ARS, can require UBS to repurchase at par value all of the ARS at any time during the period from June 30, 2010 through July 2, 2012, if such ARS have not previously been sold by Genetronics or by UBS on its behalf. In conjunction with the acceptance of the rights offering, Genetronics also amended its existing loan agreement with UBS Bank USA, increasing the existing credit line up to $12.1 million, with the ARS pledged as collateral, which Genetronics fully drew down on December 23, 2008. Although Inovio has been able to regain limited liquidity through this line of credit secured by the ARS and expects redemption of the ARS pursuant to the rights obtained, the line of credit may not provide sufficient liquidity for Inovio's current operational needs, nor provide the necessary liquidity to complete the integration process and maintain desired programs after the Merger with VGX, if completed.

        Without sufficient liquidity, Inovio, and upon completion of the Merger, the combined group, will be forced to curtail its operations, and its business will suffer. In the event current resources, including Inovio's ARS and the related line of credit, do not satisfy the combined group's needs, it may have to seek additional financing. The availability of additional financing will depend on a variety of factors such as market conditions, the general availability of credit, the volume of trading activities, the overall availability of credit to the financial services industry, our credit ratings and credit capacity, as well as the possibility that customers or lenders could develop a negative perception of our long- or short-term financial prospects if Inovio, or subsequently the combined group, incurs large investment losses or if the level of business activity decreases due to a downturn in available funding, partnership opportunities and other fluctuations. The crisis in the global financial markets currently places significant limitations on the general availability of credit and the number and level of interest of investors. Similarly, access to funds may be impaired if regulatory authorities take negative actions against the combined group. Further, even if financing becomes available, the cost to the combined group may be significantly higher than in the past. The combined group's results of operations, financial condition, and cash flows position could be materially adversely affected by these disruptions in the financial markets, including the resulting lack of liquidity in Inovio's current investments and availability of financing for future liquidity.

If the combined group does not have enough capital to fund operations, then we will have to cut costs or raise funds.

        If we are unable to raise additional funds under terms acceptable to us and in the interests of our stockholders post-Merger, then we will have to take measures to cut costs or obtain funds using alternative methods, such as:

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        If it became necessary to take one or more of the above-listed actions, then we may receive a lower valuation, which could impact our stock price. Further, the effects on our operations, financial performance and stock price may be significant if we do not or cannot take one or more of the above-listed actions in a timely manner when needed.

The market for Inovio's common stock is volatile, and the combined group anticipates that such volatility will continue indefinitely, which could adversely affect an investment in our stock.

        Historically, Inovio's share price and trading volume have been highly volatile, which is not unusual for biomedical companies of Inovio's size, age and with a discrete market niche. Inovio and VGX do not believe that the integration of the companies into the combined group will alter these factors significantly enough to lessen such volatility. It also is common for the trading volume and price of biotechnology stocks to be unrelated to a company's operations, i.e. to increase or decrease on positive or no news. Inovio's stock has exhibited this type of behavior in the past and will likely exhibit it in the future. The historically low trading volume of Inovio's stock, in relation to many other biomedical companies of its current size, and the anticipated size as the combined group, makes it more likely that a severe fluctuation in volume, either up or down, will affect the stock price.

        Some factors that we would expect to depress the price of our stock include:

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        These factors, as well as the other factors described in this joint proxy statement/prospectus, could significantly affect the price of our stock. Historically Inovio has held that quarter-to-quarter or annual comparisons of its operating results are not a good indicator of its future performance, and the companies believe that such comparisons will also be poor indicators of performance post-Merger, at least until the combined group has operated on an integrated basis for a substantial period of time, if not longer. Further, the inability to accurately compare periodic performance due to the Merger and any other fluctuations may cause Inovio's stock to perform below the expectations of public market analysts and investors post-Merger. If this happens, the price of Inovio's common stock would likely decline.

Our operating results may vary significantly from period-to-period, which may result in a decrease in the price of our common stock .

        Our future revenues and operating results may vary significantly from period-to-period due to a number of factors, many of which are outside of our control. These factors include:

        Although we acknowledge that our operating results will vary significantly from period-to-period and past periodic performance should not be relied upon as an indicator of future periodic performance, it is possible that in one or more future periods our operating results may be below the expectations of analysts and/or investors. If this happens, the price of our common stock may decrease, even if there has not been a significant adverse change in our financial condition or our operations.

Both Inovio and VGX have a history of losses, we expect to continue to incur losses and we may not achieve or maintain profitability.

        As of September 30, 2008, Inovio had an accumulated deficit of approximately $149.2 million and VGX had an accumulated deficit of approximately $63.0 million. Inovio and VGX have each operated at a loss since their respective inceptions, and the combined group anticipates such losses to continue for some time. The combined group expects its consolidated, accumulated deficit will continue to increase, as it will be expensive to continue research, development and clinical efforts, especially while integrating such efforts. If these activities are successful and if we receive approval from the FDA to market equipment and/or a therapy, then even more funding will be required to market and sell such product. The outcome of these matters cannot be predicted at this time. We anticipate maintaining current partnerships and collaborations, and expect to evaluate additional potential partnerships and collaborative agreements as a way to further fund operations, but there is no assurance we will be able

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to secure partnerships or other arrangements that will provide the required funding, if at all. We will seek to continue to rely on outside sources of financing to meet our capital needs for the initial 12 months post-Merger, however such funds may not always be readily available when needed or on terms favorable to us.

        Further, there can be no assurance, assuming we successfully raise additional funds, that we will achieve positive cash flow. If we are not able to secure additional funding, we will be required to scale back our integrated research and development programs, preclinical studies and clinical trials, general, and administrative activities and may not be able to continue in business.

VGX has a large amount of outstanding receivables from, VGXI, Inc., a wholly owned subsidiary of VGX International, which if not repaid timely could have negative cash flow impacts on VGX or the combined group.

        As a result of the sale of VGX's DNA plasmid manufacturing assets to VGXI, Inc. in June 2008, VGX has accounts receivable from VGXI, Inc totaling $6,000,000 as of September 30, 2008. This amount is to be paid in two tranches. The first tranche of $3,000,000 due on December 15, 2008 has been received while the remaining tranche of $3,000,000 is due on March 31, 2009. If VGXI, Inc. fails to pay these amounts to VGX, VGX or the combined group may suffer negative cash flow because a portion of the funds are intended to be used to repay the VGX debt and a portion of the outstanding VGX convertible debt prior to or upon closing of the Merger. Although VGX owns, and upon consummation of the Merger, if approved, the combined group will own, 30.37% of VGX International, Inc., the parent company of VGXI, Inc., VGX is not able to compel payment of the amounts owed on a timely basis, or at all, on account of this ownership interest.

Our dependence upon non-marketed products, our limited experience in manufacturing, our lack of experience marketing human-use products, and our continuing deficit may result in even further fluctuations in our trading volume and share price.

        Successful approval, marketing, and sales of our human-use equipment are critical to the financial future of our company. Our human-use products are not yet approved for sale in the U.S. and other jurisdictions and we may never obtain these approvals. Even if we do obtain approvals to sell our human-use products in the U.S., these sales may not be as large or as timely as we expect. Furthermore, the regulatory climate with respect to marketing and sales has become increasingly strict, and our lack of experience in this area may expose us to liability. These uncertainties may cause our operating results to fluctuate dramatically in the next several years. We believe that quarter-to-quarter or annual comparisons of our operating results are not a good indicator of our future performance. Nevertheless, these fluctuations may cause us to perform below the expectations of public market analysts and investors. If this happens, the price of our common shares would likely decline.

If we are unable to develop commercially successful products in various markets for multiple indications, our business will be harmed and we may be forced to curtail or cease operations.

        We cannot assure you that we will successfully develop any products, or if we do, that they will be commercially successful. If we fail to develop or successfully commercialize any products, we may be forced to refocus, curtail or cease operations. Our ability to achieve and sustain operating profitability depends on our ability, directly or with strategic partners, to successfully commercialize our therapies in Europe, Asia and in the US. This will depend in large part on our ability to commence, execute and complete clinical programs and obtain regulatory approvals for our therapies. Clinical trials are still necessary before we can seek regulatory approval to sell our products or therapies. We cannot assure you that we will receive approval for our therapies in the U.S. or in other countries or, if approved, that we or a partner will achieve a significant level of sales. If we fail to partner or commercialize our products, we may be forced to curtail or cease operations.

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        We are also in the pre-clinical stages of research and development with other new product candidates using electroporation technology. These new indications and product candidates will require significant costs to advance through the development stages. Even if such product candidates are advanced through clinical trials, the results of such trials may not gain FDA or foreign regulatory approval. Even if approved, our products may not be commercially successful.

Pre-clinical and clinical trials of human-use equipment are unpredictable, and if we experience unsuccessful trial results, our business will suffer.

        Before any of our human-use equipment can be sold, the FDA or applicable foreign regulatory authorities must determine that the equipment meets specified criteria for use in the indications for which approval is requested, including obtaining appropriate regulatory approvals. Satisfaction of regulatory requirements typically takes many years, and involves compliance with requirements covering research and development, testing, manufacturing, quality control, labeling and promotion of therapies for human use. To obtain regulatory approvals, we must, among other requirements, complete clinical trials demonstrating that our product candidates are safe and effective for a particular disease. Regulatory approval of a new treatment is never guaranteed. The FDA and each applicable foreign regulatory authority will make this determination independently, based on the results from our pre-clinical testing and clinical trials and has substantial discretion in the approval process. Despite the time and experience exerted, failure can occur at any stage, and we could encounter problems causing us to abandon clinical trials.

        In addition, any of our clinical trials for treatment using our therapies may be delayed or halted at any time for various other reasons, including:

        If any of the above events arise during our clinical trials or data review, we would expect this to have a serious negative impact on our company. Any termination of ongoing enrollment or other delay or change in the conduct of our clinical trials may not always be understood or accepted by the capital markets and announcements of such scientific results and related actions may adversely affect the market price of our common stock.

        Any delays or difficulties Inovio or VGX has encountered or the combined group will encounter in its pre-clinical research and clinical trials may delay or preclude regulatory approval. Our product development costs will increase if we experience delays in testing or regulatory approvals or if we need to perform more extensive or larger clinical trials than planned, or if we need to redirect the focus of our trials to other product candidates or medical indications. Any such events could also delay or preclude the commercialization of our therapy or any other product candidates.

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        Clinical trials are unpredictable, especially human-use trials. Results achieved in early stage clinical trials may not be repeated in later stage trials, or in trials with more patients. When early positive results were not repeated in later stage trials, pharmaceutical and biotechnology companies have suffered significant setbacks. Not only are commercialization timelines pushed back, but some companies, particularly smaller biotechnology companies with limited cash reserves, have discontinued business after releasing news of unsuccessful clinical trial results. Neither Inovio nor VGX can be certain the results it has observed in its pre-clinical testing will be confirmed in clinical trials or the results of any of its or the combined group's clinical trials will support FDA or foreign regulatory approval. If we experience unexpected, inconsistent or disappointing results in connection with a clinical or pre-clinical trial our business will suffer.

        A delay in our clinical trials, for whatever reason, will probably require us to spend additional funds to keep our product(s) moving through the regulatory process. If we do not have or cannot raise additional funds, then the testing of our human-use products could be discontinued. In the event our clinical trials are not successful, we will have to determine whether to continue to fund our programs to address the deficiencies, or whether to abandon our clinical development programs for our products in tested indications. Loss of our human-use product line would be a significant setback for our company.

        Because there are so many variables inherent in clinical trials, we cannot predict whether any of our future regulatory applications to conduct clinical trials will be approved by the FDA or other regulatory authorities, whether our clinical trials will commence or proceed as planned, and whether the trials will ultimately be deemed to be successful. Historically, the experience of both Inovio and VGX has been that submission and approval of clinical protocols has taken longer than desired or expected.

Our business is highly dependent on receiving approvals from various regulatory authorities and will be dramatically affected if approval to manufacture and sell our human-use equipment and/or gene-based therapies is not granted or is not granted in a timely manner.

        The production and marketing of our human-use equipment and related gene-based therapies, our ongoing research, development, pre-clinical testing, and clinical trial activities are subject to extensive regulation. Numerous governmental agencies in the U.S. and internationally, including the FDA, must review our applications and decide whether to grant regulatory approval. All of our human-use equipment and the therapies to be used in conjunction with such equipment must go through one or more approval processes, in some instances for each indication for which we want to label the equipment for use (such as use for transfer of a certain gene to a certain tissue). These regulatory processes are extensive and involve substantial costs and time.

        We have limited experience in, and limited resources available, for such regulatory activities. Failure to comply with applicable regulations can, among other things, result in non-approval, suspensions of regulatory approvals, fines, product seizures and recalls, operating restrictions, injunctions and criminal prosecution.

        Any of the following events can occur and, if any did occur, any one could have a material adverse effect on our business, financial conditions and results of operations:

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We cannot predict the safety profile of the use of our electroporation system when used in combination with other therapies.

        Inovio's historical clinical trials involve the use of its electroporation system in combination with certain DNA vaccines. While the data Inovio previously evaluated suggested the use of electroporation does not alone have significant adverse effects nor increase the adverse effects of other therapies, we cannot predict if this outcome will continue to be true or whether possible adverse side effects directly attributable to the vaccines provided by our partners and collaborators or developed internally will compromise the safety profile of the electroporation-based DNA delivery system when used in certain combination therapies. In some instances, clinical results may not clearly indicate whether possible adverse effects are related to our technology versus other study related factors. Even in cases where adverse effects can be shown to be attributable to other study-related factors, not to our technology, the capital markets may not always understand or accept this distinction, and announcements of such adverse events may cause a drop in the market price of our common stock.

We could be substantially damaged if the third parties we rely on to perform our clinical trials do not adhere to protocols defined in clinical trial agreements or meet expected deadlines.

        Like many companies our size, we do not have the ability to conduct preclinical or clinical studies for our product candidates without the assistance of third parties who conduct the studies on our behalf. VGX historically has worked with toxicology facilities, and Inovio and VGX have historically worked with clinical research organizations, or "CROs," that have significant resources and experience in the conduct of pre-clinical and clinical studies. The toxicology facilities conduct the pre-clinical safety studies as well as all associated tasks connected with these studies. The CROs typically perform patient recruitment, project management, data management, statistical analysis and other reporting functions. In addition, Inovio historically has worked with a number of hospitals to perform clinical trials, primarily in the field of oncology.

        The combined group anticipates working with such toxicology facilities, CROs and hospitals to perform clinical trials related to its gene-based therapy programs. We will depend on these third parties to recruit patients for our trials, to perform the trials according to our protocols, and to report the results in a thorough, accurate and consistent manner. Our reliance on these third parties for development activities reduces our control over these activities. Although we anticipate having agreements with these entities which should govern what each party is to do with respect to each protocol, patient safety and informed consent, and avoidance of conflict of interest, the risks remain that the terms of the contracts will not be followed, such as the following:

        Possible Deviations from Protocol.     The entities or the physicians and staff working at them may not perform the trials correctly. It is also possible that the occurrence of serious adverse events during a trial may require physicians and staff, in their medical judgment, to deviate from protocol in response to medical emergencies. In either case, deviations from our protocol may make the clinical data not useful and the trial could become essentially worthless.

        Potential for Conflict of Interest.     Physicians working on protocols may have an improper economic interest in our company, or other conflict of interest. When a physician has a personal stake in the success of the trial, such as when a physician owns stock, or rights to purchase stock of the trial sponsor, it can create suspicion that the trial results were improperly influenced by the physician's

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interest in economic gain. Not only can this put the clinical trial results at risk, but it can also cause serious damage to a company's reputation.

        Patient Safety and Consent Issues.     Physicians and hospitals may fail to secure formal written consent as instructed or report adverse effects that arise during the trial in the proper manner, which could put patients at unnecessary risk. Physicians and hospital staff may fail to observe proper safety measures such as the mishandling of used medical needles, which may result in the transmission of infectious and deadly diseases, such as HIV. This increases our liability, affects the data, and can damage our reputation.

        Compliance with Regulations Governing Use of Human Subjects in Research.     The use of human subjects in research is a heavily regulated area. Physicians, staff, and the Institutional Review Boards overseeing their use of human subjects may fail to comply with such regulations, potentially putting patients at risk, increasing our liability, affecting the validity of the data, and damaging our reputation.

        If these third parties do not successfully carry out their contractual duties or regulatory obligations or meet expected deadlines, or if the quality or accuracy of the clinical data they obtain is compromised due to the failure to adhere to our clinical protocols or for other reasons, our clinical trials may be extended, delayed or terminated. If these third parties do not successfully carry out their contractual duties or meet expected deadlines, we may be required to replace them. Although we believe there are a number of third-party contractors we could engage to continue these activities, replacing a third-party contractor may result in a delay of a particular trial. If any of these events were to occur, then it could have a material adverse effect on our ability to receive regulatory authorization to sell our products, and on our reputation. Negative events that arise in the performance of clinical trials sponsored by biotechnology companies of our size and with limited cash reserves have resulted in companies going out of business. While these risks are always present, to date, Inovio's and VGX's contracted physicians and clinics have been successful in collecting significant data regarding the clinical protocols under which they have operated, and neither Inovio nor VGX is aware of any conflicts of interest or improprieties regarding its protocols.

Even if our products are approved by regulatory authorities, if we fail to comply with on-going regulatory requirements, or if we experience unanticipated problems with our products, these products could be subject to restrictions or withdrawal from the market.

        Any product for which we obtain marketing approval, along with the manufacturing processes, post-approval clinical data and promotional activities for such product, will be subject to continual review and periodic inspections by the FDA and other regulatory bodies. Even if regulatory approval of a product is granted, the approval may be subject to limitations on the indicated uses for which the product may be marketed or to certain requirements resulting in costly post-marketing testing and surveillance to monitor the safety or efficacy of the product. Later discovery of previously unknown problems with our products, including unanticipated adverse events of unanticipated severity or frequency regarding manufacturer or manufacturing processes or failing to comply with regulatory requirements, may result in restrictions on such products or manufacturing processes, withdrawal of the products from the market, voluntary or mandatory recall, fines, suspension of regulatory approvals, product seizures or detention, injunctions or the imposition of civil or criminal penalties.

Failure to comply with foreign regulatory requirements governing human clinical trials and marketing approval for our human-use equipment could prevent us from selling our products in foreign markets, which may adversely affect our operating results and financial conditions.

        For marketing our electroporation systems outside the U.S., the requirements governing the conduct of clinical trials, product licensing, pricing and reimbursement vary greatly from country to country and may require additional testing. The time required to obtain approvals outside the U.S. may

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differ from that required to obtain FDA approval. We may not obtain foreign regulatory approval on a timely basis, if at all. Approval by the FDA does not ensure approval by regulatory authorities in other countries, and approval by one foreign regulatory authority does not ensure approval by regulatory authorities in other countries or by the FDA. Failure to comply with these regulatory requirements or to obtain required approvals could impair our ability to develop these markets and could have a material adverse affect on our results of operations and financial condition.

Our ability to achieve significant revenues from sales or leases of human-use products will depend on establishing effective sales, marketing and distribution capabilities or relationships and we currently lack substantial experience in these areas.

        To market our products, we will need to develop sales, marketing and distribution capabilities. In order to develop or otherwise obtain these capabilities, we may have to enter into marketing, distribution or other similar arrangements with third parties in order to sell, market and distribute our products successfully. To the extent that we enter into any such arrangements with third parties, our product revenue is likely to be lower than if we marketed and sold our products directly, and our revenues will depend upon the efforts of these third parties.

        We have limited experience in sales, marketing and distribution of clinical and human-use products and we currently have no sales, marketing or distribution capability. If we decide to market and sell our human-use products directly, we must develop a marketing and sales capability. This would involve substantial costs, training and time. We may be unable to develop sufficient sales, marketing and distribution capabilities to commercialize our products successfully. Because the laws, regulations, and industry guidelines with respect to sales, marketing and distribution of clinical and human-use products are becoming increasingly stringent, our lack of experience may cause us to fail to comply or fail to cause contracting third parties to comply, exposing us to liability. Regardless of whether we elect to use third parties or seek to develop our own marketing capability, we may not be able to successfully commercialize any product.

Delays in the approval of LifeTideTM SW 5 in other countries may affect our financial results.

        VGX has been, and the combined group will continue, actively seeking to leverage the approval of its product, LifeTideTM SW 5, in Australia to attain approval in neighboring countries such as New Zealand, Philippines and Indonesia. We have limited experience in, and limited resources available for overseeing the approval of our drug in these countries and will have to rely on third-party consultants to assist us in attaining approval. Delays in attaining regulatory approval in these countries will adversely affect future revenues.

Changes in the market conditions in the global porcine market may affect our future results.

        Our GHRH DNA therapy for porcine application, LifeTideTM SW 5, is sold through veterinarians to farmers in Australia. The demand for our product is highly correlated with the price of swine in the marketplace. As such, our expected revenue from the sale of LifeTideTM SW 5 is subject to the commodity price risk of the porcine market. We do not hedge the commodity price risk using derivatives. As the porcine market fluctuates, so will our expected revenues from this product.

We rely on collaborative and licensing relationships to fund a portion of our research and development expenses. If we are unable to maintain or expand existing relationships, or initiate new relationships, we will have to defer or curtail research and development activities in one or more areas.

        Our partners and collaborators fund a portion of our research and development expenses and assist us in the research and development of our human-use equipment and therapies. These collaborations and partnerships help pay the salaries and other overhead expenses related to research.

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In the past, Inovio has encountered operational difficulties after the termination of an agreement by a former partner. Because this partnership was terminated, Inovio did not receive significant milestone payments which it had expected and was forced to delay some clinical trials as well as some product development. Although we believe our relationships with our partners and collaborators are stable and good, we may experience such operational difficulties or termination of such relationships without anticipated payment again in the future.

        We also rely on scientific collaborators at companies and universities to further expand our research and to test our equipment. In most cases, we lend our equipment to a collaborator, teach him or her how to use it, and together design experiments to test the equipment in one of the collaborator's fields of expertise. We aim to secure agreements that restrict collaborators' rights to use the equipment outside of the agreed upon research, and outline the rights each of the parties will have in any results or inventions arising from the work.

        Nevertheless, there is always potential that:

        The results from these collaborations may not be successful. We may not be able to continue to collaborate with individuals and institutions that will further develop our products, and we may not be able to do so under terms that are not overly restrictive. If we are not able to maintain or develop new collaborative relationships, it is likely that our research pace will slow down and that it will take longer to identify and commercialize new products, or new indications for our existing products.

A small number of licensing partners and government contracts account for a substantial portion of our revenue in each period and our results of operations and financial condition could suffer if we lose these licensing partners or fail to add additional licensing partners in the future.

        We derive a significant portion of our revenue from a limited number of licensing partners and government grants and contracts in each period. Accordingly, if we fail to sign additional future contracts with major licensing partners and the government, if a contract is delayed or deferred, or if an existing contract expires or is cancelled and we fail to replace the contract with new business, our revenue could be adversely affected.

        Until commercialization of our Medpulser® Electroporation System or our gene-based therapies, we expect that a limited number of licensing partners will continue to account for a substantial portion of our revenue in each quarter in the foreseeable future. During the years ended December 31, 2007 and 2006, one licensing partner, Merck, accounted for approximately 68% and 44%, respectively, of Inovio's consolidated revenue. During the year ended December 31, 2007 another licensing partner, Wyeth, accounted for 23% of Inovio's consolidated revenue. During the three and nine months ended September 30, 2008, one licensing partner, Merck, accounted for approximately 53% and 40% of Inovio's consolidated revenue, respectively, and another licensing partner, Wyeth, accounted for 22%

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and 42% of Inovio's consolidated revenue, respectively. During the three and nine months ended September 30, 2007, Merck accounted for 55% and 69% of Inovio's consolidated revenue, respectively, and Wyeth accounted for 15% of Inovio's consolidated revenue.

        VGX to date has relied on government grants and contracts for a substantial portion of its revenues. During the years ended December 31, 2007 and 2006, government grants and contracts accounted for 95% and 100%, respectively, of VGX's consolidated revenue from its continuing operations. During the nine months ended September 30, 2007 and 2008, government grants and contracts accounted for 96% and 92%, respectively, of VGX's consolidated revenues from its continuing operations.

If we cannot maintain our existing corporate and academic arrangements and enter into new arrangements, we may be unable to develop products effectively, or at all.

        Our strategy for the research, development and commercialization of our product candidates may result in our entering into contractual arrangements with corporate collaborators, academic institutions and others. We have entered into sponsored research, license and/or collaborative arrangements with several entities, including Merck, Wyeth, Dow Global Technologies, Vical, Valentis, the U.S. Navy, Chiron, the University of Pennsylvania, Baylor University, and the University of South Florida, as well as numerous other institutions that conduct clinical trials or perform pre-clinical research for us. Our success depends upon our collaborative partners performing their responsibilities under these arrangements and complying with the regulations and requirements governing clinical trials. We cannot control the amount and timing of resources our collaborative partners devote to our research and testing programs or product candidates, or their compliance with regulatory requirements which can vary because of factors unrelated to such programs or product candidates. These relationships may in some cases be terminated at the discretion of our collaborative partners with only limited notice to us; for example, Merck can terminate its May 2004 license and collaboration agreement with us at any time in its sole discretion, without cause, by giving ninety days' advance notice to us. During the years ended December 31, 2007 and 2006, Merck accounted for approximately 68% and 44%, respectively, of Inovio's consolidated revenue, and 52%, on a pro forma basis for the year ended December 31, 2007 when combined with VGX. During the three and nine months ended September 30, 2008, Merck accounted for approximately 53% and 40% of Inovio's consolidated revenue, respectively, and 18% on a pro forma basis for the nine months ended September 30, 2008 when combined with VGX. If Merck were to terminate its agreement with us, the combined group may not be able to maintain Inovio's and VGX's existing arrangements, enter into new arrangements or negotiate current or new arrangements on acceptable terms, if at all. Some of our collaborative partners may also be researching competing technologies independently from us to treat the diseases targeted by our collaborative programs.

We rely heavily on our patents and proprietary rights to attract partnerships and maintain market position.

        The strength of our patent portfolio is an important factor that will influence our success. Patents give the patent holder the right to prevent others from using or selling its patented technology. When someone infringes upon a patent, the patent holder has the right to initiate legal proceedings against that person to prevent such infringing acts. These proceedings, however, can be lengthy and costly. Inovio and VGX historically performed, and we will perform, an ongoing review of our patent portfolio to confirm that our key technologies are adequately protected. If we determine that any of our patents require either additional disclosures or revisions to existing information, we may ask that such patents be reexamined or reissued, as applicable, by the U.S. Patent and Trademark Office.

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        The patenting process, enforcement of issued patents, and defense against claims of infringement are inherently risky. Because we rely heavily on patent protection, we face the following significant risks:

        Possibility of Inadequate Patent Protection for Product.     The U.S. Patent and Trademark Office or foreign patent offices may not grant patents of meaningful scope based on the applications we have already filed and those we intend to file. If we do not have patents that adequately protect our human-use equipment and indications for its use and other therapies, then we will not be competitive.

        Potential That Important Patents Will Be Judged Invalid.     Some of the issued patents we now own or license may be determined to be invalid. If we have to defend the validity of any of our patents, the costs of such defense could be substantial, and the outcome may not be successful. In the event an important patent related to our drug delivery technology is found to be invalid, we may lose competitive position and may not be able to receive royalties for products covered in part or whole by that patent under license agreements.

        Danger of Being Charged With Infringement.     Although neither Inovio nor VGX is currently aware of any basis for an infringement claim or any parties intending to pursue infringement claims against it, there is the possibility that the combined group may use or sell a patented technology owned by another person and/or be charged with infringement. Defending or indemnifying a third party against a charge of infringement can involve lengthy and costly legal actions, and the outcome may not be successful. Biotechnology companies comparable to us in size and financial position have discontinued business after losing infringement battles. If we or our partners were prevented from using or selling our human-use equipment, then our business would be materially adversely affected.

        Freedom to Operate Issues.     Inovio and VGX are aware that patents related to electrically-assisted drug delivery have been granted to, and patent applications have been filed by, our potential competitors. Each of Inovio and VGX or its partners have received licenses to operate under some of these patents, and the combined group will consider procuring additional licenses in the future. Nevertheless, the competitive nature of our field of business and the fact that others have sought patent protection for technologies similar to ours make these potential issues significant.

        In addition, as a result of the sale of VGX's DNA plasmid manufacturing assets to VGXI, Inc. in June 2008, VGX does not have control of certain patents relating to the current manufacturing technology for products used in VGX's pre-clinical and clinical studies and anticipated pre-clinical and clinical studies of the combined group. The rights under these patents could be lost, either by loss of rights by VGXI, Inc., for example, through abandonment of one or more patents, or by any decision of VGXI, Inc. to manufacture for other clients. If VGXI, Inc. were to lose those rights, VGX, and upon completion of the Merger, if approved, the combined group would need to expend resources to find another manufacturer and another manufacturing technology for these products.

        In addition to patents, we also rely on trade secrets and proprietary know-how. We take customary measures to protect this information with appropriate confidentiality and inventions agreements with our employees, scientific advisors, consultants, and collaborators. We cannot be sure that these agreements will not be breached, that we will be able to protect ourselves if they are breached, or that our trade secrets will not otherwise become known or be independently discovered by competitors. We also cannot be sure that academic and research institutions with which we have research arrangements may not create or improve upon our intellectual property and use that intellectual property in future research to which our competitors might have access. If any of these events occur, then we face the potential of losing control over valuable company information, which could negatively affect our competitive position.

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The rights our company relies upon to protect the intellectual property underlying our products may not be adequate, which could enable third parties to use our technology and would reduce our ability to compete in the market.

        The combined group's success will depend in part on its ability to develop or acquire commercially valuable patent rights and to protect its intellectual property. Our patent position is generally uncertain and involves complex legal and factual questions. The degree of present and future protection of our proprietary rights is uncertain.

        The risks and uncertainties that our company faces with respect to our patents and other proprietary rights include the following:

        In addition to patents, our company relies on a combination of trade secrets, nondisclosure agreements and other contractual provisions and technical measures to protect our intellectual property rights. Nevertheless, these customary measures may not be adequate to safeguard the technology underlying our products. If these measures do not protect our rights, third parties could use our technology and our ability to compete in the market would be reduced. In addition, employees, consultants and others who participate in the development of our products may breach their agreements with us regarding our intellectual property, and we may not have adequate remedies for the breach. We also may not be able to effectively protect our intellectual property rights in some foreign countries. For a variety of reasons, our company may decide not to file for patent, copyright or trademark protection or prosecute potential infringers of our patents. Our trade secrets may also become known through other means not currently foreseen by us. Despite our efforts to protect our intellectual property, our competitors or customers may independently develop similar or alternative technologies or products that are equal or superior to our technology and products without infringing on any of our intellectual property rights or design around our proprietary technologies.

Claims by others that our products infringe on their proprietary rights could adversely affect our ability to sell our products and could increase our costs.

        Substantial litigation over intellectual property rights exists in our industry. Our company expects that its products could be increasingly subject to third-party infringement claims as the number of competitors in our industry grows and the functionality of products and technology in different industry segments overlaps. Third parties may currently have, or may eventually be issued, patents which our products or technology may be alleged to infringe. Any of these third parties might make a claim of

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infringement against our company. Any litigation could result in the expenditure of significant financial resources and the diversion of management's time and resources. In addition, litigation in which our company is accused of infringement may cause negative publicity, have an impact on prospective customers, cause product shipment delays or require our company to develop non-infringing technology, make substantial payments to third parties, or enter into royalty or license agreements, which may not be available on acceptable terms, or at all. If a successful claim of infringement were made against our company and our company could not develop non-infringing technology or license the infringed or similar technology on a timely and cost-effective basis, our company's revenue may decrease and we could be exposed to legal actions by our customers.

If we are not successful in developing our current products, our business model may change as our priorities and opportunities change and our business may never develop to be profitable or sustainable.

        Inovio and VGX both have historically managed numerous programs and actively sought to develop product and program pipelines. As a result, there are many products and programs that seem promising to us which we could pursue, and a significant part of the parties' integration process, if the Merger is completed, will be to continue to focus our efforts and allocate our available resources to particular programs and products. However, with limited resources, we may decide to change priorities and shift programs away from those that Inovio and VGX have been pursuing for the purpose of exploiting the combined company's joint strengths of its core electroporation technology and development capabilities for gene-based therapeutics. The choices we make will be dependent upon numerous contemporaneous factors, some of which we cannot predict. We cannot be sure that our business model, as initially integrated or as it may evolve, will enable us to become profitable or to sustain operations.

Serious and unexpected side effects attributable to gene therapy may result in governmental authorities imposing additional regulatory requirements or a negative public perception of our products.

        The gene therapy or DNA vaccine product candidates under development could be broadly described as gene therapies. A number of clinical trials are being conducted by other pharmaceutical companies involving gene therapy, including compounds similar to, or competitive with, our product candidates. The announcement of adverse results from these clinical trials, such as serious unwanted and unexpected side effects attributable to treatment, or any response by the FDA or foreign regulatory agencies to such clinical trials, may impede the progress of our clinical trials, delay or prevent us from obtaining regulatory approval, or negatively influence public perception of our product candidates, which could harm our business and results of operations and reduce the value of our stock.

        The U.S. Senate has held hearings concerning the adequacy of regulatory oversight of gene therapy clinical trials, as well as the adequacy of research subject education and protection in clinical research in general, and to determine whether additional legislation is required to protect volunteers and patients who participate in such clinical trials. The Recombinant DNA Advisory Committee, or RAC, which acts as an advisory body to the National Institutes of Health, has expanded its public role in evaluating important public and ethical issues in gene therapy clinical trials. Implementation of any additional review and reporting procedures or other additional regulatory measures could increase the costs of or prolong our product development efforts or clinical trials.

        As of September 30, 2008, to our knowledge, there have not been any serious adverse events in any gene therapy clinical trials in which our technology was used. In the future, if one or a series of serious adverse events were to occur during a gene therapy clinical trial in which our technology was used, we would report all such events to the FDA and other regulatory agencies as required by law. Such serious adverse events, whether treatment-related or not, could result in negative public perception of our treatments and require additional regulatory review or other measures, which could

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increase the cost of or prolong our gene therapy clinical trials or require us to halt our clinical trials altogether.

        The commercial success of our products will depend in part on public acceptance of the use of gene therapy products or gene-induced products, which are a new type of disease treatment for the prevention or treatment of human diseases. Public attitudes may be influenced by claims that gene therapy products or gene-induced products are unsafe, and these treatment methodologies may not gain the acceptance of the public or the medical community. Negative public reaction to gene therapy products or gene-induced products could also result in greater government regulation and stricter clinical trial oversight.

No gene therapy products have been approved by the FDA to date and we cannot assure you that gene therapy products will ever receive approval for commercialization; this lack of precedent may undermine consumer and investor confidence in our therapies, which may depress the market price for our common stock or limit our ability to partner to advance our technologies.

        The FDA has not yet approved any human gene therapy product for sale, and the FDA deems current gene therapy efforts "experimental" on its website. There have been deaths and significant adverse effects in gene therapy clinical trials previously, and in January 2003, the FDA placed a temporary halt on all gene therapy trials using retroviral vectors in blood stem cells. Although such ban has been subsequently eased, gene therapy clinical trials still face strict standards and remain subject to potential future bans or additional oversight if there are further high-profile adverse effects in ongoing gene therapy clinical trials. As a result, investors may be hesitant to invest in or maintain a position in our common stock, creating low trading volumes and stagnant demand for our shares of common stock and limiting our ability to raise funds through equity financing on favorable terms, if at all. Further, the lack of commercial precedent may minimize the number of potential collaborators willing to partner with us long-term, limiting our other sources of operational funding and our ability to advance our gene therapy-technologies as quickly or at all.

We have the potential for product liability issues with our equipment and products.

        The testing, marketing and sale of human-use products expose us to significant and unpredictable risks of equipment product liability claims. These claims may arise from patients, clinical trial volunteers, consumers, physicians, hospitals, companies, institutions, researchers or others using, selling, or buying our equipment. Product liability risks are inherent in our business and will exist even after the products are approved for sale. If and when our human-use equipment is commercialized, we run the risk that use (or misuse) of the equipment will result in personal injury. The chance of such an occurrence will increase after a product type is on the market.

        The testing, marketing and sale of animal-use products expose us to significant and unpredictable risks of potential product liability claims. These claims may arise from farmers, veterinarians, consumers, and anyone coming in contact with our GHRH DNA therapy. We may not be successful in our attempts to manage these inherent product liability risks by using myriad of approaches including, insurance programs, quality control measures and proper training.

        Inovio and VGX have historically maintained, and we will continue to maintain, liability insurance in connection with our ongoing business and products, and we may purchase additional policies if such policies are determined by management to be necessary. However, our existing insurance and the insurance we purchase may not provide adequate coverage in the event a claim is made and we may be required to pay claims directly. If we did have to make payment against a claim, our financial ability to perform the research, development, and sales activities that we have planned would be adversely affected.

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        We also face the risk of potential product defects. Product defects can lead to loss of future sales, decrease in market acceptance, damage to our brand or reputation, product returns and warranty costs, and even product withdrawal from the market. These events can occur whether the defect resides in a component we purchased from a third party or whether it was due to our design and/or manufacture. We attempt to include provisions in our sales agreements designed to limit our exposure to product liability claims, but these provisions may not be enforceable in the countries in which the sale is made. However, we do not know whether these limitations will be enforceable in the countries in which the sale is made. Any product liability or other claim brought against us, if successful and of sufficient magnitude, could negatively impact our financial results and condition.

We cannot be certain that we will be able to manufacture our human-use equipment in sufficient volumes at commercially reasonable costs.

        Our manufacturing facilities for human-use products will be subject to quality systems regulations, international quality standards and other regulatory requirements, including pre-approval inspection for our human-use equipment and periodic post-approval inspections for all human-use products. While Inovio has previously undergone and passed a quality systems audit from an international body, we have never undergone a quality systems inspection by the FDA. We may not be able to pass an FDA inspection when and if it occurs. If our facilities are found not to be compliant with FDA standards in sufficient time, prior to a launch of our product in the U.S., then it will result in a delay or termination of our ability to produce our human-use equipment in our facility. Any delay in production will have a negative affect on our business. While there are no target dates set forth for launch of our products in the U.S., we plan on launching each product once we successfully perform a Phase III clinical study involving a particular use of our technology, obtain the requisite regulatory approval, and engage a partner who has the financial resources and marketing capacity to bring our products to market.

        Our products must be manufactured in sufficient commercial quantities, in compliance with regulatory requirements, and at an acceptable cost to be attractive to purchasers. We rely on third parties to manufacture and assemble most aspects of our equipment, and thus cannot directly control the quality, timing or quantities of equipment manufactured or assembled at any given time.

        Disruption of the manufacture of our products, for whatever reason, could delay or interrupt our ability to manufacture or deliver our products to customers in a timely basis. This would be expected to affect revenue and may affect our long-term reputation, as well. In the event we provide product of inferior quality, we run the risk of product liability claims and warranty obligations, which will negatively affect our financial performance.

There is a possibility that our technology will become obsolete or lose its competitive advantage.

        The vaccine development and delivery business is very competitive, fast moving and intense, and expected to be increasingly so in the future. Other companies and research institutions are developing drug delivery systems and gene-based therapies that, if not similar in type to our systems and therapies, are designed to address the same patient or subject population. Therefore, we cannot promise that our products will be the best, the safest, the first to market, or the most economical to manufacture and use. If competitors' products are better than ours, for whatever reason, then we could become less profitable from product sales and our products could become obsolete.

        There are many reasons why a competitor might be more successful than us, including:

        Financial Resources.     Some competitors have greater financial resources and can afford more technical and developmental setbacks than we can.

        Greater Experience.     Some competitors have been in the biomedical business longer than we have. They have greater experience than us in critical areas like clinical testing, obtaining regulatory approval

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and sales and marketing. This experience or their name recognition may give them a competitive advantage over us.

        Superior Patent Position.     Some competitors may have better patent protection over their technology than we have or will have in order to protect our technology. If we cannot use our patents to prevent others from copying our technology or developing similar technology, or if we cannot obtain a critical license to another's patent that we need to manufacture and use our equipment, then we would expect our competitive position to weaken.

        Faster to Market.     Some companies with competitive technologies may move through stages of development, approval, and marketing faster than us. If a competitor receives FDA approval, or regulatory approval in another major market outside the U.S., before us, then it will be authorized to sell its products before we can sell ours. Because the first company "to market" often has a significant advantage over others, a second place position could result in less than anticipated sales.

        Reimbursement Allowed.     In the U.S., third party payers, such as Medicare, may reimburse physicians and hospitals for competitors' products but not for our own human-use products. This would significantly affect our ability to sell our human-use products in the U.S. and would have a negative impact on revenue and our business as a whole. Outside of the U.S., reimbursement and funding policies vary widely.

The restructuring and repricing of certain VGX options and warrants may not have remedied certain issues arising under federal tax law and could expose VGX or the combined group to certain risks.

        Prior to August 2006, VGX issued options and warrants to employees and consultants that did not comply with the provisions Section 409A of the Code. In September 2008, the VGX board of directors approved two methods to bring these noncompliant options and warrants into compliance with section 409A of the Code. Each holder of non-compliant options and warrants was given the choice of either agreeing to reset the exercise price at a value that was no less than the fair market value of VGX common stock on the date of the repricing, as determined by the VGX board of directors, which considered in part preliminary work performed by an independent valuation firm, or making a forward election in which the holder was given the option to choose a date after December 31, 2008 on or after which to exercise the option or warrant. VGX cannot assure stockholders that these steps were sufficient to cure any non-compliance by VGX with respect to 409A of the Code and, if these steps are deemed insufficient, VGX, or the combined group upon closing of the Merger, could face potential tax liability under the Code.

Any acquisition we might make may be costly and difficult to integrate, may divert management resources or dilute stockholder value.

        Both Inovio and VGX have considered and made strategic acquisitions in the past, and in the future the combined group may acquire or invest in complementary companies, products or technologies. As part of our business strategy, we may acquire assets or businesses principally relating to or complementary to the combined group's integrated operations. Any acquisitions we undertake will be accompanied by issues commonly encountered in business acquisitions, which could adversely affect us, including:

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        In addition, geography and/or language barriers may make the integration of businesses more difficult. We may not be successful in overcoming these risks or any other problems encountered in connection with any of our acquisitions, and we cannot assure you that the results of any acquisition, if completed, will meet the expectations of the parties and their stockholders.

Some of VGX's officers have positions with subsidiaries and affiliates of VGX, which may have interests that could conflict with those of the combined group.

        Certain officers and directors of VGX hold officer or director positions with non-wholly owned affiliates or subsidiaries of VGX with which VGX transacts business. For example, J. Joseph Kim, VGX's chief executive officer, is a director and officer of VGX Animal Health, Inc., an 88% owned subsidiary and of VGX International, Inc., a 30% owned affiliate, each as of the record date. Dr. Kim intends to resign from his officer position with VGX International, Inc. on or before the closing of the Merger, but expects to continue as a director of that entity. Transactions and other business activities of these two entities may conflict with the interests of VGX and the combined group after the merger, and, as officers or directors of these other entities, these persons may have conflicting fiduciary duties.

We may not meet environmental guidelines and as a result could be subject to civil and criminal penalties.

        Like all companies in the biomedical industry, we are subject to a variety of governmental regulations relating to the use, storage, discharge and disposal of hazardous substances. Our safety procedures for handling, storage and disposal of such materials are designed to comply with applicable laws and regulations. While both Inovio and VGX believe they are currently in compliance with all material applicable environmental regulations, if either party or the combined group is subsequently found to not comply with environmental regulations, or is involved with contamination or injury from these materials, then we may be subject to civil and criminal penalties. This would have a negative impact on our reputation and finances, and could result in a slowdown or even complete cessation of our business.

Changes in foreign exchange rates may affect our future operating results.

        Inovio and VGX both maintain investments in foreign subsidiaries. During the years ended December 31, 2007 and 2006, Inovio AS, Inovio's wholly-owned Norwegian subsidiary, contributed approximately $159,000 and $1.1 million to Inovio's revenue, respectively, which amounted to approximately 3% and 33% of Inovio's total revenue. Inovio AS conducts its operations primarily in foreign currencies, including the Euro, Norwegian Kroner and Swedish Krona. In September 2006, Inovio established Inovio Asia Pte. Ltd., a wholly-owned company incorporated in the Republic of Singapore, which conducts its operations primarily in Singaporean dollars. VGX holds 30.37% of the outstanding shares of VGX International, a publicly-traded company on the Korean Stock Exchange whose functional currency is the Korean Won. VGX Animal Health markets its LifeTideTM SW 5 GHRH DNA therapy to the porcine market in Australia. As such, all revenues from marketing of LifeTideTM SW 5, and payments made to any vendors in Australia, will be in Australian Dollars. Fluctuation in the values of these foreign currencies relative to the U.S. dollar will affect our financial results which are reported in U.S. dollars and will cause U.S. dollar translation of such currencies to vary from one period to another. We cannot predict the scope of any fluctuations in the values of these

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foreign currencies relative to the U.S. dollar nor the effect of exchange rate fluctuations upon our future operating results.

Inovio's restructuring of its Norwegian subsidiary, Inovio AS, may not realize the efficiencies anticipated and could result in additional, unanticipated liabilities, which would have a negative effect on our financial condition.

        On December 31, 2007, Inovio's wholly-owned Norwegian subsidiary Inovio AS transferred certain patent and other intellectual property rights to Inovio's wholly-owned U.S. subsidiary, Genetronics. The value assigned to these rights was $1.9 million, which was determined by and was the responsibility of management of Inovio, who considered in part preliminary work performed by an independent valuation specialist in Norway. All Norwegian tax gains associated with this transfer of the patents and other intellectual property rights was offset by prior year tax loss carry forwards. Subsequent to year-end, Inovio changed the name of Inovio AS to Inovio Tec AS. Simultaneously, Inovio incorporated a new Norwegian wholly-owned subsidiary under the name Inovio AS, for the purpose of organizing a research effort directed towards the development of specific cancer vaccine candidates. In January 2008, all employees, employee agreements, lease agreements and fixed assets were transferred from Inovio Tec AS to Inovio AS. In December 2008, the parties entered into a Master Cross-Licensing Agreement, providing for a non-exclusive license to Inovio AS of certain Inovio intellectual property rights, relating to gene delivery for cancer treatment, as well as a non-exclusive license to Inovio of all intellectual property rights developed by Inovio AS, subject only to certain exclusive product development, manufacturing and commercialization rights retained by Inovio AS. Further, although Inovio and its board of directors retain ultimate control over and responsibility for Inovio AS, Inovio AS now has a distinct board of directors, consisting of two members of Inovio's board of directors—Dr. Avtar Dhillon and Simon Benito—and two Norwegian personnel, intended to allow more efficient balancing of U.S. legal and regulatory concerns with Norwegian legal and regulatory concerns in the course of decision-making.

        This restructuring of Inovio's Norwegian operations was intended to better focus the research and development efforts conducted in Norway on Inovio's strategic programs and ease access to previously developed intellectual property rights for Inovio and its other subsidiaries, through a Master Research Agreement among Inovio and its other subsidiaries and VGX. We expect funding for this program to be about $5.0 million over the next several years. Although designed to be tax-neutral to the parties, we cannot assure you that the tax authorities in Norway or the U.S. will agree with the valuation of the transferred assets or the procedures through which the transfers were made. If such disagreements were to arise, we may face unanticipated tax liabilities in Norway or the U.S. arising from the asset transfer. Further, as there will be an ongoing licensing relationship between the parties post-transfer, it is possible that such arrangements will receive heightened scrutiny for potential transfer pricing issues, which could result in additional liability to us. We believe that the new Inovio AS is now appropriately organized and staffed, and has the necessary resources and commitments for future resources to conduct its research and development efforts in support of our business strategy. However, we cannot assure stockholders that Inovio AS will not require further staff or financing beyond these initial commitments, or that we will be able to provide such resources if and when requested. To the extent Inovio AS or we face additional tax or transfer pricing issues, our operating results and overall financial condition may be adversely affected. In particular, if we are unable to provide additional support for Inovio AS when requested, Inovio AS may not be able to reach previously specified targets and milestones in a timely manner, undermining its financial stability and the commercial potential for its prostate cancer vaccine program.

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Some of our facilities are located near known earthquake fault zones, and the occurrence of an earthquake or other catastrophic disaster could cause damage to our facilities and equipment.

        Our San Diego facility is located near known earthquake fault zones and is vulnerable to damage from earthquakes. All of our facilities are also vulnerable to damage from other types of disasters, including fire, floods, power loss, communications failures and similar events. If any disaster were to occur, our ability to operate our business at our facilities would be seriously impaired. In addition, the unique nature of our research activities could cause significant delays in our programs and make it difficult for us to recover from a disaster. The insurance we maintain may not be adequate to cover our losses resulting from disasters or other business interruptions. Accordingly, an earthquake or other disaster could materially and adversely harm our ability to conduct business.

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THE TRANSACTION

         The discussion in this joint proxy statement/prospectus of the Merger and the principal terms of the Acquisition Agreement are subject to, and are qualified in their entirety by reference to, the Acquisition Agreement, a copy of which is attached to this joint proxy statement/prospectus as Annex A and incorporated into this joint proxy statement/prospectus by reference.

General Description of the Merger

        Inovio, its wholly-owned acquisition subsidiary referenced in this joint proxy statement/prospectus as Submerger, and VGX have agreed to a business combination pursuant to the terms of the Acquisition Agreement and in accordance with the DGCL. Upon consummation of the Merger, VGX will be merged with and into Submerger, VGX will cease to exist and Submerger will continue as the surviving entity and as a wholly-owned subsidiary of Inovio and change its name to "VGX Pharmaceuticals, LLC." The ongoing public entity will be known as Inovio Biomedical Corporation, which shall hold, as directly wholly-owned subsidiaries, VGX Pharmaceuticals, LLC and Inovio's current direct subsidiaries, including Genetronics, and the combined group shall integrate the historical operations of Inovio and VGX.

        In consideration for the Merger, Inovio will issue and otherwise allocate for issuance under options and warrants to purchase common stock and debt convertible into common stock, a total of up to 60,689,523 shares of new Inovio common stock pursuant to the terms of the Acquisition Agreement. Specifically, upon closing of the Merger, based on an exchange ratio and on the terms and conditions of which are described in this joint proxy statement/prospectus:

        Based on the respective fully-diluted share capitals of Inovio and VGX as of the record date and certain VGX option exercises anticipated prior to closing, the parties anticipate that the Merger Exchange Ratio will be approximately 0.9911488, meaning that each share of VGX common stock will be exchanged for 0.9911488 shares of Inovio common stock upon closing of the Merger.

        Other than the significant dilution resulting from the issuance of Inovio securities in conjunction with the Merger, the outstanding shares of Inovio common stock prior to the Merger will not be impacted by the Merger. Similarly, the Merger will not affect any of Inovio's other outstanding securities, other than accelerating the vesting rights of Inovio's outstanding options to purchase shares of Inovio common stock (presuming the related 2000 Plan Amendment, as discussed elsewhere in this joint proxy statement/prospectus, receives Inovio stockholder approval).

        The parties anticipate that the Merger, if completed, will result in a full integration of the existing Inovio and VGX organizations, including appointment of an integrated board of directors and management team consistent with the terms of the Acquisition Agreement, and the combination of significant administrative functions at Inovio's San Diego, California headquarters.

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Background to the Transaction

        Both Inovio and VGX regularly evaluated various strategies for improving their respective competitive positions and enhancing stockholder value. As part of these evaluations, the parties have, from time to time, considered strategic initiatives in the pursuit of their business plans, including acquisitions, divestitures and possible business combinations. Inovio's management and board of directors regularly discussed the position and prospects of Inovio within various segments of the biopharmaceutical industry, and VGX's leadership similarly evaluated its position and prospects. The parties' boards of directors regularly reviewed short and long-term business strategies, as well as market trends in the biopharmaceutical industry and the challenges confronting each company in achieving its business objectives.

        Inovio's long-term strategic plan includes diversifying its product pipeline through acquisitions, collaborations, alliances or joint ventures. Inovio's management developed criteria for identifying public and private companies that might fit its strategic plan. The criteria emphasized vaccine and immunotherapy based infectious disease and cancer companies with synergistic clinical development programs which use electroporation or a technology complimentary to electroporation assisted delivery. Starting in late 2005 through May 2008, Inovio conducted a targeted process to identify appropriate acquisition candidates, during which Inovio contacted numerous companies to assess their potential interest in engaging in an acquisition, collaboration, alliance or joint venture arrangements. As a result of these efforts, Inovio's management team met with seven of these companies to explore whether the opportunity existed for a transaction that fit the Inovio strategic plan and would potentially enhance perceived stockholder value. Inovio conducted substantive scientific due diligence on several of these companies during this period, and Inovio's management kept its board of directors informed of these discussions both informally and through reports at board meetings.

        Inovio also reviewed a larger list other non-electroporation based delivery companies, but felt it would be difficult to pursue a deal unless these companies where not able meet a significant milestone with their competing technology. Some of the additional considerations that influenced the gradual elimination of certain companies from being final candidates were the following:

        Like Inovio, VGX's long-term strategic plans for growth have included diversification through acquisitions and collaborations. The VGX management team has explored several different approaches toward growth, including:

        In 2007, the VGX board of directors made the decision to accelerate this strategy by engaging Needham and Company, LLC, or "Needham," to act as its investment advisor. Together with Needham, VGX began a systematic process of identifying and contacting those companies that potentially met its criteria for a merger or an acquisition. Merger candidates were ranked based on multiple criteria, the most important of which was the candidate's technology and its strategic fit with VGX's long-term goals. Other key criteria were the candidate's management capability, strength of its balance sheet, and its status as a public or a private company. After an extensive search and analysis, which included meetings with several companies, VGX's management and board of directors reached

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the conclusion that, given its long-term goal of becoming a dominant player in the DNA vaccines market, Inovio was the ideal candidate with whom VGX should pursue its strategy. In December 2007, the VGX board of directors and management decided to initiate inquiries to Inovio to gauge its interest in potential "merger of equals" of the two companies.

        In January 2008, representatives from VGX contacted Inovio to inquire about its interest in exploring a potential business combination transaction. Both companies' management expressed interest in exploring the feasibility of such a transaction. Shortly thereafter, the parties executed customary confidentiality agreements on January 28, 2008, allowing them to initiate due diligence. On February 11, 2008, representatives of VGX's and Inovio's management teams met at Inovio's offices in San Diego to discuss their respective businesses, programs and technology platforms, and to explore the feasibility of a business combination between VGX and Inovio. Following these general discussions, VGX and Inovio agreed that more in-depth discussions were warranted and the exchange of business information continued.

        At its regular meeting on February 15, 2008, Inovio management briefed its board of directors on the ongoing process to identify possible acquisition candidates and on management's current assessment of the degree of strategic fit for each of the active prospects. Management also presented a detailed review of the drug pipeline and potential synergies of seven possible business combination candidates viewed as the best strategic fit of the parties reviewed to date, which included VGX. After discussing these presentations, the board of directors authorized management to approach each of these companies with preliminary indications of interest for a strategic acquisition, while continuing efforts to identify other potential acquisition candidates. Subsequent to that meeting, Inovio's management conducted initial scientific diligence and engaged in detailed discussions with each of these seven candidates to assess the feasibility of a transaction that met Inovio's strategic objectives, and ultimately Inovio's management believed that VGX presented the best opportunity for Inovio and its stockholders.

        On February 20, 2008, Inovio's chief executive officer, Dr. Avtar Dhillon, met with VGX's chief executive officer, Dr. J. Joseph Kim, to advance discussions regarding a potential business combination. The chief executive officers met a number of times thereafter to discuss potential terms and conditions for a draft letter of intent for a proposed business combination to be presented to their respective boards of directors.

        On March 14, 2008, Inovio received a preliminary, non-binding indication of interest, or indicative proposal, from VGX and its financial advisor, Needham. The Inovio board of directors met later that day, during which Inovio's management reported on its meetings with VGX and the indicative proposal received from VGX and Needham regarding the proposed transaction was presented for board of directors for approval. The Inovio board of directors authorized management to continue discussions with VGX, while preparing a final summary report and presentation of initial due diligence and conclusions regarding all potential merger and acquisition candidates previously identified for presentation at the next regular meeting of the board of directors on May 5, 2008. The Inovio board of directors also asked management to contact potential consultants to assist management with operational due diligence and to contact several investment banks to assist the Inovio board in evaluating the fairness, from a financial point of view, to Inovio of the consideration payable by Inovio in connection with a potential transaction with VGX. Inovio subsequently engaged the consulting firm PRTM Management Consultants, Inc., or "PRTM," and the investment bank Oppenheimer & Co. Inc., or "Oppenheimer," for these respective purposes.

        On April 1, 2008, representatives of VGX and Inovio held a kick-off meeting regarding the proposed transaction between Inovio and VGX, including a general discussion of structure, terms and timeline. During April 2008, Inovio and VGX conducted in-person business and financial due diligence at each other's offices in San Diego, CA, Blue Bell, PA, and The Woodlands, TX, which consisted of

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in-depth evaluation of the businesses, assets and liabilities, including meetings between the parties' management teams and ongoing access to each party's separate online data room. Concurrently, PRTM was assisting management with the due diligence review of VGX. During April 2008, the management teams also met telephonically several times and reviewed in detail the profiles of the respective companies and the companies' respective scientific programs and related assets. Beginning in April 2008, the companies' counsel also drafted and negotiated a proposed form of agreement and plan of merger and ancillary documentation.

        At a regular scheduled meeting of the Inovio board of directors on May 5, 2008, Inovio's management provided the board with a detailed update of potential business combination candidates previously discussed and a report on discussions with such prospective candidates, including a detailed update on the due diligence review of such potential acquisition candidates and an assessment of the strategic fit of the active prospects. Management reported to the board that discussions with three of the prospective business combination candidates had been previously terminated in early March 2008 due to difficulties in reaching mutually beneficial economic terms, while discussions with a fourth potential candidate, which had expressed little interest in pursuing a transaction that met Inovio's strategic objectives, had been terminated in early January 2008 once it was clear that a basis for a mutually beneficial transaction did not exist. Inovio had maintained discussions with two additional companies, although neither company was interested in a business combination, as such entities remained interested in pursuing a transaction that meets Inovio's other strategic objectives. After extensive discussion, Inovio's board of directors determined that it should pursue further negotiations with VGX concerning a business combination transaction on an exclusive basis. Inovio's management and PRTM also presented the results of the preliminary diligence performed on VGX to the Inovio board of directors, including a presentation by a representative of PRTM summarizing the operational due diligence completed in support of a potential business combination transaction with VGX. Based on the scientific and business due diligence conducted by the management and PRTM, and the report of counsel on the status of negotiations for an agreement and plan of merger with VGX, Inovio's management and board of directors recommended continuing the proposed transaction with VGX.

        On June 5, 2008, Inovio's board of directors held a special meeting at which management reviewed with the board in detail the status of negotiations with VGX and the status of material open points. The board reviewed the terms of the proposed agreement and plan of merger with VGX and the company's counsel detailed the proposed structure of the transaction. Subsequently, via telephone, Oppenheimer discussed with the board the status of its financial review and the types of financial analyses it expected preliminarily to review with the Inovio board in connection with its opinion. Representatives from management then presented an assessment of the projected combined group's financial condition. The directors then further discussed the terms of the proposed merger, and agreed to postpone formal approvals of such matters until a future date due to the materiality of the unsettled items related to the merger. After such discussion, the Inovio board of directors unanimously resolved that it was in the best interests of Inovio and its stockholders to continue the negotiation, documentation and other efforts in support of the proposed merger with VGX, including the formation of Inovio Acquisition Corporation.

        On July 2, 2008, at a special telephonic meeting of the Inovio board of directors, the directors reviewed with counsel the terms of the pending agreement and plan of merger with VGX and related ancillary agreements, including all revisions made to the proposed agreements since the directors last reviewed them on June 5, 2008, and the board's fiduciary duties in evaluating the proposed transaction. Inovio's board of directors discussed at length the proposed transaction structure, the manner of calculation of the proposed consideration for the merger, the treatment of both parties' outstanding securities, and the other topics discussed under "Inovio's Reasons for the Transaction" on page 66. The Inovio board also discussed the course of negotiations with VGX and the perceived benefits that Inovio's stockholders would potentially derive as a result of the proposed transaction. Also at this

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meeting, Oppenheimer reviewed with Inovio's board of directors its financial analysis of the Merger Exchange Ratio and rendered to Inovio's board of directors an oral opinion, which was confirmed by delivery of a written opinion dated July 2, 2008, to the effect that, as of that date and based on and subject to the matters described in the opinion, the Merger Exchange Ratio provided for in the original agreement and plan of merger (prior to its amendment) was fair, from a financial point of view, to Inovio.

        After further discussion and for the reasons set forth in "Inovio's Reasons for the Transaction" on page 66, the Inovio board concluded that the proposed transaction with VGX was advisable and fair to the company and its stockholders and authorized and approved the agreement and plan of merger and the transactions contemplated thereby, and resolved to recommend that the Inovio stockholders approve the transactions contemplated by the agreement and plan of merger.

        On July 2, 2008, the VGX board of directors held a special meeting at its corporate headquarters in Blue Bell, Pennsylvania, in which the directors reviewed the terms of the pending definitive merger agreement between VGX and Inovio. A representative from Needham was also present to provide Needham's insights on the market condition and on the deal between VGX and Inovio. The evolution of the key terms of the deal and the impact the terms would have on VGX and its stockholders were discussed with the board by VGX's management, along with the prospects of the combined company and management's expectations for the combined group's contributions in the field of DNA vaccines. Management also reviewed the expected technological and financial synergies of the combined company resulting from the Merger. After further discussion, and for the reasons set forth in " VGX's Reasons for the Transaction " on page 69, the VGX board of directors unanimously concluded that the proposed transaction with Inovio was advisable and fair to VGX and its stockholders and authorized and approved the agreement and plan of merger and the transactions contemplated thereby, and resolved to recommend that the VGX stockholders approve the transactions contemplated by the agreement and plan of merger.

        The parties executed an agreement and plan of merger on July 7, 2008, which the parties announced via a joint press release, followed by a joint conference call to answer initial questions from investors and analysts.

        Subsequent to announcement of the transaction, the parties continued to analyze the potential accounting treatment of the Merger, the potential treatment of the Merger by the NYSE Alternext, the tax treatment of the Merger and the proposed combined group's operational goals. As a result, the parties negotiated an amended and restated agreement and plan of merger, adjusting the structure of the planned transaction, providing for certain shares to be issued in the Merger to be deposited into a voting trust, adjusting the combined group's proposed management and board structure and implementing other changes clarifying the terms of the Merger. The amendments did not impact the type of consideration to be issued in the Merger or the methodology for calculation of the Merger Exchange Ratio. The Inovio board of directors met on December 5, 2008, during which the directors approved the Acquisition Agreement and confirmed their recommendation to the Inovio stockholders to approve the Merger. The VGX board of directors met on December 5, 2008, during which the directors approved the Acquisition Agreement and confirmed their recommendation to the VGX stockholders to approve the Merger. The parties executed the Acquisition Agreement on December 5, 2008 and announced the Acquisition Agreement on December 8, 2008.

Inovio's Reasons for the Transaction

        In reaching its decision to approve the Merger and related agreements and proceed with the transaction with VGX, Inovio's board of directors consulted with Inovio's management regarding the

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strategic, operational and financial aspects of the transaction. These consultations included, among other things, extensive discussions regarding:

        In evaluating the Merger, Inovio's board of directors considered both Inovio's short-term and long-term interests, as well as those of its stockholders, consulted with management and legal counsel and considered the following factors, which in the aggregate it deemed favorable in reaching its decision to approve the Merger, the original agreement and plan of merger and the other transactions contemplated by the original merger agreement, and to recommend approval of the Merger to the Inovio stockholders, as well as to approve the Acquisition Agreement and reaffirm its recommendation of approval of the transaction:

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        In its review of the proposed transaction, Inovio's board of directors considered the potential adverse impact of other factors, including:

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        The above discussion of the material factors is not intended to be exhaustive, but does set forth the principal factors considered by Inovio's board of directors. After due consideration, Inovio's board of directors concluded that the potential benefits of the transaction outweighed the risks associated with the transaction. In view of the wide variety of factors considered by Inovio's board of directors in connection with the evaluation of the transaction and the complexity of these matters, Inovio's board of directors did not consider it practical to quantify, rank or otherwise assign relative weights to the foregoing factors, and it did not attempt to do so. Rather, Inovio's board of directors made its recommendation based on the totality of the information presented to it, and the investigation conducted by it. Inovio's board of directors considered all these factors and determined that these factors, as a whole, supported the conclusions and recommendations described below.

        This summary of the reasoning of Inovio's board of directors, as well as certain information presented in this section, is forward-looking in nature. This information should be read in light of the factors discussed under the section entitled "Cautionary Note Regarding Forward Looking Statements" on page 26. Inovio cannot assure you that the potential benefits or opportunities considered by Inovio's board of directors will be achieved through completion of the transaction. See the section entitled "Risk Factors" beginning on page 28.

Recommendation of Inovio's Board of Directors

        After careful consideration, Inovio's board of directors determined that the proposed transaction is fair to, and in the best interests of, Inovio and its stockholders. Inovio's board of directors recommends that Inovio stockholders vote FOR the Merger, including the issuance of Inovio securities in the transaction, as well as the related 2000 Plan Amendment. Each of the individual proposals, as recommended by the Inovio board of directors, is described in greater detail, beginning on page 209 of this joint proxy statement/prospectus.

        In considering the recommendation of Inovio's board of directors with respect to the issuance of securities pursuant to the transaction and the change of control resulting from such issuance, Inovio stockholders should be aware that certain directors and officers of Inovio have interests in the transaction that are different from, or are in addition to, the interests of Inovio's stockholders generally. See the section entitled "Interests of Directors, Officers and Affiliates" on page 86.

VGX's Reasons for the Transaction

        In reaching its decision to approve the Merger, including the original agreement and plan of merger and the Acquisition Agreement, VGX's board of directors consulted with VGX's management and financial and legal advisors regarding the strategic, operational and financial aspects of the transaction. The management team of VGX performed analyses of the business, financial performance and condition, competitive environment, and prospects of each Inovio and VGX as separate entities and on a combined basis for VGX's board of directors. The VGX board of directors also considered an assessment of other potential strategic opportunities and alternatives to the Merger, including development opportunities and other possible merger or acquisition alternatives, and determined that the Merger with Inovio was the best strategic fit and presented a unique opportunity to enhance and expand VGX's operations and product offerings and best positioned VGX for future growth.

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        In the course of reaching its decision to approve the Merger, VGX's board of directors considered a variety of factors, including but not limited to, the following:

        The VGX board of directors considered the following factors pertaining to the strategic rationale for the combination of the two companies, supporting its decision to approve the Merger:

        The VGX board of directors also considered the following financial factors pertaining to the Merger, which supported its decision to approve the Merger and enter into the related agreements:

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        The VGX board of directors also considered the following governance factors as support for its decision to approve the Merger:

        The VGX board of directors evaluated the reasonableness of terms and conditions of the Merger, including:

        The VGX board of directors weighed these advantages and opportunities against the following material factors that may weigh negatively against the Merger:

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        In reaching its decision to approve the Merger, VGX's board of directors also considered the interests that certain directors and officers of VGX have in the transaction. See the section entitled "Interests of Directors, Officers and Affiliates" on page 86.

        After consideration of these factors, the VGX board of directors determined that these risks could be mitigated or managed by VGX or Inovio or by the combined company following the Merger, were reasonably acceptable under the circumstances or, in light of the anticipated benefits, the risks were unlikely to have a materially adverse impact on the Merger or on the combined company following the Merger, and that, overall, these risks were significantly outweighed by the potential benefits of the Merger.

        Although this discussion of the information and factors considered by the VGX board of directors is believed to include the material factors considered by the VGX board of directors, it is not intended to be exhaustive and may not include all of the factors considered by the VGX board of directors. In reaching its determination to approve the Merger and approve and adopt the original agreement and plan of merger and the Acquisition Agreement, the VGX board of directors did not find it useful and did not attempt to quantify or assign any relative or specific weights to the various factors that it considered in reaching its determination that the Merger and the related agreements are advisable and fair to and in the best interests of VGX and the VGX stockholders. Rather, the VGX board of directors based its position and determination on the totality of the information presented to and factors considered by it. In addition, individual members of the VGX board of directors may have given differing weights to different factors.

        This summary of the reasoning of VGX's board of directors, as well as certain information presented in this section, is forward-looking in nature. This information should be read in light of the factors discussed under the section entitled "Cautionary Note Regarding Forward Looking Statements" on page 26. VGX cannot assure you that the potential benefits or opportunities considered by VGX's board of directors will be achieved through completion of the transaction. See the section entitled "Risk Factors" beginning on page 28.

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Recommendation of VGX's Board of Directors

        After careful consideration and with advice from Needham, VGX's board of directors determined that the Acquisition Agreement and the transactions contemplated by the Acquisition Agreement, including the terms of the Merger, are fair, reasonable and in the best interests of VGX. VGX's board of directors recommends that VGX stockholders vote FOR the proposal seeking approval of the Merger, including adoption of the Acquisition Agreement. The individual proposal, as recommended by the VGX board of directors, is described in greater detail, beginning on page 219 of this joint proxy statement/prospectus.

        In considering the determination by the VGX board of directors that the Merger and the related agreements are advisable and fair to and in the best interests of VGX and the VGX stockholders, you should be aware that certain VGX directors and officers have arrangements that may cause them to have interests in the transaction that are different from, or are in addition to, the interests of VGX stockholders generally. See the section entitled "Interests of Directors, Officers and Affiliates" on page 86.

Resulting Ownership of Inovio; Change of Control

        The Acquisition Agreement anticipates the calculation of the Merger Exchange Ratio such that the legacy holders of Inovio's securities and VGX's securities will respectively hold 50 percent of the fully-diluted share capital upon closing of the Merger, excluding the VGX convertible debt assumed in the Merger. If the Merger is consummated, based on the fully-diluted share capital outstanding of each of Inovio and VGX as of the record date, current holders of Inovio securities will own approximately [        ]% and holders of VGX securities will own approximately [        ]% of the fully-diluted share capital of the combined company (including the VGX convertible debt) and [        ]% and [        ]%, respectively, of the anticipated issued and outstanding shares of capital stock post-Merger (including the outstanding shares of Inovio Series C preferred stock on an as-converted basis). This shift in the ownership of Inovio as a result of the Merger, if completed, or the related shift in the voting power of the legacy Inovio stockholders, will constitute a "Change of Control" or "Change in Control" as defined in a number of Inovio agreements, or other qualifying triggering event, impacting the rights of Inovio and/or the other parties to such agreements, as follows:

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        In addition, Inovio has reviewed the rights of the holders of the outstanding shares of its Series C preferred stock and its outstanding warrants, and has determined that the Merger should not have any impact on the current rights of such securities, on the basis that the Merger does not qualify as a "Change of Control" or other qualifying event as defined for such securities, or if the Merger does trigger potential consequences, such adjustments are not applicable due to the significant negative differential between the pricing of the security in question and the current market price of Inovio's common stock. For example, the majority of the outstanding Inovio warrants include a Change of Control provision that, if triggered, only requires adjustment of the exercise price or allows cash redemption of the warrant if changes in rights are being made to the underlying security, the Inovio common stock, or such class of underlying security is being purchased or exchanged in a transaction, which would not occur upon closing of the Merger, if completed. However, Inovio has identified one form of warrant issued in 2004 that also provides the warrantholder, upon a "consolidation" of Inovio with another company, the ability to elect to receive cash consideration equal to the fair market value of the warrant as determined in accordance with customary valuation methodology used in the investment banking industry. Using the Black-Scholes valuation method favored by investment banks for such valuations, Inovio anticipates that its cash redemption obligation for such warrants would be significantly less than $1,000 total, if the current transaction is deemed a qualifying consolidation and the warrantholder seeks such redemption.

Opinion of Inovio's Financial Advisor

        Oppenheimer acted as a financial advisor to Inovio to evaluate, and to render an opinion to the Inovio board of directors with respect to, the fairness, from a financial point of view, to Inovio of the consideration payable by Inovio in the Merger. On July 2, 2008, at a meeting of Inovio's board of

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directors held to evaluate the Merger, Oppenheimer rendered to Inovio's board of directors an oral opinion, which was confirmed by delivery of a written opinion dated July 2, 2008, to the effect that, as of that date and based on and subject to the matters described in its opinion, the Merger Exchange Ratio provided for in the original agreement and plan of merger (prior to its amendment) was fair, from a financial point of view, to Inovio. Oppenheimer's opinion, dated July 2, 2008, relates only to the Merger Exchange Ratio provided for in the original merger agreement and does not take into account any events or developments after the date of such opinion, including any modification to the proposed Merger or the Merger Exchange Ratio provided for in the Acquisition Agreement, dated as of December 5, 2008.

        The full text of Oppenheimer's written opinion, dated July 2, 2008, which describes the assumptions made, procedures followed, matters considered and limitations on the review undertaken, is attached to this joint proxy statement/prospectus as Annex B . Oppenheimer's opinion was provided to Inovio's board of directors in connection with its evaluation of the Merger Exchange Ratio from a financial point of view to Inovio and does not address any other aspect of the Merger. Oppenheimer's opinion does not address the underlying business decision of Inovio to effect the Merger, the relative merits of the Merger as compared to any alternative business strategies that might exist for Inovio or the effect of any other transaction in which Inovio might engage and does not constitute a recommendation to any stockholder as to how such stockholder should vote or act with respect to any matters relating to the Merger. The summary of Oppenheimer's opinion described below is qualified in its entirety by reference to the full text of its opinion.

        In arriving at its opinion, Oppenheimer:

        In rendering its opinion, Oppenheimer relied upon and assumed, without independent verification or investigation, the accuracy and completeness of all of the financial and other information provided to or discussed with Oppenheimer by Inovio, VGX and their respective employees, representatives and affiliates or otherwise reviewed by Oppenheimer. Oppenheimer was advised that financial forecasts

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relating to Inovio and VGX had not been prepared by the managements of Inovio and VGX and, accordingly, Oppenheimer did not undertake an analysis of the future financial performance of Inovio and VGX. Oppenheimer assumed, with Inovio's consent, that the final terms of the merger agreement would not vary materially from those set forth in the draft reviewed by Oppenheimer. Oppenheimer also assumed, with Inovio's consent, that the Merger would qualify for federal income tax purposes as a tax-free reorganization under Section 368(a) of the Code. Oppenheimer further assumed, with Inovio's consent, that the Merger and related transactions, including the (i) sale by VGX to VGXI of certain assets relating to its DNA plasmid products for total cash consideration of $9,110,000, referred to as the VGXI asset sale, and the use of the proceeds from the VGXI asset sale and (ii) repayment of an aggregate of $7.75 million of the outstanding convertible debt of VGX not converted into Inovio common stock in the anticipated automatic conversion of certain convertible debt assumed in the Merger, referred to as the VGX convertible debt conversion, as such debt becomes due and payable, would be consummated in accordance with their respective terms without waiver, modification or amendment of any material term, condition or agreement and in compliance with all applicable laws and other requirements and that, in the course of obtaining the necessary regulatory or third party approvals, consents and releases with respect to the Merger and related transactions, no delay, limitation, restriction or condition would be imposed that would have an adverse effect on Inovio, VGX or the contemplated benefits of the Merger. Oppenheimer neither made nor obtained any independent evaluations or appraisals of the assets or liabilities, contingent or otherwise, of Inovio or VGX.

        Oppenheimer's opinion relates to the relative values of the fully diluted equity of Inovio and VGX after giving effect, in the case of VGX, to the VGX convertible debt conversion. Oppenheimer did not express any opinion as to the underlying valuation, future performance or long-term viability of Inovio or VGX, the actual value of Inovio common stock when issued or the price at which Inovio common stock would trade at any time. Oppenheimer was not requested to, and it did not, participate in the negotiation or structuring of the Merger or any related transaction. Oppenheimer expressed no view as to, and its opinion did not address, any terms or other aspects or implications of the Merger (other than the Merger Exchange Ratio to the extent expressly specified in its opinion) or any related transaction or any aspect or implication of any other agreement, arrangement or understanding entered into in connection with the Merger or otherwise, including, without limitation, the form or structure of the Merger or any related transaction, including the VGX convertible debt conversion, or any terms or aspects of the VGXI asset sale or the use of the proceeds from the VGXI asset sale. Oppenheimer also expressed no view as to, and its opinion did not address, the fairness of the amount or nature of, or any other aspect relating to, the compensation to be received by any individual officers, directors or employees of any parties to the Merger, or any class of such persons, relative to the Merger Exchange Ratio. In addition, Oppenheimer expressed no view as to, and its opinion did not address, Inovio's underlying business decision to proceed with or effect the Merger nor did its opinion address the relative merits of the Merger as compared to any alternative business strategies that might exist for Inovio or the effect of any other transaction in which Inovio might engage. Oppenheimer's opinion was necessarily based on the information available to it and general economic, financial and stock market conditions and circumstances as they existed and could be evaluated by Oppenheimer on the date of its opinion. Although subsequent developments may affect its opinion, Oppenheimer does not have any obligation to update, revise or reaffirm its opinion. Except as described above, Inovio imposed no other instructions or limitations on Oppenheimer with respect to the investigations made or the procedures followed by it in rendering its opinion.

        This summary is not a complete description of Oppenheimer's opinion or the financial analyses performed and factors considered by Oppenheimer in connection with its opinion. The preparation of a financial opinion is a complex analytical process involving various determinations as to the most appropriate and relevant methods of financial analysis and the application of those methods to the particular circumstances and, therefore, a financial opinion is not readily susceptible to summary

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description. Oppenheimer arrived at its ultimate opinion based on the results of all analyses undertaken by it and assessed as a whole, and did not draw, in isolation, conclusions from or with regard to any one factor or method of analysis for purposes of its opinion. Accordingly, Oppenheimer believes that its analyses and this summary must be considered as a whole and that selecting portions of its analyses and factors or focusing on information presented in tabular format, without considering all analyses and factors or the narrative description of the analyses, could create a misleading or incomplete view of the processes underlying Oppenheimer's analyses and opinion.

        In performing its analyses, Oppenheimer considered industry performance, general business, economic, market and financial conditions and other matters existing as of the date of its opinion, many of which are beyond the control of Inovio and VGX. No company, business or transaction used in the analyses is identical to Inovio, VGX or the Merger, and an evaluation of the results of those analyses is not entirely mathematical. Rather, the analyses involve complex considerations and judgments concerning financial and operating characteristics and other factors that could affect the acquisition, public trading or other values of the companies, business segments or transactions analyzed.

        The assumptions and estimates contained in Oppenheimer's analyses and the ranges of valuations resulting from any particular analysis are not necessarily indicative of actual values or future results, which may be significantly more or less favorable than those suggested by its analyses. In addition, analyses relating to the value of businesses or securities do not purport to be appraisals or to reflect the prices at which businesses or securities actually may be sold. Accordingly, the assumptions and estimates used in, and the results derived from, Oppenheimer's analyses are inherently subject to substantial uncertainty.

        The type and amount of consideration payable in the Merger were determined through negotiation between Inovio and VGX, and the decision to enter into the transaction was solely that of Inovio's board of directors. Oppenheimer's opinion and financial presentation were only one of many factors considered by Inovio's board of directors in its evaluation of the Merger and should not be viewed as determinative of the views of Inovio's board of directors or management with respect to the Merger or the Merger Exchange Ratio.

        The following is a summary of the material financial analyses reviewed with Inovio's board of directors in connection with Oppenheimer's opinion dated July 2, 2008. The financial analyses summarized below include information presented in tabular format. In order to fully understand Oppenheimer's financial analyses, the tables must be read together with the text of each summary. The tables alone do not constitute a complete description of the financial analyses. Considering the data in the tables below without considering the full narrative description of the financial analyses, including the methodologies and assumptions underlying the analyses, could create a misleading or incomplete view of Oppenheimer's financial analyses. For purposes of the financial analyses summarized below, the "Implied Merger Exchange Ratio" refers to the implied Merger Exchange Ratio of approximately 0.9803x calculated as set forth in the original agreement and plan of merger (prior to its amendment) based on outstanding common stock, warrant and option information for Inovio and VGX provided by the respective managements of Inovio and VGX.

        Oppenheimer performed separate sum-of-the-parts analyses of Inovio and VGX based on the sum of (i) the implied values of their respective product candidates and other operating assets, plus (ii) their respective net cash, calculated as cash and cash equivalents less debt, and the book value of their respective non-operating assets as of March 31, 2008 as adjusted, in the case of VGX's net cash, to reflect the VGXI asset sale and the VGX convertible debt conversion.

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        Inovio.     In performing the sum-of-the-parts analysis of Inovio, implied values were calculated as follows:

Transaction Date
  Parties to Transaction
12/2007   Maxygen, Inc. / Sanofi Pasteur, Inc.
2/2007   AVANT Immunotherapeutics, Inc. / Select Vaccines Limited
10/2006   Intercell AG / Merck & Co., Inc.
6/2006   Sanofi Pasteur, Inc. / Emergent BioSolutions Inc.
3/2006   Hawaii Biotech, Inc. / Avantogen Limited
7/2005   Merck & Co., Inc. / Geron Corporation
6/2004   Kirin Brewery Co., Ltd. (Pharmaceutical Division) / Merix Corporation
5/2004   Intercell AG / Merck & Co., Inc.
4/2004   Cerus Corporation / MedImmune, Inc.
3/2004   Innogenetics N.V. / Genencor International, Inc.
12/2002   Corixa Corporation / Kirin Brewery Co., Ltd. (Pharmaceutical Division)
4/2002   Bavarian Nordic A/S / PowderJect Pharmaceuticals PLC

        VGX.     In performing the sum-of-the-parts analysis of VGX, implied values were calculated as follows:

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Transaction Date
  Parties to Transaction

2/2007

  Roche Holdings, Ltd. / BioCryst Pharmaceuticals, Inc.

7/2006

  Actelion Pharmaceuticals Ltd. / Roche Holdings, Ltd.

6/2006

  Schering-Plough Corporation / Celera Genomics Group

1/2003

  Genentech, Inc. / TolerRx Inc.

5/2000

  Repligen Corporation / Tolerance Therapeutics LLC

        Based on implied per share equity reference ranges for Inovio and VGX derived from the sum of (i) the implied aggregate value of their respective product candidates and operating assets plus (ii) their respective net cash and the book value of non-operating assets as of March 31, 2008 (as adjusted, in the case of VGX's net cash, to reflect the VGXI asset sale and the VGX convertible debt conversion), the sum-of-the-parts analyses of Inovio and VGX indicated the following implied exchange ratio reference range, as compared to the Implied Merger Exchange Ratio:

Implied Exchange Ratio
Reference Range
  Implied Merger Exchange Ratio

1.1961x - 1.7544x

  0.9803x

        Oppenheimer performed separate selected companies analyses of Inovio and VGX in which Oppenheimer reviewed financial and stock market information of Inovio, VGX and the following eight selected publicly held companies with operations in the vaccine or immunotherapy segments of the biopharmaceutical industry, which are segments of such industry in which Inovio and VGX operate:

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        Oppenheimer reviewed enterprise values of the selected companies, calculated as fully-diluted market value based on closing stock prices on July 1, 2008, less cash, cash equivalents and investments in unconsolidated affiliates, plus straight debt and preferred stock, out-of-the-money convertible securities and minority interests, of the selected companies. Financial data for the selected companies were based on public filings. Based on implied per share equity reference ranges for Inovio and VGX derived by applying the amount of Inovio's and VGX's net cash as of March 31, 2008 (as adjusted, in the case of VGX's net cash, to reflect the VGXI asset sale and the VGX convertible debt conversion) to the range of enterprise values of the selected companies, the selected companies analyses of Inovio and VGX indicated the following implied exchange ratio reference range, as compared to the Implied Merger Exchange Ratio:

Implied Exchange Ratio
Reference Range
  Implied Merger Exchange Ratio

0.0646x - 11.0995x

  0.9803x

        Oppenheimer performed separate selected precedent transactions analyses of Inovio and VGX in which Oppenheimer reviewed the transaction values of the following nine selected transactions in the biopharmaceutical industry (a) involving companies with either operations in the vaccine segment of such industry, which is a segment in which Inovio and VGX operate, or product candidates in an early development stage or (b) in which the acquiror and the target had complementary technologies:

Announcement Date
  Acquiror   Target
5/12/2008   Intercell AG   Iomai Corporation
10/22/2007   Celldex Therapeutics, Inc.   AVANT Immunotherapeutics, Inc.
7/25/2007   Cell Therapeutics, Inc.   Systems Medicine, Inc.
5/7/2007   Peptech Ltd.   Evogenics Pty Ltd.
6/8/2006   Axonyx Inc.   TorreyPines Therapeutics, Inc.
4/12/2006   Infinity Pharmaceuticals, Inc.   Discovery Partners International, Inc.
1/9/2006   Cancervax Corporation   Micromet, Inc.
9/26/2005   Corgentech Inc.   AlgoRx Pharmaceuticals Inc.
9/14/2005   MedImmune, Inc.   Cellective Therapeutics, Inc.

        Oppenheimer reviewed transaction values in the selected transactions, calculated as the equity value implied for the target company based on the consideration payable in the selected transaction, including contingent payments, less cash, cash equivalents and investments in unconsolidated affiliates, plus straight debt and preferred stock, out-of-the-money convertible securities and minority interests. Financial data for the selected transactions were based on publicly available information at the time of announcement of the relevant transaction. Based on implied per share equity reference ranges for Inovio and VGX derived by applying the amount of Inovio's and VGX's net cash as of March 31, 2008 (as adjusted, in the case of VGX's net cash, to reflect the VGXI asset sale and the VGX convertible debt conversion) to the range of transaction values of the selected transactions, the selected precedent transactions analyses of Inovio and VGX indicated the following implied exchange ratio reference range, as compared to the Implied Merger Exchange Ratio:

Implied Exchange Ratio
Reference Range
 
Implied Merger Exchange Ratio

0.1471x - 5.2720x

  0.9803x

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        Inovio has agreed to pay Oppenheimer for its financial advisory services with respect to the rendering its opinion in connection with the Merger an aggregate fee of $325,000, a portion of which was payable upon Oppenheimer's engagement by Inovio and the balance of which was payable upon delivery of Oppenheimer's opinion (regardless of the conclusion reached in the opinion). Inovio also has agreed to reimburse Oppenheimer for its reasonable expenses, including reasonable fees and expenses of its legal counsel, and to indemnify Oppenheimer and related parties against liabilities, including liabilities under the federal securities laws, relating to, or arising out of, its engagement. Oppenheimer and its affiliates in the past have performed investment banking and other services for Inovio unrelated to the Merger, for which services Oppenheimer and its affiliates have received compensation, including financial advisory services to Inovio in connection with potential acquisition transactions in 2007. In the ordinary course of business, Oppenheimer and its affiliates may actively trade the securities of Inovio for Oppenheimer's and its affiliates' own accounts and for the accounts of customers and, accordingly, may at any time hold a long or short position in such securities.

        The issuance of Oppenheimer's opinion was approved by an authorized committee of Oppenheimer. Inovio selected Oppenheimer to provide certain financial advisory services in connection with the Merger based on Oppenheimer's reputation and experience and its familiarity with Inovio and its business. Oppenheimer is an internationally recognized investment banking firm and, as a part of its investment banking business, is regularly engaged in valuations of businesses and securities in connection with acquisitions and mergers, underwritings, secondary distributions of securities, private placements and valuations for other purposes.

Appraisal Rights

        Under the DGCL, holders of VGX common stock have the right to seek appraisal of their shares of VGX common stock in connection with the Merger and to receive payment in cash for the fair value of their shares of VGX common stock as determined by the Delaware Court of Chancery, or the "Chancery Court," together with a fair rate of interest, if any, in lieu of the consideration they would otherwise be entitled to pursuant to the Acquisition Agreement. These rights are known as "appraisal rights." VGX stockholders electing to exercise appraisal rights must comply with the provisions of Section 262 of the DGCL, or "Section 262," the full text of which appears in Annex E to this joint proxy statement/prospectus, in order to perfect their rights. Strict compliance with the Delaware statutory procedures will be required. For VGX stockholders who have properly exercised appraisal rights to receive the fair value of their shares, at least one VGX stockholder who has properly exercised appraisal rights must litigate an appraisal proceeding in the Chancery Court.

        The following is intended as a brief summary of the material provisions of the Delaware statutory procedures required to be followed by a VGX stockholder in order to dissent from the Merger and to perfect appraisal rights. This summary, however, is not a complete statement of all applicable requirements and is qualified in its entirety by reference to Section 262. Failure to precisely follow any of the statutory procedures set forth in Section 262 may result in a termination or waiver of a VGX stockholder's appraisal rights.

        Section 262 requires that stockholders be notified that appraisal rights will be available not less than 20 days before the stockholders' meeting to vote on the Merger. A copy of Section 262 must be included with such notice. This joint proxy statement/prospectus constitutes VGX's notice to its stockholders of the availability of appraisal rights in connection with the Merger in compliance with the requirements of Section 262. If a VGX stockholder wishes to consider exercising his or her appraisal rights, he or she should carefully review the text of Section 262 contained in Annex E since failure to timely and properly comply with the requirements of Section 262 will result in the loss of his or her appraisal rights under Delaware law.

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        If a VGX stockholder elects to demand appraisal of his or her shares, he or she must satisfy each of the following conditions:

        All demands for appraisal should be addressed to VGX Pharmaceuticals, Inc., 450 Sentry Parkway, Blue Bell, Pennsylvania 19422, Attention: Secretary, and must be delivered before the vote on the Acquisition Agreement is taken at the VGX special meeting, and should be executed by, or on behalf of, the record holder of the shares of VGX common stock. The demand must reasonably inform VGX of the identity of the stockholder and the intention of the stockholder to demand appraisal of such stockholder's shares of VGX common stock.

        To be effective, a demand for appraisal by a holder of VGX's common stock must be made by, or in the name of, such registered stockholder, fully and correctly, as the stockholder's name appears on the stock certificate(s). Beneficial owners who are not record holders may not directly make appraisal demands to VGX. The beneficial holder must, in such cases, have the registered owner, such as a broker, bank or other nominee or other nominee, submit the required demand in respect of those shares. If shares are owned of record in a fiduciary capacity, such as by a trustee, guardian or custodian, execution of a demand for appraisal should be made by or for the fiduciary; and if the shares are owned of record by more than one person, as in a joint tenancy or tenancy in common, the demand should be executed by or for all joint owners. An authorized agent, including an authorized agent for two or more joint owners, may execute the demand for appraisal for a stockholder of record; however, the agent must identify the record owner or owners and expressly disclose the fact that, in executing the demand, he or she is acting as agent for the record owner. A record owner, such as a broker, who holds shares as a nominee for others, may exercise his or her right of appraisal with respect to the shares held for one or more beneficial owners, while not exercising this right for other beneficial owners. In that case, the written demand should state the number of shares as to which appraisal is sought. Where no number of shares is expressly mentioned, the demand will be presumed to cover all shares held in the name of the record owner.

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If a VGX stockholder holds his or her shares of VGX common stock in a brokerage account or in other nominee form and he or she wishes to exercise appraisal rights, he or she should consult with his or her broker, bank or other nominee to determine the appropriate procedures for the making of a demand for appraisal by the nominee.

        Within ten days after the Effective Time of the Merger, the surviving corporation must give written notice that the Merger has become effective to each VGX stockholder who has properly filed a written demand for appraisal and who did not vote in favor of the Acquisition Agreement. At any time within 60 days after the Effective Time, any VGX stockholder who has demanded an appraisal has the right to withdraw the demand and to accept the consideration specified by the Acquisition Agreement for his or her shares of VGX common stock. Within 120 days after the Effective Time of the Merger, the surviving corporation or any stockholder who has complied with Section 262 shall, upon written request to the surviving corporation, be entitled to receive a written statement setting forth the aggregate number of shares not voted in favor of the Acquisition Agreement and with respect to which demands for appraisal rights have been received and the aggregate number of holders of such shares. Within 120 days after the Effective Time, either the surviving corporation or any VGX stockholder who has complied with the requirements of Section 262 may file a petition in the Chancery Court demanding a determination of the fair value of the shares held by all VGX stockholders entitled to appraisal. Upon the filing of the petition by a VGX stockholder, service of a copy of such petition shall be made upon the surviving corporation. The surviving corporation has no obligation to file such a petition in the event there are dissenting stockholders. Accordingly, the failure of a stockholder to file such a petition within the period specified could nullify the stockholder's previously written demand for appraisal.

        If a petition for appraisal is duly filed by a VGX stockholder and a copy of the petition is delivered to the surviving corporation, the surviving corporation will then be obligated, within 20 days after receiving service of a copy of the petition, to provide the Chancery Court with a duly verified list containing the names and addresses of all VGX stockholders who have demanded an appraisal of their shares and with whom agreements as to the value of their shares have not been reached by the surviving corporation. After notice to dissenting stockholders who demanded appraisal of their shares, the Chancery Court is empowered to conduct a hearing upon the petition, and to determine those VGX stockholders who have complied with Section 262 and who have become entitled to the appraisal rights provided thereby. The Chancery Court may require the VGX stockholders who have demanded payment for their shares to submit their stock certificates to the Register in the Chancery Court for notation thereon of the pendency of the appraisal proceedings, and if any stockholder fails to comply with that direction, the Chancery Court may dismiss the proceedings as to that stockholder.

        After determination of the VGX stockholders entitled to appraisal of their shares of VGX common stock, the appraisal proceeding shall be conducted in accordance with the rules of the Chancery Court, including any rules specifically governing appraisal proceedings. The appraisal proceeding is a litigation proceeding. At the conclusion of the litigation, the Chancery Court will appraise the shares, determining their fair value exclusive of any element of value arising from the accomplishment or expectation of the Merger, together with a fair rate of interest, if any. When the value is determined, the Chancery Court will direct the payment of such value in cash, with interest thereon accrued during the pendency of the proceeding, if the Chancery Court so determines, to the VGX stockholders entitled to receive the same, upon surrender by such holders of the certificates representing those shares.

        In determining fair value, the Chancery Court is required to take into account all relevant factors. VGX stockholders should be aware that the fair value of their shares as determined under Section 262 could be more, the same or less than the value that they are entitled to receive under the terms of the Acquisition Agreement. Stockholders also should be aware that investment banking opinions as to the fairness from a financial point of view of the consideration payable in a merger are not opinions as to "fair value" under Section 262. Unless the Chancery Court in its discretion determines otherwise for

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good cause shown, interest from the Effective Time of the Merger through the date of the payment of the judgment shall be compounded quarterly and shall accrue at 5% over the Federal Reserve discount rate (including any surcharge) as established from time to time during the period between the Effective Time of the Merger and the date of payment of the judgment.

        Costs of the appraisal proceeding may be imposed upon the surviving corporation and the VGX stockholders participating in the appraisal proceeding by the Chancery Court as the Chancery Court deems equitable in the circumstances. Upon the application of a VGX stockholder, the Chancery Court may order all or a portion of the expenses incurred by any VGX stockholder in connection with the appraisal proceeding, including, without limitation, reasonable attorneys' fees and the fees and expenses of experts, to be charged pro rata against the value of all shares entitled to appraisal. Any VGX stockholder who had demanded appraisal rights will not, after the Effective Time of the Merger, be entitled to vote shares subject to that demand for any purpose or to receive payments of dividends or any other distribution with respect to those shares, other than with respect to payment as of a record date prior to the Effective Time; however, if no petition for appraisal is filed within 120 days after the Effective Time of the Merger, or if the VGX stockholder delivers a written withdrawal of his or her demand for appraisal and an acceptance of the terms of the Merger within 60 days after the Effective Time of the Merger, then the right of that VGX stockholder to appraisal will cease and that stockholder will be entitled to receive the merger consideration for shares of VGX's common stock held by such stockholder pursuant to the Acquisition Agreement. Any withdrawal of a demand for appraisal made more than 60 days after the Effective Time of the Merger may only be made with the written approval of the surviving corporation and must, to be effective, be made within 120 days after the Effective Time.

Failure to comply with all of the procedures set forth in Section 262 will result in the loss of a stockholder's statutory appraisal rights. In view of the complexity of Section 262, VGX stockholders who may wish to dissent from the Merger and pursue appraisal rights should consult their legal advisors.

Accounting Treatment

        The Merger will be accounted for using the purchase method of accounting for business combinations under U.S. GAAP. Although the business combination of Inovio and VGX is a "merger of equals," generally accepted accounting principles require that one of the two companies in the transaction be designated as the acquirer for accounting purposes. After a review of relevant factors, in accordance with the provisions of Statement of Financial Accounting Standards No. 141, Business Combinations (SFAS 141), Inovio has been determined to be the accounting acquirer. In evaluating the appropriate accounting treatment under SFAS 141, the parties and their accountants considered all relevant facts and circumstances, including, without limitation, the entity issuing equity securities, the relative operational size of the legacy entities, the relative voting rights of the legacy holders in the combined group, the composition of the post-Merger company's board of directors and its committees, and the composition and relevant experience of senior management; a majority of these factors favored a determination of Inovio as the accounting acquirer. Accordingly, the historical consolidated financial statements of Inovio will be carried forward at their historical cost, the purchase price will be allocated to VGX's identifiable assets and liabilities based on their estimated fair values at the date of the consummation of the Merger, and any excess of the purchase price over those fair values will be accounted for as goodwill. The results of final valuations of property, plant and equipment, and intangible and other assets and the finalization of any potential plans of restructuring have not yet been completed. Inovio will revise the allocation of the purchase price based on VGX's net assets at the time of the Merger and when additional information becomes available.

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Listing or Quotation of Inovio Common Stock

        Inovio has notified the NYSE Alternext of the Acquisition Agreement, the Merger and the other transactions contemplated by the Acquisition Agreement and provided the NYSE Alternext with a copy of the Acquisition Agreement, the schedules and exhibits thereto and any other documentation requested by the NYSE Alternext for use in its evaluation of the applicability to the Merger of Section 341 of the Company Guide of the NYSE Alternext, or "Section 341," and the definition of "Reverse Merger" Section 341 provides. The parties are in continuing discussions with the NYSE Alternext regarding whether the Merger will be deemed a Reverse Merger under Section 341. If the Merger is ultimately determined not to constitute a "Reverse Merger" under Section 341, Inovio will file an additional listing application with respect to the shares of Inovio common stock to be issued or become issuable upon closing of the Merger and use commercially reasonable efforts to obtain approval of such additional listing, as well as maintain the current listing of its common stock on the NYSE Alternext. If the Merger is determined to constitute a "Reverse Merger" under Section 341, Inovio will use commercially reasonable efforts to meet the initial listing requirements of the NYSE Alternext. If Inovio is able to satisfy such initial listing requirements using commercially reasonable efforts, it will file an initial listing application with the NYSE Alternext. However, if Inovio is not able to meet the NYSE Alternext's initial listing requirements using commercially reasonable efforts, or NYSE Alternext otherwise notifies Inovio that it is out of compliance with the NYSE Alternext continued listing standards and Inovio cannot maintain the listing of its common stock using commercially reasonable efforts, then Inovio will, in consultation with VGX, pursue listing or quotation of the Inovio common stock on an alternate securities exchange or quotation system, respectively, for which it does qualify, including approval for listing or quotation of the shares of Inovio common stock to be issued or become issuable upon closing of the Merger.

Restrictions on Ability to Sell Inovio Common Stock

        The Acquisition Agreement provides that certain shares of Inovio common stock issued at closing of the Merger, or issuable pursuant to securities assumed in the Merger, will be subject to lock-up restrictions for an initial period post-Merger, in conjunction with which certain holders of Inovio and VGX securities will be asked to execute lock-up agreements. Specifically, shares of Inovio common stock held at the closing, received pursuant to the Merger, or received upon exercise or conversion of options, warrants or convertible debt assumed in the Merger (the "Restricted Securities") held by any of the following persons shall be subject to lock-up restrictions: (a) certain holders of Restricted Securities named in the Acquisition Agreement, (b) directors, executive officers and employees of VGX just prior to closing, (c) holders of the outstanding convertible debt of VGX just prior to closing, and (d) the directors, executive officers, and employees of Inovio (each a "Restricted Party" and together, the "Restricted Parties").

        For the duration of the applicable lock-up period, each Restricted Party shall not (a) sell, assign, exchange, transfer, pledge, hypothecate, distribute or otherwise dispose of (other than by operation of law where the transferee remains subject to and bound by the provisions of the Acquisition Agreement applicable during the lock-up period) (i) any Restricted Securities, or (ii) any interest (including, without limitation, an option to buy or sell) in any Restricted Securities, in whole or in part, or (b) engage in any transaction in respect to Restricted Securities or any interest in the Restricted Securities, the intent or effect of which is the effective economic disposition of such shares (the foregoing restrictions are referred to in this joint proxy statement/prospectus as the "Lock-Up Restrictions"). However, in no event shall any of the Lock-Up Restrictions restrict the transfer of the Restricted Securities pursuant to a tender offer, exchange offer or merger transaction relating to any shares of Inovio common stock subsequent to the Merger.

        The Lock-Up Restrictions shall generally apply to Restricted Securities held by the Restricted Parties, except with respect to shares of Inovio common stock issued upon conversion of the VGX

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convertible debt, for 24 months from the closing of the Merger. However, the Lock-Up Restrictions shall lapse as to 25% of the shares of Inovio common stock (held directly or underlying other Restricted Securities) initially subject to such Lock-Up Restrictions at closing upon each six-month anniversary of the date of the closing, and, if the Restricted Party is an employee and/or director of Inovio or VGX or any of their subsidiaries just prior to the Effective Time of the Merger, the Lock-Up Restrictions shall no longer apply at all upon the termination of such Restricted Party's employment or directorship with Inovio or any of its subsidiaries. The Lock-Up Restrictions shall apply to any shares of Inovio common stock issued upon conversion of the converted VGX convertible debt for six months from the closing, but shall lapse as to 50% of the shares of Inovio common stock underlying the VGX convertible debt upon the three-month anniversary of the date of closing.

        To effect the Lock-up Restrictions, upon closing Inovio will issue a stop order to its transfer agent with respect to the shares of Inovio common stock held by or issuable to the Restricted Parties, and the shares of Inovio common stock issued to the Restricted Parties in the Merger and thereafter during the effective period for the Lock-Up Restrictions shall bear a restrictive legend reflecting the Lock-Up Restrictions. Prior to the closing, Inovio shall also obtain from the chief executive officer of Inovio and shall use its best efforts to obtain from all other Inovio-affiliated Restricted Parties lock-up agreements in customary form detailing the Lock-Up Restrictions. Prior to the closing, VGX shall also obtain from the chief executive officer of VGX and shall use its best efforts to obtain from all other VGX-affiliated Restricted Parties, except those who will hold Restricted Securities consisting of solely of shares of Inovio common stock issued at the Effective Time pursuant to the Merger, lock-up agreements in customary form detailing the Lock-Up Restrictions.

        Upon the expiration of the general periods during which the Lock-Up Restrictions are applicable, Inovio shall instruct its transfer agent to remove the stop order. Prior to such times, Inovio shall also notify its transfer agent regarding the interim lapsing of the Lock-Up Restrictions as to Restricted Securities held by the Restricted Parties within five business days of each of the applicable anniversary dates. To the extent a holder of previously Restricted Securities needs assistance with the issuance of new share certificates in order to make a transfer of some or all of that portion of its shares of Inovio common stock which were previously issued with the restrictive legend, the post-Merger company intends to assist such holder in its communications with the transfer agent to effectuate such issuance and/or transfer.

Interests of Directors, Officers and Affiliates

        In considering the recommendation of Inovio's board of directors that Inovio stockholders vote in favor of the issuance of Inovio's securities in conjunction with the Merger and the resulting change of control of Inovio, Inovio stockholders should be aware that some Inovio executive officers and directors have interests in the transaction that may be different from, or in addition to, their interests as stockholders of Inovio. These interests include the execution of new employment agreements, to be effective upon closing of the Merger, between Inovio and its current executive officers, which provide for certain payments upon closing of the Merger and eligibility for future severance payments under certain terms and conditions.

        As of September 30, 2008, Inovio's directors and executive officers as a group beneficially held 2,539,212 shares of Inovio common stock including options and warrants to purchase 1,936,680 shares of Inovio common stock exercisable within 60 days of the record date also held by the Inovio directors and executive officers, equivalent to approximately 5.71% of the shares of Inovio common stock entitled to vote at the Inovio special meeting. Approval of the proposals at the Inovio special meeting requires the affirmative vote of the holders of a majority of the outstanding shares of Inovio common stock present at the Inovio special meeting, in person or by proxy duly authorized.

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        Inovio's board of directors was aware of these interests and considered them, among other matters, in making its recommendation to Inovio's stockholders that they approve the transaction and other related proposals. In addition, subsequent to such recommendation, Dr. Avtar Dhillon, Simon Benito and Chin-Cheong Chong were selected to continue service on the Inovio board as directors post-closing, for which Mr. Benito and Mr. Chong will continue to receive customary director compensation.

        In considering the recommendation of VGX's board of directors that VGX stockholders vote in favor of the issuance of Inovio's securities in conjunction with the Merger and the resulting change of control of VGX, VGX stockholders should be aware that some VGX executive officers and directors have interests in the transaction that may be different from, or in addition to, their interests as stockholders of VGX. These interests include

        Dr. Collins will receive customary director compensation for his service on the post-Merger board of directors.

        As of the record date, all directors and executive officers of VGX as a group owned approximately 30.18% of the shares of VGX common stock entitled to vote at the VGX special meeting; this percentage does not include options and warrants to purchase 4,365,000 shares of VGX common stock exercisable within 60 days of the record date also held by the VGX executive officers and directors. The affirmative vote at the VGX special meeting of the holders of a majority of the outstanding shares of VGX common stock, or approximately 20,835,120 shares based on the number of shares of outstanding VGX common stock on December 5, 2008, is required to approve the Merger and the Acquisition Agreement.

        VGX's board of directors was aware of these interests and considered them, among other matters, in making its recommendation to VGX's stockholders that they approve the transaction.

Directors and Management of Inovio Following the Transaction

        The Acquisition Agreement provides that Inovio shall identify and nominate three individuals from its current board of directors and that VGX shall identify and nominate two individuals from its current board of directors to serve on the board of directors of the post-Merger company. At least two of the individuals put forth by Inovio and one individual put forth by VGX must be "independent" pursuant to the rules and regulations of the NYSE Alternext and the Rule 10A-3(b) as promulgated under the Exchange Act. Inovio's current board of directors will take all actions necessary such that the following individuals nominated by Inovio and VGX pursuant to the terms of the Acquisition Agreement shall be appointed to the Inovio board of directors at the closing. The following is a list and brief biography of each person who is expected to serve as a director of Inovio upon and after the

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closing of the Merger pursuant to the arrangement described above, annotated with the anticipated service of such individuals on the committees of the post-Merger board of directors:

Name
  Age   Position

Avtar Dhillon, M.D. 

    47   Chairman of the Board, President, Director

J. Joseph Kim, Ph.D. 

    40   Chief Executive Officer, Director

Simon X. Benito(1)(2)(3)

    63   Director

Chin-Cheong Chong(1)(2)(3)

    48   Director

Morton Collins, Ph.D.(1)(2)(3)

    72   Director

(1)
Member of the Compensation Committee

(2)
Member of Nomination and Corporate Governance Committee

(3)
Member of the Audit Committee

         AVTAR DHILLON, M.D. joined Inovio as the President and Chief Executive Officer, and as a director, in October 2001. Post-Merger, Dr. Dhillon will remain as President and a director of the combined company and is anticipated to serve as Chairman of the Board. Prior to joining Inovio, Dr. Dhillon was engaged by MDS Capital Corp. (now Lumira Capital Corp.), one of North America's leading healthcare venture capital organizations, as a consultant in July 1998, and subsequently became Investment Manager in August 1999 and Vice President in 2000. In July 1989, Dr. Dhillon started a medical clinic and subsequently practiced family medicine for over 12 years. From March 1997 to July 1998, Dr. Dhillon served as consultant to Cardiome Pharmaceuticals., a biotechnology company listed on NASDAQ National Market and the Toronto Stock Exchange. Dr. Dhillon has a Bachelor of Science, honors degree in physiology and M.D. degree from the University of British Columbia. Dr. Dhillon is also a director of Protox Therapeutics, a publicly traded specialty pharmaceutical company and Auricle Biomedical, a capital pool company.

         J. JOSEPH KIM, PH.D. will join Inovio at closing of the Merger as its Chief Executive Officer and a director. A co-founder of VGX Pharmaceuticals and its current President, Chief Executive Officer and a director since 2000, Dr. Kim is a veteran of the biopharmaceutical industry. Prior to VGX, Dr. Kim led efforts in manufacturing and process development of several FDA-approved products and developmental therapeutics at Merck. These products include FDA-approved vaccines for Hepatitis as well as developmental vaccines and therapeutics for HIV/AIDS. Dr. Kim has published over 70 peer-reviewed scientific papers and book chapters, holds numerous patents and sits on several editorial boards and review panels. In 2002, Dr. Kim was named as one of the world's top 100 young innovators by Technology Review magazine and as one of the "40 under 40" by the Philadelphia Business Journal, which highlights most dynamic professionals who are under 40 years of age in the region. Dr. Kim was also selected on the list of the "50 Most Influential Men" in the October 2003 and in the October 2006 "Power Issue" of Details Magazine . In 2004, Dr. Kim and VGX Pharmaceuticals were selected as one of 30 Technology Pioneers by the World Economic Forum. Furthermore, Dr. Kim was featured in the "Who's Next 2005" issue of Newsweek International , which included a group of 10 leaders, scientists, and executives at the forefront of change and impact in the world. Most recently in 2006, Dr. Kim has been named a Young Global Leader by the Forum of Young Global Leaders, an affiliate of the World Economic Forum. Dr. Kim was among 175 leading executives, public figures and intellectuals under the age of 40 from 50 countries. Dr. Kim has also been featured in articles in Forbes and the New Yorker and in numerous other Media Outlets. Dr. Kim was trained in economics, engineering and biological sciences at MIT where he was a U.S. Senate Honors Scholar. He holds a Ph.D. in Biochemical Engineering from the University of Pennsylvania and an MBA in Finance from the Wharton School.

         SIMON X. BENITO has been a director of Inovio since December 2003. Prior to his retirement, Mr. Benito had a successful and extensive career serving several health care companies in senior

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executive positions, including 25 years at Merck & Co, Inc. His most recent positions included Senior Vice President, Merck Vaccine Division; Executive Vice President, Merck-Medco Managed Care; and Executive Director and Vice President, Merck Human Health, Japan. In addition, Mr. Benito was a Fellow of the Institute of Chartered Accountants in England and Wales for over thirty years until his retirement in 1999. Since April 2005, Mr. Benito has served as a director of DURECT Corporation, a publicly traded specialty pharmaceutical company.

         CHIN-CHEONG CHONG joined the Inovio board of directors in December 2008. Since October 2001, Mr. Chong has served as co-founder and Managing Director of Huios Pte Ltd (previously known as GS Excel Associates Pte Ltd), which provides consultancy services to business enterprises in the area of capital markets, fundraising, and investor relations. Mr. Chong previously worked for Goldman Sachs in New York and later started the firm's equities sales business in Singapore with a team of colleagues, covering southeast Asia. After about 10 years with Goldman Sachs, he was invited to join JP Morgan as the head of self-directed investment for south Asia in 1996 and later promoted to Co-head, Private Wealth Management Group, South Asia. From 1999 to 2000, Mr. Chong was the managing director of DBS Securities Singapore and also responsible for DBS Bank's securities and stockbroking business worldwide. Mr. Chong received his M.B.A. in Finance from Indiana University at Bloomington and he was awarded a B.Sc. in Industrial Engineering by the University of Wisconsin, Madison.

         MORTON COLLINS, PH.D. has been a director of VGX since June 2008. Dr. Collins has been a General Partner of Battelle Ventures since July 2003 and Innovations Valley Partners since August 2005. For the past 40 years, Dr. Collins has acquired broad expertise in venture capital funding of early-stage high-technology companies as a founder and managing partner of five different funds, Developmental Science Ventures I, II, III, and IV and Cardinal Partners. He chaired President Reagan's Task Force on Innovation and Entrepreneurship and served as a technology policy advisor to President George H. W. Bush. He is a former President, Director and Chairman of the National Venture Capital Association, and currently serves as Director to Kopin Corporation and Strategic Diagnostics, Inc. and several private companies. Dr. Collins holds a B.S. in Engineering from the University of Delaware, and his M.A. and Doctorate Degrees in Engineering from Princeton University.

    Executive Officers

        In addition to Dr. Kim, who shall serve as Chief Executive Officer, and Dr. Dhillon, who shall serve as President of the post-Merger company, as noted above under " Directors, " the management team of Inovio shall consist of the following persons effective as of the closing and contingent upon the occurrence of the closing:

Name
  Age   Position

Peter Kies

    45   Chief Financial Officer

C. Jo White

    54   Chief Medical Officer

Niranjan Sardesai

    41   Senior Vice President, Research and Development

Kevin Rassas

    62   Senior Vice President, Business Development

Gene Kim

    40   Vice President, Finance

Punit Dhillon

    28   Vice President, Operations

Ruxandra Draghia-Akli

    43   Vice President, Research

Iacob Mathiesen

    42   Vice President, Research and Development

Michael Fons

    49   Vice President, Corporate Development

        PETER KIES—Chief Financial Officer.     Mr. Kies has been employed by Inovio as Chief Financial Officer since June 2002. For the 15 years prior to joining Inovio, Mr. Kies acquired broad expertise in the functional and strategic management of biotechnology and high technology companies across the full spectrum of corporate growth, from Initial Public Offering to profitability. From May 1996 until

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joining Inovio, he served as Chief Financial Officer for Newgen Results Corporation, and prior to that served as Controller for Cytel Corporation and as an auditor for Ernst & Young LLP. Mr. Kies holds a B.S. in Business Administration from United States International University in San Diego, California.

        C. JO WHITE, M.D.—Chief Medical Officer.     Dr. White has served as Chief Medical Officer of VGX since 2005. She has 21 years of senior level clinical/medical affairs positions with major pharmaceutical companies including BMS, Wyeth and Merck. Her experience has been focused in the area of infectious diseases and she is trained as an Internist and Infectious Disease specialist. Dr. White has designed and conducted over 40 Phase 1-4 trials, filed several Biologics License Applications/Marketing Authorization Applications and has obtained regulatory approval for 5 different vaccines and drugs in both the U.S. and Europe. Dr. White completed a fellowship in Infectious Diseases at the National Institutes of Health (NIH) in the National Institute of Allergy and Infectious Diseases (NIAID). Dr. White is board certified in both Internal Medicine and Infectious Diseases. She graduated summa cum laude from the University of Texas in Austin with a B.A. in Microbiology. She received her medical degree with honors from Baylor College of Medicine in Houston, Texas.

        NIRANJAN SARDESAI, PH.D.—Senior Vice President, Research and Development.     Dr. Sardesai has served as Senior Vice President, Research and Development of VGX since November 2007. Dr. Sardesai is an experienced veteran of the pharmaceutical industry, with a special focus in R&D and Management of Technology. Prior to joining VGX in September 2006, Dr. Sardesai was the President of Nvision Consulting, Inc. for the period from June 2005 to September 2006. He also served as the Director of R&D and Director of Applied Research at the Fujirebio Diagnostics, Inc. from October 2000 to December 2005. At Fujirebio, Dr. Sardesai oversaw all aspects of the company's R&D activities, with a special focus on new product development. Prior to Fujirebio, he worked as a Senior Scientist at IGEN International, Inc. Dr. Sardesai received a Ph.D. in Chemistry from California Institute of Technology and an MBA in Entrepreneurial Management from the Wharton School of the University of Pennsylvania. Dr. Sardesai also completed post-doctoral fellowships at the Scripps Research Institute and the Massachusetts Institute of Technology. Dr. Sardesai received his M. Sc. in Chemistry from the Indian Institute of Technology.

        KEVIN RASSAS—Senior Vice President, Business Development.     Mr. Rassas has served as Senior Vice President, Business Development of VGX since July 2006. He first joined VGX in December 2003 to head VGX's business development efforts. Mr. Rassas has over 30 years of pharmaceutical industry experience, including senior level general management responsibility for several major international markets with Wyeth and G.D.Searle. Mr. Rassas' background includes significant experience in International Operations, P&L Management, Strategic Planning, Business Development, Finance and Administration, New Product Introductions, Joint Ventures, Project Management, and Human Resources. Mr. Rassas received a Bachelor of Arts in Economics from the University of Notre Dame and his MBA in Finance from the Kellogg School of Management at Northwestern University.

        GENE KIM—Vice President, Finance.     Mr. Kim has joined VGX in 2005 as Director of Finance and has served as Chief Financial Officer of VGX since May 2006. Mr. Kim has over 13 years of experience in the financial services and energy related industries. Prior to joining VGX, he served as a financial advisor to several small start-ups in the Washington DC area as a part of AEG Capital, a position he held from November 2003 to October 2005. He has also served as a Director of Finance for several high-tech start-ups in Silicon Valley, including Yodlee, a firm providing technology solutions for the financial services industry, and Pandesic, a joint venture between Intel and SAP. His duties included the establishment and integration of policies and procedures, implementation of accounting systems, and financial planning and analysis. Prior to his work with start-ups, he worked for Bankers Trust/Deutsche Bank as a trader in the interest rate arbitrage group. Mr. Kim began his career as a chemical engineer with Unocal where he worked as a refinery engineer. Mr. Kim has an M.B.A. in

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Finance from the Wharton School of Business at the University of Pennsylvania and a Bachelor of Science in Chemical Engineering from UCLA, and is a Certified Public Accountant.

        PUNIT DHILLON—Vice President, Operations.     Punit Dhillon was promoted by Inovio to Vice President, Finance and Operations in January 2008. Mr. Dhillon joined Inovio in September 2003 and has played a role in various corporate finance projects, including management of financing transactions, as well as day-to-day management of operational functions. Mr. Dhillon was most recently Executive Director of Finance and Operations. Prior to joining Inovio, he worked for a corporate finance law firm as a law clerk. He previously worked with MDS Capital Corp. (now Lumira) and was a consultant to several early stage health and life-science companies where he acquired broad experience in corporate management, finance and capital markets. Mr. Dhillon has a Bachelor of Arts, Honors, in Political Science and a minor in Business Administration from Simon Fraser University. Mr. Dhillon is also a director of Auricle Biomedical, a capital pool company.

        RUXANDRA DRAGHIA-AKLI, M.D., PH.D.—Vice President, Research.     Dr. Draghia-Akli has served as Vice President, Research of VGX since February 2007, and has over 15 years of experience. From November 2001 until February 2007, she served as Head of Research with ADViSYS, Inc., which VGX acquired in 2007. She is recognized as a global leader in the field of DNA delivery for therapeutic and vaccination applications. She was the co-founder of ADViSYS, Inc., developing the first plasmid-mediated growth hormone releasing hormone (GHRH) supplementation. Dr. Draghia's research activities have focused on plasmid design, gene expression and muscle-specific promoter/enhancer fragments and DNA sequences that allow for the efficient expression of either secreted or intracellular proteins for gene therapy and vaccination. Throughout her career, Dr. Draghia has published numerous scientific papers and reviews in the areas of electroporation, plasmid components for optimum transgene expression, GHRH, IGF-I and their effects on pituitary development, immune stimulation, health, and well-being. Dr. Draghia-Akli also serves as an ad hoc reviewer for granting agencies, such as European Union, USDA and NIH, annual meeting for gene therapy and endocrinology societies, and manuscripts for numerous journals. Dr. Draghia received an MD from Carol Davilla Medical School and a Ph.D. in human genetics from Romanian Academy of Medical Sciences. Dr. Draghia also completed post-doctoral fellowships at the University of Rene Descartes and the Baylor College of Medicine. She has held an adjunct faculty position at BCM.

        MICHAEL FONS, PH.D.—Vice President, Corporate Development.     Michael Fons, PhD, was promoted by Inovio to Vice President of Corporate Development in August 2007. Dr. Fons joined Inovio as Executive Director of Corporate Development in June 2004. In such capacity, he has been instrumental in defining Inovio's corporate strategy relating to DNA vaccines and DNA delivery, including assisting in securing DNA-related license agreements, acquiring valuable intellectual property assets, and establishing a strong standard for the management of Inovio's corporate relationships. From 2002 to 2004, Dr. Fons held the position of Executive Director, Business Development and Technology Assessment at Vical, Inc. Dr. Fons previously held business development roles with GeneMedicine, and Valentis. He is an Adjunct Associate Professor of Microbiology and Immunology with the University of Texas Medical Branch. Dr. Fons is a published author of 24 papers in scientific journals and numerous book chapters.

        IACOB MATHIESEN—Vice President, Research and Development.     Iacob Mathiesen is currently the managing director of Inovio's Norwegian subsidiary, Inovio AS, which is conducting preclinical research on DNA vaccines. Mr. Mathiesen joined Inovio when a company he co-founded in 1999 to pursue research and development relating to electroporation and for which he was chief executive officer was acquired by Inovio in 2005. Mr. Mathiesen has pioneered novel advancements for electroporation methods and devices for DNA delivery and has been named as inventor or co-inventor on multiple patents and co-authored numerous scientific papers relating to the use of electroporation for DNA delivery. Mr. Mathiesen received a B.Sc. in Mathematics and Natural Sciences in 1991, an

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M.Sc. in Mathematics and Natural Sciences in 1993, and a Ph.D. in Medicine in 1999, all from the University of Oslo, Norway.

        No family relationships exist between any of the directors or executive officers of Inovio or VGX or the combined group, except that Mr. Punit Dhillon, Inovio's current Vice President, Finance and Operations and the combined group's intended Vice President, Operations, is the nephew of Dr. Avtar Dhillon, Inovio's President and Chief Executive Officer and director and the combined group's intended President, director and Chairman of the Board. Neither Mr. Dhillon nor Dr. Dhillon have been party to any transaction requiring disclosure pursuant to Item 404(a) of Regulation S-K.

    Legal Proceedings

        No current Inovio or VGX directors or executive officers, nor any intended directors or executive officers of the combined group, have been involved in the certain legal proceedings listed in Item 401 of Regulation S-K.

Corporate Governance

        Inovio's Corporate Governance Policy, which includes the charters of the committees of the board of directors, is available on its website, www.inovio.com . Historically the Inovio board of directors has implicitly and explicitly acknowledged its responsibility for the stewardship of Inovio in the following ways, and the parties do not anticipate any changes in such policies and procedures upon closing of the Merger:

    Committees of the Board of Directors

      Audit Committee

        The functions of the Audit Committee include retaining Inovio's independent registered public accounting firm, reviewing its independence, reviewing and approving the planned scope of Inovio's annual audit, reviewing and approving any fee arrangements with Inovio's independent registered public accounting firm, overseeing its audit work, reviewing and pre-approving any non-audit services that may be performed by it, reviewing the adequacy of accounting and financial controls, reviewing Inovio's critical accounting policies and reviewing and approving any related party transactions. The Inovio board of directors amended the charter for the Audit Committee on March 6, 2008, to better reflect the practices and responsibilities of the Audit Committee. The Audit Committee's charter, a component of Inovio's Corporate Governance Policy, is available separately on its website at: http://media.corporate-ir.net/media_files/irol/10/105128/corpGov/AuditCommittee.pdf

        Upon closing of the Merger, the parties anticipate that Simon Benito, Chin-Cheong Chong, and Dr. Morton Collins will serve as members of the Audit Committee; each of these individuals is independent under the NYSE Alternext listing standards. The Inovio board of directors previously determined that Mr. Benito is an "audit committee financial expert" as defined under Item 407(d)(5)(ii) of Regulation S-K under the Securities Act.

      Compensation Committee

        The Compensation Committee determines the salary of the executive officers of Inovio, grants stock options under the 2007 Omnibus Incentive Plan and performs such other functions regarding compensation as the board of directors may delegate. The Inovio board of directors amended the charter for the Compensation Committee on March 27, 2008.

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        Upon closing of the Merger, the parties anticipate that Simon Benito, Chin-Cheong Chong and Dr. Morton Collins will serve as the members of the Compensation Committee. Each member of the Compensation Committee is independent under the NYSE Alternext listing standards.

      Nomination and Corporate Governance Committee

        The Nomination and Corporate Governance Committee identifies and recommends candidates for election to the Inovio board of directors. It advises the board of directors on all matters relating to directorship practices, including the criteria for selecting directors, policies relating to tenure and retirement of directors and compensation and benefit programs for non-employee directors. While the Nomination and Corporate Governance Committee has not established any minimum criteria for serving as a director, the Committee focuses on selecting individuals that have skill sets that augment the skill sets of the current directors and are most likely to assist in the building and success of Inovio. In addition, the Committee believes it appropriate for at least one member of the board of directors to meet the criteria for an "audit committee financial expert," as defined by the SEC rules, that independent members of the board who serve on the audit committee are able to read and understand fundamental financial statements, including a balance sheet, income statement, and cash flow statement and that at least a majority of the members of the board of directors meet the definition of "independent" under NYSE Alternext rules.

        The Nomination and Corporate Governance Committee also makes recommendations relating to the duties and membership of committees of the board of directors, recommends processes to evaluate the performance and contributions of individual directors and the board of directors as a whole, approves procedures designed to provide that adequate orientation and training are provided to new members of the board of directors, consults with the Chief Executive Officer in the process of recruiting new directors and assists in locating senior management personnel and selecting members for the scientific advisory board.

        The Nomination and Corporate Governance Committee has developed a policy to govern Inovio's approach to corporate governance issues and provides a forum for concerns of individual directors about matters not easily or readily discussed in a full board meeting (e.g., the performance of management). Individual directors are entitled to engage outside advisors at the expense of Inovio, with the prior approval of the Nomination and Corporate Governance Committee, and with the full knowledge of management. The board of directors amended the charter for the Nomination and Corporate Governance Committee on March 27, 2008. The Nomination and Corporate Governance Committee's charter, a component of Inovio's Corporate Governance Policy, is available separately on Inovio's website at: http://media.corporate-ir.net/media_files/irol/10/105128/corpGov/NomandCorpGov.pdf

        Upon closing of the Merger, the parties anticipate that Simon Benito, Chin-Cheong Chong and Dr. Morton Collins will serve as the members of the Nomination and Corporate Governance Committee, and each is independent under the NYSE Alternext listing standards.

    Strategic Planning and Identification of Risks

        Management prepares an annual business plan for Inovio and presents the plan to the Inovio board of directors for its review and comments. In connection therewith, the board of directors discusses various strategic matters with management and identifies business risks associated with Inovio's activities.

    Senior Management

        The board of directors takes responsibility for appointing those members of senior management who become Inovio's officers. Currently, the members of senior management of Inovio are: Dr. Avtar Dhillon, president and chief executive officer; Peter Kies, chief financial officer and human resources

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manager; Dr. Michael Fons, vice president, corporate development; and Punit Dhillon, vice president, finance and operations; however, if the Merger is completed, the executive officers of the post-Merger company will be the individuals noted under " Executive Officers" above.

    Communications Policy

        The board of directors has procedures in place to ensure effective communication between Inovio, its stockholders, prospective investors, and the public, including the dissemination of information on a regular and timely basis. Historically, the Chairman of the board of directors, the chief executive officer, the chief financial officer and the vice president, finance and operations, along with various other Inovio employees and consultants, devoted a portion of their time to dealing with stockholders and prospective investors. Stockholders who want to communicate with the board or any individual director can write to Inovio's Secretary at the following address: 11494 Sorrento Valley Road, San Diego, CA 92121-1318; such correspondence should indicate that status as an Inovio stockholder. Depending on the subject matter, management will:

    Forward the communication to the director or directors to whom it is addressed;

    Attempt to handle the inquiry directly, for example, where it is a request for information about Inovio or it is a stock-related matter; or

    Not forward the communication if it is primarily commercial in nature or if it relates to an improper or irrelevant topic.

    Internal Control and Management Information Systems

        Along with management, the board of directors is responsible for Inovio's internal control and management information systems. The Audit Committee of the board of directors meets with Inovio's independent registered public accounting firm quarterly to review Inovio's financial statements and to review Inovio's financial reporting procedures.

    Independence from Management

        To ensure that the board of directors functions independently of management, Inovio has separated the office of chairman of the Board from that of chief executive officer. Further the independent directors meet on a regular basis as often as necessary to fulfill their responsibilities, including at least annually in executive session without the presence of non-independent directors and management.

    Modified Plurality Voting Policy

        On December 5, 2008, the Inovio board of directors, upon recommendation from its Nomination and Corporate Governance Committee adopted a Modified Plurality Voting Policy as an addition to its Corporate Governance Policy. The Modified Plurality Voting Policy provides that any nominee for director in an uncontested election who receives (a) a greater number of votes "withheld" from his or her election than votes "for" his or her election and (b) votes "withheld" from his or her election that constitute thirty-five percent (35%) or more of the outstanding shares of Inovio common stock, must promptly tender his or her written resignation following the certification of the stockholder vote. The Inovio board of directors, in accordance with the procedures set out in the policy and upon a recommendation from the Nomination and Corporate Governance Committee, shall either accept such resignation or defer its acceptance for no more than thirty days to enable the Inovio board to maintain compliance with applicable rules and regulations. Inovio shall promptly disclose such determination on any pending resignation via a Current Report on Form 8-K. A copy of the Modified Plurality Voting Policy is posted to Inovio's website as part of Inovio's overall Corporate Governance Policy.

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    Code of Ethics

        Inovio has adopted a Code of Ethics, which applies to all directors, officers and employees, including the principal executive officer, principal financial and accounting officer and controller. The purpose of the Code of Ethics is to promote honest and ethical conduct. The Code of Ethics is incorporated by reference as Exhibit 14.1 to Inovio's 2007 Annual Report on Form 10-K, which was filed with the SEC on March 17, 2008, is available on Inovio's website and is also available in print, without charge, upon written request to the Secretary at 11494 Sorrento Valley Road, San Diego, CA 92121-1318. Any amendments to or waivers of the Code of Ethics will be promptly posted on the Inovio's website at www.Inovio.com or in a report on Form 8-K, as required by applicable laws.

Material Contracts and Relationships Between Inovio and VGX

        In November 2006, Inovio granted VGX a world-wide non-exclusive license to its DNA delivery technology for intratumoral delivery of a proprietary gene to control growth of melanoma and other cancers. Under the terms of the license agreement, Inovio received an upfront license fee from VGX and may receive payments from VGX based on successful completion of clinical and regulatory milestones. Inovio exclusively supplies VGX with electroporation devices for the therapy covered by the license agreement and would receive royalties on the sale of products covered by the license. As of September 30, 2008. VGX has paid Inovio $50,000 related to an upfront payment for the licensing agreement and issued Inovio 25,000 shares of VGX common stock (which were valued at $125,000 at the time of issuance in 2006).

        In December 2008, Inovio entered into a master research agreement with VGX so that Inovio may provide clinical and regulatory services as well as advanced electroporation delivery of DNA vaccines for each company's research uses. The cross-license is strictly for research use only and will permit Inovio and VGX, to conduct certain internal research on DNA vaccines delivered using electroporation and other research and development services. Under the terms of the agreement VGX will own all data and new intellectual property created by Inovio related to VGX's proprietary materials and technology and Inovio will own all data and new intellectual property created by VGX related to Inovio's proprietary materials and technology. The master research agreement can be terminated by either party with 90 days notice. The scope of each specific research project will be governed by a project agreement between Inovio and VGX. Each company will be compensated for its services based on a pre-determined hourly rate per full time employee outlined in the specific project agreement. Currently, it is contemplated that Inovio through its wholly-owned subsidiary in Norway, Inovio AS, will assist VGX to manage clinical and regulatory aspects for certain planned clinical trials.

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CERTAIN MATERIAL U.S. FEDERAL INCOME TAX CONSEQUENCES OF THE MERGER

        The following discussion summarizes the material U.S. federal income tax consequences of the Merger that are generally applicable to holders of VGX common stock. This discussion is based on the Code, judicial decisions and administrative regulations and interpretations in effect as of the date of this proxy statement/prospectus, all of which are subject to change, possibly with retroactive effect. Accordingly, the U.S. federal income tax consequences of the Merger to the holders of VGX common stock could differ from those described below.

        The discussion assumes that VGX stockholders hold their shares of VGX common stock as a capital asset. This discussion does not address all aspects of U.S. federal income taxation that may be relevant to holders of VGX common stock in light of their particular circumstances, nor does it address the U.S. federal income tax consequences to holders that are subject to special rules under U.S. federal income tax law, including:

    dealers in securities or foreign currencies;

    tax-exempt organizations;

    financial institutions or insurance companies;

    holders who have a "functional currency" other than the U.S. dollar;

    holders who own their shares indirectly through partnerships, trusts, S corporations or any other entity treated as a flow-through entity for U.S. federal income tax purposes that may be subject to special treatment;

    holders all or part of whose Inovio stock received in the Merger will be subject to forfeiture provisions;

    holders who acquired their shares in connection with stock options or stock purchase plans or other compensatory transactions; and

    holders who hold their shares as a hedge or as part of a straddle, constructive sale, conversion transaction, or other risk management transaction.

        This discussion is also limited to United States persons who hold VGX common stock (a "U.S. holder") and receive Inovio common stock therefor in the Merger. For purposes of this discussion, the term "United States person" means

    An individual citizen or resident of the United States;

    A corporation (or an entity treated as a corporation for U.S. federal income tax purposes) created or organized in or under the laws of the United States, any state thereof or the District of Columbia;

    An estate, the income of which is subject to U.S. federal income tax regardless of its source; or

    A trust that (x) is subject to the supervision of a court within the United States and the control of one or more United States persons or (y) has a valid election in effect under applicable Treasury regulations to be treated as a United States person.

        In addition, this discussion does not address the tax consequences of the Merger to a VGX option holder, warrant holder, or convertible debt holder, including the assumption by Inovio of outstanding options and warrants to acquire VGX common stock or convertible debt of VGX. In addition, this discussion does not address any tax consequences of the Merger under foreign, state or local law or U.S. federal estate and gift tax laws. No ruling has been or will be obtained from the IRS regarding any matter relating to the Merger and no assurance can be given that the IRS will not assert, or that a court will not sustain, a position contrary to any aspect of this discussion. Inovio and VGX urge holders

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of VGX common stock to consult their own tax advisors as to the U.S. federal income tax consequences of the Merger, as well as the effects of state, local and foreign tax laws in light of their own situations.

        In addition, completion of the Merger is contingent upon the receipt by (i) VGX of an opinion of its counsel, Duane Morris LLP, dated as of the closing date, to the effect that, on the basis of facts, representations and assumptions set forth in such opinion, the Merger will be treated as a reorganization within the meaning of Section 368(a) of the Code and (ii) Inovio of an opinion of its counsel, K&L Gates LLP, dated as of the closing date, to the effect that, on the basis of facts, representations and assumptions set forth in such opinion, the Merger will be treated as a reorganization within the meaning of Section 368(a) of the Code.

        The opinions of K&L Gates LLP, counsel to Inovio, and Duane Morris LLP, counsel to VGX, which are required as a condition to closing the Merger, are and will be based on U.S. federal income tax laws in effect as of the date of these opinions. An opinion of counsel is not binding on the IRS or any court. In rendering their respective opinions, Duane Morris LLP and K&L Gates LLP will rely on certain assumptions, including assumptions regarding the absence of changes in existing facts and the completion of the Merger strictly in accordance with the Merger agreement and this proxy statement/prospectus. The opinions will also rely upon certain representations and covenants made by the management of Inovio, Submerger and VGX and will assume that these representations are true, correct and complete without regard to any knowledge limitation, and that Inovio and VGX, as the case may be, will comply with these covenants. If any of these assumptions or representations is inaccurate in any way, or any of the covenants are not complied with, the opinions could be adversely affected.

        Assuming that the Merger qualifies as a reorganization within the meaning of Section 368(a) of the Code, the material U.S. federal income tax consequences of the Merger to holders of VGX common stock are as follows.

        Exchange of VGX common stock solely for Inovio common stock.     A holder of VGX common stock who exchanges such holder's shares solely for Inovio common stock in the Merger will not recognize gain or loss. Such holder will have an aggregate tax basis in the Inovio common stock received in the Merger equal to the holder's aggregate adjusted tax basis in the VGX common stock surrendered in the Merger, and the holding period for the Inovio common stock will include the holding period for the VGX common stock.

        Dissenting Stockholders.     Holders of VGX common stock are entitled to dissenters rights under Delaware law in connection with the Merger. If a U.S. holder receives cash pursuant to the exercise of dissenters' rights, that U.S. holder generally will recognize gain or loss measured by the difference between the cash received and the adjusted tax basis of such holder's shares. This gain should be long-term capital gain or loss if the U.S. holder held VGX common stock as a capital asset for more than one year. If a holder of VGX common stock who receives cash pursuant to the exercise of dissenters rights is treated as owning Inovio common stock after the Merger, as the result of the application of the constructive ownership rules, all or a portion of the cash received by the holder may be taxed as a dividend. Any holder of VGX common stock that plans to exercise dissenters' rights in connection with the Merger is urged to consult a tax advisor to determine the related tax consequences.

        Failure of the Merger to Qualify as a Reorganization.     If the Merger is not treated as a "reorganization" within the meaning of Section 368(a) of the Code, then VGX would recognize gain or loss equal to the difference between the amount realized in the Merger and the tax basis of its assets. In addition, each U.S. holder would recognize gain or loss equal to the difference between the sum of the fair market value of the Inovio common stock and such holder's tax basis in VGX common stock surrendered in exchange therefor.

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        Backup Withholding.     Non-corporate holders of VGX common stock may be subject to information reporting and backup withholding at a rate of 28% on any cash payments received. Generally, backup withholding will not apply, however, if a holder of VGX common stock:

    furnishes a correct taxpayer identification number and certifies that such holder is not subject to backup withholding on the substitute Form W-9 or successor form included in the election form/letter of transmittal received; or

    is otherwise exempt from backup withholding.

        Any amounts withheld under the backup withholding rules will generally be allowed as a refund or credit against a holder's U.S. federal income tax liability, provided the required information is furnished to the IRS.

        Reporting Requirements.     A significant holder of VGX common stock for U.S. federal income tax purposes who receives shares of Inovio common stock as a result of the Merger will be required to retain records pertaining to the Merger and to file with such holder's U.S. federal income tax return for the year in which the Merger takes place a statement setting forth certain facts relating to the Merger. Such statement must include the holder's tax basis in and fair market value of VGX common stock surrendered in the Merger.

         THIS SUMMARY IS NOT A SUBSTITUTE FOR AN INDIVIDUAL ANALYSIS OF THE TAX CONSEQUENCES OF THE MERGER TO YOU. WE URGE YOU TO CONSULT A TAX ADVISOR REGARDING THE PARTICULAR FEDERAL, STATE, LOCAL AND FOREIGN TAX CONSEQUENCES OF THE MERGER TO YOU.

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THE ACQUISITION AGREEMENT

         The following summary of the Acquisition Agreement is qualified in its entirety by reference to the complete text of the Acquisition Agreement, which is incorporated by reference and a copy of which is attached as Annex A to this joint proxy statement/prospectus. The rights and obligations of the parties are governed by the express terms and conditions of the Acquisition Agreement and not by this summary or any other information contained in this joint proxy statement/prospectus. We urge you to read the Acquisition Agreement carefully and in its entirety, as well as this joint proxy statement/prospectus, before making any decisions regarding the Merger.

         The Acquisition Agreement has been included with this joint proxy statement/prospectus to provide you additional information regarding its terms. The Acquisition Agreement sets forth the contractual rights of Inovio and VGX but is not intended to be a source of factual, business or operational information about Inovio or VGX. That kind of information can be found elsewhere in this joint proxy statement/prospectus and in the other filings Inovio makes with the SEC, which are available as described in "Where You Can Find More Information."

         As a stockholder, you are not a third party beneficiary of the Acquisition Agreement and therefore you may not directly enforce any of its terms or conditions. The parties' representations, warranties and covenants were made as of specific dates and only for purposes of the Acquisition Agreement and are subject to important exceptions and limitations, including a contractual standard of materiality different from that generally relevant to investors. In addition, the representations and warranties may have been included in the Acquisition Agreement for the purpose of allocating risk between Inovio and VGX, rather than to establish matters as facts. Certain of the representations, warranties and covenants in the Acquisition Agreement are qualified by information Inovio filed with the SEC prior to the date of the Acquisition Agreement, as well as by disclosure schedules each of Inovio and VGX delivered to the other party prior to signing the Acquisition Agreement. The disclosure schedules have not been made public because, among other reasons, they include confidential or proprietary information. The parties believe, however, that all information material to a stockholder's decision to approve the Merger is included or incorporated by reference in this document.

         You should also be aware that none of the representations or warranties has any legal effect among the parties to the Acquisition Agreement after the effective time of the Merger, nor will the parties to the Acquisition Agreement be able to assert the inaccuracy of the representations and warranties as a basis for refusing to close the transaction unless all such inaccuracies as a whole have had or would be reasonably likely to have a material adverse effect on the party that made the representations and warranties.

         Furthermore, you should not rely on the covenants in the Acquisition Agreement as actual limitations on the respective businesses of Inovio and VGX, because either party may take certain actions that are either expressly permitted in the confidential disclosure letters to the Acquisition Agreement or as otherwise consented to by the appropriate party, which may be given without prior notice to the public.

Structure of and Consideration for the Transaction

        The Acquisition Agreement contemplates that VGX will merge with and into Inovio's wholly-owned subsidiary Submerger, with Submerger surviving as the continuing entity and a wholly-owned subsidiary of Inovio, to be renamed "VGX Pharmaceuticals, LLC." In conjunction with the consummation of the merger, based upon an exchange ratio defined by the Acquisition Agreement, Inovio will exchange shares of its common stock for outstanding shares of VGX common stock and will assume and convert VGX's other outstanding securities into securities exercisable or convertible, as the case may be, for Inovio common stock. Upon issuance of such Inovio securities in conjunction with the merger of Submerger and VGX, holders of VGX securities will become holders of securities in Inovio,

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the parent, public reporting entity of the combined group. At the Effective Time of the transaction, an integrated board of directors and management team will also take over leadership of the combined group.

        Inovio stockholders will continue to own their existing shares of Inovio common stock upon closing of the Merger. The closing will not have any effect on the Inovio securities outstanding prior to the Effective Time, except that the closing may constitute a "Change of Control" or "Change in Control", as such terms are used in the Inovio incentive plans and related agreements, Inovio's organizational documents and certain of Inovio's outstanding warrants, resulting in:

        Outstanding membership interests in Submerger immediately prior to the Effective Time shall continue unchanged as membership interests in the Surviving Entity.

        Subject to the terms and conditions of the Acquisition Agreement, as a result of the Merger, and without any action on the part of Inovio, Submerger, VGX or the holder of any of VGX's outstanding securities, the following will occur:

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        Inovio and VGX also agreed that, at the Effective Time, any other contractual rights to receive shares of VGX common stock, other than the VGX options, warrants and convertible debt (which will be assumed and converted in as discussed above), shall cease to represent a right to receive shares of VGX common stock in accordance with the terms and conditions of the contract providing such rights and shall be converted into a right to receive a number of shares of Inovio common stock equal to (A) the number of shares of VGX common stock subject to such right immediately prior to the Effective Time multiplied by (B) the Merger Exchange Ratio, in accordance with the terms and conditions of the contract providing such right.

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Merger Exchange Ratio

        The Merger Exchange Ratio to be utilized to calculate the number of Inovio securities to be issued at the Effective Time, and the pricing of the assumed options and warrants, shall be equal to the quotient obtained by dividing:

Effective Time of the Transaction

        Subject to the provisions of the Acquisition Agreement, Inovio, Submerger and VGX shall cause the Merger to be consummated by filing a certificate of merger with the Secretary of State of the State of Delaware in such form as is required by, and executed and acknowledged in accordance with, the relevant provisions of the DGCL and making all other filings or recordings required under the DGCL to effect the Merger. The Certificate of Merger, when duly filed with the Secretary of State of the State of Delaware in accordance with the relevant provisions of the DGCL, shall state an effective date for the Merger of the same date as the closing date and the Effective Time of the Merger shall be the same time as the time when the closing is completed, unless Inovio and VGX shall mutually agree to a different date and time for filing and effectiveness.

Exchange of Securities

        Within three business days following the Effective Time of the Merger, Inovio shall cause Inovio's transfer agent, Computershare Trust Company, or the "Exchange Agent," to mail to each holder of record (as of the Effective Time) of a certificate or certificates prior to the Effective Time represented outstanding shares of VGX common stock and which shares were converted into the right to receive the per share applicable consideration, pursuant Acquisition Agreement: (i) a letter of transmittal (which shall specify that delivery shall be effected, and risk of loss and title to the certificates shall pass, only upon delivery of the certificates to the Exchange Agent and shall be in such form and have such other provisions as the Exchange Agent, VGX and Inovio may reasonably specify) and (ii) instructions for use in effecting the surrender of the Certificates (including a means of hand-delivery) in exchange for the applicable consideration as set forth in Acquisition Agreement. Promptly after surrender of certificates for cancellation to the Exchange Agent, together with such letter of transmittal, duly completed and validly executed in accordance with the instructions thereto and such other documents

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as may be reasonably specified in the letter of transmittal, the holder of record of such certificates shall receive in exchange therefor the applicable consideration as set forth in the Acquisition Agreement in respect of each share of VGX common stock represented by the certificates, and the certificates so surrendered shall be canceled. Until so surrendered, outstanding certificates will be deemed from and after the Effective Time, for all corporate purposes, to evidence the ownership of the applicable consideration as set forth in the Acquisition Agreement, into which such shares of VGX common stock shall have been so converted.

        From and after the Effective Time, for all corporate purposes, the instruments evidencing outstanding VGX options, VGX warrants and the VGX convertible debt will be deemed to evidence the ownership of the applicable consideration as set forth in the Acquisition Agreement into which such securities shall have been so converted. These instruments will not be automatically exchanged.

        No fraction of a share of Inovio common stock will be issued or paid by virtue of the Merger. Adjustments for fractional shares issued upon exchange of Inovio common stock for VGX common stock or issuable pursuant to assumed and converted VGX options, VGX warrants and VGX convertible debt will be made pursuant to the terms and conditions for such assumption and conversion set forth in the Acquisition Agreement.

Representations and Warranties

        The Acquisition Agreement contains customary representations and warranties of VGX relating to, among other things:

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        The Acquisition Agreement contains customary representations and warranties of Inovio and Submerger relating to, among other things:

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Conduct of Business Prior to Completion of the Transaction

        During the period prior to the Effective Time or the termination of the Acquisition Agreement, Inovio and VGX and each of its subsidiaries shall, except as otherwise expressly contemplated by the Acquisition Agreement,

        Without limiting the generality of the foregoing and without exception, VGX and/or each subsidiary will use all reasonable efforts to prepare all tax returns that are required to be filed by VGX or such subsidiary on or before the Effective Time. VGX or such subsidiary shall use all reasonable efforts to deliver each such income and franchise tax return, in a form ready to be filed, to Inovio for review at least ten business days before the due date for such income and franchise tax return.

        VGX has also agreed that, prior to the earlier of the Effective Time or the termination of the Acquisition Agreement, it will refrain from doing any of the following without the prior written consent of Inovio, which consent may not be unreasonably withheld or delayed:

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        Inovio has also agreed that, prior to the earlier of the Effective Time or the termination of the Acquisition Agreement, it will refrain from doing any of the following without the prior written consent of VGX:

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        Inovio and VGX have each granted the other party certain limited consents allowing actions otherwise barred by such provisions, related to entry into certain material agreements, issuance of securities and incurrence of cetain debt.

Regulatory Matters

        Inovio, Submerger and VGX are required to make all filings, notices, petitions, statements, registrations, submissions of information, application or submission of other documents required by any governmental entity in connection with the Merger and the transactions contemplated hereby, including:

No Solicitation

        From and after the date of the original agreement and plan of merger until the Effective Time or termination of the Acquisition Agreement, Inovio or VGX has not and will not, nor will they authorize or has either authorized any of their respective officers, directors, affiliates or employees or any investment banker, attorney or other advisor or representative retained by any of them to, directly or indirectly

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        However, until the date on which the Acquisition Agreement is approved by the required vote of the Inovio and VGX stockholders, this provision shall not prohibit Inovio or VGX from furnishing information regarding Inovio or VGX and its subsidiaries to, entering into a confidentiality agreement with or entering into discussions with, any person or group in response to a superior offer submitted by such person or group to the extent and so long as:

        At the time of the signing of the original agreement and plan of merger, Inovio and VGX and their subsidiaries immediately ceased any and all existing activities, discussions or negotiations with any parties conducted prior to signing the merger agreement with respect to any acquisition proposal.

        In addition to the foregoing, Inovio or VGX are required to: (i) provide the each other with at least forty-eight hours prior written notice (or such lesser prior written notice as provided to the members of the other party's board but in no event less than eight hours) of any board meeting at which the board is reasonably expected to consider an acquisition proposal for evaluation of whether it constitutes a superior offer and together with such notice deliver a copy of the acquisition proposal for review and (ii) provide each other with at least three business days' prior written notice of a board meeting at which the board is reasonably expected to recommend a superior offer to the stockholders in lieu of the Acquisition Agreement and the Merger and recommend withdrawal of its prior recommendation pursuant to the Acquisition Agreement and together with such notice deliver a copy of the superior offer for review.

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Other Covenants

        Some of the other material terms to which Inovio and VGX agreed, other than those related to the preparation, filing and mailing of this joint proxy statement/prospectus and holding of the Inovio and VGX special meetings, include:

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        Please see the Acquisition Agreement for additional covenants of Inovio and VGX.

Conditions to the Transaction

        Inovio's obligation to consummate the Merger and issue its securities pursuant to the Acquisition Agreement, which we refer to as the "closing," will not take place until the parties satisfy, or waive where allowable, the other conditions listed in the Acquisition Agreement. These closing conditions include but are not limited to the following:

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Termination of the Acquisition Agreement

        The Acquisition Agreement may be terminated prior to the date the registration statement, of which this joint proxy statement/prospectus is a part, becomes effective, under several circumstances, including:

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Termination Payment

        In the event that the Acquisition Agreement is terminated by Inovio pursuant to the termination provision of the Acquisition Agreement that allows for withdrawal of the Inovio board's recommendation to the Inovio stockholders in favor of the Merger in relation to receipt and recommendation of an Inovio superior offer, Inovio shall promptly, but in no event later than two business days after the date of such event, pay VGX a fee equal to $3,500,000 in immediately available funds and such payment shall be the sole and exclusive remedy relating therewith. In the event that the Acquisition Agreement is terminated by VGX pursuant to the termination provision of the Acquisition Agreement which allows for withdrawal of the VGX board's recommendation to the VGX stockholders in favor of the Merger in relation to receipt and recommendation of a VGX superior offer, VGX shall promptly, but in no event later than two business days after the date of such event, pay Inovio a fee equal to $3,500,000 in immediately available funds and such payment shall be the sole and exclusive remedy relating therewith.

Transaction Expenses

        Whether or not the transaction is completed, all fees and expenses incurred in connection with the Acquisition Agreement and the transactions contemplated by the Acquisition Agreement will be paid by the party incurring the fees or expenses.

Indemnification

        Inovio will, and will cause the Surviving Entity to, fulfill and honor all rights to indemnification existing as of the date of the Acquisition Agreement (i) in favor of an officer, director or employee of VGX or any of its subsidiaries, whether provided in the VGX charter documents or pursuant to any

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contractual agreement (as in effect as of the date of the Acquisition Agreement) to survive the Merger and be observed by the Surviving Entity to the fullest extent permitted by applicable law, and (ii) in favor of an officer, director or employee of Inovio or any of its subsidiaries, whether provided in the Inovio charter documents or pursuant to any contractual agreement (as in effect as of the date of the Acquisition Agreement) to survive the Merger and be observed by Inovio to the fullest extent permitted by applicable law, in each case until not earlier than the sixth anniversary of the Effective Time.

        Insofar as indemnification for liabilities arising under the Securities Act may be permitted to directors, officers or persons controlling the registrant pursuant to the foregoing provisions, the registrant has been informed that in the opinion of the SEC such indemnification is against public policy as expressed in the Securities Act and is therefore unenforceable.

Amendment and Waiver

        Subject to applicable law, any provision of the Acquisition Agreement may be amended by the parties thereto at anytime by execution of an instrument in writing signed on behalf of each of the parties thereto.

Governing Law

        The laws of the State of Delaware govern the Acquisition Agreement, regardless of the laws that might otherwise govern under applicable principles of conflicts of law.


OTHER AGREEMENTS RELATED TO THE TRANSACTION

VGX Support Stockholders Voting Agreements

        The Acquisition Agreement requires that four identified VGX stockholders, who collectively hold approximately 41% of the issued and outstanding VGX common stock, enter into voting agreements with Inovio. Dr. J. Joseph Kim, president, chief executive officer and director of VGX, Dr. David Weiner, a founder of VGX and significant stockholder, Dr. Morton Collins, a director of VGX, and Young K. Park, a significant stockholder of VGX (each referred to in this joint proxy statement/prospectus as a "support stockholder"), have each executed a voting agreement providing that he, in his capacity as a VGX stockholder only, shall vote or cause to be voted for approval and adoption of the Acquisition Agreement and the transactions contemplated thereby all shares of VGX common stock over which he has sole voting power, and use commercially reasonable efforts to cause any shares of VGX common stock over which he shares voting power to be voted for approval and adoption of the Acquisition Agreement and the transactions contemplated thereby, at the VGX special meeting. In the voting agreement, each support stockholder acknowledges that he will not be entitled to exercise and is therefore effectively waiving any rights of appraisal of his shares of VGX common stock that he may otherwise be entitled to with respect to such shares of VGX common stock under Section 262 of the DGCL. Further, each support stockholder agrees in the voting agreement not to offer, sell, transfer or otherwise dispose of or encumber his right to exercise the voting power of any shares of VGX common stock over which he has sole dispositive power, and to use my commercially reasonable efforts to not permit the offer, sale, transfer or other disposition or encumbrance of his right, if any, to direct the voting of any shares of VGX common stock over which he has shared dispositive power, with limited exceptions.

        The voting agreement provides for specific performance of the covenants and agreements upon any breach. The voting agreements shall terminate upon the earlier of the Effective Time of the Merger or any termination of the Acquisition Agreement. Each voting agreement may not be amended except by an instrument in writing signed on behalf of each of the parties, and is governed by the laws of the State of Delaware, without giving effect to the principles of conflicts of law thereof.

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Voting Trust Agreement

        Five significant stockholders of VGX will enter into a voting trust agreement to be signed and become effective concurrent with the closing of the Merger. These stockholders will place an aggregate of 8,000,000 shares of VGX stock into a voting trust, which will be administered by an independent committee of the board of directors of Inovio post-merger. The trustees would vote the shares in accordance with the percentage of votes cast by all stockholders on any particular matter. The trust will have a term of ten years and would terminate earlier upon a change in control of the combined group. The agreement will also terminate with respect to a stockholder if that stockholder dies or the stockholder's employment with the combined company is terminated other than for cause, as defined in the trust agreement. If Dr. J. Joseph Kim's employment with the combined group is terminated, the trust will terminate with respect to all stockholders party to the agreement upon the date of such termination. A stockholder will have the right to cause the trustees to sell the shares deposited in the trust by that stockholder, or to tender the shares in the event of a tender offer or exchange offer, for the benefit of the stockholder under certain conditions.

Lock-up Agreements

        The Acquisition Agreement provides for certain lock-up arrangements with respect to shares of Inovio common stock outstanding at the Effective Time of the Merger or issuable upon the assumption of outstanding VGX securities at the Effective Time of the Merger, as described in "Restrictions on Ability to Sell Inovio Common Stock" beginning on page 85. To support the implementation of such restrictions, Inovio agreed to obtain lock-up agreements reflecting the Lock-Up Restrictions prior to the closing from Dr. Avtar Dhillon and, using its best efforts, from all other Inovio—related Restricted Parties. Likewise, VGX agreed to obtain lock-up agreements reflecting the Lock-Up Restrictions prior to the closing from Dr. J. Joseph Kim and, using its best efforts, from all other VGX-related Restricted Parties, except those who will hold Restricted Securities consisting of solely of shares of Inovio common stock issued at the Effective Time pursuant to the Merger. In addition to setting forth the Lock-Up Restrictions as dictated by the Acquisition Agreement for acknowledgement by the Restricted Party, the lock-up agreements authorizes Inovio, during the applicable Lock-Up Period, to cause its transfer agent to decline to transfer and to note stop transfer restrictions on the transfer books and records of Inovio with respect to the shares of common stock that are restricted from transfer pursuant to the agreement. The lock-up agreement also provides the Restricted Party's acknowledgement that the lock-up agreement, and the Lock-Up Restrictions set forth in the lock-up agreement, are irrevocable on the part of the Restricted Party and survive the Restricted Party's death or incapacity, except where such death or incapacity is the cause of the Restricted Party's full termination of employment or directorship with Inovio or one of its subsidiaries.

Employment Agreements

        Inovio has executed new employment agreements with certain members of its management team and other key employees for their continued service post-Merger, to be effective at the Effective Time of the Merger. Until the Effective Time, the terms and conditions of any existing employment agreements between Inovio and these employees continue to govern the employment relationship.

    General Terms and Conditions

        All of the employment agreements to become effective upon closing of the Merger include the following general acknowledgements, covenants, terms and conditions:

    Acknowledgement that the closing of the Merger referenced above will not trigger any severance or change of control provisions of the employee's prior employment arrangements with Inovio or its subsidiaries.

    The employee's intended title, hours, duties and the ability of such title or duties to be adjusted.

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    The employee's annual salary, the employee's eligibility for salary increases, discretionary bonuses and equity incentives, and the role of other management or a committee of the Inovio board in establishing performance objectives related thereto.

    The employee's fringe benefits, including participation in health, hospitalization, life or other insurance provided by Inovio, vacation and sick leave, and reimbursement for business-related expenses.

    The agreement's initial two year term, unless terminated earlier pursuant to its termination provisions, with an automatic one year renewal on the expiration date and on each successive anniversary date thereafter, unless either party gives written notice of non-renewal and termination to the other party at least ninety (90) days prior to any expiration date.

    Occurrence of a "Change in Control" for purposes of the employment agreements as: (i) a majority of the directors elected at any annual or special general meeting of stockholders of the company are not individuals nominated by the company's then incumbent board of directors; (ii) there is occurrence of an event whereby any person or entity becomes the beneficial owner of shares representing 50% or more of the combined voting power of the voting securities of the company; or (iii) there is a merger or consolidation of the company with one or more corporations as a result of which, immediately following such merger or consolidation, the stockholders of the company as a group, as they were immediately prior to such event, will hold less than a majority of the outstanding capital stock of the surviving corporation.

    The employee's right to terminate the employment agreement: (i) at any time upon providing six weeks notice in writing to the company, (ii) upon a material breach or default of any term of the employment agreement by the company, including any reduction in salary, if such material breach or default has not been remedied within 15 days after written notice of the material breach or default has been delivered by the employee to the company, or (iii) during the initial two year period or during any one year period immediately after a Change of Control (as defined in the agreement) if (a) the employee ceases to report directly to his or her prior supervising position or (b) there is any other material reduction in the employee's duties, position, authority or responsibilities with the company relative to the duties, position, authority or responsibilities in effect immediately prior to such reduction, if the company does not cure or remedy such issues within 15 days after written notice from the employee.

    The company's right to immediately terminate the employee for "Cause" upon the occurrence of any of the following events: (i) the employee acts unlawfully, dishonestly, in bad faith or grossly negligent with respect to the business of the company as determined by the board (in some cases, upon completion of a reasonable investigation and provision of a detailed report of the results of such investigation to the employee); (ii) the employee commits any crime or fraud against the company or its property or the conviction of employee of any felony offense or crime reasonably likely to bring discredit upon the employee or the company; or (iii) a material breach or default of any term of the employment agreement by the employee if such material breach or default remains unremedied 30 days after the company delivers written notice of the material breach or default to the employee.

    The company's right to terminate the employee's employment at any time at its discretion without Cause upon certain written notice to the employee.

    The termination of employment upon the occurrence of the employee's death or permanent or extended disability.

    The types and amounts of compensation due to the employee upon termination, depending on the terms and circumstances of such termination.

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    The applicability of the laws of the State of California to the employment agreement, without regard to California's choice of law rule.

    The continued effectiveness of any confidentiality, invention assignment, non-solicit and non-compete agreement(s) previously executed in favor of the company by the employee.

    Employment Agreement for Dr. Avtar Dhillon—President

        Dr. Avtar Dhillon's agreement provides for his employment as president of Inovio post-Merger, in which role he will report to the Inovio board of directors. Pursuant to Dr. Dhillon's employment agreement, within 60 days of the beginning of each fiscal year, the Compensation Committee of Inovio's board of directors and Dr. Dhillon shall agree to his performance milestones and the amount of bonus for which Dr. Dhillon will be eligible if Dr. Dhillon as President achieves such milestones. Although Dr. Dhillon's employment agreement has a two year term, the terms and conditions of the employment agreement acknowledge that the terms of Dr. Dhillon's employment shall remain subject to further negotiation and mutual agreement in the month prior to completion of one year of service after the Effective Time. If the parties do not reach mutually agreeable terms prior to the completion of the first year of service after the Effective Time, the employment agreement will terminate, which shall be treated as a voluntary termination upon notice by Dr. Dhillon, effective as of the end of the first year of service.

        Upon the Effective Time of the Merger, Inovio will deposit a closing payment equal to 24 months of Dr. Dhillon's current annual salary into a mutually agreed upon escrow account. Inovio agreed to provision of such closing payment as an incentive to retain Dr. Dhillon's services post-Merger, in recognition of the fact that he would have been eligible for full severance under his current employment agreement had Dr. Dhillon terminated employment in conjunction with the Merger, and in recognition of Dr. Dhillon's agreement to alter the structure and scope of his current severance arrangements in his new employment agreement. An amount equal to 50% of the closing payment and any accrued interest on such amount shall be automatically released to Dr. Dhillon upon the six month anniversary of the Effective Time, and the remainder of the closing payment and any remaining accrued interest shall be released to Dr. Dhillon upon the one year anniversary of the Effective Time, unless Dr. Dhillon or Inovio terminate the employment relationship prior to such time. If Dr. Dhillon terminates the agreement other than upon voluntary notice (unrelated to a material breach or default by the company or other circumstances addressed by the agreement) or the company terminates Dr. Dhillon for any reason, the entire closing payment and any accrued interest shall be released from the escrow account upon the date of termination. If Dr. Dhillon voluntarily terminates the employment relationship without a breach by the company or under the other circumstances addressed by the agreement, then the entire closing payment and any accrued interest shall be released from the escrow account on the later of the date of termination or the six month anniversary of the Effective Time.

        In addition to the general provisions for termination of the employment agreement, Dr. Dhillon's employment agreement provides that if the company relocates Dr. Dhillon's place of employment more than 50 miles from its current location in San Diego, California, and Dr. Dhillon does not consent to such relocation, then either the company or Dr. Dhillon may terminate the employment agreement and such termination shall be treated the same as a rightful termination by the employee upon an unremedied material breach by the company.

        In the event of the termination of Dr. Dhillon's employment agreement for any reason, the company shall provide Dr. Dhillon, upon receipt of an executed release of claims in favor of Inovio: (i) any earned but unpaid salary as of the date of termination, (ii) any accrued but unused vacation pay as of such date, (iii) any unreimbursed business expenses incurred as of the termination date, (iv) any pending health care benefits, and (v) any earned but unpaid bonus amounts from the closing of the Merger. However, if Dr. Dhillon terminates the agreement due to a material breach or default by the

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company, a change in his position or duties or a company relocation of his position without his consent within the initial term of the agreement or after a Change of Control, or the company terminates Dr. Dhillon without Cause or upon death or disability, the company shall also pay Dr. Dhillon (or his estate as applicable) an amount equal to the annual bonus, if any, most recently paid to Dr. Dhillon, multiplied by the fraction of which the number of days between the fiscal year end related to the bonus and the date of termination is the numerator, and 365 is the denominator. In addition, if the employment agreement terminates under such enumerated circumstances, and Dr. Dhillon has been employed for less than one year since the Effective Time, Inovio shall pay him an amount equal to the remainder of his salary for such initial one-year period.

        Further, under any termination scenario, the company shall continue Dr. Dhillon's group health care benefits for a period of twelve months from his termination date or shall pay 100% the premiums required to continue his group health care coverage for a period of twelve months under the applicable provisions of the Consolidated Omnibus Budget Reconciliation Act of 1985, or "COBRA,", provided that Dr. Dhillon elects to continue and remains eligible for these benefits under COBRA, and does not become eligible for health coverage through another employer during such period.

    Employment Agreement for Peter Kies—Chief Financial Officer

        Mr. Kies' agreement provides for his employment as chief financial officer of Inovio post-Merger, in which role he will report to the Inovio board of directors. Pursuant to Mr. Kies' employment agreement, within 60 days of the beginning of each fiscal year, the Compensation Committee of Inovio's board of directors and Mr. Kies shall agree to his performance milestones and the amount of bonus for which Mr. Kies will be eligible if Mr. Kies as chief financial officer achieves such milestones. In addition, upon the Effective Time of the Merger, Mr. Kies shall receive a closing payment equal to six months of his current annual salary and, upon the earlier of the six-month anniversary of the Effective Time or the date of Mr. Kies' termination pursuant to the employment agreement (other than upon his voluntary termination upon notice to the company), shall receive an additional closing payment equal to six months of his current annual salary. Inovio agreed to provision of such closing payment as an incentive to retain Mr. Kies' services post-Merger, in recognition of the fact that he would have been eligible for full severance under his current employment agreement had Mr. Kies terminated employment in conjunction with the Merger, and in recognition of Mr. Kies' agreement to alter the structure and scope of his current severance arrangements in his new employment agreement.

        In addition to the general provisions for termination of the employment agreement, Mr. Kies' employment agreement provides that if the company relocates Mr. Kies' place of employment more than 50 miles from its current location in San Diego, California, and Mr. Kies does not consent to such relocation, then either the company or Mr. Kies may terminate the employment agreement and such termination shall be treated the same as a rightful termination by the employee upon an unremedied material breach by the company.

        In the event of the termination of Mr. Kies' employment agreement for any reason, the company shall provide Mr. Kies: (i) any earned but unpaid salary as of the date of termination, (ii) any accrued but unused vacation pay as of such date, (iii) any unreimbursed business expenses incurred as of the termination date, (iv) any pending health care benefits, and (v) any earned but unpaid bonus amounts from the closing of the Merger. However, if Mr. Kies terminates the agreement due to a material breach or default by the company, a change in his position or duties or a company relocation of his position without his consent within the initial term of the agreement or after a Change of Control, or the company terminates Mr. Kies without Cause or upon death or disability, the company shall also pay Mr. Kies (or his estate as applicable) an amount equal to the annual bonus, if any, most recently paid to Mr. Kies, multiplied by the fraction of which the number of days between the fiscal year end related to the bonus and the date of termination is the numerator, and 365 is the denominator. Further, under any termination scenario, the company shall continue Mr. Kies' group health care benefits for a period

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of six months from his termination date or shall pay 100% the premiums required to continue his group health care coverage for a period of six months under the applicable provisions of COBRA, provided that Mr. Kies elects to continue and remains eligible for these benefits under COBRA, and does not become eligible for health coverage through another employer during such period.

    Form of Vice President Employment Agreement

        Mr. Punit Dhillon and Mr. Michael Fons have executed employment agreements as Vice President, Operations and Vice President, Corporate Development, respectively, effective upon closing of the Merger. The form of Vice President employment agreement provides that these individuals will report to the Chief Executive Officer of Inovio, and that within 60 days of the beginning of each fiscal year, the Compensation Committee of Inovio's board of directors shall set performance milestones and the amount of bonus for which each Vice President will be eligible if he achieves such milestones. In addition, upon the Effective Time of the Merger, Mr. Dhillon and Mr. Fons shall each receive a closing payment equal to three months of his annual salary at the Effective Time.

        In addition to the general provisions for termination of the employment agreement, the form of Vice President employment agreement provides that if the company relocates a Vice President's place of employment more than 50 miles from its current location in San Diego, California, and the Vice President does not consent to such relocation, then either the company or the Vice President may terminate the employment agreement and such termination shall be treated the same as a rightful termination by the employee upon an unremedied material breach by the company.

        In the event of the termination of a Vice President's employment agreement for any reason, the company shall provide the terminating Vice President: (i) any earned but unpaid salary as of the date of termination, (ii) any accrued but unused vacation pay as of such date, and (iii) any unreimbursed business expenses incurred as of the termination date. However, if the Vice President terminates the agreement due to a material breach or default by the company, a change in his position or duties or a company relocation of his position without his consent within the initial term of the agreement or after a Change of Control, or the company terminates the Vice President without Cause, the company shall also pay the Vice President an amount equal to six months of the employee's annual salary at the time of termination, to be paid in such regular intervals over the six month period as shall be determined by the company, provided that Employee signs a standard release of all claims as presented by the company, and an amount equal to the Vice President's annual bonus, if any, most recently received, multiplied by the fraction of which the number of days between the fiscal year end related to the bonus and the date of termination is the numerator, and 365 is the denominator. However, if terminated due to death or disability, the Vice President's estate shall only also be entitled to the prorated annual bonus. Further, under any termination scenario, the company shall either continue the Vice President's healthcare benefits for a six month period post-termination or otherwise secure coverage for the Vice President for such period.

        Mr. Dhillon's agreement also allows for his duties to be performed outside of Inovio's headquarters up to five days per calendar month and provides certain travel benefits in support of such efforts.

    Form of Executive Director Employment Agreement

        Mr. Stephen Kemmerrer and Mr. Rune Kjeken have executed employment agreements as Executive Director, Engineering and Executive Director, Research & Development, respectively, effective upon closing of the Merger. The form of Executive Director employment agreement provides that these individuals will report to the Chief Executive Officer of Inovio, and that within 60 days of the beginning of each fiscal year, the Chief Executive Officer shall set performance milestones and the amount of bonus for which each Executive Director will be eligible if he achieves such milestones. In

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addition, upon the Effective Time of the Merger, Mr. Kemmerrer and Mr. Kjeken shall each receive a closing payment equal to three months of his annual salary at the Effective Time.

        In addition to the general provisions for termination of the employment agreement, the form of Executive Director employment agreement provides that if the company relocates a Executive Director's place of employment more than 50 miles from its current location in San Diego, California, and the Executive Director does not consent to such relocation, then either the company or the Executive Director may terminate the employment agreement and such termination shall be treated the same as a rightful termination by the employee upon an unremedied material breach by the company.

        In the event of the termination of a Executive Director's employment agreement for any reason, the company shall provide the terminating Executive Director: (i) any earned but unpaid salary as of the date of termination, (ii) any accrued but unused vacation pay as of such date, and (iii) any unreimbursed business expenses incurred as of the termination date. However, if the Executive Director terminates the agreement due to a material breach or default by the company, a change in his position or duties or a company relocation of his position without his consent within the initial term of the agreement or after a Change of Control, or the company terminates the Executive Director without Cause, the company shall also pay the Executive Director an amount equal to three months of the employee's annual salary at the time of termination, to be paid in such regular intervals over the three month period as shall be determined by the company, provided that the Executive Director signs a standard release of all claims as presented by the company. However, if terminated due to death or disability, the Executive Director's estate is entitled to an amount equal to the Executive Director's annual bonus, if any, most recently received, multiplied by the fraction of which the number of days between the fiscal year end related to the bonus and the date of termination is the numerator, and 365 is the denominator.

    Form of Key Employee Employment Agreement

        Ms. Maggie Campbell, Ms. Catherine Ngo and Mr. Doug Murdock have executed employment agreements as Controller, Accounting Manager and Director, Intellectual Property, respectively, effective upon closing of the Merger, and are referred to as "Key Employees." The form of Key Employee employment agreement provides that these individuals will report to the Chief Executive Officer of Inovio, and that within 60 days of the beginning of each fiscal year, the Chief Executive Officer shall set performance milestones and the amount of bonus for which each Key Employee will be eligible if she or he achieves such milestones. In addition, upon the Effective Time of the Merger, each of these Key Employees shall each receive a closing payment equal to two months of her or his annual salary at the Effective Time.

        In the event of the termination of a Key Employee's employment agreement for any reason, the company shall provide the terminating Key Employee: (i) any earned but unpaid salary as of the date of termination, (ii) any accrued but unused vacation pay as of such date, and (iii) any unreimbursed business expenses incurred as of the termination date. However, if the Key Employee terminates the agreement due to a material breach or default by the company, a change in his position or duties or a company relocation of his position without his consent within the initial term of the agreement or after a Change of Control, or the company terminates the Key Employee without Cause, the company shall also pay the Key Employee an amount equal to three months of the employee's annual salary at the time of termination, to be paid in such regular intervals over the three month period as shall be determined by the company, provided that the Key Employee signs a standard release of all claims as presented by the company. However, if terminated due to death or disability, the Key Employee's estate is entitled to an amount equal to the Key Employee's annual bonus, if any, most recently received, multiplied by the fraction of which the number of days between the fiscal year end related to the bonus and the date of termination is the numerator, and 365 is the denominator.

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INFORMATION ABOUT THE COMPANIES

Inovio Biomedical Corporation

    Overview

        Inovio Biomedical Corporation, or "Inovio," a Delaware corporation, organized in 2001, is a San Diego-based biomedical company focused on the development of next-generation vaccines to prevent or treat cancers and chronic infectious diseases. Such vaccines, which could potentially protect millions of people from debilitation or death from diseases without adequate treatments, may represent multi-billion dollar market opportunities. Historically, successful development of this new generation of vaccines—DNA vaccines—has been hindered by the lack of safe, efficient and cost effective DNA delivery methods capable of enabling their potency. However, Inovio's electroporation-based DNA delivery technology has shown potential in pre-clinical and clinical studies to play a pivotal role in facilitating delivery and enhancing the potency of preventive and therapeutic vaccines.

        Inovio is a leader in developing DNA delivery solutions based on electroporation, which uses brief, controlled electrical pulses to create temporary pores in cell membranes and enable increased cellular uptake of a useful biopharmaceutical. Once the DNA vaccine enters a cell, it can then "express" the proteins it was encoded to produce. These proteins, or antigens, are designed to be uniquely associated with a targeted cancer or infectious disease, and may then stimulate a more powerful immune response if the immune system encounters the targeted disease at a subsequent time.

        Inovio's business strategy to realize value for the company and its stockholders is as follows:

        First, Inovio has leveraged its patented technologies through licensing and collaborations, such as its licensing arrangements with Merck & Co., Inc., or "Merck," Wyeth Pharmaceuticals, or "Wyeth" and Vical Inc., or "Vical," among other research-driven biopharmaceutical companies as well as government and non-government agencies. Inovio is licensing the use of its electroporation-based DNA delivery systems for partners to use in conjunction with their proprietary DNA vaccines or DNA-based immunotherapies. These arrangements provide Inovio with some combination of upfront payments, development fees, milestone payments, royalties and a supply agreement. These partners are pursuing development of proprietary agents or conducting research using Inovio's technology.

        Second, Inovio is pursuing proprietary vaccine development or co-development, resulting in whole or partial ownership in promising vaccines to prevent or treat cancers and chronic infectious diseases.

        Inovio's technology is protected by an extensive patent portfolio covering in vivo electroporation. Inovio's patent portfolio encompasses a range of apparatuses, methodologies, conditions, and applications including oncology, gene delivery, vascular, transdermal as well as ex vivo electroporation.

    Inovio's Core Technology

        Most drugs and biologics must enter into a cell through a cell membrane in order to perform their intended function. However, gaining entry into a cell through the outer cell membrane can be a significant challenge. In the 1970s it was discovered that the brief application of high-intensity, pulsed electric fields can create temporary and reversible permeability, or pores, in the cell membrane. This pulse-induced permeabilization of the cellular membrane is generally referred to as electroporation. One observable effect of cell membrane electroporation is less restricted exchange of molecules between the cell exterior and interior—the benefit being that it allows and enhances the uptake of, for example, a biopharmaceutical agent previously injected into local tissue. The extent of membrane permeabilization depends upon various electrical, physical, chemical, and biological parameters.

        The transient, reversible nature of this electrical permeabilization of membranes is the underlying basis of Inovio's electroporation instruments, which are designed to harness this phenomenon by delivering controlled electrical pulses into tissue to facilitate the uptake of useful biopharmaceuticals. Inovio's technology generates electric fields in target tissues to induce electroporation, which increases

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cellular uptake even for large molecules such as DNA. Most cell types and tissue can be successfully electroporated as long as applicators with the appropriate configuration of needle electrodes can be used to expose cells and tissues to the electric field.

        DNA vaccines have tremendous potential as therapeutic agents for treating various diseases. One of the key obstacles to the successful development and commercialization of DNA vaccines has been the limitations associated with current delivery systems. Alternative approaches based on the use of viruses and lipids are complex and expensive, and have in the past created concerns regarding safety. Electroporation provides a straightforward, cost effective method for delivering DNA into cells with high efficiency and minimal complications (as compared to viral vectors) and, importantly, inducing clinically relevant levels of gene expression.

        Inovio has multiple systems designed to create different electroporation conditions for different applications. The current systems consist of two basic components: a pulse generator and an applicator that is inserted into selected tissue.

    MedPulser® DNA Electroporation System

        Inovio's MedPulser® DNA Delivery System was designed to create conditions to deliver DNA into tumor cells that promote optimal responses to gene-based immunotherapeutic cytokines. The cytokine-encoding plasmid is first injected with a syringe/needle into the selected tumor. Using a remote control, the pulse generator is switched on. High-voltage electrical pulses are generated and delivered through an attached electrical cord into the injected tissue through an electrode-needle array on the applicator. The electrode-needle array consists of two sets of opposite needle pairs, or a total of four needle-electrodes. The needle-electrode arrays are available in different sizes and configurations to facilitate access to tumors of different sizes and in different locations.

    MedPulser® DNA Delivery System

        The MedPulser® DNA Delivery System (DDS) was developed to optimize the delivery of DNA into muscle cells. The modified system is similar to the MedPulser® Electroporation System. The primary differences are in the parameters of the electric pulses delivered by the generator and the needle-electrode configuration of the applicator. The pulse is designed specifically for DNA delivery with a lower strength electrical field of longer duration than for tumor electroporation. The applicator has a four needle-electrode array consisting of one set of opposite pairs. They are available in a range of configurations to meet the requirements of a variety of applications.

    Elgen System

        The Elgen® DNA Delivery System, Inovio's newest generation of electroporation systems, is designed for muscle delivery. It consists of a computer-controlled, motorized two needle delivery device that injects DNA and delivers electroporation pulses through one pair of needles. This experimental system is currently under evaluation in Inovio's clinical trial for a prostate cancer vaccine at the University of Southampton in the U.K.

    Choice of Tissue for DNA Delivery

        Muscle Delivery.     Inovio's proprietary electroporation method consists of a DNA delivery system designed to introduce a plasmid vector into muscle, skin or tumor tissue. The plasmid is coded in a manner intended to cause a cell to produce an antigenic protein that the immune system will identify as foreign and against which it will mount an immune response. As with conventional vaccines, the immune will then develop memory of this antigen (and related disease) for future reference. Skeletal muscle has been a core focus because it is mainly composed of large elongated cells with multiple nuclei. Muscle cells are non-dividing, hence long-term expression can be obtained without integration of the gene of interest into the genome. Muscle cells have also been shown to have a remarkable

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capacity for secretion of proteins into the blood stream and to induce both humoral (antibody) and cellular (T-cell) immune responses after DNA delivery. Secreted antigenic proteins may therefore act systemically and produce therapeutic effects in distant tissues of the body. In this respect, the muscle functions as a factory for the production of the biopharmaceutical needed by the body. It is envisioned that delivery of DNA by electroporation to muscle cells will circumvent the costly and complicated production procedures of viral gene delivery vectors, protein-based drugs, conventional vaccines and monoclonal antibodies. In addition, this approach is designed to provide long-term stable expression of a therapeutic protein or monoclonal antibody at a sustained level. Inovio is collaborating in three clinical programs (Merck, Tripep and the University of Southampton) related to DNA delivery to muscle.

        Tumor Delivery.     Inovio has a significant intellectual property position relating to in vivo delivery of genes directly into tumor cells. Tumor cells can be readily transfected with genes encoding selected cytokines or potentially lethal proteins for the treatment of a variety of cancers. The goal of effective tumor delivery is the ultimate elimination of the transfected tumor, and Inovio has experienced very few concerns regarding the safety of the procedure in its trials to date. An ongoing Phase I/II clinical immunotherapy trial being conducted by Vical was designed to deliver IL-2 directly to accessible melanoma lesions. In December, 2008, Inovio announced final results of a similar clinical study conducted by Moffitt to deliver IL-12 directly to accessible melanoma lesions.

        Skin Delivery.     While Inovio has generated significant preclinical and preliminary clinical evidence that intramuscular electroporation-based DNA delivery will be effective for a number of vaccines, electroporation of the skin may also be a relevant route of administration. Skin or intradermal administration is important and is becoming an attractive site for immunization given its high density of antigen presenting cells (APCs). Unlike muscle, skin is the first line of defense against most pathogens and is therefore very rich in immune cells and molecules. Skin specifically contains certain cells that are known to help in generating a robust immune response. With intradermal administration of electroporation, Inovio may be able to demonstrate a comparable immune response to muscle delivery. Inovio will continue to invest research and patenting resources into developing a viable skin electroporation system for clinical evaluation.

    Applications of DNA Vaccine Technology

        Inovio and its partners are developing DNA delivery technology for two broad applications:

    Cancer

        Cancer is a disease of uncontrolled cell growth. Although cancer has been a major focus of pharmaceutical companies for decades, cancer remains one of the leading causes of death in the United States. Traditionally, three approaches have been available for treatment of cancer: surgery, radiation therapy, and chemotherapy. When detected early and still confined to a single location, cancer may be cured by surgery or radiation therapy. However, neither surgery nor radiation therapy can cure cancer that has spread throughout the body. Although chemotherapy can sometimes effectively treat cancer that has spread throughout the body, a number of non-cancerous cells, such as bone marrow cells, are also highly susceptible to chemotherapy. As a result, these types of treatments cause significant side effects and morbidity. Finally, it is common to see cancer return after apparently successful treatment by each of these means. The limitations of current cancer treatments are clearly demonstrated by the mortality rate of this disease.

        For many decades, it has been suggested that the immune system should also be able to recognize cancer cells as abnormal and destroy these cells. However, cancer cells have developed mechanisms that allow them to escape the surveillance of the immune system. Immunotherapy, a process which uses the patient's own immune system to treat cancer, may have advantages over surgery, radiation therapy, and chemotherapy. Many cancers appear to have developed the ability to "hide" from the immune

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system. A treatment that can augment the immune response against tumor cells by making the cancer more "visible" to the immune system would likely represent a significant improvement in cancer therapy. Immune-enhancing proteins such as IL-2 and IL-12, used by partners in Phase I/II trials, have shown encouraging results. There is also a need to stimulate a stronger cellular immune response (i.e. generating T-cells) to specifically attack cancerous cells. This requires the use of technology such as DNA vaccines.

        Electroporation offers effective delivery of DNA and may help Inovio develop novel cancer therapies. Inovio's current clinical-stage approaches consist of directly injecting lesions with certain plasmids followed by intratumoral electroporation as well as directly delivering certain plasmids into muscle followed by intramuscular electroporation. Upon uptake into cells, the plasmid directs the production of the encoded immunostimulatory proteins. The convenience and ability to repeat administration may offer advantages over current modalities of therapy. In addition, cancer therapies using non-viral DNA delivery may offer an added margin of safety compared with viral-based delivery, as no viral DNA/RNA or viral particles are contained in the formulation. Studies in animals have demonstrated the safety and potential efficacy of electroporation-based delivery. Subsequently, in human studies, a very low incidence of treatment-related serious adverse events has been observed.

        In addition to immunotherapy approaches, numerous cancer antigens have been identified over the past few decades and better identification tools are under development by others. Inovio will continue to evaluate opportunities to acquire or partner cancer antigens that may be useful for large market cancers such as breast, lung and prostate.

    Infectious Diseases

        DNA vaccines use portions of the genetic code of a pathogen to cause the host to produce proteins of the pathogen that may induce an immune response. Compared with conventional vaccines that use live, weakened, or dead pathogens to produce an immune response, this method potentially offers superior safety and ease of manufacturing, as well as convenient storage and handling characteristics. DNA vaccines have the potential to induce potent T-cell responses against target pathogens as well as trigger production of antibodies. Over the past decade, many scientific publications have documented the effectiveness of DNA vaccines in contributing to immune responses in dozens of species, including non-human primates and humans.

        Vaccines are generally recognized as the most cost-effective approach for infectious disease healthcare. However, the technical limitations of conventional vaccine approaches have constrained the development of effective vaccines for many diseases. Development of vaccines based on conventional methods requires significant infrastructure in research and manufacturing. In addition, the safety risks associated with certain conventional vaccine approaches may offset their potential benefits. Inovio believes its potential vaccine products may be simpler to manufacture than vaccines made using live viruses or protein subunit approaches, including those involving mammalian, avian or insect cells, or egg-based culture procedures. In addition, Inovio's DNA delivery technologies may accelerate certain aspects of vaccine product development such as non-clinical evaluation and manufacturing.

        Similar to the requirements for fighting cancer, it is apparent that an effective approach for addressing chronic infections, which are also deadly and debilitating, requires the ability to generate a strong cellular immune response. This new generation of vaccines—DNA vaccines—is showing this capability. In addition to the targets already partnered Inovio is evaluating several potential infectious disease targets in Inovio's internal development program.

    Business Strategy

        Inovio's objective is to be a biomedical company focused on developing and commercializing products that address significant unmet medical needs and, as a result, improve patients' quality of life. To achieve this objective, Inovio's business strategy currently includes the following key elements.

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    Therapeutic Drug and DNA Delivery

        Inovio develops equipment designed to enable the use of electroporation to achieve efficient and cost-effective delivery into patients of DNA vaccines targeting a variety of illnesses. Although there are many diseases for which improved drug or DNA delivery is important, Inovio believes that its greatest opportunities lie in applying electroporation to DNA-based therapies (including immunotherapy) in the areas of cancer and chronic infectious diseases.

    Advancing Inovio's Product Pipeline

        The strategy to advance Inovio's product pipeline has two key components: Inovio has leveraged its patented technologies through licensing arrangements with companies such as Merck, Wyeth and Vical, among other research-driven biopharmaceutical companies, as well as collaborations with government and non-government agencies. These partners are pursuing development of proprietary agents or conducting research using Inovio's electroporation-based DNA delivery systems. Resources used to support Inovio's partners in these efforts are funded by its partners. In addition, these arrangements provide Inovio with some combination of upfront payments, development fees, milestone payments, royalties and a supply agreement.

        In addition to expanding and providing electroporation delivery expertise, Inovio is directing resources to proprietary vaccine development or co-development, resulting in whole or partial ownership in DNA vaccine candidates. Inovio is focusing on the development of DNA-based therapies in the areas of cancer and chronic infectious diseases. The selection of targets for Inovio's independent or co-development programs is driven by three key criteria: complexity of the product development program, competition, and commercial opportunities. Inovio intends to retain significant participation in product development and commercialization of any DNA vaccines and therapeutics in pre-clinical and human trials that receive regulatory approval, although it may choose to secure additional partnerships to accelerate product development and commercialization. Inovio currently has a collaborative commercialization agreement with Tripep AB to co-develop a novel DNA hepatitis C virus (HCV) therapeutic vaccine.

    Expand Market Opportunity

        Inovio is continually evaluating and implementing opportunities to enhance its core technologies and assessing other DNA delivery technologies. Inovio is developing future product candidates based on these technologies through pre-clinical and clinical testing to determine their safety and efficacy. Inovio also seeks to develop additional applications for its technologies by testing new approaches to disease control or prevention. These efforts could lead to further independent product development or licensing opportunities. In addition, Inovio continually evaluates compatible technologies or products that may be of potential interest for in-licensing or acquisition.

    Expand the Application of Inovio's Technologies and Enable Product Development Through Strategic Collaborations

        In pre-clinical trials and early clinical trials, Inovio's technology has enabled high levels of DNA uptake and gene expression without significant acute side effects. Based on the results obtained, Inovio believes that its technology is well positioned and is as capable as competing technologies to meet the delivery requirements for DNA vaccines and immunotherapy. Inovio's strategy is to develop DNA vaccine and immunotherapy applications with major pharmaceutical, biotechnology and government agency partners wherever reasonable and/or possible to license its DNA delivery technology for specific genes or specific medical indications. In most partnering situations, Inovio provides proprietary instruments and expertise to optimize the delivery of DNA for particular applications and the partner company provides its proprietary gene, allowing Inovio access to complementary technologies or greater resources. Inovio believes that entering into selective collaborations as part of its product development

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programs can enhance the success of Inovio's product development and commercialization, diversify Inovio's product portfolio and enable Inovio to better manage its operating costs. Inovio's collaboration with partners allows pre-clinical research, clinical trials and mutually beneficial opportunities to expand Inovio's product pipeline, which may lead to the introduction of a new treatment and/or products in the marketplace at a rate and range which Inovio may not be able to support on its own. Additionally, such collaborations enable Inovio to leverage investment by its collaborators and reduce its net cash burn while retaining significant economic rights. Inovio's goal is to enter into additional agreements to license its electroporation technology for use in the delivery for specific targets.

    Products and Product Development

        Together with Inovio's licensees and collaborators, Inovio is currently developing a number of DNA-based vaccines and therapeutics for the prevention or treatment of cancer and chronic infectious diseases. Inovio's current independent development focus is on these areas as well. The table below summarizes progress in Inovio's independent, collaborative and out-licensed product development programs as of December 5, 2008.

 
   
  Pre-Clinical Studies   Development Status    
Product Area
  Product Target and
Indication(s)
  In Vitro   In Vivo   Phase
I
  Phase
II
  Phase
III
  Phase
IV
  Development

DNA Delivery
Immunotherapy

 

Malignant Melanoma

 
X
 
X
 
X
                   

Moffitt/RMR

 

Metatstatic Melanoma

 
X
 
X
 
X*
                   

Vical

DNA Delivery
Tumor-associated
antigen therapeutic
vaccines

 

HER-2 and CEA-expressing cancers

 
X
 
X
 
IP
                   

Merck

 

Prostate Cancer

 
X
 
X
 
IP
                   

Univ. of
Southampton

 

hTERT-expressing cancers

 
X
 
X
 
IP
                   

Merck

 

Unspecified Cancer

 
X
 
X
                       

Inovio

DNA Delivery Infectious
disease vaccine

 

HCV Vaccine

 
X
 
X
 
IP
                   

Tripep/Inovio

 

CMV Vaccine

 
X
 
X
                       

Vical

 

Unspecified Targets

 
X
 
IP
                       

Wyeth

 

Biodefense Targets

 
X
 
IP
                       

US Army

 

HIV Vaccine

 
X
 
IP
                       

National Cancer Institute

 

HIV Vaccine

 
X
 
IP
                       

International AIDS Vaccine Initiative

 

Unspecified Targets

 
X
 
IP
                       

Inovio


X
= Completed 

IP
= In Progress 

*
= Final data pending 

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    DNA Vaccines and Immunotherapies

        The technical limitations of conventional vaccine approaches have constrained the development of effective vaccines for many diseases. In addition, the safety risks associated with certain conventional vaccine approaches may offset their potential benefits. In the broader vaccine marketplace, it is important to note a changing dynamic. Traditionally, vaccines have been predominantly focused on the pediatric market, intended to protect children from diseases that could cause them serious harm. Today, there is a growing interest in vaccines against diseases that may affect adolescents and adults, which include both sexually transmitted diseases and infections that strike opportunistically, such as during pregnancy or in immuno-compromised individuals, including the geriatric population. Inovio believes its technologies, because of their potential safety and development time advantages, could be ideally suited for the development of this new generation of vaccines. Preclinical studies in animals have demonstrated the safety and potential efficacy of this approach.

        DNA vaccines are intended to prevent a disease (prophylactic vaccines) or to treat an existing disease (therapeutic vaccines). A DNA vaccine consists of DNA plasmid molecules encoding a selected antigen or fragment of an antigen that are introduced into cells of humans or animals with the purpose of evoking an immune response to the encoded antigen. Information encoded in the vaccine DNA plasmid molecules directs the cells to produce proteins that may then trigger the immune system to mount one or both of two responses: the production of antibodies, also known as humoral immune response, and/or the activation of T-cells and "killer cells," collectively termed cell-mediated immune response. These responses can neutralize or eliminate infectious agents (viruses, bacteria, and other microorganisms) or abnormal cells (e.g. malignant tumor cells). DNA vaccines have several advantages over traditional vaccines in that they are completely non-pathogenic (meaning they cannot cause the disease), may be effective against diseases which cannot be controlled by traditional vaccines, and are relatively fast, easy and inexpensive to design and produce. DNA vaccines are stable under normal environmental conditions for extended periods of time and do not require continuous refrigeration. A potentially major advantage of DNA vaccines is their short development cycle. For example, DNA vaccines against newly identified viral agents may be developed within weeks or months, as opposed to the years often required to develop a traditional vaccine candidate.

        DNA vaccines against cancer use a portion of the genetic code of a cancer antigen to cause a host to produce proteins of the antigen that may induce an immune response.

        Inovio has acquired considerable expertise in the delivery and efficacy evaluation of DNA vaccines, both against infectious agents and complex diseases, such as cancer. In most cases Inovio has chosen skeletal muscle as the target tissue for vaccine delivery as this muscle is known to facilitate robust and long-lasting immune responses. However, skin is also an attractive target for DNA vaccination and Inovio has developed and patented technology for DNA delivery into skin cells as well.

        Inovio is building a DNA franchise around the use of Inovio's proprietary electroporation technology together with gene-based treatments. The flagship of Inovio's development efforts involves license agreements with Wyeth, Merck and Vical, in which these companies are supporting the development and registration of therapies using Inovio's devices. To date, most of Inovio's DNA vaccine development programs have been primarily initiated by corporate partners who sustain the majority of the development expenses and have the ability to conduct the commercialization activities.

    Cancer: DNA-Based Immunotherapies

        In December 2004, Inovio initiated a Phase I clinical trial sponsored by the H. Lee Moffitt Cancer Center using its MedPulser® DNA Electroporation System to deliver plasmid DNA coding for IL-12 to tumors with the aim of treating malignant melanoma. The study was designed to assess the use of electrical pulses generated by Inovio's proprietary electroporation technology to deliver into tumor cells a plasmid DNA encoding a cytokine, interleukin-12, which stimulates adaptive and innate immunity. In December, 2008, Inovio reported that final results of this trial was presented in the peer-reviewed

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Journal of Clinical Oncology in a paper prepared by Drs. Adil Daud, Richard Heller et al, titled, "Phase I Trial of Interleukin-12 Plasmid Electroporation in Patients With Metastatic Melanoma."

        The paper concluded: "This first human trial, to our knowledge, of gene transfer utilizing in vivo DNA electroporation in metastatic melanoma showed that it is safe, effective, reproducible, and titratable." The findings showed not only regression of treated melanoma skin lesions, but also regression of distant untreated lesions, suggesting a systemic immune response to the localized treatment.

        Highlights of the study results, as reported in the paper, include:

    Twenty-four patients were enrolled in seven cohorts with escalating dose levels of plasmid IL-12 between December 2004 and February 2007. Locally injected plasmid IL-12 was followed by electroporation.

    The experimental regimen was found to be safe and well tolerated, with minimal systemic toxicity. Because there was no dose-limiting toxicity in cohorts one through five, the experimental plan was amended to add two additional cohorts. Transient pain with the administration of the electrical pulses was the most frequent adverse event experienced by patients.

    The study demonstrated significant and dose-dependent increases in intratumoral IL-12 protein expression and concomitant increases in intratumoral levels of IFN- g .

    Sixty lesions (76%) were observed to have greater than 20% necrosis (death of tumor cells), with 19 (24%) having 50% – 99% necrosis, and 25 (32%) having 100% necrosis.

    Ten subjects (53%) showed evidence of a systemic response (either stable disease or a complete response) during the study.

    Injected lesions and distant non-injected lesions showed regression after treatment. Of 19 patients with additional sites of disease outside of the treated lesions, two (10%) with untreated distant lesions and no other systemic therapy showing complete regression of all metastases. These responses occurred over 6 – 18 months, with gradual volume loss occurring at sites distinct from the electroporated sites, arguing for immune system involvement. Neither of these patients has developed any new evidence of distant disease to date. Six of 19 (32%) showed disease stabilization lasting from 4 – 20 months.

    Electroporated tumors demonstrated CD4+ and CD8+ lymphocytic infiltrate in the treated lesions.

        In July 2005, Inovio announced, along with its partner, Vical, the initiation of a human Phase I clinical study of an investigational method of delivering plasmid DNA coding for interleukin-2 (IL-2), a potent immune system stimulant, for patients with recurrent metastatic melanoma. Intravenous delivery of IL-2 protein is already approved as a treatment for metastatic melanoma, but frequently causes severe systemic toxicities. The novel treatment approach being studied in this trial involves direct injection into a tumor lesion of plasmid DNA (pDNA) encoding IL-2, followed by electroporation in which local application of electrical pulses is intended to enhance the uptake of pDNA into tumor cells. The pDNA is designed to cause cells within the tumor to produce high levels of IL-2 protein locally and thereby stimulate the immune system to attack the tumor without the systemic toxicities associated with injected IL-2. Interim results on 19 patients from this trial were presented in June, 2007, and demonstrated that intratumoral delivery of pDNA encoding IL-2 into melanoma tumors, followed by electroporation, was administered safely following sedative premedication. No serious adverse events related to the study drug or to the administration procedure were reported and the treatment was well-tolerated. The majority of related adverse events were localized to the treatment site, with the most frequent being mild injection site pain. Individual tumor responses were seen in 12 of 39 (31%) evaluated tumors after injection of different escalating doses (0.5 to 5 mg per tumor).

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Treated tumors (7 of 18, or 38%) showed local responses more frequently than did untreated tumors (5 of 21, or 24%). No overall clinical responses by standard RECIST (Response Evaluation Criteria in Solid Tumors) criteria were observed among the 19 subjects evaluated following one or two cycles of treatment. Two subjects (11%) showed activity in distant, untreated tumors, including one subject showing shrinkage and disappearance of lung tumors. This trial has completed enrollment of 26 patients.

    Cancer: DNA Vaccines

        In April 2005, The University of Southampton initiated a U.K. Medicines and Healthcare products Regulatory Agency (MHRA) approved Phase I/II clinical trial undertaken in collaboration with Inovio. The study uses Inovio's electroporation technology to deliver a therapeutic plasmid-based DNA vaccine to skeletal muscle with the aim of treating recurrent prostate cancer. The trial, sponsored and led by the University of Southampton, is investigating whether the DNA vaccine, developed at the University of Southampton, can stimulate patients to develop immune responses against prostate cancer and whether use of Inovio's electroporation system enhances this response. In June, 2008, Inovio reported that Dr. Christian H. Ottensmeier, MD, PhD, Cancer Research UK Senior Clinical Research Fellow at the University of Southampton, presented updated interim data from this clinical study at the American Society of Gene Therapy 11th Annual meeting. The data reaffirmed that, post-treatment, this therapy has proven to be safe and well-tolerated. Additional data further validated higher levels of antibody and anti-DOM CD4 responses achieved in patients treated using electroporation. This academic study is a phase I/II study of 30 HLA A2+ patients with biochemical failure of prostate cancer. The study is testing a DNA fusion vaccine, developed in Southampton, encoding for an immunostimulant sequence from tetanus linked to a sequence from prostate specific membrane antigen (PSMA27). The study is also evaluating electroporation as a novel delivery strategy for DNA vaccines compared to DNA delivered without electroporation.

        Patient enrollment for this study has been completed. Monitoring of antibody responses was completed for the 20 patients at the first and second dose levels. Monitoring of CD4 cellular immunity had been completed for the 10 patients at the lowest dose. These 10 patients had additionally been assessed for CD8 T-cell responses. Reported interim results included:

    Vaccination with and without electroporation has been safe and well-tolerated.

    14 of 20 patients developed increases in anti-DOM (the immunostimulant sequence from tetanus) antibody. Of these increased responses, 5 of 10 were in the arm not using electroporation; 9 of 10 were in the electroporation arm. Antibody responses were generally higher in patients treated using electroporation compared to those treated with the DNA vaccine alone (without electroporation).

    In 9 of 10 patients in the low dose cohort, significant increases in CD4 responses were observed relative to pre-treatment. Of these increased responses, 4 of 5 were in the electroporation arm. Patients treated exclusively with electroporation produced a higher average CD4 response; patients initially treated without electroporation and later receiving a boost in conjunction with electroporation also displayed increased CD4 responses following the electroporation boost.

    In the low dose cohort, the PSMA27 antigen induced CD8+ cytotoxic T-cells (measured by cultured IFNg ELISPOT) not detected before vaccination in 6 of 10 subjects.

        In November 2005, Merck initiated a Phase I clinical trial of a DNA cancer vaccine based on Inovio's DNA gene delivery technology that uses pDNA encoding human epidermal growth factor receptor 2, or HER-2, and carcinoembryonic antigen, or CEA. As a result of Merck reaching this milestone, Inovio received a payment of $2.0 million. The Phase I trial is evaluating the safety, tolerability and immunogenicity of the vaccine.

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        In December 2007, Inovio received an additional $2.0 million milestone payment from Merck, resulting from the filing of a second Investigational New Drug (IND) application to the Food and Drug Administration ("FDA") by Merck for a DNA-based vaccine using Inovio's DNA delivery technology. The milestone relates to Inovio's collaboration and license with Merck initiated in May 2004 for the development of certain DNA vaccines. Further development of the product may lead to additional milestone payments and royalties to Inovio. Inovio received this milestone payment for its contribution to the collaboration, which has so far demonstrated the high level of gene delivery and expression that is thought to be necessary for the induction of a therapeutic immune response. Merck has funded all clinical development costs of these candidates to date.

        As of October, 2008, Merck had begun to enroll patients for this study, which is using a DNA vaccine encoding for hTERT to target non-small cell lung and prostate cancers. The vaccine is delivered using Inovio's electroporation DNA delivery technology.

        Inovio reported in September, 2008, that in a preclinical study of a proprietary DNA-based therapeutic vaccine, in mice with metastatic melanoma treated with a DNA vaccine via intramuscular delivery, six of eight (75%) were tumor-free at the conclusion of the study.

        Numerous cancer antigens have been identified over the past few decades and better identification tools are under development by others. Inovio will continue to evaluate opportunities to acquire or partner cancer antigens that may be useful in large market cancers such as breast, lung and prostate.

    Infectious Diseases: DNA Vaccines

        In January 2006, Inovio signed an agreement with Sweden-based Tripep to co-develop a therapeutic vaccine for hepatitis C virus (HCV) using electroporation. The vaccine is based on Tripep's proprietary HCV antigen construct and delivered to infected individuals using Inovio's MedPulser® DNA Delivery System. The study is being conducted at the Karolinska Institute's University Hospital in Sweden. The terms of the development agreement call for each party to fund a portion of the Phase I and subsequent Phase II trials and thereafter share profit according to their contribution. Inovio has 33% ownership in the overall product with the option to increase this to 50% after the completion of the Phase I/II trial.

        In November, 2008, Inovio announced that Tripep had reported interim results indicating that in the third and highest dose cohort of the study, two of three subjects demonstrated reductions in viral load of 93% and 99.7%. This compares to previously reported middle dose cohort results demonstrating an 87% and 98% reduction in HCV in two of three subjects; no anti-viral effect was observed in the low dose cohort. No safety issues have been noted to date in the trial. These data suggest a potential dose response of the vaccine and support the inclusion of three additional subjects in the high dose cohort.

        In November 2006, Inovio entered into a collaboration and license agreement with Wyeth to develop DNA vaccines against multiple infectious disease targets. For further discussion about this agreement, see " Partnerships and Collaborations" below. The selection of targets for its proprietary infectious disease program is driven by three key criteria: the complexity of the product development program, competition, and commercial opportunities.

        Inovio reported in July, 2008, that in a preclinical study of a proprietary DNA-based therapeutic vaccine, 100% of immunized mice given a lethal challenge of highly pathogenic H5N1 influenza virus (A/Vietnam/1203/04) survived and showed only minor weight loss. The DNA vaccine design was based on a different influenza strain (H1N1) than the influenza strain used in the challenge, providing evidence that a universal vaccine based on conserved genes common to multiple strains of seasonal influenza and even potential pandemic influenza may have the possibility to provide widespread protection against such viruses.

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    DNA Vaccines for Biodefense

        With the adoption of the Project Bioshield Act in 2004 by the U.S. government, there is an opportunity to secure development funding for proof-of-principle DNA vaccine studies for biowarfare pathogens. Inovio has been successful in securing funding from the U.S. government. Inovio believes DNA vaccines delivered with electroporation for bio-defense have the following advantages:

    establishment of a platform technology that can be readily adapted for new threats;

    ability to rapidly manufacture and scale-up vaccine candidates for newly identified pathogens;

    rapid induction of protective immune responses following vaccination; and

    long shelf life of products for stockpiling.

        As resources obtained from government funding can be leveraged to enhance the development of technology in the area of cancer and chronic infectious disease, Inovio will continue to pursue opportunities in the area of biodefense. As an example of potential applications in the area of biodefense, one of Inovio's partners (RMR, LLC) is currently employing its skin electroporation technology in the pre-clinical development of an anthrax vaccine under a Department of Defense Small Business Innovation Research Program (SBIR) grant. Inovio currently has commercial rights to this skin electroporation system. The technology may also be useful with respect to targets such as the Lassa fever virus currently being studied by the U.S. Army in collaboration with Inovio (as further outlined under Partnerships and Collaborations below).

    Gene Therapy

        Over the past decade, classic gene therapy or treatment of inherited disorders has proven difficult. Electroporation of genes encoding therapeutic proteins has, however, demonstrated the potential to resolve these difficulties. In vivo production of proteins such as Factor IX for hemophilia or EPO for anemia represents large market opportunities. Pre-clinical studies for Inovio's partners have demonstrated multiple desirable characteristics of Inovio's approach, including:

    Long term expression of the desired gene for convenient dosing;

    Lack of immune responses to the plasmid vector;

    Ability to achieve therapeutic levels of desired protein at a steady state; and

    More natural production of the therapeutic protein than current recombinant proteins.

        The major technical hurdle for use of Inovio's technology for classic gene therapy is the induction of an unwanted immune response to the transgene product due to the highly efficient delivery and expression seen with electroporation. As this problem may take significant resources to overcome, Inovio has decided not to focus on this market in the near term.

    Animal Health/Veterinary

        While Inovio is primarily focused on the use of Inovio's technology in the development of novel human therapeutics, it retains certain rights to veterinary applications and may seek to exploit these rights in the future.

    Additional Applications of Inovio's DNA Delivery Technology

        In addition to using Inovio's electroporation technology for drug and vaccine delivery, it can be used for research to validate new drug targets and to deliver molecules. Such use of Inovio's technology may facilitate transition into clinical development. Inovio continues to pursue, on a limited basis, research and opportunities in the areas of stem cells, ex vivo applications and RNAi.

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    Partnerships and Collaborations

        In September 2008, Inovio announced it has received a contract for $933,000 from the Department of Defense (US Army) to continue research and development of DNA-based vaccines delivered via its proprietary electroporation system. The contract, titled "Design and Engineering of the Elgen Gene Delivery System for Screening and Validation of Vaccine Candidates of Military Relevance," will run through May 2010. This project is focused on identifying DNA vaccine candidates with the potential to provide rapid, robust immunity to protect against bio-warfare and bioterror attacks.

        In November 2006, Inovio entered into a collaboration and license agreement with Wyeth for a worldwide non-exclusive license to Inovio's technology for certain infectious disease targets, for which Inovio received an upfront payment of $4.5 million. Inovio will also receive research support, annual maintenance fees, royalties on any net product sales and, contingent upon the achievement of clinical and regulatory milestones, payments of up to $60.0 million over the term of the agreement.

        In October 2006, Inovio announced that it acquired from Valentis, Inc. certain DNA delivery and expression assets, including Valentis' DNAvax® polymer delivery system and GeneSwitch® gene regulation technology.

        In July 2006, Inovio announced it extended its license with RMR Technologies, LLC ("RMR") by exercising an existing option to license certain patented technology relating to the delivery of gene-based therapeutics into skin. This extends a long-standing relationship with the University of South Florida scientists and RMR founders Drs. Heller (now Executive Director, Frank Reidy Research Center for Bioelectrics, Old Dominion University), Jaroszeski, and Gilbert. This relationship dates back to the co-development of Inovio's MedPulser® Electroporation Instrument for treatment of all types of solid tumors, including head and neck cancers. RMR is the collective effort of three scientists in collaboration with the University of South Florida and the H. Lee Moffitt Cancer Center and Research Institute. The license included other patents involving the delivery of genes or drugs via ex vivo, intratumoral, and intramuscular electroporation. Recent pre-clinical studies suggest that, for certain indications, needle-less skin electroporation of DNA plasmids encoding selected antigens may also be effective at inducing desired immune responses. The patented technology licensed from RMR covers various skin electroporation electrode designs and methods, including a needle-less design using a flexible material. RMR has agreed to collaborate in an effort to develop research prototypes into commercial grade electrodes for skin delivery as well as other novel forms of electroporation-assisted DNA delivery. Inovio has agreed to provide RMR with other development expertise pertinent to projects such as RMR's SBIR-funded pre-clinical study using RMR's proprietary dermal electrodes to deliver a DNA vaccine against anthrax. In connection with the acquisition of this exclusive license, Inovio issued 86,956 shares of Inovio common stock at a price of $2.30 per share, worth $200,000 on the date of issuance.

        Inovio also licensed from RMR patents that claim the intratumoral delivery method used in the ongoing clinical trial at the Moffitt Cancer Center & Research Institute, which is delivering the gene encoding IL-12 directly to melanoma lesions. RMR, Inovio, the University of South Florida and Moffitt Cancer Center have been collaborating in the development of this novel therapy for melanoma for the past two years.

        In May 2006, Inovio announced the acquisition, under a license with Sphergen SARL, of rights to several patent families relating to the use of electroporation technology. The rights Inovio licensed included two patents with broad claims regarding electroporation of nucleic acids in muscle and tumor tissue. This intellectual property acquisition enhanced the breadth of Inovio's patent portfolio directed to the use of electroporation technology to deliver therapeutic biopharmaceuticals. The license also includes grants of rights to know-how, future improvements, and provisions for exclusivity in applications to human medicine.

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        In January 2006, Inovio signed a collaborative agreement with Tripep to co-develop a therapeutic hepatitis C virus (HCV) DNA vaccine using electroporation. Under the terms of this agreement, Inovio pledged certain electroporation equipment toward an ongoing Phase I/II study of the proprietary Tripep vaccine in exchange for a minimum of 33% of the licensing revenues or commercial income that might be derived from the vaccine. Under the terms of the agreement, Tripep will only commercialize the electroporation-based vaccine with Inovio equipment. If Inovio decides not to continue to support the co-development, Inovio will retain a profit share of sub-licensing fees or commercial revenues going forward.

        In May 2005, Inovio announced that Merck exercised an option for a non-exclusive license for an additional antigen to be used with Inovio's MedPulser® DNA Delivery System. This option exercise was provided for under the 2004 license and research collaboration agreement between Merck and Inovio, and brought the total number of antigens licensed by Merck to three. Inovio received an option fee for the additional target antigen. Under the terms of Inovio's licensing agreement with Merck, Inovio is eligible for milestone and royalty payments if certain development goals and commercialization of the device are achieved by Merck.

        In April 2005, Inovio announced the initiation of a U.K. Medicines and Healthcare products Regulatory Agency (MHRA) approved Phase I/II clinical trial undertaken in collaboration with the University of Southampton. Inovio's electroporation technology is being used to deliver a therapeutic plasmid-based DNA vaccine to skeletal muscle with the aim of treating recurrent prostate cancer. The trial, sponsored and led by the University of Southampton, is investigating whether the DNA vaccine, developed at the University of Southampton, can stimulate patients to develop immune responses against prostate cancer and whether use of Inovio's electroporation system enhances this response.

        In October 2004, Inovio announced an agreement with Vical wherein Vical licensed Inovio's DNA delivery technology for use with HIV, cytomegalovirus (CMV) and melanoma (using pDNA IL-2) targets. This agreement was based on an option agreement established with Vical in October of 2003 for a worldwide license for the use of Inovio's proprietary in vivo electroporation delivery technology in combination with Vical's proprietary vaccines.

        In May 2004, Inovio announced a significant licensing deal with Merck for the development of Merck's DNA cancer and infectious disease vaccines. The terms of the agreement include milestone and royalty payments for successful completion of the clinical development of the vaccines by Merck. Under the terms of the agreement, Merck reimbursed Inovio for the co-development of a proprietary electroporation system for the delivery of Merck's DNA vaccines. This development and commercialization agreement was an extension of an initial evaluation agreement established in 2003. Merck received the right to use Inovio's proprietary technology for two specific antigens with an option to extend the agreement to include a limited number of additional target antigens. In addition, Merck obtained a non-exclusive license to the intellectual property related to the initial two specific antigens. Merck is responsible for all development costs and clinical programs.

        The research carried out under the above agreements may result in new long-term license agreements with the other parties and may provide Inovio with additional data that Inovio believes will assist it in assessing the efficacy of using its MedPulser® DNA Electroporation System for delivery of DNA vaccines and gene therapies. The data should further assist Inovio in its licensing and commercialization efforts. In addition to the above collaboration and licensing arrangements, Inovio may develop proprietary DNA therapeutic product through early stage clinical trials and partner the product for late stage clinical development and marketing. Inovio may have to negotiate license(s) for genes or other components of the product if they are not in the public domain.

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    Market

        Inovio's product development strategy is focused on pursuing significant product opportunities where Inovio's technology is truly enabling. During 2007, Inovio prioritized its efforts after assessing different market opportunities based on an evaluation of technology risk, market size and partner interest in DNA vaccines. Based on Inovio management's assessment of the market opportunities, oncology applications appear to represent the best market opportunities, followed by applications for infectious diseases, gene therapy for protein deficiency diseases and biodefense DNA vaccines.

        Inovio believes there is a significant unmet clinical need to develop more efficacious vaccines that stimulate cellular immunity (i.e. can induce T-cell responses) and can be applied to diseases such as cancer, hepatitis C or HIV infection. For these applications, Inovio's scientists believe that DNA vaccines may offer an improvement over conventional vaccination. Inovio's scientists believe that electroporation of DNA is critical to maximizing the efficiency of DNA vaccination and meeting unmet clinical needs for therapeutic vaccines, which some industry analysts consider to be a multi-billion dollar market opportunity.

    Competition

        Although there are many competing technologies for DNA delivery, Inovio believes electroporation has a unique strategic position compared to such technologies for the following reasons:

    Minimal or no delivery related side effects, and

    Enhances DNA vaccine potency.

    Minimal or No Delivery Related Side Effects

        Any company that is developing a DNA based delivery technology, such as viral delivery systems, lipid-based systems, or electroporation technology with an aim to carry out in vivo gene delivery for the treatment of various diseases, is a potential competitor of Inovio. Currently there are five key DNA delivery technologies: viral, lipids, naked DNA, "gene gun" and electroporation. All are promising technologies, but they each also have their unique obstacles to overcome. Management believes Inovio's electroporation system is strongly positioned to succeed as the dominant delivery method for DNA vaccines.

        Viral vectors can be highly effective, however, there continue to be concerns regarding potential mutations, unwanted immune responses against the vector itself (preventing its use for re-administration or booster shots) and other side effects. Viral technology has yet to show predictable, consistent safety and is very expensive. Lipids can be effective, but may also have toxicity issues and are relatively expensive. Naked DNA is widely considered to be safe and is relatively inexpensive, but is not very effective. The gene gun technology (using gold particles as carriers of DNA for skin delivery) looks promising, however, there are data suggesting that electroporation offers equal or better efficacy and may offer broader utility without requiring a carrier. Not requiring a carrier allows electroporation to have a unique advantage over competing technologies because it eliminates one additional component that may independently propagate side effects and create manufacturing and quality control challenges.

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        Competitive advantages of electroporation over other delivery systems are summarized on Table 1 below:

Table 1: Present comparison of DNA Delivery technologies

Carrier/Vector Type
  Carrier/Vector Issues   Efficacy   Economics  

Viral

  Mutations Immune Response Infection Symptoms   +++++     $$$$$  

Lipids

  Toxicity   ++     $$  

Particle Gun

  Manufacturability   ++++     $$$  

Naked DNA

  No Vector   +     $  

(Electroporation Enhanced)

  No Vector   ++++     $  

    Enabling DNA vaccines

        Commercial and academic institutions have been trying for over 15 years to develop DNA vaccines with sufficiently potent immune responses to make them commercially viable—without much success. One facet of DNA vaccine research and development ("R&D") has been to combine an adjuvant component to help initiate a general immune response to complement the specific immune response induced by the DNA vaccine, but adjuvants complicate manufacturing and may generate additional unwanted side effects.


        In addition to being a highly efficient delivery method of plasmid to muscle cells, Inovio has shown that the mild electrical pulses of electroporation also have an adjuvant effect. This adjuvant effect seems to be related to more CpG-containing plasmid gaining access to intracellular toll-like receptors, which stimulate innate immune responses, and to slight muscle damage, which can lead to a danger signal to the immune system(1). To date, few, if any, common adjuvants seem to be required to augment immune responses observed after DNA vaccine delivery with electroporation.

(1)
Babiuk, S. et al., 2004, Increased gene expression and inflammatory cell infiltration caused by electroporation are both important for improving the efficacy of DNA vaccines. J. Biotech. 110:1

        General observations to date suggest that there has to be an increase in gene expression of at least 100-fold (compared to naked DNA) in order to achieve a therapeutic benefit in large animals including man. Electroporation is currently the only method whereby one can routinely see increases in gene expression of 100 to 1000 fold, thereby making the development of a large number of vaccines and therapeutics possible. In effect, electroporation increases the trivial levels of gene expression seen with naked DNA alone to the therapeutic levels needed for the development of successful commercial products. This puts Inovio in a unique position relative to competing technologies.

    Competitive Technologies in the Area of DNA Delivery

        Effective DNA delivery technologies are crucial for DNA vaccines. Many of the leading scientists in these fields have pointed out that the major obstacle to success has been the lack of safe, efficient, and economical methods of delivering DNA. Of the more than 800 gene therapy and DNA vaccine clinical trials started in the U.S. to date, none have progressed to regulatory approval. Inovio believes that existing DNA delivery alternatives have been a significant bottleneck to the successful development and commercialization of these promising next generation of vaccines. The following descriptions highlight the issues of the existing alternatives.

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    Viral DNA Delivery

        This technology utilizes a virus as a carrier to deliver genetic material into target cells. The method is very efficient for delivering vaccine antigens and has the advantage of mimicking real viral infection so that the recipient will mount a broad immune response against the vaccine. The greatest limitation of the technology is problems with unwanted immune responses against the viral vector, limiting its use to patients who have not been previously exposed to the viral vector and making repeated administration difficult. In addition, complexity and safety concerns increase the cost of vaccines and complicate regulatory approval.

    Ballistic DNA Delivery (Gene Gun)

        This technology utilizes micron sized DNA-coated gold particles that are shot into the skin using compressed gas. The method has matured considerably over the last 15 years and has been shown to be an efficient method to deliver a number of vaccine antigens. Since the DNA is dry coated, excellent stability of the vaccine can be achieved. The method is limited to use in skin and only a few micrograms of genetic material can be delivered each time. This may limit the utility of the method for targets such as cancer where higher doses of vaccine antigens and stronger T-cell responses are needed.

    Lipid DNA Delivery

        A number of lipid formulations have been developed that increase the effect of DNA vaccines. These work by either increasing uptake of the DNA into cells or by acting as an adjuvant, alerting the immune system. While there has been steady progress in this field, lipid delivery tends to be less efficient than viral vectors and is hampered by concerns regarding toxicity and increased complexity.

    "Naked" DNA Delivery

        The simplest DNA delivery mode is the injection of "naked" plasmid DNA into target tissue, usually skeletal muscle. This method is safe and economical but inefficient in terms of cell transfection, the process of transferring DNA into a cell across the outer cell membrane. Unfortunately, it is the least effective way of delivering DNA since only an extremely small fraction (approximately one out of twenty million) of the DNA molecules are taken up by the cells. While the method may have provided some utility for the field of gene therapy, a number of clinical studies over the last decade have shown that the method is inadequate for delivering DNA vaccines into large animals and humans.

    "Naked" DNA Delivery With Electroporation

        When naked DNA injection is followed by electroporation of the target tissue, transfection is significantly greater with resultant gene expression generally enhanced from 100 to 1000-fold. This increase makes many DNA vaccine candidates potentially feasible without unduly compromising safety or cost.

        In December 2004, the first patient was treated using Inovio's electroporation system to deliver a plasmid DNA-based immunotherapy and Inovio has initiated, together with partners, additional Phase I clinical trials using Inovio's electroporation technology to deliver DNA-based immunotherapies or DNA vaccines. To date Inovio have not observed any serious adverse events that can be attributed to the use of electroporation in these clinical DNA studies.

        Inovio believes that the greatest obstacle to making DNA vaccines and immunotherapy a reality, namely the safe, efficient, and economical delivery of DNA plasmid constructs into target cells, and also believes that electroporation may become the method of choice for DNA delivery into cells in many applications.

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        There are other companies with electroporation intellectual property and devices. Inovio believes it has significant competitive advantages over other companies focused on electroporation for multiple reasons:

    Inovio believes it has the longest history and deepest experience and insight in developing the methods and devices that will optimize the use of electroporation in conjunction with DNA-based agents. This extensive experience has been validated with multiple sets of interim data from multiple clinical studies assessing DNA-based immunotherapies against cancers and infectious disease. Inovio, in conjunction with its partners and collaborators, has been the leader in establishing proof-of-principle of electroporation-delivered DNA vaccines and immunotherapies.

    The company has a broad product line of electroporation instruments designed to enable DNA delivery in tumors, muscle, and skin.

    Inovio has been very proactive in filing for patents, as well as acquiring and licensing additional patents, to expand and strengthen Inovio's international patent estate. Inovio has, as discussed below under Intellectual Property, the leading number of patents pertaining to electroporation. Inovio's patent estate has been rigorously assessed by leading vaccine companies Merck and Wyeth prior to them consummating substantial license agreements with Inovio.

        While other companies have and continue to develop electroporation devices and possess certain patents relating to the use of electroporation, Inovio believes it has a strongly researched position and that its patent estate provides it with the potential to block competition in key areas of focus.

    Medical Device Manufacturing

        Inovio is a medical device manufacturer and, as such, operates in a regulated industry. Inovio must comply with a variety of manufacturing, product development and quality regulations in order to be able to distribute Inovio's products commercially around the world. In Europe, Inovio must comply with the MDD. Inovio has a Quality System certified by its international Notified Body to be in compliance with the international Quality System Standard, ISO13485, and meeting the Annex II Quality System requirements of the MDD. Inovio completed an Annex II Conformity Assessment procedure and achieved its CE Mark of the MedPulser® electroporation system in March 1999. Inovio completed an Annex II Conformity Assessment procedure and achieved its CE Mark of the Elgen electroporation system in November 2006.

        In the U.S., Inovio is required to maintain facilities, equipment, processes and procedures that are in compliance with quality systems regulations. Inovio's systems have been constructed to be in compliance with these regulations and its ongoing operations are conducted within these systems. Commercially distributed devices within the U.S. must be developed under formal design controls and be submitted to the FDA for clearance or approval. As Inovio prepares for U.S. marketing, all development activity is performed according to formal procedures to ensure compliance with all design control regulations.

        Inovio employs modern manufacturing methods and controls to optimize performance and control costs. Internal capabilities and core competencies are strategically determined to optimize Inovio's manufacturing efficiency. Inovio utilizes contract manufacturers for key operations, such as clean room assembly and sterilization, which are not economically conducted in-house. Inovio outsources significant sub-assemblies, such as populated printed circuit boards, for which capital requirements or manufacturing volumes do not justify vertical integration. As Inovio transitions from late-stage development activities into higher volume manufacturing activities, internal capabilities will be modified and added, as appropriate, to meet its changing priorities.

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        Currently, the durable electronic generator in the MedPulser® and Elgen system is assembled from outsourced populated printed circuit boards, and then tested, packaged and inventoried at Inovio's manufacturing facility. The disposable applicators used with the MedPulser® system are assembled and sterilized in a clean room at outside contract manufacturers. Future manufacturing of applicators for clinical trials and commercial distribution is planned to be done using a combination of internal manufacturing and outside contract manufacture.

    Intellectual Property

        Inovio's success and ability to compete depends upon its intellectual property. Inovio maintains a broad-based patent portfolio (both original and in-licensed technologies) that as of December 5, 2008, includes over 62 issued U.S. patents and 181 issued foreign counterpart patents, all of which collectively include claims to methods and/or devices for clinical use in the electroporation medical arts. Specifically, patented subject matter, as well as subject matter pending in the U.S. and foreign patent offices, includes method and device claims for delivering by electroporation medically important substances to the interior of cells in various body tissues such as a patient's muscle, skin, and other organs.

        Inovio's core technology is centered on five broad, medically relevant "indication" categories including oncology, gene therapy/delivery (including vaccination with expressible vectors), vascular administration (e.g. by catheter), transdermal administration (including delivery of substances for cancer, gene therapy, and cosmetic applications), and ex vivo administration (e.g. by electroporation of cells outside the body and introducing the created cells to the patient).

        Supporting Inovio's primary business focus, its intellectual property in gene therapy and DNA delivery enjoys a broad scope of patent protection, such as found in U.S. patent numbers 5,273,525 and in-licensed patents 6,110,161, 6,261,281, 6,610,044, 6,958,060 and 6,939,862, which include claims reciting methods and apparatus for implanting macromolecules (e.g. DNA and pharmaceutical compounds) into selected tissues of a patient by electroporation. U.S. patent number 6,763,264, with claims reciting methods of delivering expression vectors and molecules, and U.S. patent number 6,697,669, with claims reciting methods of in vivo electroporation of skin and muscle, provide broad-based coverage to the company. Other of Inovio's patents protect its proprietary methodology of electroporation wherein the electroporation process is carried out using "opposed-paired" electric field pulsing. Such patents include, and are not limited to, U.S. patent numbers 6,241,701, 6,120,493, 6,233,482, and 5,702,359C1. It is important to understand that patents having claims directed to methods of delivering substances to tissues using electroporation and devices for such methods, are generally applicable to DNA delivery and oncological applications.

        With respect to oncology, U.S. patent number 6,569,149 provides broad claim coverage directed to a method for the application of electric fields to a tissue of a patient having a "cell proliferation disorder" for the purpose of introducing molecules into cells of the tissue to treat the cell proliferation disorder. Such method comprises providing an array of multiple opposed pairs of electrodes connected to a generator, wherein at least two pairs of electrodes, after being placed in selected tissue along with the substance being electroporated, are activated simultaneously with electric pulses. Likewise, in-licensed patent 6,528,315 claims methods of electroporation of DNA to tumor cells in a broad manner.

        Inovio has a number of issued U.S. and foreign patents claiming a widely used gene regulation technology called GeneSwitch® that permits control of gene expression from DNA sequences via a small molecule that can be administered orally. For example, U.S. patents 5,364,791 and 6,599,698 claim various aspects of this unique regulation system that may be used in gene therapy products. In addition to electroporation technology for gene delivery, the company also acquired a group of patents

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claiming the delivery of DNA using polymers (e.g., 6,040,295 and 6,514,947) and lipids (e.g., 6,387,395 and 6,235,310) that are useful in the development of certain DNA vaccines.

        Inovio's patent portfolio is also active with respect to vascular, transdermal, and ex vivo applications of electroporation technology. For example, U.S. patent 5,704,908 includes claims directed to an electroporation balloon catheter. Additionally, U.S. patent 6,342,247 is directed to methods of increasing vasodilation, an important indication in maintaining blood flow in certain patients with vessel occlusion problems. U.S. patents 6,697,669, 6,654,636, 5,810,762, and 5,439,440 provide claims to transdermal application of electric fields to surface tissues, while U.S. patents 6,027,488, 6,746,441, 6,800,484, and 6,150,148 include claims to electroporation of cells in vitro. Such electroporated cells could be used either in laboratory settings or for introduction into patient blood stream or other tissues.

        Of further importance to Inovio, the currently issued patents provide a potential monopoly base for the claimed subject matter for the various indications to at least the year 2017 and numerous claims will be in force to between 2018 and 2020.

    Corporate History and Headquarters

        Inovio was originally incorporated on June 29, 1983, under the laws of California as Biotechnologies & Experimental Research, Inc. On December 10, 1991, the entity changed its corporate name to BTX, Inc. and again on February 8, 1994 changed it to Genetronics, Inc. On April 14, 1994, the board of directors approved a share exchange agreement with Consolidated United Safety Technologies Inc. On September 2, 1997, the company listed on the Toronto Stock Exchange ("TSE") as Genetronics Biomedical Ltd, under the laws of British Columbia, Canada, which wholly-owned Genetronics, Inc. On June 15, 2001, the entity completed a change in jurisdiction of incorporation from British Columbia, Canada, to the state of Delaware. This change was accomplished through a continuation of Genetronics Biomedical Ltd. into Genetronics Biomedical Corporation, a Delaware corporation. On January 17, 2003, Genetronics voluntarily de-listed from the TSE, where Inovio's common stock had been listed since September 2, 1997. On March 31, 2005, the corporate name changed from Genetronics Biomedical Corporation to Inovio Biomedical Corporation. Inovio carries out its business through its U.S. wholly-owned subsidiary, Genetronics, Inc., a Norwegian wholly-owned subsidiary, Inovio AS, and a wholly-owned subsidiary in the Republic of Singapore, Inovio Asia Pte. Ltd., which may be a platform for future research and development efforts.

        Inovio's principal executive offices are located at 11494 Sorrento Valley Road, San Diego, California 92121-1318, and the telephone number is (858) 597-6006.

    Employees

        As of January 20, 2009, Inovio employed 27 people on a full-time basis and 10 people under consulting and project employment agreements. Of the combined total, 22 were in product research, which includes research and development, quality assurance, clinical, engineering, and manufacturing, and 15 were in general and administrative, which includes corporate development, information technology, legal, investor relations, finance, and corporate administration. None of Inovio's employees are subject to collective bargaining agreements. Inovio considers its employee relations to be good.

         The following discussion and analysis of financial condition and results of operations should be read in conjunction with the Inovio Unaudited Consolidated Financial Statements and Notes thereto derived from the September 30, 2008 Quarterly Report on Form 10-Q and the Inovio Consolidated Financial Statements and Notes thereto derived from the December 31, 2007 Annual Report on Form 10-K, which statements are included elsewhere in this joint proxy statement/prospectus .

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         This discussion and analysis contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements with regards to Inovio's revenue, spending, cash flow, products, actions, plans, strategies and objectives. Forward-looking statements include, without limitation, any statement that may predict, forecast, indicate or simply state future results, performance or achievements, and may contain the words "believe," "anticipate," "expect," "estimate," "intend," "plan," "project," "will be," "will continue," "will result," "could," "should," "would," "may," "might," or any variations of such words with similar meanings. Any such statements are subject to risks and uncertainties that could cause Inovio's actual results to differ materially from those which are Inovio's management's current expectations or forecasts. Such information is subject to the risk that such expectations or forecasts, or the assumptions underlying such expectations or forecasts, become inaccurate. Such risks and uncertainties are disclosed from time to time in Inovio's reports and such risks and uncertainties are further discussed in this joint proxy statement/prospectus under "Risk Factors" beginning on page 28.

        The SEC defines critical accounting policies as those that are, in management's view, important to the portrayal of Inovio's financial condition and results of operations and require management's judgment. The following discussion and analysis of Inovio's financial condition and results of operations is based on Inovio's audited consolidated financial statements for the fiscal year ended December 31, 2007 and its unaudited condensed consolidated financial statements for the quarter ended September 30, 2008, which have been prepared in accordance with U.S. GAAP. The preparation of these consolidated financial statements requires Inovio to make estimates and judgments that affect the reported amounts of assets, liabilities, revenue and expenses. Inovio bases its estimates on experience and on various assumptions that it believes are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from those estimates. Inovio's critical accounting policies include:

        Revenue Recognition.     Revenue is recognized in accordance with SAB No. 104, Revenue Recognition in Financial Statements and EITF Issue 00-21, Revenue Arrangements with Multiple Deliverables.

        Inovio has adopted a strategy of co-developing or licensing its gene delivery technology for specific genes or specific medical indications. Accordingly, Inovio has entered into collaborative research and development agreements and have received funding for pre-clinical research and clinical trials. Payments under these agreements, which are non-refundable, are recorded as revenue as the related research expenditures are incurred pursuant to the terms of the agreements and provided collectibility is reasonably assured.

        License fees are comprised of initial fees and milestone payments derived from collaborative licensing arrangements. Inovio continues to recognize non-refundable milestone payments upon the achievement of specified milestones upon which Inovio has earned the milestone payment, provided the milestone payment is substantive in nature and the achievement of the milestone was not reasonably assured at the inception of the agreement. Inovio defers payments for milestone events which are reasonably assured and recognize them ratably over the minimum remaining period of its performance obligations. Payments for milestones which are not reasonably assured are treated as the culmination of a separate earnings process and are recognized as revenue when the milestones are achieved.

        Inovio receives non-refundable grants under available government programs. Government grants towards current expenditures are recorded as revenue when there is reasonable assurance that Inovio has complied with all conditions necessary to receive the grants, collectibility is reasonably assured, and as the expenditures are incurred.

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        Research and Development Expenses.     Since Inovio's inception, virtually all of its activities have consisted of research and development efforts related to developing its electroporation technologies. Inovio expenses all such expenditures in the period incurred. Inovio's expenses related to clinical trials are based on services received and efforts expended pursuant to contracts with multiple research institutions and clinical research organizations that conduct and manage clinical trials on Inovio's behalf. The financial terms of these agreements are subject to negotiation and vary from contract to contract and may result in uneven payment flows. Generally, these agreements set forth the scope of work to be performed at a fixed fee or unit price. Payments under the contracts depend on factors such as the successful enrollment of patients or the completion of clinical trial milestones. Expenses related to clinical trials generally are accrued based on contracted amounts applied to the level of patient enrollment and activity according to the protocol. If timelines or contracts are modified based upon changes in the clinical trial protocol or scope of work to be performed, Inovio modifies its estimates accordingly on a prospective basis.

        Valuation of Goodwill and Intangible Assets.     Inovio's business acquisitions typically result in goodwill and other intangible assets, and the recorded values of those assets may become impaired in the future. Acquired intangible assets are still being developed for the future economic viability contemplated at the time of acquisition. Inovio is concurrently conducting Phase I and pre-clinical trials using the acquired intangibles, and has entered into certain significant licensing agreements for use of these acquired intangibles.

        Inovio records patents at cost and amortize these costs using the straight-line method over the expected useful lives of the patents or 17 years, whichever is less. Patent cost consists of the consideration paid for patents and related legal costs. License costs are recorded based on the fair value of consideration paid and amortized using the straight-line method over the shorter of the expected useful life of the underlying patents or the term of the related license agreement. As of September 30, 2008, Inovio's goodwill and intangible assets resulting from acquisition costs of Inovio AS, and additional intangibles including patents and license costs, net of accumulated amortization, totaled $9.8 million.

        The determination of the value of such intangible assets requires management to make estimates and assumptions that affect Inovio's consolidated financial statements. Inovio assesses potential impairments to intangible assets when there is evidence that events or changes in circumstances indicate that the carrying amount of an asset may not be recovered. Inovio's judgments regarding the existence of impairment indicators and future cash flows related to intangible assets are based on operational performance of its acquired businesses, market conditions and other factors. If impairment is indicated, Inovio reduces the carrying value of the intangible asset to fair value. Inovio has not recognized any impairment losses through September 30, 2008.

        Although there are inherent uncertainties in this assessment process, the estimates and assumptions Inovio uses are consistent with its internal planning. If these estimates or their related assumptions change in the future, Inovio may be required to record an impairment charge on all or a portion of its goodwill and intangible assets. Furthermore, Inovio cannot predict the occurrence of future impairment-triggering events nor the impact such events might have on its reported asset values. Future events could cause Inovio to conclude that impairment indicators exist and that goodwill or other intangible assets associated with its acquired businesses are impaired. Any resulting impairment loss could have an adverse impact on its consolidated results of operations.

        Stock-Based Compensation.     Stock-based compensation cost is estimated at the grant date based on the fair-value of the award and is recognized as an expense ratably over the requisite service period of the award. Determining the appropriate fair-value model and calculating the fair value of stock-based awards at the grant date requires considerable judgment, including estimating stock price volatility, expected option life and forfeiture rates. Inovio develops its estimates based on historical

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data. If factors change and Inovio employs different assumptions in future periods, the compensation expense that Inovio records may differ significantly from what it has recorded in the current period. A small change in the estimates used may have a relatively large change in the estimated valuation. Inovio uses the Black-Scholes pricing model to value stock option awards. Inovio recognizes compensation expense using the straight-line amortization method.

        Registered Common Stock Warrants.     Inovio accounts for registered common stock warrants in accordance with EITF Issue 00-19, Accounting for Derivative Financial Instruments Indexed to, and Potentially Settled in, a Company's Own Stock, on the understanding that in compliance with applicable securities laws, the registered warrants require the issuance of registered securities upon exercise and do not sufficiently preclude an implied right to net cash settlement. Inovio classifies registered warrants on the condensed consolidated balance sheet as a current liability which is revalued at each balance sheet date subsequent to the initial issuances in October 2006 and August 2007. Determining the appropriate fair-value model and calculating the fair value of registered warrants requires considerable judgment, including estimating stock price volatility and expected warrant life. Inovio develops its estimates based on historical data. A small change in the estimates used may have a relatively large change in the estimated valuation. Inovio uses the Black-Scholes pricing model to value the registered warrants. Changes in the fair market value of the warrants are reflected in the consolidated statement of operations as " Other income and expense ."

        In May 2008, the Financial Accounting Standards Board ("FASB") issued SFAS No. 162, The Hierarchy of Generally Accepted Accounting Principles ("SFAS No. 162"). SFAS No. 162 identifies the sources of accounting principles and the framework for selecting the principles to be used in the preparation of financial statements that are presented in conformity with U.S. GAAP. Inovio is currently evaluating the impact that SFAS No. 162 will have on its condensed consolidated financial statements.

        In March 2008, the FASB issued SFAS No. 161, Disclosures about Derivative Instruments and Hedging Activities ("SFAS No. 161"). This statement changes the disclosure requirements for derivative instruments and hedging activities. Entities are required to provide enhanced disclosures about (a) how and why an entity uses derivative instruments, (b) how derivative instruments and related hedged items are accounted for under SFAS No. 133, Accounting for Derivative Instruments and Hedging Activities , and its related interpretations, and (c) how derivative instruments and related hedged items affect an entity's financial position, financial performance, and cash flows. SFAS No. 161 is effective for financial statements issued for fiscal years and interim periods beginning after November 15, 2008, with early application encouraged. This statement encourages, but does not require, comparative disclosures for earlier periods at initial adoption. The adoption of SFAS No. 161 is not expected to have a material impact on Inovio's condensed consolidated financial statements.

        In December 2007, the FASB issued SFAS No. 160, Non-controlling Interests in Consolidated Financial Statements (an amendment of Accounting Research Bulletin No. 51) ("SFAS No. 160"). SFAS No. 160 requires that non-controlling (minority) interests be reported as a component of equity, that net income attributable to the parent and to the non-controlling interest be separately identified in the income statement, that changes in a parent's ownership interest while the parent retains its controlling interest be accounted for as equity transactions, and that any retained non-controlling equity investment upon the deconsolidation of a subsidiary be initially measured at fair value. This statement is effective for fiscal years beginning after December 31, 2008, and shall be applied prospectively. However, the presentation and disclosure requirements of SFAS No. 160 are required to be applied retrospectively for all periods presented. The retrospective presentation and disclosure requirements of this statement will be applied to any prior periods presented in financial statements for the fiscal year ending December 31, 2009, and later periods during which the Company had a consolidated subsidiary with a

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non-controlling interest. As of September 30, 2008, Inovio does not have any consolidated subsidiaries in which there is a non-controlling interest.

        In December 2007, the FASB issued SFAS No. 141(R), Business Combinations ("SFAS No. 141(R)"). SFAS No. 141(R) changes the requirements for an acquirer's recognition and measurement of the assets acquired and liabilities assumed in a business combination, including the treatment of contingent consideration, pre-acquisition contingencies, transaction costs, in-process research and development and restructuring costs. In addition, under SFAS No. 141(R), changes in an acquired entity's deferred tax assets and uncertain tax positions after the measurement period will impact income tax expense. This statement will be effective for Inovio with respect to business combination transactions for which the acquisition date is after December 31, 2008. Inovio is currently evaluating the impact that SFAS No. 141(R) will have on its condensed consolidated financial statements, including specifically evaluating the impact upon consummation of the Merger with VGX, if completed.

        In November 2007, the FASB ratified EITF Issue No. 07-1, Accounting for Collaborative Agreements Related to the Development and Commercialization of Intellectual Property . EITF Issue No. 07-1 defines collaborative agreements as a contractual arrangement in which the parties are active participants to the arrangement and are exposed to the significant risks and rewards that are dependent on the ultimate commercial success of the endeavor. Additionally, it requires that revenue generated and costs incurred on sales to third parties as it relates to a collaborative agreement be recognized as gross or net based on EITF Issue No. 99-19, Reporting Revenue Gross as a Principal versus Net as an Agent . It also requires payments between participants to be accounted for in accordance with already existing generally accepted accounting principles, unless none exist, in which case a reasonable, rational, consistent method should be used. EITF Issue No. 07-1 is effective for fiscal years beginning after December 15, 2008 for all collaborative arrangements existing as of that date, with retrospective application to all periods. Inovio's management is currently evaluating the impact of this standard and does not anticipate the adoption of EITF Issue No. 07-1 to have a material impact on Inovio's condensed consolidated financial statements.

        In September 2006, the FASB issued SFAS No. 157, Fair Value Measurements ("SFAS No. 157"). SFAS No. 157 establishes a common definition for fair value to be applied to U.S. GAAP requiring use of fair value, establishes a framework for measuring fair value, and expands disclosure about such fair value measurements. SFAS No. 157 is effective for financial assets and financial liabilities for fiscal years beginning after November 15, 2007. Issued in February 2008, FSP 157-1, Application of FASB Statement No. 157 to FASB Statement No. 13 and Other Accounting Pronouncements That Address Fair Value Measurements for Purposes of Lease Classification or Measurement under Statement 13 , removed leasing transactions accounted for under Statement 13 and related guidance from the scope of SFAS No. 157. FSP 157-2 Partial Deferral of the Effective Date of Statement 157 (FSP 157-2), deferred the effective date of SFAS No. 157 for all nonfinancial assets and nonfinancial liabilities to fiscal years beginning after November 15, 2008. The partial implementation of SFAS No. 157 for financial assets and financial liabilities, effective January 1, 2008, did not have a material impact on Inovio's condensed consolidated financial statements. Inovio is currently assessing the impact of SFAS No. 157 for non-financial assets and nonfinancial liabilities on its condensed consolidated financial statements.

        In June 2007, the EITF issued EITF Issue No. 07-3, Accounting for Nonrefundable Advance Payments for Goods or Services to be Used in Future Research and Development Activities . The consensus requires companies to defer and capitalize prepaid, nonrefundable research and development payments to third parties over the period that the research and development activities are performed or the services are provided, subject to an assessment of recoverability. EITF Issue No. 07-3 is effective for

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new contracts entered into beginning on January 1, 2008. The adoption of EITF Issue No. 07-3 did not have a material impact on Inovio's condensed consolidated financial statements.

        Revenue.     Inovio had total revenue of $455,000 and $1.8 million for the three and nine months ended September 30, 2008, compared to $487,000 and $1.5 million for the three and nine months ended September 30, 2007, respectively. Revenue primarily consists of license fees, milestone payments and amounts received from collaborative research and development agreements and grants.

        Revenue from license fees and milestone payments was $215,000 and $612,000 for the three and nine months ended September 30, 2008, respectively, as compared to $137,000 and $581,000 for the three and nine months ended September 30, 2007, respectively. The increase in revenue under license fees and milestone payments for the three and nine month periods ended September 30, 2008, as compared to the comparable periods in 2007, was mainly due to higher revenue recognized from various smaller license agreements, offset by less revenue recognized from the Merck licensing agreement as this agreement was fully amortized during 2007. Revenue recognized from the Wyeth license agreement was consistent with prior periods.

        During the three and nine months ended September 30, 2008, Inovio recorded revenue under collaborative research and development arrangements of $240,000 and $1.2 million, respectively, as compared to $266,000 and $800,000 for the three and nine months ended September 30, 2007, respectively. This decrease in revenue for the three months ended September 30, 2008 was primarily due to a decrease in Merck billings based on timing of efforts related to Inovio's collaborative research agreement. The increase in revenue for the nine months ended September 30, 2008 when compared to the same period in 2007 was primarily due to an increase in Wyeth billings based on Inovio's collaborative agreement, offset by slightly lower Merck collaborative research billings. Billings from research and development work performed pursuant to the Wyeth and Merck agreements are recorded as revenue as the related research expenditures are incurred.

        There was no grant and miscellaneous revenue for the three and nine months ended September 30, 2008, as compared to $84,000 and $105,000 for the three and nine months ended September 30, 2007. The decrease in grant and miscellaneous revenue for the three and nine months ended September 30, 2008, as compared to the comparable periods in 2007, was due to no revenue recognized from the U.S. Army Grant due to the finalization of work performed. On September 26, 2008, Inovio received a new contract for $933,000 from the Department of Defense (U.S. Army) to continue research and development of DNA-based vaccines delivered via Inovio's proprietary electroporation system. The contract, titled " Design and Engineering of the Elgen Gene Delivery System for Screening and Validation of Vaccine Candidates of Military Relevance ," will run through May 2010. This project is focused on identifying DNA vaccine candidates with the potential to provide rapid, robust immunity to protect against bio-warfare and bioterror attacks.

        Research and Development Expenses.     Research and development expenses, which include clinical trial costs, for the three and nine months ended September 30, 2008, were $1.3 million and $4.6 million, respectively, compared to $2.3 million and $7.8 million for the three and nine months ended September 30, 2007, respectively. The decrease in research and development expenses for the three and nine months ended September 30, 2008, as compared to the comparable periods in 2007, was primarily due to a decrease in clinical trial expenses associated with patient enrollment, clinical site costs, data collection and monitoring costs, and decreased costs related to the use of outside Clinical Research Organizations ("CRO's") and Clinical Research Associates ("CRA's"). Additional decreases are associated with less consulting and advisory services received, offset by higher costs associated with the expansion of Inovio's in-house engineering and research expertise.

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        General and Administrative Expenses.     General and administrative expenses, which include business development expenses and the amortization of intangible assets, for the three and nine months ended September 30, 2008, were $1.9 million and $7.4 million, respectively, as compared to $3.2 million and $7.8 million for the three and nine months ended September 30, 2007, respectively. The decrease in general and administrative expenses for the three and nine months ended September 30, 2008, as compared to the comparable periods in 2007, was mainly due to a decrease in outside consulting and advisory services related to partnering Inovio's SECTA therapy program as well as a decrease in employee stock-based compensation expense, offset by increased legal fees related to the negotiation and execution of the merger agreement with VGX and ancillary documents, as well as other corporate matters.

        Stock-Based Compensation.     Stock-based compensation cost is measured at the grant date, based on the fair value of the award reduced by estimated forfeitures, and is recognized as expense over the employee's requisite service period. Total compensation cost under SFAS No. 123(R) for Inovio's equity incentive plans for the three and nine months ended September 30, 2008 was $270,000 and $797,000, respectively. From these amounts, $76,000 and $222,000 was included in research and development expenses and $194,000 and $575,000 was included in general and administrative expenses, respectively. Total compensation cost under SFAS No. 123(R) for Inovio's equity incentive plans for the three and nine months ended September 30, 2007 was $310,000 and $1.3 million, respectively. From these amounts, $75,000 and $280,000 was included in research and development expenses and $235,000 and $1.0 million was included in general and administrative expenses, respectively.

        The closing of the Merger will constitute a "Change of Control" or "Change in Control" as such terms are used in Inovio's equity incentive plans and related agreements, which will result in the acceleration of vesting for all options to purchase shares of Inovio common stock outstanding as of the Effective Date. This acceleration will result in a charge to compensation expense of approximately $930,000 subsequent to and dependent upon the closing of the Merger. Of this amount, approximately $235,000 will be recorded as research and development expenses and $695,000 will be recorded as general and administrative expenses.

        Interest Income/(Expense).     Interest income for the three and nine months ended September 30, 2008, was $97,000 and $587,000, respectively, as compared to $405,000 and $915,000 for the three and nine months ended September 30, 2007, respectively. The decrease in interest income for the three and nine months ended September 30, 2008, as compared to the comparable periods in 2007, was primarily due to lower cash and investment balances and a lower average interest rate.

        Other Income/(Expense).     Inovio recorded other income for the three and nine months ended September 30, 2008 of $307,000 and $220,000, respectively, as compared to other income of $1.9 million and $3.0 million for the three and nine months ended September 30, 2007, respectively. The decrease in other income (expense) is primarily due to the revaluation of registered common stock warrants issued by Inovio in October 2006 and August 2007. Inovio is required to revalue the warrants at each balance sheet date to fair value. If unexercised, the warrants will expire in October 2011 and August 2012, respectively.

        Imputed and Declared Dividends on Preferred Stock.     The holders of Inovio's Series C preferred stock were entitled to receive an annual dividend at the rate of 6%, payable quarterly, through May 20, 2007. These dividends were payable in cash unless the closing price of Inovio common stock for the 20 trading days immediately preceding the dividend payment date was equal to or greater than the conversion price of such shares, in which event Inovio may have elected to pay the dividends to the holders in common stock. During the nine months ended September 30, 2007, Inovio paid dividends to the holders of Inovio's Series C preferred stock in cash of $23,000. No dividends were paid during the three months ended September 2007 or during the three and nine months ended September 30, 2008.

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      Comparison of Years Ended December 31, 2007 and 2006

        The audited consolidated financial data for the years ended December 31, 2007 and December 31, 2006 is presented in the following table and the results of these two periods are used in the discussion thereafter.

 
  December 31,
2007
  December 31,
2006
  Increase/
(Decrease)
$
  Increase/
(Decrease)
%
 

Revenue:

                         

License fee and milestone payments

  $ 2,793,478   $ 1,337,105   $ 1,456,373     109 %

Revenue under collaborative research and development arrangements

    1,854,303     962,207     892,096     93  

Grants and miscellaneous revenue

    159,948     1,168,866     (1,008,918 )   (86 )
                   

Total revenue

    4,807,729     3,468,178     1,339,551     39  

Operating expenses:

                         

Research and development

    9,625,947     8,509,785     1,116,162     13  

General and administrative

    11,080,202     8,304,587     2,775,615     33  
                   

Total operating expenses

    20,706,149     16,814,372     3,891,777     23  
                   

Loss from operations

    (15,898,420 )   (13,346,194 )   2,552,226     19  

Interest and other income

    4,693,977     1,002,252     3,691,725     368  
                   

Net loss

    (11,204,443 )   (12,343,942 )   (1,139,499 )   (9 )
                   

Imputed and declared dividends on preferred stock

    (23,335 )   (2,005,664 )   (1,982,329 )   (99 )
                   

Net loss attributable to common stockholders

  $ (11,227,778 ) $ (14,349,606 ) $ (3,121,828 )   (22 )%
                   

        Revenue.     Inovio's revenue consists of license fees, milestone payments, and amounts received from collaborative research and development arrangements and grants. Inovio's total revenue increased $1.3 million or 39% for the year ended December 31, 2007, as compared to fiscal 2006 due to significant increases in license fees, milestone payments and revenue under collaborative research and development arrangements, offset partially by a large decrease in grant revenue. The $1.5 million increase in license fees and milestone payments for the year ended December 31, 2007, as compared to fiscal 2006 was primarily due to the recognition of a $2.0 million milestone payment during fiscal 2007, resulting from the achievement of a clinical milestone by Merck for the filing of an investigational new drug application for the second Merck product in a major market. Under Inovio's agreement with Merck, Inovio may receive additional future milestone payments linked to the successful development of a product. Inovio also recognized $175,000 in higher Wyeth license fee revenue in fiscal 2007 as compared to fiscal 2006, and acquired license agreements to Inovio's GeneSwitch® technology resulting in increased revenue of $130,000 during fiscal 2007. These increases were partially offset by no Valentis license fee revenue during fiscal 2007 as compared to $480,000 during fiscal 2006, and decreased revenue of $344,000 from the Merck licensing agreement in 2007 as this agreement was fully amortized in May 2007.

        The $892,000 increase in revenue under collaborative research and development arrangements during the year ended December 31, 2007, as compared to the 2006 fiscal year, was due to an $814,000 increase in Wyeth billings based on Inovio's collaborative agreement related to the commercialization of the Elgen device, and $78,000 in higher Merck collaborative research billings during 2007 as compared to 2006. Billings from research and development work performed pursuant to the Wyeth and Merck agreements are recorded as revenue as the related research expenditures are incurred.

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        The $1.0 million decrease in grant and miscellaneous revenue was due to minimal revenue recognized from U.S. Army grants during fiscal 2007 as compared to $899,000 during fiscal 2006 and a reduction in revenue recognized by Inovio AS from Inovio's European Union grant due to the timing of work performed.

        During the years ended December 31, 2007 and 2006, Inovio recognized revenue of $159,000 and $1.1 million, respectively, attributable to the operations of Inovio AS, a Norwegian company that Inovio acquired in January 2005, which amounted to approximately 3% and 33% of Inovio's total revenue. Inovio AS' revenue primarily consists of amounts received from grants and licensing revenue.

        Research and Development Expenses.     The $1.1 million increase in research and development expenses for the year ended December 31, 2007, as compared to fiscal 2006, was primarily due to an increase in clinical trial expenses associated with patient enrollment, clinical site costs, data collection and monitoring costs, and increased costs related to the use of clinical research organization and clinical research associates related to Inovio's SECTA therapy program. Additional increases are associated with the expansion of Inovio's in-house engineering and research expertise, increased consulting services, increased lab supplies related to Inovio's existing and next generation programs, increased outside lab testing performed, and expensed inventory costs. These increases were partially offset by a $672,000 decrease in expenses attributable to Inovio AS totaling $697,000 and $1.4 million during the years ended December 31, 2007 and 2006, respectively.

        Inovio's research and development activities reflect its efforts to advance its products through the various stages of product development. The expenditures that will be necessary to execute its development plans are subject to numerous uncertainties, which may affect Inovio's research and development expenditures and capital resources. Even if earlier results are positive, Inovio may obtain different results in later stages of development, which could impact Inovio's development expenditures for a particular product. Although Inovio spends a considerable amount of time planning its development activities, Inovio may be required to alter its plan based on new circumstances or events. Any deviation from Inovio's plan may require it to incur additional expenditures or accelerate or delay the timing of its development spending. Depending upon the progress of Inovio's programs, the merger with VGX and the availability of capital, Inovio expects its research and development expenses during the year ending December 31, 2008 to remain consistent when compared to the year ended December 31, 2007.

        General and Administrative Expenses.     General and administrative expenses include business development expenses and the amortization of intangible assets. The $2.8 million increase in general and administrative expenses for the year ended December 31, 2007, as compared to fiscal 2006, was primarily due to an increase in outside consulting services related to partnering Inovio's SECTA therapy program, an increase in investor relations services associated with expanding its DNA and gene therapy program, an increase in personnel expenses associated with expanding Inovio's in-house expertise, increased legal fees associated with intellectual property and business development efforts, and increased legal, accounting and auditing fees primarily attributable to matters related to correspondence with the SEC. In addition, Inovio recorded a reduction of goodwill in 2007 related to the realization of foreign net operating loss carryforwards. General and administrative costs attributable to Inovio AS were $84,000 for the year ended December 31, 2007 and were insignificant for the year ended December 31, 2006. Depending upon the progress of Inovio's programs and the availability of capital, Inovio expects its general and administrative expenses during the year ending December 31, 2008 to decrease slightly when compared to the year ended December 31, 2007.

        Share-Based Compensation.     Effective January 1, 2006, Inovio adopted Statement of Financial Accounting Standards ("SFAS") No. 123(R), Share-Based Payment , and elected to adopt the modified prospective application method. SFAS No. 123(R) requires Inovio to use a fair-value based method to account for stock-based compensation. Accordingly, stock-based compensation cost is measured at the

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grant date, based on the fair value of the award reduced by estimated forfeitures, and is recognized as expense over the employee's requisite service period. Total compensation cost under SFAS No. 123(R) for Inovio's equity incentive plans for the years ended December 31, 2007 and 2006 was $1.6 million and $1.3 million, of which $354,064 and $423,229 was included in research and development expenses and $1.2 million and $920,874 was included in general and administrative expenses, respectively. At December 31, 2007, there was $1.3 million of total unrecognized compensation cost, related to unvested stock options, which Inovio expects to recognize over a weighted-average period of one year, as compared to $946,844 for the year ended December 31, 2006. Total stock-based compensation for options granted to non-employees for the years ended December 31, 2007 and 2006 was $119,191 and $202,604, respectively.

        Interest and Other Income.     Inovio's management determined on February 6, 2008 that registered warrants issued by Inovio in October 2006 and August 2007 required reclassification from equity to liability in its consolidated financial statements for the year ended December 31, 2006 and the interim reporting periods in 2007. As a result of these reclassifications and from the net decrease in the fair value of common stock warrants issued, non-cash other income of $3.4 million and $135,000 was recognized for the years ended December 31, 2007 and 2006, respectively, resulting in an increase of $3.3 million during fiscal 2007. If unexercised, the warrants will expire in October 2011 and August 2012, respectively. The remaining increase in interest and other income for fiscal 2007, as compared to fiscal 2006, was primarily due to a larger cash and short-term investments balance and higher average interest rate.

        Imputed and Declared Dividends on Preferred Stock.     The former holders of Inovio's Series A and B preferred stock received an annual dividend at a rate of 6%, in shares of common stock or cash, payable quarterly through September 30, 2006. As a result, no dividends were paid to Series A or B preferred stockholders during the year ended December 31, 2007. Inovio paid cash of $345 and issued a total of 2,871 shares valued at $7,693 to the former holders of its Series A preferred stock, and paid $14,795 in cash to the former holders of its Series B preferred stock during fiscal 2006.

        The holders of Inovio's Series C preferred stock were entitled to receive an annual dividend at a rate of 6%, in shares of common stock or cash, payable quarterly, through May 20, 2007. As part of this dividend, Inovio paid cash of $23,335 during fiscal 2007 to holders of its Series C preferred stock. Inovio paid cash $117,204 during fiscal 2006 to holders of its Series C preferred stock and accrued $14,571 for certain holders of its Series C preferred stock who participated in an equity financing Inovio completed in October 2006.

        During 2006, Inovio recorded an imputed dividend charge of $1.9 million during the three months ended December 31, 2006, related to the investors who converted $1.2 million of their Series C preferred stock investment into 473,744 shares of Inovio common stock as part of Inovio's private placement closed in October 2006. This imputed dividend charge was calculated using guidance contained in Emerging Issues Task Force ("EITF") Issue No. 00-27, "Application of Issue No. 98-5 to Certain Convertible Instruments." As part of this private placement, these investors received 304,450 additional shares of Inovio common stock, as compared to the number of shares of Inovio common stock into which their existing Series C preferred stock could have been converted under the original terms of the Series C preferred stock. Under EITF Issue No. 00-27, this incremental number of shares of Inovio common stock was multiplied by the price of Inovio common stock on the commitment date of the original Series C preferred stock issuance, or $6.08 per share, to calculate the $1.9 million imputed dividend charge associated with this beneficial conversion.

        Income Taxes.     Since inception, Inovio has incurred operating losses and accordingly have not recorded a provision for income taxes for any of the periods presented. As of December 31, 2007, Inovio had net operating loss carry forwards for federal and state income tax purposes of approximately $55.9 million and $50.8 million, respectively. Inovio also had federal and state research and

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development tax credits of approximately $714,000 and $989,000, respectively. If not utilized, the net operating losses and credits will begin to expire in 2013. Utilization of net operating losses and credits are subject to a substantial annual limitation due to ownership change limitations provided by the Internal Revenue Code of 1986, as amended.

    Liquidity and Capital Resources

        Historically, Inovio's primary uses of cash have been to finance research and development activities including clinical trial activities in the oncology, DNA vaccines and other immunotherapy areas of its business. Since inception, Inovio has satisfied its cash requirements principally from proceeds from the sale of equity securities.

        As of September 30, 2008, Inovio had working capital of $3.4 million, as compared to $25.6 million as of December 31, 2007. The decrease in working capital during the nine months ended September 30, 2008 was primarily due to the reclassification of $12.1 million of auction rate security investments, or ARS, from short-term to non-current assets as Inovio believes with its current cash and anticipated proceeds from its line of credit secured by the ARS, that liquidity of these investments is not required for operational purposes for the next twelve months and the underlying term until recovery in value is anticipated beyond the next twelve months. In early March 2008, Inovio was informed that there was insufficient demand at auction for all six of its high-grade ARS. As a result, these affected securities are currently not liquid and Inovio could be required to hold them until they are redeemed by the issuer or to maturity. At September 30, 2008, Inovio has recorded an unrealized loss of $1.5 million on these investments, resulting in the $12.1 million carrying value. Because Inovio believes that the current decline in fair value is temporary, any difference between its estimate and an estimate that would be arrived at by another party would have no impact on Inovio's consolidated results of operations, since such difference would also be recorded to accumulated other comprehensive income. Inovio will re-evaluate each of these factors as market conditions change in subsequent periods.

        On August 26, 2008, Inovio received notice from UBS, its investment advisor in connection with its ARS, that Inovio's application had been approved for a $5.0 million uncommitted demand revolving line of credit secured by ARS held by Inovio, to provide additional working capital. As of September 30, 2008, Inovio has drawn down $1.8 million from the line of credit. On December 19, 2008, Inovio accepted an offer by UBS of certain rights to cause UBS to purchase the ARS at a future date. UBS offered the repurchase rights in connection with its obligations under settlement agreements with the SEC and other federal and state regulatory authorities, and as a result of accepting UBS's offer, Inovio, via its wholly-owned subsidiary Genetronics, which holds the ARS, can require UBS to repurchase at par value all of the ARS at any time during the period from June 30, 2010 through July 2, 2012, if such ARS have not previously been sold by Genetronics or by UBS on its behalf. In conjunction with the acceptance of the rights offering, Genetronics also obtained an increase in its the credit line up to $12.1 million, with the ARS pledged as collateral, which Genetronics fully drew down on December 23, 2008.

        The remaining decrease in working capital was primarily due to expenditures related to Inovio's research and development and clinical trial activities, as well as various general and administrative expenses related to consultants, legal, accounting and audit, corporate development, and investor relations activities.

        As of September 30, 2008, Inovio had an accumulated deficit of $149.2 million. Inovio has operated at a loss since 1994, and expects this to continue for some time. The amount of the accumulated deficit will continue to increase, as it will be expensive to continue clinical, research and development efforts. If these activities are successful and if Inovio receives approval from the FDA to market equipment, then even more funding will be required to market and sell the equipment. The outcome of the above matters cannot be predicted at this time. Inovio is evaluating potential

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partnerships as an additional way to fund operations. Inovio will continue to rely on outside sources of financing to meet its capital needs beyond next year.

        Inovio's long-term capital requirements will depend on numerous factors including:

    The progress and magnitude of the research and development programs, including preclinical and clinical trials;

    The time involved in obtaining regulatory approvals;

    The cost involved in filing and maintaining patent claims;

    Competitor and market conditions;

    The ability to establish and maintain collaborative arrangements;

    The ability to obtain grants to finance research and development projects;

    The costs associated with raising capital or obtaining liquidity and completing transactions, such as the pending Merger; and

    The cost of manufacturing scale-up and the cost of commercialization activities and arrangements.

        The ability to generate substantial funding to continue research and development activities, preclinical and clinical studies and clinical trials and manufacturing, scale-up, and selling, general, and administrative activities is subject to a number of risks and uncertainties and will depend on numerous factors including:

    The ability to raise funds in the future through public or private financings, collaborative arrangements, grant awards or from other sources;

    Inovio's potential to obtain equity investments, collaborative arrangements, license agreements or development or other funding programs in exchange for manufacturing, marketing, distribution or other rights to products developed by Inovio; and

    The ability to maintain existing collaborative arrangements.

        The global financial markets have recently experienced significant limits on available credit for companies of all sizes, and extreme volatility in market prices limiting the ability of companies to raise capital at favorable prices, if at all. This lack of liquidity and the consistently changing market conditions are currently impacting Inovio's ARS as discussed above, as well as creating significant fluctuations in the market price of Inovio's common stock. Inovio cannot project how long such conditions will last in the global financial markets, and Inovio cannot guarantee that additional funding—whether via incurrence of debt or equity sales—will be available when needed or on favorable terms. If it is not, Inovio will be required to scale back its research and development programs, preclinical studies and clinical trials, and selling, general, and administrative activities, or otherwise reduce or cease operations and Inovio's business and financial results and condition would be materially adversely affected.

        Committee Members.     The Compensation Committee of the board of directors (for purposes of this Compensation Discussion and Analysis, the "Committee") is currently composed of the following four board members: James L. Heppell (Chair), Simon Benito, Tazdin Esmail and Robert W. Rieder.

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No member of the Compensation Committee is a former or current officer or employee of Inovio, other than James L. Heppell, Inovio's Chairman of the Board. Inovio's board of directors and the Committee annually determine whether the Committee's current membership satisfies the rule of the NYSE Alternext. Each member of the Compensation Committee is independent under the NYSE Alternext listing standards and the definition of "independent" under the Sarbanes-Oxley Act of 2002.

        Charter and Functions of the Committee.     The functions of the Committee in 2007 included providing guidance to management and assisting the board of directors in matters relating to:

        The Committee's charter states that the Committee has the authority and responsibility to:

        The Nomination and Corporate Governance Committee reviews the adequacy of the Compensation Committee's charter at least annually. The Nomination and Corporate Governance Committee revised the Compensation Committee's charter as a result of the most recent review on March 27, 2008. The Compensation Committee's complete charter, a component of Corporate Governance Policy, is available separately on Inovio's web site at: http://media.corporate-ir.net/media_files/irol/10/105128/corpGov/Com pCommit.pdf

        The Committee Chairman is responsible for the Committee's meeting agendas and calendar.

        Compensation Consultant.     Inovio's Human Resources Department supports the Committee in fulfilling its charter. In addition, the Committee has the authority under its charter to engage the services of outside advisors, experts and others to assist the Committee. In accordance with this authority, the Committee, beginning in December 2006, engaged Setren, Smallberg & Associates, Inc. ("Larry Setren" or the "Consultant"), as an independent outside compensation consultant to advise the Committee on matters related to the chief executive officer and other executive compensation. The Committee plans to engage the Consultant every two to three years for this purpose.

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        The Consultant recommends the company or industry peer group (the "Peer Group") for purposes of comparison and benchmarking executive compensation and performs compensation analyses. The Consultant sometimes recommends specific pay level changes for executive officers. The Consultant's assignments are determined by the Committee Chair and/or management as directed by the Committee.

        Roles of Executives in Establishing Executive Compensation.     Inovio's chief executive officer, chief financial officer and human resources manager are also involved in the executive compensation process.

Avtar Dhillon, M.D., Inovio's chief executive officer:

Peter Kies, Inovio chief financial officer and human resources manager, provides:

        The Committee delegates to the chief executive officer and the chairman of the board the ability to approve long-term incentive awards to new hires and employees in the amount of 50,000 options or less, within defined parameters. The Committee has approved these parameters to provide appropriate incentives to different career bands within Inovio. Inovio has a written policy addressing the appropriate dating and pricing of the shares and options. Additionally, the Committee has authorized the chief executive officer to approve any base salary increases, bonuses, or new-hire offer packages with the exception of those for officers who are subject to the requirements of Section 16 of the Exchange Act.

        Committee Activity.     Each executive officer's compensation is comprised of up to three principal components: base salary, bonus and any equity awards, historically granted pursuant to Inovio's 2007 Omnibus Incentive Plan. Base salary and bonus are determined by the Committee and are reviewed at least annually. Inovio's management and the board of directors believe that the total compensation package of the executive officers should be linked to certain objective performance criteria of Inovio. Inovio uses stock options to align the long-range interests of its executive officers with the interests of stockholders. The amount of stock options that may be granted to each executive officer is determined by taking into consideration the officer's position with Inovio, overall individual performance, corporate performance and an estimate of the long-term value of the award considering current base salary and any cash bonus awarded. Inovio includes the use of other forms of equity-based awards including, but not limited to, grants of restricted shares of common stock.

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        Recognizing the importance of maintaining (i) sound principles for the development and administration of executive compensation and (ii) strong links between executive pay and performance, the Committee took the following steps, among others, in 2007:

        Using the annual reviews provided by management and the prior year competitive analysis provided by the Consultant, the Committee is able to review both the competitiveness and appropriateness of each element of executive compensation. The Committee considered several factors in these reviews, including:

        The Committee also considers the competitive market for executive compensation. The Committee seeks to maintain competitive compensation because Inovio believes that attracting and retaining exceptional talent is a key component in building a sustainable competitive advantage in the market. The Committee considers the need and rationale for each element of compensation and the amounts that are targeted and awarded in relation to Inovio's performance versus the performance of its Peer Group as periodically updated.

        After these reviews, the Committee believes that both the individual elements of compensation and the compensation in total for each NEO for 2007 is appropriate given Inovio's performance, Inovio's position in the competitive labor market, and his/her relative performance and importance to Inovio.

        During 2007, the Committee held four meetings, which were attended by all Committee members.

        Compensation Philosophy.     The primary underlying premise of Inovio's executive compensation philosophy is that pay should be performance-based, vary with the attainment of specific objectives, and be aligned with the interests of Inovio's stockholders. The Committee's primary objective is to employ compensation to differentiate and reward individual performance based on Inovio's overall business results, progress toward individual goals and objectives, and leadership behaviors consistent with Inovio's long-term success. The Committee employs the following core principles to guide its decisions.

        Pay competitively:     The Committee believes in positioning executive compensation at competitive levels necessary to attract and retain exceptional leadership talent. Performance can result in an individual's total compensation that is higher or lower than market position. The Consultant periodically compiles this competitor and market data at the request of, and by working with, the Committee.

        Have a total compensation perspective:     The Committee views all components of pay together in making compensation decisions. These components include base salary, bonuses, stock options and fringe benefits.

        The Committee reviews its compensation philosophy regularly, most recently in January 2008. The Committee believes Inovio's and its compensation philosophy is based on appropriate principles and

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did not make any changes to the overall philosophy. The Compensation Program Design section is indicated below.

        Benchmarking.     Inovio benchmark all elements of total direct compensation (base salary, bonus, total cash compensation, and all forms of long-term incentives) to the competitive marketplace. Working with the Consultant periodically, the Committee considered several factors to determine the companies in the Peer Group. The Committee has in its Peer Group companies that:

        The Committee also compared all elements of direct compensation using the Radford Biotechnology Survey during 2007.

        Compensation Program Design.     Inovio's compensation program consists primarily of base salary, bonuses and any equity awards, primarily stock options, granted pursuant to Inovio's 2007 Omnibus Incentive Plan. In general, Inovio's NEOs' compensation mix was determined by the Consultant in 2007 to be considerably below the midpoints of the Peer Group and the midpoints of the Radford Survey.

        Base Salary.     Base salaries are a non-variable element of total compensation. The Committee reviews officer salaries annually at the end of the year. They reflect each executive's responsibilities, the impact of the job, and the contributions each executive delivers to Inovio. Salaries are determined in part by competitive levels in the market—what companies in the Peer Group and executive compensation surveys pay executives with comparable responsibilities and job scope—and in part by internal equity considerations. Each year, the Committee reviews and establishes the base salary of Inovio's executive officers. Increases, if any, are based on individual performance, existing employment agreements and market conditions. To gauge market conditions, the Committee periodically evaluates the competitor and market data last compiled by the Consultant in 2006.

        At its November 2007 meeting, the Committee reviewed recommendations for salary adjustments for the chief executive officer and the other NEOs. The Committee reviews the performance and compensation of the chief executive officer in several meetings throughout each year, and in January 2008, the board voted to adjust the chief executive officer's base salary to $378,000 for the year ending December 31, 2008, effective February 1, 2008. Other salary adjustments approved for the year ending December 31, 2008 and effective February 1, 2008 include $222,600 for the chief financial officer, $200,000 for the Vice President, Corporate Development, $176,000 for the Vice President, Finance and Operations, and $179,644 for the Vice President, Research and Development.

        Bonus Compensation.     Bonuses are paid on a discretionary basis subsequent to the filing of Inovio's annual results. Bonus amounts for Inovio's NEOs and Executive Director level employees are determined based on prior year results, which include both financial indicators such as stockholder return, revenue growth and cost management in addition to other non-financial performance indicators such as the status of Inovio's clinical trials and new significant licensing arrangements. In January 2008, the Inovio board approved the chief executive officer's 2007 bonus amount of $116,375. Other 2007 bonus amounts approved include $26,600 for the chief financial officer, $16,625 for the Vice President, Corporate Development and $13,300 for the Vice President, Finance and Operations.

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        Equity-based Compensation.     For existing employees, equity based compensation generally consists of annual stock option incentive awards granted from the 2007 Omnibus Incentive Plan approved in March of each year. In January 2008, the board approved the chief executive officer's bonus of 75,000 shares of restricted stock and of options exercisable for 75,000 shares of common stock, exercisable at $0.87 per share. Other option awards approved, all exercisable at $0.87 per share, include 30,000 options for the chief financial officer, 20,000 options for the Vice President, Corporate Development, and 50,000 options for the Vice President, Finance and Operations.

        Employment Agreements.     Inovio utilizes employment agreements for all executive officers, generally when it is necessary to secure the services of a newly hired executive. Inovio currently have employment agreements with:

        The compensatory nature of the employment agreements are disclosed as required in the tabular and narrative disclosures below.

        Change-in-Control Agreements.     Inovio has change-in-control arrangements in place for its Chief Executive Officer and executive officers who are direct reports to the Chief Executive Officer. The rationale for these provisions is that in the event of a change in control of Inovio, these individuals are the most likely to lose their jobs as a result of redundancy in executive positions. Information regarding applicable payments under the change of control for the named executive officers is provided in each named executive officer's employment agreement.

        Severance.     As part of Inovio's executive officers employment agreements, any executive currently working for Inovio at the executive officer level whose employment is terminated involuntarily is eligible for severance benefits, provided each of their employment agreement requirements are met. The severance pay and benefits that are payable are stated in each executive's employment agreement.

        Stock Ownership/Retention Guidelines.     Inovio do not have any stock ownership and retention guidelines. Some companies use stock ownership and retention guidelines as a way to promote share ownership within the company and to compensate existing employees. The Committee believes that as long as executives are not exercising a significant amount of options or selling a significant amount of shares on a regular basis, there is no need for stock ownership and retention guidelines.

        Policy on Deductibility of Named Executive Officer Compensation.     Section 162(m) was added to the Code as part of the Omnibus Budget Reconciliation Act of 1993. Section 162(m) limits the deduction for compensation paid to the President and Chief Executive Officer and the other named executive officers to the extent that compensation of a particular executive exceeds $1,000,000, unless such compensation was based upon performance goals determined by a compensation committee consisting solely of two or more outside directors, the material terms of which are approved by a majority vote of the stockholders prior to the payment of such remuneration, or paid pursuant to a binding contract that was in effect on February 17, 1993. While the tax impact of any compensation arrangement is one

158


factor to be considered, such impact is evaluated in light of Inovio's overall compensation philosophy. Inovio intends to establish executive officer compensation programs that will maximize tax deduction if the Committee determines that such actions are consistent with its philosophy and in the best interests of Inovio and its stockholders. However, from time to time, Inovio may award compensation that is not fully deductible if it is determined that such award is consistent with its philosophy and in the best interest of Inovio and its stockholders.

        The Committee reviews the existing compensation program to determine the deductibility of the future compensation paid or awarded pursuant thereto and may seek guidance with respect to changes to the existing compensation program that will enable Inovio to continue to attract and retain key individuals while optimizing the deductibility to Inovio of amounts paid as compensation.

        The Committee believes that its overall executive compensation program has been successful in providing competitive compensation appropriate to attract and retain highly qualified executives and in encouraging increased performance from the executive group to foster the creation of added stockholder value.

        Code Section 409A.     Code Section 409A relates to accounting treatment for deferred compensation. The Committee has reviewed all of Inovio's compensation plans and programs to ensure that they are compliant with IRC Section 409A and has determined that, they are compliant, as long as the final regulations by the IRS do not change significantly from the proposed regulations.

        Impact of FAS 123R.     FAS 123R requires companies to record option grants as expenses at the time of grant. Option expense is one factor that the Committee considers in the design of Inovio's long-term compensation programs. Other factors include:

        The Committee monitors Inovio's FAS 123R expense to ensure that it is reasonable, although expense is not the most important factor in making decisions about Inovio's long-term incentive plans.

        The Compensation Committee reviewed and discussed the Compensation Discussion and Analysis required by Item 402(b) of SEC Regulation S-K with management. Based on such review and discussions, the Compensation Committee recommended to the board of directors that the Compensation Discussion and Analysis be included in Inovio's Proxy Statement on Schedule 14A filed with the SEC on April 1, 2008 and duplicated in this joint proxy statement/prospectus.

    Respectfully submitted,        

James L. Heppell (Chair)

 

Simon Benito

 

Tazdin Esmail

 

Robert W. Rieder

        The following table sets forth compensation information for 2007 and 2006 for Inovio's president and chief executive officer, the chief financial officer and human resources manager, the two other executive officers serving at December 31, 2007, one executive officer promoted subsequent to December 31, 2007, the managing director of Inovio AS (which Inovio collectively refers to as its

159


"named executive officers"), and two former executive officers whose salary and bonus exceeded $100,000.

Name and Principal Position
  Year   Salary
(1)
  Bonus
(2)
  Stock
Awards
(3)
  Option
Awards
(4)
  All Other
Compensation
  Total  
(a)
  (b)
  (c)
  (d)
  (e)
  (f)
  (g)
  (h)
 
Dr. Avtar Dhillon,     2007   $ 357,503   $ 116,375   $ 69,188   $ 391,394   $ 5,342   $ 939,802  
President and Chief Executive Officer     2006   $ 327,955   $ 150,500       $ 415,731   $ 4,260   $ 898,446  

Peter Kies, Chief

 

 

2007

 

$

206,966

 

$

26,600

 

 


 

$

128,244

 

 


 

$

361,810

 
Financial Officer and HR Manager     2006   $ 186,172   $ 40,000       $ 73,085       $ 299,257  

Dietmar Rabussay,

 

 

2007

 

$

185,391

 

 


 

 


 

$

63,927

 

$

5,200

 

$

254,518

 
Vice President, Research and Development(5)     2006   $ 175,012   $ 10,000       $ 66,103   $ 5,200   $ 256,315  

Michael Fons,

 

 

2007

 

$

188,180

 

$

16,625

 

 


 

$

81,877

 

$

3,324

 

$

290,006

 
Vice President, Corporate Development(6)     2006                          

Punit Dhillon,

 

 

2007

 

$

145,736

 

$

13,300

 

 


 

$

94,025

 

$

3,900

 

$

256,961

 
Vice President, Operations and Finance(7)     2006                          

Iacob Mathiesen,

 

 

2007

 

$

179,449

 

 


 

$

166,050

 

$

62,985

 

 


 

$

408,484

 
Managing Director, Inovio AS(8)     2006                          

Robert Goodenow,

 

 

2007

 

 


 

 


 

 


 

 


 

 


 

 


 
Vice President, Corporate Development(9)     2006   $ 186,110           $ 74,135       $ 260,245  

George McHugh,

 

 

2007

 

 


 

 


 

 


 

 


 

 


 

 


 
Vice President, Operations(10)     2006   $ 173,622   $ 29,014       $ 48,000   $ 85,500   $ 336,136  

(1)
Salary includes contributions made by the employee to Inovio's 401(k) plan.

(2)
Bonus payments for 2007 were made in February 2008.

(3)
Represents the compensation costs of stock awards, calculated for financial reporting purposes for the year utilizing the provisions of Statement of Financial Accounting Standards ("SFAS") No. 123R, rather than an amount paid to or realized by the named executive officer. See Note 8, "Stockholder's Equity," to Inovio's Audited Consolidated Financial Statements set forth in Inovio's Form 10-K for the year ended December 31, 2007 (the "10-K") for information concerning the SFAS 123R values, which are based on the fair value of Inovio's common stock on the date of grant. There can be no assurance that the SFAS 123R amounts will ever be realized. The stock award to Dr. Dhillon includes compensation expense related to a restricted stock award of 75,000 shares of which 18,750 shares vested immediately at a fair value of $3.69 per share. The total value of the award was $276,750, and the remaining value vests annually in May over the next three years. The stock award to Mr. Mathiesen includes compensation expense related to a restricted stock award of 90,000 shares of which 45,000 shares vested immediately at a fair value of $3.69 per share. The total value of the award was $332,100, and the remaining value will vest in December 2009.

(4)
Represents the compensation costs of stock options calculated for financial reporting purposes for the year utilizing the provisions of SFAS No. 123R, rather than an amount paid to or realized by the named executive officer. See Note 8, "Stockholder's Equity" to Inovio's Audited Consolidated Financial Statements set forth in Inovio's 10-K for the assumptions made in determining SFAS 123R values. Ratable amounts expensed for grants that were made in prior years are included. There can be no assurance that the SFAS 123R amounts will ever by realized by the named executive officer.

(5)
Dietmar Rabussay resigned effective May 2, 2008.

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(6)
Michael Fons was promoted from Executive Director of Corporate Development in August 2007.

(7)
Punit Dhillon was promoted from Executive Director, Finance and Operations in January 2008.

(8)
Managing Director of Inovio AS salary paid in Norwegian Kroners but translated to U.S. Dollars using the average exchange rate for 2007.

(9)
Robert Goodenow resigned effective March 16, 2007.

(10)
George McHugh resigned effective December 19, 2006. Amounts included in All Other Compensation reflect severance payments payable on a bi-weekly basis through June 2007.

        The following table sets forth certain information with respect to stock and option awards and other plan-based awards granted to Inovio named executive officers during 2007. Amounts representing Estimated Future Payouts Under Non-Equity Incentive Awards (i.e. thresholds, targets and minimums), and Estimated Future Payouts Under Equity Incentive Plan Awards (i.e. thresholds, targets and minimums) have not been reported in the following table as they are not applicable to Inovio compensation program during 2007.

Name
  Grant
Date
  All Other
Stock
Awards:
Number of
Shares of
Stock (#)(1)
  All Other
Option
Awards:
Number of
Securities
Underlying
Options (#)
  Exercise or
Base Price
of Option
Awards
($/Share)
  Grant Date
Fair Value
of Stock
and Option
Awards ($)
 
(a)
  (b)
  (c)
  (d)
  (e)
  (f)
 
Avtar Dhillon,     3/8/2007           225,000   $ 3.16   $ 550,328  
President and Chief Executive Officer     5/4/2007     75,000               $ 276,750  

Peter Kies,
Chief Financial Officer and HR Manager

 

 

3/8/2007

 

 

 

 

 

75,000

 

$

3.16

 

$

183,443

 

Michael Fons,

 

 

3/8/2007

 

 

 

 

 

20,000

 

$

3.16

 

$

48,918

 
Vice President, Corporate Development     5/3/2007           25,000   $ 3.75   $ 73,430  

Dietmar Rabussay,
Vice President, Research and Development

 

 

3/8/2007

 

 

 

 

 

25,000

 

$

3.16

 

$

61,148

 

Punit Dhillon,

 

 

3/8/2007

 

 

 

 

 

40,000

 

$

3.16

 

$

97,836

 
Vice President, Finance and Operations     5/3/2007           15,000   $ 3.75   $ 44,058  

Iacob Mathiesen,

 

 

3/8/2007

 

 

 

 

 

20,000

 

$

3.16

 

$

48,918

 
Managing Director, Inovio AS     5/3/2007           25,000   $ 3.75   $ 73,430  
      5/4/2007     90,000               $ 332,100  

(1)
The amount reflects the number of restricted stock awards granted on May 4, 2007 pursuant to the 2007 Omnibus Incentive Plan with a grant date fair value of $3.69 per share.

        There were no options exercised by Inovio named executive officers during 2007.

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        The following tables set forth certain information with respect to outstanding equity awards to the named executive officers under Inovio equity incentive plans during 2007. For additional information concerning the annual and long-term incentives included in Inovio's executive compensation plan, see " Compensation Discussion and Analysis—Components of the 2007 Executive Compensation Plan ."

 
  OPTION AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Options (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Options (#)
Unexercisable
  Option
Exercise
Price ($)
  Option
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 
Avtar Dhillon     100,000           2.08     10/09/2011  
  President and CEO     25,000           1.64     04/28/2012  
      124,999           1.96     06/27/2012  
      12,499           1.00     10/24/2012  
      62,500           1.08     01/09/2013  
      81,249           2.52     08/07/2013  
      37,499           5.00     11/06/2013  
      125,000           5.00     12/31/2013  
      112,500     37,500     3.82     01/14/2015  
      37,500     37,500     2.89     03/06/2016  
      56,250     168,750     3.16     03/07/2017  
                       
      774,996     243,750              
                       

Peter Kies

 

 

37,500

 

 

 

 

 

1.96

 

 

06/27/2012

 
  CFO and HR Manager     7,500           1.00     10/24/2012  
      12,500           1.24     03/24/2013  
      14,375           2.52     08/07/2013  
      15,000     5,000     4.46     02/24/2015  
      22,500     22,500     2.89     03/06/2016  
      18,750     56,250     3.16     03/07/2017  
                       
      128,125     83,750              
                       

Michael Fons

 

 

37,500

 

 

 

 

 

5.32

 

 

06/16/2014

 
  VP, Corporate Development     10,000     10,000     2.45     03/22/2016  
      5,000     15,000     3.16     03/08/2017  
      6,250     18,750     3.75     05/03/2017  
                       
      58,750     43,750              
                       

162


 
  OPTION AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Options (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Options (#)
Unexercisable
  Option
Exercise
Price ($)
  Option
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 

Dietmar Rabussay

 

 

5,499

 

 

 

 

 

9.00

 

 

07/08/2008

 
  VP, Research and Development     8,749           10.76     10/15/2008  
      3,750           16.52     02/06/2010  
      500           6.00     08/24/2010  
      6,250           6.28     05/16/2011  
      7,500           1.80     10/23/2011  
      7,500           1.64     04/28/2012  
      7,500           1.00     10/24/2012  
      12,500           1.24     03/24/2013  
      19,937           2.52     08/07/2013  
      7,500     2,500     4.46     02/24/2015  
      22,500     22,500     2.89     03/06/2016  
      6,250     18,750     3.16     03/07/2017  
                       
      115,935     43,750              
                       

Punit Dhillon

 

 

25,000

 

 

 

 

 

2.76

 

 

06/30/2013

 
  VP, Finance and Operations     6,250           2.52     08/07/2013  
      11,250     3,750     4.33     02/24/2015  
      17,500     17,500     2.45     03/22/2016  
      10,000     30,000     3.16     03/08/2017  
      3,750     11,250     3.75     05/03/2017  
                       
      73,750     62,500              
                       

Iacob Mathiesen

 

 

10,000

 

 

10,000

 

 

2.45

 

 

03/22/2016

 
  Managing Director, Inovio AS     5,000     15,000     3.16     03/08/2017  
      6,250     18,750     3.75     05/03/2017  
                       
      21,250     43,750              
                       

 

 
  RESTRICTED STOCK AWARDS  
Name
  Number of Unvested
Shares (#)(1)
  Fair Market
Value ($)
 
(a)
  (b)
  (c)
 

Avtar Dhillon
President & CEO

    56,250     207,563  

Iacob Mathiesen
Managing Director, Inovio AS

    45,000     166,050  
           

    101,250     373,613  
           

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    Compensation Committee Interlocks and Insider Participation

        In 2007, the Compensation Committee consisted of James L. Heppell (Chair), Simon Benito, Tazdin Esmail and Robert W. Rieder, each of whom is an independent director under the NYSE Alternext listing standards. Other than James L. Heppell, who is a former officer of Inovio, no member of the Compensation Committee is a former or current officer or employee of Inovio.

        During 2007, Avtar Dhillon, Inovio Chief Executive Officer, served as a director of BC Advantage (VCC) Funds, Inc. James L. Heppell, a member of Inovio Compensation Committee, serves as President and Fund Manager of BC Advantage (VCC) Funds, Inc.

        No other persons who were members of the Compensation Committee during 2007 had any relationships requiring disclosure.

    Compensation of Directors

        During 2007, Inovio paid each non-employee director of Inovio (other than the Chairman of the Board) an annual retainer fee of $19,000 and paid the Chairman of the Board an annual retainer fee of $35,000. Inovio pays or reimburses all reasonable expenses associated with directors' attendance at and participation in board and committee meetings and other company business to which a director attends. For 2007, Inovio also paid an additional $9,000 to the Compensation Committee chairman as compensation for services as that committee's chairman, an additional $14,000 to the Audit Committee chairman as compensation for services as that committee's chairman, and an additional $5,000 to the Nomination and Corporate Governance Committee chairman as compensation for services as that committee's chair. Inovio also pays each non-employee director $1,500 for attendance at each board meeting conducted in person and $750 for each board meeting conducted telephonically.

        Inovio does not pay director fees to its directors who are also Inovio employees. Thus, Dr. Dhillon does not receive director fees.

        Non-employee directors are eligible to receive, from time to time, grants of options to purchase shares of common stock under the Plan as determined by the full board of directors. During the year ended December 31, 2007, Inovio granted 10-year options to purchase a total of 90,000 shares of its common stock to its non-employee directors. at an exercise price of $3.75. Mssrs. Bandali, Benito, Esmail and Heppell received 15,000 shares each, and Mr. Reider received 30,000 shares. Mr. Rietiker, Mr. Gan and Mr. Chong did not serve as directors during 2007.

    Director Compensation Table

        The following table sets forth certain information with respect to director compensation during 2007. Amounts representing Stock Awards, Non-equity Incentive Plan Compensation, Changes in Pension Value and Nonqualified Deferred Compensation Earnings and All Other Compensation are not included in the following table as they are not applicable to Inovio compensation program during 2007.

Name
  Fees Earned or
Paid in Cash
($)
  Option
Awards
($)
  Total
($)
 
  (a)
  (b)
  (c)
  (d)
 

James Heppell

    53,750     43,567     97,317  

Simon Benito

    42,000     43,567     85,567  

Tazdin Esmail

    33,000     43,567     76,567  

Riaz Bandali

    27,250     43,567     70,817  

Robert Rieder

    20,250     18,912     39,162  

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        The narratives and tabular format requirements regarding Pension Benefits at December 31, 2007 and Nonqualified Deferred Compensation for 2007 have been excluded from this joint proxy statement/prospectus as they are not applicable to Inovio's compensation program during 2007.

VGX Pharmaceuticals, Inc.

    Overview

        VGX, a Delaware corporation founded in December 2000 by Dr. J. Joseph Kim and Professor David B. Weiner, is a biopharmaceutical company engaged in the discovery and development of novel vaccines and therapies for major infectious diseases and cancers. VGX has product candidates for the treatment of infectious diseases including HIV, as well as cancer and inflammatory diseases. The lead therapeutic programs in infectious diseases and oncology are well complemented by a research pipeline of next-generation DNA vaccines. VGX's proprietary position, coupled with a patented DNA delivery system (CELLECTRA® electroporation device), and access to cGMP plasmid manufacturing capabilities form VGX's DNA vaccines and therapies platform.

        VGX's clinical development programs include PENNVAX™-B, a DNA vaccine for the prevention of HIV in Phase I clinical trials; VGX-1027, a small molecule drug for inflammatory diseases in Phase I clinical trials; VGX-3100, a DNA therapeutic vaccine for cervical cancer in Phase I clinical trials; and the CELLECTRA® electroporator, a DNA delivery device in Phase I clinical trials. In addition, VGX has filed INDs for VGX-3200, a novel DNA therapy that utilizes GHRH for the treatment of cancer cachexia and anemia and for VGX-3400, a DNA preventative vaccine for avian influenza. VGX has established a vertically-integrated DNA Vaccines and Therapies Platform with extensive capabilities including SynCon™ DNA-based product candidates, the CELLECTRA® delivery device, and access to efficient cGMP plasmid manufacturing. Vertical control over key aspects of product development has enabled VGX to consistently develop multiple product candidates, from bench-to-IND filing, within one year. The product candidates and technology programs are protected by VGX's extensive global intellectual property portfolio.

        VGX's business strategy to realize value for the company and its stockholders is as follows:

        VGX has identified and licensed-in key technologies from world-class institutions for the treatment of infectious diseases, cancer, and inflammatory diseases. It has collaborated with various governmental agencies and organizations such as the National Institute of Allergy and Infectious Diseases (NIAID), HIV Vaccine Trials Network (HVTN), Adult Clinical Trials Group (ACTG), and the Defense Threat Reduction Agency (DTRA). These collaborations provide a third-party validation of VGX's technology as well as a means to subsidize the further development of its product pipeline in a non-dilutive manner. VGX has also secured license agreements with its affiliate, VGX International, a publicly traded company in Korea, in which the affiliate shares the development costs for some of its drug candidates.

        VGX is pursuing the development of a small molecule drug for inflammatory diseases, and building a DNA vaccines platform for the prevention and treatment of various infectious diseases and cancers. The DNA vaccines platform possessed by VGX dramatically shortens the time needed to take a potential drug candidate from bench to clinical trials—as little as a year in some cases. The efficacy of the platform was demonstrated with the recent IND opening of VGX's DNA vaccine for cervical cancer, VGX-3100, which was successfully shepherded from the research lab to preclinical toxicity studies, to an opening of an IND in approximately a year. VGX is currently leveraging its DNA vaccines platform to begin clinical trials for two other DNA vaccines candidates.

        VGX's technology is protected by an extensive patent portfolio that covers VGX's products, including VGX DNA-based Vaccines and Therapies such as PENNVAX™—DNA-based preventive and therapeutic vaccine for HIV, VGX-3100—DNA-based therapeutic vaccine for Cervical Cancer,

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VGX-3200—DNA-based therapy for treating for Cancer Cachexia, VGX-3400—DNA-based vaccine for treating Avian Flu, VGX-150—DNA-based therapy for treating Melanoma; Small Molecule Drugs, including VGX-1027 for the treatment of inflammatory diseases rheumatoid arthritis (RA) and type 1 diabetes (T1D); and Protein-based Drugs including VGX-100 for treating Lymphoma/Gastric Cancer. In addition, there is also patent coverage over VGX's DNA vaccine platform, which includes electroporation devices, such as CELLECTRA™ electroporators, and proprietary biomolecules, including a variety of DNA vectors and functional nucleotide elements, such as novel promoters. VGX's patent portfolio encompasses technologies that range from electroporation devices and their methods of use, proprietary polynucleotide and protein sequences, and a variety of proprietary vaccines and small molecules.

        VGX was incorporated in Delaware in December 2000 under the name Viral Genomics, Inc. In 2001, VGX changed its name to VGX Pharmaceuticals, Inc. In October 2005, VGX purchased a controlling interest in VGX International, Inc., a pharmaceutical and manufacturing company that is publicly traded on the Korean Stock Exchange.

        In February 2007, VGX acquired ADViSYS, Inc., a Houston, Texas-based company for its DNA plasmid manufacturing, electroporation delivery, and growth hormone releasing hormone (GHRH) technologies. In May 2007, VGX formed a subsidiary for the animal product applications of its GHRH technology, VGX Animal Health, and remains the majority stockholder of that company. VGX Animal Health's lead candidate, LifeTide™ SW5 received regulatory approval in Australia in January 2008 and became the world's first approved DNA therapy for food animals.

        In June 2008, VGX announced a strategic reorganization designed to focus its resources on developing content for DNA vaccines and therapeutics and its electroporation delivery device by selling its manufacturing operations to VGXI, Inc., a wholly-owned U.S. Subsidiary of VGX International. VGXI is a cGMP contract manufacturer of DNA plasmids utilizing 500 liter and 100 liter fermentors in the U.S. and has plans underway for a 3000 liter scale facility in Korea.

        VGX anticipates that over the next several years a number of key demographic and technological factors should accelerate growth in the market for vaccines and medical therapies to prevent and treat infectious diseases, aging associated conditions and cancer, particularly in VGX's product categories. These factors include the following:

    Rise in emerging infectious diseases and the threat of pandemics.   The attention received by the pandemic potential of avian influenza has mobilized cross-border agencies including governments, world health organizations and private and public corporations to develop effective vaccination and therapeutics strategies. VGX's candidate vaccines for avian influenza, chikungunya and dengue are intended to serve this need.

    Increased consumer awareness.   In areas such as cervical cancer, increased consumer awareness related to human papillomavirus (HPV) infection, the primary cause of cervical cancer, has led to renewed efforts for developing effective therapies. The current vaccines for cervical cancer prevention (Gardasil™ and Cervarix™), while being effective measures for prevention in the unexposed population, are ineffective in people infected with HPV.

    Large unmet need.   In areas such as human immunodeficiency virus (HIV) and hepatitis C virus (HCV) (prevention and therapy) there is a large unmet need with no vaccine options on the market. With the exit of several players in the recent years from the HIV vaccine development area, if successful, VGX believes it is positioned to obtain a significant market position.

    Increased regulatory activity.   The anti-inflammatory market represents a large market with several small molecule and antibody based therapeutics already available to patients. However, several of the disease-modifying anti-rheumatic drugs (DMARDS) have recently come under regulatory scrutiny resulting in changes to labeling due to the serious side effects of increased susceptibility

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      to opportunistic infections in patients receiving these drugs. An orally bio-available small-molecule therapeutic that can be effective and less immunosuppressive can emerge as a viable alternative to the market leaders.

    Potential Products, Technologies and Services

        Research and development expense to further the development of VGX's potential products and technologies were $12.4 million, $9.0 million and $3.4 million for the fiscal years ending December 31, 2007, 2006, and 2005, respectively.

        The following discussion describes VGX's products currently in development, the anticipated market for such products as well as the competitive environment in these markets. VGX is currently exploring strategic opportunities with each of these potential products and technologies, including the license or sale of such potential products and technologies.

    Proprietary Product Candidates

PENNVAX™-B

    Market Opportunity for Treatment of HIV

        Since its discovery in 1981, AIDS has killed more than 25 million people. In 2005, the total number of HIV-infected people worldwide reached an estimated 38.6 million, with 4.1 million newly infected individuals. In 2005, the disease claimed approximated 3.1 million lives. UNAIDS estimates that 60,000 individuals were newly infected with HIV across the U.S. and Western Europe in 2005, bringing the number of HIV-infected people to approximately 1.75 million. Over half of these individuals live in the U.S.

        In 2005, the HIV market accounted for 1.8% of global pharmaceutical sales and 17% of total anti-infective sales. Although this is relatively small compared to other therapeutic areas, the HIV market has enjoyed strong growth. It generated $7.4 billion of sales in 2005 and experienced a Compound Annual Growth Rate (CAGR) of 13.3% from 2001-2005, making it one of the fastest growing infectious disease markets.

        Effective vaccines have been actively pursued for over 20 years, without much success. The HIV represents one of the most confounding targets in medicine. The virus' high mutagenicity has made an effective vaccine development very challenging. Its outer envelope, swathed in sugar molecules, is difficult to attack, and HIV strikes the very cells that the immune system launches to thwart such an infection. Although several drugs (antiretrovirals) are available to treat the patients once they are infected, vaccines are necessary to stop the spread of disease and perhaps reduce the need for antiretroviral treatment.

        Traditional vaccines that work by exposing people to a weakened or killed microbe or proteins have failed in human testing. Noting that many long-term survivors have high counts of killer CD8+ T cells, the HIV vaccines field has turned to stimulating the immune system to generate those cells. A recent failure of HIV vaccines, which adopted the use of adenovirus or a common human cold virus that had been altered to prevent viral replication, to deliver HIV proteins as vaccines, was not effective and that a different approach is needed to develop a more effective vaccine for HIV.

    Clinical Trial Status

        VGX has initiated two separate Phase I clinical trials in 2007; one for prophylactic vaccination and the other for therapeutic vaccination for HIV. Both trials are conducted in clinical centers in the U.S. in collaboration with the University of Pennsylvania and the HIV Vaccines Trials Network (HVTN),

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which is the largest HIV vaccine testing organization in the world and funded by the U.S. National Institutes of Health (NIH).

    Competitive Landscape

        After many years of rapid development and introduction of new anti-retroviral drugs for treatment of HIV infection, the introduction of new drugs to the market for treatment of HIV infection appears to be waning. Available drugs, despite several limitations, have set a high standard that must be met in terms of efficacy. However, there is still a significant need for better HIV therapies and patents are beginning to expire on early HIV drugs. For example, zidovudine is already available as a generic drug, and other early HIV drugs will soon face such generic competition. To maintain HIV-related revenues, as well as meet the needs of HIV-infected patients, pharmaceutical companies must develop new drugs with improved profiles, especially in terms of toxicity and increased barriers to development of viral resistance. As a result, the medical and commercial needs are fueling continued interest in the development of new Nucleosides (NRTIs), Non-NRTIs, and protease inhibitors (PI) for treatment of HIV infection.

    Commercialization Plan

        Because HIV vaccine development is a high risk, and expensive proposition, the current model for development is through the formation of large networks of public and private partners. A number of government and global non-profit organizations have taken a leadership position (IAVI, Gates Foundation, NIAID/DAIDS, USMHRP and others) to support this public health crisis because private investors are reluctant to invest in these ventures. VGX plans to develop its portfolio of HIV vaccine candidates through such partnerships.

        The VGX HIV franchise consists of candidate vaccines for HIV prevention as well as therapy. Furthermore, the vaccines are differentiated according to the targeted region of the world with the greatest prevalence of a certain subtype of HIV. Thus, PENNVAX™-B is VGX's vaccine for U.S. and North America and PENNVAX™-G is its candidate product for the rest of the world. PENNVAX™-B is designed to target HIV Clade B (most commonly found in the U.S., North America, Australia and the European Union, or the EU. PENNVAX™-G is designed to target HIV Clades A, C and D most commonly found in Asia, Africa, Russia and South America.

        In 2007, VGX, The University of Pennsylvania and the HVTN agreed to collaborate on the development of PENNVAX™-B. A Phase I clinical trial for the DNA vaccine has been initiated and the first human clinical data is expected to be available in the first quarter of 2009. The consortium is presently conducting pre-clinical IND-enabling toxicology and animal safety studies for the vaccine to be delivered via electroporation using the CELLECTRA® delivery device. These studies are expected to be completed by the fourth quarter of 2008 and, if successful, will lead to the initiation of Phase I studies in the third quarter of 2009.

        A second IND is now open covering the use of PENNVAX™-B in a therapeutic setting. This study is being conducted in collaboration with the University of Pennsylvania and will target HIV positive individuals. If the Phase I studies are successful in demonstrating enhanced immunological responses to the HIV antigens, then VGX will partner with the HVTN or another governmental organization to further develop the HIV candidate vaccines through the Phase II and Phase III clinical studies. It is anticipated that given the critical need for preventive and therapeutic vaccines for HIV, the ultimate commercialization will be through a big pharma partner, for the North American and EU markets, and a world health agency for the developing world markets.

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    Therapeutic HPV-16, 18 plasmid vaccine-VGX-3100

    Market Opportunity for Treatment of Cervical Cancer

        Worldwide it is estimated that there are 473,000 cases of cervical cancer, and 253,500 deaths per year. In 2008 an estimated 3,870 women in the US will die of cervical cancer, and around 11,000 new cases are expected to be diagnosed. Cervical cancer is caused by various types of human papillomavirus (HPV). Many people who may have HPV may not show any signs or symptoms, and, therefore, they can pass the virus to others without even knowing it. Prophylactic vaccines aimed at inducing natural immunity against HPV infection in naive individuals have been approved and are effective against HPV infection, but once a person has an established infection, the vaccines are ineffective for preventing development of cervical cancer. The need for an effective therapeutic vaccine which could treat HPV infected cervical tumor cells is great, replacing surgical procedures in young women that can affect their reproductive potential. It is estimated that approximately $1.7 billion are spent in the United States each year on treatment of cervical cancer.

    Clinical Trial Status

        An IND for VGX-3100 is open. Phase I studies will examine three dose levels of the vaccine. Phase II-III studies will examine the effect of the vaccine in curing patients of intraepithelial cervical neoplasias caused by HPV.

    Competitive Landscape

        Although prophylactic vaccines for HPV, including Merck's Gardasil® and GSK's Cervarix™, have been recently approved, no therapeutic vaccine for HPV is available. Furthermore, studies suggest that these approved prophylactic vaccines do not have any therapeutic effects in women who are already infected with HPV. A number of companies are developing therapeutic vaccines for cervical cancer targeting the different subtypes of HPV. Transgene (Strasbourg, France) is likely the most advanced. Their product TG4001, based on MVA-HPV-IL2 is in Phase II studies in partnership with Roche in a deal valued at over 190 million Euros with upfront and near term milestone payments over 23 million Euros. The transgene product only targets HPV16. The VGX product is designed to treat cervical cancers arising from both HPV 16 and HPV 18. Together these two sub-types account for over 70% of the global cases of cervical cancer. MGI Pharma (ZYC 101a) and Stressgen Biopharmaceuticals Corp (HspE7) are two other companies with candidate vaccines in Phase II. Another company, Advaxis, has a HPV16 targeted candidate vaccine in Phase I studies based on a listeria vector.

    Commercialization Plan

        VGX-3100 has been manufactured under cGMP by VGXI, Inc. and has been formulated for the Phase I clinical trials. VGX anticipates partnering with a large vaccine company at the Phase II stage for further development and commercialization.

    Human Growth Hormone Releasing Hormone (GHRH) -VGX-3200

    Market Opportunity for Treatment of Cancer Cachexia

        Cachexia, an illness affecting up to 5 million people in the U.S. alone, and its associated disorders are common complications of cancer, aging, acquired immunodeficiency syndrome (AIDS), chronic obstructive pulmonary disease (from smoking), chronic kidney and heart failure. Cachexia is one of the most devastating symptoms of cancer and typically results in drastic (greater than 10% of total body weight) weight loss. This complication, which is suffered by up to 75% of cancer patients, can often be fatal before death due to the actual disease. GHRH has been shown in animal models and in dog

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cancer studies to decrease muscle wasting, correct anemia and dramatically improve the quality of life of treated patients.

        GHRH protein administered by daily injection has shown benefit in AIDS patients with metabolic disorders (lipodystrophy) associated with treatment with antiretrovirals and infection with HIV. Phase III studies with this compound are ongoing but the local reactions and the need for daily injections will limit the use of this product.

    Clinical Trial Status

        Phase I trials are planned in patients with cancer cachexia and in AIDS patients with ipodystrophy.

    Competitive Landscape

        Currently, only a progesterone analogue (Megace® ES) is licensed for treatment for cachexia. The package insert claims include modest weight gain (64% gaining five or more pounds over 12 weeks) and increased appetite. There was no effect on anemia.

    Commercialization Plan

        Treatment for cachexia, anemia and HIV related lipodystrophy are the first targets for VGX-3200. Additionally, VGX is developing the GHRH technology for a number of other indications including age-related disorders.

    Avian Influenza (H5N1) Plasmid Vaccine -VGX-3400

    Market Opportunity for Treatment of Avian Influenza

        Influenza is one of the most communicable diseases and it typically affects children and the elderly the hardest. Complications from influenza cause more than 200,000 hospitalizations and lead to approximately 36,000 deaths each year in the U.S. alone, according to the Centers for Disease Control. Worldwide, every year is typically subject to two influenza sessions (one per hemisphere), between three and five million cases of severe illness, and up to 500,000 deaths. A pandemic occurs every ten to twenty years, which infects a large proportion of the world's population, and can kill tens of millions of people as the "Spanish Flu" did in just two years (50-100 million deaths during 1918-1919).

        New influenza viruses are constantly produced by mutation or by reassortment, and can develop resistance to the standard antiviral drugs. 245 humans have died from the H5N1 strain in twelve countries according to WHO data as of September 2008. It has been spreading from Asia despite thoughts that it was under control immediately after outbreaks there in 2004. In 2005, there were reports of H5N1 in wild birds in Europe. In 2006, there were reports of avian influenza A H5N1 strain in wild birds and poultry in Africa and the Near East. Through 2006, over 140 million birds have been killed and over $10 billion have been spent to try to contain H5N1 avian influenza.

    Clinical Trial Status

        In pre-clinical studies, vaccination with VGX-3400 generated protective levels of hemagglutination inhibition (HAI) titers in 100% of the immunized animals in five separate animal models—mice, ferrets, rabbits, pigs and rhesus monkeys. Vaccination with VGX-3400 also protected 100% of the animals from an unmatched, pathogenic H5N1 virus challenge in mouse and ferret models. VGX-3400 also induced significant levels of antigen-specific CD8+ killer T cell responses. The planned Phase I trial will evaluate three levels of the vaccine for safety and immunogenicity. One dose will be chosen for expanded safety and immunogenicity (Phase II/III) studies. No efficacy studies are required for licensure of this vaccine.

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    Competitive Landscape

        Although a number of companies have well developed avian influenza programs and the lead vaccine candidates have entered into national stockpiles (U.S, and EU), there exists a need for new antigen-sparing, rapidly adaptable and easily scalable technologies to prepare for the as yet unknown target presented by the next form of avian influenza. VGX's SynCon™ platform provides protection from known avian influenza viruses (in animal studies) and has the ability to be tailored to target new and emergent ones.

    Commercialization Plan

        VGX-3400 has been manufactured under cGMP by VGXI, Inc. and has been formulated for Phase I clinical trials.

CELLECTRA® delivery device

    Market Opportunity for DNA plasmid Delivery Devices

        DNA vaccines can be developed quickly and inexpensively. In addition, they provide one of the best ways to induce cellular immune response. Unlike other delivery methods, electroporation has been shown to enhance potential immune response. This augmentation improves development and expedites clinical trials, providing additional cost effectiveness.

    Clinical Trial Status

        VGX has developed two applications in the CELLECTRA® device family. The first covers the intra-muscular (IM) delivery of DNA and the second covers the intra-dermal/subcutaneous delivery (ID) of DNA. Both devices have been validated, manufactured under cGMP and are ready for use in human clinical trials. VGX has filed a device master file (MAF) with the FDA covering the use of the CELLECTRA®-IM EP device in human clinical trials. The device is intended to be used in combination with a DNA plasmid product. VGX has finished all testing and documentation phases and is preparing to file a device master file with the FDA covering the use of the CELLECTRA®-ID EP device.

    Competitive Landscape

        Besides Inovio, Ichor and Cytopulse are other companies with an electroporation device presently in human clinical trials. Other players developing electroporation based devices include FIT Biotech, IGEA and Bio-Rad. In contrast to these devices and techniques, the technology incorporated in the CELLECTRA® device family is unique, being based on constant current and software driven pulses that are automatically adapted for each individual patient, versatile and applicable to both DNA vaccines and therapeutics delivered either IM or ID.

    Commercialization Plan

        VGX's innovative DNA delivery technology allows efficient delivery of DNA plasmids to cover a broad range of applications including gene therapy and vaccines. VGX intends to develop the CELLECTRA® device in combination with its own internally developed products as well as through partnering with external partners via appropriate licensing arrangements. It is anticipated that the device will be used in combination with VGX-3100, VGX-3200, VGX-3400 and the family of PENNVAX™ vaccines. VGX is also in early stage licensing discussions with other biotechnology companies for the use of the device in combination with their proprietary vaccine candidates. VGX has in place supported research agreements and CRADAs with academic institutions and research organizations. Commercial terms have not been discussed with these entities.

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    VGX-1027

    Market Opportunity for Treatment of Rheumatoid Arthritis and Type 1 Diabetes

        In the U.S. alone, 1.3 million people suffer from rheumatoid arthritis (RA) according to the National Institute of Arthritis and Musculoskeletal Skin Diseases (NIAMS). Overall, the prevalence in North America and the European Union is expected to increase until at least 2010, due to the aging population. With significant unmet clinical need and the progressive introduction of higher value and effective biopharmaceuticals, the rheumatoid arthritis market is expected to more than double in value to $27 billion by 2015.

        As of 2007, 23.6 million Americans—7.8 percent of the population—have diabetes, of which an estimated 5.7 million people are undiagnosed. Type 1 Diabetes (T1D), which can be fatal if untreated, usually strikes children and young adults, although it can strike at any age. In adults, T1D accounts for 5 to 10 percent (0.9 million -1.8 million people) of all diagnosed cases of diabetes in the U.S. alone. Risk factors for T1D may be autoimmune, genetic, or environmental. No known way to prevent type 1 diabetes exists.

    Clinical Trial Status

        Phase I studies are underway and indicate that the compound is orally bioavailable and well tolerated to date. After completion of Phase I studies, Phase II/III studies will be conducted in patients with RA to evaluate its effects on pain relief and joint destruction.

        Clinical studies of VGX-1027 in patients with T1D are planned after completion of the ongoing Phase I studies for RA. Under the terms of the license agreement between VGX and VGXI, VGXI was granted worldwide rights to VGX-1027 for T1D. As such, VGXI will lead the Phase II and Phase III clinical trial efforts for T1D. VGX, in return, will receive various milestone payments and a royalty payment based on percentage of net sales.

    Competitive Landscape

        Treatments for RA include primarily non-steroidal anti-inflammatory drugs (NSAID) for pain and inflammation relief, and disease-modifying anti-rheumatic drugs (DMARDs) for slowing RA's progress. A trend toward the use of DMARDs earlier in the disease demonstrates a reduction in RA's severity, so physicians are prescribing them more often. Advances in biologic DMARDs, which are more effective and targeting, but also more expensive. Studies indicate that as disease severity increases, patients take multiple drugs, though this has also been linked with compliance issues, especially with the elderly. Blockbuster therapeutic agents on the market include Enbrel® (Global Sales of $4.4 Billion in 2006, by Amgen), Remicade® ($3.6 Billion, Johnson & Johnson), and Humira® ($1.9 Billion, Abbott). However, all of these agents require IV or IM delivery. VGX-1027 offers a distinct advantage over such products because it can be taken as a once or twice-a-day pill.

        There are very few treatment options available currently for T1D patients other than daily insulin injections. Therefore, there is an unmet demand for a once-a-day, bioavailable small-molecule drug that can be administered orally.

    Commercialization Plan

        VGX has completed manufacturing of clinical supplies under cGMP to support the Phase I studies. The Phase I-SAD studies have been completed and VGX has demonstrated oral bioavailability and a satisfactory safety profile in the human studies to-date. VGX intends to develop VGX-1027 through the Phase I (SAD and MAD) and Phase IIa studies prior to licensing to a relevant pharma partner. Small molecule therapeutics for inflammatory diseases continues to be an active area of interest from a licensing point of view with several recently announced deals.

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    LifeTide™ SW5

    Market Opportunity for Growth Hormone Release Hormone in Food Animals

        LifeTide™ SW5 was shown to decrease perinatal morbidity and mortality in offspring of pigs housed in farm conditions, and in large licensing studies shown to exert its effects for at least three consecutive pregnancies of the treated female pig. Other similar GHRH-expressing plasmids have been used in dairy cows, beef, horses and young pigs. Animals in normal or heat stress conditions showed decreased morbidity, and optimized production parameters—milk production and fertility are positively impacted, while laminitis or hoof problems are resolved

    Clinical Trial Status

        LifeTide™ SW5 was approved for use in pigs by the Australian Pesticides and Veterinary Medicines Authority (APVMA) on January 5, 2008. Optimizations made to the LifeTide™ SW5 plasmid meant to reduce the plasmid dose (from 5 mg to 1 mg) are currently tested. Preliminary data from these studies show similar outcome in groups treated with LifeTide™ SW5 or the newer construct. At the end of these trials, data will be submitted for review to APVMA and used for future applications for approval.

    Competitive Landscape

        VGX does not believe there are any other comparable products in the food animal market for the moment. The recombinant growth hormone protein preparations from Monsanto are currently the closest competitor—Posilac indicated to increase milk production in dairy cows (used in approximately 30% of all dairy in the US), and porcine somatotropin used in the finishing phase in pigs in Australia. These products have the disadvantage of requiring frequent administrations (once every 14 days in dairy cows; every day for the last two weeks before slaughter in pigs) and often resulting in adverse effects in treated animals.

    Commercialization Plan

        On September 10, 2008, VGX Animal Health, Inc., or VGXAH, a majority-owned subsidiary of VGX, signed a Marketing & Distribution Agreement with Country Vet Wholesaling Pty Ltd, an Australian proprietary company, for the sale of LifeTide™ SW5. In addition, VGXAH has submitted an application for approval in New Zealand, and plans to seek approval in several other countries in South East Asia including The Philippines and Indonesia. VGX has also initiated studies to support regulatory approval of this technology in other major markets, including the U.S. and China.

    Management's Discussion and Analysis of Financial Condition and Results of Operations

         The following discussion and analysis of VGX's financial condition and results of operations should be read in conjunction with VGX's Unaudited Consolidated Financial Statements and Notes thereto and Consolidated Financial Statements and Notes thereto included elsewhere in this joint proxy statement/prospectus. This discussion and analysis contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements with regards to VGX's revenue, spending, cash flow, products, actions, plans, strategies and objectives. Forward-looking statements include, without limitation, any statement that may predict, forecast, indicate or simply state future results, performance or achievements, and may contain the words "believe," "anticipate," "expect," "estimate," "intend," "plan," "project," "will be," "will continue," "will result," "could," "should," "would," "may," "might," or any variations of such words with similar meanings. Any such statements are subject to risks and uncertainties that could cause our actual results to differ materially from those which are VGX's management's current expectations or forecasts. Such information is subject to the risk that such expectations or forecasts, or the assumptions underlying such expectations or forecasts, become inaccurate.

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Such risks and uncertainties are further discussed in this joint proxy statement/prospectus under "Risk Factors" beginning on page 28.

    Critical Accounting Policies

        The SEC defines critical accounting policies as those that are, in management's view, important to the portrayal of VGX's financial condition and results of operations and require management's judgment. VGX's discussion and analysis of its financial condition and results of operations is based on its unaudited consolidated financial statements, which have been prepared in accordance with U.S. GAAP. The preparation of these consolidated financial statements requires VGX to make estimates and judgments that affect the reported amounts of assets, liabilities, revenue and expenses. VGX bases its estimates on experience and on various assumptions that VGX believes are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from those estimates. VGX's critical accounting policies include:

        Revenue Recognition.     Revenue is recognized in accordance with SAB No. 104, Revenue Recognition in Financial Statements and EITF Issue 00-21, Revenue Arrangements with Multiple Deliverables. VGX has been awarded a contract from the government as well as grants from certain third-party organizations to help fund research for the technologies and drugs that VGX is attempting to bring to full commercial use. Once research and development expenditures qualifying under the grant are incurred, grant reports are periodically completed and submitted to the granting agency for review. If approved, the granting agency will then remit payment to VGX. Such amounts are recorded as revenue upon receipt.

        License fees are comprised of initial fees and milestone payments derived from collaborative licensing arrangements. VGX recognizes non-refundable milestone payments upon the achievement of specified milestones upon which VGX has earned the milestone payment, provided the milestone payment is substantive in nature and the achievement of the milestone was not reasonably assured at the inception of the agreement. VGX defers payments for milestone events which are reasonably assured and recognize them ratably over the minimum remaining period of its performance obligations. Payments for milestones which are not reasonably assured are treated as the culmination of a separate earnings process and are recognized as revenue when the milestones are achieved.

        With regards to revenue recognition related to product sales, VGX recognizes revenue in accordance with SAB No. 104 and records revenue when it has satisfied all the requirements under SAB No. 104.

        Research and Development Expenses.     Since VGX's inception, virtually all of its activities have consisted of research and development efforts related to developing its DNA vaccines and electroporation technologies. VGX expenses all such expenditures in the period incurred. VGX's expenses related to clinical trials are based on services received and efforts expended pursuant to contracts with multiple research institutions and clinical research organizations that conduct and manage clinical trials on its behalf. The financial terms of these agreements are subject to negotiation and vary from contract to contract and may result in uneven payment flows. Generally, these agreements set forth the scope of work to be performed at a fixed fee or unit price. Payments under the contracts depend on factors such as the successful enrollment of patients or the completion of clinical trial milestones. Expenses related to clinical trials generally are accrued based on contracted amounts applied to the level of patient enrollment and activity according to the protocol. If timelines or contracts are modified based upon changes in the clinical trial protocol or scope of work to be performed, VGX modifies its estimates accordingly on a prospective basis.

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        Valuation of Goodwill and Intangible Assets.     VGX's business acquisitions typically result in goodwill and other intangible assets, and the recorded values of those assets may become impaired in the future. Acquired intangible assets are still being developed for the future economic viability contemplated at the time of acquisition. VGX is concurrently conducting Phase I and pre-clinical trials using the acquired intangibles, and VGX has entered into certain significant licensing agreements for use of these acquired intangibles.

        As of September 30, 2008, VGX's goodwill and intangible assets resulting from acquisition costs of ADViSYS, Inc., net of accumulated amortization, totaled $4.1 million. The determination of the value of such intangible assets requires management to make estimates and assumptions that affect VGX's consolidated financial statements. VGX assesses potential impairments to intangible assets when there is evidence that events or changes in circumstances indicate that the carrying amount of an asset may not be recovered. VGX's judgments regarding the existence of impairment indicators and future cash flows related to intangible assets are based on operational performance of VGX's acquired businesses, market conditions and other factors. If impairment is indicated, VGX reduces the carrying value of the intangible asset to fair value. As of September 30, 2008, VGX has recognized impairment costs associated with the customer lists and a portion of the assembled workforce acquired from ADViSYS, Inc. when the manufacturing operations based in The Woodlands, TX were sold to a related party.

        Although there are inherent uncertainties in this assessment process, the estimates and assumptions VGX uses are consistent with VGX's internal planning. If these estimates or their related assumptions change in the future, VGX may be required to record an impairment charge on all or a portion of VGX's goodwill and intangible assets. Furthermore, VGX cannot predict the occurrence of future impairment-triggering events nor the impact such events might have on VGX's reported asset values. Future events could cause VGX to conclude that impairment indicators exist and that goodwill or other intangible assets associated with VGX's acquired businesses are impaired. Any resulting impairment loss could have an adverse impact on VGX's consolidated results of operations.

        VGX expenses patent and related legal costs as well as trademark and license costs as they are incurred.

        Stock-Based Compensation.     Stock-based compensation cost is estimated at the grant date based on the fair-value of the award and is recognized as an expense ratably over the requisite service period of the award. Determining the appropriate fair-value model and calculating the fair value of stock-based awards at the grant date requires considerable judgment, including estimating stock price volatility, expected option life and forfeiture rates. VGX develops its estimates based on historical data. If factors change and VGX employs different assumptions in future periods, the compensation expense that is to be recorded may differ significantly from what has been recorded in the current period. A small change in the estimates used may have a relatively large change in the estimated valuation. VGX uses the Black-Scholes pricing model to value stock option awards. VGX recognizes compensation expense using the straight-line amortization method.

    Recent Accounting Pronouncements

        In May 2008, the Financial Accounting Standards Board ("FASB") issued SFAS No. 162, The Hierarchy of Generally Accepted Accounting Principles ("SFAS No. 162"). SFAS No. 162 identifies the sources of accounting principles and the framework for selecting the principles to be used in the preparation of financial statements that are presented in conformity with U.S. GAAP. VGX is currently evaluating the impact that SFAS No. 162 will have on its consolidated financial statements.

        Effective January 1, 2008, VGX has adopted the provisions of Financial Accounting Standards Board Statement No. 157, Fair Value Measurements ("SFAS No. 157") to measure assets and liabilities. SFAS No. 157 establishes a common definition for fair value to be applied to U.S. GAAP requiring use

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of fair value, establishes a framework for measuring fair value, and expands disclosure about such fair value measurements. SFAS No. 157 is effective for financial assets and financial liabilities for fiscal years beginning after November 15, 2007. Issued in February 2008, FSP 157-1, Application of FASB Statement No. 157 to FASB Statement No. 13 and Other Accounting Pronouncements That Address Fair Value Measurements for Purposes of Lease Classification or Measurement under Statement 13 , removed leasing transactions accounted for under Statement 13 and related guidance from the scope of SFAS No. 157. FSP 157-2 Partial Deferral of the Effective Date of Statement 157 (FSP 157-2), deferred the effective date of SFAS No. 157 for all nonfinancial assets and nonfinancial liabilities to fiscal years beginning after November 15, 2008. The partial implementation of SFAS No. 157 for financial assets and financial liabilities, effective January 1, 2008, did not have a material impact on VGX's consolidated financial statements. VGX is currently assessing the impact of SFAS No. 157 for non-financial assets and non-financial liabilities on its consolidated financial statements.

        VGX management anticipates, based on the composition of its existing assets and liabilities, which the valuations used to estimate the fair value will rely on observable and unobservable inputs. Observable inputs are those that reflect a public market, whereas unobservable inputs are those that reflect management's assumptions about the assumptions market participants would use in pricing the underlying asset or liability. VGX management does not believe that SFAS No. 157 will have a material impact on the amounts reported in the financial statements; however, additional disclosures about the inputs used to develop the measurements of fair value and the effects of certain measurements reported in the consolidated statements of operations for a fiscal period will be required.

        Effective January 1, 2008, VGX adopted Financial Accounting Standards Board Statement No. 159, The Fair Value Option for Financial Assets and Financial Liabilities ("SFAS No. 159"). SFAS No. 159 provides companies with an option to report selected financial assets and liabilities at fair value. The Statement also establishes presentation and disclosure requirements designed to facilitate comparisons between companies that choose different measurement attributes for similar types of assets and liabilities. SFAS No. 159 requires companies to provide additional information that will help investors and other users of financial statements to more easily understand the effect of a company's choice to use fair value on its earnings. Adoption of SFAS No. 159 did not have an impact on VGX's consolidated results of operations and financial position.

        In December 2007, the Financial Accounting Standards Board issued Statement No. 141 (revised 2007), Business Combinations ("SFAS No. 141(R)"), which is effective for financial statements issued for fiscal years beginning on or after December 15, 2008. SFAS No. 141(R) establishes principles and requirements for how an acquirer recognizes and measures in its financial statements the identifiable assets acquired, the liabilities assumed, any non-controlling interest in the acquiree, and the goodwill acquired in the business combination. SFAS No. 141(R) also establishes disclosure requirements to enable the evaluation of the nature and financial effects of the business combination. FAS 141(R) will be applied prospectively. VGX expects the adoption of SFAS 141(R) to not have a material impact on the consolidated financial statements.

        In December 2007, the FASB issued SFAS No. 160, Non-controlling Interests in Consolidated Financial Statements (an amendment of Accounting Research Bulletin No. 51) ("SFAS No. 160"). SFAS No. 160 requires that non-controlling (minority) interests be reported as a component of equity, that net income attributable to the parent and to the non-controlling interest be separately identified in the income statement, that changes in a parent's ownership interest while the parent retains its controlling interest be accounted for as equity transactions, and that any retained non-controlling equity investment upon the deconsolidation of a subsidiary be initially measured at fair value. This statement is effective for fiscal years beginning after December 31, 2008, and shall be applied prospectively. However, the presentation and disclosure requirements of SFAS No. 160 are required to be applied retrospectively for all periods presented. The retrospective presentation and disclosure requirements of this statement will be applied to any prior periods presented in financial statements for the fiscal year

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ending December 31, 2009, and later periods during which VGX had a consolidated subsidiary with a non-controlling interest. As of September 30, 2008, VGX does not have any consolidated subsidiaries in which there is a non-controlling interest.

        In November 2007, the FASB ratified EITF Issue No. 07-1, Accounting for Collaborative Agreements Related to the Development and Commercialization of Intellectual Property. EITF Issue No. 07-1 defines collaborative agreements as a contractual arrangement in which the parties are active participants to the arrangement and are exposed to the significant risks and rewards that are dependent on the ultimate commercial success of the endeavor. Additionally, it requires that revenue generated and costs incurred on sales to third parties as it relates to a collaborative agreement be recognized as gross or net based on EITF Issue No. 99-19, Reporting Revenue Gross as a Principal versus Net as an Agent . It also requires payments between participants to be accounted for in accordance with already existing generally accepted accounting principles, unless none exist, in which case a reasonable, rational, consistent method should be used. EITF Issue No. 07-1 is effective for fiscal years beginning after December 15, 2008 for all collaborative arrangements existing as of that date, with retrospective application to all periods. VGX management is currently evaluating the impact of this standard and does not anticipate the adoption of EITF Issue No. 07-1 to have a material impact on VGX's consolidated financial statements.

        In July 2006, the FASB issued Interpretation No. 48, "Accounting for Uncertainty in Income Taxes" ("FIN 48"). FIN 48 prescribes detailed guidance for the financial statement recognition, measurement and disclosure of uncertain tax positions recognized in an enterprise's financial statements in accordance with FASB Statement No. 109, "Accounting for Income Taxes" ("SFAS No. 109"). Tax positions must meet a more-likely-than-not recognition threshold at the effective date to be recognized upon the adoption of FIN 48 and in subsequent periods. FIN 48 will be applied to all tax positions accounted for under SFAS No. 109 upon initial adoption.

        VGX adopted FIN 48 effective January 1, 2008 with no impact on its consolidated financial statements. VGX recognizes interest and penalties, if any, related to uncertain tax positions in income tax expense. Upon adoption of FIN 48, VGX had no interest or penalties accrued related to uncertain tax positions, due to the net operating loss carryforwards that VGX has available.

    Results of Operations for the Nine Months Ended September 30, 2008 Compared to the Nine Months Ended September 30, 2007

        Revenue.     VGX had total revenue from continuing operations of $2,216,000 and $695,000 for the nine months ended September 30, 2008 and 2007, respectively, and $4,069,000 for the period from December 12, 2000 (inception) through September 30, 2008. Revenue primarily consists of product sales of Animal Health's Lifetide™ SW5 product in Australia, government contract and grant revenue, R&D license and cost sharing fees, and other sources including rental of VGX's electroporation devices, sales of associated arrays, and sales of animals used in research activities.

        For the nine months ended September 30, 2008 and the period from December 12, 2000 (inception) to September 30, 2008, revenue from sales of Animal Health's Lifetide™ SW5 product in Australia totaled $40,000. Since marketing approval for this product was received in January 2008, there were no sales recorded in 2007.

        Revenue from the contract with the Defense Threat Reduction Agency (DTRA) to develop VGX's constant current electroporation technology for intradermal (ID) delivery of DNA vaccines and therapeutics was $1,962,000 for the nine months ended September 30, 2008 as well as for the period from December 12, 2000 (inception) to September 30, 2008. No revenue from this contract was recognized in 2007, even though work was started when the contract was awarded in August. Vouchers were not approved for reimbursement until the DCAA audit was completed and VGX was established as an approved vendor.

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        From May 2003 to April 2008, VGX was granted a sub-award, in conjunction with the University of Pennsylvania, to conduct research activities on a smallpox vaccine for approximately $80,000 per annum. During the nine months ended September 30, 2008 and 2007, revenue from this grant of $86,000 and $43,000, respectively, was recorded. As noted this sub-award for the development of smallpox vaccines ended on April 30, 2008; it is not expected to be renewed. The remaining $626,000 in grant revenues recognized in the nine months ended September 30, 2007 consisted of an NIH grant for the Preclinical Test of Biodefense Drug for SEB Toxin Exposure. The reduction in this revenue is indicative of the terms of the award, with the majority of activities being conducted in previous years. For the period from December 12, 2000 (inception) to September 30, 2008, revenue from government grants totaled $1,828,000.

        For the nine months ended September 30, 2008, VGX recognized $100,000 of license fee revenue which represents a cost sharing fee to partially cover the costs of patents, product enhancement and other associated R&D efforts related to VGX's CELLECTRATM Device in Korea. This license agreement was executed in April of 2008; thus no revenue was recognized in 2007. Revenue from all license fees received by VGX from December 12, 2000 (inception) to September 30, 2008 totaled $175,000.

        Other operating revenue for the nine months ended September 30, 2008 reflects $24,000 in revenue from the sale of research animals no longer needed for studies, and $4,000 from sales of electroporation arrays. Other operating revenue for the nine months ended September 30, 2007 was $26,000, which represents rental of electroporation devices, sales of associated arrays and research consulting fees. For the period from December 12, 2000 (inception) to September 30, 2008, other operating revenue totaled $64,000.

        Cost of Product Sales Expenses.     Cost of product sales from continuing operations for the nine months ended September 30, 2008 as well as for the period from December 12,2000 (inception) to September 30, 2008, reflect expenses associated with the first shipment of Animal Health's Lifetide™ SW5 product for sale in Australia, totaling $112,000. Collaborative efforts between manufacturing and research are currently underway to evaluate processes and dosages with the intent of developing a more cost effective product for sale to customers.

        Research and Development Expenses.     Research and development expenses in continuing operations, which include clinical trial costs and pre-clinical research activities, for the nine months ended September 30, 2008 and 2007, were $10.0 million and $8.2 million, respectively. The increase in research and development expenses for the nine months ended September 30, 2008, as compared to the same period in 2007, was primarily related to the milestone payment incurred in conjunction with the acquisition of ADViSYS, and increased spending for preclinical and research projects, including the DTRA contract. For the period from December 12, 2000 (inception) to September 30, 2008, total research and development expenses from continuing operations totaled $36,240,000.

        General and Administrative Expenses.     General and administrative expenses in continuing operations, which include marketing expenses, business development expenses and the amortization of intangible assets, for the nine months ended September 30, 2008 and 2007 were $6.4 million and $4.0 million, respectively. The increase in general and administrative expenses for the nine months ended September 30, 2008 as compared to 2007 was primarily related to an increase in stock-based compensation as a result of the option re-pricing that took place in September 2008, as well as increased intangible asset amortization for two additional months in 2008, production of marketing materials and product samples and supplies associated with Animal Health's Lifetide™ SW5 product approved for sale in Australia in January 2008, and increased spending for outside consulting services and legal and accounting fees related to the execution of the definitive merger agreement with INOVIO. These increases are partially offset by a reduction in stock-based compensation for a former related party employee whose options vested completely in June of 2007. For the period from

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December 12, 2000 (inception) to September 30, 2008, general and administrative expenses from continuing operations totaled $31,435,000.

        Stock-Based Compensation.     Stock-based compensation cost is measured at the grant date, based on the fair value of the award reduced by estimated forfeitures, and is recognized as expense over the employee's requisite service period. Total compensation cost under SFAS No. 123(R) for VGX's stock plans for the nine months ended September 30, 2008 was $8,093,000, of which $1,852,000 was included in research and development expenses and $6,241,000 was included in general and administrative expenses. Total compensation cost under SFAS No. 123(R) for VGX's stock plans for the nine months ended September 30, 2007 was $4,810,000, of which $789,000 was included in research and development expenses and $4,021,000 was included in general and administrative expenses. The increase in stock-based compensation expenses for research and development in the nine month period ended September 30, 2008 as compared to 2007 is attributable to the issuance of shares upon the attainment of a key milestone. The increase in stock-based compensation expenses for general and administrative in the nine month period ended September 30, 2008 as compared to 2007 reflects the option re-pricing that took place in September 2008. For the period from December 12, 2000 (inception) to September 30, 2008, total stock-based compensation recorded by VGX is $37,299,000.

        Losses from Equity Investment.     VGX recorded expense for the nine months ended September 30, 2008 and 2007 of $818,000 and $563,000, respectively, which reflects VGX's ownership share of the losses of VGX International, Inc., which is accounted for by the equity method in VGX's financial statements. The increase in losses in for the period in question is attributable to the increased R&D spending by VGX International related to the clinical trial support of VGX-1027. For the period from December 12, 2000 (inception) through September 30, 2008, VGX's portion of losses in VGX International reflected in the statements of operations is $2,834,000.

        Interest Income.     Interest income for the nine months ended September 30, 2008 and 2007 was $394,000 and $703,000, respectively. The decrease in interest income for the nine months ended September 30, 2008, as compared to 2007, was primarily due to lower cash and investment balances and a lower average interest rate. Interest income from December 12, 2000 (inception) to September 30, 2008 totaled $2,260,000.

        Interest Expense.     VGX recorded interest expense for the nine months ended September 30, 2008 and 2007 of $476,000 and $840,000, respectively. Included in this expense is interest accrued on loans from investors of $476,000 and $735,000 for the nine months ended September 30, 2008 and 2007, respectively. The reduction in interest expense is reflective of loans that have been repaid in 2007 and 2008. Also reflected in interest expense is amortization of debt issuance costs of $105,000 for the nine months ended September 30, 2007. These costs were being amortized over the term of the borrowings, and the reduction in expense is indicative of the settlement of the outstanding liability related to these costs with the issuance of 71,000 stock options in September 2008. For the period from December 12, 2000 (inception) to September 30, 2008, interest expense totaled $2,807,000, which consists of $2,456,000 of interest on loans to investors, $257,000 of debt issuance cost amortization, and $94,000 of foreign currency losses related to repayment of certain loans issued in foreign currency during 2007.

        Other Income (Expense), net.     For the nine months ended September 30, 2008 and the period from December 12, 2000 (inception) to September 30, 2008, VGX reflected $97,000 in other income, representing the gain realized on the settlement of the liability related to debt issuance costs, which is indicative of a reduction in the stock price from the time the liability was incurred until September 2008, when it was satisfied with the issuance of 71,000 stock options to the investor who was instrumental in assisting VGX with raising funds for the company.

        Minority Interest.     For the nine months ended September 30, 2008 and 2007, VGX reflected $254,000 and $6,000, respectively, in minority interest, reflecting the portion of Animal Health's losses

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attributable to third party stockholders. For the period from December 12, 2000 (inception) through September 30, 2008, VGX reflected $297,000 of minority interest in its consolidated statements of operations.

        Discontinued Operations.     On June 10, 2008, an Asset Purchase Agreement was executed whereby all of the manufacturing assets of VGX were sold to a related party. VGX had not previously contemplated the sale of it manufacturing assets, as it was considered to be a part of its overall strategy of penetrating the DNA Vaccines industry. The proceeds from the sale of the assets could be used to fund VGX's clinical trials as well as redeem convertible debt. While having an internal DNA plasmid manufacturing operation allowed VGX the flexibility and control over the manufacturing of its DNA plasmids, VGX management believed that any potential manufacturing risk could be mitigated through the use of alternate sourcing and supply agreements. The purchase price allocation was determined by, and was the responsibility of, VGX management, who considered in part preliminary work performed by an independent third party valuation firm who used various valuation methodologies including DCF, Revenue Multiples, Comp Analysis, etc, to arrive at the purchase price allocation. As such, the board of VGX approved the asset sale and the deal was consummated on June 10, 2008.

        Gain on Sale of Manufacturing Assets.     For the nine months ended September 30, 2008 and the period from December 12, 2000 (inception) to September 30, 2008, VGX recognized a gain on the sale of its manufacturing assets of $6,653,000, net of tax, which consists of the gross gain of $9,555,000 partially offset by a reduction in the investment of the related party of $2,902,000, representing the share of the gain related to VGX's ownership percentage in that entity.

        Loss from Discontinued Operations.     Operating losses from discontinued operations, related to the sale of the manufacturing assets, for the nine months ended September 30, 2008 and 2007 were $1,587,000 and $1,045,000, respectively.

        For the nine months ended September 30, 2008, revenue from product sales to customers of the DNA manufacturing facility totaled $566,000, which represents shipments to a customer in the United Kingdom, in response to their supply needs, along with reimbursement for the associated shipping costs totaling $22,000, which were billed to the customer at the completion of the manufacturing campaign. Offsetting this revenue was the cost of manufacturing these products of $331,000, and unabsorbed labor and overhead of $1,562,000, as well as general and administrative expenses of $282,000 related to amortization of the intangible assets related to customer contracts acquired as part of the asset purchase agreement executed with ADViSYS, Inc. in February 2007.

        For the nine months ended September 30, 2007, revenue from sales of manufactured plasmids totaled $309,000. Offsetting this revenue were costs incurred by VGX related to the production of these products of $302,000, as well as unabsorbed labor and overhead incurred at the production facility of $994,000, and general and administrative expenses of $58,000 related to amortization of the intangible assets related to customer contracts acquired as part of the assets purchase agreement executed with ADViSYS, Inc. in February 2007.

        For the period from December 12, 2000 (inception) to September 30, 2008, operating losses from the discontinued manufacturing operations totaled $2,996,000.

    Results of Operations for the Year Ended December 31, 2007 Compared to the Year Ended December 31, 2006

        Revenue.     VGX reported total revenue of $705,000 and $337,000 for the years ended December 31, 2007 and 2006, respectively, and $1,853,000 for the period from December 12, 2000 (inception) through December 31, 2007. Revenue consists of government grant reimbursements, R&D licensing fees, and other sources including rental of electroporation devices, sales of associated arrays, and research consulting activities.

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        Revenue from government grant reimbursements for the years ended December 31, 2007 and 2006 amounted to $669,000 and $337,000, respectively. The increase in this revenue is indicative of VGX's revenue recognition policy of recognizing grant revenues only upon receipt of funds as well of the terms of the awards, with the majority of activities being conducted in 2007. For the period from December 12, 2000 (inception) to December 31, 2007, revenue from government grants totaled $1,741,000.

        Other operating revenue for the year ended December 31, 2007 and the period from December 12, 2000 (inception) to December 31, 2007 totaled $36,000, which represents rental of electroporation devices, sales of associated arrays to research organizations, and research consulting activities.

        VGX did not receive any revenue from licensing fees in either 2007 or 2006. However, license fee revenue recognized from December 12, 2000 (inception) to December 31, 2007 totaled $75,000.

        Research and Development Expenses.     Research and development expenses in continuing operations, which include clinical trial costs and pre-clinical research activities, for the years ended December 31, 2007 and 2006, were $10.9 million and $9.0 million, respectively. The increase in research and development expenses from 2006 to 2007 was primarily related to staffing increases, expanded pre-clinical research activities, and new programs resulting from the acquisition of additional technologies purchased from ADViSYS, Inc. in February 2007. This increase was partially offset by the reduction in expenses incurred for the manufacturing of API (Active Pharmaceutical Ingredient) required for clinical trials as well as a reduction in outside services costs related to clinical trials. For the period from December 12, 2000 (inception) to December 31, 2007, total research and development expenses in continuing operations totaled $26,213,000.

        General and Administrative Expenses.     General and administrative expenses in continuing operations, which include business development expenses and the amortization of intangible assets, for the years ended December 31, 2007 and 2006, were $5.0 million and $8.7 million, respectively. The reduction in general and administrative expenses from 2006 to 2007 is primarily related to higher stock-based compensation expenses in 2006 for options and warrants granted to key executives and consultants in lieu of cash. VGX has always used non-cash stock-based compensation as a means to conserve cash and to align the interests of its executive and consultants with other stockholders of the company. In 2006, there was a grant of warrants to a former employee of the company for his efforts in a successful round of financing which was a key reason for the higher G&A costs compared to 2007. 2007 did see an increase in expenses related to staffing, as well as professional fees and services associated with VGX's expanded organizational structure, and intangible asset amortization related to the technologies acquired through the asset purchase agreement with ADViSYS, Inc.; however, it was not enough to offset the one-time charge related to the issuance of options and warrant in 2006. For the period from December 12, 2000 (inception) to December 31, 2007, general and administrative expenses totaled $25,078,000.

        Stock-Based Compensation.     Stock-based compensation cost is measured at the grant date, based on the fair value of the award reduced by estimated forfeitures, and is recognized as expense over the employee's requisite service period. Total compensation cost under SFAS No. 123(R) for VGX's stock plans for the year ended December 31, 2007 was $5,473,000, of which $1,150,000 was included in research and development expenses and $4,323,000 was included in general and administrative expenses. Total compensation cost under SFAS No. 123(R) for VGX's stock plans for the year ended December 3, 2006 was $12,152,000, of which $567,000 was included in research and development expenses and $11,585,000 was included in general and administrative expenses. As noted in the above paragraph, the majority of the difference in stock-based compensation expenses between 2006 and 2007 is attributable to a grant of warrants to a former employee for his contributions to a successful round

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of financing in 2006. For the period from December 12, 2000 (inception) to December 31, 2007, total stock-based compensation recorded by VGX is $29,206,000.

        Losses from Equity Investment.     VGX recorded expense for the years ended December 31, 2007 and 2006 of $990,000 and $700,000, respectively, which reflects VGX's ownership share of the losses of VGX International, Inc., which is accounted for by the equity method in VGX's financial statements. For the period from December 12, 2000 (inception) through December 31, 2007, VGX's portion of losses in VGX International reflected in the statements of operations is $2,016,000.

        Interest Income.     Interest income for the years ended December 31, 2007 and 2006 was $919,000 and $846,000, respectively. VGX invests its excess cash in short-term money market funds; its investment philosophy holds liquidity and preservation of capital as paramount. The increase in interest income realized in 2007 was primarily due to higher cash and investment balances for part of 2007, offset by the decrease in yields on short-term certificates of deposits reflecting the state of the fixed-income markets. Interest income from December 12, 2000 (inception) to December 31, 2007 totaled $1,866,000.

        Interest Expense.     VGX recorded interest expense for the years ended December 31, 2007 and 2006 of $1,129,000 and $957,000, respectively. Included in this expense is interest accrued on loans from investors of $909,000 and $826,000 for the years ended December 31, 2007 and 2006, respectively. The increase in interest expense is reflective of increased loan balances for most of 2007. Also reflected in interest expense is amortization of debt issuance costs of $126,000 and $131,000 for the years ended December 31, 2007 and 2006, respectively. These costs are being amortized over the term of the borrowings, and the reduction in expense is indicative of the maturities and repayments made by VGX. For the year ended December 31, 2007, VGX recognized $94,000 of foreign currency losses related to the repayment of a loan denominated in Korean Won, which is classified as interest expense in the consolidated statements of operations. For the period from December 12, 2000 (inception) to December 31, 2007, interest expense totaled $2,331,000, which consists of $1,980,000 of interest on loans to investors, $257,000 of debt issuance cost amortization, and $94,000 of foreign currency losses incurred upon the repayment of a loan denominated in Korean Won.

        Minority Interest.     For the year ended December 31, 2007, and the period from December 12, 2000 (inception) to December 31, 2007, VGX reflected $44,000 in minority interest, reflecting the portion of Animal Health's losses attributable to third party stockholders. Animal Health was carved out as a subsidiary of VGX during the second quarter of 2007, and issued common stock to a third party in the third quarter of 2007. As a result, no minority interest was recognized prior to 2007.

        Discontinued Operations.     On June 10, 2008, an Asset Purchase Agreement was executed whereby all of the manufacturing assets of VGX were sold to a related party. VGX had not previously contemplated the sale of it manufacturing assets, as it was considered to be a part of its overall strategy of penetrating the DNA Vaccines industry. The proceeds from the sale of the assets could be used to fund VGX's clinical trials as well as redeem convertible debt. While having an internal DNA plasmid manufacturing operation allowed VGX the flexibility and control over the manufacturing of its DNA plasmids, VGX management believed that any potential manufacturing risk could be mitigated through the use of alternate sourcing and supply agreements. The purchase price allocation was determined by, and was the responsibility of, VGX management, who considered in part preliminary work performed by an independent third party valuation firm who used various valuation methodologies including DCF, Revenue Multiples, Comp Analysis, etc, to arrive at the purchase price allocation. As such, the board of VGX approved the asset sale and the deal was consummated on June 10, 2008.

        Loss from Discontinued Operations.     Operating losses from discontinued operations, related to the manufacturing assets held for sale, for the year ended December 31, 2007 and the period from December 12, 2000 (inception) to December 31, 2007 were $1,410,000.

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        Income Taxes.     Since inception, VGX has incurred operating losses and accordingly has not recorded a provision for income taxes for any of the periods presented. As of December 31, 2007, VGX had net operating loss carry forwards for federal and state income tax purposes of approximately $27.6 million and $23.3 million, respectively, which will expire in 2021 through 2027 if not utilized. Utilization of net operating losses are subject to a substantial annual limitation due to ownership change limitations provided by the Internal Revenue Code of 1986, as amended.

    Liquidity and Capital Resources

        Historically, VGX's primary uses of cash have been to finance research and development activities including clinical trial activities in its small molecule drug programs as well in the DNA vaccines and other immunotherapy areas of its business. Since inception, VGX has satisfied its cash requirements principally from loans from investors and proceeds from the sale of equity securities.

        As of September 30, 2008, VGX had working capital from continuing operations of $2.7 million, as compared to $3.4 million as of December 31, 2007. The decrease in working capital during the nine months ended September 30, 2008 was primarily due to repayment of notes payable and accrued interest to investors, increased spending for research and development activities, maintenance of VGX's patent portfolio, and general and administrative expenses related to consulting, legal, accounting, audit and other professional services in conjunction with the definitive merger agreement executed with INOVIO. This reduction is partially offset by the anticipated proceeds from the sale of the manufacturing assets through an asset purchase agreement with a related party in June 2008.

        From the period from inception (December 12, 2000) through September 30, 2008, cash provided by discontinued operations amounted to $1.2 million. This was the result of the $6.7 million gain on the sale of the manufacturing assets which took place in June 2008, offset by cash used in discontinued operations of $5.5 million. Following the sale of the manufacturing assets, VGX believes that it will be in a better position to focus on its strategic objectives and devote its resources exclusively to research and clinical development of novel product candidates.

        As of September 30, 2008, VGX had an accumulated deficit of $63.0 million. VGX has operated at a loss since December 12, 2000 (inception), and expects this to continue for some time. The amount of the accumulated deficit will continue to increase, as it will be expensive to continue clinical, research and development efforts. If these activities are successful and if VGX receives approval from the FDA to market products and / or equipment, then even more funding will be required to market and sell the products and equipment. The outcome of the above matters cannot be predicted at this time. VGX will evaluate potential partnerships as an additional way to fund operations, and will continue to rely on outside sources of financing to meet capital needs beyond next year.

        VGX's long-term capital requirements will depend on numerous factors including:

    The progress and magnitude of the research and development programs, including preclinical and clinical trials;

    The time involved in obtaining regulatory approvals;

    The cost involved in filing and maintaining patent claims;

    Competitor and market conditions;

    The ability to establish and maintain collaborative arrangements;

    The ability to obtain grants to finance research and development projects; and

    The cost of manufacturing scale-up and the cost of commercialization activities and arrangements.

183


        The ability to generate substantial funding to continue research and development activities, preclinical and clinical studies and clinical trials and manufacturing, scale-up, and selling, general, and administrative activities is subject to a number of risks and uncertainties and will depend on numerous factors including:

    The ability to raise funds in the future through private financings, collaborative arrangements, grant awards or from other sources;

    VGX's potential to obtain equity investments, collaborative arrangements, license agreements or development or other funding programs in exchange for manufacturing, marketing, distribution or other rights to products developed by VGX; and

    The ability to maintain existing collaborative arrangements.

        VGX cannot guarantee that additional funding will be available when needed or on favorable terms. If it is not, VGX will be required to scale back research and development programs, preclinical studies and clinical trials, and selling, general, and administrative activities, or otherwise reduce or cease operations and VGX's business and financial results and condition would be materially adversely affected.

    Executive Compensation

        The following table sets forth compensation information for 2007 for VGX's president and chief executive officer, the chief financial officer, and other key executives of VGX who will become executive officers of the combined company.

    Summary Compensation Table

Name and Principal Position(1)
  Year   Salary ($)   Bonus
($)(2)
  Option
Awards
($)(3)
  All Other
Compensation
($)(4)
  Total ($)  

J. Joseph Kim
CEO and President

    2007     240,000     40,000     1,766,456     4,260     2,050,716  

Kevin Rassas
Sr. VP of Business Development

    2007     131,667     10,000     186,177     1,467     329,311  

Gene J. Kim
CFO

    2007     151,603     15,000     1,090,721     1,967     1,259,290  

N. Sardesai
Sr. VP of Research

    2007     131,060     14,000     76,775     1,633     223,468  

C. Jo White
CMO

    2007     210,000     42,000     209,782     2,767     464,549  

R. Draghia-Akli(5)
VP of Research

    2007     158,000     7,000     23,611     7,131     195,742  

(1)
The information set forth in this table relates to the executive officer's position at VGXP during the 2007 fiscal year

(2)
Includes bonus earned in 2007 but which were paid in 2008.

(3)
The amounts in the Option Awards column reflect the estimated dollar amounts to be recognized for financial purposes for the fiscal year ended December 31, 2007 in accordance with FAS 123(R), for awards pursuant to the VGX 2001 Equity Incentive Plan, and thus includes amounts attributable to awards granted before 2007.

(4)
Consists of matching contribution to VGXP 401(K) plan, life insurance premium payment in which the beneficiary is not VGX, and unused vacation payout, which resulted from a change VGX's policy regarding the number of days of unused vacation days that can be carried over to the following fiscal year. VGX ended its policy of matching contribution to the VGX 401(K) plan in the second quarter of 2007.

(5)
R. Draghia-Akli joined VGX as a result of the asset purchase agreement between ADViSYS and VGX signed in February 21, 2007. Her salary reflects those paid by VGX only.

184


    Employment Agreements

        VGX utilizes employment agreements for all executive officers, generally when it is necessary to secure the services of a newly hired executive. VGX currently has employment agreements with:

    J. Joseph Kim, Ph.D., VGX's President and Chief Executive Officer, effective as of March 31, 2008

    Gene J. Kim, VGX's Chief Financial Officer, effective October 1, 2005, amended as of August 20, 2008;

    Kevin Rassas, VGX's Senior Vice President, Business Development, effective as of December 17, 2005, amended as of August 20, 2008; and

    C. Jo. White, Chief Medical Officer, effective as of August 1, 2005, amended as of August 20, 2008;

    Niranjan Sardesai, Ph.D., Senior Vice President, Research and Development, effective as of November 1, 2007, amended as of August 20, 2008 and October 1, 2008; and

    Ruxandra Draghia-AKli, Vice President, Research effective as of November 14, 2001, amended as of September 2, 2008.

        J. Joseph Kim, Ph.D., Employment Agreement.     Under an executive employment agreement, J. Joseph Kim, Ph.D. serves as VGX's President and CEO. Under the terms of the agreement, Dr. Kim is entitled to receive an annual salary of $240,000. He is also eligible to receive an incentive cash bonus up to the amount, based upon the criteria, as may be determined by the board and targeted at 30% or more of the base salary. In addition to the salary and cash bonus, he is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by the VGX board of directors.

        Under VGX's employment agreement with Dr. Kim, if VGX terminates his employment at any time without cause, as defined in the employment agreement, he is entitled to receive severance compensation in the form of monthly payments of his then-current base salary and of the pro rata bonus amount for a period of 24 months following the effective date of such termination. The pro rata bonus amount shall mean one-twelfth of the greater of (A) the most recent annual cash bonus paid prior to his termination, or (B) the average of the three most recent annual cash bonuses paid prior to his termination. VGX will also continue to pay his COBRA premiums for 18 months thereafter.

        VGX has change-in-control agreements in place for the chief executive officer. The rationale for the agreement is that in the event of a change in control of VGX, this individual is most likely to lose his job as a result of redundancy in executive position. If Dr. Kim is terminated as a result of change-in-control, Dr. Kim is entitled to receive payments due him under the conditions of termination without cause as outlined above and a lump sum cash severance payment equal to his then-current monthly base salary and the pro rata bonus amount multiplied by 24 but discounted to present value based on applicable federal rate under the Code.

        Gene J. Kim Employment Agreement.     Under an executive employment agreement, Gene J. Kim serves as VGX's Chief Financial Officer. Under the terms of the agreement, Mr. Kim is entitled to receive an annual salary of $170,400. He is also eligible to receive an incentive cash bonus up to the amount, based upon the criteria, as may be determined by the board and targeted at 20% or more of the base salary. In addition to the salary and cash bonus, he is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by the VGX board of directors.

        Under VGX's employment agreement with Mr. Kim, if VGX terminates his employment at any time without cause, as defined in the employment agreement, he is entitled to receive severance

185



compensation in the form of monthly payments of his then-current base salary and of the pro rata bonus amount for a period of 12 months following the effective date of such termination. The pro rata bonus amount shall mean one-twelfth of the greater of (A) the most recent annual cash bonus paid prior to his termination, or (B) the average of the three most recent annual cash bonuses paid prior to his termination. VGX will also continue to pay his COBRA premiums for six months thereafter.

        Kevin W. Rassas Employment Agreement.     Under an executive employment agreement, Kevin W. Rassas serves as VGX's Senior Vice President of Business Development. Under the terms of the agreement, Mr. Rassas is entitled to receive an annual salary of $150,700. He is also eligible to receive an incentive cash bonus up to the amount, based upon the criteria, as may be determined by the board and targeted at 30% or more of the base salary. In addition to the salary and cash bonus, he is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by VGX board of directors.

        Under VGX's employment agreement with Mr. Rassas, if VGX terminates his employment at any time without cause, as defined in the employment agreement, he is entitled to receive severance compensation in the form of monthly payments of his then-current base salary and of the pro rata bonus amount for a period of six months following the effective date of such termination. The pro rata bonus amount shall mean one-twelfth of the greater of (A) the most recent annual cash bonus paid prior to his termination, or (B) the average of the three most recent annual cash bonuses paid prior to his termination. VGX will also continue to pay his COBRA premiums for six months thereafter.

        C. Jo White, M.D. Employment Agreement.     Under an executive employment agreement, C. Jo White serves as VGX's Chief Medical Officer. Under the terms of the agreement, Dr. White is entitled to receive an annual salary of $216,300. She is also guaranteed to receive a minimum cash bonus of 20% of her annual salary. In addition to the salary and cash bonus, she is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by the VGX board of directors.

        Under VGX's employment agreement with Dr. White, if VGX terminates her employment at any time without cause, as defined in the employment agreement, she is entitled to receive severance compensation in the form of monthly payments of her then-current base salary and of the pro rata bonus amount for a period of six months following the effective date of such termination. The pro rata bonus amount shall mean one-twelfth of the greater of (A) the most recent annual cash bonus paid prior to her termination, or (B) the average of the three most recent annual cash bonuses paid prior to her termination. VGX will also continue to pay her COBRA premiums for six months thereafter.

        Niranjan Sardesai, Ph.D. Employment Agreement.     Under an executive employment agreement, Niranjan Sardesai, Ph.D. serves as VGX's Senior Vice President of Research and Development. Under the terms of the agreement, Dr. Sardesai is entitled to receive an annual salary of $170,000 per annum. He is also eligible to receive an incentive cash bonus up to the amount, based upon the criteria, as may be determined by the board and targeted at twenty percent (20%) or more of the base salary. In addition to the salary and cash bonus, he is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by the VGX board of directors.

        Under VGX's employment agreement with Dr. Sardesai, if VGX terminates his employment at any time without cause, as defined in the employment agreement, he is entitled to receive severance compensation in the form of monthly payments of his then-current base salary and of the pro rata bonus amount for a period of six months following the effective date of such termination. The pro rata bonus amount shall mean one-twelfth of the greater of (A) the most recent annual cash bonus paid prior to his termination, or (B) the average of the three most recent annual cash bonuses paid prior to his termination. VGX will also continue to pay his COBRA premiums for six months thereafter.

186


        Ruxandra Draghia-Akli, M.D. Employment Agreement.     Under an executive employment agreement, C. Jo White serves as VGX's Chief Medical Officer. Under the terms of the agreement, Dr. Draghia-Akli is entitled to receive an annual salary of $189,571.00 per annum. She is also eligible to receive an incentive cash bonus up to the amount, based upon the criteria, as may be determined by the board and targeted at 20% or more of the base salary. In addition to the salary and cash bonus, she is also entitled to participate in such employee benefit plans or programs of VGX, and shall be entitled to such other fringe benefits, as are from time to time adopted by the VGX board of directors.

        Under VGX's employment agreement with Dr. Draghia-Akli, if VGX terminates her employment at any time without cause, as defined in the employment agreement, she is entitled to receive severance compensation in the form of monthly payments of her then-current base salary for a period of six months following the effective date of such termination. VGX will also continue to pay her COBRA premiums for 6 months thereafter.

    Elements of Post-Termination Compensation

        Change-in-Control Agreements.     VGX has change-in-control agreements in place for the chief executive officer. The rationale for the agreement is that in the event of a change in control of VGX, this individual is most likely to lose his job as a result of redundancy in executive position. Information regarding applicable payments under the change of control for the named executive officer is provided in executive officer's employment agreement.

        Severance.     As part of VGX's executive officers employment agreements, any executive currently working for VGX at the executive officer level whose employment is terminated involuntarily is eligible for severance benefits, provided each of their employment agreement requirements are met. The severance pay and benefits that are payable are stated in each executive's employment agreement.

    Internal Revenue Code Section 409A

        Code Section 409A relates to accounting treatment for deferred compensation. VGX is aware that it had granted options and warrants which did not comply with the provisions of Section 409A of the Code. In September 2008, the VGX board of directors approved two methods to bring these non-compliant stock options and warrants into compliance with section 409A of the Code. Each holder of non-compliant options and warrants was given the choice of either agreeing to reset the exercise price at a value that was no less than the fair market value of VGX common stock on the date of repricing, or making a forward election in which the holder was given the option to choose a date after December 31, 2008 on or after which to exercise the stock option and warrant. The new grant prices were determined and were the responsibility of VGX Board of Directors and management, which considered in part preliminary work performed by an independent valuation firm.

    Impact of FAS 123R

        FAS 123R requires companies to record option grants as expenses at the time of grant. Option expense is one factor that VGX considers in the design of VGX's long-term compensation programs. Other factors include:

    the link to performance that each type of equity award provides;

    the degree of upside leverage and downside risk inherent in each type of award;

    the impact on dilution and overhang that the different equity awards have; and

    the role that each type of equity award has in the attraction, retention, and motivation of VGX's executive and key employee talent.

187


        VGX monitors its FAS 123R expense to ensure that it is reasonable, although expense is not the most important factor in making decisions about VGX's long-term incentive plans.

    Option Repricing

        In September 2008, the VGX board of directors approved a re-pricing of certain high priced options issued to employee and consultants to lower the grant price in order to improve employee morale. The options were re-priced to new grant prices which ranged from $1.00 to $2.25. The new grant prices were determined and were the responsibility of the VGX Board of Directors and management, which considered in part preliminary work performed by an independent valuation firm. The grant price prior to the re-pricing was $5.00. The repricing of the options was done in accordance with FAS 123R. Using the Black-Scholes Option Pricing Model, the fair values of the modified options at the modification date were calculated. This was then compared against the fair values of the original options at the modification date. The differences between the two were recognized as compensation expense over the remaining life of the options. If the vesting schedule of the options were accelerated, the additional compensations expenses were recognized immediately as opposed to over the length of the vesting schedule. The re-pricing will create an additional non-cash compensation charge of $2,968,745, $324,123, and $52,734 in 2008, 2009, and 2010, respectively.

        There was an additional re-pricing of options that were not compliant with Section 409A. In this case, the grant prices of the options were adjusted upwards from $.025 to $.50 to $1.00 to $1.25. As the fair values of the modified options at the modification date was lower than the fair values of the original options at the modification date, no additional compensations expenses were recognized; this is consistent with the fact that the grantees were giving up lower-priced options for the higher-priced ones.

    Options Exercised

        There were no options exercised by VGX named executive officers during 2007.

      Outstanding Equity Awards as of December 31, 2008

        The following tables set forth certain information with respect to outstanding equity awards to the named executive officers under VGX equity incentive plans during 2007.

 
  OPTION AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Options (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Options (#)
Unexercisable
  Option
Exercise
Price ($)
  Option
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 

J. Joseph Kim

    1,000,000           1.25     05/01/2016  
 

President and CEO

    200,000     400,000     1.25     1/18/2017  

    83,333     166,667     1.25     09/28/2017  

          200,000     1.25     09/12/2018  
                       

    1,283,333     766,667              
                       

188


 
  OPTION AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Options (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Options (#)
Unexercisable
  Option
Exercise
Price ($)
  Option
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 

Gene J. Kim

    150,000           1.25     10/1/2015  
 

CFO

    500,000           1.25     5/1/2016  

    233,333     116,667     1.25     1/18/2018  

    66,667     133,333     1.25     9/28/2017  

          200,000     1.25     9/12/2018  
                       

    950,000     450,000              
                       

Kevin Rassas

   
200,000
         
0.05
   
12/16/2013
 
 

Sr. VP, Business Development

    400,000           0.20     12/1/2014  

    120,000           0.30     12/17/2015  

    20,000     10,000     2.25     10/2/2016  

    33,333     16,667     2.25     1/18/2017  

    5,000     10,000     2.25     11/1/2017  

          20,000     1.5     9/12/2018  
                       

    778,333     56,667              
                       

Niranjan Sardesai

   
95,000
   
40,000
   
1.50
   
8/28/2016
 
 

Sr. VP, Research and Development

    16,667     8,333     1.50     1/5/2017  

    10,000     5,000     1.50     1/18/2017  

    45,000     30,000     1.50     11/1/2017  

          50,000     1.50     9/12/2018  
                       

    166,667     133,333              
                       

C. Jo White

   
100,000
         
0.03
   
10/01/2012
 
 

Chief Medical Officer

    100,000           1.25     10/01/2012  

    100,000           0.20     12/01/2014  

    300,000           1.25     09/01/2015  

    33,333     16,667     1.25     01/18/2017  

          55,000     1.25     09/12/2018  
                       

    633,333     71,667              
                       

189


 
  OPTION AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Options (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Options (#)
Unexercisable
  Option
Exercise
Price ($)
  Option
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 

Ruxandra Draghia-Akli

    13,333     26,667     1.50     05/01/2017  
 

VP, Research

          45,000     1.50     09/12/2018  
                       

    13,333     71,667              
                       

 

 
  WARRANT AWARDS  
Name
  Number of
Securities
Underlying
Unexercised
Warrants (#)
Exercisable
  Number of
Securities
Underlying
Unexercised
Warrants (#)
Unexercisable
  Warrant
Exercise
Price ($)
  Warrant
Expiration
Date
 
(a)
  (b)
  (c)
  (d)
  (e)
 

J. Joseph Kim

    1,250,000           1.25     8/1/2015  
                       

    1,250,000                    
                       

    Compensation of Directors

        VGX pays each non-employee director of VGX (other than the chairman of the board) an annual retainer fee of $30,000. VGX pays or reimburses all reasonable expenses associated with directors' attendance at and participation in board and VGX stockholder's meetings and other company business to which a director attends. VGX did not pay director fees in 2007 because Dr. Kim served as the sole director of VGX.

        VGX does not pay director fees to its directors who are also VGX employees. Therefore, Dr. Kim does not receive director fees.

        Non-employee directors are eligible to receive, from time to time, grants of options to purchase shares of common stock under the VGX equity incentive plan as determined by the full VGX board of directors. During 2008, VGX granted ten-year options to purchase a total of 10,000 shares of its common stock to each of its non-employee directors at an exercise price of $1.50.

190



SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT

Security Ownership of Certain Beneficial Owners and Management of Inovio Prior to the Transaction

        The following table sets forth information as of December 31, 2008, with respect to the beneficial ownership of Inovio's common stock by (i) each person known to Inovio to be the beneficial owners of more than 5% of its common stock, (ii) each of Inovio's directors and nominees for director, (iii) each of Inovio's executive officers, and (iv) all of Inovio's directors and executive officers as a group.

        Beneficial ownership is determined in accordance with the rules of the SEC. In computing the number of shares beneficially owned by a stockholder and the percentage of ownership of that stockholder, shares of common stock underlying shares of convertible preferred stock, options or warrants held by that stockholder that are convertible or exercisable, as the case may be, within 60 days of December 31, 2008 are included. Those shares, however, are not deemed outstanding for the purpose of computing the percentage ownership of any other person. Each stockholder's percentage of ownership in the following table is based upon 44,023,050 shares of Inovio common stock outstanding as of December 31, 2008.

Beneficial Owner of Shares of Common
Stock(1)(2)
  Amount and Nature
of Beneficial
Ownership of
Shares of Common
Stock
  Percent of Class of Shares of Common Stock  

5% Stockholders:(3)

             

None

             

Directors and Executive Officers:

             

Avtar Dhillon(4)

    1,089,357     2.42 %

James L. Heppell(5)

    207,769     *  

Riaz Bandali(6)

    80,404     *  

Simon X. Benito(7)

    93,732     *  

Tazdin Esmail(8)

    144,472     *  

Robert W. Rieder(9)

    28,748     *  

Stephen Rietiker(10)

    326,249     *  

Patrick Gan(11)

    7,499     *  

Chin-Cheong Chong(12)

    150,375     *  

Peter Kies(13)

    205,201     *  

Michael Fons(14)

    105,025     *  

Punit Dhillon(15)

    158,714     *  

All directors and executive officers as a group (12 persons)

    2,597,545     5.65 %

*
Less than 1%

(1)
This table is based upon information supplied by officers, directors and principal stockholders. Except as shown otherwise in the table, the address of each stockholder listed is in care of Inovio at 11494 Sorrento Valley Rd., San Diego, California 92121-1318.

(2)
Except as otherwise indicated in the footnotes of this table and pursuant to applicable community property laws, the persons named in the table have sole voting and investment power with respect to all shares of common stock. Beneficial ownership is determined in accordance with the rules of the SEC and generally includes voting or investment power with respect to securities.

(3)
To Inovio's knowledge, as of December 31, 2008, no individual or group beneficiary held 5% or more of its common stock.

191


(4)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, 949,996 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008, and 18,750 shares of restricted stock which vests within 60 days of December 31, 2008.

(5)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 194,059 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(6)
Includes 2,941 shares underlying Series C preferred stock and 1,029 shares underlying warrants that are convertible or exercisable, respectively, within 60 days of December 31, 2008, and 76,249 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(7)
Includes 1,544 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 84,999 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(8)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 134,999 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(9)
Includes 28,748 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(10)
Includes 26,249 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(11)
Includes 7,499 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(12)
Includes 1,666 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008. Does not include 37,800 shares of common stock held of record for which Mr. Chong disclaims beneficial ownership.

(13)
Includes 514 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 203,125 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(14)
Includes 105,000 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(15)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 157,500 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

Security Ownership of Certain Beneficial Owners and Management of VGX Prior to the Transaction

        The following table sets forth certain information regarding beneficial ownership of the shares in VGX's share capital as of December 31, 2008 by: (i) each stockholder who is known by VGX to own beneficially more than five percent of the capital stock of VGX; (ii) each executive officer named below; (iii) each director of VGX; and (iv) all of VGX's current directors and executive officers as a group.

        Beneficial ownership is determined in accordance with the rules of the SEC. In computing the number of shares beneficially owned by a stockholder and the percentage of ownership of that stockholder, shares of common stock underlying options, warrants or convertible debt (excluding any

192



shares issuable upon conversion of accrued interest on such convertible debt) held by that stockholder that are exercisable or convertible, as the case may be, within 60 days of December 31, 2008 are included. Those shares, however, are not deemed outstanding for the purpose of computing the percentage ownership of any other person. Each stockholder's percentage of ownership in the following table is based upon 41,870,240 shares of VGX common stock outstanding as of December 31, 2008.

 
  Beneficial Ownership  
Name of Beneficial Owner(1)
  Amount and Nature of
Beneficial Ownership of
Shares of Common Stock
  Percent of Class of Shares
of Common Stock
 

5% Stockholders

             

University of Pennsylvania

    3,603,604     8.6 %

David Weiner

    3,550,000     8.5 %

Ernest Shin(2)

    4,592,850     10.3 %

Bryan Chung(3)

    2,310,375     5.5 %

Directors and Executive Officers

             

J. Joseph Kim(4)

    14,593,333     32.9 %

Gene J. Kim(5)

    950,000     2.2 %

C. Jo White(6)

    633,333     1.5 %

Kevin Rassas(7)

    720,869     1.7 %

Niranjan Sardesai(8)

    166,667     *  

Ruxandra Draghia-Akli(9)

    13,333     *  

Morton Collins(10)

    230,000     *  

All directors and executive officers as a group (7 persons)

    17,321,666     37.03 %

*
Less than one % of shares outstanding.

(1)
This table is based upon information supplied by officers, directors and principal stockholders. Unless otherwise indicated, the address of each beneficial holder listed is 450 Sentry Parkway, Blue Bell, Pennsylvania 19422. Except as otherwise indicated in the footnotes of this table and pursuant to applicable community property laws, the persons named in the table have sole voting and investment power with respect to all shares of common stock. Beneficial ownership is determined in accordance with the rules of the SEC and generally includes voting or investment power with respect to securities.

(2)
Includes 2,625,000 shares underlying warrants that are exercisable within 60 days of December 31, 2008.

(3)
Includes 52,000 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(4)
Includes 1,250,000 shares underlying warrants that are exercisable within 60 days of September 30, 2008, and 1,283,333 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(5)
Includes 950,000 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(6)
Includes 633,333 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

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(7)
Includes 58,233 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008 and 542,536 shares to be issued on February 15, 2009 via a cashless exercise of options exercisable for up to 720,000 shares.

(8)
Includes 166,667 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(9)
Includes 13,333 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(10)
Includes 10,000 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

Security Ownership of Certain Beneficial Owners and Management of Inovio Following the Completion of the Transaction

        The following table sets forth certain information regarding the amount and percentage of the beneficial ownership of the Inovio's common stock, giving effect to the transaction presuming a Merger Exchange Ratio of 0.9911488, by: (i) each stockholder who VGX and Inovio believe will own beneficially more than five percent of Inovio's common stock upon completion of the Merger, based on ownership of capital stock of Inovio and/or VGX as of December 31, 2008, presuming approval of the Acquisition Agreement and Merger; (ii) each director anticipated to be appointed to Inovio's board of directors and each employee anticipated to be appointed or continue as an executive officer of Inovio at the Effective Time; and (iii) all of the anticipated directors and executive officers as a group.

        Beneficial ownership is determined in accordance with the rules of the SEC. In computing the number of shares beneficially owned by a stockholder and the percentage of ownership of that stockholder, shares of common stock underlying options, warrants, convertible preferred stock or convertible debt (excluding any shares issuable upon conversion of accrued interest on such convertible debt) held by that stockholder that are exercisable or convertible, as the case may be, within 60 days of December 31, 2008 are included, including giving effect to any acceleration of vesting, and resulting increase in beneficial ownership, that may occur for holders of Inovio options at the Effective Time of the Merger. Those shares, however, are not deemed outstanding for the purpose of computing the percentage ownership of any other person. Each stockholder's percentage of ownership in the following table is based upon the projected 86,634,003 shares of Inovio common stock anticipated to be outstanding upon completion of the Merger presuming no exercises or conversion of outstanding options, warrants or convertible debt prior to the closing. The figures below are not definitive and may change based on actual differences in the Merger Exchange Ratio as calculated at closing, the

194



additional vesting of securities prior to closing and changes in the number of shares of Inovio common stock actually outstanding immediately post-Merger.

 
  Beneficial Ownership  
Name of Beneficial Owner(1)
  Amount and Nature of
Beneficial Ownership of
Shares of Common Stock
  Percent of Class of Shares
of Common Stock
 

5% Stockholders

             

Ernest Shin(2)

    3,571,708     4.00 %

Directors and Executive Officers

             

J. Joseph Kim(3)

    14,464,165     16.23 %

Avtar Dhillon(4)

    1,408,107     3.11 %

Simon X. Benito(5)

    99,983     *  

Chin-Cheong Chong(6)

    178,709     *  

Morton Collins(7)

    227,965     *  

Peter Kies(8)

    343,951     *  

C. Jo White(9)

    627,728     *  

Niranjan Sardesai(10)

    165,192     *  

Kevin Rassas(11)

    714,489     *  

Gene Kim(12)

    941,592     1.08 %

Punit Dhillon(13)

    317,464     *  

Ruxandra Draghia-Akli(14)

    13,215     *  

Iacob Mathiesen(15)

    205,000     *  

Michael Fons(16)

    202,525     *  

All directors and executive officers as a group (14 persons)

    19,910,085     21.32 %

*
Less than one % of shares outstanding.

(1)
This table is based upon information supplied by officers, directors and principal stockholders. The address of each beneficial holder listed is the same as designated in the current beneficial ownership tables presented above. Except as otherwise indicated in these footnotes and pursuant to community property laws, to the extent applicable, the persons named in the table have sole voting and investment power with respect to all shares of common stock. Beneficial ownership is determined in accordance with the rules of the SEC and generally includes voting or investment power with respect to securities.

(2)
Includes 2,601,766 shares underlying warrants that are exercisable within 60 days of December 31, 2008.

(3)
Includes 1,238,936 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 1,271,974 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(4)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, 1,193,746 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing, and 93,750 shares of restricted stock which shall become fully vested upon closing.

(5)
Includes 1,544 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 91,250 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing.

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(6)
Includes 30,000 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing. Does not include 37,800 shares of common stock held of record for which Mr. Chong disclaims beneficial ownership.

(7)
Includes 9,912 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(8)
Includes 514 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 341,875 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing.

(9)
Includes 627,728 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(10)
Includes 151,976 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(11)
Includes 57,718 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008 and 537,734 shares to be issued on February 15, 2009 via a cashless exercise of options exercisable for up to 713,628 shares.

(12)
Includes 941,592 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(13)
Includes 1,029 shares underlying warrants that are exercisable within 60 days of December 31, 2008, and 316,250 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing.

(14)
Includes 13,215 shares of common stock issuable pursuant to options exercisable within 60 days of December 31, 2008.

(15)
Includes 115,000 shares of common stock underlying options which shall become fully vested and exercisable upon closing and 45,000 shares of restricted common stock that shall become fully vested upon closing.

(16)
Includes 202,500 shares of common stock issuable pursuant to options which shall become fully vested and exercisable upon closing.

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QUANTITATIVE AND QUALITATIVE DISCLOSURE ABOUT MARKET RISKS

Interest Rate Risk

        Market risk represents the risk of loss that may impact Inovio's, VGX's, or if the Merger is completed, the combined group's, consolidated financial position, results of operations or cash flows due to adverse changes in financial and commodity market prices and rates. Inovio is exposed to market risk primarily in the area of changes in United States interest rates and conditions in the credit markets, and the recent and consistent fluctuations in interest rates and availability of funding in the credit markets primarily impacts the performance of Inovio's investments. Inovio does not have any material foreign currency or other derivative financial instruments. Under Inovio's current policies, Inovio does not use interest rate derivative instruments to manage exposure to interest rate changes. Inovio attempts to increase the safety and preservation of its invested principal funds by limiting default risk, market risk and reinvestment risk. Inovio mitigates default risk by investing in investment grade securities.

        VGX currently does not have any substantial interest rate risk. VGX does not hold or issue financial instruments for trading or speculative purposes. VGX's unrestricted cash is invested in money market accounts and are held for working capital purposes. Due to the short-term nature of these investments, VGX believes that it does not have any material exposure to changes in the fair value of its investment portfolio as a result of changes in interest rates. Declines in interest rates, however, would reduce future investment income.

Fair Value Measurements

        All of Inovio's investment securities are classified as available-for-sale and therefore reported on the consolidated balance sheet at market value. Inovio's investment securities consist of high-grade ARS, corporate debt securities and government agency securities. As of September 30, 2008, Inovio's investments included $12.1 million of high-grade (AAA rated) ARS issued primarily by municipalities. Inovio's ARS are debt instruments with a long-term maturity and with an interest rate that is reset in short intervals through auctions. The recent conditions in the global credit markets have prevented some investors from liquidating their holdings of auction rate securities because the amount of securities submitted for sale has exceeded the amount of purchase orders for such securities. In early March 2008, Inovio was informed that there was insufficient demand at auctions for six of its high-grade auction rate securities, representing approximately $12.1 million. As a result, these affected securities are currently not liquid and the interest rates have been reset to the predetermined higher rates. When auctions for these securities fail, the investments may not be readily convertible to cash until a future auction of these investments is successful or they are redeemed or mature. If the credit ratings of the security issuers deteriorate and any decline in market value is determined to be other than temporary, Inovio would be required to adjust the carrying value of the investment through a permanent impairment charge. In the event Inovio needs to access the funds that are in an illiquid state, Inovio will not be able to do so without the possible loss of principal, until a future auction for these investments is successful or they are redeemed by the issuer or they mature. At this time, Inovio's management has not obtained sufficient evidence to conclude that these investments are permanently impaired or that they will not be settled in the short term, although the market for these investments is presently uncertain. If Inovio is unable to sell these securities in the market or they are not redeemed, then Inovio may be required to hold them to maturity. Inovio will continue to monitor and evaluate these investments on an ongoing basis for permanent impairment.

        Inovio adopted the provisions of SFAS No. 157 effective January 1, 2008 and have determined that Inovio utilizes unobservable (Level 3) inputs in determining the fair value of its ARS investments held at September 30, 2008. The estimated fair value of all Inovio's ARS holdings at September 30, 2008 is $12.1 million, which reflects a $1.5 million adjustment to the principal value (cost) of $13.6 million as of September 30, 2008. All of the $12.1 million of ARS are classified within non current assets in

197



Inovio's unaudited condensed consolidated balance sheet as of September 30, 2008. Inovio currently believes that the temporary decline in fair value is due entirely to liquidity issues in the market. All of Inovio's ARS have maintained their credit ratings of AAA, continue to pay interest obligations and the underlying assets for the majority of securities are almost entirely backed by the U.S. government or free from subprime lending issues currently being experienced in the financial markets. In addition, Inovio believes with is current cash and anticipated proceeds from its line of credit secured by the ARS, that its holdings of ARS will not be required for operational purposes for the next twelve months, which Inovio believes allows sufficient time for the securities to return to full value. Inovio will re-evaluate each of these factors as market conditions change in subsequent periods.

        On December 19, 2008, Inovio accepted an offer by UBS of certain rights to cause UBS to purchase the ARS at a future date. UBS offered the repurchase rights in connection with its obligations under settlement agreements with the SEC and other federal and state regulatory authorities, and as a result of accepting UBS's offer, Inovio, via its wholly-owned subsidiary Genetronics, which holds the ARS, can require UBS to repurchase at par value all of the ARS at any time during the period from June 30, 2010 through July 2, 2012, if such ARS have not previously been sold by Genetronics or by UBS on its behalf. In conjunction with the acceptance of the rights offering, Genetronics also obtained an increase in its the credit line up to $12.1 million, with the ARS pledged as collateral, which Genetronics fully drew down on December 23, 2008.

Foreign Currency Risk

        Inovio has operated primarily in the United States and most transactions during the three and nine months ended September 30, 2008, have been made in U.S. dollars. Accordingly, Inovio does not have any material exposure to foreign currency rate fluctuations, nor does it have any foreign currency hedging instruments in place.

        Inovio has conducted clinical trials in Europe in conjunction with several clinical research organizations, where Inovio has clinical sites being monitored by clinical research associates. While invoices relating to these clinical trials are generally denominated in U.S. dollars, Inovio's financial results could be affected by factors such as inflation in foreign currencies, in relation to the U.S. dollar, in markets where these vendors have assisted Inovio in conducting these clinical trials. Certain transactions related to Inovio and its subsidiaries Inovio AS and Inovio Asia Pte. Ltd. ("IAPL"), are denominated primarily in foreign currencies, including Euros, British Pounds, Canadian Dollars, Norwegian Kroner, Swedish Krona, and Singapore Dollars. As a result, Inovio's financial results could be affected by factors such as changes in foreign currency exchange rates or weak economic conditions in foreign markets where Inovio conducts business, including the impact of the existing crisis in the global financial markets in such countries and the impact on both the U.S. dollar and the noted foreign currencies.

        Inovio does not use derivative financial instruments for speculative purposes. Inovio does not engage in exchange rate hedging or hold or issue foreign exchange contracts for trading purposes. Currently, Inovio does not expect the impact of fluctuations in the relative fair value of other currencies to be material in 2008.

        VGX does have a foreign exchange rate risk with regards to its investment in its affiliate, VGX International, of which it holds 30.37% of outstanding shares. VGX International is a publicly-traded company on the Korean Stock Exchange. VGX recognizes its investment in VGX International using the equity method of reporting for the treatment of investments. Therefore, any losses or gains of VGX International, whose functional currency is Korean Wons, is translated into U.S. Dollars and recognized in the financials of VGX. In the event of sale of shares of VGX International, VGX would be subject to both equity price risk as well as foreign exchange rate risk. There are no current plans to reduce VGX's stake in VGX International.

        VGX also owns 88.1% of outstanding shares in VGX Animal Health, which sells its LifeTide™ SW 5 GHRH DNA therapy to the porcine market in Australia, and is thus subject to the commodity price risk of the porcine market. The ability to meet the revenue projections of LifeTide™ SW 5 is highly correlated with the health of the swine industry in Australia.

198



CAPITAL STRUCTURE OF INOVIO

Capital Stock

        The authorized capital stock of Inovio consists of 300,000,000 shares of Inovio common stock, par value $0.001 per share and 10,000,000 shares of Inovio preferred stock, par value $0.001 per share. As of the record date:

    [                        ] shares of Inovio common stock were issued and [                        ] shares were outstanding;

    [                        ] shares of Inovio preferred stock were issued, of which 71 shares of Inovio Series C Cumulative Convertible Preferred Stock were outstanding;

    [                        ] shares of Inovio common stock were reserved for issuance upon exercise of outstanding options granted pursuant to the Inovio's equity incentive plans; and

    [                        ] shares of Inovio common stock were reserved for issuance upon exercise of outstanding Inovio warrants.

        No shares of Inovio common stock are owned or held by any subsidiary of Inovio. All of the outstanding shares of capital stock of Inovio are, and all shares of capital stock of Inovio which may be issued pursuant to the Inovio options or the Inovio warrants will be, when issued, duly authorized and validly issued, fully paid and nonassessable and not subject to any preemptive rights. No outstanding shares of Inovio common stock are subject to a repurchase option or risk of forfeiture in favor of Inovio. Inovio has no obligation to issue any shares of the Inovio preferred stock and the Inovio preferred stock is not subject to any demand rights.

Stock Options

        Except for the Inovio's previously reported equity incentive plans, as filed with the SEC and listed on the exhibit index to the registration statement of which this joint proxy statement/prospectus is a part, Inovio does not have any stock option plan or any other plan, program, agreement or arrangement providing for any equity or equity-based compensation for any person. Inovio has a current reserve of 57,938 shares of Inovio common stock for future issuances of awards under its equity incentive plans, and as of the record date [                        ] shares are subject to outstanding Inovio options.

Warrants

        As of the record date, Inovio has a reserve of [                        ] shares of common stock for issuance upon exercise of the Inovio warrants outstanding.

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COMPARISON OF RIGHTS OF HOLDERS OF INOVIO COMMON STOCK
AND VGX COMMON STOCK

        Inovio is incorporated in the State of Delaware and the rights of Inovio stockholders are currently governed by the DGCL, by Inovio's certificate of incorporation (including the Certificates of Designations, Rights and Preferences for Inovio's preferred stock) and Inovio's bylaws. VGX is incorporated in the State of Delaware and the rights of VGX stockholders are currently governed by the DGCL, by VGX's certificate of incorporation and VGX's bylaws. After the completion of the Merger, stockholders of VGX will become stockholders of Inovio, and will become subject to Inovio's certificate of incorporation and bylaws.

        The following is a summary of the material differences between the rights of Inovio common stockholders and the rights of VGX common stockholders. While Inovio and VGX believe that this summary covers the material differences between the two, this summary may not contain all of the information that is important to you. This summary is not intended to be a complete discussion of the respective rights of Inovio common stockholders and VGX common stockholders and it is qualified in its entirety by reference to Delaware law and the various documents of Inovio and VGX referenced in this summary. This summary should be carefully read, along with this entire joint proxy statement/prospectus and the other documents referenced in this joint proxy statement/prospectus, for a more complete understanding of the differences between being a stockholder of Inovio and being a stockholder of VGX. Inovio has filed with the SEC certain documents referred to this summary and will send copies of these documents to you upon your request. See the section entitled " Where You Can Find More Information About Inovio " on page 223.

 
  Inovio   VGX

Capitalization

  The authorized capital stock of Inovio consists of: (i) 300,000,000 shares of common stock, par value $0.001 per share and (ii) 10,000,000 shares of preferred stock, par value $0.001 per share.   The authorized capital stock of VGX consists of: (i) 100,000,000 shares of common stock, par value $0.0001 per share and (ii) 1,000,000 shares of preferred stock, par value $0.0001 per share.

 

As of the record date, 2008 (i)  [                        ] shares of common stock were issued and outstanding; (ii)  [                        ] shares of preferred stock were issued and outstanding, of which [                        ] were Series C Cumulative Convertible Preferred Stock; (iii)  [                        ] shares of common stock were reserved for issuance upon exercise of outstanding options granted pursuant to the Inovio incentive plans; and (iv) [                        ] shares of common stock were reserved for issuance upon exercise of outstanding Inovio warrants.

 

As of the record date, 2008, (i)  [                        ] shares of common stock were issued and outstanding; (ii)  [                        ] shares of preferred stock were issued and outstanding; (iii)  [                        ] shares of common stock were reserved for issuance upon exercise of outstanding options granted pursuant to the VGX option plan; (iv) [                        ] shares of common stock were reserved for issuance upon exercise of outstanding VGX warrants; and (v) [                        ] shares of common stock were reserved for issuance upon conversion of outstanding notes evidencing the VGX convertible debt.

Number of Directors             

 

The Inovio certificate of incorporation and bylaws provide that the number of directors shall initially be set at eight, and Inovio currently has nine directors.

 

The VGX bylaws provide that the board of directors shall initially consist of three members, and VGX currently has three directors.

200


 
  Inovio   VGX

Election and Term of Directors

 

The Inovio certificate of incorporation and bylaws provide that the directors shall be elected at each annual meeting of the stockholders and shall hold office until the expiration of the term for which he or she was elected and until his or her respective successor is elected, except in the case of the death, resignation or removal of any director.

 

The VGX bylaws provide that the stockholders shall elect directors at the annual meeting of stockholders and a director shall hold office until the expiration of the term for which he or she was selected and until a successor shall have been elected and qualified or until his or her earlier death, resignation or removal.

Removal of Directors

 

The Inovio certificate of incorporation provides that, subject to the rights of the holders of any series of preferred stock then outstanding, any director, or the entire board of directors, may be removed from office at any time, with or without cause, but only by the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of capital stock of the corporation entitled to vote generally in the election of directors, voting together as a single class.

 

The VGX bylaws provide that any director or the entire board of directors may, unless otherwise provided by law, be removed with or without cause by the holders of shares entitled to cast a majority of the votes which all stockholders are entitled to cast at an election of directors.

Vacancies on the Board of Directors

 

The Inovio certificate of incorporation provides that subject to the rights of the holders of any series of preferred stock then outstanding, newly created directorships resulting from any increase in the authorized number of directors or any vacancies in the board of directors resulting from death, resignation or other cause ( other than removal from office by a vote of the stockholders ) may be filled only by a majority vote of the directors then in office, though less than a quorum, and directors so chosen shall hold office for a term expiring at the next annual meeting of stockholders at which the term of office expires, and until their respective successors are elected, except in the case of the death, resignation, or removal of any director. No decrease in the number of directors constituting the board of directors shall shorten the term of any incumbent director. Further, subject to the rights of the holders of any series of preferred stock then outstanding, a vacancy resulting from the removal of a director by the stockholders may be filled at a special meeting of the stockholders held for that purpose.

 

The VGX bylaws provide that vacancies and newly created directorships resulting from any increase in the authorized number of directors elected by all of the stockholders having a right to vote as a single class may be filled by a majority of the directors then in office, through less than a quorum, or by a sole remaining director, and the directors so chosen shall hold office until their successors are elected and qualified or until their earlier death, resignation or removal. If there are no directors in office, then an election of directors may be held in the manner provided by statute. Whenever the holders of any class or classes of stock or series thereof are entitled to elect one or more directors by the provisions of the amended and restated certificate of incorporation, vacancies and newly created directorships of such class or classes or series may be filled by a majority of the directors elected by such class or classes or series thereof then in office, or by a sole remaining director so elected.

201


 
  Inovio   VGX

Amendment to Certificate of Incorporation

  The Inovio certificate of incorporation provides that Inovio may amend or repeal any provision contained in its certificate of incorporation; provided , however , that, notwithstanding any other provision of its certificate of incorporation or any provision of law which might otherwise permit a lesser vote or no vote, but in addition to any vote of the holders of any class or series of the stock of Inovio required by law or by its certificate of incorporation, the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of the capital stock of Inovio entitled to vote generally in the election of directors, voting together as a single class, shall be required to amend or repeal certain articles of Inovio's certificate of incorporation regarding board procedures and indemnification.   The VGX certificate of incorporation provides that VGX has the right at any time, and from time to time, to amend, alter, change or repeal any provision contained in its certificate of incorporation.

Amendment to Bylaws

 

The Inovio certificate of incorporation provides that the Inovio board of directors is expressly empowered to adopt, amend or repeal Inovio's bylaws. The stockholders shall also have power to adopt, amend or repeal Inovio's bylaws. Any adoption, amendment or repeal of Inovio's bylaws by the stockholders shall require, in addition to any vote of the holders of any class or series of stock of Inovio required by law or by the certificate of incorporation, the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of Inovio's capital stock entitled to vote generally in the election of directors, voting together as a single class.

 

The VGX bylaws provide that such bylaws may be altered, amended or repealed or new bylaws may be adopted either (1) by vote of the stockholders at a duly organized annual or special meeting of stockholders, or (2) by vote of a majority of the board of directors at any regular or special meeting of directors.

202


 
  Inovio   VGX

General Meeting of Stockholders

 

Inovio's bylaws provide that the annual meeting of stockholders for the election of directors and for the transaction of such other business as may properly be brought before the meeting shall be held on a date to be fixed by the board of directors or the president and chief executive officer at the time and place to be fixed by the board of directors or the president and stated in the notice of the meeting.

 

VGX's bylaws provide that the board of directors may fix and designate the date and time of the annual meeting of the stockholders, but if no such date and time is fixed and designated by the board, the meeting for any calendar year shall be held on the first day of March in such year, if not a legal holiday under the laws of Delaware, and, if a legal holiday, then on the next succeeding business day, not a Saturday, at 9:00 a.m., and at said meeting the stockholders then entitled to vote shall elect directors and shall transact such other business as may properly be brought before the meeting.

Special Meeting of Stockholders

 

Inovio's bylaws provide that special meetings of stockholders may be called at any time by the board of directors.

 

The VGX bylaws provide that special meetings of the stockholders of the corporation may be called at any time by the chairman of the board, a majority of the board of directors, the president, or at the request, in writing, of stockholders entitled to cast at least a majority of the votes that all stockholders are entitled to cast at the particular meeting.

Notice of Stockholder Meetings

 

Inovio's bylaws provide that written notice of each annual or special meeting of stockholders shall be given not less than 10 nor more than 60 days before the date on which the meeting is to be held. The notice required shall be given to each stockholder entitled to vote at such annual or special meeting and shall state the place, date and hour and purpose or purposes of the meeting.

 

The VGX bylaws provide that written notice of the place, date and hour of every meeting of the stockholders, whether annual or special, shall be given to each stockholder of record entitled to vote at a the meeting not less than 10 nor more than 60 days before the date of the meeting. Every notice of a special meeting shall state the purpose or purposes thereof.

Stockholder Nominations and Proposals

 

Inovio's bylaws provide that at an annual meeting of stockholders, only such business shall be conducted as shall have been properly brought before the meeting. For business to be properly brought before an annual meeting by a stockholder, the stockholder must have given timely notice thereof in writing to the secretary of Inovio, the period for which will depend on the nature of the proposal and whether such proposal is subject to SEC Rule 14a-8.

 

VGX has no comparable provision in its organizational documents and thus any stockholder proposals would be governed by the DGCL.

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  Inovio   VGX

Nomination of Director Candidates

 

The Inovio bylaws provide that subject to the rights of holders of any class or series of preferred stock then outstanding, nominations for the election of directors may be made by the board of directors or a proxy committee appointed by the board of directors or by any stockholder entitled to vote in the election of directors generally.

 

VGX has no comparable provision in its organizational documents and thus any director nominations or appointments would be governed by the DGCL.

Proxy

 

Inovio's bylaws provide that each stockholder of record entitled to vote at a meeting of stockholders may authorize any other person or persons to vote or act for him by written proxy executed by the stockholder. No stockholder may authorize more than one proxy for his shares.

 

The VGX bylaws provide that a stockholder may execute a writing authorizing another person or persons to act for the stockholder as proxy.

The VGX bylaws also provide that no proxy shall be voted or acted upon after 3 years from its date, unless the proxy provides for a longer period.

Furthermore, a duly executed proxy shall be irrevocable if it states that it is irrevocable and if, and only so long as, it is coupled with an interest sufficient in law to support an irrevocable power.

Voting Rights

 

Inovio's bylaws provide that each stockholder shall have one vote for each share of stock entitled to vote held of record by such stockholder and a proportionate vote for each fractional share so held, unless otherwise provided by law. Inovio's preferred stockholders generally vote with Inovio's common stockholders on an as-converted basis.

 

VGX's certificate of incorporation and bylaws provide that each stockholder shall be entitled to one vote, in person or by proxy, for each share of capital stock having voting power held by such stockholder. Further, VGX's certificate of incorporation provides that the holders of common stock shall vote together as a single class on all matters submitted to stockholders for a vote and VGX stockholders shall not have the right to cumulate their votes for the election of the corporation's directors.

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  Inovio   VGX

Stockholder Action at a Meeting

 

Inovio's bylaws provide that when a quorum is present at any meeting, any election shall be determined by a plurality of the votes cast by the stockholders entitled to vote at the election, and all other matters shall be determined by a majority of the votes cast affirmatively or negatively on the matter (or if there are two or more classes of stock entitled to vote as separate classes, then in the case of each such class, a majority of each such class present or represented and voting affirmatively or negatively on the matter) shall decide such matter, except when a different vote is required by express provision of law, the certificate of incorporation or the bylaws.

 

The VGX bylaws provide that directors shall be elected by a plurality of the votes of the shares present in person or represented by proxy at the meeting and entitled to vote on the election of directors.

In all matters other than the election of directors, the affirmative vote of the majority in voting power of shares present in person or represented by proxy at the meeting and entitled to vote thereon shall be the act of the stockholders, unless the question is one upon which, by express provision of the applicable statute, the amended and restated certificate of incorporation or the VGX bylaws, a different vote is required in which case such express provision shall govern and control the decision of the question.

Stockholder Action by Written Consent

 

Inovio's certificate of incorporation provides that any action required or permitted to be taken by the stockholders of Inovio must be effected at a duly called annual or special meeting of stockholders of Inovio and may not be effected by any consent in writing by such stockholders.

 

The VGX bylaws provide that any action required to be taken at any annual or special meeting of stockholders of the corporation, or any action which may be taken at any annual or special meeting of such stockholders, may be taken without a meeting, without prior notice and without a vote, if a consent or consents in writing, setting forth the action so taken, shall be signed by the holders of outstanding stock having not less than the minimum number of votes that would be necessary to authorize or take such action at a meeting at which all shares entitled to vote thereon were present and voted.

Dividends

 

Inovio has no comparable provision in its organizational documents and thus any dividends would be governed by Sections 170 through 174 of the DGCL.

 

The VGX certificate of incorporation provides that subject to provisions of law, the certificate of incorporation and any certificate of designation with respect to any preferred stock, the holders of common stock shall be entitled to receive dividends out of funds legally available therefor at such times and in such amounts as the board of directors may determine in its sole discretion.

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  Inovio   VGX

Liquidation

 

Liquidation of Inovio would be governed by the provisions of the Certificates of Designations, Rights and Preferences for any Inovio preferred stock outstanding, with Inovio common stock participating in distributions upon satisfaction of the liquidation preferences of the outstanding Inovio preferred stock.

 

The VGX certificate of incorporation provides that upon any liquidation, dissolution or winding up of the corporation, whether voluntary or involuntary, after the payment or provision for payment of all debts and liabilities of the corporation and all preferential amounts to which the holders of the preferred stock are entitled with respect to the distribution of assets in liquidation, the holders of common stock shall be entitled to share ratably in the remaining assets of the corporation available for distribution.

Right of Inspection

 

Inovio has no comparable provision in its organizational documents and thus any rights of inspection would be governed by Section 220 of the DGCL which provides that any stockholder, in person or by attorney or other agent, shall, upon written demand under oath stating the purpose thereof, have the right during the usual hours for business to inspect for any proper purpose, and to make copies and extracts from Inovio's stock ledger, a list of its stockholders, and its other books and records.

 

VGX's bylaws provide that every stockholder shall, upon written demand under oath stating the purpose thereof, have a right to examine, in person or by agent or attorney, during the usual hours for business, for any proper purpose, the stock ledger, list of stockholders, books or records of account, and records of the proceedings of the stockholders and directors of the corporation, and to make copies or extracts therefrom. A proper purpose shall mean a purpose reasonably related to such person's interest as a stockholder.

Liability of Director and Officer

 

Inovio's certificate of incorporation provides that a director of Inovio shall not be personally liable to the corporation or its stockholders for monetary damages for breach of fiduciary duty as a director, except for liability (i) for any breach of the director's duty of loyalty to the corporation or its stockholders, (ii) for acts or omissions not in good faith or which involved intentional misconduct or a knowing violation of law, (iii) under Section 174 of the DGCL, or (iv) for any transaction from which the director derived an improper personal benefit.

 

The VGX certificate of incorporation provides that the directors of the corporation shall be entitled to the benefits of all limitations on the liability of directors generally that are now or hereafter become available under the DGCL. Without limiting the generality of the foregoing, no director of the corporation shall be liable to VGX or its stockholders for monetary damages for breach of fiduciary duty as a director, except for liability (i) for any breach of the director's duty of loyalty to corporation or its stockholders, (ii) for acts or omissions not in good faith or which involve intentional misconduct or a knowing violation of law, (iii) under Section 174 of the DGCL, or (iv) for any transaction from which the director derived an improper personal benefit.

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  Inovio   VGX

Indemnification of Directors and Officers

 

Inovio's bylaws provide that each person who was or is made a party or is threatened to be made a party to or is involved in any action, suit or proceeding, whether civil, criminal, administrative or investigative ("proceeding"), by reason of the fact that he or she or a person of whom he or she is the legal representative, is or was a director or officer of Inovio or is or was serving at the request of the corporation as a director or officer of another corporation, or of a partnership, joint venture, trust or other enterprise, including service with respect to employee benefit plans, whether the basis of such proceeding is alleged action in an official capacity as a director, officer or employee or in any other capacity while serving as a director, officer or employee, shall be indemnified and held harmless by Inovio to the fullest extent authorized by Delaware Law, as the same exists or may hereafter be amended (but, in the case of any such amendment, only to the extent that such amendment permits the corporation to provide broader indemnification rights than said law permitted the corporation to provide prior to such amendment) against all expenses, liability and loss reasonably incurred or suffered by such person in connection therewith and such indemnification shall continue as to a person who has ceased to be a director, officer or employee and shall inure to the benefit of his or her heirs, executors and administrators; provided , however , that, except as provided in Section 7.2 of Article 7 of Inovio's bylaws, Inovio shall indemnify any such person seeking indemnity in connection with an action, suit or proceeding (or part thereof) initiated by such person only if (a) such indemnification is expressly required to be made by law, (b) the action, suit or proceeding (or part thereof) was authorized by the board of directors of Inovio, (c) such indemnification is provided by the corporation, in its sole discretion, pursuant to the powers vested in the corporation under the DGCL, or (d) the action, suit or proceeding (or

 

VGX's certificate of incorporation provides that VGX shall indemnify any person who was or is an authorized representative of the corporation, and who was or is a party, or is threatened to be made a party to any third party proceeding, by reason of the fact that such person was or is an authorized representative of the corporation, against expenses, judgments, fines and amounts paid in settlement actually and reasonably incurred by such person in connection with such third party proceeding if such person acted in good faith and in a manner such person reasonably believed to be in, or not opposed to, the best interests of the corporation and, with respect to any criminal third party proceeding, had no reasonable cause to believe such conduct was unlawful. The termination of any third party proceeding by judgment, order, settlement, conviction or upon a plea of nolo contender or its equivalent, shall not of itself create a presumption that the authorized representative did not act in good faith and in a manner which such person reasonably believed to be in or not opposed to, the best interests of the corporation, and, with respect to any criminal third party proceeding, had reasonable cause to believe that such conduct was unlawful.

Further, VGX shall indemnify any person who was or is an authorized representative of the corporation, and who was or is a party, or is threatened to be made a party to any corporate proceeding, by reason of the fact that such person was or is an authorized representative of the corporation, against expenses actually and reasonably incurred by such person in connection with the defense or settlement of such corporate proceedings if such person acted in good faith and in a manner reasonably believed to be in, or not opposed to, the best interests of the corporation and except that no indemnification shall be made in respect of any claim issue or matter as to which such person shall have been adjudged to be

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  Inovio   VGX

  part thereof) is brought to establish or enforce a right to indemnification under an indemnity agreement or any other statute or law or otherwise as required under Section 145 of the DGCL. Such right shall be a contract right and shall include the right to be paid by Inovio expenses incurred in defending any such proceeding in advance of its final disposition; provided , however , that, unless the DGCL then so prohibits, the payment of such expenses incurred by a director or officer of Inovio in his or her capacity as a director or officer (and not in any other capacity in which service was or is tendered by such person while a director or officer, including, without limitation, service to an employee benefit plan) in advance of the final disposition of such proceeding, shall be made only upon delivery to Inovio of an undertaking, by or on behalf of such director or officer, to repay all amounts so advanced if it should be determined ultimately that such director or officer is not entitled to be indemnified.   liable to the corporation unless and only to the extent that the Court of Chancery or the court in which such corporate proceeding was brought shall determine upon application that, despite the adjudication of liability but in view of all the circumstances of the case, such authorized representative is fairly and reasonably entitled to indemnity for such expenses which the Court of Chancery or such other court shall deem proper.

To the extent that a present or former authorized representative of the corporation has been successful on the merits or otherwise in defense of any third party or corporate proceeding or in defense of any claim, issue or matter therein, such person shall be indemnified against expenses actually and reasonably incurred by such person in connection therewith.

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SPECIAL MEETING OF INOVIO STOCKHOLDERS

Questions and Answers About The Inovio Special Meeting

        The Inovio special meeting will be held on [                        ], 2009 at [                        ], local time, at Inovio's principal executive offices, located at 11494 Sorrento Valley Road, San Diego, California 92121. Inovio is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because Inovio's board of directors is soliciting their proxy to vote at the Inovio special meeting.

        There are two matters scheduled for a vote at the Inovio special meeting:

        Only Inovio's stockholders of record at the close of business on [                        ], 2009, the "record date," will be entitled to vote at the Inovio special meeting. On the record date, there were [                        ] shares of Inovio common stock outstanding and entitled to vote.

        If on the record date, the shares of an Inovio stockholder were registered directly in such stockholder's name with Inovio's transfer agent, Computershare Trust Company, then such Inovio stockholder is a "stockholder of record." As a stockholder of record, the Inovio stockholder may vote in person at the meeting or vote by proxy. Whether or not an Inovio stockholder of record plans to attend the meeting, Inovio urges such stockholders to fill out and return the enclosed proxy card to ensure his or her or its vote is counted.

        If on the record date, the shares of an Inovio stockholder were held, not in such stockholder's name, but rather in an account at a brokerage firm, bank, dealer or other similar organization, then such Inovio stockholder is the beneficial owner of shares held in "street name" and these proxy materials are being forwarded to such stockholder by that organization. The organization holding such Inovio stockholder's account is considered to be the stockholder of record for purposes of voting at the special meeting. As a beneficial owner, the Inovio stockholder has the right to direct such stockholder's broker or other agent on how to vote the shares in such stockholder's account. These Inovio stockholders are also invited to attend the special meeting. However, since such Inovio stockholders are

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not the stockholder of record, they may not vote their shares in person at the meeting unless they request and obtain a valid proxy from their broker or other agent.

        Inovio stockholders may vote "For" or "Against" each proposal or abstain from voting. The procedures for voting are as follows:

        If an Inovio stockholder is a stockholder of record, such stockholder may vote in person at the Inovio special meeting or vote by proxy using the enclosed proxy card. Whether or not such Inovio stockholder plans to attend the meeting, Inovio urges such stockholder to vote by proxy to ensure such stockholder's vote is counted. An Inovio stockholder may still attend the meeting and vote in person if such Stockholder has already voted by proxy.

        To vote in person, as Inovio stockholder must come to the special meeting and Inovio will give each stockholder a ballot when he, she or its authorized representative arrives.

        To vote using the proxy card, an Inovio stockholder must complete, sign and date the enclosed proxy card and return it promptly in the envelope provided. If an Inovio stockholder returns such stockholder's signed proxy card to Inovio before the special meeting, or brings his or her proxy card to the meeting, Inovio will vote such stockholder's shares as he, she or it directs.

        If an Inovio stockholder is a beneficial owner of shares registered in the name of a broker, bank or other agent, such stockholder should have received a proxy card and voting instructions with these proxy materials from that organization rather than from Inovio. An Inovio stockholder shall simply complete and mail the proxy card to ensure that such stockholder's vote is counted.

        To vote in person at the Inovio special meeting, an Inovio stockholder must obtain a valid proxy from such stockholder's broker, bank or other agent. An Inovio stockholder shall follow the instructions from such stockholder's broker or bank included with these proxy materials, or contact such stockholder's broker or bank to request a proxy form.

        On each matter to be voted upon, an Inovio stockholder has one vote for each share of common stock and 1,470 votes for each share of Series C preferred stock he, she or it owns as of the record date.

        If an Inovio stockholder returns a signed and dated proxy card without marking any voting selections, such stockholder's shares will be voted "For" all proposals presented for voting as described in this joint proxy statement/prospectus, including the issuance of Inovio securities in the Merger and the amendment to the Inovio 2000 Plan. If any other matter is properly presented at the meeting, such Inovio stockholder's proxy (one of the individuals named on such stockholder's proxy card) will vote such stockholder's shares using his or her best judgment.

        Inovio will pay for the entire cost of soliciting proxies from its stockholders. In addition to these mailed proxy materials, Inovio's directors and employees may also solicit proxies in person, by

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telephone or by other means of communication. Directors and employees will not be paid any additional compensation for soliciting proxies. Inovio will also reimburse brokerage firms, banks and other agents for the cost of forwarding proxy materials to beneficial owners.

        If an Inovio stockholder receives more than one proxy card, such stockholder's shares are registered in more than one name or are registered in different accounts. Such Inovio stockholder must complete, sign and return each proxy card to ensure that all of the shares are voted.

        Yes. An Inovio stockholder can revoke such stockholder's proxy at any time before the final vote at the meeting. An Inovio stockholder who is the record holder of the Inovio shares may revoke such stockholder's proxy by any one of three ways:

        If an Inovio stockholder's shares are held by a broker or bank as a nominee or agent, such stockholder should follow the instructions provided by the Inovio stockholder's broker or bank.

        Votes will be counted by the inspector of election appointed for the meeting, who will separately count "For" and "Against" votes, abstentions and broker non-votes. Abstentions will be counted towards the vote total for each proposal and will have the same effect as "Against" votes.

        If an Inovio stockholder does not give instructions to such stockholder's broker, the broker can vote such shares with respect to discretionary items, but not with respect to non-discretionary items. On non-discretionary items for which an Inovio stockholder does not give such stockholder's broker instructions, the shares will be treated as "broker non-votes." All of the proposals to be presented at the Inovio special meeting may be considered non-discretionary items, and thus Inovio encourages its stockholders holding shares in street name to instruct their brokers on how to vote. The effect of a broker non-vote will depend on the number and method of calculation of votes needed to approve each proposal.

        To be approved, Proposal 1, the Merger, pursuant to the terms of the Acquisition Agreement, including the issuance of Inovio securities, must receive a "For" vote from holders of a majority of the shares of Inovio common stock entitled to vote and present at the Inovio special meeting, either in person or by proxy duly authorized. Abstentions will have the same effect as a vote "Against" the proposal; although present for a quorum, broker non-votes are not deemed entitled to vote and will have no effect. As of the record date, there were [                                    ] shares of Inovio common stock outstanding and [71] shares of Inovio Series C preferred stock outstanding. Inovio cannot predict how many shares of Inovio capital stock entitled to vote will do so, and thus cannot specify a minimum numbers of votes "For" the Merger, including adoption of the Acquisition Agreement and the resulting issuance of Inovio securities, necessary to approve the proposal.

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        To be approved, Proposal 2, the amendment and restatement of the Inovio 2000 Plan to clarify the acceleration of vesting of Inovio options issued and outstanding thereunder at the Effective Time and to remove the termination of unexercised Inovio options issued and outstanding thereunder at the Effective Time, must receive a "For" vote from holders of a majority of the shares of Inovio common stock entitled to vote and present at the Inovio special meeting, either in person or by proxy duly authorized. If an Inovio stockholder "Abstains" from voting, it will have the same effect as an "Against" vote; although present for a quorum, broker non-votes are not deemed entitled to vote and thus will have no effect. As of the record date, there were [                                    ] shares of Inovio common stock outstanding and [71] shares of Series C preferred stock outstanding. Inovio cannot predict how many shares of Inovio capital stock entitled to vote will do so, and thus cannot specify a minimum numbers of votes "For" the amendment and restatement of Inovio's 2000 Plan regarding the vesting of Inovio options issued and outstanding and to remove the termination of unexercised Inovio options issued and outstanding under the Inovio 2000 Plan, to approve the proposal.

        A quorum of stockholders is necessary to hold a valid meeting. A quorum will be present if the holders of at least one-third of the the outstanding shares of Inovio capital stock entitled to vote are present at the Inovio special meeting, either in person or by proxy duly authorized. On the record date, there were [                                    ] shares of Inovio common stock outstanding and entitled to vote; plus 71 outstanding shares of Series C preferred stock entitled to vote with the common stock as a combined class, on an as-converted basis. Thus, [                                    ] shares of Inovio capital stock must be represented by stockholders present at the meeting either in person or by proxy to have a quorum.

        The shares an Inovio stockholder holds will be counted towards the quorum only if he, she or it submits a valid proxy (or one is submitted on such stockholder's behalf by such stockholder's broker, bank or other nominee) or if the stockholder votes at the meeting. Abstentions and broker non-votes will be counted towards the quorum requirement. If there is no quorum, the meeting may be adjourned either by the chairman of the meeting or by vote of the holders of a majority of the shares represented at the meeting.

        If you are an Inovio stockholder and you do not submit a proxy card, directly or through your broker, or vote at the Inovio special meeting, it will make it difficult for Inovio to establish a quorum necessary to transact business at the Inovio special meeting. If you are an Inovio stockholder and you submit a proxy card and affirmatively elect to abstain from voting, your proxy will be counted as present for the purpose of determining the presence of a quorum but will not be voted on any of the proposals relating to the Merger. If a quorum is established, but you do not vote in person or by proxy, or if a broker fails to vote your shares, such failure may interfere with Inovio's ability to close the proposed Merger as Inovio may not receive the votes required to approve the proposals described in this joint proxy statement/prospectus.

        Yes. The closing of the Merger which is the subject of Proposal 1 is conditioned on the approval of Proposal 2. Additionally, if Proposal 1 is not approved by the Inovio stockholders, but Proposal 2 is, the Inovio board in its discretion can determine whether to take action to consummate the changes anticipated by Proposal 2.

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        Preliminary voting results will be announced at the Inovio special meeting. Final voting results will be published in the earlier of a Current Report on Form 8-K announcing the closing of the Merger, if the proposals are approved by the Inovio stockholders and the VGX stockholders provide necessary approvals at the VGX special meeting, or Inovio's periodic report for the reporting period during which the Inovio special meeting occurs.

        Inovio does not currently intend to seek an adjournment of the Inovio special meeting. However, adjournments may be made for the purpose of, among other things, soliciting additional proxies. Under Inovio's bylaws, the Inovio special meeting may be adjourned from time to time either by the chairman of the meeting or by the vote of a majority of the shares represented thereat. When the Inovio special meeting is adjourned to another time or place, notice need not be given of the adjourned meeting if the time and place are announced at the meeting at which the adjournment is taken. At the adjourned meeting, Inovio may transact any business which might have been transacted at the original meeting.

Proposal 1—Approval of Merger and Acquisition Agreement, Including Issuance of Inovio Securities

        As discussed elsewhere in this joint proxy statement/prospectus, the holders of Inovio common stock are being asked to approve a business combination with VGX, pursuant the Acquisition Agreement between Inovio, Submerger and VGX, whereby VGX will merge with and into Submerger, Inovio will issue shares of its common stock to VGX stockholders in exchange for all outstanding shares of common stock of VGX and Inovio will assume all outstanding VGX options, warrants and, on a consolidated basis, convertible debt, on the terms and conditions set forth elsewhere in this joint proxy statement/prospectus. Holders of Inovio common stock should read carefully this joint proxy statement/prospectus, including the Annexes, in its entirety for more detailed information concerning the Acquisition Agreement and the Merger. In particular, holders of Inovio common stock are directed to:

        As discussed elsewhere in this joint proxy statement/prospectus, receipt of the requisite approvals from the Inovio and VGX stockholders for the Merger is only one condition of many to the consummation of the Merger. If approved, Inovio and VGX hope to complete the Merger shortly after obtaining the requisite stockholder approvals at the Inovio special meeting and the VGX special meeting, and believe the closing will occur prior to March 31, 2009. However, Inovio and VGX cannot predict the exact timing of the completion of the Merger because the Merger is subject to several conditions. There may be a substantial period of time between the Inovio and VGX special meetings and the completion of the Merger, and Inovio and VGX may not complete the Merger by March 31, 2009. For a detailed description of the conditions to the transaction, see the section entitled

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"Conditions to the Transaction" on page 113. The Merger will not be effective, including the issuance of the Inovio securities as consideration for the Merger, until such time as Submerger and VGX file the necessary certificate of merger with the Secretary of State of Delaware.

        To be approved, the Merger, including adoption of the Acquisition Agreement and the issuance of Inovio securities pursuant thereto, must receive a "For" vote from holders of a majority of the shares of Inovio common stock (including the outstanding shares of Series C preferred stock voting on an as-converted basis) entitled to vote and present at the Inovio special meeting, either in person or by proxy duly authorized. Abstentions will have the same effect as a vote "Against" the proposal; although present for a quorum, broker non-votes are not deemed entitled to vote and will have no effect. As of the record date, there were [                                    ] shares of Inovio common stock outstanding and [71] shares of Inovio Series C preferred stock outstanding. Inovio cannot predict how many shares of Inovio capital stock entitled to vote on this proposal will do so, and thus cannot specify a minimum numbers of votes "For" the Merger, including adoption of the Acquisition Agreement and the resulting issuance of Inovio securities, necessary to approve the proposal.

THE INOVIO BOARD OF DIRECTORS RECOMMENDS A VOTE "FOR" THE MERGER, INCLUDING ADOPTION OF THE ACQUISITION AGREEMENT AND ISSUANCE OF INOVIO SECURITIES PURSUANT THERETO—PROPOSAL 1

Proposal 2—Approval of Amendment to the Inovio 2000 Plan

        Inovio initially adopted and obtained stockholder approval of its 2000 Stock Option Plan in 2000, pursuant to which 1,850,000 shares of common stock were reserved for issuance to executive officers, directors, employees and consultants of Inovio. Subsequent to amendments adopted by the board of directors and approved by stockholders in 2002, 2004 and 2005, increasing the maximum number of common shares reserved for issuance pursuant to such Plan, Inovio's board of directors adopted the current Amended Inovio 2000 Stock Option Plan, or the Inovio 2000 Plan, on March 6, 2006, which the stockholders of Inovio subsequently approved on May 5, 2006, increasing the number of shares available to be issued under the Inovio 2000 Plan to 4,750,000. At September 12, 2008, options covering an aggregate of 5,454,461 shares, less exercised and canceled shares, of Inovio common stock had been granted under the Inovio 2000 Plan, and only 210,937 shares of Inovio common stock (plus any shares that might in the future be returned to the Inovio 2000 Plan as a result of cancellations or expiration of options) remained available for future grants under the Inovio 2000 Plan. Inovio does not intend to make any further grants under this Plan.

        On July 2, 2008, the board of directors approved an amendment and restatement of the Inovio 2000 Plan, subject to stockholder approval, to clarify the acceleration of vesting of Inovio options issued and outstanding thereunder at the Effective Time of the Merger and to remove termination of unexercised Inovio options issued and outstanding thereunder at the Effective Time of the Merger, if the Merger is completed. If Proposal 2 receives Inovio stockholder approval, but Proposal 1 is not approved or the transaction otherwise fails to close, the Inovio board of directors reserves the right to determine in its discretion whether to take action to consummate the changes anticipated by Proposal 2.

        The essential features of the proposed Amended and Restated Inovio 2000 Plan (for purposes of this Overview, the "Plan") are outlined below; however the following summary of the Plan is qualified

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in its entirety by the specific language of the Plan, provided as Annex D hereto and incorporated by reference in its entirety.

        General.     The Plan provides for the grant of Incentive Stock Options ("ISOs") and Nonstatutory Stock Options ("NSOs"). As of September 30, 2008, Inovio had outstanding options under the prior Inovio 2000 Plan to purchase an aggregate of 3,167,402 shares of Inovio common stock at per share exercise prices ranging from $1.00 to $6.76. See " Compensation Discussion and Analysis " beginning on page 153 for additional information about Inovio's other equity incentive plans and the securities issued and outstanding thereunder.

        Shares subject to the Plan.     A maximum of 4,750,000 shares of the authorized but unissued or reacquired common stock of Inovio may be issued pursuant to the Plan. In the event of any stock dividend, stock split, reverse stock split, recapitalization, combination, reclassification, or similar change in the capital structure of Inovio, appropriate adjustments will be made to the shares subject to the Plan, and to outstanding options. To the extent any outstanding option under the Plan expires or terminates prior to exercise in full or if Inovio repurchases shares issued upon exercise of an option, the shares of common stock for which that option is not exercised or the repurchased shares are returned to the Plan and will again be available for issuance under the Plan.

        Administration.     The Compensation Committee of Inovio's board of directors administers the Plan. All option grants are approved by the Compensation Committee, except that Inovio's Chief Executive Officer and/or Chairman of the board of directors may approve option grants to persons below the level of Vice President of Inovio to a maximum individual grant of 50,000 options. With respect to the participation of individuals whose transactions in Inovio's equity securities are subject to Section 16 of the Exchange Act, the Plan must be administered in compliance with the requirements, if any, of Rule 16b-3 under the Exchange Act. Subject to the provisions of the Plan, the Compensation Committee determines the persons to whom options are to be granted, the number of shares to be covered by each option, whether an option is to be an ISO or a NSO, the terms of vesting and exercisability of each option, including the effect thereon of an optionee's termination of service, the type of consideration to be paid to Inovio upon exercise of an option, the duration of each option, and all other terms and conditions of the options. Inovio does not intend to make any further grants pursuant to the Plan, and makes it current compensatory grants pursuant to the Inovio 2007 Omnibus Incentive Plan instead.

        Eligibility.     Generally, all employees, directors and consultants of Inovio or of any present or future parent or subsidiary corporations of Inovio are eligible to participate in the Plan. In addition, the Plan also permits the grant of options to prospective employees, consultants and directors in connection with written offers of employment or engagement. Any person eligible under the Plan may be granted a NSO. However, only employees may be granted ISOs.

        Terms and conditions of options.     Each option granted under the Plan is evidenced by a written agreement between Inovio and the optionee specifying the number of shares subject to the option and the other terms and conditions of the option, consistent with the requirements of the Plan. The exercise price per share must equal at least the fair market value of a share of Inovio's common stock on the date of grant of the stock option. The exercise price of any ISO granted to a person who at the time of grant owns stock possessing more than 10% of the total combined voting power of all classes of stock of Inovio or any parent or subsidiary corporation of Inovio, referred to as a 10% Stockholder, must be at least 110% of the fair market value of a share of Inovio's common stock on the date of grant.

        Generally, the exercise price may be paid in cash, by check, or in cash equivalent, by tender of shares of Inovio's common stock owned by the optionee having a fair market value not less than the exercise price, by the assignment of the proceeds of a sale or a loan with respect to some or all of the

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shares of common stock being acquired upon the exercise of the option, by means of a promissory note, by any lawful method approved by the board or by any combination of these. The Compensation Committee may nevertheless restrict the forms of payment permitted in connection with any option grant.

        The Compensation Committee will specify when options granted under the Plan will become exercisable and vested. Shares subject to options generally vest and become exercisable in installments, subject to the optionee's continued employment or service or achievement of specified milestones.

        Change of Control; Reorganization.     Upon a change of control, as defined in the Plan, all options outstanding under the Plan on the date of such change in control shall become immediately and fully vested and exercisable, except to the extent that an option grant triggers a change of control resulting from an increase in such optionee's beneficial ownership (within the meaning of Rule 13d-3 under the Exchange Act) of Inovio securities. In the event of a reorganization, as defined in the Plan, in which Inovio is not the surviving or acquiring corporation, or in which Inovio is or becomes a wholly-owned subsidiary of another corporation after the effective date of the reorganization, outstanding options shall be subject to the agreement governing the reorganization, which may provide, without limitation, for the assumption of each option granted under this Plan or its parent or subsidiary, for the substitution by surviving corporation or its parent or subsidiary of its own options for such options, for accelerated vesting and accelerated expiration, or for settlement in cash or cash equivalents. An event of reorganization may also constitute a change of control.

        Termination or amendment.     Unless sooner terminated, no ISOs may be granted under the Plan after July 30, 2010. The board may terminate or amend the Plan at any time, but, no amendment may adversely affect an outstanding option without the consent of the optionee, unless the amendment is required to preserve the option's status as an ISO or is necessary to comply with any applicable law.

        The following summary is intended only as a general guide as to the U.S. federal income tax consequences under current law of participation in the Plan and does not attempt to describe all possible federal or other tax consequences of such participation or tax consequences based on particular circumstances.

        ISOs.     An optionee recognizes no taxable income for regular income tax purposes as the result of the grant or exercise of an ISO qualifying under Section 422 of the Code. Optionees who do not dispose of their shares for two years following the date the option was granted or within one year following the exercise of the option will normally recognize a long-term capital gain or loss equal to the difference, if any, between the sale price and the purchase price of the shares. If an optionee satisfies such holding periods upon a sale of the shares, Inovio will not be entitled to any deduction for federal income tax purposes. If an optionee disposes of shares within two years after the date of grant or within one year from the date of exercise, referred to as a disqualifying disposition, the difference between the fair market value of the shares on the exercise date, and the option exercise price, not to exceed the gain realized on the sale if the disposition is a transaction with respect to which a loss, if sustained, would be recognized, will be taxed as ordinary income at the time of disposition. Any gain in excess of that amount will be a capital gain. If a loss is recognized, there will be no ordinary income, and such loss will be a capital loss. A capital gain or loss will be long-term if the optionee's holding period is more than 12 months. Generally, for federal income tax purposes, Inovio should be able to deduct any ordinary income recognized by the optionee upon the disqualifying disposition of the shares, except to the extent the deduction is limited by applicable provisions of the Code or the regulations thereunder.

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        The difference between the option exercise price and the fair market value of the shares on the exercise date of an ISO is an adjustment in computing the optionee's alternative minimum taxable income and may be subject to an alternative minimum tax which is paid if the tax exceeds the regular tax for the year. Special rules may apply with respect to certain subsequent sales of the shares in a disqualifying disposition, certain basis adjustments for purposes of computing the alternative minimum taxable income on a subsequent sale of the shares and certain tax credits that may arise with respect to optionees subject to the alternative minimum tax.

        NSOs.     Options not designated or qualifying as ISOs will be NSOs. NSOs have no special tax status. An optionee generally recognizes no taxable income as the result of the grant of such an option. Upon exercise of a NSO, the optionee normally recognizes ordinary income in an amount equal to the difference between the option exercise price and the fair market value of the shares on the exercise date. If the optionee is an employee, the ordinary income generally is subject to withholding of income and employment taxes. Upon the sale of stock acquired by the exercise of a NSO, any gain or loss, based on the difference between the sale price and the fair market value on the exercise date, will be taxed as capital gain or loss. A capital gain or loss will be long-term if the optionee's holding period is more than 12 months. No tax deduction is available to Inovio with respect to the grant of a NSO or the sale of the stock acquired pursuant to that grant. Inovio generally should be entitled to a deduction equal to the amount of ordinary income recognized by the optionee as a result of the exercise of a NSO, except to the extent the deduction is limited by applicable provisions of the Code or the regulations thereunder.

        Stockholders are requested in this Proposal 2 to approve the amendment to the Inovio 2000 Plan. The affirmative vote of the holders of a majority of the shares of Inovio common stock (including the outstanding shares of the Series C preferred stock voting on an as-converted basis) present in person or represented by proxy and entitled to vote at the meeting will be required to approve the amendment to the Inovio 2000 Plan. Abstentions will be counted toward the tabulation of votes cast on the proposal and will have the same effect as negative votes. Broker non-votes are counted towards a quorum, but will not be counted for any purpose in determining whether this matter has been approved.

        For the reasons set forth in " Inovio's Reasons for the Transaction " beginning on page 66, the board of directors of Inovio that it is advisable and in the best interests of Inovio and its stockholders to amend the Inovio 2000 Plan, subject to stockholder approval, to clarify the acceleration of vesting of Inovio options issued and outstanding thereunder and to remove the termination of unexercised Inovio options issued and outstanding thereunder upon the Effective Time of the Merger, if the transaction is completed.

THE BOARD OF DIRECTORS UNANIMOUSLY RECOMMENDS A VOTE "FOR"
THE AMENDMENT TO THE INOVIO 2000 PLAN—PROPOSAL 2

Other Matters

        Inovio's board of directors knows of no other matters that will be presented for consideration at the special meeting. If any other matters are properly brought before the meeting, it is the intention of the persons named in the accompanying proxy to vote on such matters in accordance with their best judgment.

Householding of Proxy Materials

        The SEC has adopted rules that permit companies and intermediaries (e.g., brokers) to satisfy the delivery requirements for proxy statements and annual reports with respect to two or more stockholders sharing the same address by delivering a single proxy statement addressed to those stockholders. This

217



process, which is commonly referred to as "householding," potentially means extra convenience for stockholders and cost savings for companies.

        This year, a number of brokers with account holders who are Inovio stockholders will be "householding" Inovio's proxy materials. A single proxy statement will be delivered to multiple stockholders sharing an address unless contrary instructions have been received from the affected stockholders.

        Once an Inovio stockholder has received notice from such stockholder's broker that the broker will be "householding" communications to such stockholder's address, "householding" will continue until the broker is notified otherwise or until such stockholder revokes such stockholder's consent. If at any time, an Inovio stockholder no longer wishes to participate in "householding" and would prefer to receive a separate proxy statement and annual report, such stockholder shall notify such stockholder's broker, direct a written request to: Investor Relations, Inovio Biomedical Corporation, 11494 Sorrento Valley Road, San Diego, California 92121 or at (858) 597-6006. Stockholders who currently receive multiple copies of the proxy statement at their address and would like to request "householding" of their communications should contact their broker.

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SPECIAL MEETING OF VGX STOCKHOLDERS

Questions and Answers About The VGX Special Meeting

When and where is the VGX special meeting?

        The VGX special meeting will be held on [                  ], 2009 at [            ], local time, at VGX's principal executive offices, located at 450 Sentry Parkway, Blue Bell, Pennsylvania 19422. VGX is sending this joint proxy statement/prospectus and the enclosed proxy card to its stockholders because VGX's board of directors is soliciting their proxy to vote at the VGX special meeting.

What are VGX stockholders voting on at the VGX special meeting?

        VGX stockholders are being asked to consider and vote upon a proposal to approve a business combination pursuant to the Acquisition Agreement, whereby VGX will merge with and into Submerger, and Inovio will issue shares of its common stock to VGX stockholders in exchange for all outstanding shares of common stock of VGX and assume all outstanding VGX options, warrants and, on a consolidated basis, convertible debt, on the terms and conditions set forth elsewhere in this joint proxy statement/prospectus. The Merger would result in holders of VGX common stock owning approximately 49.06% of Inovio's outstanding capital stock immediately after the closing and holders of VGX securities owning approximately 51.82% of Inovio on a fully-diluted basis immediately after the closing.

Who can vote at the VGX special meeting?

        Only VGX's stockholders of record at the close of business on [                  ], 2009, the "record date," will be entitled to vote at the VGX special meeting. On the record date, there were [            ] shares of VGX common stock outstanding and entitled to vote. Whether or not a VGX stockholder plans to attend the meeting, VGX urges such stockholders to fill out and return the enclosed proxy card to ensure his or her or its vote is counted.

How do VGX stockholders vote?

        VGX stockholders may vote "For" or "Against" the proposal or abstain from voting. If a VGX stockholder is a stockholder of record, such stockholder may vote in person at the VGX special meeting or vote by proxy using the enclosed proxy card. Whether or not such VGX stockholder plans to attend the meeting, VGX urges such stockholder to vote by proxy to ensure such stockholder's vote is counted. A VGX stockholder may still attend the meeting and vote in person if such Stockholder has already voted by proxy.

        To vote in person, a VGX stockholder must come to the special meeting and VGX will give each stockholder a ballot when he, she or its authorized representative arrives.

        To vote using the proxy card, a VGX stockholder must complete, sign and date the enclosed proxy card and return it promptly in the envelope provided. If a VGX stockholder returns such stockholder's signed proxy card to VGX before the special meeting, or brings his or her proxy card to the meeting, VGX will vote such stockholder's shares as he, she or it directs.

How many votes does a VGX stockholder have?

        On each matter to be voted upon, a VGX stockholder has one vote for each share of common stock he, she or it owns as of the record date.

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What if a VGX stockholder returns a proxy card but does not make specific choices?

        If a VGX stockholder returns a signed and dated proxy card without marking any voting selections, such stockholder's shares will be voted "For" all proposals presented for voting by VGX stockholders as described in this joint proxy statement/prospectus, including the Merger. If any other matter is properly presented at the meeting, such VGX stockholder's proxy (one of the individuals named on such stockholder's proxy card) will vote such stockholder's shares using his or her best judgment.

Who is paying for this proxy solicitation?

        Inovio is paying for the costs of the joint proxy statement/prospectus and VGX will pay for the cost of soliciting proxies from its stockholders. In addition to these mailed proxy materials, VGX's directors and employees may also solicit proxies in person, by telephone or by other means of communication. Directors and employees will not be paid any additional compensation for soliciting proxies. VGX will also reimburse brokerage firms, banks and other agents for the cost of forwarding proxy materials to beneficial owners.

What does it mean if a VGX stockholder receives more than one proxy card?

        If a VGX stockholder receives more than one proxy card, such stockholder's shares are registered on VGX's stock ledger in more than one name or are registered in different accounts. Such VGX stockholder must complete, sign and return each proxy card to ensure that all of the shares are voted.

Can a VGX stockholder change the VGX stockholder's vote after submitting the proxy?

        Yes. A VGX stockholder can revoke such stockholder's proxy at any time before the final vote at the meeting. A VGX stockholder who is the record holder of the VGX shares may revoke such stockholder's proxy by any one of three ways:

How are votes counted?

        Votes will be counted by the inspector of election appointed for the meeting, who will separately count "For" and "Against" votes and abstentions. Abstentions will be counted towards the vote total for each proposal and will have the same effect as "Against" votes.

How many votes are needed to approve each proposal?

        To be approved, the Merger and Acquisition Agreement, must receive a "For" vote from holders of a majority of the shares of VGX common stock entitled to vote at the VGX special meeting. Abstentions will have the same effect as a vote "Against" the proposal. As of the record date, there were [                  ] shares of VGX common stock outstanding. Therefore, stockholders holding at least [                  ] shares of VGX common stock must vote "For" the Merger, including adoption of the Acquisition Agreement.

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What is the quorum requirement?

        A quorum of stockholders is necessary to hold a valid meeting. A quorum will be present if the holders of a majority of the outstanding shares of VGX common stock entitled to vote are present at the VGX special meeting, either in person or by proxy duly authorized. On the record date, there were [                  ] shares of VGX common stock outstanding and entitled to vote. Therefore, [                  ] shares of VGX common stock must be represented by stockholders present at the meeting either in person or by proxy to have a quorum.

        The shares a VGX stockholder holds will be counted towards the quorum only if he, she or it submits a valid proxy or if the stockholder votes at the meeting. Abstentions will be counted towards the quorum requirement. If there is no quorum, the meeting may be adjourned either by the chairman of the meeting or by vote of the holders of a majority of the shares represented at the meeting.

As a VGX stockholder, what happens if I do not vote on any of the proposals?

        If you are a VGX stockholder and you do not submit a proxy card or vote at the VGX special meeting, it will make it difficult for VGX to establish a quorum necessary to transact business at the VGX special meeting and to obtain the requisite vote to approve the Merger proposal. If you are a VGX stockholder and you submit a proxy card and affirmatively elect to abstain from voting, your proxy will be counted as present for the purpose of determining the presence of a quorum but will not be voted on the Merger proposal. If a quorum is established, but you do not vote in person or by proxy, such failure may interfere with VGX's ability to close the proposed Merger as VGX may not receive the votes required to approve the proposal described in this joint proxy statement/prospectus.

How can VGX stockholders find out the results of the voting at the VGX special meeting?

        Preliminary voting results will be announced at the VGX special meeting. Final voting results will be published in the earlier of an Inovio Current Report on Form 8-K announcing the closing of the Merger, if the proposals are approved by the VGX stockholders and the Inovio stockholders provide necessary approvals at the Inovio special meeting, or Inovio's periodic report for the reporting period during which the VGX special meeting occurs.

Will the VGX special meeting be adjourned for the purpose of soliciting additional proxies?

        VGX does not currently intend to seek an adjournment of the VGX special meeting. However, adjournments may be made for the purpose of, among other things, soliciting additional proxies. Under VGX's bylaws, the VGX special meeting may be adjourned from time to time either by the chairman of the meeting or by the vote of a majority of the shares represented thereat. When the VGX special meeting is adjourned to another time or place, notice need not be given of the adjourned meeting if the time and place are announced at the meeting at which the adjournment is taken. At the adjourned meeting, VGX may transact any business that might have been transacted at the original meeting.

Proposal 1—Approval of Merger and Acquisition Agreement

        As discussed elsewhere in this joint proxy statement/prospectus, the holders of VGX common stock are being asked to approve a business combination with Inovio, pursuant the Acquisition Agreement between VGX, Submerger and Inovio, whereby VGX will merge with and into Submerger, Inovio will issue shares of its common stock to VGX stockholders in exchange for all outstanding shares of common stock of VGX and Inovio will assume all outstanding VGX options, warrants and, on a consolidated basis, convertible debt, on the terms and conditions set forth elsewhere in this joint proxy statement/prospectus. Holders of VGX common stock should read carefully this joint proxy statement/prospectus, including the Annexes, in its entirety for more detailed information concerning

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the Acquisition Agreement and the Merger. In particular, holders of VGX common stock are directed to:

        As discussed elsewhere in this joint proxy statement/prospectus, receipt of the requisite approvals from the VGX and Inovio stockholders for the Merger is only one condition of many to the consummation of the Merger. If approved, VGX and Inovio hope to complete the Merger shortly after obtaining the requisite stockholder approvals at the VGX special meeting and the Inovio special meeting, and believe the closing will occur prior to March 31, 2009. However, VGX and Inovio cannot predict the exact timing of the completion of the Merger because the Merger is subject to several conditions. There may be a substantial period of time between the VGX and Inovio special meetings and the completion of the Merger, and VGX and Inovio may not complete the Merger by March 31, 2009. For a detailed description of the conditions to the transaction, see the section entitled "Conditions to the Transaction" on page 112. The Merger will not be effective, including the issuance of the Inovio securities as consideration for the Merger, until such time as Submerger and VGX file the necessary certificate of merger with the Secretary of State of Delaware.

        To be approved, the Merger, including adoption of the Acquisition Agreement, must receive a "For" vote from holders of a majority of the shares of VGX common stock entitled to vote at the VGX special meeting. Abstentions will have the same effect as a vote "Against" the proposal. As of the record date, there were [                  ] shares of VGX common stock outstanding. Therefore, stockholders holding at least [                  ] shares of VGX common stock must vote "For" the Merger proposal including the adoption of the Acquisition Agreement.

THE VGX BOARD OF DIRECTORS RECOMMENDS A VOTE "FOR" THE MERGER,
INCLUDING ADOPTION OF THE ACQUISITION AGREEMENT—PROPOSAL 1

Other Matters

        VGX's board of directors knows of no other matters that will be presented for consideration at the special meeting. If any other matters are properly brought before the meeting, it is the intention of the persons named in the accompanying proxy to vote on such matters in accordance with their best judgment.


LEGAL MATTERS

        The validity of the Inovio securities offered by this joint proxy statement/prospectus has been passed upon for Inovio by K&L Gates LLP, Los Angeles, California. Certain U.S. federal income tax consequences relating to the Merger will be passed upon for Inovio by K&L Gates LLP, San Francisco, California, and for VGX by Duane Morris LLP, Philadelphia, Pennsylvania.

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EXPERTS

        The consolidated financial statements of Inovio Biomedical Corporation at December 31, 2007 and 2006, and for each of the three years in the period ended December 31, 2007 included in the joint proxy statement/prospectus of Inovio Biomedical Corporation and VGX Pharmaceuticals, Inc., which is referred to and made part of this Prospectus and Registration Statement, have been audited by Ernst & Young LLP, independent registered public accounting firm, as set forth in their report thereon appearing elsewhere herein, and are included in reliance upon such report given on the authority of such firm as experts in accounting and auditing.

        The consolidated financial statements of VGX Pharmaceuticals, Inc. at December 31, 2007 and 2006, and for the years ended December 31, 2007 and 2006 and the period from December 12, 2000 (inception) through December 31, 2007, included in the joint proxy statement/prospectus of Inovio Biomedical Corporation and VGX Pharmaceuticals, Inc., which is referred to and made part of this Prospectus and Registration Statement, have been audited by Ernst & Young LLP, independent registered public accounting firm, as set forth in their report thereon appearing elsewhere herein, and are included in reliance upon such report given on the authority of such firm as experts in accounting and auditing.


WHERE YOU CAN FIND MORE INFORMATION ABOUT INOVIO

        Inovio files annual, quarterly and current reports, proxy statements and other information with the SEC. Inovio's SEC filings are available to the public from commercial document retrieval services and at the website maintained by the SEC at http://www.sec.gov . You may also read and copy any document Inovio files with the SEC at, or obtain copies of the documents at prescribed rates by writing to the SEC's Public Reference Section at 100 F Street, N.E., Washington, D.C. 20549. Please call the SEC at 1-800-SEC-0330 for further information on the operation of its Public Reference Room.

        Inovio has filed a registration statement on Form S-4 with the SEC with respect to Inovio securities to be issued to VGX stockholders in the transaction. This joint proxy statement/prospectus is a part of that registration statement and constitutes both the prospectus of Inovio and proxy statements of Inovio and VGX for their special meetings. This registration statement, including the attached annexes, exhibits and schedules, contains additional relevant information about Inovio, Inovio capital stock and VGX. This joint proxy statement/prospectus does not contain all of the information set forth in the registration statement because parts of the registration statement are omitted in accordance with the rules and regulations of the SEC. The registration statement and its exhibits are available for inspection and copying at the SEC's offices as set forth above.

        This joint proxy statement/prospectus also incorporates by reference all documents that Inovio may file with the SEC under Sections 13(a), 13(c), 14 or 15(d) of the Exchange Act between the date of this joint proxy statement/prospectus and the date of the special meeting and the date of the Inovio special meeting (other than portions of those documents that are furnished and not filed). Those documents are considered to be part of this joint proxy statement/prospectus, effective as of the date they are filed. In the event of conflicting information in these documents, the information in the latest-filed document should be considered correct.

        Inovio has supplied all information contained in this joint proxy statement/prospectus relating to Inovio, and VGX has supplied all information in this joint proxy statement/prospectus relating to VGX.


INFORMATION ON INOVIO'S WEBSITE

        Inovio's website is www.inovio.com ; however, information on Inovio's website is not a part of, or incorporated by reference in, this joint proxy statement/prospectus, and should not be relied upon in evaluating the proposals set forth for approval by the Inovio stockholders or approval by the VGX stockholders.

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INFORMATION ON VGX'S WEBSITE

        VGX's website is www.vgxp.com ; however, information on VGX's website is not part of, or incorporated by reference in, this joint proxy statement/prospectus, and should not be relied upon in evaluating the proposals set forth for approval by the Inovio stockholders or approval by the VGX stockholders.

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INOVIO BIOMEDICAL CORPORATION

Index to Consolidated Financial Statements

 
  Page

Report of Independent Registered Public Accounting Firm

  F-2

Consolidated Balance Sheets as of December 31, 2007 and December 31, 2006 (as restated)

 
F-3

Consolidated Statements of Operations for the years ended December 31, 2007, 2006 (as restated) and 2005

 
F-4

Consolidated Statements of Stockholders' Equity for the years ended December 31, 2007, 2006 (as restated) and 2005

 
F-5

Consolidated Statements of Cash Flows for the years ended December 31, 2007, 2006 (as restated) and 2005

 
F-6

Notes to Consolidated Financial Statements

 
F-7

Condensed Consolidated Balance Sheets as of September 30, 2008 (Unaudited) and December 31, 2007

 
F-54

Condensed Consolidated Statements of Operations for the Three and Nine Months Ended September 30, 2008 and 2007 (Unaudited)

 
F-55

Condensed Consolidated Statements of Cash Flows for the Nine Months Ended September 30, 2008 and 2007 (Unaudited)

 
F-56

Notes to Condensed Consolidated Financial Statements (Unaudited)

 
F-57

F-1



Report of Independent Registered Public Accounting Firm

The Board of Directors and Stockholders
Inovio Biomedical Corporation

        We have audited the accompanying consolidated balance sheets of Inovio Biomedical Corporation as of December 31, 2007 and 2006 (as restated), and the related consolidated statements of operations, stockholders' equity and cash flows for each of the years ended December 31, 2007, December 31, 2006 (as restated) and December 31, 2005. These financial statements are the responsibility of Inovio's management. Our responsibility is to express an opinion on these financial statements based on our audits.

        We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (U.S.). Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accounting principles used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion.

        In our opinion, the financial statements referred to above present fairly, in all material respects, the consolidated financial position of Inovio Biomedical Corporation at December 31, 2007 and 2006 (as restated), and the consolidated results of its operations and its cash flows for the years ended December 31, 2007, December 31, 2006 (as restated) and December 31, 2005, in conformity with U.S. generally accepted accounting principles.

        As discussed in Note 3 to the consolidated financial statements, effective January 1, 2006, the Company changed its method of accounting for share-based payments in accordance with Statement of Financial Accounting Standards ("SFAS") No. 123 (revised 2004), "Share-Based Payment."

        We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (U.S.), Inovio Biomedical Corporation's internal control over financial reporting as of December 31, 2007, based on criteria established in Internal Control—Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission and our report dated March 12, 2008 expressed an unqualified opinion thereon.

    /s/ Ernst & Young LLP

San Diego, California
March 12, 2008

 

 

F-2



Inovio Biomedical Corporation

CONSOLIDATED BALANCE SHEETS

 
  December 31,
2007
  December 31,
2006
 
 
   
  As restated(1)
 

ASSETS

 

Current assets:

             

Cash and cash equivalents

  $ 10,250,929   $ 8,321,606  

Short-term investments

    16,999,600     14,700,000  

Accounts receivable

    1,139,966     326,071  

Prepaid expenses and other current assets

    613,656     1,124,262  
           

Total current assets

    29,004,151     24,471,939  

Fixed assets, net

    401,727     390,789  

Intangible assets, net

    6,186,430     6,514,293  

Goodwill

    3,900,713     4,290,594  

Other assets

    282,000     282,000  
           

Total assets

  $ 39,775,021   $ 35,949,615  
           

LIABILITIES, MINORITY INTEREST AND STOCKHOLDERS' EQUITY

 

Current liabilities:

             

Accounts payable and accrued expenses

  $ 1,807,305   $ 2,009,972  

Accrued clinical trial expenses

    573,767     675,330  

Common stock warrants

    367,071     3,540,692  

Deferred revenue

    544,410     583,147  

Deferred rent

    61,946     50,581  
           

Total current liabilities

    3,354,499     6,859,722  

Deferred revenue, net of current portion

    4,335,806     4,396,875  

Deferred rent, net of current portion

    99,712     177,909  

Deferred tax liabilities

    950,250     1,013,250  
           

Total liabilities

    8,740,267     12,447,756  
           

Minority Interest

        5,349,995  

Stockholders' equity:

             

Preferred stock—par value $0.001; Authorized shares: 10,000,000, issued and outstanding: 113,382 and 1,028,069 at December 31, 2007 and 2006, respectively

    113     1,028  

Common stock—par value $0.001; Authorized shares: 300,000,000, issued and outstanding: 43,870,989 and 43,814,739 at December 31, 2007 and 35,639,521 and 35,639,521 at December 31, 2006, respectively

    43,815     35,639  

Additional paid-in capital

    170,730,621     146,783,730  

Receivables from stockholders

    (50,000 )   (86,030 )

Accumulated deficit

    (139,847,326 )   (128,619,548 )

Accumulated other comprehensive income

    157,531     37,045  
           

Total stockholders' equity

    31,034,754     18,151,864  
           

Total liabilities, minority interest and stockholders' equity

  $ 39,775,021   $ 35,949,615  
           

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 to reflect certain accounting reclassifications, as described more fully in Note 2.

The accompanying notes are an integral part of these consolidated financial statements.

F-3



Inovio Biomedical Corporation

CONSOLIDATED STATEMENTS OF OPERATIONS

 
  Year ended
December 31,
2007
  Year ended
December 31,
2006
  Year ended
December 31,
2005
 
 
  As restated(1)
 

Revenue:

                   

License fee and milestone payments

  $ 2,793,478   $ 1,337,105   $ 2,563,283  

Revenue under collaborative research and development arrangements

    1,854,303     962,207     1,492,145  

Grants and miscellaneous revenue

    159,948     1,168,866     1,411,825  
               

Total revenue

    4,807,729     3,468,178     5,467,253  
               

Operating expenses:

                   

Research and development

    9,625,947     8,509,785     11,454,773  

General and administrative

    11,080,202     8,304,587     6,187,450  

Charge for acquired in-process research and development

            3,332,000  
               

Total operating expenses

    20,706,149     16,814,372     20,974,223  
               

Loss from operations

    (15,898,420 )   (13,346,194 )   (15,506,970 )

Other income

    3,421,580     320,706     2,443  

Interest income

    1,272,397     681,546     207,675  
               

Net loss

    (11,204,443 )   (12,343,942 )   (15,296,852 )

Imputed dividends on common stock

            (8,329,112 )

Imputed and declared dividends on preferred stock

    (23,335 )   (2,005,664 )   (2,736,658 )
               

Net loss attributable to common stockholders

  $ (11,227,778 ) $ (14,349,606 ) $ (26,362,622 )
               

Amounts per common share—basic and diluted:

                   

Net loss

  $ (0.27 ) $ (0.40 ) $ (0.81 )

Imputed dividends on common stock

            (0.44 )

Imputed and declared dividends on preferred stock

        (0.06 )   (0.14 )
               

Net loss attributable to common stockholders

  $ (0.27 ) $ (0.46 ) $ (1.39 )
               

Weighted average number of common shares outstanding—basic and diluted

    41,493,412     31,511,683     19,009,189  
               

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 to reflect certain accounting reclassifications, as described more fully in Note 2.

The accompanying notes are an integral part of these consolidated financial statements.

F-4



Inovio Biomedical Corporation

CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY

 
  Preferred stock   Common stock    
   
   
   
   
 
 
   
   
   
  Accumulated
other
Comprehensive
(loss) income
   
 
 
  Number
of shares
  Amount   Number
of shares
  Amount   Additional
paid-in
capital
  Receivables
From
stockholders
  Accumulated
deficit
  Total
stockholders'
equity
 
 
   
   
   
   
  As restated(1)
   
  As restated(1)
  As restated(1)
  As restated(1)
 

Balance at December 31, 2004

    1,441   $ 2     18,420,427   $ 18,420   $ 103,438,408   $   $ (87,907,320 ) $   $ 15,549,510  

Exercise of stock options for cash

            34,980     35     59,441                 59,476  

Exercise of warrants for cash

            136,250     136     256,014                 256,150  

Cashless exercise of warrants

            43,130     43     (43 )                

Issuance of common stock for cash, net of issuance costs of $997,682

            6,834,408     6,835     15,398,064                 15,404,899  

Issuance of Series D preferred stock for acquisition of Inovio AS

    1,966,292     1,966             7,902,528                 7,904,494  

Conversions of preferred stock to common stock

    (405,309 )   (406 )   3,944,043     3,944     (3,538 )                

Warrants issued for services

                    120,913                 120,913  

Share-based compensation

                    116,382                 116,382  

Imputed and declared dividends

            55,518     56     10,451,785                 10,451,841  

Comprehensive income:

                                                       
 

Net loss attributable to common stockholders

                            (26,362,622 )       (26,362,622 )
 

Foreign currency translation loss

                                (30,295 )   (30,295 )

Total comprehensive income

                                    (26,392,917 )
                                       

Balance at December 31, 2005

    1,562,424     1,562     29,468,756     29,469     137,739,954         (114,269,942 )   (30,295 )   23,470,748  

Exercise of stock options for cash

            148,629     148     251,280                 251,428  

Issuance of common stock for patents and other assets

            86,956     87     128,835                 128,922  

Issuance of stockholder note receivable

                    86,030     (86,030 )            

Issuance of common stock for cash, net of issuance costs of $1,161,070, as restated(1)

            4,074,067     4,074     5,058,931                 5,063,005  

Issuance of common stock for consulting services

            49,261     49     99,951                 100,000  

Conversions of preferred stock to common stock

    (534,355 )   (534 )   1,763,981     1,764     (1,230 )                

Share-based compensation

            45,000     45     1,546,662                 1,546,707  

Imputed and declared dividends

            2,871     3     1,873,317                 1,873,320  

Comprehensive income:

                                                       
 

Net loss attributable to common stockholders, as restated(1)

                            (14,349,606 )       (14,349,606 )
 

Foreign currency translation gain

                                67,340     67,340  

Total comprehensive income

                                    (14,282,266 )
                                       

Balance at December 31, 2006, as restated(1)

    1,028,069   $ 1,028     35,639,521   $ 35,639   $ 146,783,730   $ (86,030 ) $ (128,619,548 ) $ 37,045   $ 18,151,864  
                                       

Balance at December 31, 2006, as restated(1)

    1,028,069   $ 1,028     35,639,521   $ 35,639   $ 146,783,730   $ (86,030 ) $ (128,619,548 ) $ 37,045   $ 18,151,864  

Exercise of stock options for cash

            94,563     94     218,407                 218,501  

Exercise of warrants for cash

            3,082     3     7,394                 7,397  

Cashless exercise of warrants

            38,097     38     (38 )                

Conversions of preferred stock to common stock

    (914,687 )   (915 )   960,238     961     (46 )                

Conversions of ordinary shares to common stock

            2,201,644     2,202     5,347,793                 5,349,995  

Cash receipt towards shareholder notes receivable

                        36,030             36,030  

Issuance of common stock for consulting services

            263,750     264     610,762                 611,026  

Issuance of common stock for cash, net of issuance costs of $110,313

            4,595,094     4,595     16,059,829                 16,064,424  

Share-based compensation

            18,750     19     1,702,790                 1,702,809  

Comprehensive income:

                                                       
 

Net loss attributable to common stockholders

                            (11,227,778 )       (11,227,778 )
 

Unrealized gain (loss) on investments

                                9,945     9,945  
 

Foreign currency translation gain

                                110,541     110,541  
                                       

Total comprehensive income

                                    (11,107,292 )
                                       

Balance at December 31, 2007

    113,382   $ 113     43,814,739   $ 43,815   $ 170,730,621   $ (50,000 ) $ (139,847,326 ) $ 157,531   $ 31,034,754  
                                       

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 to reflect certain accounting reclassifications as described more fully in Note 2.

The accompanying notes are an integral part of these consolidated financial statements.

F-5



Inovio Biomedical Corporation

CONSOLIDATED STATEMENTS OF CASH FLOWS

 
  Year ended
December 31,
2007
  Year ended
December 31,
2006
  Year ended
December 31,
2005
 
 
  As restated(1)
 

Cash flows from operating activities:

                   

Net loss

  $ (11,204,443 ) $ (12,343,942 ) $ (15,296,852 )

Adjustments to reconcile net loss to net cash used in operating activities:

                   
 

Depreciation

    185,683     206,743     147,129  
 

Amortization of intangible assets

    831,958     767,900     709,938  
 

Change in value of common stock warrants

    (3,173,621 )   (135,182 )    
 

Stock-based compensation

    1,702,809     1,546,707     116,382  
 

Compensation for services paid in common stock

    611,026     100,000      
 

Amortization of deferred tax liabilities

    (63,000 )   (63,000 )   (57,750 )
 

Charge for acquired in-process research and development

            3,332,000  
 

Deferred rent

    (66,832 )   (57,385 )   (29,520 )
 

Realization of loss carryforwards

    389,881          
 

Revenue from conversion of note payable

        (10,810 )    
 

Accretion of discount on available-for-sale securities

    (86,670 )        

Changes in operating assets and liabilities:

                   
 

Accounts receivable

    (726,884 )   (57,631 )   152,471  
 

Prepaid expenses and other

    507,230     (400,417 )   (150,644 )
 

Accounts payable and accrued expenses

    (321,080 )   (233,894 )   (1,259,924 )
 

Deferred revenue

    (99,806 )   3,637,763     28,747  
               

Net cash used in operating activities

    (11,513,749 )   (7,043,148 )   (12,308,023 )
               

Cash flows from investing activities:

                   

Purchase of available-for-sale securities

    (18,602,985 )   (24,000,000 )    

Proceeds from sales of available-for-sale securities

    16,400,000     9,300,000      

Acquisition of business, net of cash acquired

            (2,341,028 )

Purchases of capital assets

    (141,635 )   (46,744 )   (286,907 )

Capitalization of patents and other assets

    (504,095 )   (1,318,431 )   (447,764 )
               

Net cash used in investing activities

    (2,848,715 )   (16,065,175 )   (3,075,699 )
               

Cash flows from financing activities:

                   

Proceeds from issuance of common stock, net of issuance costs

    16,290,322     8,975,735     15,304,716  

Repayment of stockholder note receivable

    36,030          

Proceeds from issuance of shares to minority interest

        5,349,995      

Payment of preferred stock cash dividend

    (23,335 )   (132,343 )   (613,929 )
               

Net cash provided by financing activities

    16,303,017     14,193,387     14,690,787  
               

Effect of exchange rate changes on cash

    (11,230 )   69,975     (30,295 )

Increase (decrease) in cash and cash equivalents

    1,929,323     (8,844,961 )   (723,230 )

Cash and cash equivalents, beginning of period

    8,321,606     17,166,567     17,889,797  
               

Cash and cash equivalents, end of period

  $ 10,250,929   $ 8,321,606   $ 17,166,567  
               

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 to reflect certain accounting reclassifications, as described more fully in Note 2.

The accompanying notes are an integral part of these consolidated financial statements.

F-6



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS

1. The Company

        Inovio Biomedical Corporation, a Delaware corporation, organized in 2001, is a San Diego-based biomedical company focused on the development of next-generation vaccines to prevent or treat cancers and chronic infectious diseases. Such vaccines, which could potentially protect millions of people from debilitation or death from diseases without adequate treatments, may represent multi-billion dollar market opportunities. Historically, successful development of this new generation of vaccines—DNA vaccines—has been hindered by the lack of safe, efficient and cost effective DNA delivery methods capable of enabling their potency. However, Inovio's electroporation-based DNA delivery technology has shown potential in pre-clinical and clinical studies to play a pivotal role in facilitating delivery and enhancing the potency of preventive and therapeutic vaccines.

        Inovio's business strategy to realize value for the company and its stockholders is as follows:

        First, Inovio has leveraged its patented technologies through licensing and collaborations, such as its licensing arrangements with Merck & Co., Inc., or Merck, Wyeth Pharmaceuticals, or Wyeth and Vical Inc., or Vical, among other research-driven biopharmaceutical companies as well as government and non-government agencies. Inovio is licensing the use of its electroporation-based DNA delivery systems for partners to use in conjunction with their proprietary DNA vaccines or DNA-based immunotherapies. These arrangements provide the Company with some combination of upfront payments, development fees, milestone payments, royalties and a supply agreement. These partners are pursuing development of proprietary agents or conducting research using Inovio's technology.

        Second, Inovio is pursuing proprietary vaccine development or co-development, resulting in whole or partial ownership in promising vaccines to prevent or treat cancers and chronic infectious diseases. Inovio currently has a collaborative commercialization agreement with Tripep AB, or Tripep, to co-develop a novel DNA hepatitis C therapeutic vaccine (HCV), for which they received approvals from the Swedish Medical Products Agency (MPA) and local ethics committees to initiate a Phase I/II clinical trial, which has now begun enrollment. Inovio also has two undisclosed programs underway in pre-clinical studies to generate a protective immune response with electroporation mediated delivery of an antigen in relevant animal models.

        Inovio incurred a net loss attributable to common stockholders of $11.2 million for the year ended December 31, 2007. Inovio had working capital of $25.6 million and an accumulated deficit of $139.8 million as of December 31, 2007. Inovio's ability to continue as a going concern is dependent upon Inovio's ability to achieve profitable operations and to obtain additional capital. Inovio will continue to rely on outside sources of financing to meet its capital needs. The outcome of these matters cannot be predicted at this time. Further, there can be no assurance, assuming the Company successfully raises additional funds, that it will achieve positive cash flow. If Inovio is not able to secure additional funding, the Company will be required to scale back on research and development programs, preclinical studies and clinical trials, and general and administrative activities and may not be able to continue in business. These consolidated financial statements do not include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should the Company be unable to continue in business. Inovio's consolidated financial statements as of and for the year ended December 31, 2007 have been prepared on a going concern basis, which contemplates the realization of assets and the settlement of liabilities and commitments in the normal course of business for the foreseeable future.

F-7



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented

        Inovio has restated previously issued consolidated financial statements to reflect certain accounting adjustments. As disclosed in the Current Report on Form 8-K filed February 12, 2008, the staff of the Securities and Exchange Commission (the "SEC Staff") reviewed and issued comments pertaining to Inovio's Form 10-K for the year ended December 31, 2006 and the Form 10-Q for the three and nine month periods ended September 30, 2007. After substantial correspondence and discussions with the SEC Staff regarding certain comments received pertaining to the classification of registered warrants issued by us in October 2006 and August 2007, management determined that such registered warrants require reclassification from equity to liability in Inovio's consolidated financial statements for the year ended December 31, 2006 and the interim reporting periods in 2007.

        In October 2006, Inovio issued 4,074,067 registered shares of common stock and registered warrants exercisable for 1,425,919 shares of common stock for approximately $9.9 million in a registered direct financing solely involving offshore investors. In August 2007, Inovio issued 230,000 registered shares of Inovio's common stock and registered warrants exercisable for 150,000 shares of Inovio's common stock to Asia Life Sciences Venture Consulting Inc. ("ALVC"), in consideration for identifying opportunities for the license or sale of all or part of one of Inovio's SECTA therapy programs. Inovio originally classified the registered warrants issued in both transactions as equity, however after substantial discussions with the SEC Staff regarding the legal and accounting principles applicable to the facts and circumstances surrounding the issuance of these registered warrants, the Company determined that the warrants should be classified as a liability pursuant to EITF Issue 00-19, "Accounting for Derivative Financial Instruments Indexed to, and Potentially Settled in, a Company's Own Stock" on the understanding that in compliance with applicable securities laws, the registered warrants require the issuance of registered securities upon exercise and do not sufficiently preclude an implied right to net cash settlement. If unexercised, the warrants will expire in October 2011 and August 2012, respectively.

        The decision to restate Inovio's consolidated financial statements was made by management, in consultation with Inovio's independent registered public accounting firm, Ernst & Young LLP. Due to the error in the initial classification of the registered warrants, Inovio's previously issued consolidated financial statements for the fiscal year ended December 31, 2006 and the subsequent interim periods in 2007 and the related reports of Ernst & Young LLP and all earnings and similar communications issued by us since December 31, 2006 should no longer be relied upon and are restated to reflect the impact of the required reclassification of the registered warrants. The restatement resulted in the reclassification of the fair value of the registered warrants upon issuance from equity to a liability in the amounts of $3.7 million for the October 13, 2006 issuance and $232,000 for the August 3, 2007 issuance. Subsequent to the issuance, the warrants are required to be marked-to-market to their current fair value for each reporting period. The revaluation of the registered warrants at each subsequent balance sheet date resulted in a reduction in the carrying value of the liability to $3.5 million as of the year ended December 31, 2006, $3.2 million as of the quarter ended March 31, 2007, $2.5 million as of the quarter ended June 30, 3007, and $790,000 as of the quarter ended September 30, 2007. Also, the revaluation of the registered warrants at each subsequent balance sheet date is reflected in the consolidated Statements of Operations as "Other income" or "Other expense", which resulted in an increase to other income of $135,000 for the year ended December 31, 2006, of $330,000 for the quarter ended March 31, 2007, of $727,000 for the quarter ended June 30, 3007, and of $1.9 million for the quarter ended September 30, 2007. There is no effect on the consolidated Statement of Cash Flows as a result of this change as the mark-to-market adjustment would have been reflected as a non-cash

F-8



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)


charge within Inovio's consolidated Statements of Operations. The impact on the Statement of Changes in Stockholder's Equity is reflected in reduced Accumulated Deficit for the periods indicated.

        The following quarterly data has been derived from Inovio's unaudited consolidated financial statements and, in Inovio's opinion, reflect all recurring adjustments necessary to fairly present Inovio's financial information when read in conjunction with Inovio's Consolidated Financial Statements and Notes. The following data for the year ended December 31, 2006 (as restated) has been derived from Inovio's audited consolidated financial statements and, in Inovio's opinion, reflect all recurring adjustments necessary to fairly present Inovio's financial information when read in conjunction with Inovio's Consolidated Financial Statements and Notes. This quarterly and annual information has been restated for, and as of the end of, all quarters of fiscal 2007 and the fourth quarter of fiscal 2006 from previously reported information filed on Form 10-Q and Form 10-K, as a result of the restatement of

F-9



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

Inovio's financial results as discussed above. The results of operations for any period are not necessarily indicative of the results to be expected for any future period.

 
  Quarter Ended
September 30,
2007
  Adjustments(A)   Quarter Ended
September 30,
2007
 
 
  As reported
   
  As restated
 

Consolidated Statement of Operations:

                   

Revenue:

                   

License fee and milestone payments

  $ 136,870   $     $ 136,870  

Revenue under collaborative research and development arrangements

    265,970           265,970  

Grants and miscellaneous revenue

    83,671           83,671  
                 

Total revenue

    486,511           486,511  

Operating Expenses:

                   

Research and development

    2,335,378           2,335,378  

General and administrative

    3,177,723           3,177,723  
                 

Total operating expenses

    5,513,101           5,513,101  
                 

Loss from operations

    (5,026,590 )         (5,026,590 )

Interest income

    405,023           405,023  

Other income/(expense)

    576     1,926,488     1,927,064  
               

Net loss

    (4,620,991 )   1,926,488     (2,694,503 )

Imputed and declared dividends on preferred stock

               
               

Net loss attributable to common stockholders

  $ (4,620,991 ) $ 1,926,488   $ (2,694,503 )
               

Amounts per common share—basic and diluted:

                   

Net loss

  $ (0.11 ) $ 0.05   $ (0.06 )

Imputed and declared dividends on preferred stock

             
               

Net loss attributable to common stockholders

  $ (0.11 ) $ 0.05   $ (0.06 )
               

Weighted average number of common shares—basic & diluted

    43,699,683           43,699,683  
                 

(A)
Marked-to-market adjustment for current fair value of warrants.

F-10



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  Quarter Ended
June 30,
2007
  Adjustments(A)   Quarter Ended
June 30,
2007
 
 
  As reported
   
  As restated
 

Consolidated Statement of Operations:

                   

Revenue:

                   

License fee and milestone payments

  $ 209,265   $     $ 209,265  

Revenue under collaborative research and development arrangements

    286,312           286,312  

Grants and miscellaneous revenue

               
                 

Total revenue

    495,577           495,577  

Operating Expenses:

                   

Research and development

    2,907,836           2,907,836  

General and administrative

    2,344,551           2,344,551  
                 

Total operating expenses

    5,252,387           5,252,387  
                 

Loss from operations

    (4,756,810 )         (4,756,810 )

Interest income

    286,792           286,792  

Other income/(expense)

    470     726,835     727,305  
               

Net loss

    (4,469,548 )   726,835     (3,742,713 )

Imputed and declared dividends on preferred stock

    (8,244 )         (8,244 )
                 

Net loss attributable to common stockholders

  $ (4,477,792 ) $ 726,835   $ (3,750,957 )
               

Amounts per common share—basic and diluted:

                   

Net loss

  $ (0.11 ) $ 0.02   $ (0.09 )

Imputed and declared dividends on common & preferred stock

             
               

Net loss attributable to common stockholders

  $ (0.11 ) $ 0.02   $ (0.09 )
               

Weighted average number of common shares—basic & diluted

    40,674,947           40,674,947  
                 

(A)
Marked-to-market adjustment for current fair value of warrants.

F-11



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  Quarter Ended
March 31,
2007
  Adjustments(A)   Quarter Ended
March 31,
2007
 
 
  As reported
   
  As restated
 

Consolidated Statement of Operations:

                   

Revenue:

                   

License fee and milestone payments

  $ 234,489   $     $ 234,489  

Revenue under collaborative research and development arrangements

    247,990           247,990  

Grants and miscellaneous revenue

    21,423           21,423  
                 

Total revenue

    503,902           503,902  

Operating Expenses:

                   

Research and development

    2,516,411           2,516,411  

General and administrative

    2,291,161           2,291,161  
                 

Total operating expenses

    4,807,572           4,807,572  
                 

Loss from operations

    (4,303,670 )         (4,303,670 )

Interest income

    223,068           223,068  

Other income/(expense)

    9,786     329,519     339,305  
               

Net loss

    (4,070,816 )   329,519     (3,741,297 )

Imputed and declared dividends on common & preferred stock

    (15,091 )         (15,091 )
                 

Net loss attributable to common stockholders

  $ (4,085,907 ) $ 329,519   $ (3,756,388 )
               

Amounts per common share—basic and diluted:

                   

Net loss

  $ (0.11 ) $ 0.01   $ (0.10 )

Imputed and declared dividends on preferred stock

             
               

Net loss attributable to common stockholders

  $ (0.11 ) $ 0.01   $ (0.10 )
               

Weighted average number of common shares—basic & diluted

    37,694,634           37,694,634  
                 

(A)
Marked-to-market adjustment for current fair value of warrants.

F-12



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  Quarter Ended
December 31,
2006
  Adjustments(A)   Quarter Ended
December 31,
2006
 
 
  As reported
   
  As restated
 

Consolidated Statement of Operations:

                   

Revenue:

                   

License fee and milestone payments

  $ 810,290   $     $ 810,290  

Revenue under collaborative research and development arrangements

    199,489           199,489  

Grants and miscellaneous revenue

    521,887           521,887  
                 

Total revenue

    1,531,666           1,531,666  

Operating Expenses:

                   

Research and development

    2,701,534           2,701,534  

General and administrative

    2, 623,888           2,623,888  
                 

Total operating expenses

    5,325,422           5,325,422  
                 

Loss from operations

    (3,793,756 )         (3,793,756 )

Interest income

    230,638           230,638  

Other income/(expense)

    175,505     135,182     310,687  
               

Net loss

    (3,387,613 )   135,182     (3,252,431 )

Imputed and declared dividends on common & preferred stock

    (1,867,170 )         (1,867,170 )
               

Net loss attributable to common stockholders

  $ (5,254,783 ) $ 135,182   $ (5,119,601 )
               

Amounts per common share—basic and diluted

                   

Net loss

  $ (0.10 ) $   $ (0.10 )

Imputed and declared dividends on preferred stock

    (0.05 )       (0.05 )
               

Net loss attributable to common stockholders

  $ (0.15 ) $   $ (0.15 )
               

Weighted average number of common shares—basic & diluted

    34,902,998           34,902,998  
                 

(A)
Marked-to-market adjustment for current fair value of warrants.

F-13



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  Year Ended
December 31,
2006
  Adjustments(A)   Year Ended
December 31,
2006
 
 
  As reported
   
  As restated
 

Consolidated Statement of Operations:

                   

Revenue:

                   

License fee and milestone payments

  $ 1,337,105   $     $ 1,337,105  

Revenue under collaborative research and development arrangements

    962,207           962,207  

Grants and miscellaneous revenue

    1,168,866           1,168,866  
                 

Total revenue

    3,468,178           3,468,178  

Operating Expenses:

                   

Research and development

    8,509,785           8,509,785  

General and administrative

    8,304,587           8,304,587  
                 

Total operating expenses

    16,814,372           16,814,372  
                 

Loss from operations

    (13,346,194 )         (13,346,194 )

Interest income

    681,546           681,546  

Other income/(expense)

    185,524     135,182     320,706  
               

Net loss

    (12,479,124 )   135,182     (12,343,942 )
 

Imputed and declared dividends on preferred stock

    (2,005,664 )         (2,005,664 )
               

Net loss attributable to common stockholders

  $ (14,484,788 ) $ 135,182   $ (14,349,606 )
               

Amounts per common share—basic and diluted:

                   

Net loss

  $ (0.40 ) $   $ (0.40 )

Imputed and declared dividends on preferred stock

    (0.06 )       (0.06 )
               

Net loss attributable to common stockholders

  $ (0.46 ) $   $ (0.46 )
               

Weighted average number of common shares—basic & diluted

    31,511,683           31,511,683  
                 

(A)
Marked-to-market adjustment for current fair value of warrants.

F-14



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

CONSOLIDATED BALANCE SHEET

 
  September 30,
2007
  Adjustments(B)   September 30,
2007
 
 
  As reported
   
  As restated
 

ASSETS

                   

Current assets:

                   

Cash and cash equivalents

  $ 7,086,719   $     $ 7,086,719  

Short-term investments

    21,362,700           21,362,700  

Accounts receivable

    292,643           292,643  

Prepaid expenses and other current assets

    878,917           878,917  
               

Total current assets

    29,620,979           29,620,979  

Fixed assets, net

    370,972           370,972  

Intangible assets, net

    6,300,705           6,300,705  

Goodwill

    4,290,594           4,290,594  

Other assets

    282,000           282,000  
               

Total assets

  $ 40,865,250   $   $ 40,865,250  
               

LIABILITIES, MINORITY INTEREST AND
STOCKHOLDERS' EQUITY

                   

Current liabilities:

                   

Accounts payable and accrued expenses

  $ 1,894,086   $     $ 1,894,086  

Accrued clinical trial expenses

    653,321           653,321  

Common stock warrants

        789,739     789,739  

Deferred revenue

    496,566           496,566  

Deferred rent

    61,947           61,947  
               

Total current liabilities

    3,105,920     789,739     3, 895,659  

Deferred revenue, net of current portion

    4,146,829           4,146,829  

Deferred rent, net of current portion

    115,198           115,198  

Deferred tax liabilities

    966,000           966,000  
               

Total liabilities

    8,333,947     789,739     9,123,686  
               

Minority Interest

               

Stockholders' equity:

                   

Preferred stock—par value $0.001; Authorized shares: 10,000,000, issued and outstanding: 113,382 and 1,028,069 at September 30, 2007 and December 31, 2006, respectively

    113           113  

Common stock—par value $0.001; Authorized shares: 300,000,000, issued and outstanding: 43,859,739 and 43,803,489 at September 30, 2007 and 35,639,521 and 35,639,521 at December 31, 2006, respectively

    43,803           43,803  

Additional paid-in capital

    174,309,742     (3,907,763 )   170,401,979  

Receivables from stockholders

    (50,000 )         (50,000 )

Accumulated deficit

    (141,939,420 )   3,118,024     (138,821,396 )

Accumulated other comprehensive income

    167,065           167,065  
               

Total stockholders' equity

    32,531,303     (789,739 )   31,741,564  
               

Total liabilities, minority interest and stockholders' equity

  $ 40,865,250   $   $ 40,865,250  
               

(B)
Reclassification of warrants from equity to liability.

F-15



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  June 30,
2007
  Adjustments(B)   June 30,
2007
 
 
  As reported
   
  As restated
 

ASSETS

                   

Current assets:

                   

Cash and cash equivalents

  $ 7,785,789   $     $ 7,785,789  

Short-term investments

    23,811,160           23,811,160  

Accounts receivable

    362,522           362,522  

Prepaid expenses and other current assets

    1,025,935           1,025,935  
               

Total current assets

    32,985,406           32,985,406  

Fixed assets, net

    385,916           385,916  

Intangible assets, net

    6,409,122           6,409,122  

Goodwill

    4,290,594           4,290,594  

Other assets

    282,000           282,000  
               

Total assets

  $ 44,353,038   $   $ 44,353,038  
               

LIABILITIES, MINORITY INTEREST AND
STOCKHOLDERS' EQUITY

                   

Current liabilities:

                   

Accounts payable and accrued expenses

  $ 1,649,413   $     $ 1,649,413  

Accrued clinical trial expenses

    775,796           775,796  

Common stock warrants

        2,484,338     2,484,338  

Deferred revenue

    478,262           478,262  

Deferred rent

    69,447           69,447  
               

Total current liabilities

    2,972,918     2,484,338     5,457,256  

Deferred revenue, net of current portion

    4,237,021           4,237,021  

Deferred rent, net of current portion

    143,185           143,185  

Deferred tax liabilities

    981,750           981,750  
               

Total liabilities

    8,334,874     2,484,338     10,819,212  
               

Minority Interest

               

Stockholders' equity:

                   

Preferred stock—par value $0.001; Authorized shares: 10,000,000, issued and outstanding: 113,397 and 1,028,069 at June 30, 2007 and December 31, 2006, respectively

    113           113  

Common stock—par value $0.001; Authorized shares: 300,000,000, issued and outstanding: 43,605,184 and 43,548,934,739 at June 30, 2007 and 35,639,521 and 35,639,521 at December 31, 2006, respectively

    43,549           43,549  

Additional paid-in capital

    173,226,341     (3,675,874 )   169,550,467  

Receivables from stockholders

    (50,000 )         (50,000 )

Accumulated deficit

    (137,318,429 )   1,191,536     (136,126,893 )

Accumulated other comprehensive income

    116,590           116,590  
               

Total stockholders' equity

    36,018,164     (2,484,338 )   33,533,826  
               

Total liabilities, minority interest and stockholders' equity

  $ 44,353,038   $   $ 44,353,038  
               

(B)
Reclassification of warrants from equity to liability.

F-16



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  March 31,
2007
  Adjustments(B)   March 31,
2007
 
 
  As reported
   
  As restated
 

ASSETS

                   

Current assets:

                   

Cash and cash equivalents

  $ 6,333,607   $     $ 6,333,607  

Short-term investments

    12,700,000           12,700,000  

Accounts receivable

    248,738           248,738  

Prepaid expenses and other current assets

    1,147,448           1,147,448  
               

Total current assets

    20,429,793           20,429,793  

Fixed assets, net

    414,267           414,267  

Intangible assets, net

    6,502,289           6,502,289  

Goodwill

    4,290,594           4,290,594  

Other assets

    282,000           282,000  
               

Total assets

  $ 31,918,943   $   $ 31,918,943  
               

LIABILITIES, MINORITY INTEREST AND
STOCKHOLDERS' EQUITY

                   

Current liabilities:

                   

Accounts payable and accrued expenses

  $ 1,475,453   $     $ 1,475,453  

Accrued clinical trial expenses

    720,346           720,346  

Common stock warrants

        3,211,173     3,211,173  

Deferred revenue

    439,814           439,814  

Deferred rent

    69,447           69,447  
               

Total current liabilities

    2,705,060     3,211,173     5,916,233  

Deferred revenue, net of current portion

    4,308,346           4,308,346  

Deferred rent, net of current portion

    160,546           160,546  

Deferred tax liabilities

    997,500           997,500  
               

Total liabilities

    8,171,452     3,211,173     11,382,625  
               

Minority Interest

               

Stockholders' equity:

                   

Preferred stock—par value $0.001; Authorized shares: 10,000,000, issued and outstanding: 113,413 and 1,028,069 at March 31, 2007 and December 31, 2006, respectively

    113           113  

Common stock—par value $0.001; Authorized shares: 300,000,000, issued and outstanding: 38,788,666 and 35,639,521 at March 31, 2007 and 35,639,521 and 35,639,521 at December 31, 2006, respectively

    38,789           38,789  

Additional paid-in capital

    156,493,314     (3,675,874 )   152,817,440  

Receivables from stockholders

    (50,000 )         (50,000 )

Accumulated deficit

    (132,840,637 )   464,701     (132,375,936 )

Accumulated other comprehensive income

    105,912           105,912  
               

Total stockholders' equity

    23,747,491     (3,211,173 )   20,536,318  
               

Total liabilities, minority interest and stockholders' equity

  $ 31,918,943   $   $ 31,918,943  
               

(B)
Reclassification of warrants from equity to liability.

F-17



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

2. Restatement of Prior Periods Presented (Continued)

 
  December 31,
2006
  Adjustments(B)   December 31,
2006
 
 
  As reported
   
  As restated
 

ASSETS

                   

Current assets:

                   

Cash and cash equivalents

  $ 8,321,606   $     $ 8,321,606  

Short-term investments

    14,700,000           14,700,000  

Accounts receivable

    326,071           326,071  

Prepaid expenses and other current assets

    1,124,262           1,124,262  
               

Total current assets

    24,471,939           24,471,939  

Fixed assets, net

    390,789           390,789  

Intangible assets, net

    6,514,293           6,514,293  

Goodwill

    4,290,594           4,290,594  

Other assets

    282,000           282,000  
               

Total assets

  $ 35,949,615   $   $ 35,949,615  
               

LIABILITIES, MINORITY INTEREST AND
STOCKHOLDERS' EQUITY

                   

Current liabilities:

                   

Accounts payable and accrued expenses

  $ 2,009,972   $     $ 2,009,972  

Accrued clinical trial expenses

    675,330           675,330  

Common stock warrants

        3,540,692     3,540,692  

Deferred revenue

    583,147           583,147  

Deferred rent

    50,581           50,581  
               

Total current liabilities

    3,319,030     3,540,692     6,859,722  

Deferred revenue, net of current portion

    4,396,875           4,396,875  

Deferred rent, net of current portion

    177,909           177,909  

Deferred tax liabilities

    1,013,250           1,013,250  
               

Total liabilities

    8,907,064     3,540,692     12,447,756  
               

Minority Interest

    5,349,995           5,349,995  

Stockholders' equity:

                   

Preferred stock—par value $0.001; Authorized shares: 10,000,000, issued and outstanding: 1,028,069 and 1,562,424 at December 31, 2006 and 2005, respectively

    1,028           1,028  

Common stock—par value $0.001; Authorized shares: 300,000,000, issued and outstanding: 35,639,521 and 29,468,756 at December 31, 2006 and 2005, respectively,

    35,639           35,639  

Additional paid-in capital

    150,459,604     (3,675,874 )   146,783,730  

Receivables from stockholders

    (86,030 )         (86,030 )

Accumulated deficit

    (128,754,730 )   135,182     (128,619,548 )

Accumulated other comprehensive income

    37,045           37,045  
               

Total stockholders' equity

    21,692,556     (3,540,692 )   18,151,864  
               

Total liabilities, minority interest and stockholders' equity

  $ 35,949,615   $   $ 35,949,615  
               

(B)
Reclassification of warrants from equity to liability.

F-18



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies

Consolidation

        The accompanying consolidated financial statements include the accounts of Inovio Biomedical Corporation and its domestic and foreign subsidiaries. In January 2007, Inovio acquired the minority interest of Inovio's Singapore subsidiary, IAPL. Inovio now wholly owns all of its subsidiaries. All intercompany accounts and transactions have been eliminated in consolidation.

Use of estimates

        The preparation of consolidated financial statements in accordance with U.S. generally accepted accounting principles requires the Company to make estimates and judgments that affect the reported amounts of assets, liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. Inovio bases its estimates on historical experience and on various other assumptions that are believed to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions. On an ongoing basis, Inovio reviews its estimates to ensure that these estimates appropriately reflect changes in the business or as new information become available.

Fair Value of Financial Instruments

        Inovio's financial instruments consist of cash and cash equivalents, short-term investments, and accounts receivables and payables. The carrying amounts of these instruments approximate fair value because of their short-term maturities and variable interest rates.

Cash and Cash equivalents

        Cash equivalents are highly liquid investments purchased with original maturities of three months or less and are stated at cost, which approximates market value. At December 31, 2007 and 2006, cash equivalents included $3.7 million and $2.0 million in money market funds, respectively.

Short-term Investments

        Inovio's short-term investments consist of auction rate securities classified as available-for sale, which are on deposit with a major financial institution and are stated at market value. All of Inovio's short-term investments are classified as municipal debt securities as of December 31, 2007 and 2006, and are auction rate securities which have contractual maturities in excess of ten years and reset to par on a monthly basis.

Accounts receivable

        Trade accounts receivable are recorded at invoiced amounts and do not bear interest. Inovio performs ongoing credit evaluations of its customers' financial condition. Credit is extended to customers as deemed necessary and generally does not require collateral. Management believes that the risk of loss is significantly reduced due to the quality and financial position of Inovio's customers. No allowance for doubtful accounts was deemed necessary at December 31, 2007 and 2006.

F-19



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)

Fixed assets

        Property and equipment are stated at cost and depreciated using the straight-line method over the estimated useful life of the assets, generally three to five years. Leasehold improvements are amortized over the shorter of the remaining term of the related leases or the estimated economic useful lives of the improvements. Repairs and maintenance are expensed as incurred.

Cost method investments

        Investments in corporate entities with less than a 20% voting interest are accounted for under the cost method. Inovio monitors these investments for impairment and makes appropriate reductions in carrying values if the Company determines an impairment charge is required, based primarily on the financial condition and near-term prospects of these companies. As of December 31, 2007 no impairments have been noted.

        The Company's cost method investments consist of minor investments in two non-public companies of $125,000 and $25,000, for both years ended December 31, 2007 and 2006. The fair value of Inovio's cost method investments is not estimated if there are no identified events or changes in circumstances that may have a significant adverse effect on the fair value of the investments. The Company has determined, in accordance with SFAS 107, "Disclosures about Fair Value of Financial Instruments," that it is not practicable to estimate the fair value of the investments because the cost basis investments are in non-public companies and there is no recognized exchange for which these investments are sold.

Goodwill

        Goodwill represents costs which were in excess of the fair value in Inovio's acquisition of Inovio AS.

        In accordance with SFAS No. 142, "Goodwill and Other Intangible Assets," goodwill and intangible assets with indefinite lives are not amortized but instead are measured for impairment annually, or when events indicate that impairment exists. Inovio's accounting policy with respect to reviewing goodwill for impairment is a two step process. The first step of the impairment test compares the fair value of Inovio's reporting unit with its carrying value including allocated goodwill. If the carrying value of Inovio's reporting unit exceeds its fair value, then the second step of the impairment test is performed to measure the impairment loss, if any. Inovio tests goodwill for impairment at the entity level which is considered its reporting unit. Inovio's estimate of fair value is determined using both the Discounted Cash Flow method of the Income Approach and the Guideline Public Company method of the Market Approach. The Discounted Cash Flow method estimates future cash flows of Inovio's business for a certain discrete period and then discounts them to their present value. The Guideline Public Company method computes value indicators ("multiples") from the operating data of the selected publicly traded guideline companies. After these multiples were evaluated, appropriate value indicators were selected and applied to the operating statistics of the reporting unit to arrive at indications of value. Specifically, Inovio relied upon the application of Total Invested Capital based valuation multiples for each guideline company. In applying the Income and Market Approaches, premiums and discounts were determined and applied to estimate the fair values of the reporting unit. To arrive at the indicated value of equity under each approach, Inovio then assigned a relative weighting to the resulting values from each approach to determine whether the carrying value of the reporting unit exceeds its fair value, thus requiring step 2 of the impairment test.

F-20



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)

        Inovio conducts the impairment test annually on November 30th for each fiscal year for which goodwill is evaluated for impairment. The Company is also aware of the requirement to evaluate goodwill for impairment at other times should circumstances arise pursuant to the guidance provided in SFAS 142, paragraph 26. To date, Inovio has concluded that the fair value of the reporting unit significantly exceeded the carrying value and therefore, step 2 of the impairment test has never been performed.

Intangible Assets

        Intangible assets acquired as part of the Inovio AS acquisition (see Note 16) are amortized using the straight-line method over their estimated period of contractual and cash flow benefit, which is 18 years.

        Patents are recorded at cost and amortized using the straight-line method over the expected useful lives of the patents or 17 years, whichever is less. Cost is comprised of the consideration paid for patents and related legal costs. If management determines that development of products to which patent costs relate is not reasonably certain or that costs exceed recoverable value, such costs are charged to operations.

        License costs are recorded based on the fair value of consideration paid and amortized using the straight-line method over the shorter of the expected useful life of the underlying patents or the term of the related license agreement.

        As disclosed in Inovio's consolidated financial statements, intangible assets subject to amortization and long-lived assets are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable in accordance with SFAS No. 144 discussed below. Additional factors Inovio considers include the operational performance of its acquired businesses, estimates of future cash flows, market conditions, and other qualitative factors. Any estimates and assumptions Inovio uses for reviewing potential impairments are consistent with internal planning. See Notes 6 and 16 for further discussion of Inovio's goodwill and intangible assets.

Minority Interest

        In a private placement completed in October 2006, Inovio's Singapore subsidiary IAPL issued 2,201,644 ordinary shares to outside investors which created a minority interest. As a result of this transaction, Inovio retained a 75% ownership interest in its IAPL subsidiary with the minority interest shareholders holding 25% as of December 31, 2006. In January 2007, Inovio acquired the minority interest and wholly own IAPL as of December 31, 2007 (see Note 9).

Income taxes

        Inovio accounts for income taxes using the liability method of tax allocation. Future income taxes are recognized for the future income tax consequences attributable to differences between the carrying values of assets and liabilities and their respective income tax bases. Future income tax assets and liabilities are measured using enacted income tax rates expected to apply to taxable income in the years in which temporary differences are expected to be recovered or settled. The effect on future income tax assets and liabilities of a change in rates is included in earnings in the period that includes the

F-21



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)


enactment date. Future income tax assets are recorded in the consolidated financial statements if realization is considered more likely than not.

Revenue recognition

        Revenue is recognized in accordance with SAB No. 104, "Revenue Recognition in Financial Statements" and EITF Issue 00-21, "Revenue Arrangements with Multiple Deliverables".

        Inovio has adopted a strategy of co-developing or licensing its gene delivery technology for specific genes or specific medical indications. Accordingly, Inovio has entered into collaborative research and development agreements and has received funding for pre-clinical research and clinical trials. Payments under these agreements, which are non-refundable, are recorded as revenue as the related research expenditures are incurred pursuant to the terms of the agreements and provided collectibility is reasonably assured.

        License fees are comprised of initial fees and milestone payments derived from collaborative licensing arrangements. Inovio continues to recognize non-refundable milestone payments upon the achievement of specified milestones upon which the Company has earned the milestone payment, provided the milestone payment is substantive in nature and the achievement of the milestone was not reasonably assured at the inception of the agreement. Inovio defers payments for milestone events which are reasonably assured and recognizes them ratably over the minimum remaining period of Inovio's performance obligations. Payments for milestones which are not reasonably assured are treated as the culmination of a separate earnings process and are recognized as revenue when the milestones are achieved.

        Inovio receives non-refundable grants under available government programs. Inovio records government grants applicable towards current expenditures as revenue when there is reasonable assurance that the Company has complied with all conditions necessary to receive the grants, collectibility is reasonably assured, and the related expenditures have been incurred.

Research and development expenses

        Since Inovio's inception, virtually all of Inovio's activities have consisted of research and development efforts related to developing electroporation technologies. Inovio expenses all such expenditures in the period incurred. Inovio's expenses related to clinical trials are based on services received and efforts expended pursuant to contracts with multiple research institutions and clinical research organizations that conduct and manage clinical trials on Inovio's behalf. The financial terms of these agreements are subject to negotiation and vary from contract to contract and may result in uneven payment flows. Generally, these agreements set forth the scope of work to be performed at a fixed fee or unit price. Payments under the contracts depend on factors such as the successful enrollment of patients or the completion of clinical trial milestones. Expenses related to clinical trials generally are accrued based on contracted amounts applied to the level of patient enrollment and activity according to the protocol. If timelines or contracts are modified based upon changes in the clinical trial protocol or scope of work to be performed, the Company modifies its estimates accordingly on a prospective basis. In-process research and development ("IPR&D") costs realized upon the acquisition of Inovio AS (see Note 16) were valued using the royalty savings method. Under this method, the value of acquired technology is a function of the projected revenues attributable to the products utilizing the asset, the royalty rate that would hypothetically be charged by a licensor of the

F-22



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)


technology to a licensee and an appropriate discount rate to reflect the inherent risk of the projected cash flows.

Net loss per share

        Net loss per share is calculated in accordance with the Financial Accounting Standards Board's ("FASB") Statement of Financial Accounting Standards ("SFAS") No. 128, "Earnings Per Share." Basic loss per share is computed by dividing the net loss for the year by the weighted average number of common shares outstanding during the year. Diluted loss per share is calculated in accordance with the treasury stock method and reflects the potential dilution that would occur if securities or other contracts to issue common stock were exercised or converted to common stock. Since the effect of the assumed exercise of common stock options and other convertible securities was anti-dilutive for all periods presented, basic and diluted loss per share are the same.

        The following table summarizes potential common shares that were excluded from historical basic and diluted net loss per share calculation because of their anti-dilutive effect:

Common stock equivalents
  As of
December 31,
2007
  As of
December 31,
2006
  As of
December 31,
2005
 

Options to purchase common stock

    3,465,462     2,798,900     1,141,267  

Warrants to purchase common stock

    8,892,000     8,663,700     5,648,036  

Convertible preferred stock

    217,720     1,177,959     2,631,512  

Non-vested restricted common stock

    101,250          
               
 

Total

    12,676,432     12,640,559     9,420,815  
               

Leases

        Leases are classified as either capital or operating leases. Leases which transfer substantially all of the benefits and risks incidental to the ownership of assets are accounted for as if there was an acquisition of an asset and incurrence of an obligation at the inception of the lease. All other leases are accounted for as operating leases. Inovio's San Diego headquarter facility lease, which has escalating payments, is expensed on a straight-line basis over the term of five years. At the end of the original lease term, Inovio has the option of renewing this lease for an additional five-year lease term at an annual rate equal to the fair market rental value of the property, as defined in the lease agreement. This lease represents the primary expense and commitment as indicated in Note 10 "Commitments" below. Other leases exist for the Norway facility and for office machinery, such as copiers, wherein lease expense is recorded as incurred.

Share-based compensation

        Effective January 1, 2006 Inovio adopted SFAS No. 123(R) using the modified prospective application method. Accordingly, stock-based compensation cost is measured at the grant date, based on the fair value of the award, and is recognized as an expense over the employee's requisite service period. Because the Company elected to use the modified prospective application method, results for prior periods have not been restated. In March 2005, the Securities and Exchange Commission issued Staff Accounting Bulletin ("SAB") No. 107, which provides supplemental implementation guidance for

F-23



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)


SFAS No. 123(R). Inovio has applied the provisions of SAB No. 107 in its adoption of SFAS No. 123(R).

        Inovio estimates the fair value of stock options granted using the Black-Scholes option pricing model. The Black-Scholes option pricing model was developed for use in estimating the fair value of traded options, which have no vesting restrictions and are fully transferable. In addition, option valuation models require the input of highly subjective assumptions, including the expected stock price volatility and expected option life. Inovio amortizes the fair value of the awards on a straight-line basis. All options grants are amortized over the requisite service period of the awards. Expected volatility is based on historical volatility. The expected life of options granted is calculated using the simplified method based on the terms and conditions of the options as provided in SAB No. 107. The risk-free interest rate is based on the U.S. Treasury yield in effect at the time of grant. The forfeiture rate is based on historical data and Inovio records share-based compensation expense only for those awards that are expected to vest. The dividend yield is based on the fact that no dividends have been paid on common stock historically, and none are currently expected to be paid.

        For the purpose of calculating pro-forma information under SFAS No. 123 for periods prior to January 1, 2006, Inovio accounted for forfeitures as they occurred. Assumptions used in the Black-Scholes model are presented below:

 
  Year Ended December 31,  
 
  2007   2006   2005  

Risk-free interest rate

    4.07% - 4.67%     4.68% - 4.96%     3.97 %

Expected volatility

    93% - 98%     98% - 109.%     104 %

Expected life in years

    6     6     6  

Dividend yield

             

Other Accumulated Comprehensive Income

        Components of comprehensive income are reported in the consolidated financial statements in the period in which they are recognized. The components of comprehensive income include net loss, unrealized gains and losses on investments and foreign currency translation adjustments. The components of accumulated other comprehensive income are indicated on the Consolidated Statements of Stockholder's Equity.

Pending accounting pronouncements

        In February 2007, the FASB issued SFAS No. 159, "The Fair Value Option for Financial Assets and Financial Liabilities—Including an amendment of FASB Statement No. 115" ("SFAS 159"). Under SFAS 159, the Company may elect to measure certain financial instruments and other items at fair value on an instrument by instrument basis subject to certain restrictions. SFAS 159 becomes effective for the Company on January 1, 2008. The impact of the adoption of SFAS 159 will be dependent on the extent to which Inovio elects to measure eligible items at fair value.

        In September 2006, the FASB issued SFAS No. 157, "Fair Value Measurements," ("SFAS 157"). SFAS 157 defines fair value, establishes a framework for measuring fair value in generally accepted accounting principles, and expands disclosures about fair value measurements. The provisions of this

F-24



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

3. Summary of Significant Accounting Policies (Continued)


standard apply to other accounting pronouncements that require or permit fair value measurements. SFAS 157 becomes effective for the Company on January 1, 2008. Upon adoption, the provisions of SFAS 157 are to be applied prospectively with limited exceptions. Management is currently evaluating the impact of this standard and does not expect the adoption of SFAS 157 to have a material impact on its consolidated financial statements. In December 2007, the SEC issued Staff Accounting Bulletin ("SAB") No. 110 which expresses views regarding the use of a "simplified" method, as discussed in SAB No. 107, in developing an estimate of expected term of "plain vanilla" share options in accordance with SFAS No. 123(R). The impact of this bulletin will not have a material impact on Inovio's consolidated financial statements.

Adoption of Recent Accounting Pronouncements

        In July 2006, the FASB issued FASB Interpretation No. 48 ("FIN No. 48"), "Accounting for Uncertainty in Income Taxes, an interpretation of FASB Statement No. 109". This interpretation prescribes a "more-likely-than-not" recognition threshold and measurement attribute (the largest amount of benefit that is greater than 50% likely of being realized upon ultimate settlement with tax authorities) for the financial statement recognition and measurement of a tax position taken or expected to be taken in a tax return. This interpretation also provides guidance on derecognition, classification, interest and penalties, accounting in interim periods, disclosure and transition. FIN No. 48 is effective for fiscal years beginning after December 15, 2006. The Company adopted FIN No. 48 on January 1, 2007, and there was no impact from adoption on Inovio's financial condition and results of operations for the year ended December 31, 2007.

4. Major Customers and Concentration of Credit Risk

Customer
  2007   % of Total
Revenue
  2006   % of Total
Revenue
  2005   % of Total
Revenue
 

Merck

  $ 3,268,884     68 % $ 1,535,540     44 % $ 2,822,634     52 %

Wyeth

    1,118,023     23                  

Valentis

            655,123     19          

U.S Army grant

    21,423         898,932     26     684,646     13  

All other

    399,399     9     378,583     11     1,959,973     35  
                           

Total Revenue

  $ 4,807,729     100 % $ 3,468,178     100 % $ 5,467,253     100 %
                           

        In May 2004, Inovio announced that the Company had signed a collaboration and licensing agreement with Merck & Co., Inc. (Merck) to develop and commercialize Inovio's MedPulser® DNA Delivery System, which will be developed for use with certain of Merck's DNA vaccine programs. Under the terms of the agreement, Merck receives the right to use Inovio's proprietary technology initially for two specific antigens with an option to extend the agreement to include a limited number of additional target antigens. Inovio received an upfront license payment under this agreement, and may receive milestone payments linked to the successful development of a product. As of December 31, 2007 and 2006, $239,580 or 21%, and $199,489 or 61% of Inovio's total accounts receivable balance of $1.1 million and $326,071, respectively, was attributable to Merck.

F-25



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

4. Major Customers and Concentration of Credit Risk (Continued)

        During the year ended December 31, 2007, Inovio recognized revenue from Inovio's collaboration and licensing agreement with Wyeth which was executed in November 2006. As of December 31, 2007, $889,451 or 78% of Inovio's total accounts receivable balance of $1.1 million was attributable to Wyeth. None of Inovio's accounts receivable balance was attributable to Wyeth at December 31, 2006.

        In October 2006, Inovio acquired various licenses, patents and the rights to existing customer agreements from Valentis in exchange for future cash payments of $540,000 and the settlement of a royalty obligation of $320,000. As part of this arrangement, the Company was discharged of all other outstanding obligations in connection with a previous licensing arrangement, and received approximately $159,000 of funds previously held in escrow. During the year ended December 31, 2007 and 2006 Inovio recorded $0 and $655,123 revenue from Valentis, respectively. None of Inovio's total accounts receivable balance as of December 31, 2007 or 2006 was attributable to Valentis.

        There is minimal credit risk with these customers based upon collection history and their size and financial condition. Accordingly, Inovio does not consider it necessary to record a reserve for uncollectible accounts receivable.

5. Fixed Assets

 
  Cost   Accumulated
depreciation
and
amortization
  Net book value  

As of December 31, 2007

                   

Machinery, equipment and office furniture

  $ 2,026,992   $ (1,836,966 ) $ 190,026  

Leasehold improvements

    734,317     (522,616 )   211,701  

Equipment under capital leases

             
               

  $ 2,761,309   $ (2,359,582 ) $ 401,727  
               

As of December 31, 2006

                   

Machinery, equipment and office furniture

  $ 1,886,946   $ (1,720,498 ) $ 166,448  

Leasehold improvements

    677,742     (453,401 )   224,341  

Equipment under capital leases

    119,671     (119,671 )    
               

  $ 2,684,359   $ (2,293,570 ) $ 390,789  
               

        Depreciation and amortization expense for the years ending December 31, 2007, 2006 and 2005 was $185,683, $206,743 and $147,129, respectively. In accordance with SFAS No. 144, the Company determined that the carrying value of these long-lived assets was not impaired for the periods presented.

F-26



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

6. Goodwill and Intangible Assets

        In accordance with SFAS No. 142, "Goodwill and Other Intangible Assets," Inovio's goodwill is not amortized, but is subject to an annual impairment test. The following sets forth the intangible assets by major asset class:

 
   
  December 31, 2007   December 31, 2006  
 
  Useful
Life (Yrs)
  Gross   Accumulated
Amortization
  Net Book
Value
  Gross   Accumulated
Amortization
  Net Book
Value
 

Non-Amortizing:

                                           
 

Goodwill(a)

        $ 3,900,713   $   $ 3,900,713   $ 4,290,594   $   $ 4,290,594  

Amortizing:

                                           
 

Patents

    8-17     5,224,109     (2,775,713 )   2,448,396     4,829,597     (2,409,080 )   2,420,517  
 

Licenses

    8-17     1,198,781     (854,497 )   344,284     1,198,781     (723,755 )   475,026  
 

Other(b)

    18     4,050,000     (656,250 )   3,393,750     4,050,000     (431,250 )   3,618,750  
                                 
 

Total Intangible assets

          10,472,890     (4,286,460 )   6,186,430     10,078,378     (3,564,085 )   6,514,293  
                                 
 

Total goodwill and intangible assets

        $ 14,373,603   $ (4,286,460 ) $ 10,087,143   $ 14,368,972   $ (3,564,085 ) $ 10,804,887  
                                 

(a)
Goodwill was recorded from the Inovio AS acquisition in January 2005 (See Note 16). In 2007 Inovio recorded a reduction in Goodwill of $389,881 related to the realization of foreign net operating loss carry forwards.

(b)
Other intangible assets represent the fair value of acquired contracts and intellectual property from the Inovio AS acquisition (See Note 16). At the time of the acquisition, Inovio determined the remaining useful life for the acquired contractual relationships to be approximately 18 years, reflecting the period over which the contractual relationships would contribute to Inovio's cash flows, consistent with the guidance in SFAS 142, paragraph 11. Inovio evaluated the useful life of the acquired contractual relationships based upon a review of the legal life of the underlying patents and discussions with the management of Inovio AS regarding estimates of each patent's useful economic life as it related to the acquired contracts. Based on these factors, Inovio determined that its relevant market sales and cash flows would likely decline after 18 years, when the key patents related to the acquired contracts expire. The Company expects that the acquired contractual relationships will continue to provide positive cash flows through at least 18 years, as determined at the time of acquisition.

        Aggregate amortization expense on intangible assets was $831,958, $767,900 and $709,938 for the years ended December 31, 2007, 2006 and 2005, respectively. Amortization expense related to intangible assets at December 31, 2007 for each of the next five fiscal years and beyond is expected to be incurred as follows:

2008

  $ 767,767  

2009

    645,811  

2010

    595,093  

2011

    545,417  

2012

    497,070  

Thereafter

    3,135,272  
       

  $ 6,186,430  
       

        In accordance with SFAS No. 142, the Company has completed its annual impairment tests and fair value analysis for goodwill and other non-amortizing intangible assets, respectively, held throughout the year. There were no impairments or impairment indicators present and no loss was recorded during the year ended December 31, 2007.

F-27



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

7. Accounts Payable and Accrued Expenses

 
  As of
December 31,
2007
  As of
December 31,
2006
 

Trade accounts payable

  $ 394,786   $ 555,323  

Accrued compensation

    559,685     735,993  

Accrued clinical trial expenses

    573,767     675,330  

Other accrued expenses

    852,834     718,656  
           

  $ 2,381,072   $ 2,685,302  
           

8. Deferred Revenue

        Inovio defers revenue recognition of cash receipts from licensing and other agreements and recognizes them ratably over the minimum remaining period of Inovio's performance obligations. The combined current and long-term deferred revenue balance of $4.9 million consists primarily of an unrecognized balance of $4.2 million arising from the $4.5 million payment received from Wyeth in November 2006 for the 15 year collaborative and licensing agreement.

9. Stockholders' Equity

Preferred Stock

 
   
   
  Outstanding as of
December 31,
 
 
  Authorized   Issued   2007   2006  

Series A Preferred Stock, par $0.001

    1,000     817          

Series B Preferred Stock, par $0.001

    1,000     750          

Series C Preferred Stock, par $0.001

    1,091     1,091     71     102  

Series D Preferred Stock, par $0.001

    1,966,292     1,966,292     113,311     1,027,967  

        The following is a summary of changes in the number of outstanding shares of Inovio's preferred stock for the years ended December 31, 2005, 2006 and 2007:

 
  Series A   Series B   Series C   Series D  

Shares Outstanding as of January 1, 2005

    291     110     1,040      

Preferred Shares issued

                1,966,292  

Preferred Shares converted

    (239 )   (10 )   (703 )   (404,357 )

Shares Outstanding as of December 31, 2005

    52     100     337     1,561,935  

Preferred Shares converted

    (52 )   (100 )   (235 )   (533,968 )

Shares Outstanding as of December 31, 2006

            102     1,027,967  

Preferred Shares converted

            (31 )   (914,656 )

Shares Outstanding as of December 31, 2007

            71     113,311  

        The shares of Inovio's outstanding Series C and Series D Preferred Stock have the following pertinent rights and privileges, as set forth in Inovio's Amended and Restated Certificate of Incorporation and its Certificates of Designations, Rights and Preferences related to the various series of preferred stock.

F-28



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

Dividend Preferences

        The holders of all series of Inovio's preferred stock are entitled to receive dividends on a pari passu basis with the holders of common stock, when, if and as declared by Inovio's board of directors.

        In addition, the holders of the Series C Preferred Stock received a mandatory dividend rate of 6% per annum per outstanding share of Series C Preferred Stock, payable quarterly, based on the $10,000 Liquidation Preference of such share through the period ending on May 20, 2007. These dividends were paid in cash or common stock equal to the equivalent cash amount divided by the 20 day preceding average closing price. The Company could only elect to pay the dividends in shares of common stock if the average closing price of the shares of common stock for the 20 days immediately preceding the dividend payment date was equal to or greater than the conversion price of either of the relevant series of Preferred Stock. All dividends were paid to outstanding Series C Preferred Stockholders on each quarter-end payment date. Inovio paid cash dividends to holders of Series C Preferred Stock of $23,335 and $117,204 during the years ended December 31, 2007 and 2006.

Rights on Liquidation

        In the event of any voluntary or involuntary liquidation, dissolution or winding up of the Company (a "liquidation event"), before any distribution of assets of the Company shall be made to or set apart for the holders of common stock, the holders of Series C Preferred Stock, pari passu, are entitled to receive payment of such assets of the Company in an amount equal to $10,000 per share of such series of preferred stock, plus any accumulated and unpaid dividends thereon (whether or not earned or declared). In the event of any liquidation event, the holders of the Series D Preferred Stock are entitled to be paid out of the assets of the Company available for distribution to its stockholders (i) before any distribution of assets of the Company shall be made to or set apart for the holders of common stock or any class or series of stock ranking on liquidation junior to the Series D Preferred Stock, (ii) ratably with any class or series of stock ranking on liquidation on a parity with the Series D Preferred Stock, and (iii) after and subject to the payment in full of all amounts required to be distributed to the holders of Inovio's Series C Preferred Stock and any other class or series of stock of the Company ranking on liquidation prior and in preference to the Series D Preferred Stock, an amount equal to $3.204 per share of Series D Preferred Stock.

        If the assets of the Company available for distribution to stockholders exceed the aggregate amount of the liquidation preferences payable with respect to all shares of each series of preferred stock then outstanding, then, after the payment of such preferences is made or irrevocably set aside, the holders of Inovio's common stock are entitled to receive a pro rata portion of such assets based on the aggregate number of shares of common stock held by each such holder. The holders of Inovio's outstanding preferred stock shall participate in such a distribution on a pro-rata basis, computed based on the number of shares of common stock which would be held by such preferred holders if immediately prior to the liquidation event all of the outstanding shares of the preferred stock had been converted into shares of common stock at the then current conversion value applicable to each series.

        A Change of Control of the Company (as defined in the Certificates of Designations, Rights and Preferences) is not a liquidation event triggering the preferences described above, and is instead addressed by separate terms in the Series C and Series D Certificates of Designations, Rights, and Preferences.

F-29



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        Although the liquidation preferences are in excess of the par value of $0.001 per share of Inovio's preferred stock, these preferences are equal to or less than the stated value of such shares based on their original purchase price.

Voting Rights

        The holders of all series of Inovio's preferred stock outstanding have full voting rights and powers equal to the voting rights and powers of holders of Inovio's common stock and are entitled to notice of any stockholders' meeting in accordance with Inovio's Bylaws. Holders of Inovio's preferred stock are entitled to vote on any matter upon which holders of Inovio's common stock have the right to vote, including, without limitation, the right to vote for the election of directors together with the holders of common stock as one class.

Actions Requiring the Consent of Holders of Convertible Preferred Stock

        As long as at a certain number of shares of each series of Inovio's preferred stock issued on the respective "Date of Original Issue" for such series are outstanding, the consent of at least a majority of the shares of that series of preferred stock outstanding are necessary to approve:

            (a)   Any amendment, alteration or repeal of (i) any of the provisions of the relevant series' Certificate of Designation, including any increase in the number of authorized shares of such series or (ii) Inovio's Certificate of Incorporation or Bylaws in a manner that would adversely affect the rights of the holders of the relevant series of preferred stock;

            (b)   the authorization, creation, offer, sale or increase in authorized shares by the Company of any stock of any class, or any security convertible into stock of any class, or the authorization or creation of any new series of preferred stock ranking in terms of liquidation preference, redemption rights or dividend rights, pari passu with or senior to, the relevant series of preferred stock in any manner;

            (c)   the declaration or payment of any dividend or other distribution (whether in cash, stock or other property) with respect to Inovio's capital stock or that of any subsidiary, other than a dividend or other distribution pursuant to the terms of the relevant series of preferred stock or other series of preferred stock noted in the relevant Certificate of Designation; and

            (d)   except for the holders of the Series D Preferred Stock, the redemption, purchase or other acquisition, directly or indirectly, of any shares of Inovio's capital stock or any of its subsidiaries or any option, warrant or other right to purchase or acquire any such shares, or any other security, other than certain accepted redemptions of preferred stock, certain outstanding warrants, the repurchase of shares at cost from employees of the Company upon termination of employment in accordance with written agreements pursuant to which the shares were issued, or other specified repurchase or redemption rights pursuant to written agreements outstanding at the time of original issuance of the preferred stock in question.

        These specific voting rights are applicable for the Series C Preferred Stock as long as at least 35% of the number of shares of Series C Preferred Stock issued on the Date of Original Issue remain outstanding, and the same threshold applies to the Series D Preferred Stock. As of December 31, 2007, only the outstanding shares of Inovio's Series D Preferred Stock had such series voting rights remaining.

F-30



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

Participation Rights

        Holders of the Series C Preferred Stock have the right to participate with respect to Inovio's issuance of any equity or equity-linked securities or debt convertible into equity or in which there is an equity component ("Additional Securities") on the same terms and conditions as offered by the Company to the other purchasers of such Additional Securities. However securities issued or issuable upon any of the following are not deemed "Additional Securities": (A) the conversion of outstanding preferred stock or exercise of related warrants, or the issuance of shares of common stock as payment of dividends to holders of preferred stock, (B) the exercise of any warrants or options outstanding prior to the authorization or issuance of the series of preferred stock in question (C) the issuance (at issuance or exercise prices at or above fair market value) of common stock, stock awards or options under, or the exercise of any options granted pursuant to, any Board-approved employee stock option or similar plan for the issuance of options or capital stock of the Company, (D) the issuance of shares of common stock pursuant to a stock split, combination or subdivision of the outstanding shares of common stock, and (E) for evaluation of the rights of the Series C Preferred Stock only, in connection with a bona fide joint venture or development agreement or strategic partnership, the primary purpose of which is not to raise equity capital.

        Each time the Company proposes to offer any Additional Securities, it is obligated to provide each holder of shares of the Series C Preferred Stock notice of such intention including the terms of such intended offering (including size and pricing) and the anticipated closing date of the sale. These preferred stockholders then have a specified period in which to respond to the Company to elect to purchase or obtain, at the price and on the terms specified in Inovio's notice, up to that number of such Additional Securities which equals such holder's Pro Rata Amount. The "Pro Rata Amount" for any given holder of shares of the Series C Preferred Stock equals that portion of the Additional Securities offered by the Company which equals the proportion that the number of shares of common stock that such preferred stockholder owns or has the right to acquire to the total number of shares of common stock then outstanding (assuming in each case the full conversion and exercise of all convertible and exercisable securities then outstanding).

        The holders of the Series C Preferred Stock have the right to pay the consideration for the Additional Securities purchasable upon such participation with shares of such series of Preferred Stock, which will be valued for such purpose at the applicable series' Liquidation Preference plus any accrued and unpaid dividends for such purpose. However, when shares of such preferred stock are used as participation consideration, then such holder's Pro Rata Amount is increased (but not decreased) to the extent necessary to equal that number of Additional Securities as are convertible into or exchangeable for such number of shares of Common Stock as is obtained by dividing (a) the Liquidation Preference attributable to such holder's shares of the applicable series of Preferred Stock plus any accrued and unpaid dividends on such Preferred Stock by (b) the Conversion Value then in effect for such shares, and in such event the Company shall be obligated to sell such number of Additional Securities to each such holder, even if the aggregate Pro Rata Amount for all such holders exceeds the aggregate amount of Additional Securities that the Company had initially proposed to offer. To the extent that not all holders of a particular series of preferred stock elect to participate up to their full Pro Rata Amounts, the participating holders of that series of preferred stock have the right to increase their participation accordingly.

F-31



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        The participation rights of the holders of the Series C Preferred Stock may not be assigned or transferred, other than assignment to any wholly-owned subsidiary or parent of, or to any corporation or entity that is, within the meaning of the Securities Act, controlling, controlled by or under common control with, any such holder. As a result of transfers, the holders of the Series C Preferred Stock outstanding as of December 31, 2007 no longer had such participation rights.

        The Series D Preferred Stock has no participation rights.

        During Inovio's October 2006, December 2005 and January 2005 common stock offerings, Inovio informed holders of Inovio's outstanding Series A, B, and C Cumulative Convertible Preferred Stock with participation rights, of their ability to participate in the respective offering based upon the pricing of the transaction and the applicable liquidation preference for the series of preferred share participating. These participating stockholders obtained incremental shares of common stock as a result of exercising their participation rights, thereby converting their outstanding shares of Cumulative Convertible Preferred Stock at a lower offering price compared to their current conversion price. The right to participate was available only for a limited period time in relation to the specific transaction and the exercise of the existing participation right did not reflect or create a lasting change in the holders' conversion privileges. Some of the participating stockholders had previously converted a portion of their shares of Inovio's preferred stock pursuant to their optional conversion rights, and most of the participating stockholders wholly converted their remaining shares of Inovio's preferred stock through exercise of their participation rights in the noted offerings.

Conversion Rights

        The Series C Preferred Stock each provide the holder of such shares an optional conversion right and provide a mandatory conversion upon certain triggering events.

        Right to Convert     The holder of any share or shares of Series C Preferred Stock has the right at any time, at such holder's option, to convert all or any lesser portion of such holder's shares of the Preferred Stock into such number of fully paid and non-assessable shares of Common Stock as is determined by dividing (i) the aggregate Liquidation Preference applicable to the particular series of preferred shares, plus accrued and unpaid dividends thereon by (ii) the applicable Conversion Value (as defined in the relevant series' Certificate of Designations, Rights and Preferences) then in effect for such series of preferred shares. The Company is not obligated to issue any fractional shares or scrip representing fractional shares upon such conversion and instead shall pay the holder an amount in cash equal to such fraction multiplied by the current market price per share of Inovio's common stock.

        Mandatory Conversion     The Company has the option upon thirty (30) days prior written notice, to convert all of the outstanding shares of the Series C Preferred Stock into such number of fully paid and non-assessable shares of common stock as is determined by dividing (i) the aggregate Liquidation Preference of the shares of the relevant series of preferred stock to be converted plus accrued and unpaid dividends thereon by (ii) the applicable Conversion Value (as defined in the relevant series' Certificate of Designations, Rights and Preferences) then in effect, if at any time after twelve months following the Original Issue Date of each such series of preferred stock all of the following triggering events occur:

              (i)  The registration statement covering all of the shares of common stock into which the particular series of preferred stock is convertible is effective (or all of the shares of common stock

F-32



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

    into which the preferred stock is convertible may be sold without restriction pursuant to Rule 144 under the Securities Act of 1933, as amended);

             (ii)  the Daily Market Price (as defined in the applicable Certificates of Designations, Rights and Preferences) of the common stock crosses a specified pricing threshold for twenty of the thirty consecutive trading days prior to the date the Company provides notice of conversion to the holders; and

            (iii)  the average daily trading volume (subject to adjustment for stock dividends, subdivisions and combinations) of the common stock for at least twenty of the thirty consecutive trading days prior to the date the Company provides notice of conversion to the holders exceeds 25,000 shares.

        As of December 31, 2007, Inovio's outstanding shares of the Series C Preferred Stock were convertible into 104,410 shares of Inovio's common stock at a conversion price of $6.80 per share, and the applicable Daily Market Price of the common stock for triggering mandatory conversion equaled $18.00 per share.

        The Series D Preferred Stock only provides the holder of such shares an optional conversion right. As of December 31, 2007, 113,311 shares of the Series D Preferred Stock were convertible into Inovio's common stock on a one-for-one basis.

    Imputed and Declared Dividends on Preferred Stock

        The holders of Inovio's Series A and B Preferred Stock were entitled to receive an annual dividend at the rate of 6%, payable quarterly, through September 30, 2006. These dividends were payable in cash unless the closing price of Inovio's common shares for the 20 trading days immediately preceding the dividend payment date was equal to or greater than the conversion price of such shares, in which event the Company may have elected to pay the dividends to the holders in common stock. As part of this dividend to holders of Series A and B Preferred Stock, Inovio issued a total of 2,871 common shares valued at $7,693, and paid $15,140 in cash during 2006. Inovio issued a total of 55,518 common shares valued at $179,956 and paid $60,235 in cash during 2005. There were no shares of Series A or B Preferred Stock outstanding on December 31, 2007 and 2006, respectively. As of December 31, 2005, 52 shares of Series A Preferred Stock and 100 shares of Series B Preferred Stock remained outstanding.

        The holders of Inovio's Series C Preferred Stock are entitled to receive an annual dividend at the rate of 6%, payable quarterly, through May 20, 2007. These dividends are payable in cash unless the closing price of Inovio's common shares for the 20 trading days immediately preceding the dividend payment date is equal to or greater than the conversion price of such shares, in which event Inovio may elect to pay the dividends to the holders in common stock. As part of this dividend, Inovio paid cash of $23,335 during fiscal 2007 to holders of Series C Preferred Stock. Inovio paid cash $117,204 during fiscal 2006 to holders of Series C Preferred Stock and accrued $14,571 for certain holders of Series C Preferred Stock who participated in Inovio's October 2006 equity financing, during fiscal 2006. Inovio paid dividends in cash of $553,694 during 2005.

F-33



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        During 2006, Inovio recorded an imputed dividend charge of $1.9 million during the three months ended December 31, 2006, related to the investors who converted $1.2 million of their Series C Preferred Stock investment into 473,744 shares of common stock as part of Inovio's October 2006 private placement. This imputed dividend charge was calculated using guidance contained in Emerging Issues Task Force ("EITF") Issue No. 00-27, "Application of Issue No. 98-5 to Certain Convertible Instruments." As part of this private placement, these investors received 304,450 additional shares of Inovio's common stock, as compared to the number of shares of common stock into which their existing Series C Preferred Stock could have been converted under the original terms of the Series C Preferred Stock. Under EITF Issue No. 00-27, this incremental number of shares of common stock was multiplied by the price of common stock on the commitment date of the original Series C Preferred Stock issuance, or $6.08 per share, to calculate the $1.9 million imputed dividend charge associated with this beneficial conversion.

        During 2005, Inovio recorded an imputed dividend charge of $1.9 million related to the investors who converted $3.2 million of their previous Series C Preferred Stock investment into 790,123 shares of common stock as part of Inovio's January 2005 private placement. As part of this private placement, these investors received 319,535 additional shares of common stock by participating, as compared to the number of shares of common stock into which their existing Series C Preferred Stock could have been converted under the original terms of the Series C Preferred Stock. This incremental number of shares of common stock was multiplied by the price of common stock on the commitment date of the original Series C Preferred Stock issuance, or $6.08 per share, to calculate the $1.9 million imputed dividend charge associated with this beneficial conversion.

        During 2005, Inovio also recorded an imputed dividend charge related to common stockholders of $8.3 million to the investors who converted their Series B and C Preferred Stock and common stock investments into shares of common stock as part of Inovio's December 2005 private placement. As part of this private placement, these investors received 1,670,406 additional shares of common stock by participating, as compared to the number of shares of common stock into which their existing common or preferred stock could have been converted under the original terms of their agreements. This incremental number of shares of common stock was multiplied by the price of Inovio's common stock on the commitment date of the original issuance, to calculate the $8.3 million imputed dividend charge associated with this beneficial conversion.

    Common Stock

        In August 2007, Inovio entered into an agreement with an outside consulting advisor pursuant to which the Company issued 230,000 registered shares of common stock and registered warrants to purchase 150,000 shares of common stock, as payment of a non-refundable retainer in connection with the engagement of its services.

        In May 2007, Inovio completed a registered equity financing, whereby the Company sold 4,595,094 shares of its common stock resulting in gross aggregate cash proceeds of $16.2 million.

        In March 2007, Inovio entered into an agreement in which the Company agreed to issue a total of 90,000 restricted shares of its common stock in equal quarterly installments in exchange for consulting services. As of December 31, 2007, Inovio had issued 33,750 restricted common shares and recorded a consulting expense and related liability of $10,350 as of December 31, 2007 for the 11,250 common shares which were issued in January 2008. During the remaining term of the agreement, the Company

F-34



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)


will continue to issue 11,250 restricted shares of its common stock at each quarter-end in exchange for the consulting services the Company will receive each quarter.

        In January 2007, Inovio exchanged for 2,201,644 restricted shares of its common stock and warrants to purchase up to 770,573 restricted shares of its common stock for 2,201,644 ordinary shares of Inovio's Singapore subsidiary Inovio Asia Pte. Ltd. (IAPL), pursuant to the terms of the Securities Purchase and Exchange Agreement under which the ordinary shares were originally issued by IAPL in October 2006 for $5.3 million.

        In March 2007, Inovio terminated its exclusive royalty-free license to IAPL allowing Inovio's subsidiary to use certain of Inovio's intellectual property, which had been issued in October 2006 prior to the ordinary share financing described above, in exchange for 6,584,365 ordinary shares of IAPL. Upon termination Inovio retained the IAPL ordinary shares received in the license transaction.

        In October 2006, Inovio completed a registered offering with foreign investors, whereby the Company sold 4,074,067 shares of its common stock and issued warrants to purchase 1,425,919 shares of its common stock which resulted in gross aggregate cash proceeds of $9.9 million. As part of this offering, Inovio informed holders of the then outstanding Series C Preferred Stock who held participation rights, of their ability to participate in the respective offering based upon the pricing of the transaction and the applicable liquidation preference for their series of preferred shares with such rights. Some of these participating stockholders had previously converted a portion of their shares of preferred stock pursuant to their optional conversion rights, and most of these participating stockholders wholly converted their remaining shares of Inovio's preferred stock through exercise of their participation rights in this offering. By electing to participate in this offering, these participating preferred stockholders converted 115.12 shares of previously issued Series C Preferred Stock and $14,571 of accrued dividends into 479,722 restricted shares of Inovio's common stock and warrants to purchase 167,902 restricted shares of Inovio's common stock. These participating stockholders received 304,450 additional restricted shares of common stock as compared to the number of shares of common stock into which their existing Series C Preferred Stock could have been converted under the original terms of the Series C Preferred Stock. As a result, Inovio recorded an imputed dividend charge of $1.9 million related to the participating stockholders who converted $1.2 million of their previous Series C Preferred Stock investment. Inovio calculated this imputed dividend charge pursuant to the guidance contained in Emerging Issues Task Force ("EITF") Issue No. 00-27, "Application of Issue No. 98-5 to Certain Convertible Instruments," where the incremental number of shares of its common stock which was received by participating Series C Preferred Stockholders was multiplied by the price of Inovio's common stock on the commitment date of the original Series C Preferred Stock issuance, or $6.08 per share, to calculate the imputed dividend charge associated with this beneficial conversion.

        In July and October 2006, Inovio issued 25,000 and 24,261 shares of Inovio's common stock, respectively, to an outside consulting company in payment of a non-refundable retainer in connection with the engagement of its services.

        In June 2006, Inovio issued 86,956 common shares to a licensing company in exchange for various patents and other assets and a $50,000 shareholder note receivable.

        In December 2005, Inovio completed a private placement of an aggregate of $15.8 million in gross cash proceeds through the sale of Inovio's common stock to institutional and accredited investors that included Merck and Vical, two of Inovio's strategic partners. At the closing, Inovio issued to the

F-35



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)


investors an aggregate of 9,892,735 shares of common stock and warrants to purchase an aggregate of 3,462,451 shares of common stock, and received in exchange (1) gross cash proceeds of $15.8 million; (2) an aggregate of 734 shares of outstanding Series A, B and C Cumulative Convertible Preferred Stock; and (3) 1,142,593 shares of outstanding common stock. In addition, Inovio issued to the investors five-year warrants to purchase 35% of the number of shares of common stock they acquired in the offering at an exercise price of approximately $2.93 per share.

        In January 2005, Inovio completed a private placement to accredited investors whereby the Company sold 1,540,123 shares of common stock at a purchase price of $4.05 per share and issued warrants to purchase 508,240 shares of common stock at an exercise price of $5.50 per share, which resulted in aggregate cash proceeds of $3.0 million. Of the aggregate proceeds, 20% was due upon the closing of the offering in January 2005, and 80% was due six months after the closing in June 2005, which resulted in the receipt of a promissory note from these 80% investors, for which the Company later granted an extension to December 2005. Prior to December 2005, Inovio received the remaining amount due from one of the three investors and therefore issued this investor its previously subscribed shares of common stock. A portion of this private placement involved investors who converted $3.2 million of their previous investment in Inovio's Series C Preferred Stock into 790,123 shares of the common stock issued as part of this private placement with no associated cash proceeds to the Company.

        The Company offered to exchange all or a portion of the remaining two subscribed investors January 2005 shares of common stock for new common stock and new warrants issued in the December 2005 offering. These participating investors were offered the same securities and pricing offered to new outside investors in the December 2005 offering, and the two remaining subscribed investors accepted the exchange offer. Therefore, in the December 2005 offering, the first previously subscribed investor exchanged 750,000 shares of previously subscribed common stock for 1,265,625 shares of new common stock in addition to 442,969 new warrants to purchase shares of common stock. The second previously subscribed investor exchanged 392,593 shares of previously subscribed common stock for 662,500 shares of new common stock and 231,875 new warrants to purchase shares of common stock. Because the purchase price in the December 2005 offering was lower than the January 2005 offering, the exchange resulted in a repricing of the shares subscribed to by these investors from $4.05 per share in the January 2005 offering to $2.40 per common share.

        To account for this transaction, Inovio followed the guidance contained in EITF 00-27 when calculating the imputed dividend charge related to this offering.

    Warrants

        In addition to warrants granted in connection with Inovio's Common and Preferred Stock offerings, as discussed above, the Company has issued the following additional warrants.

        In connection with the leasing of Inovio's new corporate headquarters, the Company issued a warrant to purchase 50,000 shares of common stock at $5.00 per share to the landlord of this leased facility in December 2004. This warrant is immediately exercisable and expires five years from the date of issuance. This warrant was valued on the date of issuance using the Black-Scholes pricing model. The fair value of this warrant, $120,913, will be recognized ratably over the five-year term of the lease as rent expense. As of December 31, 2007, this warrant remained outstanding.

F-36



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        On June 6, 2002, Inovio granted warrants to a placement agent to acquire 166,250 shares of common stock for $1.88 per share. In September 2003, warrants to purchase 30,000 shares of common stock were exercised totaling $56,400 in gross proceeds. In March 2005, warrants to purchase 136,250 shares of common stock were exercised totaling $256,150 in gross proceeds.

        On September 15, 2000, Inovio entered into an exclusive license agreement with the University of South Florida Research Foundation, Inc. (USF), whereby USF granted the Company an exclusive, worldwide license to USF's rights in patents and patent applications generally related to needle electrodes ("License Agreement"). Pursuant to the License Agreement, Inovio granted USF and its designees warrants to acquire 150,000 common shares for $9.00 per share until September 14, 2010. Of the total warrants granted, 75,000 vested at the date of grant and the remainder will vest upon the achievement of certain milestones. The 75,000 non-forfeitable vested warrants were valued at $553,950 using the Black- Scholes pricing model and were recorded as other assets with a credit to additional paid-in capital. The remaining 75,000 warrants are forfeitable and will be valued at the fair value on the date of vesting using the Black- Scholes pricing model. As of December 31, 2007, no warrants issued in connection with this licensing agreement had been exercised.

    Stock options

        Inovio has one active stock and cash-based incentive plan, the 2007 Omnibus Incentive Plan (the "Incentive Plan"), pursuant to which the Company has granted stock options and restricted stock awards to executive officers, directors and employees. The plan was adopted on March 31, 2007 and approved by the stockholders on May 4, 2007. The Incentive Plan reserves 750,000 shares of Inovio's common stock for issuance as or upon exercise of incentive awards granted and to be granted at future dates. At December 31, 2007, Inovio had 539,375 shares of common stock available for future grant and had outstanding 101,250 shares of unvested restricted common stock, 63,750 shares of vested restricted stock, and options to purchase 45,625 shares of common stock. The awards granted and available for future grant under the Incentive Plan generally have a term of ten years and generally vest over a period of three years. The Incentive Plan terminates by its terms on March 31, 2017.

        The Incentive Plan supersedes all of Inovio's previous stock option plans, which include the 1997 Stock Option Plan, under which the Company had options to purchase 41,498 shares of common stock outstanding and the Amended 2000 Stock Option Plan, under which the Company had options to purchase 3,378,339 shares of common stock outstanding at December 31, 2007. The terms and conditions of the options outstanding under these plans remain unchanged.

        Total compensation cost under SFAS No. 123(R) for Inovio's stock plans for the years ended December 31, 2007 and 2006 was $1.6 million and $1.3 million, of which $354,064 and $423,229 was included in research and development expenses and $1.2 million and $920,874 was included in general and administrative expenses, respectively.

        At December 31, 2007 and 2006, there was $1.3 million and $946,844 of total unrecognized compensation cost, respectively, related to unvested stock options, which is expected to be recognized over a weighted-average period of one year.

        Prior to January 1, 2006, Inovio accounted for employee stock options under the measurement and recognition provisions of APB No. 25. Accordingly, the Company recorded no share-based compensation expense for employee stock option grants as all options granted had exercises prices

F-37



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)


greater than the fair market value of the underlying stock on the date of grant. In accordance with SFAS No. 123, "Accounting for Stock-Based Compensation," the Company provided pro forma net loss and net loss per share disclosures for each period presented in these consolidated financial statements prior to the adoption of SFAS No. 123(R) as if Inovio had applied the fair value-based method in measuring compensation expense for share-based compensation plans. The following table illustrates the effect on net loss attributable to common stockholders as if the fair value-based method had been applied to all outstanding and unvested awards during the year ended December 31, 2005.

 
  Year ended
December 31, 2005
 

Net loss attributable to common stockholders, as reported

  $ (26,362,622 )

Deduct: Stock-based employee compensation expense determined under fair value method for all awards

    (1,375,703 )
       

Pro forma net loss attributable to common stockholders

  $ (27,738,325 )
       

Basic and diluted net loss attributable to common stockholders per share, as reported

  $ (1.39 )
       

Basic and diluted pro forma net loss attributable to common stockholders per share

  $ (1.46 )
       

        Inovio accounts for options granted to non-employees in accordance with Emerging Issues Task Force ("EITF") No. 96-18, "Accounting for Equity Instruments That Are Issued to Other Than Employees for Acquiring, or in Conjunction with Selling, Goods or Services," and Statement of Financial Accounting Standard ("SFAS") No. 123(R), "Share-Based Payment." The fair value of these options at the measurement dates was estimated using the Black-Scholes pricing model.

        Total stock-based compensation for options granted to non-employees for the years ended December 31, 2007, 2006 and 2005, was $119,191, $202,604, and $116,382, respectively. As of December 31, 2007 and 2006, 455,937 and 280,937 options remained outstanding, respectively.

        The following table summarizes total stock options outstanding at December 31, 2007:

 
  Options outstanding   Options exercisable  
Exercise price
  Options
outstanding
  Weighted-
average
remaining
contractual life
(in years)
  Weighted average
exercise price
  Options
exercisable
  Weighted-
average
exercise
price
 

$0.00 - $2.00

    508,280     4.8   $ 1.51     495,623   $ 1.50  

$2.01 - $4.00

    2,445,435     7.7   $ 2.96     1,360,142   $ 2.84  

$4.01 - $6.00

    401,499     6.1   $ 4.97     378,999   $ 5.00  

$6.01 - $8.00

    72,500     5.1   $ 6.27     72,500   $ 6.27  

$8.01 - $22.00

    37,748     0.9   $ 12.22     37,748   $ 12.22  
                             

    3,465,462     6.9   $ 3.15     2,345,012   $ 3.17  
                             

        At December 31, 2007, the aggregate intrinsic value of options outstanding was $150, the aggregate intrinsic value of options exercisable was $150, and the weighted average remaining contractual term of options exercisable was 6.1 years.

F-38



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        At December 31, 2006, the aggregate intrinsic value of options outstanding was $1.9 million; the aggregate intrinsic value of options exercisable was $1.5 million and the weighted average remaining contractual term of options exercisable was 6.3 years.

        Stock option activity under Inovio's stock option plans was as follows:

 
  Number of
shares
  Weighted-average
exercise price
 

Balance, December 31, 2004

    2,093,713   $ 3.47  

Granted

    622,000     3.77  

Exercised

    (34,980 )   1.70  

Cancelled

    (296,845 )   3.68  
             

Balance, December 31, 2005

    2,383,888     3.55  

Granted

    872,750     2.56  

Exercised

    (148,628 )   1.69  

Cancelled

    (309,110 )   4.64  
             

Balance, December 31, 2006

    2,798,900     3.22  

Granted

    963,125     3.20  

Exercised

    (94,563 )   2.31  

Cancelled

    (202,000 )   4.57  
             

Balance, December 31, 2007

    3,465,462   $ 3.15  
             

        The weighted average exercise price was $6.36 for the 118,250 options which expired during the year ended December 31, 2007, $5.53 for the 167,687 options which expired during the year ended December 31, 2006 and $4.24 for the 139,913 options which expired during the year ended December 31, 2005.

        The weighted average grant date fair value per share was $2.51 for options granted during the year ended December 31, 2007, $2.18 for options granted during the year ended December 31, 2006 and $3.05 for options granted during the year ended December 31, 2005.

        The aggregate intrinsic value of options exercised was $94,876 during the year ended December 31, 2007; $158,042 during the year ended December 31, 2006 and $32,556 during the year ended December 31, 2005.

        A summary of Inovio's nonvested restricted shares as of December 31, 2007 and activity during the year is as follows:

 
  Number of shares   Weighted-average grant-date fair value  

Nonvested at January 1, 2007

         

Granted

    165,000   $ 3.69  

Vested

    (63,750 ) $ 3.69  

Forfeited

         
             

Nonvested at December 31, 2007

    101,250   $ 3.69  
             

F-39



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

9. Stockholders' Equity (Continued)

        As of December 31, 2007, there was $278,991 of total unrecognized compensation cost related to nonvested share-based compensation arrangements. That cost is expected to be recognized over a weighted-average period of 2 years.

10. Commitments

        Rent expense was $490,069, $488,774, and $553,229 for the years ended December 31, 2007, 2006 and 2005, respectively. This amount is net of sublease income of $37,679 and $37,950 in 2007 and 2006, respectively. Future minimum lease payments under non-cancelable operating leases as of December 31, 2007 are as follows:

2008

  $ 508,907  

2009

    522,049  

2010

    103,036  

2011

    5,640  

Thereafter

     
       

Total

  $ 1,139,632  
       

        In the normal course of business, the Company is a party to a variety of agreements pursuant to which they may be obligated to indemnify the other party. It is not possible to predict the maximum potential amount of future payments under these types of agreements due to the conditional nature of Inovio's obligations and the unique facts and circumstances involved in each particular agreement. Historically, payments made by the Company under these types of agreements have not had a material effect on Inovio's business, results of operations or financial condition.

11. Income Taxes

        In accordance with SFAS 109, "Accounting for Income Taxes," a deferred tax asset or liability is determined based on the difference between the financial statement and tax basis of assets and liabilities as measured by the enacted tax rates which will be in effect when these differences reverse. Inovio provides a valuation allowance against net deferred tax assets unless, based upon the available evidence, it is more likely than not that the deferred tax asset will be realized.

F-40



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

11. Income Taxes (Continued)

        The components of the provision (benefit) for income taxes are shown below:

 
  As of
December 31,
2007
  As of
December 31,
2006
  As of
December 31,
2005
 

Current:

                   
 

Federal

  $   $   $  
 

State

             
 

Foreign

             
               

  $   $   $  
               

Deferred:

                   
 

Federal

  $   $   $  
 

State

             
 

Foreign

    327,000     (63,000 )   (58,000 )
               

  $ 327,000   $ (63,000 ) $ (58,000 )
               

        The reconciliation of income tax attributable to operations computed at the statutory tax rates to income tax expense (recovery), using a 35% statutory tax rate, is:

 
  Year ended
December 31,
2007
  Year ended
December 31,
2006
  Year ended
December 31,
2005
 

Income taxes at statutory rates

  $ (3,786,000 ) $ (4,368,000 ) $ (5,374,000 )

State income tax, net of federal benefit

    (742,000 )   (659,000 )   (676,000 )

Change in valuation allowance

    (6,445,000 )   4,636,000     4,486,000  

IRC Section 382 limitation

    12,749,000          

Write off of in-process research and development

            1,166,000  

Fair value warrant

    (1,192,000 )        

Other

    (257,000 )   328,000     340,000  
               

  $ 327,000   $ (63,000 ) $ (58,000 )
               

        The income tax expense has been recorded as an increase to general and administrative expenses, as its effect is immaterial.

F-41



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

11. Income Taxes (Continued)

        Significant components of Inovio's deferred tax assets and liabilities as of December 31, 2007 and 2006 are shown below:

 
  As of
December 31,
2007
  As of
December 31,
2006
 

Deferred tax assets:

             
 

Capitalized research expense

  $ 929,000   $ 785,000  
 

Net operating loss carry forwards

    23,019,000     30,650,000  
 

Research and development and other tax credits

    1,356,000     1,732,000  
 

Other

    4,028,000     3,001,000  
           

    29,332,000     36,168,000  

Valuation allowance

    (29,332,000 )   (36,168,000 )
           

Total deferred tax assets

         
           

Deferred tax liabilities:

             
 

Difference between book and tax basis for patent and license costs

         
 

Acquired intangibles

    (950,250 )   (1,013,250 )
           

Net deferred tax liabilities

  $ (950,250 ) $ (1,013,250 )
           

        Inovio has established a valuation allowance for all deferred tax assets, including those for net operating loss ("NOL") and tax credit carry forwards. Such a valuation allowance is recorded when it is more likely than not that the deferred tax assets will not be realized.

        The net deferred tax liability of $950,250 as of December 31, 2007, resulted from the acquisition of Inovio AS and reflects the net effect of temporary differences between the carrying amount of intangible assets for financial statement reporting purposes and the amount used for income tax purposes. The liability will be amortized over the life of the underlying intangible, which is 18 years and will be accounted for as an income tax recovery.

        As of December 31, 2007, Inovio had federal and California tax net operating loss carry forwards of approximately $55.9 million and $50.8 million, respectively. The federal loss carry forwards will begin to expire in 2019 unless previously utilized. The California loss carry forwards will begin to expire in 2013. The difference between the federal and California tax loss carry forwards is primarily attributable to the capitalization of research and development expenses for California income tax purposes and the 50% to 60% limitation of California loss carry forwards. In addition, Inovio had federal and state research tax credit carry forwards of $713,542 and $988,523, respectively. The federal tax credit carry forwards will begin to expire in 2022. The California research tax credit carry forwards do not expire. At December 31, 2007, the Company had foreign tax loss carry forwards related to the acquisition of Inovio AS of approximately $2.2 million. The foreign net operating loss carry forwards begin to expire in 2011. Future realization of this asset will result in a reduction to the extent of any remaining goodwill, then to any remaining long-term intangibles, and the remainder, if any, as a reduction of income tax expense. During 2007, $389,881 was recognized and recorded as a reduction of goodwill.

        Utilization of the NOL and tax credit carryforwards will be subject to a substantial annual limitation under Section 382 of the Internal Revenue Code of 1986, and similar state provisions due to

F-42



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

11. Income Taxes (Continued)


ownership change limitations that have occurred previously or that could occur in the future. These ownership changes will limit the amount of NOL and tax credit carryforwards and other deferred tax assets that can be utilized to offset future taxable income and tax, respectively. In general, an ownership change, as defined by Section 382, results from transactions increasing ownership of certain stockholders or public groups in the stock of the corporation by more than 50 percentage points over a three-year period. An analysis was performed which indicated that multiple ownership changes have occurred in previous years which created annual limitations on Inovio's ability to utilize NOL and tax credit carryovers. Such limitations will result in approximately $12.7 million of tax benefits related to NOL and tax credit carryforwards that will expire unused. Accordingly, the related NOL and R&D credit carryforwards have been removed from deferred tax assets accompanied by a corresponding reduction of the valuation allowance. Due to the existence of the valuation allowance, limitations created by future ownership changes, if any, related to Inovio's operations in the U.S. will not impact Inovio's effective tax rate.

        In July 2006, the FASB issued FIN 48, which clarifies the accounting for uncertainty in income taxes recognized in a company's financial statements in accordance with Statement of Financial Accounting Standards No. 109, "Accounting for Income Taxes." FIN 48 prescribes a recognition threshold and measurement process for recording in the financial statements uncertain tax positions taken or expected to be taken in a tax return. Additionally, FIN 48 provides guidance on the de-recognition, classification, interest and penalties, accounting in interim periods, and disclosure requirements for uncertain tax positions. Inovio adopted the provisions of FIN 48 beginning January 1, 2007. The adoption of FIN 48 did not impact Inovio's financial condition, results of operations or cash flows. As of December 31, 2007, the Company has not recorded any uncertain tax benefits.

        Inovio files income tax returns in the U.S. and various foreign and state jurisdictions. Due to losses incurred, the Company is essentially subject to income tax examination by tax authorities from Inovio's inception to date. Inovio's policy is to recognize interest expense and penalties related to income tax matters as tax expense. At December 31, 2007, Inovio does not have any significant accruals for interest related to unrecognized tax benefits or tax penalties.

12. 401(k) Plan

        In 1995, Inovio's U.S. subsidiary adopted a 401(k) Profit Sharing Plan (the "Plan") covering substantially all of its employees. The defined contribution plan allows the employees to contribute a percentage of their compensation each year. Inovio currently matches 50% of Inovio's employees' contributions, up to 6% of their annual compensation. The Company's contributions are recorded as expense in the accompanying consolidated statements of operations and totaled $54,965, $44,529 and $62,450 for the years ended December 31, 2007, 2006 and 2005, respectively.

13. Segment Information

        Pursuant to the Inovio's acquisition of Inovio AS (see Note 16), the Company operates in one business segment in the U.S. and Europe. Revenues are attributable to the geographical area based on the location of the customer. During the years ending December 31, 2007 revenues in Europe and the U.S. totaled $138,525 and $4.7 million, respectively. During the years ending December 31, 2006 revenues in Europe and the U.S. totaled $261,935 and $3.2 million, respectively, and during the year ending December 31, 2005 revenues in Europe and the U.S. totaled $379,250 and $5.1 million,

F-43



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

13. Segment Information (Continued)


respectively. Long-lived assets within the U.S. consist primarily of patents and other intellectual property. Long-lived assets outside the U.S. consist primarily of goodwill and intangible assets. As of December 31, 2007, long-lived assets in Europe and the U.S. totaled $7.7 million and $2.8 million, respectively. As of December 31, 2006, long-lived assets in Europe and the U.S. totaled $7.9 million and $2.9 million, respectively, and as of December 31, 2005, long-lived assets in Europe and the U.S. totaled $8.2 million and $2.3 million, respectively.

14. Related Party Transactions

        During the years ended December 31, 2007, 2006 and 2005, Inovio made payments of $0, $4,828, and $20,930, respectively, for legal services formerly provided by Catalyst Corporate Lawyers, where one of the former partners is the Chairman of the Company. All transactions are recorded at their exchange amounts.

        In March 2004, Inovio announced the selection of Quintiles Transnational Corp., a global pharmaceutical services organization, as the clinical research organization ("CRO") for clinical trials in the U.S. and Europe. In addition, the investment division of this CRO, Qfinance, Inc., is an investor in Inovio's Series A, B and C Preferred Stock. During the year ended December 31, 2006, Qfinance, Inc. converted 50, 100 and 109 shares respectively, of Inovio's Series A, B and C Preferred Stock into a total of 725,788 of Inovio's common shares. Total clinical trial expenses paid to Quintiles Transnational Corp. for the years ended December 31, 2007, 2006, and 2005, were $22,536, $371,018 and $3.5 million, respectively.

F-44



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

15. Supplemental Disclosures of Cash Flow Information

 
  Year ended
December 31,
2007
  Year ended
December 31,
2006
  Year ended
December 31,
2005
 

Supplemental schedule of financing activities:

                   

Conversion of minority interest into common stock

  $ 5,349,995   $   $  

Imputed dividends on preferred stock

  $   $ 1,851,056   $ 10,271,885  

Common stock issued in connection with declared dividends on preferred stock

  $   $ 22,264   $ 179,900  

Cashless exercise of warrants

  $ 38   $   $ 43  

Conversions of preferred stock to common stock

  $ 961   $ 1,764   $ 3,944  

Issuance of series D preferred stock for Inovio AS acquisition

  $   $   $ 7,904,494  

Issuance of common stock for patents and other assets

  $   $ 128,922   $  

Issuance of common stock in exchange for shareholder note receivable

  $   $ 86,030   $  

Leasehold improvements financed by landlord

  $ 92,486   $ 172,054   $  

Investment received in exchange for licensing agreement

  $   $ 125,000   $  

16. Inovio AS Acquisition

        In January 2005, the Company acquired Inovio AS for purposes of utilizing Inovio AS's electroporation for gene therapy and DNA vaccines as a complement to Inovio's existing electroporation therapy program. The acquisition expanded Inovio's intellectual property in electroporation and expanded its number of agreements with pharmaceutical companies. The Company's acquired in-process research and development consists of a prototype of a pulse-generating instrument and pulse applicator (the "Technology Platform") acquired in connection with the acquisition of Inovio AS.

        At the time of the acquisition of Inovio AS, the Technology Platform acquired had not yet reached economic viability and required an estimated additional $3.0 million investment to produce a product capable of being mass-produced. Further, prior to generating market sales, the Technology Platform would be required to go through clinical trials with each drug, DNA vaccine, or gene with which it would be partnered. As of the date of acquisition, clinical trials had not commenced for any combination of a specific payload and the Technology Platform.

        Given the fact that the Technology Platform had no alternative future use, the costs associated with producing a product capable of being mass-produced, and the requirements for FDA approval prior to generating any market sales, the Company determined the future expense levels to be significant and margins using a discounted cash flow method to be insignificant. Therefore, the Technology Platform was classified as IPR&D upon acquisition and valued using the royalty savings

F-45



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

16. Inovio AS Acquisition (Continued)


method. Under this method, the value of the technology is a function of the projected revenues attributable to the products utilizing the asset, the royalty rate that would hypothetically be charged by a licensor of the technology to a licensee and an appropriate discount rate to reflect the inherent risk of the projected cash flows.

    Royalty Rate

        To determine an appropriate royalty rate for the Technology Platform, the Company considered factors such as the age of the technology, market competition, quality, absolute and relative profitability, and the prevailing rates for similar properties. Inovio's analysis indicated an appropriate pretax royalty rate of 10 percent. This royalty rate was based on an analysis of royalty rates paid for similar drug delivery technologies.

    Cost to Complete

        As previously mentioned, an additional $3.0 million would be required in order to complete the Technology Platform. Based on discussions with Inovio AS's management, it was estimated that this $3.0 million would be spent during the next three years.

    Discount Rate

        The discount rate utilized for the Section 197 tax benefit calculation was based on the perceived risk associated with the technology platform. In developing a discount rate for the technology platform, the Company applied the acquired company's weighted average cost of capital of 43 percent.

        The major risks and uncertainties associated with the timely and successful completion of the Technology Platform include both the ability to confirm its safety and efficacy based on data obtained from clinical trials and the ability to obtain necessary regulatory approvals. Additionally, the major risks and uncertainties include the ability to successfully complete the Technology Platform within the estimated costs. The above assumptions were prepared solely for the purposes of estimating fair values of these items as of the date of their acquisition. No assurance can be given that the underlying assumptions used to forecast the cash flows or the timely and successful completion of such projects will materialize, as estimated. For these reasons, among others, actual results may vary significantly from the estimated results.

        The acquired IPR&D is still being developed for the future economic viability contemplated at the time of acquisition. Inovio is concurrently conducting Phase I and pre-clinical trials using the Technology Platform acquired, and the Company has entered into certain significant licensing agreements for use of this acquired technology.

        Under the terms of the transaction, Inovio acquired the entire share capital of Inovio for an aggregate purchase price of $10.9 million; $3.0 million of the purchase price consisted of cash and $7.9 million consisted of shares of Inovio's Series D Convertible Preferred Stock, par value $0.001 per share, net of transaction costs. Inovio issued 1,966,292 shares of the Series D Preferred Stock in the transaction, based on the average closing price of Inovio's common stock as reported on the NYSE Alternext during the 30 trading day period immediately preceding the closing. As of December 31, 2007, 1,852,981 shares of the Series D Preferred Stock had been converted into 1,852,981 shares of common stock.

F-46



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

16. Inovio AS Acquisition (Continued)

        When valuing the Series D Preferred Stock issued as part of the Acquisition for accounting purposes, Inovio followed guidance set forth in SFAS No. 141, Business Combinations . Under SFAS No. 141, the fair value of securities issued as part of an acquisition should be valued based on the market price of those securities for a reasonable period before and after the date that the terms of the acquisition are agreed to and announced. For purposes of valuing the Series D Preferred Stock issued as part of the Acquisition, the Company used an average fair value of $4.02 per share of Series D Preferred Stock. This average was based on the closing prices of Inovio's common stock on each of the three days prior to the Acquisition, the day of Acquisition and the three days following the Acquisition.

        Those shareholders of Inovio AS who received shares of Series D Preferred Stock in the transaction (the "Series D Holders") will also be entitled to additional issuances of Series D Preferred Stock in the event the Company achieves certain strategic and commercial milestones, as set forth in the Stock Purchase Agreement and summarized below. None of the following milestones were achieved:

    In the event that the Company received payment commitments of at least $8.0 million, of which at least $1.0 million must be in the form of upfront payments, through the signing of contracts involving Inovio AS' technology through September 30, 2006, the Company was required to issue an additional $2.0 million of Series D Preferred Stock to the shareholders of Inovio AS ("the Second Payment"). The value of each share of Series D Preferred Stock issued in connection with the Second Payment would have equaled the average of the closing price of Inovio's common stock as reported on the NYSE Alternext during the 30 day trading period immediately preceding the Second Payment date.

    In the event that the Company received payment commitments of at least $16.0 million (including the $8.0 million in payment commitments noted above), of which at least $2.0 million (including the $1.0 million in upfront payments noted above) must be in the form of upfront payments, through the signing of contracts involving Inovio AS' technology through September 30, 2006, the Company was required to issue an additional $1.0 million of Series D Preferred Stock to the shareholders of Inovio AS ("the Third Payment"). The value of each share of Series D Preferred Stock issued in connection with the Third Payment would have equaled the average of the closing price of Inovio's common stock as reported on the NYSE Alternext during the 30 day trading period immediately preceding the Third Payment date.

        Under the purchase method of accounting, the total consideration as shown in the table below was allocated to Inovio AS' tangible and intangible assets and liabilities based on their estimated fair values as of the date of the completion of the Acquisition. The total consideration was as follows:

Fair value of Series D Preferred Stock issued(a)

  $ 7,904,494  

Cash

    3,000,000  

Transaction costs

    121,517  
       

Total consideration

  $ 11,026,011  
       

      (a)
      There is no market price for the Series D Convertible Preferred Stock, thus the market price of Inovio's common stock was used in determining the fair value of the Series D Convertible Preferred Stock on the basis that such shares are convertible into common

F-47



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

16. Inovio AS Acquisition (Continued)

        stock on a one-for-one conversion ratio and the dividend, participation and liquidation rights of the Series D Convertible Preferred Stock closely resemble Inovio's common stock.

        The allocation of the above purchase price is as follows:

Fair value of net tangible assets acquired and liabilities assumed

  $ 487,417  

Fair value of identifiable intangible assets acquired

    7,382,000  

Deferred tax liabilities

    (1,134,000 )

Goodwill

    4,290,594  
       

Total purchase price allocation

  $ 11,026,011  
       

        Inovio AS' results of operations for the period from the date of acquisition (January 25, 2005) through December 31, 2005, were included in Inovio's consolidated statement of operations for the year ended December 31, 2005. Identifiable acquired intangible assets include in-process research and development of $3.3 million, and an intangible asset related to acquired contracts and intellectual property of approximately $4.1 million. At the close of the acquisition, Inovio determined that the acquired contractual relationships represented a valuable asset due to the expectation of future business opportunities to be leveraged from the existing relationship with each partner. Inovio used the excess earnings method to value the contractual relationships, examining the economic returns contributed by the identified tangible and intangible assets of the acquired company, and then isolating the excess return attributable to contractual relationships. Under this method, the value of the contractual relationship was calculated as a function of:

    an estimated attrition rate of contracts as of the acquisition date;

    the expected future operating income generated by the contracts;

    the contributory asset charge that would be paid to the requisite operating assets from operating income; and

    a discount rate that reflects the level of risk associated with future cash flows attributable to the contractual relationships.

        Acquired contracts expected to generate future cash flows upon the date of acquisition included the acquired contractual relationships and the acquired Company's customer contracts which were expected to generate future market sales. Inovio used projections to determine the base revenue projections related to the contractual relationships as well as the associated expenses. The cash flows generated by the contractual relationships represented a return on all of the assets employed in the generation of those cash flows, including tangible as well as identifiable intangible assets, consistent with the value and the relative risk of the asset. As part of this analysis, the Company determined individual rates of return applicable to each acquired asset or asset class, and estimated the effective "contributory asset charge" to be applied to the cash flows generated by the acquired contractual relationships. Contributory asset charges were made for returns related to the following: working capital, fixed assets, technology platform and assembled workforce. An effective tax rate of 40 percent was applied to the projected cash flows generated by the acquired contractual relationships. The calculated contributory asset charge was then applied to the expected future operating income generated by the surviving contracts to estimate the excess cash flow from the contractual relationships

F-48



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

16. Inovio AS Acquisition (Continued)


and then discounted to present value at a discount rate that reflected the amount of risk associated with the hypothetical cash flows generated. In valuing the contractual relationships, the Company used a discount rate of 43 percent. In accordance with SFAS No. 142, the Company determined a useful life for remaining contractual relationships of approximately 18 years. After employing this method, the Company then added the present value of the Section 197 tax benefits to arrive at the indicated fair value of the contractual relationships, as of the acquisition date of $4.1 million, to be amortized over 18 years.

        The $3.3 million assigned to acquired in-process research and development ("IPR&D") was recorded as an expense in the consolidated statement of operations for the year ended December 31, 2005. Inovio believes that electroporation is one of the key enabling technologies to make vaccines efficacious, practical and cost effective. A complete electroporation solution consists of three components: a pulse generating instrument; a line of pulse applicators; and a "payload" consisting of a drug, DNA vaccine, or gene that will typically be provided by a third party, but which is integral to the solution submitted for regulatory approval and ultimately marketed and sold. At the time of acquisition, the Company being acquired had a prototype of a pulse- generating instrument and pulse applicator (the "Technology Platform"); however, this Technology Platform had not yet reached economic viability and was estimated to require an additional $3.0 million investment to produce a product capable of being mass-produced. Further, prior to generating market sales the Technology Platform would be required to go through clinical trials with each drug, DNA vaccine, or gene with which it would be partnered. As of the date of acquisition, clinical trials had not started for any combination of a specific payload and the Technology Platform. The Technology Platform had no alternative future use, there were significant remaining costs associated with producing a product capable of being mass-produced, and the requirements for FDA approval prior to generating any market sales. In addition, Inovio determined that future expense levels were significant and that the margins using a discounted cash flow method were insignificant. Based on these considerations, the Technology Platform was classified as IPR&D upon acquisition and valued using the royalty savings method. Under this method, the value of the technology is a function of the projected revenues attributable to the products utilizing the asset, the royalty rate that would hypothetically be charged by a licensor of the technology to a licensee, and an appropriate discount rate to reflect the inherent risk of the projected cash flows

        On December 31, 2007, Inovio's wholly-owned Norwegian subsidiary Inovio AS transferred certain patent and other intellectual property rights ("IPR") to Inovio's wholly owned U.S. subsidiary Genetronics Inc. The value assigned to these rights was $1.9 million, which was determined by and was the responsibility of management of Inovio, who considered in part preliminary work performed by an independent valuation specialist in Norway. All Norwegian tax gains associated with this transfer of the patents and IPR was offset by prior year tax loss carry forwards. Subsequent to year-end, the Company changed the name of Inovio AS to Inovio Tec AS. Simultaneously, the Company incorporated a new Norwegian wholly-owned subsidiary under the name Inovio AS, for the purpose of organizing a research effort directed towards the development of specific cancer vaccine candidates. The Company expects funding for this program to be about $5.0 million over the next several years. In January 2008, all employees, employee agreements, lease agreements and fixed assets were transferred from Inovio Tec AS to Inovio AS.

F-49



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

17. Quarterly Financial Information (Unaudited and Restated, as indicated)

        The following unaudited quarterly financial information reflects all normal recurring adjustments, which are, in the opinion of management, necessary for a fair statement of the results of the interim periods. The four quarters for per share figures may not add for the year because of the different number of shares outstanding during the year. This quarterly information has been restated for, and as of the end of, all quarters of fiscal 2007 and the fourth quarter of fiscal 2006 from previously reported information filed on Form 10-Q, as a result of the restatement of Inovio's financial results as discussed in Note 2. The results of operations for any period are not necessarily indicative of the results to be

F-50



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

17. Quarterly Financial Information (Unaudited and Restated, as indicated) (Continued)


expected for any future period. Summarized unaudited quarterly data for the years ended December 31, 2007 and 2006, are as follows:

 
  Quarter Ended
December 31,
2007
  Quarter Ended
September 30,
2007
  Quarter Ended
June 30,
2007
  Quarter Ended
March 31,
2007
 
 
   
  As restated(1)
  As restated(1)
  As restated(1)
 

Consolidated Statement of Operations:

                         

Revenue:

                         

License fee and milestone payments

  $ 2,212,854   $ 136,870   $ 209,265   $ 234,489  

Revenue under collaborative research and development arrangements

    1,054,031     265,970     286,312     247,990  

Grants and miscellaneous revenue

    54,854     83,671         21,423  
                   

Total revenue

    3,321,739     486,511     495,577     503,902  

Operating Expenses:

                         

Research and development

    1,866,322     2,335,378     2,907,836     2,516,411  

General and administrative

    3,266,767     3,177,723     2, 344,551     2,291,161  
                   

Total operating expenses

    5,133,089     5,513,101     5,252,387     4,807,572  
                   

Loss from operations

    (1,811,350 )   (5,026,590 )   (4,756,810 )   (4,303,670 )

Interest income

    357,514     405,023     286,792     223,068  

Other income

    427,906     1,927,064     727,305     339,305  
                   

Net loss

    (1,025,930 )   (2,694,503 )   (3,742,713 )   (3,741,297 )

Imputed and declared dividends on preferred stock

            (8,244 )   (15,091 )
                   

Net loss attributable to common stockholders

    (1,025,930 ) $ (2,694,503 ) $ (3,750,957 ) $ (3,756,388 )
                   

Amounts per common share—basic and diluted:

                         

Net loss

  $ (0.02 ) $ (0.06 ) $ (0.09 ) $ (0.10 )

Imputed and declared dividends on preferred stock

                 
                   

Net loss attributable to common stockholders

  $ (0.02 ) $ (0.06 ) $ (0.09 ) $ (0.10 )
                   

Weighted average number of common shares—basic and diluted

    43,812,905     43,699,683     40,674,947     37,694,634  

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 and quarterly periods in 2007 to reflect certain accounting reclassifications, as described more fully in Note 2.

F-51



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

17. Quarterly Financial Information (Unaudited and Restated, as indicated) (Continued)

 
  Quarter Ended
December 31,
2006
  Quarter Ended
September 30,
2006
  Quarter Ended
June 30,
2006
  Quarter Ended
March 31,
2006
 
 
  As restated(1)
   
   
   
 

Consolidated Statement of Operations:

                         

Revenue:

                         

License fee and milestone payments

  $ 810,290   $ 204,699   $ 171,062   $ 151,054  

Revenue under collaborative research and development arrangements

    199,489     254,137     232,351     276,230  

Grants and miscellaneous revenue

    521,887     116,993     259,277     270,709  
                   

Total revenue

    1,531,666     575,829     662,690     697,993  

Operating Expenses:

                         

Research and development

    2,701,534     2,185,931     1,981,895     1,640,425  

General and administrative

    2,623,888     1,926,628     1,883,521     1,870,550  
                   

Total operating expenses

    5,325,422     4,112,559     3,865,416     3,510,975  
                   

Loss from operations

    (3,793,756 )   (3,536,730 )   (3,202,726 )   (2,812,982 )

Interest income

    230,638     124,398     152,503     174,007  

Other income

    310,687     3,451     1,453     5,115  
                   

Net loss

    (3,252,431 )   (3,408,881 )   (3,048,770 )   (2,633,860 )

Imputed and declared dividends on preferred stock

    (1,867,170 )   (31,706 )   (34,423 )   (72,365 )
                   

Net loss attributable to common stockholders

  $ (5,119,601 ) $ (3,440,587 ) $ (3,083,193 ) $ (2,706,225 )
                   

Amounts per common share—basic and diluted:

                         

Net loss

  $ (0.10 ) $ (0.11 ) $ (0.10 ) $ (0.09 )

Imputed and declared dividends on preferred stock

    (0.05 )            
                   

Net loss attributable to common stockholders

  $ (0.15 ) $ (0.11 ) $ (0.10 ) $ (0.09 )
                   

Weighted average number of common shares—basic and diluted

    34,902,998     30,902,644     30,568,369     29,621,372  

(1)
Inovio has restated the previously issued consolidated financial statements for the year ended December 31, 2006 and quarterly periods in 2007 to reflect certain accounting reclassifications, as described more fully in Note 2.

18. Subsequent Events

        The Company's short-term investments included $14.1 million and $13.6 million of auction rate securities issued primarily by municipalities as of December 31, 2007 and February 29, 2008, respectively. In early March 2008, the Company was informed that there was insufficient demand at auction (also known as failure to settle) for six of its auction rate securities. As a result, these affected

F-52



INOVIO BIOMEDICAL CORPORATION

NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS (Continued)

18. Subsequent Events (Continued)


securities are currently not liquid. However, the Company now earns a higher interest rate on these specific investments. In the event the Company needs to access the funds that are in an illiquid state, it will not be able to do so without the possible loss of principal, until a future auction for these investments is successful or they are redeemed by the issuer or they mature. At this time, management has not obtained sufficient evidence to conclude that these investments are impaired or that they will not be settled in the short term, although the market for these investments is presently uncertain. If the Company is unable to sell these securities in the market or they are not redeemed, then the Company could be required to hold them to maturity. The Company does not have a need to access these funds for operational purposes for the foreseeable future. The Company will continue to monitor and evaluate these investments on an ongoing basis for impairment or for the need to reclassify to long term investments.

F-53



INOVIO BIOMEDICAL CORPORATION

CONDENSED CONSOLIDATED BALANCE SHEETS

 
  September 30,
2008
  December 31,
2007
 
 
  (Unaudited)
   
 

ASSETS

 

Current assets:

             

Cash and cash equivalents

  $ 6,411,494   $ 10,250,929  

Short-term investments

        16,999,600  

Accounts receivable

    740,368     1,139,966  

Prepaid expenses and other current assets

    747,971     613,656  
           

Total current assets

    7,899,833     29,004,151  

Investments

    12,057,775      

Fixed assets, net

    403,609     401,727  

Intangible assets, net

    5,937,549     6,186,430  

Goodwill

    3,900,713     3,900,713  

Other assets

    282,000     282,000  
           

Total assets

  $ 30,481,479   $ 39,775,021  
           

LIABILITIES AND STOCKHOLDERS' EQUITY

 

Current liabilities:

             

Accounts payable and accrued expenses

  $ 1,478,016   $ 1,807,305  

Accrued clinical trial expenses

    491,922     573,767  

Line of credit

    1,763,845      

Common stock warrants

    145,833     367,071  

Deferred revenue

    497,676     544,410  

Deferred rent

    77,953     61,946  
           

Total current liabilities

    4,455,245     3,354,499  

Deferred revenue, net of current portion

    4,084,065     4,335,806  

Deferred rent, net of current portion

    37,245     99,712  

Deferred tax liabilities

    903,000     950,250  
           

Total liabilities

    9,479,555     8,740,267  
           

Commitments and contingencies

             

Stockholders' equity:

             

Preferred stock

        113  

Common stock

    44,011     43,815  

Additional paid-in capital

    171,616,752     170,730,621  

Receivables from stockholders

    (50,000 )   (50,000 )

Accumulated deficit

    (149,237,215 )   (139,847,326 )

Accumulated other comprehensive (loss) income

    (1,371,624 )   157,531  
           

Total stockholders' equity

    21,001,924     31,034,754  
           

Total liabilities and stockholders' equity

  $ 30,481,479   $ 39,775,021  
           

See accompanying notes.

F-54



INOVIO BIOMEDICAL CORPORATION

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(Unaudited)

 
  Three Months Ended
September 30,
  Nine Months Ended
September 30,
 
 
  2008   2007   2008   2007  

Revenue:

                         

License fee and milestone payments

  $ 214,825   $ 136,870   $ 611,578   $ 580,624  

Revenue under collaborative research and development arrangements

    239,912     265,970     1,159,207     800,272  

Grant and miscellaneous revenue

        83,671         105,094  
                   

Total revenue

    454,737     486,511     1,770,785     1,485,990  
                   

Operating expenses:

                         

Research and development

    1,274,387     2,335,378     4,551,039     7,759,625  

General and administrative

    1,928,928     3,177,723     7,416,613     7,813,435  
                   

Total operating expenses

    3,203,315     5,513,101     11,967,652     15,573,060  
                   

Loss from operations

    (2,748,578 )   (5,026,590 )   (10,196,867 )   (14,087,070 )

Interest income, net

    97,008     405,023     587,128     914,883  

Other income, net

    307,162     1,927,064     219,850     2,993,674  
                   

Net loss

    (2,344,408 )   (2,694,503 )   (9,389,889 )   (10,178,513 )

Imputed and declared dividends on preferred stock

                (23,335 )
                   

Net loss attributable to common stockholders

  $ (2,344,408 ) $ (2,694,503 ) $ (9,389,889 ) $ (10,201,848 )
                   

Amounts per common share—basic and diluted:

                         

Net loss per share attributable to common stockholders

  $ (0.05 ) $ (0.06 ) $ (0.21 ) $ (0.25 )
                   

Weighted average number of common shares outstanding—basic and diluted

    43,929,654     43,699,683     43,881,047     40,711,751  

See accompanying notes.

F-55



INOVIO BIOMEDICAL CORPORATION

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

 
  Nine Months
Ended
September 30,
2008
  Nine Months
Ended
September 30,
2007
 

Cash flows from operating activities:

             
 

Net loss

  $ (9,389,889 ) $ (10,178,513 )
 

Adjustments to reconcile net loss to net cash used in operating activities:

             
   

Depreciation

    142,000     124,831  
   

Amortization of intangible assets

    615,094     622,929  
   

Change in value of common stock warrants

    (221,238 )   (2,750,953 )
   

Stock-based compensation

    844,401     1,389,324  
   

Compensation for services to be paid in common stock

    40,725     595,857  
   

Amortization of deferred tax liabilities

    (47,250 )   (47,250 )
   

Deferred rent

    (46,460 )   (51,345 )
   

Loss on disposal of fixed assets

    5,473      
   

Accretion of discount on available-for-sale securities

    (60,345 )   (49,410 )
   

Changes in operating assets and liabilities:

             
     

Accounts receivable

    413,065     24,813  
     

Prepaid expenses and other current assets

    (184,906 )   308,877  
     

Accounts payable and accrued expenses

    (408,413 )   (153,934 )
     

Deferred revenue

    (298,475 )   (336,627 )
           

Net cash used in operating activities

    (8,596,218 )   (10,501,401 )
           

Cash flows from investing activities:

             

Purchases of available-for-sale securities

    (4,500,000 )   (16,602,985 )

Proceeds from sales of available-for-sale securities

    8,000,000     10,000,000  

Purchases of capital assets

    (114,144 )   (105,014 )

Capitalization of patents and other assets

    (366,213 )   (409,341 )
           

Net cash provided by (used in) investing activities

    3,019,643     (7,117,340 )
           

Cash flows from financing activities:

             

Proceeds from issuance of common stock, net of issuance costs

    1,088     16,290,322  

Proceeds from line of credit

    1,803,036      

Repayment of line of credit

    (39,191 )      

Repayment of stockholder note receivable

        36,030  

Payment of preferred stock cash dividend

        (23,335 )
           

Net cash provided by financing activities

    1,764,933     16,303,017  
           

Effect of exchange rate changes on cash

    (27,793 )   80,837  
           

Decrease in cash and cash equivalents

    (3,839,435 )   (1,234,887 )

Cash and cash equivalents, beginning of period

    10,250,929     8,321,606  
           

Cash and cash equivalents, end of period

  $ 6,411,494   $ 7,086,719  
           

See accompanying notes.

F-56



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(Unaudited)

1. Basis of Presentation

        The accompanying unaudited condensed consolidated financial statements of Inovio Biomedical Corporation (the "Company") have been prepared in accordance with United States generally accepted accounting principles ("U.S. GAAP") for interim financial information and with instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by U.S. GAAP for complete financial statements. The condensed consolidated balance sheet as of September 30, 2008, condensed consolidated statements of operations for the three and nine months ended September 30, 2008 and 2007, and the condensed consolidated statements of cash flows for the nine months ended September 30, 2008 and 2007, are unaudited, but include all adjustments (consisting of normal recurring adjustments) that the Company considers necessary for a fair presentation of the financial position, results of operations and cash flows for the periods presented. The results of operations for the three and nine months ended September 30, 2008, shown herein are not necessarily indicative of the results that may be expected for the year ending December 31, 2008, or for any other period. These unaudited condensed consolidated financial statements, and notes thereto, should be read in conjunction with the audited consolidated financial statements for the year ended December 31, 2007, included in the Company's Form 10-K filed with the U.S. Securities and Exchange Commission ("SEC") on March 17, 2008.

        The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets, liabilities, disclosures of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates.

        The Company incurred a net loss attributable to common stockholders of $2.3 million and $9.4 million for the three and nine months ended September 30, 2008, respectively. The Company had working capital of $3.4 million, in addition to $12.1 million of long-term investments, and an accumulated deficit of $149.2 million as of September 30, 2008. The Company's ability to continue as a going concern is dependent upon its ability to achieve profitable operations and to obtain additional capital. The Company will continue to rely on outside sources of financing to meet its capital needs. The outcome of these matters cannot be predicted at this time. Further, there can be no assurance, assuming the Company successfully raises additional funds, that the Company will achieve positive cash flow. If the Company is not able to secure additional funding, the Company will be required to scale back its research and development programs, preclinical studies and clinical trials, and general and administrative activities and may not be able to continue in business. These unaudited condensed consolidated financial statements do not include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should the Company be unable to continue in business.

2. Principles of Consolidation

        These unaudited condensed consolidated financial statements include the accounts of Inovio Biomedical Corporation, incorporated in the state of Delaware, and its wholly-owned subsidiaries, Genetronics, Inc., a company incorporated in the state of California; Inovio AS and Inovio Tec AS, companies incorporated in Norway; and Inovio Asia Pte. Ltd. ("IAPL"), a company incorporated in the Republic of Singapore. All intercompany accounts and transactions have been eliminated upon consolidation.

F-57



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

3. Investment Securities and Fair Value Measurements

        All of the Company's investment securities are classified as available-for-sale and are reported on the condensed consolidated balance sheet at estimated fair value. Unrealized gains and losses associated with these investments are reported in stockholders' equity in accordance with Statement of Financial Accounting Standards ("SFAS") No. 115, Accounting for Certain Investments in Debt and Equity Securities.

        As of September 30, 2008, the Company's investments included $12.1 million of high-grade (AAA rated) auction rate securities ("ARS") issued primarily by municipalities. The Company's ARS are debt instruments with a long-term maturity and with an interest rate that is reset in short intervals through auctions. The recent conditions in the global credit markets have prevented some investors from liquidating their holdings of ARS because the amount of securities submitted for sale has exceeded the amount of purchase orders for such securities. The Company has been informed that there is insufficient demand at auction for all of its high-grade ARS. As a result, these affected securities are currently not liquid and the interest rates have been reset to the predetermined higher rates. When auctions for these securities fail, the investments may not be readily convertible to cash until a future auction of these investments is successful or they are redeemed or mature. If the credit ratings of the security issuers deteriorate and any decline in market value is determined to be other-than-temporary, the Company would be required to adjust the carrying value of the investment through a permanent impairment charge.

        During the three and nine months ended September 30, 2008 the Company has recorded an unrealized loss of $430,000 and $1.5 million, respectively, on its ARS holdings. The unrealized loss reduced the estimated fair value of ARS holdings as of September 30, 2008 to $12.1 million. The Company has determined this reduction in fair value to be temporary. All of the $12.1 million of ARS are classified within non-current assets in the unaudited condensed consolidated balance sheet as of September 30, 2008.

        Subsequent to September 30, 2008, the Company received a proposal from its investment advisor to redeem its ARS at par on June 30, 2010. The Company has entered into an appeals process to expedite this timeline, seeking earlier redemption. In addition, the Company is reviewing a proposal from its investment advisor to increase the Line of Credit (See Note 4—Line of Credit) from $5.0 million to $9.0 million in order to provide additional liquidity.

        On January 1, 2008 the Company adopted the provisions of SFAS No. 157, Fair Value Measurements ("SFAS 157"), for its financial assets and liabilities. SFAS 157 defines fair value as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants on the measurement date. SFAS 157 also establishes a fair value hierarchy that requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value. The standard describes three levels of inputs that may be used to measure fair value:

            Level 1 Inputs     Quoted prices for identical instruments in active markets. The Company has determined that its investments in money market funds meet the criteria for definition within the level 1 hierarchy.

F-58



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

3. Investment Securities and Fair Value Measurements (Continued)

            Level 2 Inputs     Quoted prices for similar instruments in active markets; and quoted prices for identical or similar instruments in markets that are not active. The Company has determined that no items meet the criteria for definition within the level 2 hierarchy.

            Level 3 Inputs     Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities. The Company has determined that its investments in ARS meet the criteria for definition within the level 3 hierarchy. The Company has used a discounted cash flow model to determine the estimated fair value of its investment in ARS as of September 30, 2008. The assumptions used in preparing the discounted cash flow model include estimates for interest rates, timing and amount of cash flows and expected holding period of the ARS. Based on this assessment of fair value, the Company recorded an unrealized loss of approximately $1.5 million related to its ARS as of September 30, 2008. Management believes this unrealized loss is primarily attributable to the limited liquidity of these investments and has no reason to believe that any of the underlying issuers are presently at risk of credit default.

        The Company endeavors to utilize the best available information in measuring fair value. Financial assets and liabilities are classified in their entirety based on the lowest level of input that is significant to the fair value measurement. The following table sets forth the Company's financial assets that were accounted for at fair value on a recurring basis as of September 30, 2008:

 
  Total   Quoted Prices
in Active
Markets for
Identical
Assets
(Level 1)
  Significant
Unobservable
Inputs
(Level 3)
 

Cash and cash equivalents(1)

  $ 5,381,534   $ 5,381,534   $  

Available-for-sale investments, long-term(2)

    12,057,775         12,057,775  
               

Total

  $ 17,439,309   $ 5,381,534   $ 12,057,775  
               

(1)
Cash and cash equivalents consist primarily of money market funds with original maturity dates of three months or less.

(2)
Available-for-sale investments consist of ARS issued primarily by municipalities. Unrealized gains or losses on available-for-sale securities are recorded in accumulated other comprehensive loss at each measurement date.

F-59



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

3. Investment Securities and Fair Value Measurements (Continued)

        The following table presents a summary of changes in fair value of the Company's assets measured on a recurring basis using significant unobservable inputs (Level 3) as defined in SFAS 157 for the nine months ended September 30, 2008:

 
  Auction Rate
Securities
 

Balance at January 1, 2008

  $  

Transfers in to Level 3

    14,050,000  

Total unrealized losses included in other comprehensive loss

    (1,492,225 )

Purchases and settlements (net)

    (500,000 )
       

Balance at September 30, 2008

  $ 12,057,775  
       

Total change in unrealized losses included in other comprehensive loss

  $ (1,492,225 )
       

4. Line of Credit

        On August 26, 2008, the Company received notice from UBS Bank USA ("UBS") that the Company's application had been approved for a $5.0 million uncommitted demand revolving line of credit ("Line of Credit") secured by ARS held by the Company in an account with UBS Financial Services, Inc. (the "Collateral Account"), to provide additional working capital. Advances under the Line of Credit bear interest at LIBOR plus 1.00% (the "Spread Over LIBOR"). UBS may change the Spread Over LIBOR at its discretion when the Collateral consisting of ARS may be sold, exchanged or otherwise conveyed by the Company for gross proceeds that are, in the aggregate, not less than the par value of such securities. As of September 30, 2008 the Company has drawn down $1.8 million from the Line of Credit.

        Subsequent to September 30, 2008, the Company has been reviewing a proposal from UBS to increase the Line of Credit to $9.0 million in order to provide additional liquidity.

F-60



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

5. Goodwill and Intangible Assets

 
  Useful
Life
Years
  Cost   Accumulated
amortization
  Net book
value
 

As of September 30, 2008

                         

Non-amortizing:

                         

Goodwill(a)

      $ 3,900,713   $   $ 3,900,713  

Amortizing:

                         

Patents

    8 - 17   $ 5,590,322   $ (3,133,380 ) $ 2,456,942  

Licenses

    8 - 17     1,198,781     (943,174 )   255,607  

Other(b)

    18     4,050,000     (825,000 )   3,225,000  
                     
 

Total Intangible Assets

          10,839,103     (4,901,554 )   5,937,549  
                     

Total Goodwill and Intangible Assets

        $ 14,739,816   $ (4,901,554 ) $ 9,838,262  
                     

As of December 31, 2007

                         

Non-amortizing:

                         

Goodwill(a)

      $ 3,900,713   $   $ 3,900,713  

Amortizing:

                         

Patents

    8 - 17   $ 5,224,109   $ (2,775,713 ) $ 2,448,396  

Licenses

    8 - 17     1,198,781     (854,497 )   344,284  

Other(b)

    18     4,050,000     (656,250 )   3,393,750  
                     
 

Total Intangible Assets

          10,472,890     (4,286,460 )   6,186,430  
                     

Total Goodwill and Intangible Assets

        $ 14,373,603   $ (4,286,460 ) $ 10,087,143  
                     

(a)
Goodwill was recorded from the Inovio AS acquisition in January 2005.

(b)
Other intangible assets represent the fair value of acquired contracts and intellectual property from the Inovio AS acquisition.

        Aggregate amortization expense on intangible assets for the three and nine months ended September 30, 2008 was $200,000 and $615,000, respectively, and for the three and nine months ended September 30, 2007 was $208,000 and $623,000, respectively. The estimated aggregate amortization expense for each of the five succeeding fiscal years is $227,000 for the remainder of fiscal year 2008, $875,000 for 2009, $736,000 for 2010, $628,000 for 2011, and $566,000 for 2012.

F-61



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity

        The following is a summary of the Company's authorized and issued common and preferred stock as of September 30, 2008 and December 31, 2007:

 
   
   
  Outstanding as of  
 
  Authorized   Issued   September 30,
2008
  December 31,
2007
 

Common Stock, par $0.001

    300,000,000     44,105,550     44,011,800     43,814,739  

Series A Preferred Stock, par $0.001

    1,000     817          

Series B Preferred Stock, par $0.001

    1,000     750          

Series C Preferred Stock, par $0.001

    1,091     1,091     71     71  

Series D Preferred Stock, par $0.001

    1,966,292     1,966,292         113,311  

Preferred Stock

        The following is a summary of changes in the number of outstanding shares of the Company's preferred stock for the three months ended September 30, 2008 and 2007:

 
  Series C   Series D  

Shares Outstanding as of July 1, 2008

    71     113,311  

Preferred Shares converted

        (113,311 )
           

Shares Outstanding as of September 30, 2008

    71      
           

Shares Outstanding as of July 1, 2007

    86     113,311  

Preferred Shares converted

    (15 )    
           

Shares Outstanding as of September 30, 2007

    71     113,311  
           

        The following is a summary of changes in the number of outstanding shares of the Company's preferred stock for the nine months ended September 30, 2008 and 2007:

 
  Series C   Series D  

Shares Outstanding as of January 1, 2008

    71     113,311  

Preferred Shares converted

        (113,311 )
           

Shares Outstanding as of September 30, 2008

    71      
           

Shares Outstanding as of January 1, 2007

    102     1,027,967  

Preferred Shares converted

    (31 )   (914,656 )
           

Shares Outstanding as of September 30, 2007

    71     113,311  
           

        The shares of the Company's outstanding Series C and Series D Preferred Stock have the following pertinent rights and privileges, as set forth in the Company's Amended and Restated Certificate of Incorporation and its Certificates of Designations, Rights and Preferences related to the various series of preferred stock.

F-62



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)

Dividend Preferences

        The holders of all series of the Company's preferred stock are entitled to receive dividends on a pari passu basis with the holders of common stock, when, if and as declared by the Company's Board of Directors.

        In addition, the holders of the Series C Preferred Stock received a mandatory dividend rate of 6% per annum per outstanding share of Series C Preferred Stock, payable quarterly, based on the $10,000 Liquidation Preference of such share through the period ending on May 20, 2007. These dividends were paid in cash or common stock equal to the equivalent cash amount divided by the 20 day preceding average closing price. The Company could only elect to pay the dividends in shares of common stock if the average closing price of the shares of common stock for the 20 days immediately preceding the dividend payment date was equal to or greater than the conversion price of either of the relevant series of Preferred Stock. All dividends were paid to outstanding Series C Preferred Stockholders on each quarter-end payment date. As part of this dividend, the Company paid cash of $23,000 during the nine months ended September 30, 2007 to holders of Series C Preferred Stock. No dividends were paid during the three months ended September 30, 2007 or during the three and nine months ended September 30, 2008.

Rights on Liquidation

        In the event of any voluntary or involuntary liquidation, dissolution or winding up of the Company (a "liquidation event"), before any distribution of assets of the Company shall be made to or set apart for the holders of common stock, the holders of Series C Preferred Stock, pari passu, are entitled to receive payment of such assets of the Company in an amount equal to $10,000 per share of such series of preferred stock, plus any accumulated and unpaid dividends thereon (whether or not earned or declared). In the event of any liquidation event, the holders of the Series D Preferred Stock are entitled to be paid out of the assets of the Company available for distribution to its stockholders (i) before any distribution of assets of the Company shall be made to or set apart for the holders of common stock or any class or series of stock ranking on liquidation junior to the Series D Preferred Stock, (ii) ratably with any class or series of stock ranking on liquidation on a parity with the Series D Preferred Stock, and (iii) after and subject to the payment in full of all amounts required to be distributed to the holders of the Company's Series C Preferred Stock and any other class or series of stock of the Company ranking on liquidation prior and in preference to the Series D Preferred Stock, an amount equal to $3.204 per share of Series D Preferred Stock.

        If the assets of the Company available for distribution to stockholders exceed the aggregate amount of the liquidation preferences payable with respect to all shares of each series of preferred stock then outstanding, then, after the payment of such preferences is made or irrevocably set aside, the holders of the Company's common stock are entitled to receive a pro rata portion of such assets based on the aggregate number of shares of common stock held by each such holder. The holders of the Company's outstanding preferred stock shall participate in such a distribution on a pro-rata basis, computed based on the number of shares of common stock which would be held by such preferred holders if immediately prior to the liquidation event all of the outstanding shares of the preferred stock had been converted into shares of common stock at the then current conversion value applicable to each series.

F-63



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)

        A Change of Control of the Company (as defined in the Certificates of Designations, Rights and Preferences) is not a liquidation event triggering the preferences described above, and is instead addressed by separate terms in the Series C and Series D Certificates of Designations, Rights, and Preferences. In addition to the default adjustment of conversion and other rights of the Series C and Series D Preferred Stock upon a Change of Control of the Company, holders of Series C Preferred Stock are entitled to notice of a proposed Change of Control transaction prior to its consummation and have the ability to elect redemption of the holder's Series C Preferred Stock at a premium to the liquidation preference applicable to such shares.

        Although the liquidation preferences are in excess of the par value of $0.001 per share of the Company's preferred stock, these preferences are equal to or less than the stated value of such shares based on their original purchase price.

Voting Rights

        The holders of all series of the Company's preferred stock outstanding have full voting rights and powers equal to the voting rights and powers of holders of the Company's common stock and are entitled to notice of any stockholders' meeting in accordance with the Company's Bylaws. Holders of the Company's preferred stock are entitled to vote on any matter upon which holders of the Company's common stock have the right to vote, including, without limitation, the right to vote for the election of directors together with the holders of common stock as one class.

Actions Requiring the Consent of Holders of Convertible Preferred Stock

        As long as a certain number of shares of each series of the Company's preferred stock issued on the respective "Date of Original Issue" for such series are outstanding, the consent of at least a majority of the shares of that series of preferred stock outstanding are necessary to approve:

            (a)   Any amendment, alteration or repeal of (i) any of the provisions of the relevant series' Certificate of Designation, including any increase in the number of authorized shares of such series or (ii) the Company's Certificate of Incorporation or Bylaws in a manner that would adversely affect the rights of the holders of the relevant series of preferred stock;

            (b)   the authorization, creation, offer, sale or increase in authorized shares by the Company of any stock of any class, or any security convertible into stock of any class, or the authorization or creation of any new series of preferred stock ranking in terms of liquidation preference, redemption rights or dividend rights, pari passu with or senior to, the relevant series of preferred stock in any manner;

            (c)   the declaration or payment of any dividend or other distribution (whether in cash, stock or other property) with respect to the Company's capital stock or that of any subsidiary, other than a dividend or other distribution pursuant to the terms of the relevant series of preferred stock or other series of preferred stock noted in the relevant Certificate of Designation; and

            (d)   except for the holders of the Series D Preferred Stock, the redemption, purchase or other acquisition, directly or indirectly, of any shares of the Company's capital stock or any of its subsidiaries or any option, warrant or other right to purchase or acquire any such shares, or any

F-64



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)


    other security, other than certain accepted redemptions of preferred stock, certain outstanding warrants, the repurchase of shares at cost from employees of the Company upon termination of employment in accordance with written agreements pursuant to which the shares were issued, or other specified repurchase or redemption rights pursuant to written agreements outstanding at the time of original issuance of the preferred stock in question.

        These specific voting rights are applicable for the Series C Preferred Stock as long as at least 35% of the number of shares of Series C Preferred Stock issued on the Date of Original Issue remain outstanding, and the same threshold applies to the Series D Preferred Stock. As of September 30, 2008, no Preferred Stock holders had such series voting rights remaining.

Participation Rights

        Holders of the Series C Preferred Stock have the right to participate with respect to the Company's issuance of any equity or equity-linked securities or debt convertible into equity or in which there is an equity component ("Additional Securities") on the same terms and conditions as offered by the Company to the other purchasers of such Additional Securities. However securities issued or issuable upon any of the following are not deemed "Additional Securities": (A) the conversion of outstanding preferred stock or exercise of related warrants, or the issuance of shares of common stock as payment of dividends to holders of preferred stock, (B) the exercise of any warrants or options outstanding prior to the authorization or issuance of the series of preferred stock in question (C) the issuance (at issuance or exercise prices at or above fair market value) of common stock, stock awards or options under, or the exercise of any options granted pursuant to, any Board-approved employee stock option or similar plan for the issuance of options or capital stock of the Company, (D) the issuance of shares of common stock pursuant to a stock split, combination or subdivision of the outstanding shares of common stock, and (E) for evaluation of the rights of the Series C Preferred Stock only, in connection with a bona fide joint venture or development agreement or strategic partnership, the primary purpose of which is not to raise equity capital.

        Each time the Company proposes to offer any Additional Securities, it is obligated to provide each holder of shares of the Series C Preferred Stock notice of such intention including the terms of such intended offering (including size and pricing) and the anticipated closing date of the sale. These preferred stockholders then have a specified period in which to respond to the Company to elect to purchase or obtain, at the price and on the terms specified in the Company's notice, up to that number of such Additional Securities which equals such holder's Pro Rata Amount. The "Pro Rata Amount" for any given holder of shares of the Series C Preferred Stock equals that portion of the Additional Securities offered by the Company which equals the proportion that the number of shares of common stock that such preferred stockholder owns or has the right to acquire to the total number of shares of common stock then outstanding (assuming in each case the full conversion and exercise of all convertible and exercisable securities then outstanding).

        The holders of the Series C Preferred Stock have the right to pay the consideration for the Additional Securities purchasable upon such participation with shares of such series of Preferred Stock, which will be valued for such purpose at the applicable series' Liquidation Preference plus any accrued and unpaid dividends for such purpose. However, when shares of such preferred stock are used as participation consideration, then such holder's Pro Rata Amount is increased (but not decreased) to

F-65



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)


the extent necessary to equal that number of Additional Securities as are convertible into or exchangeable for such number of shares of Common Stock as is obtained by dividing (a) the Liquidation Preference attributable to such holder's shares of the applicable series of Preferred Stock plus any accrued and unpaid dividends on such Preferred Stock by (b) the Conversion Value then in effect for such shares, and in such event the Company shall be obligated to sell such number of Additional Securities to each such holder, even if the aggregate Pro Rata Amount for all such holders exceeds the aggregate amount of Additional Securities that the Company had initially proposed to offer. To the extent that not all holders of a particular series of preferred stock elect to participate up to their full Pro Rata Amounts, the participating holders of that series of preferred stock have the right to increase their participation accordingly.

        The participation rights of the holders of the Series C Preferred Stock may not be assigned or transferred, other than assignment to any wholly-owned subsidiary or parent of, or to any corporation or entity that is, within the meaning of the Securities Act, controlling, controlled by or under common control with, any such holder. As a result of transfers, the holders of the Series C Preferred Stock outstanding as of September 30, 2008 no longer had such participation rights.

        The Series D Preferred Stock has no participation rights.

        During the Company's October 2006, December 2005 and January 2005 common stock offerings, the Company informed holders of its outstanding Series A, B, and C Cumulative Convertible Preferred Stock with participation rights, of their ability to participate in the respective offering based upon the pricing of the transaction and the applicable liquidation preference for the series of preferred share participating. These participating stockholders obtained incremental shares of common stock as a result of exercising their participation rights, thereby converting their outstanding shares of Cumulative Convertible Preferred Stock at a lower offering price compared to their current conversion price. The right to participate was available only for a limited period time in relation to the specific transaction and the exercise of the existing participation right did not reflect or create a lasting change in the holders' conversion privileges. Some of the participating stockholders had previously converted a portion of their shares of the Company's preferred stock pursuant to their optional conversion rights, and most of the participating stockholders wholly converted their remaining shares of the Company's preferred stock through exercise of their participation rights in the noted offerings.

Conversion Rights

        The Series C Preferred Stock each provide the holder of such shares an optional conversion right and provide a mandatory conversion upon certain triggering events.

Right to Convert

        The holder of any share or shares of Series C Preferred Stock has the right at any time, at such holder's option, to convert all or any lesser portion of such holder's shares of the Preferred Stock into such number of fully paid and non-assessable shares of Common Stock as is determined by dividing (i) the aggregate Liquidation Preference applicable to the particular series of preferred shares, plus accrued and unpaid dividends thereon by (ii) the applicable Conversion Value (as defined in the relevant series' Certificate of Designations, Rights and Preferences) then in effect for such series of

F-66



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)


preferred shares. The Company is not obligated to issue any fractional shares or scrip representing fractional shares upon such conversion and instead shall pay the holder an amount in cash equal to such fraction multiplied by the current market price per share of the Company's common stock.

Mandatory Conversion

        The Company has the option upon thirty (30) days prior written notice, to convert all of the outstanding shares of the Series C Preferred Stock into such number of fully paid and non-assessable shares of common stock as is determined by dividing (i) the aggregate Liquidation Preference of the shares of the relevant series of preferred stock to be converted plus accrued and unpaid dividends thereon by (ii) the applicable Conversion Value (as defined in the relevant series' Certificate of Designations, Rights and Preferences) then in effect, if at any time after twelve months following the Original Issue Date of each such series of preferred stock all of the following triggering events occur:

              (i)  The registration statement covering all of the shares of common stock into which the particular series of preferred stock is convertible is effective (or all of the shares of common stock into which the preferred stock is convertible may be sold without restriction pursuant to Rule 144 under the Securities Act of 1933, as amended);

             (ii)  the Daily Market Price (as defined in the applicable Certificates of Designations, Rights and Preferences) of the common stock crosses a specified pricing threshold for twenty of the thirty consecutive trading days prior to the date the Company provides notice of conversion to the holders; and

            (iii)  the average daily trading volume (subject to adjustment for stock dividends, subdivisions and combinations) of the common stock for at least twenty of the thirty consecutive trading days prior to the date the Company provides notice of conversion to the holders exceeds 25,000 shares.

        As of September 30, 2008, the Company's outstanding shares of the Series C Preferred Stock were convertible into 104,410 shares of common stock at a conversion price of $6.80 per share, and the applicable Daily Market Price of the common stock for triggering mandatory conversion equaled $18.00 per share.

        The Series D Preferred Stock only provides the holder of such shares an optional conversion right. As of September 30, 2008, all shares of Series D Preferred Stock had been converted.

Imputed and Declared Dividends on Preferred Stock

        The holders of the Company's Series C Preferred Stock were entitled to receive an annual dividend at the rate of 6%, payable quarterly, through May 20, 2007. These dividends were payable in cash unless the closing price of the Company's common shares for the 20 trading days immediately preceding the dividend payment date was equal to or greater than the conversion price of such shares, in which event the Company may have elected to pay the dividends to the holders in common stock. As part of this dividend, the Company paid cash of $23,000 during the nine months ended September 30, 2007, to holders of Series C Preferred Stock. No dividends were paid during the three months ended September 30, 2007 or during the three and nine months ended September 30, 2008.

F-67



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)

Common Stock

        In August 2007, the Company entered into an agreement with an outside consulting advisor pursuant to which the Company issued 230,000 registered shares of common stock and registered warrants to purchase 150,000 shares of common stock, as payment of a non-refundable retainer in connection with the engagement of its services.

        In May 2007, the Company completed a registered equity financing, whereby it sold 4,595,094 shares of common stock resulting in gross aggregate cash proceeds of $16.2 million.

        In March 2007, the Company entered into an agreement in which it agreed to issue a total of 90,000 restricted shares of the Company's common stock in equal quarterly installments in exchange for consulting services. As of September 30, 2008, the Company had issued 78,750 restricted common shares. During the remaining term of the agreement, the Company will continue to issue 11,250 restricted shares of common stock at each quarter-end in exchange for the consulting services the Company will receive each quarter.

        In January 2007, the Company exchanged for 2,201,644 restricted shares of common stock and warrants to purchase up to 770,573 restricted shares of common stock for 2,201,644 ordinary shares of the Company's Singapore subsidiary Inovio Asia Pte. Ltd. (IAPL), pursuant to the terms of the Securities Purchase and Exchange Agreement under which the ordinary shares were originally issued by IAPL in October 2006 for $5.3 million.

        In March 2007, the Company terminated its exclusive royalty-free license to IAPL allowing its subsidiary to use certain of the Company's intellectual property, which had been issued in October 2006 prior to the ordinary share financing described above, in exchange for 6,584,365 ordinary shares of IAPL. Upon termination the Company retained the IAPL ordinary shares received in the license transaction.

        In October 2006, the Company completed a registered offering with foreign investors, whereby the Company sold 4,074,067 shares of common stock and issued warrants to purchase 1,425,919 shares of common stock which resulted in gross aggregate cash proceeds of $9.9 million. As part of this offering, the Company informed holders of the then outstanding Series C Preferred Stock who held participation rights, of their ability to participate in the respective offering based upon the pricing of the transaction and the applicable liquidation preference for their series of preferred shares with such rights. Some of these participating stockholders had previously converted a portion of their shares of preferred stock pursuant to their optional conversion rights, and most of these participating stockholders wholly converted their remaining shares of the Company's preferred stock through exercise of their participation rights in this offering. By electing to participate in this offering, these participating preferred stockholders converted 115.12 shares of previously issued Series C Preferred Stock and $15,000 of accrued dividends into 479,722 restricted shares of common stock and warrants to purchase 167,902 restricted shares of common stock. These participating stockholders received 304,450 additional restricted shares of common stock as compared to the number of shares of common stock into which their existing Series C Preferred Stock could have been converted under the original terms of the Series C Preferred Stock. As a result, the Company recorded an imputed dividend charge of $1.9 million related to the participating stockholders who converted $1.2 million of their previous Series C Preferred Stock investment. The Company calculated this imputed dividend charge pursuant

F-68



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)


to the guidance contained in Emerging Issues Task Force ("EITF") Issue No. 00-27, Application of Issue No. 98-5 to Certain Convertible Instruments , where the incremental number of shares of common stock which was received by participating Series C Preferred Stockholders was multiplied by the price of the Company's common stock on the commitment date of the original Series C Preferred Stock issuance, or $6.08 per share, to calculate the imputed dividend charge associated with this beneficial conversion.

Warrants

        All warrants issued as partial consideration for the previously mentioned August 2007 consulting advisor agreement are exercisable at an exercise price of $3.00 per share through August 2012. As of September 30, 2008 no warrants issued in connection with the consulting agreement had been exercised and all were outstanding.

        All warrants issued in the October 2006 registered offering are exercisable at an exercise price of $2.87 per share through October 2011. As of September 30, 2008, no warrants issued in connection with the Company's registered offering and preferred stock conversion had been exercised and all were outstanding.

        All warrants issued in the October 2006 participating preferred stock conversion and the January 2007 IAPL ordinary share exchange are exercisable at an exercise price of $2.87 per share through October 2011. As of September 30, 2008, no warrants issued in connection with the IAPL private placement had been exercised and all were outstanding.

        In the December 2005 private placement to accredited investors, the Company issued warrants to purchase an aggregate of 3,462,451 shares of common stock at an exercise price of approximately $2.93 per share, which are exercisable through December 2010. As of September 30, 2008, no warrants issued in connection with this private placement had been exercised, and all were outstanding.

        In the January 2005 private placement to accredited investors, the Company issued warrants to purchase 508,240 shares of common stock at an exercise price of $5.50 per share, which are exercisable through January 2010. As of September 30, 2008, no warrants issued as part of this private placement had been exercised and all were outstanding.

        In connection with the leasing of the new corporate headquarters, the Company issued a warrant to purchase 50,000 shares of common stock at $5.00 per share to the landlord of the leased facility in December 2004, which is exercisable through December 2009. This warrant was valued on the date of issuance using the Black-Scholes pricing model. The fair value of this warrant, $121,000, is being recognized ratably over the five-year term of the lease as rent expense. As of September 30, 2008, this warrant remains unexercised and outstanding.

        In the May 2004 offering of Series C Preferred Stock, the Company issued warrants to the investors to purchase 561,084 shares of common stock at an exercise price of $8.80 per share and warrants to the placement agents to purchase 152,519 shares of common stock at an exercise price of $6.80 per share, in each case exercisable through May 10, 2009. As of September 30, 2008, none of these warrants had been exercised and all were outstanding.

F-69



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Stockholders' Equity (Continued)

        At the closing of the July 2003 sale of previously issued and subsequently converted Series A and Series B Preferred Stock, the Company issued warrants to the investors to purchase 2,433,073 shares of common stock at an exercise price of $3.00 per share and warrants to the placement agents to purchase 447,060 shares of common stock at an exercise price of between $2.40 and $2.80 per share, both of which expired on July 13, 2008. Of these July 2003 warrants, warrants to purchase 878,582 shares had been exercised as of September 30, 2008, resulting in gross cash proceeds of $2.0 million.

        On September 15, 2000, the Company entered into an exclusive license agreement with the University of South Florida Research Foundation, Inc. ("USF"), whereby USF granted us an exclusive, worldwide license to USF's rights in patents and patent applications generally related to needle electrodes (the "License Agreement"). Pursuant to the License Agreement, the Company granted USF and its designees a warrant to acquire 150,000 common shares for $9.00 per share. This warrant expires on September 14, 2010. At the date of grant, 75,000 shares underlying the warrant vested, and the remaining shares will vest upon the achievement of certain milestones. The 75,000 non-forfeitable vested shares underlying the warrant were valued at $554,000 using the Black-Scholes pricing model and were recorded as capitalized license fees. The remaining 75,000 shares underlying the non-vested warrant are forfeitable and will be valued at the fair value on the date of vesting using the Black-Scholes pricing model. As of September 30, 2008, none of these warrants had been exercised and all were outstanding.

Stock Options

        The Company has one active stock and cash-based incentive plan, the 2007 Omnibus Incentive Plan (the "Incentive Plan"), pursuant to which the Company has granted stock options and restricted stock awards to executive officers, directors and employees. The plan was adopted on March 31, 2007, approved by the stockholders on May 4, 2007, and approved by the stockholders as amended on May 2, 2008. The Incentive Plan reserves 1,750,000 shares of common stock for issuance as or upon exercise of incentive awards granted and to be granted at future dates. At September 30, 2008, the Company had 393,000 shares of common stock available for future grant and had outstanding 138,750 shares of unvested restricted common stock, 101,250 shares of vested restricted stock, and options to purchase 1,115,750 shares of common stock. The awards granted and available for future grant under the Incentive Plan generally have a term of ten years and generally vest over a period of three years. The Incentive Plan terminates by its terms on March 31, 2017.

        The Incentive Plan supersedes all of the Company's previous stock option plans, which include the 1997 Stock Option Plan, under which the Company had options to purchase 23,499 shares of common stock outstanding and the Amended 2000 Stock Option Plan, under which the Company had options to purchase 3,167,402 shares of common stock outstanding at September 30, 2008. The terms and conditions of the options outstanding under these plans remain unchanged.

7. Net Loss Per Share

        Net loss per share is calculated in accordance with SFAS No. 128, Earnings Per Share . Basic loss per share is computed by dividing the net loss for the year by the weighted average number of common shares outstanding during the year. Diluted loss per share is calculated in accordance with the treasury stock method and reflects the potential dilution that would occur if securities or other contracts to

F-70



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

7. Net Loss Per Share (Continued)


issue common stock were exercised or converted to common stock. Since the effect of the assumed exercise of common stock options and other convertible securities was anti-dilutive for all periods presented, there is no difference between basic and diluted loss per share.

8. Stock-Based Compensation

        The Company accounts for stock-based compensation in accordance with SFAS No. 123(R), Share-Based Payment. The Company estimates the fair value of stock options granted using the Black-Scholes option pricing model. The Black-Scholes option pricing model was developed for use in estimating the fair value of traded options, which have no vesting restrictions and are fully transferable. In addition, option valuation models require the input of highly subjective assumptions, including the expected stock price volatility and expected option life. The Company amortizes the fair value of the awards on a straight-line basis. All options grants are amortized over the requisite service period of the awards. Expected volatility is based on historical volatility. The expected life of options granted is based on historical expected life. The risk-free interest rate is based on the U.S. Treasury yield in effect at the time of grant. The forfeiture rate is based on historical data and the Company records stock-based compensation expense only for those awards that are expected to vest. The dividend yield is based on the fact that no dividends have been paid historically and none are currently expected to be paid.

        The assumptions used to estimate the fair value of stock options granted in the nine month period ended September 30, 2008 and 2007 are presented below:

 
  Nine Months Ended September 30,
 
  2008   2007

Risk-free interest rate

  2.65% – 3.18%   4.07% – 4.95%

Expected volatility

  69%   94% – 98%

Expected life in years

  4   6

Dividend yield

   

        Total compensation cost under SFAS No. 123(R) for the Company's stock plans that has been recognized in the condensed consolidated statement of operations for the three and nine months ended September 30, 2008 was $270,000 and $797,000, respectively, of which $76,000 and $222,000 was included in research and development expenses and $194,000 and $575,000 was included in general and administrative expenses, respectively.

        Total compensation cost under SFAS No. 123(R) for the Company's stock plans that has been recognized in the condensed consolidated statement of operations for the three and nine months ended September 30, 2007 was $310,000 and $1.3 million, respectively, of which $75,000 and $280,000 was included in research and development expenses and $235,000 and $1.0 million was included in general and administrative expenses, respectively.

        As of September 30, 2008, there was $978,000 of total unrecognized compensation cost related to non-vested stock-based compensation arrangements, which is expected to be recognized over a weighted-average period of one year. As of September 30, 2007, there was $1.7 million of total unrecognized compensation cost related to non-vested stock-based compensation arrangements, which was expected to be recognized over a weighted-average period of 1.1 years.

F-71



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

8. Stock-Based Compensation (Continued)

        The weighted average grant date fair value per share was $1.06 and $0.98 for employee stock options granted during the three and nine months ended September 30, 2008, respectively, and $1.72 and $2.17 for employee stock options granted during the three and nine months ended September 30, 2007, respectively.

        The weighted average grant date fair value per share was $0.87 for non-vested restricted stock granted during the nine months ended September 30, 2008. There was no restricted stock granted during the three months ended September 30, 2008. The weighted average grant date fair value per share was $3.69 for non-vested restricted stock granted during nine months ended September 30, 2007. There was no restricted stock granted during the three months ended September 30, 2007.

        At September 30, 2008, there was $216,000 of total unrecognized compensation cost related to non-vested restricted stock, which is expected to be recognized over a weighted-average period of 1.3 years. At September 30, 2007, there was $314,000 of total unrecognized compensation cost related to non-vested restricted stock, which was expected to be recognized over a weighted-average period of 1.9 years.

        The Company accounts for options granted to non-employees in accordance with EITF No. 96-18, Accounting for Equity Instruments That Are Issued to Other Than Employees for Acquiring, or in Conjunction with Selling, Goods or Services , and SFAS No. 123(R). The fair value of these options at the measurement dates was estimated using the Black-Scholes pricing model. Total stock-based compensation for options granted to non-employees for the three and nine months ended September 30, 2008 was $8,000 and $47,000, respectively. Total stock-based compensation for options granted to non-employees for the three and nine months ended September 30, 2007 was $11,000 and $103,000, respectively.

9. Comprehensive Loss

        Comprehensive loss for the three and nine months ended September 30, 2008 and September 30, 2007 includes net loss, foreign currency translation gains and losses, and unrealized gains and losses on investments. A summary of the Company's comprehensive loss is as follows:

 
  Three Months Ended
September 30,
  Nine Months Ended
September 30,
 
 
  2008   2007   2008   2007  

Comprehensive loss:

                         

Net loss

  $ (2,344,408 ) $ (2,694,503 ) $ (9,389,889 ) $ (10,178,513 )
 

Unrealized gains (losses) on available-for-sale securities

    (430,125 )   14,280     (1,502,170 )   10,305  
 

Foreign currency translation adjustments

    (76,518 )   36,195     (26,985 )   119,715  
                   

Comprehensive loss

  $ (2,851,051 ) $ (2,644,028 ) $ (10,919,044 ) $ (10,048,493 )
                   

F-72



INOVIO BIOMEDICAL CORPORATION

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

10. Supplemental Disclosures of Cash Flow Information

 
  Nine Months Ended
September 30,
 
 
  2008   2007  

Supplemental schedule of financing activities:

             

Conversion of minority interest into common stock

  $   $ 5,349,995  

Leasehold improvements financed by landlord

  $ 35,211   $  

Conversions of preferred stock to common stock

  $ 113   $ 961  

Interest paid

  $ 3,036   $  

Non-cash warrant exercise for common stock

  $   $ 38  

F-73



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Consolidated Financial Statements

YEARS ENDED DECEMBER 31, 2007 AND 2006 AND THE PERIOD
FROM DECEMBER 12, 2000 (INCEPTION) THROUGH DECEMBER 31, 2007

Contents

Report of Independent Auditors

  F-75

Audited Consolidated Financial Statements

   
 

CONSOLIDATED BALANCE SHEETS

 
F-76
 

CONSOLIDATED STATEMENTS OF OPERATIONS

 
F-77
 

CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY (DEFICIT)

 
F-78
 

CONSOLIDATED STATEMENTS OF CASH FLOWS

 
F-80
 

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

 
F-81

F-74



Report of Independent Auditors

The Board of Directors
VGX Pharmaceuticals, Inc.

        We have audited the accompanying consolidated balance sheets of VGX Pharmaceuticals, Inc. (a development-stage company) as of December 31, 2007 and 2006, and the related consolidated statements of operations, stockholders' equity (deficit), and cash flows for each of the two years in the period ended December 31, 2007 and for the period from December 12, 2000 (inception) through December 31, 2007. These financial statements are the responsibility of the Company's management. Our responsibility is to express an opinion on these financial statements based on our audits.

        We conducted our audits in accordance with auditing standards generally accepted in the United States. Those standards require that we plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. We were not engaged to perform an audit of the Company's internal control over financial reporting. Our audits included consideration of internal control over financial reporting as a basis for designing audit procedures that are appropriate in the circumstances, but not for the purpose of expressing an opinion on the effectiveness of the Company's internal control over financial reporting. Accordingly, we express no such opinion. An audit also includes examining, on a test basis, evidence supporting the amounts and disclosures in the financial statements, assessing the accounting principles used and significant estimates made by management, and evaluating the overall financial statement presentation. We believe that our audits provide a reasonable basis for our opinion.

        In our opinion, the financial statements referred to above present fairly, in all material respects, the consolidated financial position of VGX Pharmaceuticals, Inc. as of December 31, 2007 and 2006, and the results of its operations and its cash flows for each of the two years in the period ended December 31, 2007 and for the period from December 12, 2000 (inception) through December 31, 2007, in conformity with accounting principles generally accepted in the United States.

        The accompanying financial statements have been prepared assuming that VGX Pharmaceuticals, Inc. will continue as a going concern. As more fully described in Note 2, the Company has historically incurred operating losses. These conditions raise substantial doubt about the Company's ability to continue as a going concern. Management's plans in regard to these matters are described in Note 1. The financial statements do not include any adjustments to reflect the possible future effects on the recoverability and classification of assets or the amounts and classification of liabilities that may result from the outcome of this uncertainty.

GRAPHIC

Philadelphia, Pennsylvania
June 30, 2008, except for Note 3, as to which the date is January 19, 2009

F-75



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Consolidated Balance Sheets

 
  December 31  
 
  2007   2006  

Assets

             

Current assets:

             
 

Cash and cash equivalents

  $ 15,814,097   $ 20,915,863  
 

Accounts receivable

    2,100      
 

Inventories

    26,925      
 

Restricted cash

    1,000,000     1,000,000  
 

Prepaid expenses and other current assets

    317,797     32,552  
 

Assets of discontinued operations

    3,840,104      
           

Total current assets

    21,001,023     21,948,415  

Property and equipment, net of accumulated depreciation of $138,933 and $19,819, at December 31, 2007 and 2006, respectively

    409,768     70,024  

Equity investment

    7,966,143     8,928,205  

Intangible assets, net of accumulated amortization of $397,604

    3,578,896      

Goodwill

    907,076      

Debt issuance cost, net

    129,037     83,611  

Other assets

    130,147     27,038  
           

Total assets

  $ 34,122,090   $ 31,057,293  
           

Liabilities and stockholders' equity

             

Current liabilities:

             
 

Accounts payable

  $ 724,466   $ 160,773  
 

Accrued expenses

    2,339,591     2,309,259  
 

Current portion of long-term debt

    10,310,000     9,789,435  
 

Other current liabilities

    354,305     185,000  
 

Liabilities of discontinued operations

    4,051,013      
           

Total current liabilities

    17,779,375     12,444,467  

Long-term debt

    2,940,000     4,000,000  

Other noncurrent liabilities

         
           

Total liabilities

    20,719,375     16,444,467  

Minority interest

    956,497      

Stockholders' equity:

             
 

Preferred stock, $0.0001 par value; 1,000,000 shares authorized, no shares outstanding

         
 

Common stock, $0.0001 par value; 100,000,000 shares authorized, 44,798,574 shares and 42,634,355 shares issued and outstanding at December 31, 2007 and 2006, respectively

    4,480     4,263  
 

Additional paid-in capital

    65,085,032     49,506,617  
 

Accumulated other comprehensive income

    642,036     591,235  
 

Deficit accumulated during the development stage

    (53,285,330 )   (35,489,289 )
           

Total stockholders' equity

    12,446,218     14,612,826  
           

Total liabilities and stockholders' equity

  $ 34,122,090   $ 31,057,293  
           

See accompanying notes.

F-76



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Consolidated Statements of Operations

 
  Year Ended December 31   Period From
December 12,
2000 (Inception)
to December 31,
 
 
  2007   2006   2007  

Revenue:

                   
 

Grant revenue

  $ 668,955   $ 337,178   $ 1,741,408  
 

License fee revenue

            75,000  
 

Other operating revenue, net

    36,448         36,448  
               

Total revenue

    705,403     337,178     1,852,856  

Operating expenses:

                   
 

Research and development

    10,936,149     9,007,334     26,213,298  
 

General and administrative

    4,999,391     8,679,153     25,078,334  
               

Total operating expenses

    15,935,540     17,686,487     51,291,642  
               

Loss from operations

   
(15,230,137

)
 
(17,349,309

)
 
(49,438,786

)
 

Losses from equity investment

   
(990,338

)
 
(700,451

)
 
(2,015,869

)
 

Interest income

    919,026     846,219     1,866,364  
 

Interest expense

    (1,128,464 )   (957,153 )   (2,330,911 )
 

Minority interests

    43,503         43,503  
               

Loss from continuing operations

    (16,386,410 )   (18,160,694 )   (51,875,699 )

Discontinued operations:

                   

Loss from discontinued operations

    (1,409,631 )       (1,409,631 )
               

Net loss

 
$

(17,796,041

)

$

(18,160,694

)

$

(53,285,330

)
               

See accompanying notes.

F-77


VGX Pharmaceuticals, Inc.
(A Development-Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit)

 
   
   
   
   
   
   
  Deficit
Accumulated
During the
Development
Stage
   
 
 
  Common Stock    
   
   
  Accumulated
Other
Comprehensive
Income
   
 
 
  Additional
Paid-in
Capital
  Deferred
Stock
Compensation
  Equity
Financing
Receivable
   
 
 
  Shares   Amount   Total  

Issuance of common stock to Founders

    14,050,000   $ 1,405   $ 291,470   $   $   $   $   $ 292,875  
 

Net loss

                            (292,875 )   (292,875 )
                                   

Balance, December 31, 2000

    14,050,000     1,405     291,470                 (292,875 )    
 

Issuance of common stock for patents

    3,550,000     355     (355 )                    
 

Issuance and exercise of options to non-employees

    150,000     15     24,728                     24,743  
 

Note conversion

    1,800,000     180     299,820                     300,000  
 

Issuance of warrants in connection with debt

            62,079                     62,079  
 

Issuance of warrants to employees and related party

            113,828                     113,828  
 

Net loss

                            (730,410 )   (730,410 )
                                   

Balance, December 31, 2001

    19,550,000     1,955     791,570                 (1,023,285 )   (229,760 )
 

Issuance of common stock at $0.50

    930,000     93     232,407                     232,500  
 

Note conversion

    440,000     44     103,200                     103,244  
 

Options to non-employees

            62,855     (59,465 )               3,390  
 

Amortization of deferred stock compensation

                6,632                 6,632  
 

Issuance of warrants to employees and related party

            37,618                     37,618  
 

Net loss

                            (413,367 )   (413,367 )
                                   

Balance, December 31, 2002

    20,920,000     2,092     1,227,650     (52,833 )           (1,436,652 )   (259,743 )
 

Issuance of common stock at $0.60

    433,890     43     118,535                     118,578  
 

Note conversion/retirement

    837,200     84     157,596                     157,680  
 

Exercise of stock options and warrants

    105,000     11     23,115                     23,126  
 

Issuance of options and warrants to employees

            601,234     (211,614 )               389,620  
 

Issuance of warrants in connection with debt

            51,309                     51,309  
 

Issuance of options and warrants to non-employees

            87,600                     87,600  
 

Amortization of deferred stock compensation

                94,535                 94,535  
 

Net loss

                            (748,545 )   (748,545 )
                                   

Balance, December 31, 2003

    22,296,090     2,230     2,267,039     (169,912 )           (2,185,197 )   (85,840 )
 

Issuance of common stock at $0.60

    41,110     4     12,329                     12,333  
 

Issuance of common stock at $1.00

    1,447,000     145     617,519                     617,664  
 

Issuance of common stock to non-employees

    24,000     2     7,140                     7,142  
 

Issuance of common stock to employees

    130,000     13     64,987                     65,000  
 

Issuance of common stock at $2.00

    1,851,750     185     3,703,315         (2,065,500 )           1,638,000  
 

Exercise of warrants

    6,042,725     604     (604 )                    
 

Issuances of common stock to non-employees

    53,604     6     53,598                     53,604  
 

Note conversion

    50,601     5     11,062                     11,067  
 

Issuance of options and warrants to employees

            3,366,004     (1,855,657 )               1,510,347  
 

Issuance of options and warrants to non-employees

            440,100                     440,100  
 

Amortization of deferred stock compensation

                276,810                 276,810  
 

Net loss

                            (3,808,249 )   (3,808,249 )
                                   

Balance, December 31, 2004

    31,936,880     3,194     10,542,489     (1,748,759 )   (2,065,500 )       (5,993,446 )   737,978  

F-78


VGX Pharmaceuticals, Inc.
(A Development-Stage Company)
Consolidated Statements of Stockholders' Equity (Deficit) (Continued)

 
   
   
   
   
   
   
  Deficit
Accumulated
During the
Development
Stage
   
 
 
  Common Stock    
   
   
  Accumulated
Other
Comprehensive
Income
   
 
 
  Additional
Paid-in
Capital
  Deferred
Stock
Compensation
  Equity
Financing
Receivable
   
 
 
  Shares   Amount   Total  

Balance, December 31, 2004 (from previous page)

    31,936,880     3,194     10,542,489     (1,748,759 )   (2,065,500 )       (5,993,446 )   737,978  
 

Collection of share purchase contract

                    2,065,500             2,065,500  
 

Issuance of common stock at $2.25

    1,261,546     126     2,583,903                     2,584,029  
 

Issuance of common stock at $3.00

    310,211     31     808,493                     808,524  
 

Issuance of common stock to non-employees

    13,000     1     25,999                     26,000  
 

Issuance of options and warrants to employees

            9,204,972     (3,333,418 )               5,871,554  
 

Issuance of options and warrants to non-employees

            882,675                     882,675  
 

Exercise of stock options and warrants

    2,679,933     268     (268 )                    
 

Amortization of deferred stock compensation

                1,816,241                 1,816,241  
 

Change in foreign currency translation

                          113,052         113,052  
 

Net loss

                            (11,335,149 )   (11,335,149 )
                                   

Balance, December 31, 2005

    36,201,570     3,620     24,048,263     (3,265,936 )       113,052     (17,328,595 )   3,570,404  
 

Reclassification of deferred compensation on the adoption of SFAS No. 123(R)

            (3,265,936 )   3,265,936                  
 

Issuance of common stock at $3.00

    3,347,812     335     9,491,866                     9,492,201  
 

Issuance of common stock at $5.00

    1,383,000     138     6,522,075                     6,522,213  
 

Issuance of common stock to non-employees

    125,000     12     424,988                     425,000  
 

Compensation expense for stock option and warrant awards

            11,016,997                     11,016,997  
 

Expense for options and warrants to non-employees

            455,510                     455,510  
 

Issuance of options related to equity financing activities

            254,682                     254,682  
 

Exercise of stock options and warrants

    1,330,800     133     4,358                     4,491  
 

Note conversion

    246,173     25     553,814                     553,839  
 

Change in foreign currency translation

                        478,183         478,183  
 

Net loss

                            (18,160,694 )   (18,160,694 )
                                   

Balance, December 31, 2006

    42,634,355     4,263     49,506,617             591,235     (35,489,289 )   14,612,826  
 

Issuance of common stock at $5.00

    2,024,219     203     10,105,892                     10,106,095  
 

Issuance of common stock to non-employees

    130,000     13     649,987                     650,000  
 

Issuance of common stock to employees

    10,000     1     49,999                     50,000  
 

Compensation expense for stock option and warrant awards

            4,604,190                     4,604,190  
 

Expense for options and warrants to non-employees

            168,347                     168,347  
 

Change in foreign currency translation

                        50,801         50,801  
 

Net loss

                            (17,796,041 )   (17,796,041 )
                                   

Balance, December 31, 2007

    44,798,574   $ 4,480   $ 65,085,032   $   $   $ 642,036   $ (53,285,330 ) $ 12,446,218  
                                   

See accompanying notes.

F-79



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Consolidated Statements of Cash Flows

 
  Year Ended December 31   Period from
December 12, 2000
(Inception) to
December 31, 2007
 
 
  2007   2006  

Cash flows from operating activities

                   

Net loss

  $ (17,796,041 ) $ (18,160,694 ) $ (53,285,330 )

Adjustments to reconcile net loss to net cash used in operating activities:

                   
 

Depreciation and amortization

    1,523,163     147,070     1,683,535  
 

Stock-based compensation

    5,472,537     12,152,189     29,206,419  
 

Interest converted into common stock

        53,839     53,839  
 

Loss on disposal

        1,598     2,164  
 

Minority interest in net loss

    (43,503 )       (43,503 )
 

Losses from equity investment

    990,338     700,451     2,015,869  
 

Changes in operating assets and liabilities:

                   
   

Accounts receivable

    6,048         6,048  
   

Inventories

    (1,811,812 )       (1,811,812 )
   

Prepaid expenses and other assets

    (383,812 )   10,911     (443,402 )
   

Accounts payable and accrued expenses

    297,900     1,053,073     2,767,932  
   

Deferred revenue from manufacturing operations

    3,412,089         3,412,089  
   

Other current liabilities

    169,305     157,000     354,305  
               

Net cash used in operating activities

    (8,163,788 )   (3,884,563 )   (16,081,847 )

Cash flows from investing activities

                   

Purchase of ADViSYS, Inc., net of cash acquired

    (2,058,762 )       (2,058,762 )

Equity investment

        (4,464,277 )   (9,362,501 )

Investment in third-party stock

    (60,000 )       (60,000 )

Purchases of property and equipment

    (614,814 )   (46,018 )   (715,985 )

Proceeds from sale of minority interest

    1,000,000         1,000,000  
               

Net cash used in investing activities

    (1,733,576 )   (4,510,295 )   (11,197,248 )

Cash flows from financing activities

                   

Increase in restricted cash

            (1,000,000 )

Proceeds from debt borrowings

    1,600,000     8,789,435     15,889,435  

Repayment of debt to investors

    (2,139,435 )       (2,139,435 )

Debt issuance costs

    (171,500 )   (215,000 )   (386,500 )

Proceeds from issuance of common stock

    5,485,000     16,018,905     30,708,159  
               

Net cash provided by financing activities

    4,774,065     24,593,340     43,071,659  
               

Net (decrease) increase in cash and cash equivalents

    (5,123,299 )   16,198,482     15,792,564  

Effects of exchange rates on cash and cash equivalents

    21,533         21,533  

Cash and cash equivalents, beginning of period

    20,915,863     4,717,381      
               

Cash and cash equivalents, end of period

  $ 15,814,097   $ 20,915,863   $ 15,814,097  
               

Supplemental schedule of noncash investing and financing cash flow activities

                   

Capital lease for office equipment

  $ 9,562   $   $ 9,562  
               

Issuance of common stock to acquire ADViSYS, Inc. 

  $ 4,621,095   $   $ 4,621,095  
               

Conversion of long-term debt and accrued interest to common stock

  $   $ 553,839   $ 553,839  
               

Issuance of warrants in connection with debt

  $   $   $ 58,953  
               

Supplemental schedule of cash flow information

                   

Interest paid

  $ 909,681   $   $ 924,681  
               

See accompanying notes.

F-80



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements

December 31, 2007

1. Description of the Business and Basis of Presentation

        VGX Pharmaceuticals, Inc. (the Company) is a development-stage company incorporated in Delaware as Viral Genomix, Inc. on December 12, 2000 (inception). The Company began operations on January 1, 2001. The Company is a biopharmaceutical company engaged in the discovery and development of drugs and DNA vaccines for the treatment of infectious diseases, including the HIV and hepatitis C viruses, as well as cancer and inflammatory diseases. The Company has built a broad product pipeline encompassing these major disease categories, and these product candidates and technology programs are protected by the Company's extensive global intellectual property patents. The Company has generated an accumulated deficit of $53.3 million since inception. The Company anticipates incurring additional losses for the foreseeable future. Substantial additional financing will be needed by the Company to fund its operations and to develop its products. There is no assurance that such financing will be available when needed.

        VGX Animal Health, Inc. (Animal Health) is a biotechnology company engaged in the development and commercialization of products designed to add to the economic value of livestock and improve the health of companion animals. The Animal Health franchise was acquired as part of the acquisition of ADViSYS in February 2007. The Company carved out the acquired Animal Health franchise into a separate company in order to clearly segregate the Animal Health franchise from its core technology dedicated to developing drugs for human application. Animal Health's lead candidate Lifetide™ SW5 for porcine application was approved for marketing in Australia in January 2008. The Company owns 86% of the outstanding stock of Animal Health as of December 31, 2007. Animal Health is consolidated in the results of the Company's consolidated financial statements.

        The Company is subject to those risks associated with biotechnology companies in a similar stage of development. There can be no assurance that the Company's research and development activities will be successful, that products developed will obtain necessary regulatory approval, or that any approved product will be commercially viable. In addition, the Company operates in an environment of rapid technological change and is largely dependent on the services of its employees and consultants.

        The financial statements of the Company have been prepared assuming the Company will continue as a going concern, which contemplates the realization of assets and the satisfaction of liabilities in the normal course of business. Accordingly, the financial statements do not include any adjustments to recorded asset values that might be necessary should the Company be unable to continue in existence. The Company has incurred continued operating losses, and has experienced increasing cash outflow from operating activities since inception. Despite the additional funding obtained in fiscal year 2007, the Company is a developmental-stage entity, and has not established a consistent revenue stream. In addition, it is uncertain whether the Company will become profitable in the foreseeable future, or if the Company will continue to be able to obtain capital financing as needed to sustain its operations. These factors raise substantial doubt about the Company's ability to continue as a going concern. Management believes that actions presently being taken will allow for the Company to continue as a going concern. These actions include the issuance of convertible debt securities, the sale of equity securities, and the continued research and development of its products to achieve a sustainable revenue stream.

F-81



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies

Principles of Consolidation

        The consolidated financial statements of the Company include the accounts of its majority-owned subsidiary, Animal Health. All significant intercompany transactions and balances have been eliminated.

Use of Estimates

        The preparation of financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Actual results could differ from such estimates.

Fair Value of Financial Instruments

        Management believes that the carrying amounts of the Company's financial instruments, including cash and cash equivalents, restricted cash, accounts payable, accrued expenses, and current portion of long-term debt approximate fair value due to the short-term nature of those instruments.

Cash and Cash Equivalents

        Cash and cash equivalents are stated at market value. Cash equivalents include only securities having a maturity of three months or less at the time of purchase. The Company limits its credit risk associated with cash and cash equivalents by placing them with banks it believes are highly creditworthy. As of December 31, 2007 and 2006, cash and cash equivalents consisted of bank deposits only. The Company had restricted cash of $1,000,000 as of December 31, 2007 and 2006. This cash is restricted as collateral for one of the Company's creditors.

Inventories

        Inventories are stated at the lower of cost or market. Cost is determined by the first-in, first-out method. Inventory includes the cost of raw materials used in production, direct labor costs, and an allocated portion of manufacturing overhead. Overhead costs include electricity, depreciation, and other manufacturing costs that cannot be linked to the production of goods. At December 31, 2007, all manufacturing inventory has been classified as assets of discontinued operations, and the balance of EP array inventory at December 31, 2007 was $26,925.

Property and Equipment

        Property and equipment consists of research lab equipment, office furniture, and computers and is recorded at cost. Maintenance and repairs are charged to expense as incurred, and costs of improvements are capitalized. Depreciation is recognized using the straight-line method based on an estimated useful life of 3-7 years for the related assets. Total depreciation expense was $916,757 and $15,681 for the years ended December 31, 2007 and 2006, respectively, of which $120,150 and $15,681, respectively, are included in continuing operations. Total depreciation expense for the period from

F-82



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)


December 12, 2000 (inception) through December 31, 2007 was $945,740, of which $149,133 is included in continuing operations.

Long-Lived Assets

        In accordance with Statement of Financial Accounting Standards (SFAS) No. 144, Accounting for the Impairment of Long-Lived Assets , long-lived assets, such as property and equipment, are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. Recoverability of assets to be held and used is measured by a comparison of the carrying amount of an asset to estimated undiscounted future cash flows expected to be generated by the asset. If the carrying amount of an asset exceeds its estimated future cash flows, an impairment charge is recognized by the amount by which the carrying amount of the asset exceeds the fair value of the asset. As of December 31, 2007, management believes that no revision to the remaining useful lives or write-down of long-lived assets is required.

Goodwill and Intangible Assets

        The Company accounts for goodwill and intangible assets in accordance with Statement of Financial Accounting Standards (SFAS) No. 142, Goodwill and Other Intangible Assets . Goodwill represents the excess of the purchase price over fair value of net assets acquired and totaled $1,084,844 at December 31, 2007, of which $177,768 is attributable to the manufacturing operation's assembled workforce, and has been moved to assets of discontinued operations. In accordance with SFAS No. 142, goodwill is not amortized, rather it is tested for impairment at least annually. The Company determined there was no impairment during 2007.

        Intangible assets with finite lives, primarily customer contracts and proprietary technology, are amortized over their estimated useful lives from 3 to 9 years. Amortization of intangible assets for the five years subsequent to December 31, 2007 is expected to be: $759,297 in 2008 and $477,125 for each of 2009, 2010, 2011 and 2012, of which $477,125 in 2008 and $477,125 for each of 2009, 2010, 2011 and 2012 will be from continuing operations.

Deferred Issuance Costs

        The Company capitalizes costs associated with obtaining financing and amortizes them on a straight-line basis over the term of the underlying debt. Amortized deferred issuance costs are classified as interest expense in the consolidated statement of operations and totaled $126,074, $131,389 and $257,463, for the years ended December 31, 2007, 2006 and for the period from December 12, 2000 (inception) to December 31, 2007, respectively.

Equity Investment

        The Company accounts for its investment in VGX International, Inc. using the equity method of accounting. Should circumstances change, such as a change in the percentage of ownership, the Company will review its accounting treatment for its investment. The equity investment is presented on

F-83



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)


the consolidated balance sheets, net of unamortized acquisition costs. Acquisition costs are being amortized using the straight-line method over five years.

Revenue Recognition

        The Company has been awarded grants from certain third-party organizations to help fund research for the drugs that the Company is attempting to bring to full commercial use. Once research and development expenditures qualifying under the grant are incurred, grant reports are periodically completed and submitted to the granting agency for review. If approved, the granting agency will then remit payment to the Company. Such amounts are recorded as revenue upon receipt.

        With regard to contract manufacturing services, VGX recognizes revenue from the DNA plasmids it produces for its customers, to their specifications, only upon shipment from its premises, at which time title and all benefits and risks of ownership pass to the customer. The value of the inventory includes the cost of raw materials, direct labor and facility overhead. Overhead costs include indirect manufacturing costs such as utilities and depreciation that cannot be directly linked to the production of specific products.

        In 2007, all revenue from product sales was related to contract manufacturing services, and these activities and processes were sold to a related party in June 2008. As a result, revenue from sales of these products has been reflected as discontinued operations on the consolidated statements of operations.

        Deferred revenue represents billings for products and services which will be recognized when the products are shipped or the services provided. VGX manufactures DNA plasmids for its customers, to their specifications, in compliance with the terms and conditions outlined in a contract or master services agreement. The agreements typically consist of a series of payments, to be made to VGX at specified points during the production process, which typically spans several months. As a result, payments are made to VGX for these contracted services in advance of, and during, the production process, and are recorded as deferred revenue on the balance sheet until the product is shipped to the customer, at which time revenue is recognized. During 2007, several progress payments were made to VGX from its customers; however, at the request of the customer, VGX stored the inventory in its facility, thus resulting in a significant amount of deferred revenue at December 31, 2007, which is included in liabilities of discontinued operations.

        Since these services were sold as part of the asset purchase agreement executed in 2008, the deferred revenue on the consolidated balance sheet at the time of the sale was considered in the calculation of the gain on the sale of these assets.

Foreign Currency Translation

        The Company complies with SFAS No. 52, Foreign Currency Translation , which established standards for reporting on investments in foreign companies. The foreign currency translation adjustment represents the foreign currency translation related to the Company's equity investment, and is included in accumulated other comprehensive income on the consolidated balance sheets. For the

F-84



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)


year ended December 31, 2007, $93,975 of foreign currency losses were included in the consolidated statement of operations.

Research and Development Expenses

        Research and development costs are charged to expense as incurred. Research and development expenses include, among other costs, salaries and other personnel-related costs, consultant fees, preclinical costs, costs to conduct clinical trials, costs to manufacture drug candidates and clinical supplies, laboratory supplies costs, patent application costs, and facility-related costs. Costs incurred under agreements with third parties are charged to expense as incurred in accordance with the specific contractual performance terms of such agreements. Costs of third parties include costs associated with preclinical and clinical support activities.

Income Taxes

        Income taxes are accounted for under the liability method. Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Valuation allowances are established when necessary to reduce deferred tax assets to the amount expected to be realized. Deferred tax assets and liabilities are measured at the balance sheet date using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in the period such tax rate changes are enacted.

Acquisitions

        Acquisitions are accounted for under the purchase method of accounting in accordance with SFAS No. 141, Business Combinations , whereby the purchase price is allocated to the underlying net assets based on management's estimates of the fair value of intangible and tangible assets acquired and liabilities assumed. The excess of purchase price over estimated fair value is recorded as goodwill.

Stock-Based Compensation—VGX Pharmaceuticals

        In December 2004, the Financial Accounting Standards Board (FASB) issued SFAS No. 123(R), Share-Based Payment , a revision of SFAS No. 123, Accounting for Stock-Based Compensation , that addresses the accounting for share-based payment transactions in which an enterprise receives employee services in exchange for (a) equity instruments of the enterprise or (b) liabilities that are based on the fair value of the enterprise's equity instruments or that may be settled by the issuance of such equity investments. SFAS No. 123(R) requires that an entity measure the cost of equity-based service awards based on the grant-date fair value of the award and recognize the cost of such awards over the period during which the employee is required to provide service in exchange for the award (the vesting period). SFAS No. 123(R) requires that an entity measure the cost of liability-based service awards based on current fair value that is remeasured subsequently at each reporting date through the settlement date. The Company had previously adopted the fair-value method of SFAS No. 123, using the Black-Scholes Model to account for equity-based awards issued to employees and directors and has

F-85



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)


adopted this new standard effective January 1, 2006 under the modified prospective transition method. The modified prospective transition method requires the Company to recognize share-based compensation expense in the consolidated statements of operations for all share-based payments granted, modified, or settled after the date of adoption as well as for any awards that were granted prior to the adoption date for which the requested service has not been provided as of the adoption date.

        The per-share weighted-average fair value of the options granted during 2007 and 2006 was estimated at $2.66 and $4.07, respectively, on the date of grant using the Black-Scholes option-pricing model with the following weighted-average assumptions:

 
  2007   2006  

Expected dividend yield

    0 %   0 %

Expected volatility

    50 %   50 %

Risk-free interest rate

    4.7 %   4.9 %

Expected life

    6 years     6 years  

        The weighted-average valuation assumptions were determined as follows:

    Expected stock price volatility: The expected volatility used is based on historical volatilities of similar entities within the Company's industry which were commensurate with the Company's expected term assumption as described in Securities and Exchange Commission staff accounting bulletin (SAB) No. 107 relating to SFAS No. 123(R).

    Expected term of options: The expected term of options represents the period of time options are expected to be outstanding. The expected term of the options granted is derived from the "simplified" method as described in SAB No. 107 relating to SFAS No. 123(R).

    Risk-free interest rate: The Company bases the risk-free interest rate on the interest rate payable on U.S. Treasury securities in effect at the time of grant for a period that is commensurate with the assumed expected option term.

    Expected annual dividends: The estimate for annual dividends is $0.00, because the Company has not historically paid, and does not expect for the foreseeable future to pay, a dividend.

    Estimated forfeiture rate: The Company's estimated annual forfeiture rate on 2007 stock option grants ranges between 0.00% and 4.14%, based on the historical forfeiture experience of various employee groups.

        The compensation expense under SFAS No. 123(R) for the year ended December 31, 2007 was $5,472,537, net of estimated forfeiture. The compensation expense under SFAS No. 123 for the year ended December 31, 2006 was $12,152,189. The Company accounts for stock-based compensation to non-employees using the fair-value method in accordance with SFAS No. 123(R) and EITF Issue No. 96-18, Accounting for Equity Instruments That Are Issued to Other Than Employees for Acquiring, or in Conjunction with Selling Goods or Services . For the years ended December 31, 2007 and 2006, the Company granted stock options to consultants of 75,200 and 274,633, respectively, and recorded stock-based compensation expense of $168,347 and $455,510, respectively. These options generally vest over a

F-86



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)


period of three years, though some vest over a period less than three years or immediately upon grant. The Company valued the stock option grants to non-employees using the same method and assumptions as stock option grants to employees. In addition to the awards of stock options, the Company awarded 140,000 and 125,000 shares of common stock, during the years ended December 31, 2007 and 2006, respectively, to employees and non-employees. In connection with awards of stock, the Company recorded compensation expense of $700,000 and $425,000, respectively.

Stock-Based Compensation for Subsidiary—Animal Health

        Animal Health, a subsidiary of the Company, has adopted a 2007 equity incentive plan for the issuance of options to employees and consultants. Animal Health uses the same accounting policies as the Company regarding stock-based compensation.

        The per-share weighted-average fair value of the options granted by Animal Health during 2007 was $.04, on the date of grant using the Black-Scholes option-pricing model with the following weighted-average assumptions:

 
  2007  

Expected dividend yield

    0 %

Expected volatility

    50 %

Risk-free interest rate

    4.7 %

Expected life

    6 years  

        The weighted-average valuation assumptions were determined as follows:

    Expected stock price volatility: The expected volatility used is based on historical volatilities of similar entities within Animal Health's industry which were commensurate with Animal Health's expected term assumption as described in Securities and Exchange Commission staff accounting bulletin (SAB) No. 107 relating to SFAS No. 123(R).

    Expected term of options: The expected term of options represents the period of time options are expected to be outstanding. The expected term of the options granted is derived from the "simplified" method as described in SAB No. 107 relating to SFAS No. 123(R).

    Risk-free interest rate: Animal Health bases the risk-free interest rate on the interest rate payable on U.S. Treasury securities in effect at the time of grant for a period that is commensurate with the assumed expected option term.

    Expected annual dividends: The estimate for annual dividends is $0.00, because Animal Health has not historically paid, and does not expect for the foreseeable future to pay, a dividend.

    Estimated forfeiture rate: Animal Health did not estimate the forfeiture rate for 2007 because it had no historical data in which to make an assumption. The total size of the expense was also deemed to be immaterial; therefore, making forfeiture assumption less significant.

        The compensation expense under SFAS No. 123(R) for the Animal Health 2007 equity incentive plan for the year ended December 31, 2007 was insignificant.

F-87



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

2. Summary of Significant Accounting Policies (Continued)

Reclassifications

        Certain prior-year balances have been reclassified to conform with the current presentation.

Recent Accounting Pronouncements

        Effective January 1, 2008, the Company will adopt the provisions of Financial Accounting Standards Board Statement No. 157, Fair Value Measurements (FAS 157) to measure assets and liabilities. FAS 157 defines fair value, establishes a framework for measuring fair value in accounting principles generally accepted in the United States and expands the required disclosures about fair value measurements. The provisions of FAS 157 provide a hierarchy of inputs to valuation techniques which are comprised of observable and unobservable inputs and/or a combination thereof.

        Management anticipates, based on the composition of the Company's existing assets and liabilities, that the valuations used to estimate the fair value will rely on a observable and unobservable inputs. Observable inputs are those that reflect a public market, whereas unobservable inputs are those that reflect management's assumptions about the assumptions market participants would use in pricing the underlying asset or liability. Management does not believe that FAS 157 will have a material impact on the amounts reported in the financial statements; however, additional disclosures about the inputs used to develop the measurements of fair value and the effects of certain measurements reported in the consolidated statements of operations for a fiscal period will be required.

        Effective January 1, 2008, the Company will adopt Financial Accounting Standards Board Statement No. 159, The Fair Value Option for Financial Assets and Financial Liabilities (FAS 159). FAS 159 provides companies with an option to report selected financial assets and liabilities at fair value. The Statement also establishes presentation and disclosure requirements designed to facilitate comparisons between companies that choose different measurement attributes for similar types of assets and liabilities. FAS 159 requires companies to provide additional information that will help investors and other users of financial statements to more easily understand the effect of a company's choice to use fair value on its earnings. Management does not believe that FAS 159 will have a material impact on the amounts reported in the consolidated financial statements.

        In December 2007, the Financial Accounting Standards Board issued Statement No. 141 (revised 2007), Business Combinations (FAS 141(R)), which is effective for financial statements issued for fiscal years beginning on or after December 15, 2008. FAS 141(R) establishes principles and requirements for how an acquirer recognizes and measures in its financial statements the identifiable assets acquired, the liabilities assumed, any non-controlling interest in the acquiree, and the goodwill acquired in the business combination. FAS 141(R) also establishes disclosure requirements to enable the evaluation of the nature and financial effects of the business combination. FAS 141(R) will be applied prospectively. The Company expects the adoption of FAS 141(R) to not have a material impact on the consolidated financial statements.

3. Discontinued Operations

        In June 2008, VGX decided to sell its DNA plasmid manufacturing business to its affiliate VGXI, Inc. The sale included the patents related to the manufacturing of DNA plasmids as well as all

F-88



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

3. Discontinued Operations (Continued)


other assets related to manufacturing of DNA plasmids. Other assets acquired through the ADViSYS acquisition—Cellectra and the GHRH technology for veterinary applications were not part of the sale to VGXI, Inc. There were two primary reasons for the sale of the manufacturing assets. First, as predicted, operating a DNA plasmid manufacturing business took considerable time and resources. It was beginning to affect the focus of some of the key management personnel, as a substantial amount of management's time was being allocated to the manufacturing business instead of drug development. Second, management felt that divesting some of its non-core assets, such as DNA manufacturing, was preferable to raising capital through the sale of equity.

        As a result of this decision, VGX has classified the results of operations of the DNA plasmid manufacturing operations as discontinued operations in the consolidated balance sheet and statements of operations for the year ended December 31, 2007. This was done in accordance with the SFAS No. 144.

4. Inventories

        Inventories related to continuing operations consist of the following:

 
  December 31
 
 
  2007   2006  

Other—EP arrays

    26,925      
           

Total inventories

  $ 26,925   $  
           

5. Accrued Expenses

        Accrued expenses related to continuing operations consist of the following:

 
  December 31
 
 
  2007   2006  

Payroll and related expenses

  $ 279,142   $ 248,761  

Professional fees

    246,052     66,682  

Accrued research costs

    745,801     1,012,551  

Accrued interest

    1,055,084     962,127  

Other

    13,512     19,138  
           

  $ 2,339,591   $ 2,309,259  
           

F-89



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

6. Debt

        Debt consists of the following:

 
  December 31
 
 
  2007   2006  

Unsecured convertible notes payable

  $ 12,250,000   $ 10,650,000  

Secured convertible note payable

    1,000,000     1,000,000  

Note payable

        2,139,435  
           

Total debt

    13,250,000     13,789,435  

Current portion of long-term debt

    10,310,000     9,789,435  
           

Long-term debt

  $ 2,940,000   $ 4,000,000  
           

        In November 2005, the Company issued a $500,000 unsecured six-month maturity convertible note with an annual interest rate of 20% to an existing shareholder. The note and accrued interest was subsequently converted to common shares in 2006 upon maturity.

        In June 2005, the Company issued a $1,000,000 two-year maturity convertible note with an annual interest rate of 5%. The note is convertible into common shares and is collateralized by a check for the same amount, which is recognized as restricted cash on the Company's consolidated balance sheets.

        From August 2005 to December 2005, the Company reached an agreement with various investors to issue $4,000,000 in convertible notes ranging in maturity from 18 months to 24 months with annual interest rates ranging from 5% to 40%. Additionally, $6,650,000 in convertible notes were issued during the first half of 2006 with an annual interest rate of 5%. Of the total debt, $3,350,000 was secured by equity securities of a related party. In November of 2006, the Company entered into an agreement with an investor to issue a short-term note in the amount of 2,010,000,000 Korean Wons or $2,116,863 secured by equity securities of a related party. The note was repaid in 2007. During 2007, the Company reached an agreement with various investors to issue $1,600,000 in convertible notes ranging in maturity from 19 to 20 months.

        The convertible notes are convertible into shares of common stock at a defined conversion ratio (dollar for dollar). In addition, the notes shall automatically convert upon an initial public offering or a majority approval by the board of directors. Minimum principal repayments of long-term debt as of December 31, 2007 are as follows:

2008

  $ 10,310,000  

2009

    2,940,000  
       

  $ 13,250,000  
       

F-90



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

7. Minority Interest

        The Company owns 86% of the outstanding stock of Animal Health, a biotechnology company engaged in the development and commercialization of products designed to add to the economic value of livestock and improve the health of companion animals. Animal Health is consolidated in the results of the Company's consolidated financial statements. The minority interest liability represents, in aggregate, that portion of the combined total equity that is owned by the minority investor. The minority investor's share of the combined net loss is separately disclosed in the consolidated statement of operations.

8. Stockholders' Equity (Deficit)

        As of December 31, 2007, the Company is authorized to issue up to 100,000,000 shares of common stock and 1,000,000 shares of preferred stock. As of December 31, 2007, the Company had not issued any preferred stock.

Common Stock

2001 Equity Compensation Plan

        In August 2001 (and as amended in January 2007), the Company adopted the 2001 Equity Compensation Plan (the Plan) that authorizes the Company to grant up to 11,000,000 shares of common stock to eligible employees, directors, and consultants to the Company in the form of restricted stock and stock options. The amount and terms of grants are determined by the board of directors. The term of the options may be up to 10 years, and options are exercisable in cash or as

F-91



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

8. Stockholders' Equity (Deficit) (Continued)


otherwise determined by the board of directors. Generally, options vest 33% per year on each anniversary of the date of grant. Information relative to the Plan from inception is as follows:

 
  Options   Weighted Average Exercise Price   Aggregate Exercise Price  

Balance December 31, 2000

      $ 0.00005   $  
 

Granted

    150,000     0.00005     7.50  
 

Exercised

    (150,000 )   0.00005     (7.50 )
               

Balance December 31, 2001

        —            
 

Granted

    350,000     0.095     33,250  
               

Balance December 31, 2002

    350,000     0.095     33,250  
 

Granted

    1,252,224     0.04     50,056  
 

Exercised

    (50,000 )   0.19     (7,500 )
 

Cancelled/Forfeited

    (75,000 )   0.05     (3,750 )
               

Balance December 31, 2003

    1,477,224     0.05     72,056  
 

Granted

    1,686,000     0.14     243,300  
               

Balance December 31, 2004

    3,163,224     0.10     315,356  
 

Granted

    1,699,450     0.27     452,613  
 

Exercised

    (120,000 )   0.17     (20,400 )
               

Balance December 31, 2005

    4,742,674     0.16     747,569  
 

Granted

    2,702,633     0.82     2,218,290  
 

Exercised

    (968,000 )   0.19     (182,500 )
 

Cancelled/Forfeited

    (150,000 )   0.30     (45,000 )
               

Balance December 31, 2006

    6,327,307     0.43     2,738,359  
 

Granted

    2,616,700     5.00     13,083,500  
 

Exercised

        —            
 

Cancelled/Forfeited

    (229,000 )   0.87     (200,000 )
               

Balance December 31, 2007

    8,715,007   $ 1.80   $ 15,621,859  
               

        As of December 31, 2007, options to purchase 8,715,007 shares of common stock were outstanding, and the weighted-average remaining contractual life of all options was 7.8 years.

F-92



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

8. Stockholders' Equity (Deficit) (Continued)

        The following table summarizes information about stock options outstanding at December 31, 2007:

 
  Options Outstanding   Options Exercisable  
Range of
Exercise Prices
  Outstanding   Weighted-
Average Remaining
Contractual
Life (Years)
  Weighted-
Average Exercise Price
  Exercisable   Weighted-
Average Remaining
Contractual
Life (Years)
  Weighted-
Average Exercise Price
 
  $0.05 – $0.10     1,503,224     5.8   $ 0.09     1,503,224     5.8   $ 0.09  
  $0.11 – $0.25     1,854,450     7.1     0.22     1,654,450     7.1     0.21  
  $0.26 – $0.50     2,540,633     8.0     0.43     1,193,300     7.8     0.39  
  $0.51 – $5.00     2,816,700     9.2   $ 5.00     132,000     9.0   $ 5.00  
                                     
        8,715,007                 4,482,974              
                                     

        The total fair value of shares vested during 2007 totaled $4,772,537. As of December 31, 2007, there was $9,668,620 of total unrecognized compensation expense, net of estimated forfeitures, related to unvested options granted under the Stock Plans. That expense is expected to be recognized as follows:

Year ended December 31, 2008

  $ 4,715,049  

Year ended December 31, 2009

    3,953,783  

Year ended December 31, 2010

    999,788  
       

  $ 9,668,620  
       

        As of December 31, 2007, 996,993 shares were available for future grants under the Plan. Certain employee option vesting may be accelerated in the event of a change in control of the Company.

Warrants to Acquire Common Stock

        As of December 31, 2007, in connection with prior-year debt issuances, the Company had outstanding 10-year warrants to purchase 233,933 shares of common stock at a weighted-average exercise price of $0.31 per share, exercisable through various dates through December 2013. The total expense recognized under the Black-Scholes option pricing model for these warrants was $50,203. As of December 31, 2007 the Company had outstanding 10-year warrant to purchase 1,100,000 shares of common stock at an average exercise price of $0.50 per share, exercisable through April 2016; this warrant was issued to an employee who is not currently with the Company. The total expense recognized under the Black-Scholes option pricing model for this warrant was $5,097,548.

F-93



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

8. Stockholders' Equity (Deficit) (Continued)

Shares Reserved for Future Issuance

        At December 31, 2007, the Company has reserved the following shares of common stock for issuance:

Common stock options outstanding

    8,715,007  

Common stock options available for future grant

    996,993  

Common stock warrants

    1,333,933  
       

    11,045,933  
       

Common Stock—Animal Health

        As of December 31, 2007, Animal Health is authorized to issue up to 20,000,000 shares of common stock.

2007 Equity Compensation Plan

        In May 2007, Animal Health adopted the 2007 Equity Compensation Plan (the Plan) that authorizes Animal Health to grant up to 1,500,000 shares of common stock to eligible employees, directors, and consultants to Animal Health in the form of restricted stock and stock options. The Plan was subsequently amended in February 2008, with both board and stockholder approval to increase the number of shares eligible to be granted under the plan to 2,000,000 shares of Animal Health common shares. The amount and terms of grants are determined by the board of directors. The term of the options may be up to 10 years, and options are exercisable in cash or as otherwise determined by the board of directors. Generally, options vest 33% per year on each anniversary of the date of grant.

        Information relative to the Plan from inception is as follows:

 
  Options   Weighted-
Average
Exercise Price
  Aggregate
Exercise Price
 

Balance December 31, 2006

      $   $  
 

Granted

    1,255,667     0.07     87,614  
 

Exercised

             
               

Balance December 31, 2007

    1,255,667   $ 0.07   $ 87,614  
               

        As of December 31, 2007, options to purchase 1,255,667 shares of common stock were outstanding, and the weighted-average remaining contractual life of all options was 9.5 years.

F-94



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

8. Stockholders' Equity (Deficit) (Continued)

        The following table summarizes information about stock options outstanding at December 31, 2007:

 
  Options Outstanding   Options Exercisable  
Range of
Exercise Prices
  Outstanding   Weighted-
Average Remaining
Contractual
Life (Years)
  Weighted-
Average Exercise Price
  Exercisable   Weighted-
Average Remaining
Contractual
Life (Years)
  Weighted-
Average Exercise Price
 
  $0.0001 – $0.50     1,139,000     9.42     0.0001              
  $0.51     – $1.00     116,667     9.87     0.75     107,223     9.87     0.75  
                                     
        1,255,667                 107,223              
                                     

        As of December 2007, there were no exercises of any stock options.

        The total fair value of shares vested during 2007 equals $42,080. As of December 31, 2007, there was $3,646 of total unrecognized compensation expense, net of estimated forfeitures, related to unvested options granted under the Stock Plans. That expense is expected to be recognized as follows:

Year ended December 31, 2008

  $ 1,328  

Year ended December 31, 2009

    1,329  

Year ended December 31, 2010

    989  
       

  $ 3,646  
       

        As of December 31, 2007, 244,333 shares were available for future grants under the Plan. Certain employee option vesting may be accelerated in the event of a change in control of Animal Health.

Shares Reserved for Future Issuance

        At December 31, 2007, Animal Health has reserved the following shares of common stock for issuance:

Common stock options outstanding

    1,255,667  

Common stock options available for future grant

    244,333  
       

    1,500,000  
       

9. Commitments

Leases

        In May 2005, the Company signed a facility lease with a lessor for a lease through May 2010. The lease provides for one additional five-year renewal option. In addition, the Company has entered into equipment leases consisting of a three-year operating lease for a copier expiring in June 2009, and a five-year telecommunications lease expiring in February 2010. The five-year telecommunications lease automatically renews for another five years under the same terms unless notified within 30 days of

F-95



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

9. Commitments (Continued)


expiration. In 2006, the Company entered into a three-year lease with a broadband network provider to enhance connectivity. All leases contain renewal options. In 2007, the Company signed a capital equipment lease for a copy machine for a three-year term expiring August 2010. There was a bargain purchase option which made the copier a capital lease. The value of the copier is properly booked as a fixed asset. In November 2007, the Company signed a facility lease in Houston through October 2017. The agreement is a renewal of a lease that was assigned to the Company when it acquired the assets of ADViSYS in February 2007. Future minimum lease payments under the facility lease as well as the other equipment leases are as follows:

 
  Equipment   Facility  

2008

  $ 19,291   $ 397,805  

2009

    16,766     406,101  

2010

    4,688     304,398  

2011

        254,361  

Thereafter

        1,549,238  
           

Total minimum lease payments

  $ 40,745   $ 2,911,903  
           

        Rent expense under operating lease was $303,186 in 2007, of which $159,936 was for continuing operations. In 2006, rent expense under operating lease was $136,910. Rent expense from inception to December 31, 2007 for continuing operations was $497,159.

License Agreements

        In May 2003, the Company entered into a research and development agreement with a pharmaceutical company in China in which the Company granted to the aforementioned company exclusive rights in The People's Republic of China, Taiwan, Hong Kong, and Macao to research, develop, and market recombinant Viral Protein r (Vpr) protein and Adeno-Vpr-based products as treatments for cancer and sepsis. The license agreement required a $75,000 up-front payment, which was recorded as revenue in the accompanying consolidated statements of operations for the year ended December 31, 2003. The license agreement also requires milestone payments upon the enrollment of the first patient in Phase II trial and royalty payments equal to a specified percentage of future commercial sales of products manufactured using the licensed technology, through the later of the expiration of the licensed patents or 10 years after the first commercial sale of covered product. In March of 2007, the Company terminated the agreement with this party for its failure to comply with the terms of the agreement.

        In November 2001, the Company entered into a license agreement with a university to license certain patent rights. The license agreement required issuance of Company stock in lieu of an up-front cash payment, which was recorded as research and development expense in 2001. The license agreement requires various milestone payments. They include a $500,000 payment for the enrollment of the first patient in Phase III trials, a $500,000 payment for the filing of the NDA for the first licensed product, a $500,000 payment on the anniversary of the filing, a $1,500,000 payment upon the receipt of an NDA approval letter for the first licensed product, and a $1,500,000 payment on the first

F-96



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

9. Commitments (Continued)


anniversary of the receipt of an approval for the first licensed product. These payments are in effect through the later of the expiration of the licensed patents or ten years after the first commercial sale of covered product. The agreement is valid through the later of 25 years from the effective date or the expiration of the last to expire or abandonment of the patent rights.

        In December 2005, the Company entered into an alliance agreement with a European pharmaceutical company for the worldwide rights to conduct research and development and market a drug with indications in rheumatoid arthritis and psoriasis. The license agreement required issuance of Company stock as well as an up-front cash payment, which was recorded as research and development expense in the accompanying consolidated statement of operations for the year ended December 31, 2005. The license agreement requires various milestone payments upon the completion of patient enrollment for a Phase II trial product for $50,000, a $250,000 payment upon completion of the first Phase III trial product, and a $2,000,000 payment upon NDA approval of a trial product. These payments are in effect through the later of the expiration of the licensed patents or ten years after the first commercial sale of covered product. The agreement is valid through the later of 20 years from the effective date or the expiration of the last to expire or abandonment of the patent rights.

        In November 2006, the Company entered into a license agreement with a U.S.-based company for its patented DNA-delivery technology to use in the intratumoral delivery of a proprietary gene to control the growth of melanoma and other cancers. Under the terms of the agreement, the Company paid the licensor an up-front license fee in cash and equity. There will also be payments based on successful completion of clinical and regulatory milestones. They include a payment upon beginning of a Phase II trial, a payment upon completion of the Phase II trial, payment upon the completion of Phase III trial, a payment upon the NDA approval, and a payment upon sale of licensed product in any of France, Germany, Italy, the U.S., or the United Kingdom. The Company will in return be exclusively supplied with the licensor's electroporation devices for the therapy included in the license agreement and will also pay the licensor royalties on the sale of products covered by the license. The term of the agreement will extend until the last to expire of any royalty period for any licensed product. Royalty period will be, with respect to any particular licensed product in any country, the period of time beginning on the first commercial sale of such licensed product in such a country and extending until the earlier of (1) the date when there is not any valid claim included in any licensor patent right in any country which would be infringed by the sale of the licensed product in any country for a license granted by licensor to the Company or (2) 10 years from the date of the first commercial sale of such licensed product in such country.

        In December 2006, the Company entered into an R&D collaboration and license agreement with a related party in which the Company granted the licensee exclusive worldwide rights to conduct research, development activities, sales, licensing, and marketing of VGX-1027 for Type I Diabetes. There are milestone and royalty payments due to the Company from the licensee. The milestone payments are due upon 1) The completion of a Phase I study, 2) Upon completion of patient accrual for T1D Phase II trial, 3) Upon completion of patient accrual for Phase III clinical trial, 4) Upon NDA submission, and 5) Upon NDA approval. However, the actual amount of the milestone payments had been contractually agreed to be negotiated at a later time. The two parties have agreed to also share R&D costs on a mutually agreeable basis. The terms of the agreement shall terminate the earlier of

F-97



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

9. Commitments (Continued)


(1) expiration of the last-to-expire patent or (2) 20 years from the effective date. In October 2007 an amendment was made to the agreement in which the sharing of the R&D costs between the Company and the related-party was clarified. The related-party agreed to be responsible for all third-party costs related to the completion of Phase I clinical trials.

        In April 2007, the Company entered into a commercial license agreement with a U.S.-based company to license its proprietary technology for the clinical and commercial production of Vpr protein. The license agreement requires various milestone and royalty payments. This includes payments to be made annually on each anniversary of the acceptance of an IND until an NDA is filed, a payment upon submission of NDA or BLA, and a payment upon receipt of marketing approval for the product.

        In April 2007, the Company entered into a license agreement with a university to license certain patent rights. Upon the execution of this agreement, the Company made an initial payment of $100,000 to the University. The license agreement requires various milestone payments. They include a $125,000 payment upon filing of an IND application, a $250,000 payment upon enrollment of first subject in Phase II clinical trial, a payment of $375,000 upon enrollment of first subject in Phase III clinical trial, a payment of $250,000 upon filing of NDA and a payment of $1,500,000 upon receipt of approval in the U.S., the EU, or Japan (whichever is first to occur). In addition, the Company is required to make minimum payments related to research and development activities of $200,000 in the first 12-month period, $250,000 in the second 12-month period, $300,000 in the third 12-month period, and a total of $400,000 for all years subsequent to the third 12-month period until the termination of the agreement. The agreement is valid through the later of 10 years after the first sale of the first licensed product, or the expiration or abandonment of the last patent to expire or become abandoned.

        In May 2007, the Company entered into a license agreement with a university to license certain patent rights. The license agreement requires various milestone payments. They include an annual maintenance fee of $25,000, a $75,000 payment upon beginning of Phase I trial, a $100,000 payment upon beginning of Phase II trial, a $250,000 payment upon the initiation of Phase III trial, and a $500,000 payment upon the first commercial sale of the licensed product. The agreement also calls for a royalty payment on net sales. There is a sliding scale of milestone payments for achievement of clinical milestones for second and third clinical indications. The agreement is valid through 10 years after the first sale of the first licensed product.

        In June 2007, the Company entered into a license agreement with a related party in which it grants to the licensee exclusive world-wide rights to conduct research, development activities, sale, licensing, and marketing of VGX-100 for gastric cancer in humans. There are milestone and royalty payments due to the Company from the licensee. The milestone payments are due upon 1) The completion of a Phase I study, 2) Upon completion of patient accrual for Gastric Cancer Phase II trial, 3) Upon completion of patient accrual for Phase III clinical trial, 4) Upon NDA submission, and 5) Upon NDA approval. . However, the actual amount of the milestone payments had been contractually agreed to be negotiated at a later time. The two parties have agreed to also share R&D costs on a mutually agreeable basis. The terms of the agreement shall terminate the earlier of (1) expiration of the last-to-expire patent or (2) 20 years from the effective date.

F-98



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

9. Commitments (Continued)

        In September 2007, the Company entered into a license agreement with a related party to license out certain patent rights related to its Animal Health Franchise. The license agreement requires various milestone and royalty payments from the related-party to the Company. These include a $250,000 payment for the filing of an INAD, $500,000 payment upon initiation of Phase III or pivotal trial, $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the U.S., $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the EU, and $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the territories outside the EU and the U.S. Notwithstanding the above payment schedule, the related party does not have to make any milestone payments to the Company unless it has raised at least $5,000,000 in capital. In connection with this agreement the Company and the related party also reached a nonexclusive agreement in which the Company grants device and manufacturing patent rights to the aforementioned related party. Also as part of the agreement, the related party has agreed to make certain royalty payments to the seller of ADViSYS assets that the Company was obligated to make under the terms of the asset purchase agreement. The seller has recourse to the Company should the related-party fail to make proper payment to the seller.

        In October 2007, the Company entered into an agreement with a related party in which it grants to the licensee exclusive, nonsublicensable, royalty-bearing patent rights for certain manufacturing processes related to the production of plasmids. The territory covered under the agreement is Asia. The agreement requires royalty payments as a percentage of net sales.

    Research Agreements

        In December 2005, the Company entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is five years. The Company has committed a total of $1,035,000 ($207,000 per year) during the term of this agreement. The payments are to be made in increments of $207,000 during the term of the sponsored research agreement.

        In June 2006, the Company entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is two years but can be extended to five years upon review of the progress of the research. The total value of the agreement is not to exceed $1,000,000. The maximum liability of the Company during the two-year term of the agreement is $400,000. This agreement was cancelled on April 13, 2008 through mutual agreement.

    Supply Agreements

        In July 2005, the Company entered into a supply agreement with a manufacturer to purchase a minimum annual amount of 500 kilograms of the active pharmaceutical ingredient (API). The supply agreement is contingent upon the receipt of the regulatory approval of the VGX NDA for the product. The term of the agreement is 10 years from receipt of the approval of the NDA. There is an automatic renewal for successive terms of two years unless a written notice is provided to the other party within 180 days prior to the end of the term.

F-99



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

9. Commitments (Continued)

        In July 2005, the Company entered into a supply agreement with a manufacturer to purchase a minimum annual amount of 1,000 kilograms of the API. The supply agreement is contingent upon the receipt of the regulatory approval for sale of the product. The term of the agreement is five years from receipt of the approval for sale of the product. This agreement will be in force after the initial five-year term unless a written notice is provided to the other party requesting that the agreement be terminated.

        In March 2006, the Company entered into a supply agreement with a related party to purchase a minimum annual amount of 20,000 kilograms of the API. The supply agreement is contingent upon the receipt of the regulatory approval for sale of the product in the U.S. The term of the agreement is the later of five years from receipt of the approval for sale of the product or from May 1, 2009 to April 2014. This agreement will be in force after the initial five-year term unless a written notice is provided to the other party requesting that the agreement be terminated.

    Sales and Marketing Agreements

        In February 2007, the Company entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market PICTOVIR in Asia, Africa, and the Middle East. There are milestone and royalty payments associated with the agreement. This includes a $3,000,000 payment to the Company upon completion of Phase III trials for PICTOVIR, a $3,000,000 payment to the Company upon submission of NDA for PICTOVIR, and a $5,000,000 payment to the Company upon NDA approval. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date.

        In April 2007, the Company entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market VGX-410C in Asia, Africa, and the Middle East. There are milestone and royalty payments associated with the agreement. They include a $3,000,000 payment to the Company upon completion of Phase III trials for VGX-410C, a $3,000,000 payment to the Company upon submission of NDA for VGX-410C, a $5,000,000 payment for NDA approval in Japan, and a $5,000,000 payment to the Company upon NDA approval in any country except for Japan. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date. The Company decided in December 2007 to discontinue the VGX-410C program to concentrate its efforts on other candidates in its pipeline.

        In August 2007, Animal Health entered into a sales and marketing agreement with an Australia-based company to import, warehouse, and distribute its products to veterinarians in Australia. A $5,000 payment was made to the Australian company upon execution of this agreement, and another $5,000 payment was due upon receipt of final regulatory approval of Animal Health's product in Australia. The additional payment was made in 2008 upon the announcement of the approval. Additionally, under the terms of the agreement, Animal Health will pay the distributor a commission based on a percentage of all sales in Australia.

F-100



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

10. Income Taxes

        At December 31, 2007, the Company had federal net operating loss carryforwards of approximately $27,604,700, which will expire in 2021 through 2027 if not utilized. In addition, the Company had state net operating loss carryforwards of approximately $23,339,300. The state net operating losses are subject to an annual limitation of $3,000,000 or 12.5% of taxable income, whichever is greater, and expire in 2021 through 2027.

        The Tax Reform Act of 1986 (the Act) provides for a limitation on the annual use of net operating loss and research and development tax credit carryforwards following certain ownership changes (as defined by the Act) that could limit the Company's ability to utilize these carryforwards. The Company may have experienced an ownership change, as defined by the Act, as a result of past financings. Accordingly, the Company's ability to utilize the aforementioned carryforwards may be limited. Additionally, U.S. tax laws limit the time during which these carryforwards may be applied against future taxes; therefore, the Company may not be able to take full advantage of these carryforwards for federal income tax purposes.

        The components of the net deferred tax assets are as follows:

 
  December 31  
 
  2007   2006  

Net operating losses

  $ 11,028,000   $ 9,897,000  

Other temporary differences

    12,167,700     5,235,700  
           

Gross deferred tax assets

    23,195,700     15,132,700  

Deferred tax asset valuation allowance

    (23,195,700 )   (15,132,700 )
           

  $   $  
           

        In assessing the realizability of deferred tax assets, the Company considers whether it is more likely than not that some portion or all of the deferred tax assets will not be realized. The ultimate realization of deferred tax assets is dependent upon the generation of future taxable income during the periods in which the temporary differences representing net future deductible amounts become deductible. Due to the Company's history of losses, the deferred tax assets are fully offset by a valuation allowance at December 31, 2007 and 2006. The valuation allowance in 2007 increased by 8,063,000 over 2006 and related primarily to additional net operating losses incurred by the Company.

11. Acquisition

        On February 21, 2007, the Company acquired all of the assets as defined in the asset purchase agreement of ADViSYS, Inc. whose primary operations comprise DNA plasmid manufacturing for customers, R&D activities for CELLECTRA™ and GHRH for veterinary applications. The results of the acquired company's operations have been included in the consolidated financial statements since the acquisition date. The aggregate purchase price at the time of the purchase consisted of $2,211,000 in cash and 924,219 shares of common stock, valued at their estimated fair value, of the Company. The Company is to pay the seller additional consideration upon completion of certain milestones. In

F-101



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

11. Acquisition (Continued)


January 2008, the Company issued an additional 200,000 shares of Company stock upon the achievement of marketing approval of LifeTide™ SW 5.0 in Australia.

        The purchase price has been allocated as follows, as of the acquisition date:

Inventories

  $ 318,118  

Current assets

    367,937  

Property and equipment and other long-term assets

    1,784,737  

Intangible assets

    4,341,400  

Goodwill

    1,084,844  
       

Total assets acquired

    7,897,036  

Less total liabilities assumed

    (926,479 )
       

Net assets acquired

  $ 6,970,557  
       

        The Company believes that its market position and diverse range of products were the primary reasons for a total purchase price that resulted in the recognition of goodwill.

        The $4,341,400 of acquired intangible assets has a weighted-average useful life of approximately eight years. The intangible assets include customer lists of $364,900 (weighted-average useful life of 3.9 years), and proprietary technology of $3,976,500 (weighted-average useful life of 8.4 years). As of December 31, 2007, the intangible assets related to customer lists are reflected in assets of discontinued operations.

        The expense for amortization of intangibles in 2007 was $480,332; the amortization expense for intangibles since the inception of the Company is $480,332, of which $397,604 is included in continuing operations in each respective period.

        Included in total liabilities assumed above is deferred revenue of $376,010. In accordance with Emerging Issues Task Force Issue (EITF) 01-3, Accounting in a Business Combination for Deferred Revenue of an Acquiree , the Company has determined that it has assumed a legal performance obligation of the acquiree. In order to record the deferred revenue at fair value in accordance with EITF 01-3, the Company has excluded revenue related to efforts completed prior to the acquisition date of approximately $921,000. As of December 31, 2007, deferred revenue is reflected in liabilities of discontinued operations.

12. Equity Investment

        In October 2005, the Company purchased 250,000 shares of a Korean-based company, Dong-IL Fabrics, at an aggregate purchase price of $4,787,824. At the date of purchase, the Company's ownership represented 33% of the total outstanding shares of Dong-IL Fabrics. Additionally, the Company incurred $110,400 of acquisition costs associated with the investment. In 2006, the name of Dong-IL Fabrics was officially changed to VGX International (VGXI). Also in 2006, the Company invested an additional $4,408,065 in VGXI. Finally, during 2006, VGXI had a secondary offering in which the Company elected not to fully participate. Prior to that offering, the Company's ownership percentage was 38%. Accordingly, the December 31, 2007 carrying value of the investment in VGXI is

F-102



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

12. Equity Investment (Continued)


less than the Company's ownership percentage of VGXI's equity. The Company's current ownership percentage in VGXI is 30%.

        Under the equity method of accounting in accordance with APB 18, The Equity Method of Accounting for Investments in Common Stock , the Company has recorded an interest in the earnings or losses of VGXI beginning from the date of purchase. The Company's interest in the losses of VGXI from the date of purchase through December 31, 2007 is $2,015,869, which includes $47,840 of amortized acquisition costs. VGXI is a publicly traded company on the Korean Stock Exchange and, therefore, the equity investment on the balance sheet is based upon the quoted market price of the stock, net of unamortized acquisition costs.

        The financial position and results of operations of VGXI as of and for the year ended December 31, 2007 are as follows:

    Financial Position:

 
  December 31, 2007  

Assets

       

Current assets

  $ 32,237,728  

Fixed assets

    6,958,811  

Other assets

    7,074,560  
       

Total assets

  $ 46,271,099  
       

Liabilities

       

Current liabilities

  $ 8,289,305  

Long-term liabilities

    246,946  
       

Total liabilities

    8,536,251  

Total equity

    37,734,848  
       

Total liabilities and equity

  $ 46,271,009  
       

    Results of Operations:

 
  Year Ended December 31, 2007  

Revenues

  $ 10,788,501  

Cost of sales

    9,328,418  
       

Gross profit

    1,460,083  

Operating expenses

    6,741,753  
       

Operating loss

  $ (5,281,670 )
       

Net loss

  $ (3,103,624 )
       

F-103



VGX Pharmaceuticals, Inc.
(A Development-Stage Company)

Notes to Consolidated Financial Statements (Continued)

December 31, 2007

12. Equity Investment (Continued)

        In October 2007, the Company made a strategic investment of $60,000 in a biotechnology company based in Colorado. The two companies have also agreed to cooperate on various future research projects. The investee is a private company in which the company holds less than 10% of outstanding shares.

13. Subsequent Events

        In January 2008, Animal Health received an approval by the Australian Pesticides and Veterinary Medicines Authority (APVMA) for LifeTide™ SW 5, the Company's leading Growth Hormone Releasing Hormone (GHRH) product for swine therapy. LifeTide™ SW 5 is an injectable DNA plasmid encoding for porcine GHRH, and is administered as a once in a lifetime treatment for use in sows of breeding age to increase the number of piglets weaned.

        In February 2008, the Company entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market VGX-1027 for Rheumatoid Arthritis (RA), in Asia (excluding Japan), Africa, and the Middle East. There are milestone and royalty payments associated with the agreement due to the Company. They include a $1,500,000 payment for the initiation of a Phase II trial for RA, a $3,000,000 payment for the initiation of a Phase III trial, a $3,000,000 payment for the submission of NDA, and a $5,000,000 payment upon approval of NDA. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date.

        In March 2008, the Company entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is five years and the total value of the agreement is not to exceed $1,180,000.

        In April 2008, the Company entered into a license agreement with a related party in which it grants to the licensee exclusive rights in Korea to the development, sales, licensing, and marketing for the CELLECTRA™ Device. There are milestone and royalty payments due to the Company from the licensee. These include a $100,000 payment to VGX upon filing of each IND using Cellectra, $150,000 payment upon initiation of each Phase II trial, $250,000 payment upon initiation of each Phase III trial, $500,000 payment upon each BLA approval, and a $750,000 payment upon first commercial sale of Cellectra for each BLA. The licensee also agreed to pay $100,000 cost sharing fee as well as $25,000 annually to partially cover the costs of patents, product enhancement, and other associated R&D efforts. The terms of the agreement shall terminate the earlier of (1) expiration of the last-to-expire patent or (2) 20 years from the effective date.

        In June 2008, the Company entered into an Asset Purchase Agreement with a related party to sell the assets of the plasmid manufacturing division in The Woodlands, Texas, in exchange for $9,110,000 in cash. The plasmid manufacturing division was originally acquired by the Company as part of the acquisition of assets of ADViSYS, Inc. in February of 2007. The payment is to be structured so that the last tranche of the purchase price will be received by March 31, 2009. There are no other milestone or royalty payments owed by either party to the Agreement.

F-104



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

Consolidated Financial Statements
For the Period Ended September 30, 2008

 
  Page

Consolidated Balance Sheets as of September 30, 2008 (Unaudited) and December 31, 2007

  F-106

Consolidated Statements of Operations for the Nine Months Ended September 30, 2008 and 2007 and the Period from December 12, 2000 (Inception) to September 30, 2008

 
F-107

Consolidated Statements of Cash Flows for the Nine Months Ended September 30, 2008 and 2007 and the Period from December 12, 2000 (Inception) to September 30, 2008 (Unaudited)

 
F-108

Notes to Consolidated Financial Statements (Unaudited)

 
F-109

F-105



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

CONSOLIDATED BALANCE SHEETS

 
  September 30,
2008
  December 31,
2007
 
 
  (Unaudited)
   
 

ASSETS

             

Current assets:

             

Cash and cash equivalents

  $ 6,760,395   $ 15,814,097  

Accounts receivable

    42,625     2,100  

Receivables due from related parties

    6,351,489      

Inventories

    37,475     26,925  

Restricted cash

        1,000,000  

Prepaid expenses and other current assets

    208,872     317,797  

Assets of discontinued operations

        3,840,104  
           

Total current assets

   
13,400,856
   
21,001,023
 

Equity investment

   
2,578,924
   
7,966,143
 

Fixed assets, net

    398,998     409,768  

Intangible assets, net

    3,221,052     3,578,896  

Goodwill

    907,076     907,076  

Debt issuance costs, net

        129,037  

Other assets

    130,147     130,147  
           

Total assets

 
$

20,637,053
 
$

34,122,090
 
           

LIABILITIES AND STOCKHOLDERS' EQUITY

             

Current liabilities:

             

Accounts payable

  $ 814,914   $ 724,466  

Accrued expenses

    1,961,896     2,339,591  

Current portion of long-term debt

    7,900,000     10,310,000  

Other current liabilities

    47,097     354,305  

Liabilities of discontinued operations

        4,051,013  
           

Total current liabilities

   
10,723,907
   
17,779,375
 

Long-term debt

   
100,000
   
2,940,000
 
           

Total liabilities

   
10,823,907
   
20,719,375
 

Minority interest

   
702,835
   
956,497
 

Stockholders' equity:

             

Common stock

    4,167     4,480  

Additional paid-in capital

    73,179,654     65,085,032  

Accumulated deficit

    (63,048,018 )   (53,285,330 )

Accumulated other comprehensive (loss) income

    (1,025,492 )   642,036  
           

Total stockholders' equity

   
9,110,311
   
12,446,218
 
           

Total liabilities and stockholders' equity

 
$

20,637,053
 
$

34,122,090
 
           

See accompanying notes.

F-106



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

CONSOLIDATED STATEMENTS OF OPERATIONS

(Unaudited)

 
  Nine Months Ended
September 30
   
 
 
  Period from
December 12, 2000 (Inception)
to September 30, 2008
 
 
  2008   2007  

Revenue:

                   

Revenue from product sales

  $ 40,000   $   $ 40,000  

Government contract revenue

    1,962,305         1,962,305  

Government grant revenue

    86,120     668,955     1,827,528  

License fee revenue

    100,000         175,000  

Other operating revenue, net

    27,625     25,562     64,073  
               

Total revenue

   
2,216,050
   
694,517
   
4,068,906
 

Operating expenses:

                   

Cost of product sales

    112,153         112,153  

Research and development

    10,026,912     8,225,442     36,240,210  

General and administrative

    6,356,794     3,976,436     31,435,138  
               

Total operating expenses

   
16,495,859
   
12,201,878
   
67,787,501
 
               

Loss from operations

   
(14,279,809

)
 
(11,507,361

)
 
(63,718,595

)

Losses from equity investment

   
(817,935

)
 
(562,638

)
 
(2,833,804

)

Interest income

    393,783     703,365     2,260,147  

Interest expense

    (476,403 )   (839,849 )   (2,807,314 )

Other income (expense), net

    97,497         97,497  

Minority interest

    253,662     5,853     297,165  
               

Loss from continuing operations

   
(14,829,205

)
 
(12,200,630

)
 
(66,704,904

)

Discontinued operations:

                   

Gain on sale of manufacturing assets, net of tax

    6,653,153         6,653,153  

Loss from discontinued operations

    (1,586,636 )   (1,044,779 )   (2,996,267 )
               

Net loss

 
$

(9,762,688

)

$

(13,245,409

)

$

(63,048,018

)
               

Amounts per common share—basic and diluted:

                   

Loss from continuing operations per share

 
$

(0.34

)

$

(0.28

)
     

Income / (loss) from discontinued operations per share

  $ 0.12   $ (0.02 )      

Net loss per share

  $ (0.22 ) $ (0.30 )      

Weighted average number of common shares outstanding—basic and diluted

   
43,959,706
   
43,641,329
       

See accompanying notes.

F-107



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

CONSOLIDATED STATEMENTS OF CASH FLOWS

(Unaudited)

 
  Nine Months
Ended
September 30,
2008
  Nine Months
Ended
September 30,
2007
  Period From
December 12, 2000
(Inception) to
September 30,
2008
 

Cash flows from operating activities:

                   
 

Net loss

  $ (9,762,688 ) $ (13,245,409 ) $ (63,048,018 )
 

Adjustments to reconcile net loss to net cash used in operating activities:

                   
   

Gain on sale of manufacturing assets

    (6,653,153 )       (6,653,153 )
   

Depreciation and amortization

    852,102     1,194,694     2,535,637  
   

Stock-based compensation

    8,092,559     4,810,343     37,298,978  
   

Interest converted into common stock

            53,839  
   

Loss on disposal of fixed assets

    617         2,781  
   

Minority interest in net loss

    (253,662 )   5,853     (297,165 )
   

Losses from equity investment

    817,935     562,638     2,833,804  
   

Changes in operating assets and liabilities:

                   
     

Accounts receivable

    (20,525 )   (546,337 )   (14,477 )
     

Receivables due from related parties

    (351,489 )       (351,489 )
     

Inventories

    (163,653 )   (1,397,841 )   (1,975,465 )
     

Prepaid expenses and other assets

    221,906     (331,169 )   (221,496 )
     

Accounts payable and accrued expenses

    (432,182 )   75,479     2,335,750  
     

Deferred revenue from manufacturing operations

    83,789     3,619,271     3,495,878  
     

Other current liabilities

    (307,208 )   101,483     47,097  
               

Net cash used in operating activities

   
(7,875,652

)
 
(5,162,701

)
 
(23,957,499

)

Cash flows from investing activities:

                   

Purchase of ADViSYS, Inc., net of cash acquired

        (2,058,762 )   (2,058,762 )

Payment received on sale of manufacturing assets

    3,110,000         3,110,000  

Equity investment

            (9,362,501 )

Investment in third party stock

            (60,000 )

Purchases of property and equipment

    (167,557 )   (279,004 )   (883,542 )

Proceeds from sale of minority interest

        1,000,000     1,000,000  
               

Net cash provided by (used in) investing activities

   
2,942,443
   
(1,337,766

)
 
(8,254,805

)

Cash flows from financing activities:

                   

Decrease in restricted cash

    1,000,000          

Proceeds from debt borrowings

    100,000     960,000     15,989,435  

Repayment of debt to investors

    (5,350,000 )       (7,489,435 )

Debt issuance costs

    129,037     (102,900 )   (257,463 )

Proceeds from issuance of common stock

    1,750     5,500,000     30,709,909  
               

Net cash (used in) provided by financing activities

   
(4,119,213

)
 
6,357,100
   
38,952,446
 

Effect of exchange rate changes on cash

   
(1,280

)
 
(376

)
 
20,253
 
               

(Decrease) increase in cash and cash equivalents

   
(9,053,702

)
 
(143,743

)
 
6,760,395
 

Cash and cash equivalents, beginning of period

    15,814,097     20,915,863      
               

Cash and cash equivalents, end of period

 
$

6,760,395
 
$

20,772,120
 
$

6,760,395
 
               

See accompanying notes.

F-108



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(Unaudited)

1. Basis of Presentation and Description of the Business

        The accompanying unaudited consolidated financial statements of VGX Pharmaceuticals, Inc. ("VGX") have been prepared in accordance with United States generally accepted accounting principles ("U.S. GAAP") for interim financial information. Accordingly, they do not include all of the information and footnotes required by U.S. GAAP for complete financial statements. The consolidated balance sheet as of September 30, 2008, consolidated statements of operations for the nine months ended September 30, 2008 and 2007, and the consolidated statements of cash flows for the nine months ended September 30, 2008 and 2007, are unaudited, but include all adjustments (consisting of normal recurring adjustments) that VGX considers necessary for a fair presentation of the financial position, results of operations and cash flows for the periods presented. The results of operations for the nine months ended September 30, 2008, shown herein are not necessarily indicative of the results that may be expected for the year ending December 31, 2008, or for any other period. These unaudited consolidated financial statements, and notes thereto, should be read in conjunction with the audited consolidated financial statements for the year ended December 31, 2007.

        VGX Pharmaceuticals, Inc. is a development-stage company incorporated in Delaware as Viral Genomix, Inc. on December 12, 2000 (inception). VGX began operations on January 1, 2001, and is a biopharmaceutical company engaged in the discovery and development of drugs and DNA vaccines for the treatment of infectious diseases, including the HIV virus, as well as cancer and inflammatory diseases. VGX has built a broad product pipeline encompassing these major disease categories, and these product candidates and technology programs are protected by VGX's extensive global intellectual property patents. VGX has generated an accumulated deficit of $63.0 million since inception. VGX anticipates incurring additional losses for the foreseeable future. Substantial additional financing will be needed by VGX to fund its operations and to develop its products. There is no assurance that such financing will be available when needed.

        VGX Animal Health, Inc. (Animal Health) is a biotechnology company engaged in the development and commercialization of products designed to add to the economic value of livestock and improve the health of companion animals. The Animal Health franchise was acquired as part of the acquisition of ADViSYS in February 2007. VGX carved out the acquired Animal Health franchise into a separate company in order to clearly segregate the Animal Health franchise from its core technology dedicated to developing drugs for human application. Animal Health's lead candidate is Lifetide™ SW5 for porcine. In January 2008, Animal Health received an approval by the Australian Pesticides and Veterinary Medicines Authority (APVMA) for LifeTide™ SW 5, VGX's leading Growth Hormone Releasing Hormone (GHRH) product for swine therapy. LifeTide™ SW 5 is an injectable DNA plasmid encoding for porcine GHRH, and is administered as a once in a lifetime treatment for use in sows of breeding age to increase the number of piglets weaned. VGX owns 88% of the outstanding stock of Animal Health as of September 30, 2008. Animal Health is consolidated in the results of VGX's consolidated financial statements.

        On June 10, 2008, VGX entered into an Asset Purchase Agreement with a related party to sell the assets of the plasmid manufacturing division in The Woodlands, Texas, in exchange for $9,110,000 in cash. The plasmid manufacturing division was originally acquired by VGX as part of the acquisition of assets of ADViSYS, Inc. in February of 2007. The payment is to be structured so that the last tranche of the purchase price will be received by March 31, 2009. There are no other milestone or royalty

F-109



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

1. Basis of Presentation and Description of the Business (Continued)


payments owed by either party to the Agreement. VGX has reflected a gain on the sale of these assets in its consolidated statement of operations of $6.7 million, net of taxes, for the nine months ended September 30, 2008.

        VGX is subject to those risks associated with biotechnology companies in a similar stage of development. There can be no assurance that VGX's research and development activities will be successful, that products developed will obtain necessary regulatory approval, or that any approved product will be commercially viable. In addition, VGX operates in an environment of rapid technological change and is largely dependent on the services of its employees and consultants.

        VGX incurred a loss from continuing operations of $14.8 million for the nine months ended September 30, 2008. VGX had working capital of $2.7 million, and an accumulated deficit of $63.0 million as of September 30, 2008. VGX's ability to continue as a going concern is dependent upon its ability to achieve profitable operations and to obtain additional capital. VGX will continue to rely on outside sources of financing to meet its capital needs. The outcome of these matters cannot be predicted at this time. Further, there can be no assurance, assuming VGX successfully raises additional funds, that VGX will achieve positive cash flow. If VGX is not able to secure additional funding, VGX will be required to scale back its research and development programs, preclinical studies and clinical trials, and general and administrative activities and may not be able to continue in business. These unaudited consolidated financial statements do not include any adjustments to the specific amounts and classifications of assets and liabilities, which might be necessary should VGX be unable to continue in business. VGX's unaudited consolidated financial statements as of and for the period ended September 30, 2008 have been prepared on a going concern basis, which contemplates the realization of assets and the settlement of liabilities and commitments in the normal course of business for the foreseeable future.

2. Summary of Significant Accounting Policies

Principles of Consolidation

        These unaudited consolidated financial statements include the accounts of VGX's majority-owned subsidiary, Animal Health. All intercompany accounts and transactions have been eliminated upon consolidation.

Use of Estimates

        The preparation of financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of expenses during the reporting period. Actual results could differ from such estimates.

F-110



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

Fair Value of Financial Instruments

        Management believes that the carrying amounts of VGX's financial instruments, including cash and cash equivalents, restricted cash, accounts payable, accrued expenses, and current portion of long-term debt approximate fair value due to the short-term nature of those instruments.

Cash and Cash Equivalents

        Cash and cash equivalents are stated at market value. Cash equivalents include only securities having a maturity of three months or less at the time of purchase. VGX limits its credit risk associated with cash and cash equivalents by placing them with banks it believes are highly creditworthy. As of September 30, 2008 and December 31, 2007, cash and cash equivalents consisted of bank deposits only. VGX had restricted cash of $1,000,000 as of December 31, 2007 and 2006, which was restricted as collateral for one of VGX's creditors. The restriction was removed in June 2008 when the debt to this creditor was repaid in full.

Inventories

        Inventories are stated at the lower of cost or market. Cost is determined by the first-in, first-out method. Inventory includes the cost of raw materials used in production, direct labor costs, and an allocated portion of manufacturing overhead. Overhead costs include electricity, depreciation, and other manufacturing costs that cannot be linked to the production of goods. At September 30, 2008, all manufacturing inventory had been sold to a related party in conjunction with an asset purchase agreement, and the balance of EP array inventory at September 30, 2008 was $37,475.

Property and Equipment

        Property and equipment consists of research lab equipment, office furniture, and computers and is recorded at cost. Maintenance and repairs are charged to expense as incurred, and costs of improvements are capitalized. Depreciation is recognized using the straight-line method based on an estimated useful life of 3-7 years for the related assets. Total depreciation expense for the nine months ended September 30, 2008 was $212,086, of which $98,715 is included in continuing operations. Total depreciation expense for the nine months ended September 30, 2007 was $753,885, of which $89,368 is included in continuing operations. Total depreciation expense for the period from December 12, 2000 (inception) through September 30, 2008 was $1,157,827, of which $247,849 is included in continuing operations.

Long-Lived Assets

        In accordance with Statement of Financial Accounting Standards (SFAS) No. 144, Accounting for the Impairment of Long-Lived Assets , long-lived assets, such as property and equipment, are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may not be recoverable. Recoverability of assets to be held and used is measured by a comparison of the carrying amount of an asset to estimated undiscounted future cash flows expected to be generated by the asset. If the carrying amount of an asset exceeds its estimated future cash flows, an

F-111



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)


impairment charge is recognized by the amount by which the carrying amount of the asset exceeds the fair value of the asset. As of September 30, 2008, VGX management believes that no revision to the remaining useful lives or write-down of long-lived assets is required.

Goodwill and Intangible Assets

        VGX accounts for goodwill and intangible assets in accordance with Statement of Financial Accounting Standards (SFAS) No. 142, Goodwill and Other Intangible Assets . Goodwill represents the excess of the purchase price over fair value of net assets acquired and totaled $907,076 at September 30, 2008. In accordance with SFAS No. 142, goodwill is not amortized; rather it is tested for impairment at least annually.

        When VGX acquired the assets of ADViSYS, Inc. in February 2007, a portion of the goodwill associated with the transaction was attributable to the purchase of the assembled workforce, both in the manufacturing and research areas of the operation. In June 2008, VGX sold its manufacturing assets that were previously acquired from ADViSYS to a related party, along with the assembled workforce supporting those operations. The indicated value of the assembled workforce was allocated proportionately between manufacturing and research personnel, based on the number of employees in each functional area at the time of the acquisition. As a result of the subsequent divestiture in June 2008, VGX recognized an impairment charge of $177,768 (the portion of the original value of assembled workforce allocated to manufacturing operations) in the consolidated statement of operations for the nine months ended September 30, 2008 as an offset to the gain on the sale of manufacturing assets, net of tax, in discontinued operations.

        Intangible assets with finite lives, primarily customer contracts and proprietary technology, are amortized over their estimated useful lives from 3 to 9 years. Total amortization expense of intangible assets for the nine months ended September 30, 2008 was $640,016, of which $357,844 was included in continuing operations. Total amortization expense of intangible assets for the nine months ended September 30, 2007 was $336,241, of which $278,323 is included in continuing operations. Total amortization expense of intangible assets for the period from December 12, 2000 (inception) through September 30, 2008 was $1,120,348, of which $755,448 is included in continuing operations. Included in intangible asset amortization expense for discontinued operations for the nine months ended September 30, 2008 is an impairment charge of $240,808 related to the manufacturing contracts that were sold to a related party as part of the asset purchase agreement.

        When VGX acquired the assets of ADViSYS, Inc. in February 2007, a portion of the purchase price was allocated to intangible assets related to two DNA plasmid manufacturing customer contracts that were assigned to VGX in conjunction with the asset purchase agreement. In June 2008, VGX sold its manufacturing assets to a related party and, as part of that transaction, recognized the remaining unamortized intangible asset values for the two customer contracts of $240,808 as an impairment charge, since VGX no longer had any involvement with those customers from a manufacturing perspective. This impairment expense is included in the loss from discontinued operations in the consolidated statement of operations for the nine months ended September 30, 2008.

F-112



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

Deferred Issuance Costs

        VGX capitalizes costs associated with obtaining financing and amortizes them on a straight-line basis over the term of the underlying debt. Amortized deferred issuance costs are classified as interest expense in the consolidated statements of operations and totaled $0, $104,577 and $257,463, for the nine months ended September 30, 2008 and 2007, and for the period from December 12, 2000 (inception) to September 30, 2008, respectively. In September 2008, stock options for 71,000 shares of common stock were issued to settle the outstanding liability related to these deferred issuance costs. As the equity value of VGX's stock had declined since the incurrence of the liability, fair market value of the stock options for 71,000 shares also decreased. The value of the liability carried on the books of VGX reflected the fair market value of the stock options at the time of the incurrence of the liability; when the options were finally issued, and the associated deferred asset and liability were removed from the books of VGX, the result was a gain of $97,497, which is reflected in other income for the nine months ended September 30, 2008 and the period from December 12, 2000 (inception) to September 30, 2008.

Equity Investment

        VGX accounts for its investment in VGX International, Inc. using the equity method of accounting. Should circumstances change, such as a change in the percentage of ownership, VGX will review its accounting treatment for its investment. The equity investment is presented on the consolidated balance sheets, net of unamortized acquisition costs. Acquisition costs are being amortized using the straight-line method over five years.

Revenue Recognition

        VGX has been awarded grants from certain third-party organizations to help fund research for the drugs that it is attempting to bring to full commercial use. Once research and development expenditures qualifying under the grant are incurred, grant reports are periodically completed and submitted to the granting agency for review. If approved, the granting agency will then remit payment to VGX. Such amounts are recorded as revenue upon receipt. With regard to revenue recognition related to product sales, VGX recognizes revenue in accordance with SEC Staff Accounting Bulletin (SAB) No. 104 and records revenue when it has satisfied all the requirements under SAB No. 104.

Foreign Currency Translation

        VGX complies with SFAS No. 52, Foreign Currency Translation , which established standards for reporting on investments in foreign companies. The foreign currency translation adjustment represents the foreign currency translation related to VGX's equity investment, and to loans received from investors in foreign currency, and is included in accumulated other comprehensive income on the consolidated balance sheets.

F-113



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

Research and Development Expenses

        Research and development costs are charged to expense as incurred. Research and development expenses include, among other costs, salaries and other personnel-related costs, consultant fees, preclinical costs, costs to conduct clinical trials, costs to manufacture drug candidates and clinical supplies, laboratory supplies costs, patent application costs, and facility-related costs. Costs incurred under agreements with third parties are charged to expense as incurred in accordance with the specific contractual performance terms of such agreements. Costs of third parties include costs associated with preclinical and clinical support activities.

Income Taxes

        Income taxes are accounted for under the liability method. Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases and operating loss and tax credit carryforwards. Valuation allowances are established when necessary to reduce deferred tax assets to the amount expected to be realized. Deferred tax assets and liabilities are measured at the balance sheet date using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The effect on deferred tax assets and liabilities of a change in tax rates is recognized in the period such tax rate changes are enacted.

Acquisitions

        Acquisitions are accounted for under the purchase method of accounting in accordance with SFAS No. 141, Business Combinations , whereby the purchase price is allocated to the underlying net assets based on management's estimates of the fair value of intangible and tangible assets acquired and liabilities assumed. The excess of purchase price over estimated fair value is recorded as goodwill.

Warrants to Acquire Common Stock

        As of September 30, 2008, in connection with prior-year debt issuances, VGX had outstanding 10-year warrants to purchase 208,933 shares of common stock at a weighted-average exercise price of $0.28 per share, exercisable through various dates through December 2013. The total expense recognized under the Black-Scholes option pricing model for these warrants was $46,108. As of September 30, 2008 VGX had outstanding 10-year warrant to purchase 4,808,800 shares of common stock at an average exercise price of $1.11 per share, exercisable through April 2016; these were issued to current and former employees of VGX. The total expense recognized under the Black-Scholes option pricing model for these warrants was $13,278,687.

Stock-Based Compensation—VGX Pharmaceuticals

        In December 2004, the Financial Accounting Standards Board (FASB) issued SFAS No. 123(R), Share-Based Payment , a revision of SFAS No. 123, Accounting for Stock-Based Compensation , that addresses the accounting for share-based payment transactions in which an enterprise receives employee services in exchange for (a) equity instruments of the enterprise or (b) liabilities that are

F-114



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)


based on the fair value of the enterprise's equity instruments or that may be settled by the issuance of such equity investments. SFAS No. 123(R) requires that an entity measure the cost of equity-based service awards based on the grant-date fair value of the award and recognize the cost of such awards over the period during which the employee is required to provide service in exchange for the award (the vesting period). SFAS No. 123(R) requires that an entity measure the cost of liability-based service awards based on current fair value that is remeasured subsequently at each reporting date through the settlement date. VGX had previously adopted the fair-value method of SFAS No. 123, using the Black-Scholes Model to account for equity-based awards issued to employees and directors and has adopted this new standard effective January 1, 2006 under the modified prospective transition method. The modified prospective transition method requires VGX to recognize share-based compensation expense in the consolidated statements of operations for all share-based payments granted, modified, or settled after the date of adoption as well as for any awards that were granted prior to the adoption date for which the requested service has not been provided as of the adoption date.

        The assumptions used to estimate the fair value of stock options granted in the nine month periods ended September 30, 2008 and 2007 are presented below:

 
  Nine Months Ended September 30  
 
  2008   2007  

Expected dividend yield

    0 %   0 %

Expected volatility

    51 %   50 %

Risk-free interest rate

    3.0 %   4.6 %

Expected life

    6 years     6 years  

        The weighted-average valuation assumptions were determined as follows:

    Expected stock price volatility: The expected volatility used is based on historical volatilities of similar entities within VGX's industry which were commensurate with VGX's expected term assumption as described in Securities and Exchange Commission staff accounting bulletin (SAB) No. 107 relating to SFAS No. 123(R).

    Expected term of options: The expected term of options represents the period of time options are expected to be outstanding. The expected term of the options granted is derived from the "simplified" method as described in SAB No. 107 relating to SFAS No. 123(R).

    Risk-free interest rate: VGX bases the risk-free interest rate on the interest rate payable on U.S. Treasury securities in effect at the time of grant for a period that is commensurate with the assumed expected option term.

    Expected annual dividends: The estimate for annual dividends is $0.00, because VGX has not historically paid, and does not expect for the foreseeable future to pay, a dividend.

    Estimated forfeiture rate: VGX's estimated annual forfeiture rate on 2007 stock option grants ranges between 0.00% and 4.14%, based on the historical forfeiture experience of various employee groups.

F-115



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

        Total compensation expense under SFAS No. 123(R) for the nine months ended September 30, 2008 was $8,092,559. The compensation expense under SFAS No. 123 for the nine months ended September 30, 2007 was $4,810,343. The increase in compensation expense for the nine months ended September 30, 2008 was due to the charge related to option re-pricing and acceleration that took place in September of 2008. The total estimated increase in compensation expenses due to the re-pricing and acceleration is $2,968,747, $324,123, and $52,734 in 2008, 2009, and 2010, respectively.

        VGX accounts for options granted to non-employees in accordance with EITF No. 96-18, Accounting for Equity Instruments That Are Issued to Other Than Employees for Acquiring, or in Conjunction with Selling, Goods or Services , and SFAS No. 123(R). The fair value of these options at the measurement dates was estimated using the Black-Scholes pricing model. Total stock-based compensation for options granted to non-employees for the nine months ended September 30, 2008 and 2007 were $49,193 and $187,639, respectively. These options generally vest over a period of three years, though some vest over a period less than three years or immediately upon grant. VGX valued the stock option grants to non-employees using the same method and assumptions as stock option grants to employees.

        In addition to the awards of stock options, VGX awarded 200,000 shares of stock to a non-employee related to a milestone payment identified in the Assets Purchase Agreement executed with ADViSYS, Inc. in February 2007, due upon the approval of Animal Health's LifeTide™ SW 5 product for sale in Australia, 70,000 shares of stock to non-employees for assistance with fund raising activities, and 10,000 shares of stock to an employee for the nine months ended September 30, 2008. For the nine months ended September 30, 2007, 60,000 shares of stock were awarded to non-employees for assistance with fund raising activities and Korean business consultations. During the same period 10,000 shares of stock were awarded to an employee as part of his employment agreement. In connection with awards of stock, VGX recorded compensation expense of $1,056,800 for the nine months ended September 30, 2008 and $350,000 for the nine months ended September 30, 2007.

        As of September 30, 2008, there was $3,739,453 of total unrecognized compensation cost related to non-vested stock-based compensation arrangements.

        The weighted average grant date fair value per share was $1.49 for employee stock options granted during the nine months ended September 30, 2008, and $2.66 for employee stock options granted during the nine months ended September 30, 2007.

Stock-Based Compensation for Subsidiary—Animal Health

        Animal Health, a subsidiary of VGX, has adopted a 2007 equity incentive plan for the issuance of options to employees and consultants. Animal Health uses the same accounting policies as VGX regarding stock-based compensation.

F-116



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

        The assumptions used to estimate the fair value of stock options granted in the nine month periods ended September 30, 2008 and 2007 are presented below:

 
  Nine Months Ended September 30  
 
  2008   2007  

Expected dividend yield

    0 %   0 %

Expected volatility

    51 %   50 %

Risk-free interest rate

    3.0 %   4.9 %

Expected life

    6 years     6 years  

        The weighted-average valuation assumptions were determined as follows:

    Expected stock price volatility: The expected volatility used is based on historical volatilities of similar entities within Animal Health's industry which were commensurate with Animal Health's expected term assumption as described in Securities and Exchange Commission staff accounting bulletin (SAB) No. 107 relating to SFAS No. 123(R).

    Expected term of options: The expected term of options represents the period of time options are expected to be outstanding. The expected term of the options granted is derived from the "simplified" method as described in SAB No. 107 relating to SFAS No. 123(R).

    Risk-free interest rate: Animal Health bases the risk-free interest rate on the interest rate payable on U.S. Treasury securities in effect at the time of grant for a period that is commensurate with the assumed expected option term.

    Expected annual dividends: The estimate for annual dividends is $0.00, because Animal Health has not historically paid, and does not expect for the foreseeable future to pay, a dividend.

    Estimated forfeiture rate: Animal Health did not estimate the forfeiture rate for 2007 because it had no historical data in which to make an assumption. The total size of the expense was also deemed to be immaterial; therefore, making forfeiture assumption less significant.

        The compensation expense under SFAS No. 123(R) for the Animal Health 2007 equity incentive plan for the nine months ended September 30, 2008 and 2007 were insignificant.

Reclassifications

        Certain prior period balances have been reclassified to conform with the current presentation.

Recent Accounting Pronouncements

        In May 2008, the Financial Accounting Standards Board ("FASB") issued SFAS No. 162, The Hierarchy of Generally Accepted Accounting Principles ("SFAS No. 162"). SFAS No. 162 identifies the sources of accounting principles and the framework for selecting the principles to be used in the preparation of financial statements that are presented in conformity with U.S. GAAP. VGX is currently evaluating the impact that SFAS No. 162 will have on its consolidated financial statements.

F-117



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)

        Effective January 1, 2008, VGX has adopted the provisions of Financial Accounting Standards Board Statement No. 157, Fair Value Measurements ("SFAS No. 157") to measure assets and liabilities. SFAS No. 157 establishes a common definition for fair value to be applied to U.S. GAAP requiring use of fair value, establishes a framework for measuring fair value, and expands disclosure about such fair value measurements. SFAS No. 157 is effective for financial assets and financial liabilities for fiscal years beginning after November 15, 2007. Issued in February 2008, FSP 157-1, Application of FASB Statement No. 157 to FASB Statement No. 13 and Other Accounting Pronouncements That Address Fair Value Measurements for Purposes of Lease Classification or Measurement under Statement 13 , removed leasing transactions accounted for under Statement 13 and related guidance from the scope of SFAS No. 157. FSP 157-2 Partial Deferral of the Effective Date of Statement 157 (FSP 157-2), deferred the effective date of SFAS No. 157 for all nonfinancial assets and nonfinancial liabilities to fiscal years beginning after November 15, 2008. The partial implementation of SFAS No. 157 for financial assets and financial liabilities, effective January 1, 2008, did not have a material impact on VGX's consolidated financial statements. VGX is currently assessing the impact of SFAS No. 157 for non-financial assets and non-financial liabilities on its consolidated financial statements. See Note 4, Fair Value Measurements.

        VGX management anticipates, based on the composition of its existing assets and liabilities, that the valuations used to estimate the fair value will rely on observable and unobservable inputs. Observable inputs are those that reflect a public market, whereas unobservable inputs are those that reflect management's assumptions about the assumptions market participants would use in pricing the underlying asset or liability. VGX management does not believe that SFAS No. 157 will have a material impact on the amounts reported in the financial statements; however, additional disclosures about the inputs used to develop the measurements of fair value and the effects of certain measurements reported in the consolidated statements of operations for a fiscal period will be required.

        Effective January 1, 2008, VGX adopted Financial Accounting Standards Board Statement No. 159, The Fair Value Option for Financial Assets and Financial Liabilities ("SFAS No. 159"). SFAS No. 159 provides companies with an option to report selected financial assets and liabilities at fair value. The Statement also establishes presentation and disclosure requirements designed to facilitate comparisons between companies that choose different measurement attributes for similar types of assets and liabilities. SFAS No. 159 requires companies to provide additional information that will help investors and other users of financial statements to more easily understand the effect of a company's choice to use fair value on its earnings. Adoption of SFAS No. 159 did not have an impact on VGX's consolidated results of operations and financial position.

        In December 2007, the Financial Accounting Standards Board issued Statement No. 141 (revised 2007), Business Combinations ("SFAS No. 141(R)"), which is effective for financial statements issued for fiscal years beginning on or after December 15, 2008. SFAS No. 141(R) establishes principles and requirements for how an acquirer recognizes and measures in its financial statements the identifiable assets acquired, the liabilities assumed, any non-controlling interest in the acquiree, and the goodwill acquired in the business combination. SFAS No. 141(R) also establishes disclosure requirements to enable the evaluation of the nature and financial effects of the business combination. FAS 141(R) will

F-118



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

2. Summary of Significant Accounting Policies (Continued)


be applied prospectively. VGX expects the adoption of SFAS 141(R) to not have a material impact on the consolidated financial statements.

        In December 2007, the FASB issued SFAS No. 160, Non-controlling Interests in Consolidated Financial Statements (an amendment of Accounting Research Bulletin No. 51) ("SFAS No. 160"). SFAS No. 160 requires that non-controlling (minority) interests be reported as a component of equity, that net income attributable to the parent and to the non-controlling interest be separately identified in the income statement, that changes in a parent's ownership interest while the parent retains its controlling interest be accounted for as equity transactions, and that any retained non-controlling equity investment upon the deconsolidation of a subsidiary be initially measured at fair value. This statement is effective for fiscal years beginning after December 31, 2008, and shall be applied prospectively. However, the presentation and disclosure requirements of SFAS No. 160 are required to be applied retrospectively for all periods presented. The retrospective presentation and disclosure requirements of this statement will be applied to any prior periods presented in financial statements for the fiscal year ending December 31, 2009, and later periods during which VGX had a consolidated subsidiary with a non-controlling interest. As of September 30, 2008, VGX does not have any consolidated subsidiaries in which there is a non-controlling interest.

        In November 2007, the FASB ratified EITF Issue No. 07-1, Accounting for Collaborative Agreements Related to the Development and Commercialization of Intellectual Property . EITF Issue No. 07-1 defines collaborative agreements as a contractual arrangement in which the parties are active participants to the arrangement and are exposed to the significant risks and rewards that are dependent on the ultimate commercial success of the endeavor. Additionally, it requires that revenue generated and costs incurred on sales to third parties as it relates to a collaborative agreement be recognized as gross or net based on EITF Issue No. 99-19, Reporting Revenue Gross as a Principal versus Net as an Agent . It also requires payments between participants to be accounted for in accordance with already existing generally accepted accounting principles, unless none exist, in which case a reasonable, rational, consistent method should be used. EITF Issue No. 07-1 is effective for fiscal years beginning after December 15, 2008 for all collaborative arrangements existing as of that date, with retrospective application to all periods. VGX management is currently evaluating the impact of this standard and does not anticipate the adoption of EITF Issue No. 07-1 to have a material impact on our consolidated financial statements.

        In July 2006, the FASB issued Interpretation No. 48, "Accounting for Uncertainty in Income Taxes" ("FIN 48"). FIN 48 prescribes detailed guidance for the financial statement recognition, measurement and disclosure of uncertain tax positions recognized in an enterprise's financial statements in accordance with FASB Statement No. 109, "Accounting for Income Taxes" ("SFAS No. 109"). Tax positions must meet a more-likely-than-not recognition threshold at the effective date to be recognized upon the adoption of FIN 48 and in subsequent periods. FIN 48 will be applied to all tax positions accounted for under SFAS No. 109 upon initial adoption.

        VGX adopted FIN 48 effective January 1, 2008 with no impact on its consolidated financial statements. VGX recognizes interest and penalties, if any, related to uncertain tax positions in income tax expense. Upon adoption of FIN 48, VGX had no interest or penalties accrued related to uncertain tax positions, due to the net operating loss carryforwards that VGX has available.

F-119



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

3. Discontinued Operations

        On June 10, 2008, VGX entered into an asset purchase agreement with VGXI, Inc, a Delaware incorporated wholly-owned subsidiary of VGX International, a publicly traded company in Korea of which VGX owns 30.37% of outstanding shares. Under the agreement, VGX divested its assets related to the DNA plasmid manufacturing business; a business which it had acquired in February of 2007 under an asset purchase agreement with ADViSYS. The aggregate sale price was for $9,110,000 in cash which is to be paid in installments, the first of which, amounting to $1,750,000, was received in June 2008. The second installment of $1,360,000 was received in July 2008 by VGX; the remaining $6,000,000 is to be received in tranches of $4,000,000 and $2,000,000 in December 2008 and March 2009, respectively. There are no milestone or contingent payments as part of this agreement.

        VGX recorded a one-time gain on the sale of manufacturing assets, net of tax of $69,500, of $6,653,153, net of $2,901,856 adjustment for VGX's 30.37% stake in VGX International. Operating results of VGX's discontinued operations are shown separately as a single line item in the accompanying consolidated statements of operations. Operating losses from discontinued operations for the nine months ended September 30, 2008 and 2007 were $1,586,636 and $1,044,779, respectively, and $2,996,267 from December 12, 2000 (inception) through September 30, 2008. In conjunction with the sale of the manufacturing assets, VGX wrote off the value of intangible assets associated with the plasmid manufacturing business—namely the value of customer contracts acquired through the asset purchase agreement with ADViSYS. The unamortized amount of these contracts was $240,808 just prior to the sale of the business and is reflected in the loss from discontinued operations for the nine months ended September 30, 2008. VGX also adjusted its goodwill attributable to the assembled workforce acquired from ADViSYS in February 2007 for the manufacturing operations, determined to be $177,768, and offset this charge against the gain on the sale of these assets.

4. Fair Value Measurements

        On January 1, 2008, VGX adopted SFAS No. 157, Fair Value Measurements. SFAS No. 157 defines fair value and establishes a framework for measuring fair value in accordance with generally accepted accounting principles. In February 2008, the FASB issued Staff Position No. 157-2, Effective Date of FASB Statement No. 157 , which deferred the effective date of SFAS No. 157 for one year for nonfinancial assets and liabilities recorded at fair value on a non-recurring basis. As defined by SFAS No. 157, the fair value of an asset or liability would be based on an "exit price" basis rather than an "entry price" basis. Additionally, the fair value should be market-based and not an entity-based measurement. SFAS No. 157 also establishes a fair value hierarchy which requires an entity to maximize the use of observable inputs and minimize the use of unobservable inputs when measuring fair value. SFAS No. 157 describes three levels of input that may be used to measure fair value.

         Level 1 —Financial assets and liabilities whose values are based on unadjusted quoted prices for identical assets or liabilities in an active market that the company has the ability to access at the measurement date.

F-120



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

4. Fair Value Measurements (Continued)

         Level 2 —Financial assets and liabilities whose values are based on quoted prices in markets where trading occurs infrequently or whose values are based on quoted prices of instruments with similar attributes in active markets. Level 2 inputs include the following:

    Quoted prices for similar assets or liabilities, in active markets;

    Quoted prices for identical or similar assets or liabilities in non-active markets;

    Inputs other than quoted prices that are observable for substantially the full term of the asset or liability; and

    Inputs that are derived principally from or corroborated by observable market data for substantially the full term of the asset or liability.

         Level 3 —Financial assets and liabilities whose values are based on prices or valuation techniques that require inputs that are both unobservable and significant to the overall fair value measurement. These inputs reflect management's own assumptions about the assumptions a market participant would use in pricing the asset or liability.

 
  Fair Value Measurements at September 30, 2008  
 
  Fair Value at
September 30,
2008
  Quoted Prices
in Active Markets
(Level 1)
  Significant Other
Observable Inputs
(Level 2)
  Significant
Unobservable Inputs
(Level 3)
 

Assets measured at fair value on a recurring basis

                         

Cash and cash equivalents(1)

  $ 6,670,127   $ 6,670,127   $   $  
                   

Total

  $ 6,670,127   $ 6,670,127   $   $  
                   

(1)
Cash and cash equivalents consist primarily of money market funds with original maturity dates of three months or less.

        VGX has no liabilities that are financial instruments which would be required to be disclosed as of September 30, 2008 under FAS 157.

5. Inventories

        Inventories related to continuing operations consist of the following:

 
  September 30,
2008
  December 31,
2007
 

Other—EP arrays

    37,475     26,925  
           

Total inventories

  $ 37,475   $ 26,925  
           

        Manufacturing inventories at December 31, 2007, totaling $2,103,005, have been reclassified to assets from discontinued operations in the current balance sheet presentation.

F-121



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

6. Accrued Expenses

        Accrued expenses related to continuing operations consist of the following:

 
  September 30,
2008
  December 31,
2007
 

Payroll and related expenses

  $ 72,521   $ 279,142  

Professional fees

    165,832     246,052  

Accrued research costs

    680,836     745,801  

Accrued interest

    945,068     1,055,084  

Accrued Texas franchise tax

    69,500      

Other

    28,139     13,512  
           

  $ 1,961,896   $ 2,339,591  
           

7. Debt

        Debt consists of the following:

 
  September 30,
2008
  December 31,
2007
 

Unsecured convertible notes payable

  $ 8,000,000   $ 12,250,000  

Secured convertible note payable

        1,000,000  
           

Total debt

    8,000,000     13,250,000  

Current portion of long-term debt

    7,900,000     10,310,000  
           

Long-term debt

  $ 100,000   $ 2,940,000  
           

        In June 2005, VGX issued a $1,000,000 two-year maturity convertible note with an annual interest rate of 5%. The note was convertible into common shares and was collateralized by a check for the same amount, which was recognized as restricted cash on VGX's consolidated balance sheets. In June 2008 this debt was repaid and the related restriction on cash was eliminated.

        From August 2005 to December 2005, VGX reached an agreement with various investors to issue $4,000,000 in convertible notes ranging in maturity from 18 months to 24 months with annual interest rates ranging from 5% to 40%. Additionally, $6,650,000 in convertible notes were issued during the first half of 2006 with an annual interest rate of 5%. Of the total debt, $3,350,000 was secured by equity securities of a related party. In November of 2006, VGX entered into an agreement with an investor to issue a short-term note in the amount of 2,010,000,000 Korean Wons or $2,116,863 secured by equity securities of a related party. The note was repaid in 2007. During 2007, VGX reached an agreement with various investors to issue $1,600,000 in convertible notes ranging in maturity from 19 to 20 months. In June 2008 VGX secured an additional $100,000 note with a maturity term of 24 months; this note is to be automatically converted to equity upon a public event for VGX. Also, of the $8,000,000 in total notes outstanding at September 30, 2008, agreements have been reached with note holders of $4,400,000 in principal in which the conversion price would be automatically set to $1.05 and converted to equity upon a public event.

F-122



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

7. Debt (Continued)

        The convertible notes are convertible into shares of common stock at a defined conversion ratio (dollar for dollar). Minimum principal repayments of debt as of September 30, 2008 are as follows:

October 1, 2008 to September 30, 2009

  $ 7,900,000  

October 1, 2009 to September 30, 2010

    100,000  
       

  $ 8,000,000  
       

8. Minority Interest

        VGX owns 88% of the outstanding stock of Animal Health, a biotechnology company engaged in the development and commercialization of products designed to add to the economic value of livestock and improve the health of companion animals. Animal Health is consolidated in the results of VGX's consolidated financial statements. The minority interest liability represents, in aggregate, that portion of the combined total equity that is owned by the minority investor. The minority investor's share of the combined net loss is separately disclosed in the consolidated statements of operations.

9. Commitments

Government Contract Awards

        In August 2007, VGX was awarded a contract from the Defense Threat Reduction Agency (DTRA) to develop its constant current electroporation technology for intradermal (ID) delivery of DNA vaccines and therapeutics. The contract is for $1,990,411 over 12 months. Under the contract, VGX will demonstrate in vivo efficacy of novel vaccines derived from DNA plasmid-based pox virus antigens delivered using a skin micro-electroporation system. Revenue is being recognized when reimbursement for incurred expenses is received, which began in February 2008. For the nine months ended September 30, 2008, revenue from government contracts was $1,962,305.

        In September 2008, VGX was awarded a contract with the National Institute of Allergy and Infectious Diseases ("NIAID") to study novel micro-electrodes for delivery of optimized DNA vaccines for human immunodeficiency virus (HIV). The contract is effective September 30, 2008 and is for five years with two one year options (period of performance September 30, 2008—September 29, 2015 including the two options). The value for the five years is $21,269,154 with two option years six and seven valued at $1,193,230 and $1,132,465 respectively for a total value of $23,594,849. No revenue or expenses have been reflected in the financial statements as of September 30, 2008.

Leases

        In May 2005, VGX signed a facility lease with a lessor for a lease through May 2010. The lease provides for one additional five-year renewal option. In addition, VGX has entered into equipment leases consisting of a three-year operating lease for a copier expiring in June 2009, and a five-year telecommunications lease expiring in February 2010. The five-year telecommunications lease automatically renews for another five years under the same terms unless notified within 30 days of expiration. In 2006, VGX entered into a three-year lease with a broadband network provider to

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(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


enhance connectivity. All leases contain renewal options. In 2007, VGX signed a capital equipment lease for a copy machine for a three-year term expiring August 2010. There was a bargain purchase option which made the copier a capital lease. The value of the copier is properly booked as a fixed asset, and was subsequently transferred to a related party as part of the asset purchase agreement executed in June 2008. In November 2007, VGX signed a facility lease in Houston through October 2017. The agreement is a renewal of a lease that was assigned to VGX when it acquired the assets of ADViSYS in February 2007. In June 2008 a sublease agreement was executed between VGX and the related party that purchased the manufacturing assets at the Houston facility, whereby 87.5% of the lease expenses are reimbursed to VGX monthly.

License Agreements

        In November 2001, VGX entered into a license agreement with a university to license certain patent rights. The license agreement required issuance of VGX stock in lieu of an up-front cash payment, which was recorded as research and development expense in 2001. The license agreement requires various milestone payments. They include a $500,000 payment for the enrollment of the first patient in Phase III trials, a $500,000 payment for the filing of the NDA for the first licensed product, a $500,000 payment on the anniversary of the filing, a $1,500,000 payment upon the receipt of an NDA approval letter for the first licensed product, and a $1,500,000 payment on the first anniversary of the receipt of an approval for the first licensed product. These payments are in effect through the later of the expiration of the licensed patents or ten years after the first commercial sale of covered product. The agreement is valid through the later of 25 years from the effective date or the expiration of the last to expire or abandonment of the patent rights.

        In December 2005, VGX entered into an alliance agreement with a European pharmaceutical company for the worldwide rights to conduct research and development and market a drug with indications in rheumatoid arthritis and psoriasis. The license agreement required issuance of VGX stock as well as an up-front cash payment, which was recorded as research and development expense in the accompanying consolidated statement of operations for the year ended December 31, 2005. The license agreement requires various milestone payments upon the completion of patient enrollment for a Phase II trial product for $50,000, a $250,000 payment upon completion of the first Phase III trial product, and a $2,000,000 payment upon NDA approval of a trial product. These payments are in effect through the later of the expiration of the licensed patents or ten years after the first commercial sale of covered product. The agreement is valid through the later of 20 years from the effective date or the expiration of the last to expire or abandonment of the patent rights.

        In November 2006, VGX entered into a license agreement with a U.S.-based company for its patented DNA-delivery technology to use in the intratumoral delivery of a proprietary gene to control the growth of melanoma and other cancers. Under the terms of the agreement, VGX paid the licensor an up-front license fee in cash and equity. There will also be payments based on successful completion of clinical and regulatory milestones. They include a payment upon beginning of a Phase II trial, a payment upon completion of the Phase II trial, payment upon the completion of Phase III trial, a payment upon the NDA approval, and a payment upon sale of licensed product in any of France, Germany, Italy, the U.S., or the United Kingdom. VGX will in return be exclusively supplied with the

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(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


licensor's electroporation devices for the therapy included in the license agreement and will also pay the licensor royalties on the sale of products covered by the license. The term of the agreement will extend until the last to expire of any royalty period for any licensed product. Royalty period will be, with respect to any particular licensed product in any country, the period of time beginning on the first commercial sale of such licensed product in such a country and extending until the earlier of (1) the date when there is not any valid claim included in any licensor patent right in any country which would be infringed by the sale of the licensed product in any country for a license granted by licensor to VGX or (2) 10 years from the date of the first commercial sale of such licensed product in such country.

        In December 2006, VGX entered into an R&D collaboration and license agreement with a related party in which VGX granted the licensee exclusive worldwide rights to conduct research, development activities, sales, licensing, and marketing of VGX-1027 for Type I Diabetes. There are milestone and royalty payments due to VGX from the licensee. The milestone payments are due upon 1) The completion of a Phase I study, 2) Upon completion of patient accrual for T1D Phase II trial, 3) Upon completion of patient accrual for Phase III clinical trial, 4) Upon NDA submission, and 5) Upon NDA approval. However, the actual amount of the milestone payments had been contractually agreed to be negotiated at a later time. The two parties have agreed to also share R&D costs on a mutually agreeable basis. The terms of the agreement shall terminate the earlier of (1) expiration of the last-to-expire patent or (2) 20 years from the effective date. In October 2007 an amendment was made to the agreement in which the sharing of the R&D costs between VGX and the related-party was clarified. The related-party agreed to be responsible for all third-party costs related to the completion of Phase I clinical trials. In August 2008, an amendment between VGX and the related party was reached in which VGX agreed to pay for the cost of the Multiple Ascending Dose ("MAD") Study which is expected to cost approximately USD 1.2 Million. The related-party will in turn reimburse VGX for the cost of the study within 60 days of the study closure. Costs incurred for the MAD study as of September 30, 2008 were $251,739.

        In April 2007, VGX entered into a commercial license agreement with a U.S.-based company to license its proprietary technology for the clinical and commercial production of Vpr protein. The license agreement requires various milestone and royalty payments. This includes payments to be made annually on each anniversary of the acceptance of an IND until an NDA is filed, a payment upon submission of NDA or BLA, and a payment upon receipt of marketing approval for the product.

        In April 2007, VGX entered into a license agreement with a university to license certain patent rights. Upon the execution of this agreement, VGX made an initial payment of $100,000 to the University. The license agreement requires various milestone payments. They include a $125,000 payment upon filing of an IND application, a $250,000 payment upon enrollment of first subject in Phase II clinical trial, a payment of $375,000 upon enrollment of first subject in Phase III clinical trial, a payment of $250,000 upon filing of NDA and a payment of $1,500,000 upon receipt of approval in the U.S., the EU, or Japan (whichever is first to occur). In addition, VGX is required to make minimum payments related to research and development activities of $200,000 in the first 12-month period, $250,000 in the second 12-month period, $300,000 in the third 12-month period, and a total of $400,000 for all years subsequent to the third 12-month period until the termination of the agreement.

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(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


The agreement is valid through the later of 10 years after the first sale of the first licensed product, or the expiration or abandonment of the last patent to expire or become abandoned.

        In May 2007, VGX entered into a license agreement with a university to license certain patent rights. The license agreement requires various milestone payments. They include an annual maintenance fee of $25,000, a $75,000 payment upon beginning of Phase I trial, a $100,000 payment upon beginning of Phase II trial, a $250,000 payment upon the initiation of Phase III trial, and a $500,000 payment upon the first commercial sale of the licensed product. The agreement also calls for a royalty payment on net sales. There is a sliding scale of milestone payments for achievement of clinical milestones for second and third clinical indications. The agreement is valid through 10 years after the first sale of the first licensed product.

        In June 2007, VGX entered into a license agreement with a related party in which it grants to the licensee exclusive world-wide rights to conduct research, development activities, sale, licensing, and marketing of VGX-100 for gastric cancer in humans. There are milestone and royalty payments due to VGX from the licensee. The milestone payments are due upon 1) The completion of a Phase I study, 2) Upon completion of patient accrual for Gastric Cancer Phase II trial, 3) Upon completion of patient accrual for Phase III clinical trial, 4) Upon NDA submission, and 5) Upon NDA approval. . However, the actual amount of the milestone payments had been contractually agreed to be negotiated at a later time. The two parties have agreed to also share R&D costs on a mutually agreeable basis. The terms of the agreement shall terminate the earlier of (1) expiration of the last-to-expire patent or (2) 20 years from the effective date.

        In September 2007, VGX entered into a license agreement with a related party to license out certain patent rights related to its Animal Health Franchise. The license agreement requires various milestone and royalty payments from the related-party to VGX. These include a $250,000 payment for the filing of an INAD, $500,000 payment upon initiation of Phase III or pivotal trial, $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the U.S., $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the EU, and $1,000,000 payment upon receipt of NADA approval letter for the first licensed product in the territories outside the EU and the U.S. Notwithstanding the above payment schedule, the related party does not have to make any milestone payments to VGX unless it has raised at least $5,000,000 in capital. In connection with this agreement VGX and the related party also reached a nonexclusive agreement in which VGX grants device and manufacturing patent rights to the aforementioned related party. Also as part of the agreement, the related party has agreed to make certain royalty payments to the seller of ADViSYS assets that VGX was obligated to make under the terms of the asset purchase agreement. The seller has recourse to VGX should the related-party fail to make proper payment to the seller.

        In October 2007, VGX entered into an agreement with a related party in which it grants to the licensee exclusive, nonsublicensable, royalty-bearing patent rights for certain manufacturing processes related to the production of plasmids. The territory covered under the agreement is Asia. The agreement requires royalty payments as a percentage of net sales.

        In April 2008, VGX entered into a license agreement with a related party in which it grants to the licensee exclusive rights in Korea to the development, sales, licensing, and marketing for the

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(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


CELLECTRA™ Device. There are milestone and royalty payments due to VGX from the licensee. These include a $100,000 payment to VGX upon filing of each IND using Cellectra, $150,000 payment upon initiation of each Phase II trial, $250,000 payment upon initiation of each Phase III trial, $500,000 payment upon each BLA approval, and a $750,000 payment upon first commercial sale of Cellectra for each BLA. The licensee also agreed to pay $100,000 cost sharing fee as well as $25,000 annually to partially cover the costs of patents, product enhancement, and other associated R&D efforts. The terms of the agreement shall terminate the earlier of (1) expiration of the last-to-expire patent or (2) 20 years from the effective date.

Research Agreements

        In December 2005, VGX entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is five years. VGX has committed a total of $1,035,000 ($207,000 per year) during the term of this agreement. The payments are to be made in increments of $207,000 during the term of the sponsored research agreement.

        In June 2006, VGX entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is two years but can be extended to five years upon review of the progress of the research. The total value of the agreement is not to exceed $1,000,000. The maximum liability of VGX during the two-year term of the agreement is $400,000. This agreement was cancelled on April 13, 2008 through mutual agreement.

        In March 2008, VGX entered into a sponsored research agreement with a university to reimburse the university for all direct and indirect costs incurred in the conduct of the sponsored research. The term of the agreement is five years and the total value of the agreement is not to exceed $1,180,000.

Supply Agreements

        In July 2005, VGX entered into a supply agreement with a manufacturer to purchase a minimum annual amount of 500 kilograms of the active pharmaceutical ingredient (API). The supply agreement is contingent upon the receipt of the regulatory approval of the VGX NDA for the product. The term of the agreement is 10 years from receipt of the approval of the NDA. There is an automatic renewal for successive terms of two years unless a written notice is provided to the other party within 180 days prior to the end of the term. In July 2008, VGX sent a written notice to the manufacturer stating VGX's intent to terminate the agreement. With the discontinuation of the Pictovir and the Hep-C small molecule drug programs, VGX no longer requires the supply of the API.

        In July 2005, VGX entered into a supply agreement with a manufacturer to purchase a minimum annual amount of 1,000 kilograms of the API. The supply agreement is contingent upon the receipt of the regulatory approval for sale of the product. The term of the agreement is five years from receipt of the approval for sale of the product. This agreement will be in force after the initial five-year term unless a written notice is provided to the other party requesting that the agreement be terminated. In July 2008, VGX sent a written notice to the manufacturer stating VGX's intent to terminate the

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(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


agreement. With the discontinuation of the Pictovir and the Hep-C small molecule drug programs, VGX no longer requires the supply of the API.

        In March 2006, VGX entered into a supply agreement with a related party to purchase a minimum annual amount of 20,000 kilograms of the API. The supply agreement is contingent upon the receipt of the regulatory approval for sale of the product in the U.S. The term of the agreement is the later of five years from receipt of the approval for sale of the product or from May 1, 2009 to April 2014. This agreement will be in force after the initial five-year term unless a written notice is provided to the other party requesting that the agreement be terminated.

        In June 2008, in conjunction with the Asset Purchase Agreement between VGX and VGXI, Inc, VGX entered into a supply agreement with a related-party in which the related-party was granted Most Favored Status as a supplier of DNA plasmids. As a part of this agreement, VGX issued a purchase order for $1,764,503 to the related-party to supply VGX with needed DNA plasmids for the upcoming Phase I and Phase II clinical trials. VGX Animal Health also issued a purchase order to the related-party for $248,518 for a supply of LifeTide™ SW 5, its Growth Hormone Releasing Hormone ("GHRH") DNA therapy approved for use in Australia. This supply agreement is in effect for ten (10) years from the effective date.

Sales and Marketing Agreements

        In February 2007, VGX entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market PICTOVIR in Asia, Africa, and the Middle East. There are milestone and royalty payments associated with the agreement. This includes a $3,000,000 payment to VGX upon completion of Phase III trials for PICTOVIR, a $3,000,000 payment to VGX upon submission of NDA for PICTOVIR, and a $5,000,000 payment to VGX upon NDA approval. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date.

        In April 2007, VGX entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market VGX-410C in Asia, Africa, and the Middle East. There are milestone and royalty payments associated with the agreement. They include a $3,000,000 payment to VGX upon completion of Phase III trials for VGX-410C, a $3,000,000 payment to VGX upon submission of NDA for VGX-410C, a $5,000,000 payment for NDA approval in Japan, and a $5,000,000 payment to VGX upon NDA approval in any country except for Japan. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date. VGX decided in December 2007 to discontinue the VGX-410C program to concentrate its efforts on other candidates in its pipeline.

        In August 2007, Animal Health entered into a sales and marketing agreement with an Australia-based company to import, warehouse, and distribute its products to veterinarians in Australia. A $5,000 payment was made to the Australian company upon execution of this agreement, and another $5,000 payment was due upon receipt of final regulatory approval of Animal Health's product in Australia. The additional payment was made in 2008 upon the announcement of the approval. Additionally, under

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VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)


the terms of the agreement, Animal Health will pay the distributor a commission based on a percentage of all sales in Australia.

        In February 2008, VGX entered into a sales and marketing agreement with a related party in which the licensee was granted exclusive rights to sell and market VGX-1027 for Rheumatoid Arthritis (RA), in Asia (excluding Japan), Africa, and the Middle East. There are milestone and royalty payments associated with the agreement due to VGX. They include a $1,500,000 payment for the initiation of a Phase II trial for RA, a $3,000,000 payment for the initiation of a Phase III trial, a $3,000,000 payment for the submission of NDA, and a $5,000,000 payment upon approval of NDA. The terms of the agreement shall terminate upon the earlier of (1) expiration of the last-to-expire patent, or (2) 20 years after the effective date.

        In August 2008, VGX Animal Health entered into Marketing and Distribution Agreement with an Australia-based company in which the Australian company becomes the exclusive distributor of LifeTide™ SW 5 in Australia. The term of the agreement is three (3) years from the signing of the agreement, with automatic one (1) year extension.

Definitive Merger Agreement

        On July 7, 2008, Inovio Biomedical Corporation (AMEX:INO / "INOVIO"), a developer of electroporation-based DNA vaccine delivery technology, and VGX Pharmaceuticals, Inc. ("VGX"), a privately held DNA vaccine developer, executed a definitive merger agreement (the "Merger Agreement"), which provides for the issuance of INOVIO's securities in exchange for all of the outstanding securities of VGX, and the merger of an acquisition subsidiary of INOVIO with and into VGX (the "Merger"). Each company's board of directors has approved the Merger Agreement and the all-stock transaction it contemplates. The transaction is subject to completion of the registration of the INOVIO securities to be issued with the U.S. Securities and Exchange Commission (SEC), receipt of approval from both companies' stockholders of the transaction, and other customary closing conditions. The parties expect to complete the merger in the first quarter of 2009; however, the actual timing of the transaction will depend on a number of factors, some of which are beyond either company's control. Upon closing of the merger, INOVIO anticipates changing its name to VGX Pharmaceuticals, Inc.

        The Merger Agreement anticipates that at the time of closing of the merger, a wholly-owned acquisition subsidiary of INOVIO will merge into VGX, with VGX surviving as a wholly-owned subsidiary of INOVIO. Concurrently, INOVIO will issue shares of its common stock in exchange for all of the outstanding shares of VGX common stock based on an exchange ratio derived from the comparative fully diluted share capitalization of the companies, excluding the shares of VGX common stock underlying $5.5 million of VGX convertible debt (the "Excluded Debt"). INOVIO will also assume all outstanding VGX options and warrants and all VGX convertible debt in excess of the Excluded Debt, which will be adjusted based on the exchange ratio and become exercisable or convertible, as applicable, for INOVIO's common stock. The Excluded Debt will also be assumed at closing, but unlike the VGX convertible debt discussed above, the principal outstanding under the Excluded Debt at closing will be immediately converted into shares of INOVIO's common stock at $1.05 per share.

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VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

9. Commitments (Continued)

        INOVIO is required to use commercially reasonable efforts to register the securities to be issued in the merger under the Securities Act of 1933, as amended, on a registration statement on Form S-4 to be filed with the Securities and Exchange Commission. Registered shares of INOVIO common stock received in the transaction by certain significant holders of VGX common stock and certain affiliates and all employees of VGX and shares of INOVIO common stock held by all affiliates and employees of INOVIO at the time of consummation of the transaction will be subject to lock-up arrangements that will provide for 25% of the shares initially subject to the lock-up per individual to be released from such restrictions upon each six-month anniversary of the closing date of the transaction, such that all shares will be released from the lock-up arrangements upon the two-year anniversary of the closing date of the transaction. The lock-up restrictions will also apply to the shares of INOVIO common stock issued upon assumption and conversion of VGX convertible debt for six-months after the closing date of the transaction, and will provide for 50% of the shares initially subject to the lock-up to be released upon the three-month anniversary of the closing date of the transaction. INOVIO anticipates listing the securities to be issued in the merger with the American Stock Exchange ("AMEX").

        INOVIO must submit information about the proposed transaction to the AMEX for review and determination of whether the transaction qualifies as a "reverse merger" under Company Guide Section 341, which if applicable could require INOVIO to re-qualify for initial listing of its securities on the AMEX. The parties do not believe that the transaction is a "reverse merger" as defined by the AMEX and believes that additional listing criteria should apply.

10. Income Taxes

        VGX accounts for income taxes under the liability method. Under this method, deferred tax assets and liabilities are determined based on the difference between the financial statement and tax bases of assets and liabilities using enacted tax rates in effect for the year in which the differences are expected to affect taxable income. Valuation allowances are established when necessary to reduce deferred tax assets to the amounts expected to be realized.

        VGX incurred losses from continuing operations for the nine months ended September 30, 2008 and September 30, 2007. In accordance with SFAS No. 109, VGX has continued to maintain a valuation allowance for it U.S. deferred tax assets.

        Federal tax net operating loss carryforwards (NOLs) aggregated approximately $27.6 million at December 31, 2007. To the extent NOLs are utilized, VGX will reverse a portion of its valuation allowance.

        VGX has not yet undertaken a study to determine if it has undergone any ownership change as defined in IRC Section 382. An ownership change could cause an annual limitation on the usage of the above NOLs.

        VGX adopted the provisions of FASB Interpretation 48, "Accounting for Uncertainty in Income Taxes—an Interpretation of FASB Statement No. 109", or FIN 48, on January 1, 2008. VGX did not have any unrecognized tax positions and there was no material effect on its financial condition or results of operations as a result of adopting FIN 48.

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VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

10. Income Taxes (Continued)

        VGX's policy is to recognize interest and penalties accrued on any unrecognized tax positions as a component of income tax expense. As of the date of adoption of FIN 48, VGX did not have any accrued interest or penalties associated with any unrecognized tax benefits, nor was any interest expense recognized during the period.

11. Equity Investment

        In October 2005, VGX purchased 250,000 shares of a Korean-based company, Dong-IL Fabrics, at an aggregate purchase price of $4,787,824. At the date of purchase, VGX's ownership represented 33% of the total outstanding shares of Dong-IL Fabrics. Additionally, VGX incurred $110,400 of acquisition costs associated with the investment. In 2006, the name of Dong-IL Fabrics was officially changed to VGX International (VGXI). Also in 2006, VGX invested an additional $4,408,065 in VGXI. Finally, during 2006, VGXI had a secondary offering in which VGX elected not to fully participate. Prior to that offering, VGX's ownership percentage was 38%. Accordingly, the September 30, 2008 carrying value of the investment in VGXI is less than VGX's ownership percentage of VGXI's equity. VGX's current ownership percentage in VGXI is 30%.

        Under the equity method of accounting in accordance with APB 18, The Equity Method of Accounting for Investments in Common Stock , VGX has recorded an interest in the earnings or losses of VGXI beginning from the date of purchase. VGX's interest in the losses of VGXI from the date of purchase through September 30, 2008 is $5,735,660, which includes $64,400 of amortized acquisition costs, as well as VGXI's share of the gain on the sale of manufacturing assets realized by VGX of $2,901,856. VGXI is a publicly traded company on the Korean Stock Exchange and, therefore, the equity investment on the balance sheet is based upon the quoted market price of the stock, net of unamortized acquisition costs.

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VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

11. Equity Investment (Continued)

        The financial position and results of operations of VGXI as of and for the nine months ended September 30, 2008 are as follows:

    Financial Position:

 
  September 30, 2008  
 
  (Unaudited)
 

Assets

       

Current assets

  $ 16,888,351  

Fixed assets

    5,373,706  

Other assets

    12,097,859  
       

Total assets

  $ 34,359,916  
       

Liabilities

       

Current liabilities

  $ 6,938,973  

Long-term liabilities

    594,491  
       

Total liabilities

    7,533,464  

Total equity

    26,826,452  
       

Total liabilities and equity

  $ 34,359,916  
       

    Results of Operations:

 
  Nine Months Ended September 30, 2008  
 
  (Unaudited)
 

Revenues

  $ 7,741,460  

Cost of sales

    6,830,935  
       

Gross profit

    910,525  

Operating expenses

    4,831,859  
       

Operating loss

  $ (3,921,334 )
       

Net loss

  $ (2,638,910 )
       

        In October 2007, VGX made a strategic investment of $60,000 in a biotechnology company based in Colorado. The two companies have also agreed to cooperate on various future research projects. The investee is a private company in which VGX holds less than 10% of outstanding shares.

12. Net Loss Per Share

        Net loss per share is calculated in accordance with SFAS No. 128, Earnings Per Share . Basic loss per share is computed by dividing the net loss for the year by the weighted average number of common shares outstanding during the year. Diluted loss per share is calculated in accordance with the treasury

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VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

12. Net Loss Per Share (Continued)


stock method and reflects the potential dilution that would occur if securities or other contracts to issue common stock were exercised or converted to common stock. Since the effect of the assumed exercise of common stock options and other convertible securities was anti-dilutive for all periods presented, there is no difference between basic and diluted loss per share.

13. Comprehensive Loss

        Comprehensive loss for the nine months ended September 30, 2008 and September 30, 2007 includes net loss, unrealized losses on foreign bank account activity, and foreign currency translation gains and losses. A summary of VGX's comprehensive loss is as follows:

 
  Nine Months Ended September 30, 2008   Nine Months Ended September 30, 2007   Period from December 12, 2000 (Inception) to September 30, 2008  

Comprehensive loss:

                   

Net loss

  $ (9,762,688 ) $ (13,245,409 ) $ (63,048,018 )

Unrealized losses on foreign bank activity

    (101 )   (66 )   (33,788 )

Foreign currency translation adjustments

    (1,667,427 )   232,605     (991,704 )
               

Comprehensive loss

  $ (11,430,216 ) $ (13,012,870 ) $ (64,073,510 )
               

14. Supplemental Disclosures of Cash Flow Information

 
  Nine Months Ended September 30, 2008   Nine Months Ended September 30, 2007   Period from December 12, 2000 (Inception) to September 30, 2008  

Supplemental schedule of investing activities:

                   

Capital lease for office equipment

  $   $   $ 9,562  

Issuance of common stock to acquire ADViSYS, Inc. 

  $   $ 4,621,095   $ 4,621,095  

Conversion of long-term debt and accrued interest to common stock

  $   $   $ 553,839  

Issuance of warrants in connection with debt

  $   $   $ 58,953  

Supplemental schedule of cash flow information:

                   

Interest paid

  $ 586,791   $ 772,335   $ 1,511,472  
               

15. Subsequent Events

        In November 2008, an agreement was reached with three convertible note holders representing a total of $2,140,000 in principal in which the convertible feature of the aforementioned notes were removed; in effect, they are now straight debt. In return, VGX agreed to repay the debt at the earlier of the maturity date or the closing date of the transaction. The maturity dates of the notes in question

F-133



VGX PHARMACEUTICALS, INC.
(A Development-Stage Company)

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Continued)

(Unaudited)

15. Subsequent Events (Continued)


all fall during April, 2009. Also, VGX and a group of investors mutually agreed to abrogate the commitment to fund $1.1 million in two-year notes. These notes were originally to be converted to equity at $1.05 conversion price upon a public event and were part of (the "Excluded Debt"). As such, the total value of the Excluded Debt decreased from $5.5 million to $4.4 million.

        Also in November 2008, an agreement was reached with the holders of $4.4 million of Excluded Debt, to either extend the notes until 2010 or be extendable at VGX's discretion to 2010. As part of this agreement, the terms related to the automatic conversion of these notes at a public event at a conversion price of $1.05 was removed. The notes will still be automatically converted to equity at $1.05 if the shares of the combined company trade at or above $2.10 for five consecutive trading days.

        In November 2008, an agreement was reached between VGXP and VGXI, Inc., in which the parties agreed to modify the payment structure of the remaining $6.0 million due from VGXI, Inc. The remaining $6.0 million will now be received in two equal $3.0 million tranches in December 2008 and March 2009. Previously, they were to be paid in two tranches of $4.0 million and $2.0 million in December 2008 and March 2009.

        In December 2008, VGX repaid $1.5 million in short term notes due on December 31, 2008. VGX decided to prepay the debt several weeks before the maturity date.

        In December 2008, VGX entered into a license agreement with a related party in which it grants to the licensee exclusive rights to the development, sales, licensing, and marketing of VGX-3400, its candidate for Avian Influenza, in humans in the Republic of Korea. There is a $100,000 upfront licensing fee as well a royalty payment on net sales due to VGX from the licensee. The licensee is also responsible for filing and maintenance fees related to the patents for VGX-3400 in the Republic of Korea. There are no other additional milestone payments due from the licensee. The term of the agreement shall terminate upon later of: (a) the last to expire patent or (b) twenty (20) years after the effective date.

        In December 2008, VGX agreed to participate in the secondary offering of VGX International due to be completed in the first quarter of 2009. The total amount of participation is $200,000. VGX's ownership percentage is expected to be lowered from the current 30% to approximately 25% after the secondary offering.

        In December 2008, VGX issued 200,000 shares of the Company stock in accordance with the Asset Purchase Agreement of ADViSYS, Inc signed on February 21, 2007. VGX had triggered a milestone payment upon the usage of CELLECTRA™ in a clinical trial.

F-134



ANNEX I

INDEX TO UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS

 
   
 

Unaudited Pro Forma Combined Balance Sheet as of September 30, 2008

    I-4  

Unaudited Pro Forma Combined Statement of Operations for the year ended December 31, 2007

    I-5  

Unaudited Pro Forma Combined Statement of Operations for the nine months ended September 30, 2008

    I-6  

Notes to Unaudited Pro Forma Combined Financial Statements

    I-7  

I-1



INOVIO BIOMEDICAL CORPORATION

VGX PHARMACEUTICALS, INC.

UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS

        The following unaudited pro forma condensed combined statements of earnings combine the historical consolidated statements of earnings of Inovio Biomedical Corporation (Inovio) and VGX Pharmaceuticals, Inc. (VGX) giving effect to the merger and related events, as if they had been consummated on January 1, 2007. The unaudited pro forma condensed combined balance sheet combines the historical unaudited consolidated balance sheet of Inovio as of September 30, 2008 and the historical unaudited consolidated balance sheet of VGX as of September 30, 2008 giving effect to the merger and related events, as if they had been consummated on September 30, 2008.

        The unaudited pro forma condensed combined statement of operations for the year ended December 31, 2007 is based on the historical statement of operations of Inovio and combines the results of operations of VGX for the year ended December 31, 2007 as if the transaction had occurred as of January 1, 2007. The unaudited pro forma condensed combined statement of operations for the nine months ended September 30, 2008 is based on the historical statements of operations of Inovio and combines the results of operations for VGX for the nine months ended September 30, 2008 as if the acquisition had occurred as of January 1, 2007. The fiscal year ends of Inovio and VGX are both December 31.

        The pro forma information is preliminary, is being furnished solely for informational purposes and is not necessarily indicative of the combined financial position or results of operations that might have been achieved for the periods or dates indicated, nor is it necessarily indicative of the future results of the combined company. The pro forma information is based on preliminary estimates and assumptions set forth in the notes to the unaudited pro forma condensed combined financial statements. The pro forma information does not reflect cost savings expected to be realized from the elimination of certain expenses and from synergies expected to be created or the costs to achieve such cost savings or synergies. No assurance can be given that cost savings or synergies will be realized.

        Pro forma adjustments are necessary to reflect the estimated purchase price, including the new equity structure, and to adjust VGX's net tangible and intangible assets and liabilities to preliminary estimated fair values. Pro forma adjustments are also necessary to reflect the amortization expense related to amortizable intangible assets, changes in depreciation and amortization expense resulting from fair value adjustments to net tangible assets, and costs to finance the merger, related to the pro forma adjustments.

        The pro forma adjustments to VGX's assets and liabilities and allocation of purchase price are preliminary and are based on Inovio management's estimates of the fair value of the assets to be acquired and liabilities to be assumed. Inovio made estimates of fair value of the VGX assets acquired and liabilities assumed using reasonable assumptions based on historical experience and information obtained from VGX management. The valuation methodology used to estimate the value of the identified intangible assets acquired was the excess earnings method. This method reflects the present value of the operating cash flows generated by the intangible asset after taking into account the cost to realize the revenue, and an appropriate discount rate to reflect the time value and risk associated with the invested capital. To value a particular intangible asset, the value and required rate of return for other assets that contribute to the generation of the revenue earned by that intangible asset must be determined. The required returns on these other assets are deducted from the future net operating income to determine the returns specifically earned by the intangible asset. A discount rate percent was then applied that considered the reasonable expectation of the risk profile of the proprietary technology in order to bring the future income to a present value.

I-2



INOVIO BIOMEDICAL CORPORATION

VGX PHARMACEUTICALS, INC.

UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS (Continued)

        The final purchase price allocation will be completed after asset and liability valuations are finalized. A final determination of these fair values, which cannot be made prior to the completion of the transaction, will include Inovio management's consideration of a final valuation based on the actual net tangible and intangible assets of VGX that exist as of the consummation of the merger. Any final adjustments may change the allocation of the purchase price, which could affect the fair value assigned to the assets and liabilities and could result in a change to the unaudited pro forma condensed combined financial statements presented herein. Amounts preliminarily allocated to assets and liabilities, and the estimated useful lives of intangible assets with indefinite and definite lives, may change significantly, which could result in a material increase or decrease in amortization of definite lived intangible assets. Estimates related to the determination of the lives of assets acquired may also change, which could result in a material increase or decrease in depreciation or amortization expense.

        Certain reclassifications have been made to conform VGX's historical amounts to Inovio's presentation.

        The unaudited pro forma condensed combined financial information should be read in conjunction with the audited and unaudited financial statements and accompanying notes of Inovio and VGX included elsewhere in this joint proxy statement/prospectus.

I-3



Inovio Biomedical Corporation

Unaudited Pro Forma Condensed Balance Sheet

As of September 30, 2008

 
  Inovio   VGX   Pro Forma
Adjustments
   
  Combined  
ASSETS                              

Current assets:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 
Cash and cash equivalents   $ 6,411,494   $ 6,760,395             $ 13,171,889  
Accounts receivable     740,368     42,625               782,993  
Prepaid expenses and other current assets     747,971     208,872               956,843  
Receivables due from related parties         6,351,489               6,351,489  
Inventories         37,475               37,475  
                       
  Total current assets:     7,899,833     13,400,856             21,300,689  
                       
Investments     12,057,775                   12,057,775  
Fixed assets, net     403,609     398,998     (238,695 ) A     563,912  
Intangible assets, net     5,937,549     3,221,052     (17,160,947 ) A     17,462,541  
                  (4,784,122 ) A        
                  (3,221,052 ) B        
                  28,685,939   B        
                  7,997,055   B        
                  (3,212,933 ) F        
Goodwill     3,900,713     907,076     (907,076 ) A     3,900,713  
Other assets     282,000     130,147     (125,000 ) I     287,147  
Equity investment         2,578,924     (1,542,804 ) A     1,036,120  
                       
  Total assets:   $ 30,481,479   $ 20,637,053   $ 5,490,365       $ 56,608,897  
                       

LIABILITIES AND STOCKHOLDERS EQUITY

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 
Current liabilities:                              
Accounts payable and accrued expenses   $ 1,478,016   $ 2,776,810     500,000   C   $ 4,754,826  
Accrued clinical trial expenses     491,922                   491,922  
Line of credit     1,763,845                   1,763,845  
Common stock warrants     145,833                   145,833  
Deferred revenue     497,676                   497,676  
Deferred rent     77,953                   77,953  
Current portion of long-term debt         7,900,000               7,900,000  
Other current liabilities         47,097               47,097  
                       
  Total current liabilities:     4,455,245     10,723,907     500,000         15,679,152  
                       
Deferred revenue, net of current portion     4,084,065                   4,084,065  
Deferred rent, net of current portion     37,245                   37,245  
Deferred tax liabilities     903,000                   903,000  
Long-term debt         100,000               100,000  
                       
  Total liabilities:     9,479,555     10,823,907     500,000         20,803,462  
                       
Commitments and contingencies                      
Minority Interest         702,835               702,835  
Stockholders' equity:                              
Preferred stock                        
Common stock     44,011     4,167     (4,167 ) D     86,541  
                  42,533   E        
                  (3 ) I        
Additional paid-in capital     171,616,752     73,179,654     (73,179,654 ) D     189,002,581  
                  17,396,076   E        
                  (10,247 ) I        
Receivables from stockholders     (50,000 )                 (50,000 )
Accumulated deficit     (149,237,215 )   (63,048,018 )   63,048,018   D     (152,564,898 )
                  (3,212,933 ) F        
                  (114,750 ) I        
Accumulated other comprehensive (loss) income     (1,371,624 )   (1,025,492 )   1,025,492   D     (1,371,624 )
                       
  Total stockholders' equity     21,001,924     9,110,311     4,990,365         35,102,600  
                       
    Total liabilities, minority interest and stockholders' equity   $ 30,481,479   $ 20,637,053   $ 5,490,365       $ 56,608,897  
                       

I-4



Inovio Biomedical Corporation

Unaudited Pro Forma Condensed Combined Statement of Operations

For the Year Ended December 31, 2007

 
  Inovio   VGX   Pro Forma Adjustments    
  Combined  

Revenue:

                             

License fee and milestone payments

  $ 2,793,478   $   $       $ 2,793,478  

Revenue under collaborative research and development arrangements

    1,854,303                   1,854,303  

Grant and miscellaneous revenue

    159,948     668,955               828,903  

Other operating revenue, net

        36,448               36,448  
                       

Total revenue:

    4,807,729     705,403             5,513,132  
                       

Operating Expenses:

                             

Research and development

    9,625,947     10,936,149     1,024,401   G     21,586,497  

General and administrative

    11,080,202     4,999,391     (72,090 ) J     16,122,253  

                114,750   I        
                       

Total operating expenses

    20,706,149     15,935,540     1,067,061         37,708,750  
                       

Loss from operations

    (15,898,420 )   (15,230,137 )   (1,067,061 )       (32,195,618 )
                       

Interest income (expense)

    1,272,397     (209,438 )             1,062,959  

Other income (expense)

    3,421,580                   3,421,580  

Losses from equity investment

        (990,338 )             (990,338 )

Minority interests

        43,503               43,503  
                       

Loss from continuing operations

    (11,204,443 )   (16,386,410 )   (1,067,061 )       (28,657,914 )
                       

Discontinued operations:

                             

Loss from discontinued operations

        (1,409,631 )             (1,409,631 )
                       

Net loss

    (11,204,443 )   (17,796,041 )   (1,067,061 )       (30,067,545 )
                       

Imputed and declared dividends on preferred stock

    (23,335 )                 (23,335 )
                       

Net loss attributable to common stockholders

  $ (11,227,778 ) $ (17,796,041 ) $ (1,067,061 )     $ (30,090,880 )
                       

Amounts per common share—basic and diluted:

                             

Net loss from continuing operations

  $ (0.27 ) $ (0.37 )           $ (0.34 )

Net gain/loss from discontinued operations

  $   $ (0.03 )           $ (0.02 )
                       

Net loss per common share attributable to common stockholders

  $ (0.27 ) $ (0.40 )           $ (0.36 )
                         

Weighted average number of common shares outstanding—basic and diluted

    41,493,412     43,915,950     42,609,442         84,102,854  
                       

I-5



Inovio Biomedical Corporation

Unaudited Pro Forma Condensed Combined Statement of Operations

For the Nine Months Ended September 30, 2008

 
  Inovio   VGX   Pro Forma
Adjustments
  Combined  

Revenue:

                         

License fee and milestone payments

  $ 611,578   $ 100,000         $ 711,578  

Revenue under collaborative research and development arrangements

    1,159,207               1,159,207  

Grant and miscellaneous revenue

        113,745           113,745  

Revenue from product sales

        40,000           40,000  

Government contract revenue

        1,962,305           1,962,305  
                   

Total revenue:

    1,770,785     2,216,050         3,986,835  
                   

Operating Expenses:

                         

Research and development

    4,551,039     10,026,912     768,301    H   15,346,252  

General and administrative

    7,416,613     6,356,794     (59,229 ) K   13,714,178  

Cost of product sales

        112,153           112,153  
                   

Total operating expenses

    11,967,652     16,495,859     709,072     29,172,583  
                   

Loss from operations

    (10,196,867 )   (14,279,809 )   (709,072 )   (25,185,748 )
                   

Interest income (expense)

    587,128     (82,620 )         504,508  

Other income (expense)

    219,850     97,497           317,347  

Losses from equity investment

        (817,935 )         (817,935 )

Minority Interest

        253,662           253,662  
                   

Loss from continuing operations

    (9,389,889 )   (14,829,205 )   (709,072 )   (24,928,166 )
                   

Discontinued operations:

                         

Gain on sale of manufacturing assets, net of tax

        6,653,153           6,653,153  

Loss from discontinued operations

        (1,586,636 )         (1,586,636 )
                   

Net loss

    (9,389,889 )   (9,762,688 )   (709,072 )   (19,861,649 )
                   

Imputed and declared dividends on preferred stock

                 
                   

Net loss attributable to common stockholders

  $ (9,389,889 ) $ (9,762,688 ) $ (709,072 ) $ (19,861,649 )
                   

Amounts per common share—basic and diluted:

                         

Net loss from continuing operations

  $ (0.21 ) $ (0.34 )       $ (0.29 )

Net gain/loss from discontinued operations

  $   $ 0.12           0.06  
                     

Net loss per common share attributable to common stockholders

  $ (0.21 ) $ (0.22 )       $ (0.23 )
                     

Weighted average number of common shares outstanding- basic and diluted

    43,881,047     43,959,706     42,646,942     86,527,989  
                   

I-6



INOVIO BIOMEDICAL CORPORATION

NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS

Note 1—Basis of Presentation

        On July 7, 2008, Inovio Biomedical Corporation (the "registrant") and VGX Pharmaceuticals, Inc., a privately-held Delaware corporation ("VGX"), executed a definitive merger agreement (the "Merger Agreement"), which provides for the issuance of the registrant's securities in exchange for all of the outstanding securities of VGX and the merger of an acquisition subsidiary with VGX. On December 5, 2008, the registrant and VGX executed an amended and restated merger agreement (the "Amended Agreement"), as approved by both the registrant's and VGX's boards of directors.

        The Amended Agreement provides that at the time of closing of the merger contemplated by the Amended Agreement, VGX will merge with and into a wholly-owned acquisition subsidiary of the registrant, with that subsidiary surviving the merger (the "Merger").

        Concurrent with the Merger, the registrant will issue shares of the registrant's common stock in exchange for all of the outstanding shares of VGX common stock based on an exchange ratio derived from the comparative fully diluted share capitalization of the companies, excluding the shares of VGX common stock underlying outstanding VGX convertible debt. The registrant will also assume all outstanding VGX options, VGX warrants and, on a consolidated basis, VGX convertible debt, which will become exercisable or convertible, as applicable, for the registrant's common stock; the pricing and shares into which the VGX options and VGX warrants are exercisable will be adjusted based on the exchange ratio, and the VGX convertible debt will become convertible at $1.05 per share of the registrant's common stock.

        Due to the structure of the exchange ratio calculation, it is not possible for the parties to state with certainty at this time the total number of shares of the registrant's common stock, options and warrants to be issued at closing of the Merger. However, the exchange ratio is designed to result in the legacy holders of the registrant's and VGX securities each holding on an aggregate basis 50% of the combined company's fully-diluted equity interests, excluding from the calculation the shares issuable upon the conversion of the VGX convertible debt. For purposes of determining the estimated purchase price, based on the current exchange ratio, the registrant estimated it would issue approximately 42,508,192 shares of its common stock in exchange for all the outstanding securities of VGX. The fair value of the registrants shares used to determining the purchase price was $0.41 per share. The Agreement also provides that five significant stockholders of VGX will place 8,000,000 shares of the registrant's common stock received in the Merger into a voting trust, effective concurrent with the closing of the Merger, to be administered by an independent committee of the board of directors of the combined company. The trustees would vote the shares in accordance with the percentage of votes cast by all stockholders on any particular matter. Based on current capitalization information and the impact of the anticipated voting trust agreement, the parties anticipate that legacy registrant capital stock holders and legacy VGX common stock holders will share voting power over the combined company approximately 50.94% and 39.83%, respectively, based on the anticipated number of shares of Inovio capital stock to be outstanding, with the remainder of voting power to be allocated by the voting trust. However, the exact percentage split of the equity interests in and voting power over the combined company will depend on a number of factors, including the registrant's pre-closing capitalization and VGX's pre-closing capitalization, thus these projected percentages may change prior to closing.

        The determination of the purchase price and the allocation of purchase price is preliminary. The determination of the final purchase price will be determined upon consummation of the merger. The final determination of the purchase price allocation will be based on the fair values of assets acquired,

I-7



INOVIO BIOMEDICAL CORPORATION

NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS (Continued)

Note 1—Basis of Presentation (Continued)


including fair values of acquired in-process research and development and other identifiable intangibles, and the fair value of liabilities assumed as of the date that the acquisition is consummated. The excess of the fair value of assets and liabilities over the purchase price of the acquired entity is allocated on a pro rata reduction of amounts that otherwise would have been assigned to all of the acquired assets. The purchase price allocation will remain preliminary until Inovio completes a final valuation of significant tangible and identifiable intangible assets acquired (including in-process research and development), evaluates the integration plan, which is to be undertaken upon the consummation of the merger, and determines the fair values of other assets and liabilities acquired. The final determination of the purchase price allocation is expected to be completed as soon as practicable after the consummation of the merger. The final amounts allocated to assets and liabilities could cause material differences in the information presented in the unaudited pro forma combined condensed financial statements.

        The amount allocated to acquired in-process research and development represents an estimate of the fair value of purchased in-process technology for research projects that, as of the date of the expected consummation of the merger, will not have reached technological feasibility and do not have a future alternative use. The values of the research projects will be determined based on analyses using estimated cash flows to be generated by the products that results from the in-process projects. These cash flows will be estimated by forecasting total revenues expected from these products and then deducting appropriate operating expenses, cash flow adjustments and contributory asset returns to establish a forecast of net cash flows arising from the in-process technology. These cash flows will be substantially reduced to take into account the time value of money and the risk associated with the inherent difficulties and uncertainties given the projected stage of development of these projects at closing. For purposes of the unaudited pro forma combined condensed balance sheet as of September 30, 2008, $3.2 million of the total purchase price has been allocated to acquired in-process research and development, net of negative goodwill allocation, which is not expected to have reached technological feasibility at the consummation date of the merger and have no future alternative use. The amounts allocated to in-process research and development will be charged to expense in the statement of earnings in the period the acquisition is consummated.

        The acquired in-process research and development consists of VGX's drug candidates for rheumatoid arthritis (VGX-1027), cervical cancer (VGX-3100), and influenza (VGX-3400). VGX has developed all three drug candidates and they are either currently in clinical trials or INDs to begin clinical trials have been filed with the FDA; specifically:

        VGX-1027.     VGX's small molecule drug for rheumatoid arthritis is currently in Phase I clinical trials. A single ascending dose study was completed in 2008 and a multiple ascending dose study should be completed during the first quarter of 2009, which would mark the end of the Phase 1 trial. VGX, or if the Merger has been completed, the combined group, expects to begin a Phase II trial later in 2009. VGX hopes to license the drug to a large pharmaceutical company for a milestone based licensing fee and royalty as a percentage of sales and as a result does not expect to incur the cost of a phase III trial, as it would rely on its licensing partner to bear that portion of the cost. VGX expects the product to attain marketing approval and sales by 2016 and expects achieving such results will require approximately $18 million of additional expenses.

        VGX-3100.     The VGX DNA vaccine for therapeutic treatment of cervical cancer entered Phase 1 clinical trials in the second half of 2008. The Phase 1 trial is expected to end in late 2009 and VGX

I-8



INOVIO BIOMEDICAL CORPORATION

NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS (Continued)

Note 1—Basis of Presentation (Continued)


anticipates initiating a Phase II trial in 2010. The Phase II trial is expected to last two years, ending in 2011. VGX hopes to license the drug to a third party after the Phase II trial, such that the cost of a Phase III trial would be borne by the third-party licensee. VGX is aiming to obtain a BLA approval and first sales of this vaccine in 2016. VGX projects expected costs from 2009 to first sales to be approximately $6 million.

        VGX-3400.     VGX's DNA vaccine for influenza has completed preclinical toxicity studies and an IND has been filed with the FDA. VGX is currently working with the FDA to address some safety related questions. VGX is hoping to initiate Phase I clinical trials in 2009. Once completed, VGX expects to license the drug to a third party since demonstration of an immune response from Phase I study patients should be sufficient proof of concept of its drug and electroporation, and expects any additional clinical trial costs after the Phase I trial is expected to be borne by the licensee, including dose ranging studies, as well as larger population studies (Phase IIa/b; Phase III). VGX hopes to obtain a BLA approval and first sales in 2015. VGX projects its costs to be incurred from 2009 to first sales to be approximately $2 million.

        The development of these technologies remains a risk due to the remaining efforts to achieve technical viability, rapidly changing customer markets, uncertain standards for new products, and significant competitive threats from our competitors. Failure to develop these technologies into commercially viable products and/or failure to bring them to market in a timely manner could result in a loss of market share, which could have a material adverse impact on the combined group's business and operating results, could negatively impact the return on investment that we expected at the time that the merger was completed and may result in impairment charges.

        The total purchase price of the acquisition is estimated as follows:

Value of Inovio shares issued

  $ 17,438,609  

Transaction costs

    500,000  
       

Total

  $ 17,938,609  
       

        The fair value of the Inovio shares used in determining the purchase price was $0.41 per share based on the average of the closing price of Inovio common stock for the period two days before and two days after the December 5, 2008 Amended Agreement announcement date.

I-9



INOVIO BIOMEDICAL CORPORATION

NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS (Continued)

Note 1—Basis of Presentation (Continued)

        The estimated purchase price has been allocated to the acquired tangible and intangible assets and liabilities assumed based on their fair values as of September 30, 2008. The allocation to assets and liabilities is summarized below:

 
  Fair Value   Negative
Goodwill
Allocation
  Fair Value
After Negative
Goodwill
Allocation
 
Tangible assets   $ 16,508,925   $ (1,781,499 ) $ 14,727,426  
Assumed liabilities     (10,823,907 )       (10,823,907 )
Assumed minority interest     (702,835 )       (702,835 )
Intangible assets (developed technology)     28,685,939     (17,160,947 )   11,524,992  
In-process research and development     7,997,055     (4,784,122 )   3,212,933  
Negative Goodwill     (23,726,568 )   23,726,568      
               
Total   $ 17,938,609   $   $ 17,938,609  
               

Note 2—Pro Forma Adjustments

        

(A)
To eliminate historical goodwill of VGX of $907,076 and allocate negative goodwill of $23,726,568 due to the fair value of purchased net assets exceeding the cost of the acquired entity. Negative goodwill has been allocated on a pro rata basis to fixed assets in the amount of $238,695, equity investment in the amount of $1,542,804, intangible assets in the amount of $17,160,947, and in-process research and development in the amount of $4,784,122.

    According to Statement of Financial Accounting Standards No. 141, if the amounts assigned to the acquired net assets exceed their costs, the excess is commonly referred to as negative goodwill. Negative goodwill was allocated on a pro rata basis to all VGX acquired assets except for long-term deposits included in other assets.

(B)
To eliminate existing VGX intangible assets of $3,221,052 and adjust identifiable intangible assets and in-process research and development to estimated fair value by $28,685,939 and $7,997,055, respectively.

(C)
To record transaction costs of $500,000.

(D)
To eliminate historical equity accounts and accumulated deficit of VGX including common stock of $4,167, additional paid-in capital of $73,179,654, accumulated deficit of $63,048,018 and accumulated other comprehensive loss of $1,025,492.

(E)
To record $42,533 to common stock and $17,396,076 to additional paid-in capital related to the fair value of Inovio's common stock issued in connection with the merger.

(F)
Reflects the portion of the purchase price allocated to acquired in-process research and development projects that, as of the consummation date of the merger, will not have reached technological feasibility and have no future alternative use. Because this is directly attributable to the acquisition and will not have a continuing impact in excess of one year, it is not reflected in the unaudited pro forma combined condensed statement of operations. However, acquired in-process research and development will be recorded as an expense in the period that the acquisition is completed.

I-10



INOVIO BIOMEDICAL CORPORATION

NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS (Continued)

Note 2—Pro Forma Adjustments (Continued)

(G)
To amortize incremental increase in intangible assets by $1,024,401 for the twelve months ended December 31, 2007 for the two developed technologies with estimated useful lives of eight and nine years. The estimate for the useful lives was based upon the expected remaining life of the patents related to the two technologies, the landscape of the competing technologies, as well as the expected market acceptance.

(H)
To amortize incremental increase in intangible assets by $768,301 for the nine months ended September 30, 3008 for the two developed technologies with estimated useful lives of eight and nine years. The estimate for the useful lives was based upon the expected remaining life of the patents related to the two technologies, the landscape of the competing technologies, as well as the expected market acceptance.

(I)
To eliminate Inovio's equity investment in VGX of $125,000, including an $114,750 impairment adjustment based on the current fair market value of VGX common stock.

(J)
To reverse depreciation expense for the twelve months ended December 31, 2007 related to reduction of fixed assets due to allocation of negative goodwill.

(K)
To reverse depreciation expense for the nine months ended September 30, 2008 related to reduction of fixed assets due to allocation of negative goodwill.

(L)
Pro forma basic and diluted net loss per share is calculated by dividing the pro forma combined net loss attributable to common stockholders by the pro forma weighted average common shares outstanding. A reconciliation of the shares used to calculate Inovio's historical basic and diluted net loss per share to shares used to calculate the pro forma basic and diluted net loss per share follows:
 
  Nine Months
Ended September 30,
2008
  Year Ended
December 31,
2007
 

Shares used to calculate Inovio's historical basic and diluted net loss per common share

    43,881,047     41,493,412  

Estimated shares issued in connection with the merger

    42,533,192     42,533,192  

Accelerated vesting of restricted common shares subsequent to and dependent upon the closing of the merger

    138,750     101,250  

Less shares previously owned by Inovio

    (25,000 )   (25,000 )
           

Shares used to calculate pro forma basic and diluted net loss per common share

    86,527,989     84,102,854  
           

I-11



ANNEX A

AMENDED AND RESTATED

AGREEMENT AND PLAN OF MERGER

BY AND AMONG

INOVIO BIOMEDICAL CORPORATION,

INOVIO ACQUISITION, LLC

AND

VGX PHARMACEUTICALS, INC.

Dated as of December 5, 2008


TABLE OF CONTENTS

 
   
  Page

ARTICLE I THE PLAN OF MERGER

  A-2
 

1.1

 

The Merger

 
A-2
 

1.2

 

The Closing

 
A-2
 

1.3

 

Effective Time of the Merger

 
A-2
 

1.4

 

General Effects of the Merger

 
A-2
 

1.5

 

Surviving Entity Certificate of Formation and Operating Agreement

 
A-2
 

1.6

 

Manager, Directors and Officers

 
A-3
 

1.7

 

Effect of Merger on VGX Securities

 
A-3
 

1.8

 

Dissenting Shares

 
A-7
 

1.9

 

Exchange Procedures; Surrender of Certificates

 
A-8
 

1.10

 

No Further Ownership Rights in VGX Common Stock or Interest in Surviving Entity

 
A-9
 

1.11

 

Lost, Stolen or Destroyed Certificates

 
A-9
 

1.12

 

Further Action

 
A-9
 

1.13

 

Effect of Merger on Inovio Securities

 
A-10

ARTICLE II REPRESENTATIONS AND WARRANTIES OF VGX

 
A-10
 

2.1

 

Organization; Standing and Power; Charter Documents; Subsidiaries

 
A-10
 

2.2

 

Capital Structure

 
A-11
 

2.3

 

Authority; Non-Contravention; Necessary Consents

 
A-13
 

2.4

 

Records; Financial Information

 
A-13
 

2.5

 

Absence of Certain Changes or Events

 
A-14
 

2.6

 

Taxes

 
A-16
 

2.7

 

Intellectual Property

 
A-18
 

2.8

 

Regulatory Compliance; Permits

 
A-25
 

2.9

 

Litigation

 
A-27
 

2.10

 

Brokers' and Finders' Fees; Fees and Expenses

 
A-27
 

2.11

 

Employee Matters and Benefit Plans

 
A-27
 

2.12

 

Title to Properties

 
A-30
 

2.13

 

Environmental Matters

 
A-30
 

2.14

 

Contracts

 
A-31
 

2.15

 

Board Approval

 
A-32
 

2.16

 

Transactions with Related Parties

 
A-32
 

2.17

 

Insurance

 
A-32

A-i


 
   
  Page
 

2.18

 

Liabilities

  A-33
 

2.19

 

Product Claims

 
A-33
 

2.20

 

Accounts Receivable

 
A-33
 

2.21

 

Anti-Takeover Statute Not Applicable

 
A-33
 

2.22

 

Foreign Corrupt Practices

 
A-33

ARTICLE III REPRESENTATIONS AND WARRANTIES OF INOVIO AND SUBMERGER

 
A-33
 

3.1

 

Organization; Standing and Power; Charter Documents; Subsidiaries

 
A-34
 

3.2

 

Capital Structure

 
A-34
 

3.3

 

Authority; Non-Contravention; Necessary Consents

 
A-36
 

3.4

 

Records; SEC Reports; Financial Statements; Controls

 
A-37
 

3.5

 

Absence of Certain Changes or Events

 
A-38
 

3.6

 

Tax Returns and Audits

 
A-39
 

3.7

 

Intellectual Property

 
A-41
 

3.8

 

Regulatory Compliance; Permits

 
A-46
 

3.9

 

Litigation

 
A-48
 

3.10

 

Brokers' and Finders' Fees; Fees and Expenses

 
A-48
 

3.11

 

Employee Matters and Benefit Plans

 
A-48
 

3.12

 

Title to Properties

 
A-51
 

3.13

 

Environmental Matters

 
A-51
 

3.14

 

Contracts

 
A-52
 

3.15

 

Board Approval

 
A-53
 

3.16

 

Transactions with Related Parties

 
A-53
 

3.17

 

Insurance

 
A-53
 

3.18

 

Liabilities

 
A-54
 

3.19

 

Product Claims

 
A-54
 

3.20

 

Accounts Receivable

 
A-54
 

3.21

 

Anti-Takeover Statute Not Applicable

 
A-54
 

3.22

 

Foreign Corrupt Practices

 
A-54
 

3.23

 

Listing and Maintenance Requirements

 
A-54
 

3.24

 

Opinion of Financial Advisor

 
A-55
 

3.25

 

Operations of Submerger

 
A-55

ARTICLE IV CONDUCT PRIOR TO THE EFFECTIVE TIME

 
A-55
 

4.1

 

Conduct of Business of VGX and its Subsidiaries

 
A-55

A-ii


 
   
  Page
 

4.2

 

Conduct of Business of Inovio and its Subsidiaries

  A-58
 

4.3

 

Sale of Assets; Reduction of VGX Convertible Debt

 
A-61

ARTICLE V ADDITIONAL AGREEMENTS

 
A-61
 

5.1

 

Registration Pursuant to the Securities Act

 
A-61
 

5.2

 

Solicitation Pursuant to the Exchange Act

 
A-62
 

5.3

 

VGX Stockholder Solicitation and Approval

 
A-62
 

5.4

 

VGX and Inovio Information

 
A-63
 

5.5

 

Confidentiality; Access to Information

 
A-64
 

5.6

 

No VGX Solicitation

 
A-65
 

5.7

 

No Inovio Solicitation

 
A-67
 

5.8

 

Public Disclosure

 
A-69
 

5.9

 

Regulatory Filings; Reasonable Efforts

 
A-70
 

5.10

 

Notification of Certain Matters

 
A-71
 

5.11

 

Employee Benefits

 
A-72
 

5.12

 

Reservation of Shares

 
A-72
 

5.13

 

Listing or Quotation

 
A-72
 

5.14

 

Continuation of Indemnification

 
A-73
 

5.15

 

FIRPTA Compliance

 
A-73
 

5.16

 

Submerger Compliance

 
A-73
 

5.17

 

Certain Litigation

 
A-74
 

5.18

 

Treatment as Reorganization

 
A-74
 

5.19

 

Financial Statements

 
A-74
 

5.20

 

Affiliates

 
A-74
 

5.21

 

Identification of Directors

 
A-74
 

5.22

 

Employment Agreements

 
A-75
 

5.23

 

No Severance Obligations

 
A-75
 

5.24

 

Expenses

 
A-75
 

5.25

 

Line of Credit

 
A-75
 

5.26

 

Headquarters

 
A-75

ARTICLE VI CONDITIONS TO THE MERGER

 
A-75
 

6.1

 

Conditions to Obligations of Each Party to Effect the Merger

 
A-75
 

6.2

 

Additional Conditions to Obligations of VGX

 
A-76
 

6.3

 

Additional Conditions to the Obligations of Inovio

 
A-77

A-iii


 
   
  Page

ARTICLE VII TERMINATION, AMENDMENT AND WAIVER

  A-79
 

7.1

 

Termination

 
A-79
 

7.2

 

Notice of Termination; Effect of Termination

 
A-80
 

7.3

 

Amendment

 
A-80
 

7.4

 

Extension; Waiver

 
A-80
 

7.5

 

Termination Payments

 
A-81

ARTICLE VIII [RESERVED]

 
A-81

ARTICLE IX GENERAL PROVISIONS

 
A-81
 

9.1

 

Survival of Representations and Warranties

 
A-81
 

9.2

 

Certain Definitions

 
A-81
 

9.3

 

Notices

 
A-88
 

9.4

 

Interpretation

 
A-89
 

9.5

 

Counterparts

 
A-89
 

9.6

 

Entire Agreement; Third Party Beneficiaries

 
A-89
 

9.7

 

Severability

 
A-89
 

9.8

 

Other Remedies; Specific Performance

 
A-90
 

9.9

 

Governing Law; Forum Selection

 
A-90
 

9.10

 

Rules of Construction

 
A-90
 

9.11

 

Assignment

 
A-90
 

9.12

 

Waiver of Jury Trial

 
A-90
 

9.13

 

Time is of the Essence

 
A-90
 

9.14

 

Legal Representation

 
A-90

A-iv


INDEX OF EXHIBITS

Exhibit A   VGX Support Stockholders

Exhibit B

 

Form of Support Stockholder Voting Agreement

Exhibit C

 

Form of Voting Trust Agreement

Exhibit D

 

Form of Affiliates Letter

Exhibit E

 

Form of Inovio Vice President Employment Agreement

Exhibit F

 

Form of Inovio Executive Director Employment Agreement

Exhibit G

 

Form of Inovio Key Employee Employment Agreement

Exhibit H

 

Form of Employment Agreement for Peter Kies

Exhibit I

 

Form of Employment Agreement for Dr. Avtar Dhillon

Exhibit J

 

Form of Legal Opinion of K&L Gates LLP

Exhibit K

 

Form of Legal Opinion of Duane Morris LLP

SCHEDULES

VGX Disclosure Letter

Inovio Disclosure Letter

Schedule 1.6(d)

 

Officers of Inovio Post-Closing

Schedule 1.7(d)(ii)

 

Certain VGX Convertible Debt

Schedule 1.7(h)

 

Certain Restricted Parties for Lock-Up Arrangement

Schedule 4.3

 

Asset Purchase Agreement Between VGXI, Inc. and VGX Pharmaceuticals, Inc. dated June 10, 2008

Schedule 5.9(d)

 

Necessary Consents

Schedule 5.22

 

Closing Employment Agreements

         [Exhibits and schedules to this agreement which do not contain information material to understanding the terms of this agreement, and which are not otherwise required to be disclosed at this time are omitted from this Annex A. Those agreements listed above as exhibits to this agreement which are material to Inovio and the proposed combined group have been filed as exhibits to the registration statement of which this proxy statement/prospectus is a part.]

A-v


AMENDED AND RESTATED AGREEMENT AND PLAN OF MERGER

        This AGREEMENT AND PLAN OF MERGER (the " Agreement ") is made and entered into as of December 5, 2008, by and among Inovio Biomedical Corporation, a Delaware corporation (" Inovio "), Inovio Acquisition, LLC, a Delaware limited liability company and wholly-owned subsidiary of Inovio (" Submerger "), and VGX Pharmaceuticals, Inc. (" VGX "). Certain capitalized terms that are used herein shall have the respective meanings ascribed thereto in Article IX hereof.

RECITALS

        A.    Inovio, VGX and Submerger's predecessor, Inovio Acquisition Corporation, previously entered into a certain Agreement and Plan of Merger dated as of July 7, 2008 (the " Prior Agreement "). The parties hereto wish by this Agreement to amend and restate the Prior Agreement.

        B.    Inovio Acquisition Corporation, a Delaware corporation, converted into Submerger on October 31, 2008, and Submerger is a successor to Inovio Acquisition Corporation.

        C.    Upon the terms and subject to the conditions of this Agreement and in accordance with the Delaware General Corporation Law (the " DGCL "), Inovio, Submerger and VGX will enter into a business combination pursuant to which VGX will be merged with and into Submerger (the " Merger ") and upon consummation of the Merger, VGX will cease to exist and Submerger will continue as the surviving entity and as a wholly owned subsidiary of Inovio and change its name to VGX Pharmaceuticals, LLC.

        D.    The VGX Board (i) has determined that the Merger and the transactions contemplated hereby are fair to, advisable and in the best interests of, VGX and its stockholders, (ii) has approved this Agreement, the Merger and the other transactions contemplated by this Agreement and (iii) has determined, subject to the terms of this Agreement, to recommend the approval of this Agreement and the Merger by the VGX Stockholders.

        E.    The Inovio Board (i) has determined that the Merger and the other transactions contemplated hereby are fair to, advisable and in the best interests of, Inovio and its stockholders, (ii) has approved this Agreement, the Merger and the other transactions contemplated by this Agreement and (iii) has determined, subject to the terms of this Agreement, to recommend the approval of this Agreement and the Merger by the Inovio Stockholders.

        F.     As a result of the Merger, among other things, (i) all of the issued and outstanding VGX Common Stock as of the Effective Time shall be canceled and converted into the right to receive the consideration as set forth herein, (ii) all outstanding VGX Options as of the Effective Time shall be assumed by Inovio and converted into options to purchase Inovio Common Stock on the terms set forth herein, (iii) all outstanding VGX Warrants as of the Effective Time shall be assumed by Inovio and converted into warrants to purchase Inovio Common Stock on the terms set forth herein and (iv) all outstanding VGX Convertible Debt as of the Effective Time shall be assumed and converted into debt convertible into Inovio Common Stock on the terms set forth herein.

        G.    Promptly after the execution and delivery of this Agreement, each of the persons and entities identified in Exhibit A (the " VGX Support Stockholders ") shall enter into a voting agreement substantially in the form attached hereto as Exhibit B (the " Support Stockholder Voting Agreement "), which Support Stockholder Voting Agreement shall when executed (i) become effective without any action on the part of Inovio, Submerger, VGX or the VGX Support Stockholders immediately upon the VGX Solicitation Date and (ii) bind the VGX Support Stockholders to vote their shares of VGX Common Stock for approval of the VGX Voting Proposal.

A-1


        H.    The Merger is intended to qualify as a reorganization within the meaning of Section 368(a) of the Code, and this Agreement is intended to constitute a "plan of reorganization" within the meaning of the regulations promulgated under Section 368 of the Code.

         NOW, THEREFORE , in consideration of the covenants, promises and representations set forth herein, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties, intending to be legally bound, agree as follows:

ARTICLE I
THE PLAN OF MERGER

        1.1     The Merger .    At the Effective Time, upon the terms and subject to the conditions set forth in this Agreement and in accordance with the applicable provisions of the DGCL, VGX shall be merged with and into Submerger, the separate existence of VGX shall thereupon cease and Submerger shall continue as the surviving entity and as a wholly owned subsidiary of Inovio and shall change its name to VGX Pharmaceuticals, LLC. VGX Pharmaceuticals, LLC, as the surviving entity after the Merger, is sometimes referred to herein as the " Surviving Entity ".

        1.2     The Closing .    Upon the terms and subject to the conditions set forth in Article VI of this Agreement, the closing of the transactions contemplated hereby (the " Closing ") shall take place as promptly as practicable (but in no event later than the second business day) after the satisfaction or waiver of the conditions set forth in Article VI of this Agreement (other than those that by their terms are to be satisfied or waived at the Closing, which shall be satisfied or waived at the Closing), or such other date upon which the parties hereto shall mutually agree (the " Closing Date "), at the offices of K&L Gates LLP at 10100 Santa Monica Boulevard, 7 th  Floor, Los Angeles, California 90067, or such other date, time and/or location upon which the parties hereto shall mutually agree. The Closing may occur by the exchange of documents by facsimile or other electronic means.

        1.3     Effective Time of the Merger.     Subject to the provisions of this Agreement, the parties hereto shall cause the Merger to be consummated by filing a certificate of merger (the " Certificate of Merger ") with the Secretary of State of the State of Delaware in such form as is required by, and executed and acknowledged in accordance with, the relevant provisions of the DGCL and making all other filings or recordings required under the DGCL to effect the Merger. The Certificate of Merger, when duly filed with the Secretary of State of the State of Delaware in accordance with the relevant provisions of the DGCL, shall state an effective date for the Merger of the same date as the Closing Date and the effective time of the Merger shall be the same time as the time when the Closing is completed, unless the parties hereto shall mutually agree to a different date and time for filing and effectiveness. The effective time of the Merger is sometimes referred to herein as the " Effective Time ."

        1.4     General Effects of the Merger .    From and after the Effective Time, the Merger shall have all of the effects provided in this Agreement, the Certificate of Merger and applicable law, including the provisions of the DGCL. Without limiting the generality of the foregoing, and subject thereto, at the Effective Time, all the property, rights, privileges, powers and franchises of Submerger and VGX, respectively, shall vest in the Surviving Entity, and all debts, liabilities and duties of Submerger and VGX, respectively, shall become the debts, liabilities and duties of the Surviving Entity, with the VGX Options, VGX Warrants, VGX Convertible Debt, Other VGX Rights and VGX Debt treated in accordance with Section 1.7 hereof.

        1.5     Surviving Entity Certificate of Formation and Operating Agreement.     

A-2


        1.6     Manager, Directors and Officers.     

        1.7     Effect of Merger on VGX Securities.     

A-3


A-4


A-5


A-6


        (j)     Other Rights to VGX Common Stock .    Inovio and VGX agree that at the Effective Time any contractual rights to receive shares of VGX Common Stock, other than the VGX Options, VGX Warrants and VGX Convertible Debt (which shall be assumed and converted in accordance with Sections 1.7(b) and (c) hereof) (" Other VGX Rights "), shall cease to represent a right to receive shares of VGX Common Stock in accordance with the terms and conditions of the contract providing such Other VGX Right and shall be converted into a right to receive a number of shares of Inovio Common Stock equal to (A) the number of shares of VGX Common Stock subject to such Other VGX Right immediately prior to the Effective Time multiplied by (B) the Merger Exchange Ratio, in accordance with the terms and conditions of the contract providing such Other VGX Right.

        1.8     Dissenting Shares.     

A-7


        1.9     Exchange Procedures; Surrender of Certificates.     

A-8


        1.10     No Further Ownership Rights in VGX Common Stock or Interest in Surviving Entity .    The Merger Consideration paid pursuant to the Merger upon the surrender for exchange of shares of VGX Common Stock in accordance with the terms hereof shall be deemed to have been paid in full satisfaction of all rights pertaining to such shares of VGX Common Stock, and there shall be no further registration of transfers on the records of the Surviving Entity of shares of VGX Common Stock that were outstanding immediately prior to the Effective Time nor any allocation of membership interests in the Surviving Entity with respect to such shares of VGX Common Stock. If, after the Effective Time, Certificates are presented to the Surviving Entity for any reason, they shall be canceled and exchanged as provided in this Article I.

        1.11     Lost, Stolen or Destroyed Certificates .    In the event any Certificates evidencing shares of VGX Common Stock shall have been lost, stolen or destroyed, the Exchange Agent shall deliver in exchange for such lost, stolen or destroyed Certificates, upon receiving notice from the holder thereof and upon the making of an affidavit of that fact by such holder, such amount as may be required pursuant to Section 1.7 hereof; provided, however, that Inovio may, in its discretion and, as a condition precedent to the issuance thereof, require the owner of such lost, stolen or destroyed Certificates to deliver an agreement of indemnity against any claim that may be made against Inovio, the Exchange Agent or the Surviving Entity with respect to the Certificates alleged to have been lost, stolen or destroyed.

        1.12     Further Action .    At and after the Effective Time, the officers and directors of Inovio and the Surviving Entity will be authorized to execute and deliver, in the name and on behalf of VGX and the Submerger, as the case may be, any deeds, bills of sale, assignments or assurances and to take and do, in the name and on behalf of VGX and the Submerger, any other actions and things to vest, perfect or confirm of record or otherwise in the Surviving Entity any and all right, title and interest in, to and

A-9



under any of the rights, properties or assets acquired or to be acquired by the Surviving Entity as a result of, or in connection with, the Merger.

        1.13     Effect of Merger on Inovio Securities .    The Closing shall not have any effect on the Inovio Securities outstanding prior to the Effective Time, except that the Closing shall constitute a "Change of Control" or "Change in Control" as such terms are used in the Inovio Incentive Plans and related agreement, in the Inovio Charter Documents and in the Inovio Warrants, resulting in:

ARTICLE II
REPRESENTATIONS AND WARRANTIES OF VGX

        VGX represents and warrants to Inovio and Submerger, subject to such exceptions and disclosures as set forth in the disclosure letter supplied by VGX to Inovio and Submerger dated as of the date of the Prior Agreement and an updated disclosure letter as of the date hereof (together, the " VGX Disclosure Letter "), as follows:

        2.1     Organization; Standing and Power; Charter Documents; Subsidiaries.     

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        2.2     Capital Structure.     

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        2.3     Authority; Non-Contravention; Necessary Consents.     

        2.4     Records; Financial Information.     

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        2.5     Absence of Certain Changes or Events.     Since the date of VGX Balance Sheet, VGX and each of its Subsidiaries has conducted its business in the ordinary course consistent with past practice and, since such date, (i) with respect to VGX and its Subsidiaries other than VGXI there has not been or (ii) with respect to VGXI only, to the Knowledge of VGX, there has not been nor has VGX been asked to act in any management or stockholder capacity to allow for or approve:

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        2.6     Taxes.     

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        2.7     Intellectual Property.     

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        2.8     Regulatory Compliance; Permits.     

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        2.9     Litigation.     There are no claims, suits, actions or proceedings (" Legal Proceedings ") pending or, to the Knowledge of VGX, threatened against VGX or any of its Subsidiaries or any of their respective properties or relating to any of the executive officers and directors of VGX or any of its Subsidiaries in their capacity as such, before any court, Governmental Entity, or any arbitrator that seeks to restrain, enjoin or prevent the consummation of the transactions contemplated hereby or which, if adversely decided, would reasonably be expected, either individually or in the aggregate with all such claims, actions or proceedings, to be material to VGX or any of its Subsidiaries. Section 2.9 of VGX Disclosure Letter further sets forth a list as of the date hereof of all litigation settlement agreements to which VGX or any of its Subsidiaries is a party.

        2.10     Brokers' and Finders' Fees; Fees and Expenses.     VGX has not incurred, nor will it incur, directly or indirectly, any liability for brokerage or finders' fees or agents' commissions or any similar charges in connection with this Agreement or the transactions contemplated hereby.

        2.11     Employee Matters and Benefit Plans.     

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        2.12     Title to Properties.     

        2.13     Environmental Matters.     

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        2.14     Contracts.     

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        2.15     Board Approval.     As of the date hereof, the VGX Board has, by resolutions duly adopted at a meeting duly called and held and not subsequently rescinded or modified in any way, (i) determined the Merger to be advisable, (ii) approved this Agreement and the transactions contemplated thereby, including the Merger, and (iii) recommended that the VGX Stockholders approve this Agreement and the Mergers and directed that such matters be submitted to the VGX Stockholders for approval.

        2.16     Transactions with Related Parties.     As of the date hereof, VGX is not a party to any transaction of the type described in Item 404(a) of Regulation S-K of the rules and regulations of the SEC.

        2.17     Insurance.     

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        2.18     Liabilities.     Neither VGX nor any of its Subsidiaries has any liabilities (absolute, accrued, contingent or otherwise) of a nature required by US GAAP to be disclosed on a consolidated balance sheet or in the related notes thereto, or any off-balance sheet liabilities, other than (a) any liabilities which did not have or would not have had, individually or in the aggregate, a Material Adverse Effect on VGX or any of its Subsidiaries, and (b) liabilities incurred in connection with the transactions contemplated hereby.

        2.19     Product Claims.     To the Knowledge of VGX, there has not been any claim under any contractual warranty, guaranty or other indemnity, or any claims of product liability arising from allegations of personal injury, property damage, or medical malpractice, with respect to the VGX Products or services of VGX or its Subsidiaries through the date hereof.

        2.20     Accounts Receivable.     As of the date hereof, VGX does not reasonably expect that the collections rate of its currently outstanding accounts receivable will be materially worse than its historical collection rate.

        2.21     Anti-Takeover Statute Not Applicable.     No "business combination," "fair price," "moratorium," "control share acquisition" or other similar anti-takeover statute or regulation under the laws of the State of Delaware is applicable to VGX, the shares of VGX Common Stock or other VGX Securities, the Merger or any of the other transactions contemplated by this Agreement.

        2.22     Foreign Corrupt Practices.     Neither VGX nor any of its Subsidiaries nor, to the knowledge of VGX, any director, officer, agent, employee or other Person acting on behalf of VGX or any of its Subsidiaries has, in the course of its actions for, or on behalf of, VGX or its Subsidiaries (a) used any corporate funds of VGX or any of its Subsidiaries for any unlawful contribution, gift, entertainment or other unlawful expenses relating to political activity; (b) made any direct or indirect unlawful payment to any foreign or domestic government official or employee from corporate funds; (c) violated or is in violation of any provision of the U.S. Foreign Corrupt Practices Act of 1977, as amended; or (d) made any unlawful bribe, rebate, payoff, influence payment, kickback or other unlawful payment to any foreign or domestic government official or employee.


ARTICLE III
REPRESENTATIONS AND WARRANTIES OF INOVIO AND SUBMERGER

        Inovio and Submerger represent and warrant to VGX, subject to such exceptions and disclosures as set forth in the disclosure letter supplied by Inovio to VGX dated as of the date of the Prior

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Agreement and an updated disclosure letter as of the date hereof (together, the " Inovio Disclosure Letter "), as follows:

        3.1     Organization; Standing and Power; Charter Documents; Subsidiaries.     

        3.2     Capital Structure.     

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        3.3     Authority; Non-Contravention; Necessary Consents.     

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        3.4     Records; SEC Reports; Financial Statements; Controls.     

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        3.5     Absence of Certain Changes or Events.     Since the date of the most recent SEC Report, Inovio has conducted its business in the ordinary course consistent with past practice and, since such date, there has not been:

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        3.6     Tax Returns and Audits.     

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        3.7     Intellectual Property.     

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        3.8     Regulatory Compliance; Permits.     

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        3.9     Litigation.     There are no Legal Proceedings pending or, to the Knowledge of Inovio, threatened against Inovio or any of its Subsidiaries or any of their respective properties or relating to any of the executive officers and directors of Inovio or any of its Subsidiaries in their capacity as such, before any court, Governmental Entity, or any arbitrator that seeks to restrain, enjoin or prevent the consummation of the transactions contemplated hereby or which, if adversely decided, would reasonably be expected, either individually or in the aggregate with all such claims, actions or proceedings, to be material to Inovio or any of its Subsidiaries. Section 3.9 of Inovio Disclosure Letter further sets forth a list as of the date hereof of all litigation settlement agreements to which Inovio or any of its Subsidiaries is a party.

        3.10     Brokers' and Finders' Fees; Fees and Expenses.     Inovio has not incurred, nor will it incur, directly or indirectly, any liability for brokerage or finders' fees or agents' commissions or any similar charges in connection with this Agreement or the transactions contemplated hereby.

        3.11     Employee Matters and Benefit Plans.     

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        3.12     Title to Properties.     

        3.13     Environmental Matters.     

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        3.14     Contracts.     

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        3.15     Board Approval.     As of the date hereof, the Inovio Board has, by resolutions duly adopted at a meeting duly called and held and not subsequently rescinded or modified in any way, (i) determined the Merger to be advisable, (ii) approved this Agreement and the transactions contemplated thereby, including the Merger, and (iii) recommended that the Inovio Stockholders approve this Agreement and the Mergers and directed that such matters be submitted to the Inovio Stockholders for approval.

        3.16     Transactions with Related Parties.     As of the date hereof, Inovio is not a party to any transaction of the type described in Item 404(a) of Regulation S-K of the rules and regulations of the SEC.

        3.17     Insurance.     

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        3.18     Liabilities.     Except as disclosed in Section 3.18 of the Inovio Disclosure Letter, since the date of the most recent SEC Report prior to the date hereof, neither Inovio nor any of its Subsidiaries has any liabilities (absolute, accrued, contingent or otherwise) of a nature required by US GAAP to be disclosed on a consolidated balance sheet or in the related notes thereto, or any off-balance sheet liabilities, other than (i) any liabilities which did not have or would not have had, individually or in the aggregate, a Material Adverse Effect on Inovio, (ii) liabilities incurred in the ordinary course of business and (iii) liabilities incurred in connection with the transactions contemplated hereby.

        3.19     Product Claims.     To the Knowledge of Inovio, there has not been any claim under any contractual warranty, guaranty or other indemnity, or any claims of product liability arising from allegations of personal injury, property damage, or medical malpractice, with respect to the products or services of Inovio or its Subsidiaries through the date hereof.

        3.20     Accounts Receivable.     As of the date hereof, Inovio does not reasonably expect that the collections rate of its currently outstanding accounts receivable will be materially worse than its historical collection rate.

        3.21     Anti-Takeover Statute Not Applicable.     No "business combination," "fair price," "moratorium," "control share acquisition" or other similar anti-takeover statute or regulation under the laws of the State of Delaware is applicable to Inovio, the shares of Inovio Common Stock or other Inovio Securities, the Merger or any of the other transactions contemplated by this Agreement.

        3.22     Foreign Corrupt Practices.     Neither Inovio nor any of its Subsidiaries nor, to the knowledge of Inovio, any director, officer, agent, employee or other Person acting on behalf of Inovio or any of its Subsidiaries has, in the course of its actions for, or on behalf of, Inovio or its Subsidiaries (i) used any corporate funds for any unlawful contribution, gift, entertainment or other unlawful expenses relating to political activity; (ii) made any direct or indirect unlawful payment to any foreign or domestic government official or employee from corporate funds; (iii) violated or is in violation of any provision of the U.S. Foreign Corrupt Practices Act of 1977, as amended; or (iv) made any unlawful bribe, rebate, payoff, influence payment, kickback or other unlawful payment to any foreign or domestic government official or employee.

        3.23     Listing and Maintenance Requirements.     Inovio has not, in the twelve months preceding the date hereof, received notice (written or oral) from the NYSE Alternext to the effect that Inovio is not in compliance with the listing or maintenance requirements of such market.

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        3.24     Opinion of Financial Advisor.     Inovio's Board of Directors has received an opinion from Oppenheimer & Co. Inc. to the effect that, as of the date of such opinion specified therein, the Merger Exchange Ratio is fair to Inovio from a financial point of view.

        3.25     Operations of Submerger.     Submerger is a direct, wholly owned subsidiary of Inovio, formed solely for the purpose of engaging in the transactions contemplated by this Agreement, and has engaged in no other business activities and has conducted its operations only as contemplated by this Agreement.


ARTICLE IV
CONDUCT PRIOR TO THE EFFECTIVE TIME

        4.1     Conduct of Business of VGX and its Subsidiaries.     

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        4.2     Conduct of Business of Inovio and its Subsidiaries.     

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        4.3     Sale of Assets; Reduction of VGX Convertible Debt.     Notwithstanding anything to contrary in this Article IV , VGX may take all necessary actions to fulfill its obligations under that certain Asset Purchase Agreement between VGX and VGXI, Inc. dated as of June 10, 2008, as provided as Schedule 4.3 hereof, including transfer of the assets identified to be transferred therein (including the schedules and exhibits to such agreement) (the " Transferred Assets "), without any further written consent from Inovio, provided, however (i) VGX shall receive at least $7,750,000 in aggregate in cash from VGXI, Inc. in consideration of the sale of the Transferred Assets; (ii) regardless of the timing of actual receipt of proceeds for the Transferred Assets from VGXI, Inc., VGX shall reduce an aggregate of $7,750,000 owed pursuant to the VGX Convertible Debt outstanding as of the date of the Prior Agreement, as such VGX Convertible Debt becomes due and payable, and (iii) VGX shall perform its obligations under and maintain the agreement dated June 25, 2008 between VGXI, Inc. and VGX pursuant to which VGXI shall manufacture and supply product to VGX for preclinical studies and/or clinical trials use and future commercialization (the " Manufacturing Agreement ").


ARTICLE V
ADDITIONAL AGREEMENTS

        5.1     Registration Pursuant to the Securities Act.     Inovio shall use commercially reasonable efforts to prepare and, within forty-five (45) business days of the date of this Agreement file with the SEC a registration statement on Form S-4 to register the offer and sale of Inovio Common Stock in the Merger, including registering the assumption of and shares of Inovio Common Stock underlying the VGX Options, VGX Warrants and VGX Convertible Debt (the " Registration Statement "). The Registration Statement will include (i)(a) prospectus with respect to the Inovio Common Stock, Inovio Options, Inovio Warrants and other Inovio securities, if any, to be issued in the Merger (the " Prospectus "), (b) proxy materials which shall constitute the proxy statement for the Inovio Stockholders' Meeting, including description of the Additional Inovio Proposals (the " Inovio Proxy Statement "), and (iii) proxy materials which shall constitute the proxy statement for the VGX Stockholders' Meeting (the " VGX Proxy Statement "; the Prospectus, Inovio Proxy Statement and VGX Proxy Statement together, and any amendments or supplements thereto, the " Proxy Statement/Prospectus "). VGX and its counsel shall be given reasonable opportunity to review, comment on and approve, which approval shall not be unreasonably withheld, the Registration Statement prior to the filing thereof with the SEC. Inovio shall accept all reasonable comments provided to the Registration Statement by VGX. Inovio agrees to provide in writing to VGX and its counsel any comments Inovio or its counsel may receive from the SEC or its staff with respect to the Registration Statement promptly after receipt of such comments and shall provide VGX and its counsel with a reasonable opportunity to participate in the response of Inovio to such comments. Inovio will respond to any comments from the SEC on the Registration Statement, and VGX will work with Inovio in good faith to answer any comments from the SEC in a timely manner. Inovio shall provide VGX with copies of any written responses to the SEC or its staff and shall notify VGX with respect to any oral responses to the SEC or its staff. Inovio will work in good faith and use all reasonable efforts to have the Registration Statement declared effective as soon as practicable after the Form S-4 Filing Date and to maintain such effectiveness for so long as shall be required for the issuance of the Merger Consideration pursuant to the Merger; provided , however , that no party shall be required to modify any of the terms of this Agreement or the Merger, or the transactions contemplated hereby, in order to have the Registration Statement declared effective. Within two (2) business days following the

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Registration Effective Date, Inovio shall file the final Proxy Statement/Prospectus included therein under Rule 424(b) promulgated pursuant to the Securities Act.

        5.2     Solicitation Pursuant to the Exchange Act.     

        5.3     VGX Stockholder Solicitation and Approval.     

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        5.4     VGX and Inovio Information.     

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        5.5     Confidentiality; Access to Information.     

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        5.6     No VGX Solicitation.     

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        5.7     No Inovio Solicitation.     

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        5.8     Public Disclosure.     Inovio and VGX will consult with each other and agree before issuing any press release, making any public statement or otherwise making any disclosure with respect to the Merger, this Agreement (including the VGX and Inovio Disclosure Letters), a VGX Acquisition Proposal or an Inovio Acquisition Proposal and will not issue any such press release or make any such public statement or other disclosure prior to such agreement, except to the extent necessary in order to comply with (i)  Section 5.9 (Regulatory Filings; Reasonable Efforts), (ii) applicable law or any listing agreement with a national securities exchange and (iii) seeking the consents and waivers necessary to consummate the transactions contemplated hereby. Each of Inovio and VGX acknowledge that public disclosures related to this Agreement and the Merger are subject to the limitations and filing requirements set forth by Rules 165 and 425 as promulgated under the Securities Act.

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        5.9     Regulatory Filings; Reasonable Efforts.     

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        5.10     Notification of Certain Matters.     

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        5.11     Employee Benefits.     

        5.12     Reservation of Shares.     Inovio shall take all corporate action necessary to reserve for issuance a sufficient number of shares of Inovio Common Stock for delivery upon exercise of the assumed and converted VGX Options and VGX Warrants, conversion of the assumed and converted VGX Convertible Debt and satisfaction of the converted Other VGX Rights.

        5.13     Listing or Quotation.     

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        5.14     Continuation of Indemnification.     

        5.15     FIRPTA Compliance.     On the Closing Date, VGX shall deliver to Inovio a properly executed statement in a form reasonably acceptable to Inovio for purposes of satisfying Inovio's obligations under Treasury Regulation Section 1.1445-2(c)(3).

        5.16     Submerger Compliance.     Inovio shall cause Submerger to comply with all of its obligations under or relating to this Agreement. Prior to the Effective Time, Submerger shall not engage in any business which is not in connection with the Merger pursuant to this Agreement.

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        5.17     Certain Litigation.     From the date hereof, VGX shall use all reasonable efforts to provide Inovio with periodic updates (upon the request of Inovio) of the status and developments in the litigation referenced in Section 2.9 of the VGX Disclosure Letter. From the date hereof, Inovio shall use all reasonable efforts to provide VGX with periodic updates (upon the request of VGX) of the status and developments in the litigation referenced in Section 3.9 of the Inovio Disclosure Letter.

        5.18     Treatment as Reorganization.     The parties hereby adopt this Agreement as a "plan of reorganization" within the meaning of Section 1.368-2(g) and 1.368-3(a) of the United States Treasury Regulations. Each of Inovio, VGX and Submerger shall deliver officer's certificates as requested by counsel for purposes of rendering the opinions described in Section 6.1(g) hereto. Neither VGX nor Inovio has taken or will take any action, either before or after the Closing, which could cause the Merger to fail to qualify as a reorganization. The parties hereto shall timely satisfy or cause to be satisfied all applicable tax reporting and filing requirements with respect to the transactions contemplated hereby, including the reporting requirements of Treasury Regulations Section 1.368-3T.

        5.19     Financial Statements.     

        5.20     Affiliates.     Within ten (10) business days following the date of this Agreement, VGX shall deliver to Inovio a letter identifying all known Persons who, as known to VGX, would be deemed affiliates of the VGX for purposes of Rule 144 of the Securities Act (the " Affiliate Letter "), and VGX shall update such Affiliate Letter from time to time prior to the Effective Time if and when VGX learns that additional Persons would be deemed affiliates of VGX for such purposes. VGX shall use its reasonable efforts to obtain a written agreement from each Person who may be so deemed an affiliate for such purposes as soon as reasonably practicable and, in any event, prior to the Effective Time, substantially in the form of Exhibit D hereto. Inovio and Submerger acknowledge that the requirement in Section 5.20 of the Prior Agreement for delivery of the Affiliate Letter within ten (10) business days of the date of the Prior Agreement has been previously waived.

        5.21     Identification of Directors.     No later than five (5) business days prior to the Form S-4 Filing Date, (i) Inovio shall have identified and put forth to VGX the names of two (2) individuals from the Inovio Board as of the date of this Agreement and (ii) VGX shall have identified and put forth to Inovio the name of one (1) individual from the VGX Board as of the date of this Agreement, each to serve as directors of Inovio after the Closing. No later than five (5) business days prior to the filing of the first pre-effective amendment to the Registration Statement, each of Inovio and VGX shall have identified and put forth to the other party the name of one (1) additional individual from each of the Inovio Board and the VGX Board to serve as directors of Inovio after the Closing. At least two (2) of the individuals put forth by Inovio and one (1) of the individuals put forth by VGX must be "independent" pursuant to the rules and regulations of the NYSE Alternext and the Rule 10A-3(b) as promulgated under the Exchange Act. If a named individual is not satisfactory to the other party, the

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party shall notify the other party of its objections within two (2) business days and the nominating party shall identify an alternate individual promptly. No later than two (2) business days prior to the Form S-4 Filing Date, (a) each of Inovio and VGX shall have approved the initial four (4) individuals proposed as directors, and (b) each of the identified individuals shall have signed an acknowledgement indicating his or her consent to serve as a director for Inovio after the Closing and providing consent to being identified as a prospective director in the Registration Statement, the VGX Soliciting Materials and other Merger-related documentation. The two (2) additional individuals must provide such executed acknowledgment and consent no later than two (2) business days prior to the filing of the first pre-effective amendment to the Registration Statement. Inovio and VGX agree that one of the appointees from the Inovio Board shall serve as Chairman of the Board of Directors after Closing.

        5.22     Employment Agreements.     On or prior to the Effective Time, Inovio shall execute employment agreements with those individuals set forth on Schedule 5.22 for the positions and at the salary levels noted thereon, in substantially the form provided in Exhibits E, F, G, H and I as referenced in such Schedule (the " Closing Employment Agreements "), which shall solely become effective as of the Effective Time.

        5.23     No Severance Obligations.     Each party will use its reasonable best efforts to obtain appropriate agreements, acknowledgement or waivers from its officers and its Subsidiaries' officers that the Merger will not constitute a "Change of Control" or "Change in Control" within the meaning of their respective employment, change in control or other compensatory or employment-related agreements, other than as provided in Section 5.23(a).

        5.24     Expenses.     All fees and expenses incurred in connection with this Agreement and the transactions contemplated hereby shall be paid by the party incurring such expenses whether or not the Merger is consummated.

        5.25     Line of Credit.     Upon request of VGX subsequent to the Registration Effective Date and subject to approval of the Inovio Board at such time, Inovio shall provide VGX with a line of credit up to $2,000,000 for use to fund continuing operations, to be documented upon issuance with customary terms and conditions.

        5.26     Headquarters.     Inovio and VGX agree to use commercially reasonable efforts to maintain Inovio's headquarters in San Diego, California after the Effective Time.

ARTICLE VI
CONDITIONS TO THE MERGER

        6.1     Conditions to Obligations of Each Party to Effect the Merger.     The respective obligations of each party to this Agreement to effect the Merger shall be subject to the satisfaction at or prior to the Effective Time of the following conditions, any of which may be waived, in writing, solely by VGX and Inovio together, except as otherwise noted below:

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        6.2     Additional Conditions to Obligations of VGX.     The obligation of VGX to consummate and effect the Merger shall be subject to the satisfaction at or prior to the Effective Time of each of the following conditions, any of which may be waived, in writing, exclusively by VGX:

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        6.3     Additional Conditions to the Obligations of Inovio.     The obligations of Inovio to consummate and effect the Merger shall be subject to the satisfaction at or prior to the Effective Time of each of the following conditions, any of which may be waived, in writing, exclusively by Inovio:

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ARTICLE VII
TERMINATION, AMENDMENT AND WAIVER

        7.1     Termination.     This Agreement may be terminated at any time prior to the Effective Time, by action taken or authorized by the board of directors of the terminating party or parties as provided below, whether before or after the requisite approvals of the VGX Stockholders and/or the Inovio Stockholders:

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        7.2     Notice of Termination; Effect of Termination.     Any termination of this Agreement under Section 7.1 above will be effective immediately upon the delivery of written notice of the terminating party to the other parties hereto (or such later time as may be contemplated by Sections 7.1(b), (d), (e) ). In the event of the termination of this Agreement as provided in Section 7.1 , this Agreement shall be of no further force or effect and no party hereto shall have any liability hereunder, except (i) as set forth in Section 5.5(a) , this Section 7.2 , Section 7.3 , and Article IX (General Provisions), each of which shall survive the termination of this Agreement, and (ii) nothing herein shall relieve any party from liability for any willful breach of this Agreement. This Section 7.2 shall not impair the right of any party to compel specific performance by another party of its obligations hereunder.

        7.3     Amendment.     Subject to applicable law, this Agreement may be amended by the parties hereto at any time by execution of an instrument in writing signed on behalf of each of the parties hereto.

        7.4     Extension; Waiver.     At any time prior to the Effective Time any party hereto may, to the extent legally allowed, (i) extend the time for the performance of any of the obligations or other acts of the other parties hereto, (ii) waive any inaccuracies in the representations and warranties made to such party contained herein or in any document delivered pursuant hereto and (iii) waive compliance with any of the agreements or conditions for the benefit of such party contained herein. Any agreement on the part of a party hereto to any such extension or waiver shall be valid only if set forth in an instrument in writing signed on behalf of such party. Delay in exercising any right under this Agreement shall not constitute a waiver of such right. To the extent that any matter disclosed in the VGX Disclosure Letter, as updated from the disclosure letter of VGX attached to the Prior Agreement, would have constituted a breach of Section 4.1 of the Prior Agreement, Inovio and Submerger hereby waive such breach. In addition, to the extent that any matter disclosed in the Inovio Disclosure Letter, as updated from the disclosure letter of Inovio and Submerger attached to the Prior Agreement, would have constituted a breach of Section 4.2 of the Prior Agreement, VGX hereby waives such breach.

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        7.5     Termination Payments.     In the event that this Agreement is terminated by Inovio pursuant to Section 7.1(g) , Inovio shall promptly, but in no event later than two (2) business days after the date of such event, pay VGX a fee equal to $3,500,000 in immediately available funds and such payment shall be the sole and exclusive remedy relating therewith. In the event that this Agreement is terminated by VGX pursuant to Section 7.1(f) , VGX shall promptly, but in no event later than two (2) business days after the date of such event, pay Inovio a fee equal to $3,500,000 in immediately available funds and such payment shall be the sole and exclusive remedy relating therewith.

ARTICLE VIII
[RESERVED]

ARTICLE IX
GENERAL PROVISIONS

        9.1     Survival of Representations and Warranties.     The representations and warranties contained in this Agreement shall survive until the Effective Time; provided, however, that the foregoing shall not affect the date the representations and warranties set forth herein are deemed made.

        9.2     Certain Definitions.     For all purposes of and under this Agreement, the following terms shall have the following respective meanings:

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        9.3     Notices.     All notices and other communications hereunder shall be in writing and shall be deemed duly given (i) on the date of delivery if delivered personally, (ii) on the date of confirmation of receipt (or, the first business day following such receipt if the date is not a business day or if sent after business hours) of transmission by telecopy, facsimile, or electronic mail, or (iii) on the date of confirmation of receipt (or, the first business day following such receipt if the date is not a business day) if delivered by a nationally recognized courier service. All notices hereunder shall be delivered as set forth below, or pursuant to such other instructions as may be designated in writing by the party to receive such notice:

    Inovio Biomedical Corporation
11494 Sorrento Valley Road
San Diego, California 92121-1318
    Attention:   Dr. Avtar Dhillon
Peter Kies
    Facsimile: (858) 597-0451

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K&L Gates LLP
10100 Santa Monica Boulevard, 7 th  Floor
Los Angeles, CA 90067
    Attention:   Thomas J. Poletti, Esq.
Shoshannah Katz, Esq.
    Facsimile:  (310) 552-5001/(310) 552-5008
    VGX Pharmaceuticals, Inc.
450 Sentry Parkway
Blue Bell, PA 19422
    Attention:   Dr. J. Joseph Kim
Gene Kim
    Facsimile:  (267) 440-4242
    Duane Morris LLP
30 South 17th Street
Philadelphia, PA 19103-4196
    Attention:   Kathleen Shay, Esq.
Sandra G. Stoneman, Esq.
    Facsimile:  (215) 979-1020

        9.4     Interpretation.     When a reference is made in this Agreement to Exhibits, such reference shall be to an Exhibit to this Agreement unless otherwise indicated. The words " include ," " includes " and " including " when used herein shall be deemed in each case to be followed by the words " without limitation ." The table of contents and headings contained in this Agreement are for reference purposes only and shall not affect in any way the meaning or interpretation of this Agreement. When reference is made herein to " the business of " an entity, such reference shall be deemed to include the business of all direct and indirect Subsidiaries of such entity. Reference to the Subsidiaries of an entity shall be deemed to include all direct and indirect Subsidiaries of such entity.

        9.5     Counterparts.     This Agreement may be executed in one or more counterparts, all of which shall be considered one and the same agreement and shall become effective when one or more counterparts have been signed by each of the parties and delivered to the other party, it being understood that all parties need not sign the same counterpart.

        9.6     Entire Agreement; Third Party Beneficiaries.     This Agreement and the documents and instruments and other agreements among the parties hereto as contemplated by or referred to herein, including the VGX Disclosure Letter and the Inovio Disclosure Letter: (a) constitute the entire agreement among the parties with respect to the subject matter hereof and supersede all prior agreements and understandings, both written and oral, among the parties with respect to the subject matter hereof including, without limitation, that certain Indicative Proposal dated March 14, 2008 addressed to Inovio from VGX; it being understood that the Confidentiality Agreement shall continue in full force and effect until the Closing and shall survive any termination of this Agreement in accordance with its terms; and (b) are not intended to confer upon any other person any rights or remedies hereunder, except the persons specified in Section 5.14 . This Agreement amends and restates, and replaces and supersedes in its entirety, the Prior Agreement.

        9.7     Severability.     In the event that any provision of this Agreement or the application thereof, becomes or is declared by a court of competent jurisdiction to be illegal, void or unenforceable, the

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remainder of this Agreement will continue in full force and effect and the application of such provision to other persons or circumstances will be interpreted so as reasonably to effect the intent of the parties hereto. The parties further agree to replace such void or unenforceable provision of this Agreement with a valid and enforceable provision that will achieve, to the extent possible, the economic, business and other purposes of such void or unenforceable provision.

        9.8     Other Remedies; Specific Performance.     Except as otherwise provided herein, any and all remedies herein expressly conferred upon a party will be deemed cumulative with and not exclusive of any other remedy conferred hereby, or by law or equity upon such party, and the exercise by a party of any one remedy will not preclude the exercise of any other remedy. The parties hereto agree that irreparable damage would occur in the event that any of the provisions of this Agreement were not performed in accordance with their specific terms or were otherwise breached. It is accordingly agreed that the parties shall be entitled to seek an injunction or injunctions to prevent breaches of this Agreement and to enforce specifically the terms and provisions hereof in any court of the United States or any state having jurisdiction, this being in addition to any other remedy to which they are entitled at law or in equity.

        9.9     Governing Law; Forum Selection.     

        9.10     Rules of Construction.     The parties hereto agree that they have been represented by counsel during the negotiation and execution of this Agreement and, therefore, waive the application of any law, regulation, holding or rule of construction providing that ambiguities in an agreement or other document will be construed against the party drafting such agreement or document.

        9.11     Assignment.     No party may assign either this Agreement or any of its rights, interests, or obligations hereunder without the prior written approval of the other parties and any such attempted assignment without such consent shall be null and void. Subject to the preceding sentence, this Agreement shall be binding upon and shall inure to the benefit of the parties hereto and their respective successors and permitted assigns.

        9.12     Waiver of Jury Trial.     TO THE EXTENT PERMISSIBLE BY LAW, EACH OF INOVIO, SUBMERGER AND VGX HEREBY IRREVOCABLY WAIVES ALL RIGHT TO TRIAL BY JURY IN ANY ACTION, PROCEEDING OR COUNTERCLAIM (WHETHER BASED ON CONTRACT, TORT OR OTHERWISE) ARISING OUT OF OR RELATING TO THIS AGREEMENT OR THE ACTIONS OF INOVIO, SUBMERGER OR VGX IN THE NEGOTIATION, ADMINISTRATION, PERFORMANCE AND ENFORCEMENT HEREOF.

        9.13     Time is of the Essence.     The parties hereby agree that time is of the essence in connection with this Agreement.

        9.14     Legal Representation.     The parties' respective legal rights and obligations and the practical and legal effects of this Agreement have been fully explained to each of the parties by his or her respective counsel, and each party acknowledges that it has sought and obtained independent legal advice from counsel of its own selection; that each fully understands its legal rights and obligations; and that having had such advice and with such knowledge, each party clearly understands and assents to all the provisions hereof and each of them is signing this Agreement freely and voluntarily.

[ Remainder of page intentionally left blank ]

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        IN WITNESS WHEREOF, the undersigned have caused this Agreement to be executed by their duly authorized respective officers, as of the date first written above.

    INOVIO BIOMEDICAL CORPORATION

 

 

By:

 

/s/ AVTAR S. DHILLON

    Name:   Dr. Avtar Dhillon
    Title:   Chief Executive Officer

 

 

INOVIO ACQUISITION, LLC

 

 

By:

 

/s/ AVTAR S. DHILLON

    Name:   Dr. Avtar Dhillon
    Title:   Chief Executive Officer

 

 

VGX PHARMACEUTICALS, INC.

 

 

By:

 

/s/ J. JOSEPH KIM

    Name:   Dr. J. Joseph Kim
    Title:   Chief Executive Officer

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ANNEX B

[LETTERHEAD OF OPPENHEIMER & CO. INC.]

July 2, 2008

The Board of Directors
Inovio Biomedical Corporation
11494 Sorrento Valley Road
San Diego, California 92121-1318

Members of the Board:

        You have asked Oppenheimer & Co. Inc. ("Oppenheimer") to render a written opinion ("Opinion") to the Board of Directors of Inovio Biomedical Corporation ("Inovio") as to the fairness, from a financial point of view, to Inovio of the Exchange Ratio (as defined below) provided for in an Agreement and Plan of Merger (such agreement, the "Merger Agreement") to be entered into among Inovio, Inovio Acquisition Corporation, a wholly owned subsidiary of Inovio ("Merger Sub"), and VGX Pharmaceuticals, Inc. ("VGX"). The Merger Agreement provides for, among other things, the merger of Merger Sub with and into VGX (the "Merger"), as a result of which VGX will become a wholly owned subsidiary of Inovio and each outstanding share of the common stock, par value $0.0001 per share, of VGX ("VGX Common Stock") will be converted into the right to receive a number of shares of the common stock, par value $0.001 per share, of Inovio ("Inovio Common Stock") equal to the quotient obtained by dividing (a) the sum of the total number of outstanding shares of Inovio Common Stock plus the total number of shares of Inovio Common Stock issuable upon (i) conversion of outstanding shares of the preferred stock of Inovio, (ii) exercise of outstanding options to purchase Inovio Common Stock, whether vested or unvested, issued pursuant to Inovio's incentive plans and (iii) exercise of outstanding warrants to purchase Inovio Common Stock, by (b) the sum of the total number of outstanding shares of VGX Common Stock plus the total number of shares of VGX Common Stock issuable upon (i) exercise of outstanding options and other compensatory rights to acquire VGX Common Stock, whether vested or unvested, and (ii) exercise of outstanding warrants to purchase VGX Common Stock (such resulting quotient, the "Exchange Ratio"). The Merger Agreement further provides that, immediately subsequent to the effective time of the Merger, a portion of the outstanding convertible debt of VGX will be converted into shares of Inovio Common Stock at a conversion price equal to the average of the closing prices of Inovio Common Stock for the 10 trading-day period ending on the trading day prior to public announcement of the execution of the Merger Agreement (the "VGX Convertible Debt Conversion").

        In arriving at our Opinion, we:

(a)
reviewed a draft, dated July 1, 2008, of the Merger Agreement;

(b)
reviewed audited financial statements of Inovio and VGX for fiscal years ended December 31, 2007, 2006 and 2005 and unaudited financial statements of Inovio and VGX for the three months ended March 31, 2008;

(c)
reviewed historical market prices and trading volumes of Inovio Common Stock;

(d)
held discussions with the senior managements of Inovio and VGX with respect to the businesses and prospects of Inovio and VGX;

(e)
reviewed and analyzed the market values of companies that we deemed relevant in evaluating Inovio and VGX;

(f)
reviewed and analyzed publicly available financial terms of transactions that we deemed relevant in evaluating the Merger;

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(g)
reviewed and analyzed publicly available financial terms of licensing transactions that we deemed relevant in evaluating the product candidates of Inovio and VGX;

(h)
discussed with the management of Inovio its assessments as to the anticipated pro forma funding needs of, and cash available to, Inovio;

(i)
reviewed public information concerning Inovio and VGX; and

(j)
performed such other analyses, reviewed such other information and considered such other factors as we deemed appropriate.

        In rendering our Opinion, we relied upon and assumed, without independent verification or investigation, the accuracy and completeness of all of the financial and other information provided to or discussed with us by Inovio, VGX and their respective employees, representatives and affiliates or otherwise reviewed by us. We have been advised that financial forecasts relating to Inovio and VGX have not been prepared by the managements of Inovio and VGX and, accordingly, we have not undertaken an analysis of the future financial performance of Inovio and VGX. We have assumed, with the consent of Inovio, that the final terms of the Merger Agreement will not vary materially from those set forth in the draft reviewed by us. We also have assumed, with the consent of Inovio, that the Merger will qualify for federal income tax purposes as a tax-free reorganization under Section 368(a) of the Internal Revenue Code of 1986, as amended. We further have assumed, with the consent of Inovio, that the Merger and related transactions, including the (i) pending sale by VGX of certain assets relating to its DNA plasmid products for total cash consideration of $9,110,000 (the "Asset Sale") and the use of the proceeds therefrom and (ii) repayment of an aggregate of $7.75 million of the outstanding convertible debt of VGX not converted into Inovio Common Stock in the VGX Convertible Debt Conversion, as such debt becomes due and payable, will be consummated in accordance with their respective terms without waiver, modification or amendment of any material term, condition or agreement and in compliance with all applicable laws and other requirements and that, in the course of obtaining the necessary regulatory or third party approvals, consents and releases with respect to the Merger and related transactions, no delay, limitation, restriction or condition will be imposed that would have an adverse effect on Inovio, VGX or the contemplated benefits of the Merger. We have neither made nor obtained any independent evaluations or appraisals of the assets or liabilities, contingent or otherwise, of Inovio or VGX.

        Our opinion as set forth herein relates to the relative values of the fully diluted equity of Inovio and VGX after giving effect, in the case of VGX, to the VGX Convertible Debt Conversion. We are not expressing any opinion as to the underlying valuation, future performance or long-term viability of Inovio or VGX, the actual value of Inovio Common Stock when issued or the price at which Inovio Common Stock will trade at any time. We were not requested to, and we did not, participate in the negotiation or structuring of the Merger or any related transaction. We express no view as to, and our Opinion does not address, any terms or other aspects or implications of the Merger (other than the Exchange Ratio to the extent expressly specified herein) or any related transaction or any aspect or implication of any other agreement, arrangement or understanding entered into in connection with the Merger or otherwise, including, without limitation, the form or structure of the Merger or any related transaction, including the VGX Convertible Debt Conversion, or any terms or aspects of the Asset Sale or the use of the proceeds therefrom. We also express no view as to, and our Opinion does not address, the fairness of the amount or nature of, or any other aspect relating to, the compensation to be received by any individual officers, directors or employees of any parties to the Merger, or any class of such persons, relative to the Exchange Ratio. In addition, we express no view as to, and our Opinion

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does not address, the underlying business decision of Inovio to proceed with or effect the Merger nor does our Opinion address the relative merits of the Merger as compared to any alternative business strategies that might exist for Inovio or the effect of any other transaction in which Inovio might engage. Our Opinion is necessarily based on the information available to us and general economic, financial and stock market conditions and circumstances as they exist and can be evaluated by us on the date hereof. It should be understood that, although subsequent developments may affect this Opinion, we do not have any obligation to update, revise or reaffirm the Opinion.

        The issuance of this Opinion was approved by an authorized committee of Oppenheimer. As part of our investment banking business, we are regularly engaged in valuations of businesses and securities in connection with acquisitions and mergers, underwritings, secondary distributions of securities, private placements and valuations for other purposes.

        We have acted as financial advisor to Inovio solely for purposes of this Opinion and will receive a fee for our services, a portion of which was payable upon our engagement by Inovio and a significant portion of which will be payable upon delivery of this Opinion. We and our affiliates in the past have performed investment banking and other services for Inovio unrelated to the Merger, for which services we and our affiliates have received compensation, including financial advisory services to Inovio in connection with potential acquisition transactions in 2007. In the ordinary course of business, we and our affiliates may actively trade securities of Inovio for our and our affiliates' own accounts and for the accounts of customers and, accordingly, may at any time hold a long or short position in such securities.

        Based upon and subject to the foregoing, and such other factors as we deemed relevant, it is our opinion, that, as of the date hereof, the Exchange Ratio provided for in the Merger is fair, from a financial point of view, to Inovio. This Opinion is for the use of the Board of Directors of Inovio in its evaluation of the Merger and does not constitute a recommendation to any stockholder as to how such stockholder should vote or act with respect to any matters relating to the Merger.

  Very truly yours,

 

/s/ OPPENHEIMER & CO. INC.  

 

OPPENHEIMER & CO. INC.

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ANNEX C

STATE OF DELAWARE
CERTIFICATE OF MERGER OF
DOMESTIC CORPORATION INTO
DOMESTIC LIMITED LIABILITY COMPANY

        Pursuant to Title 8, Section 264(c) of the Delaware General Corporation Law and Title 6, Section 18-209 of the Limited Liability Company Act, the undersigned limited liability company executed the following Certificate of Merger:

        FIRST:     The name of the surviving limited liability company is Inovio Acquisition, LLC and the name of the corporation being merged into this surviving limited liability company is VGX Pharmaceuticals, Inc.

        SECOND:     The Agreement of Merger has been approved, adopted, certified, executed and acknowledged by the surviving limited liability company and the merging corporation.

        THIRD:     The name of the surviving limited liability company is VGX Pharmaceuticals, LLC.

        FOURTH:     The merger is to become effective on                                        .

        FIFTH:     The Agreement of Merger is on file at 11494 Sorrento Valley Rd. San Diego, CA 92121, the place of business of the surviving limited liability company.

        SIXTH:     A copy of the Agreement of Merger will be furnished by the surviving limited liability company on request, without cost, to any member of any constituent limited liability company or stockholder of any constituent corporation.

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         IN WITNESS WHEREOF, said limited liability company has caused this certificate to be signed by an authorized person, the                         day of                        , A.D.,            .

    By:     

        Authorized Person

 

 

Name:

 

Dr. Avtar Dhillon

        Print or Type

 

 

Title:

 

Chief Executive Officer

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ANNEX D

INOVIO BIOMEDICAL CORPORATION
AMENDED AND RESTATED 2000 STOCK OPTION PLAN
(as amended by the Board of Directors through July 2, 2008
with approvals by stockholders through [                                    ], 2008)

1.     INTERPRETATION     

         1.1    Defined Terms— For the purposes of this Plan, the following terms shall have the following meanings:

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2.     STATEMENT OF PURPOSE     

         2.1    Principal Purposes— The principal purposes of the Plan are to provide the Company and its shareholders with the advantages of the incentive inherent in stock ownership on the part of employees, officers, directors, and consultants responsible for the continued success of the Company; to create in such individuals a proprietary interest in, and a greater concern for, the welfare and success of the Company; to encourage such individuals to remain with the Company; and to attract new employees, officers, directors and consultants to the Company.

         2.2    ISOs and Non-ISOs— Under this Plan, the Company may grant either ISOs or Non-ISOs. Each ISO granted hereunder is intended to constitute an "incentive stock option," for the purposes of section 422 of the Code, and this Plan and each such ISO is intended to comply with all of the requirements of Section 422 of the Code and of all other provisions of the Code applicable to incentive stock options and to plans issuing the same. Each Non-ISO granted hereunder is intended to constitute an Option that is not an "incentive stock option" for the purposes of section 422 of the Code, and that does not comply with the requirements of Section 422 of the Code.

3.     ADMINISTRATION     

         3.1    Board or Committee— The Plan shall be administered by the Board or by a committee of the Board appointed in accordance with Section 3.2 or 3.4 below.

         3.2    Appointment of Committee— The Board may at any time appoint a Committee, consisting of not less than two of its members, to administer the Plan on behalf of the Board in accordance with such terms and conditions as the Board may prescribe, consistent with this Plan. Once appointed, the Committee shall continue to serve until otherwise directed by the Board. From time to time, the Board may increase the size of the Committee and appoint additional members, remove members (with or without cause) and appoint new members in their place, fill vacancies however caused, or remove all members of the Committee and thereafter directly administer the Plan. In the discretion of the Board, a Committee may consist solely of two (2) or more Non-Employee Directors, and/or Outside Directors. Notwithstanding anything in this Section 3 to the contrary, the Board or the Committee may delegate to a Committee of one or more members of the Board the authority to grant Options to eligible persons who (a) are not then subject to Section 16 of the Exchange Act and/or (b) are either (i) not then Covered Employees and are not expected to be Covered Employees at the time of recognition of income resulting from such Options, or (ii) not persons with respect to whom the Company wishes to comply with Section 162(m) of the Code.

         3.3    Quorum and Voting— A majority of the members of the Committee shall constitute a quorum, and, subject to the limitations in this Section 3, all actions of the Committee shall require the affirmative vote of members who constitute a majority of such quorum.

         3.4    Committee Complying with Section 162(m) of the Code— If the Company is a "publicly held corporation" within the meaning of Section 162(m), the Board may establish a Committee of "outside directors" within the meaning of Section 162(m) to approve the grant of any Option which might reasonably be anticipated to result in the payment of employee remuneration that would otherwise exceed the limit on employee remuneration deductible for income tax purposes pursuant to Section 162(m) of the Code.

         3.5    Powers of Committee— Any Committee appointed under Section 3.2 or 3.4 above shall have the authority to do the following:

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         3.6    Administration by Committee— The Committee's exercise of the authority set out in Section 3.4 shall be consistent with the intent that ISOs issued under the Plan be qualified under the terms of Section 422 of the Code, and that Non-ISOs shall not be so qualified. All determinations made by the Committee in good faith on matters referred to in Section 3.4 shall be final, conclusive, and binding upon all Persons. The Committee shall have all powers necessary or appropriate to accomplish its duties under this Plan. In addition, the Committee's administration of the Plan shall in all respects be consistent with the policies and rules of any stock exchange or over the counter market on which the Shares are listed.

4.     ELIGIBILITY     

         4.1    Eligibility for ISOs— An ISO may only be granted to a person who is an employee of the Company or an Affiliate of the Company, including directors or officers who are employees of the Company or an Affiliate of the Company.

         4.2    Eligibility for Non-ISOs— Non-ISOs may be granted to any employee, officer, director or consultant of the Company or an Affiliate of the Company.

         4.3    No Violation of Securities Laws— No Option shall be granted to any Optionee unless the Committee has determined that the grant of such Option and the exercise thereof by the Optionee will not violate applicable securities laws.

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         4.4    Limit on Maximum Grant to any Optionee Notwithstanding anything in this Plan to the contrary, no officer or employee of the Company or an Affiliate of the Company shall receive Options exercisable for more than two million one hundred thousand (2,100,000) Shares over any three year period, nine hundred thirty-five thousand (935,000) Shares over any one year period or 5% of the outstanding Shares.

5.     SHARES SUBJECT TO THE PLAN     

         5.1    Number of Shares— The Committee, from time to time, may grant Options to purchase an aggregate of up to four million seven hundred fifty thousand (4,750,000) Shares, subject to regulatory approval, to be made available from authorized, but unissued or reacquired, Shares. In calculating the foregoing four million seven hundred fifty thousand (4,750,000) Shares, the Committee shall include the 1,116,819 Shares subject to options outstanding as of the Effective Date of the Plan. The foregoing number of Shares shall be adjusted, where necessary, to take account of the events referred to in Section 11 hereof.

         5.2    Decrease in Number of Shares Subject to Plan— Upon exercise of an Option, the number of Shares thereafter available under the Plan and under the Option shall decrease by the number of Shares as to which the Option was exercised.

         5.3    Expiry of Option— If an Option expires or terminates for any reason without having been exercised in full, the unpurchased Shares subject thereto shall again be available for the purposes of the Plan.

         5.4    Reservation of Shares— The Company will at all times reserve and keep available such number of Shares as shall be sufficient to satisfy the requirements of the Plan.

6.     OPTION TERMS     

         6.1    Option Agreement— With respect to each Option to be granted to an Optionee, the Committee shall specify the following terms in the Option Agreement between the Company and the Optionee:

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         6.2    No Grant After Ten Years From Effective Date— No Option shall be granted under the Plan later than ten (10) years from the Effective Date of the Plan. Except as expressly provided herein, nothing contained in this Plan shall require that the terms and conditions of Options granted under the Plan be uniform.

         6.3    No Disposition for Six Months— An Optionee who is subject to Section 16 of the Exchange Act and whose Option grant is not exempt from Section 16 under Rule 16b-3 shall not make a Disposition of any Shares issued upon exercise of an Option unless at least six (6) months has elapsed between the Date of Grant of the Option and the date of Disposition of the Shares issued upon exercise of such Option. Notwithstanding the foregoing, other than termination for just cause, if a sale within the applicable time periods set forth in this Section 6 or Section 9 of Shares acquired upon the exercise of an Option would subject the Optionee to suit under Section 16(b) of the Exchange Act, the Option shall remain exercisable until the earliest to occur of (i) the tenth (10th) day following the date on which a sale of such Shares by the Optionee would no longer be subject to suit, (ii) the one hundred and ninetieth (190th) day after the Optionee's termination of employment, or (iii) the Option Expiry Date.

7.      LIMITATION ON GRANTS OF OPTIONS     

         7.1    US$100,000 Limit on ISOs .— If the aggregate Fair Market Value (valued as of the Date of Grant of each ISO) of:

exceeds US$100,000, as such amount may be adjusted from time to time under Section 422(d) of the Code, then to the extent of such excess such options shall be treated as options that are not "incentive stock options" for purposes of the Code.

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8.      EXERCISE OF OPTION     

         8.1    Method of Exercise Subject to any limitations or conditions imposed upon an Optionee pursuant to the Option Agreement or Section 6 above, an Optionee may exercise an Option by giving written notice thereof to the Company at its principal place of business, provided that any Options granted after the Plan is approved by the required regulatory authorities but prior to the date on which shareholder approval to the Plan is given, may not be exercised unless and until the Plan receives shareholder approval.

         8.2    Payment of Option Price The notice described in Section 8.1 shall be accompanied by full payment of the aggregate Option Price to the extent the Option is so exercised, and full payment of any amounts the Company determines must be withheld for tax purposes from the Optionee pursuant to the Option Agreement. Such payment shall be:

         8.3    Issuance of Stock Certificate As soon as practicable after exercise of an Option in accordance with Sections 8.1 and 8.2 above, the Company shall issue a stock certificate evidencing the Shares with respect to which the Option has been exercised. Until the issuance of such stock certificate, no right to vote or receive dividends or any other rights as a shareholder shall exist with respect to such Shares, notwithstanding the exercise of the Option. No adjustment will be made for a dividend or other right for which the record date is prior to the date the stock certificate is issued, except as provided in Section 11 below.

         8.4    Tax Withholding in General The Company shall have the right to deduct from any and all payments made under the Plan, or to require the Optionee, through cash payment or otherwise, to make adequate provision for, the federal, state, local and foreign taxes, if any, required by law to be withheld by the Company with respect to an Option or the Shares acquired pursuant thereto. The Company shall have no obligation to deliver Shares or to release Shares from an escrow established pursuant to an Option Agreement until the Company's tax withholding obligations have been satisfied by the Optionee.

9.      TRANSFERABILITY OF OPTIONS     

         9.1    Non-Transferable Unless otherwise specified in an Option Agreement, and except as provided otherwise in this Section 9, Options are non-assignable and non-transferable.

         9.2    Death of Optionee If the employment of an Optionee as an employee or consultant of the Company or an Affiliate of the Company, or the position of an Optionee as a director of the Company or an Affiliate of the Company, terminates as a result of Optionee's death, any Options held by such Optionee shall pass to the Qualified Successor of the Optionee, and shall be exercisable by the

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Qualified Successor on or before the date which is the earlier of twelve (12) months following the date of death or the last day of the Term.

         9.3    Disability of Optionee If the employment of an Optionee as an employee or consultant of the Company or an Affiliate of the Company, or the position of an Optionee as a director of the Company or an Affiliate of the Company, terminates as a result of the Optionee's Disability, any Option held by such Optionee that could have been exercised immediately prior to such termination of service shall be exercisable by such Optionee, or by such Optionee's Guardian, on or before the date which is the earlier of twelve (12) months following the termination of service of such Optionee, and the last day of the Term.

         9.4    Disability and Death of Optionee If an Optionee who has ceased to be employed by the Company or an Affiliate of the Company by reason of such Optionee's Disability dies within six (6) months after the termination of such employment, any Option held by such Optionee that could have been exercised immediately prior to such Optionee's death shall pass to the Qualified Successor of such Optionee, and shall be exercisable by the Qualified Successor:

         9.5    Deemed Non-Interruption of Employment Employment shall be deemed to continue intact during any military or sick leave or other bona fide leave of absence if the period of such leave does not exceed ninety (90) days or, if longer, for so long as the Optionee's right to re-employment with the Company or an Affiliate of the Company is guaranteed either by statute or by contract. If the period of such leave exceeds ninety (90) days and the Optionee's re-employment is not so guaranteed, then such Optionee's employment shall be deemed to have terminated ninety-one (91) days from the date such leave commenced.

10.      TERMINATION OF OPTIONS     

         10.1  Termination of Options To the extent not earlier exercised or terminated in accordance with section 9 above, an Option shall terminate at the earliest of the following dates:

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         10.2  Vesting In the event that an Optionee's position as an employee, officer, consultant or director of the Company or of an Affiliate of the Company is terminated, and the Optionee has no continuing business relationship with the Company or an Affiliate of the Company as an employee, officer, consultant, or director, the Option held by such Optionee shall cease to vest as at the date of termination, regardless of whether the Optionee is subject to restricted trading periods due to his or her status as an insider, as determined by the Company.

11.      ADJUSTMENTS TO OPTIONS     

         11.1  Alteration in Capital Structure If there is a material alteration in the capital structure of the Company resulting from a recapitalization, stock split, reverse stock split, stock dividend, or otherwise, the Committee shall make such adjustments to this Plan (and to the Options then outstanding under this Plan) as the Committee determines to be appropriate and equitable under the circumstances, so that the proportionate interest of each holder of any such Option shall, to the extent practicable, be maintained as before the occurrence of such event. Such adjustments may include, without limitation (a) a change in the number or kind of shares of stock of the Company covered by such Options, or other property for which Shares are exchanged as part of such adjustment, and (b) a change in the Option Price payable per share; provided, however, that the aggregate Option Price applicable to the unexercised portion of existing Options shall not be altered, it being intended that any adjustments made with respect to such Options shall apply only to the price per share and the number of shares subject thereto. For purposes of this Section 11.1, neither (i) the issuance of additional shares of stock of the Company in exchange for adequate consideration (including services), nor (ii) the conversion of outstanding preferred shares of the Company into Shares shall be deemed to be material alterations of the capital structure of the Company.

         11.2  Corporate Reorganization In the event of a reorganization as defined in this Section 11.2 in which the Company is not the surviving or acquiring corporation, or in which the Company is or becomes a wholly-owned subsidiary of another corporation after the effective date of the reorganization, outstanding Options shall be subject to the agreement governing the reorganization, which may provide, without limitation, for the assumption of each Option granted under this Plan or its parent or subsidiary, for the substitution by surviving corporation or its parent or subsidiary of its own options for such Options, for accelerated vesting and accelerated expiration, or for settlement in cash or cash equivalents. In any event, the exercise and/or vesting of any Option that was permissible solely be reason of this Section 11.2 shall be conditioned upon the consummation of the reorganization. For purposes of this Section 11.2, "reorganization" shall mean any statutory merger, statutory consolidation, sale of all or substantially all of the assets of the Company, or sale, pursuant to an agreement with the Company, of securities of the Company pursuant to which the Company is or becomes a wholly-owned subsidiary of another corporation after the effective date of the reorganization.

         11.3  Acceleration of Vesting Schedule The Committee shall have the right, in its sole discretion, to accelerate the vesting schedule of any Option.

         11.4  Change of Control Unless otherwise provided by the Committee in the applicable Option Agreement, in the event of a Change of Control, all Options outstanding on the date of such Change of Control shall become immediately and fully exercisable. The provisions of this Section 11.4 shall not be applicable to any Options granted to an Optionee if any Change of Control results from such Optionee's beneficial ownership (within the meaning of Rule 13d-3 under the Exchange Act) of Shares or Company Voting Securities.

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         11.5  Determinations to be Made By Committee Adjustments and determinations under this Section 11 shall be made by the Committee, whose decisions as to what adjustments or determination shall be made, and the extent thereof, shall be final, binding, and conclusive.

12.      TERMINATION AND AMENDMENT OF PLAN     

         12.1  Termination of Plan Unless earlier terminated as provided in Section 12.2 below, the Plan shall terminate on, and no Option shall be granted under the Plan, after the end of the day prior to the tenth (10 th ) anniversary of the Effective Date.

         12.2  Power of Committee to Terminate or Amend Plan Subject to the approval of any stock exchange on which the Company is listed, the Committee may terminate, suspend or amend the terms of the Plan; provided, however, that no amendment shall be effective unless approved by the shareholders of the Company within twelve (12) months before or after the adoption of the amendment, where the amendment will: (a) increase the number of shares reserved for Options under the Plan; (b) modify the requirements as to eligibility for participation in the Plan (to the extent such modification requires shareholder approval in order for the Plan to satisfy the requirements of Section 422 of the Code); or (c) modify the Plan in any other way if such modification requires shareholder approval in order for the Plan to satisfy the requirements of Section 422 of the Code, Rule 16b-3 or any Nasdaq or securities exchange listing requirements. Upon any termination, suspension or amendment of the Plan, the Company shall notify the Optionees then holding Options under the Plan of such termination, suspension or amendment, and upon receipt of such notification, all Optionees will then be deemed to be bound by such termination, suspension or the provisions of such amendment to the Plan, as the case may be.

         12.3  No Grant During Suspension of Plan No Option may be granted during any suspension, or after termination, of the Plan. Amendment, suspension, or termination of the Plan shall not, without the consent of the Optionee, impair any rights or increase any obligations of the Optionee under any Option previously granted prior to such amendment, suspension or termination.

13.      CONVERSION OF ISOS INTO NON-ISOS     

         13.1  Conversion of ISOs into Non-ISOs At the written request of any ISO Optionee, the Committee may in its discretion take such actions as may be necessary to convert such Optionee's ISOs (or any installments or portions of installments thereof) that have not been exercised on the date of conversion into Non-ISOs at any time prior to the expiration of such ISOs, regardless of whether the Optionee is an employee of the Company or an Affiliate of the Company at the time of such conversion. Such actions include, but shall not be limited to, extending the exercise period of such ISOs. At the time of such conversion, the Committee, with the consent of the Optionee, may impose such conditions on the exercise of the resulting Non-ISOs as the Committee in its discretion may determine, provided that such conditions are consistent with this Plan. Nothing in the Plan shall be deemed to give any Optionee the right to have such Optionee's ISOs converted into Non-ISOs, and no such conversion shall occur until and unless the Committee takes appropriate action, unless such conversion is required by applicable law. The Committee, with the consent of the Optionee, may also terminate any portion of any ISO that has not been exercised at the time of such conversion.

14.      CONDITIONS PRECEDENT TO ISSUANCE OF SHARES     

         14.1  Compliance with Securities Laws Options shall not be granted and Shares shall not be issued pursuant to the exercise of any Option unless the grant and exercise of such Option and the issuance and delivery of such Shares comply with all relevant provisions of law, including, without limitation, the Securities Act, the Exchange Act, any applicable state or provincial securities law, the rules and regulations promulgated thereunder, and the requirements of any stock exchange upon which the Shares may then be listed or otherwise traded.

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         14.2  Regulatory Approval to Issuance of Shares The Company shall seek to obtain from regulatory commission or agency having jurisdiction over the Plan such authority as may be required to issue and sell Shares upon the exercise of any Option; provided, however, that this undertaking shall not require the Company to register under the Securities Act (or any other applicable law for the registration and sale of securities) either the Plan, any Option or any Shares issued or issuable pursuant to any such Option. If, after reasonable efforts, the Company is unable to obtain from any such regulatory commission or agency the authority which counsel for the Company deems necessary for the lawful issuance and sale of stock under the Plan, the Company shall be relieved from any liability for failure to issue and sell stock upon exercise of any such Options unless and until such authority is obtained.

15.      USE OF PROCEEDS     

         15.1  Use of Proceeds Proceeds from the sale of Shares made pursuant to the exercise of an Option shall constitute general funds of the Company and shall be used for general corporate purposes.

16.      NOTICES     

         16.1  Notices All notices, requests, demands and other communications required or permitted to be given under this Plan and the Options granted under this Plan shall be in writing and shall be either served personally on the party to whom notice is to be given, in which case notice shall be deemed to have been duly given on the date of such service; telefaxed, in which case notice shall be deemed to have been duly given on the date the telefax is sent; or mailed to the party to whom notice is to be given, by registered or certified first class mail, return receipt requested, postage prepaid, and addressed to the party at his, her or its most recent known address, in which case such notice shall be deemed to have been duly given on the tenth (10 th ) postal delivery day following the date of such mailing.

17.      MISCELLANEOUS PROVISIONS     

         17.1  No Obligation to Exercise An Optionee shall be under no obligation to exercise such Optionee's Option.

         17.2  No Obligation to Retain Optionee Nothing contained in this Plan shall obligate the Company or an Affiliate of the Company to retain an Optionee as an employee, officer, director, or consultant for any period, nor shall this Plan interfere in any way with the right of the Company or an Affiliate of the Company to reduce such Optionee's compensation.

         17.3  Binding Agreement The provisions of this Plan and each Option Agreement with an Optionee shall be binding upon such Optionee and any Qualified Successor or Guardian of such Optionee.

         17.4  Use of Terms Where the context so requires, references herein to the singular shall include the plural, and vice versa.

         17.5  Headings The headings used in this Plan are for convenience of reference only and shall not in any way affect or be used in interpreting any of the provisions of this Plan.

18.      SHAREHOLDER APPROVAL OF PLAN     

         18.1  Shareholder Approval of Plan This Plan must be approved by a majority of the votes cast at a meeting of the shareholders of the Company, other than votes attaching to securities beneficially owned by:

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19.      MERGER OF FORMER STOCK OPTION PLANS     

         19.1  Upon receipt of shareholder and regulatory approval, the 1997 Stock Option Plan and the 1995 Stock Option Plan of the Company, as amended, shall both be deemed to be merged herein, such that all options outstanding under the 1997 Stock Option Plan of the Company (the "1997 Options") and the 1995 Stock Option Plan of the Company (the "1995 Options") shall be deemed to be outstanding under the Plan to the same extent as if they were originally granted hereunder, and shall be governed hereby and entitled to all of the benefits and obligations herein. The Committee shall be authorized to amend, at any time and from time to time, all or any of the 1997 Options and the 1995 Options as the Committee may determine necessary or advisable or may otherwise deem appropriate, to conform such agreements to this Plan.

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ANNEX E

SECTION 262 OF THE GENERAL CORPORATION LAW OF THE STATE OF DELAWARE

        § 262. Appraisal rights.

        (a) Any stockholder of a corporation of this State who holds shares of stock on the date of the making of a demand pursuant to subsection (d) of this section with respect to such shares, who continuously holds such shares through the effective date of the merger or consolidation, who has otherwise complied with subsection (d) of this section and who has neither voted in favor of the merger or consolidation nor consented thereto in writing pursuant to § 228 of this title shall be entitled to an appraisal by the Court of Chancery of the fair value of the stockholder's shares of stock under the circumstances described in subsections (b) and (c) of this section. As used in this section, the word "stockholder" means a holder of record of stock in a stock corporation and also a member of record of a nonstock corporation; the words "stock" and "share" mean and include what is ordinarily meant by those words and also membership or membership interest of a member of a nonstock corporation; and the words "depository receipt" mean a receipt or other instrument issued by a depository representing an interest in one or more shares, or fractions thereof, solely of stock of a corporation, which stock is deposited with the depository.

        (b) Appraisal rights shall be available for the shares of any class or series of stock of a constituent corporation in a merger or consolidation to be effected pursuant to § 251 (other than a merger effected pursuant to § 251(g) of this title), § 252, § 254, § 257, § 258, § 263 or § 264 of this title:

        (1) Provided, however, that no appraisal rights under this section shall be available for the shares of any class or series of stock, which stock, or depository receipts in respect thereof, at the record date fixed to determine the stockholders entitled to receive notice of and to vote at the meeting of stockholders to act upon the agreement of merger or consolidation, were either (i) listed on a national securities exchange or (ii) held of record by more than 2,000 holders; and further provided that no appraisal rights shall be available for any shares of stock of the constituent corporation surviving a merger if the merger did not require for its approval the vote of the stockholders of the surviving corporation as provided in subsection (f) of § 251 of this title.

        (2) Notwithstanding paragraph (1) of this subsection, appraisal rights under this section shall be available for the shares of any class or series of stock of a constituent corporation if the holders thereof are required by the terms of an agreement of merger or consolidation pursuant to §§ 251, 252, 254, 257, 258, 263 and 264 of this title to accept for such stock anything except:

        a. Shares of stock of the corporation surviving or resulting from such merger or consolidation, or depository receipts in respect thereof;

        b. Shares of stock of any other corporation, or depository receipts in respect thereof, which shares of stock (or depository receipts in respect thereof) or depository receipts at the effective date of the merger or consolidation will be either listed on a national securities exchange or held of record by more than 2,000 holders;

        c. Cash in lieu of fractional shares or fractional depository receipts described in the foregoing subparagraphs a. and b. of this paragraph; or

        d. Any combination of the shares of stock, depository receipts and cash in lieu of fractional shares or fractional depository receipts described in the foregoing subparagraphs a., b. and c. of this paragraph.

        (3) In the event all of the stock of a subsidiary Delaware corporation party to a merger effected under § 253 of this title is not owned by the parent corporation immediately prior to the merger, appraisal rights shall be available for the shares of the subsidiary Delaware corporation.

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        (c) Any corporation may provide in its certificate of incorporation that appraisal rights under this section shall be available for the shares of any class or series of its stock as a result of an amendment to its certificate of incorporation, any merger or consolidation in which the corporation is a constituent corporation or the sale of all or substantially all of the assets of the corporation. If the certificate of incorporation contains such a provision, the procedures of this section, including those set forth in subsections (d) and (e) of this section, shall apply as nearly as is practicable.

        (d) Appraisal rights shall be perfected as follows:

        (1) If a proposed merger or consolidation for which appraisal rights are provided under this section is to be submitted for approval at a meeting of stockholders, the corporation, not less than 20 days prior to the meeting, shall notify each of its stockholders who was such on the record date for such meeting with respect to shares for which appraisal rights are available pursuant to subsection (b) or (c) hereof that appraisal rights are available for any or all of the shares of the constituent corporations, and shall include in such notice a copy of this section. Each stockholder electing to demand the appraisal of such stockholder's shares shall deliver to the corporation, before the taking of the vote on the merger or consolidation, a written demand for appraisal of such stockholder's shares. Such demand will be sufficient if it reasonably informs the corporation of the identity of the stockholder and that the stockholder intends thereby to demand the appraisal of such stockholder's shares. A proxy or vote against the merger or consolidation shall not constitute such a demand. A stockholder electing to take such action must do so by a separate written demand as herein provided. Within 10 days after the effective date of such merger or consolidation, the surviving or resulting corporation shall notify each stockholder of each constituent corporation who has complied with this subsection and has not voted in favor of or consented to the merger or consolidation of the date that the merger or consolidation has become effective; or

        (2) If the merger or consolidation was approved pursuant to § 228 or § 253 of this title, then either a constituent corporation before the effective date of the merger or consolidation or the surviving or resulting corporation within 10 days thereafter shall notify each of the holders of any class or series of stock of such constituent corporation who are entitled to appraisal rights of the approval of the merger or consolidation and that appraisal rights are available for any or all shares of such class or series of stock of such constituent corporation, and shall include in such notice a copy of this section. Such notice may, and, if given on or after the effective date of the merger or consolidation, shall, also notify such stockholders of the effective date of the merger or consolidation. Any stockholder entitled to appraisal rights may, within 20 days after the date of mailing of such notice, demand in writing from the surviving or resulting corporation the appraisal of such holder's shares. Such demand will be sufficient if it reasonably informs the corporation of the identity of the stockholder and that the stockholder intends thereby to demand the appraisal of such holder's shares. If such notice did not notify stockholders of the effective date of the merger or consolidation, either (i) each such constituent corporation shall send a second notice before the effective date of the merger or consolidation notifying each of the holders of any class or series of stock of such constituent corporation that are entitled to appraisal rights of the effective date of the merger or consolidation or (ii) the surviving or resulting corporation shall send such a second notice to all such holders on or within 10 days after such effective date; provided, however, that if such second notice is sent more than 20 days following the sending of the first notice, such second notice need only be sent to each stockholder who is entitled to appraisal rights and who has demanded appraisal of such holder's shares in accordance with this subsection. An affidavit of the secretary or assistant secretary or of the transfer agent of the corporation that is required to give either notice that such notice has been given shall, in the absence of fraud, be prima facie evidence of the facts stated therein. For purposes of determining the stockholders entitled to receive either notice, each constituent corporation may fix, in advance, a record date that shall be not more than 10 days prior to the date the notice is given, provided, that if the notice is given on or after the effective date of the merger or consolidation, the record date shall be

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such effective date. If no record date is fixed and the notice is given prior to the effective date, the record date shall be the close of business on the day next preceding the day on which the notice is given.

        (e) Within 120 days after the effective date of the merger or consolidation, the surviving or resulting corporation or any stockholder who has complied with subsections (a) and (d) of this section hereof and who is otherwise entitled to appraisal rights, may commence an appraisal proceeding by filing a petition in the Court of Chancery demanding a determination of the value of the stock of all such stockholders. Notwithstanding the foregoing, at any time within 60 days after the effective date of the merger or consolidation, any stockholder who has not commenced an appraisal proceeding or joined that proceeding as a named party shall have the right to withdraw such stockholder's demand for appraisal and to accept the terms offered upon the merger or consolidation. Within 120 days after the effective date of the merger or consolidation, any stockholder who has complied with the requirements of subsections (a) and (d) of this section hereof, upon written request, shall be entitled to receive from the corporation surviving the merger or resulting from the consolidation a statement setting forth the aggregate number of shares not voted in favor of the merger or consolidation and with respect to which demands for appraisal have been received and the aggregate number of holders of such shares. Such written statement shall be mailed to the stockholder within 10 days after such stockholder's written request for such a statement is received by the surviving or resulting corporation or within 10 days after expiration of the period for delivery of demands for appraisal under subsection (d) of this section hereof, whichever is later. Notwithstanding subsection (a) of this section, a person who is the beneficial owner of shares of such stock held either in a voting trust or by a nominee on behalf of such person may, in such person's own name, file a petition or request from the corporation the statement described in this subsection.

        (f) Upon the filing of any such petition by a stockholder, service of a copy thereof shall be made upon the surviving or resulting corporation, which shall within 20 days after such service file in the office of the Register in Chancery in which the petition was filed a duly verified list containing the names and addresses of all stockholders who have demanded payment for their shares and with whom agreements as to the value of their shares have not been reached by the surviving or resulting corporation. If the petition shall be filed by the surviving or resulting corporation, the petition shall be accompanied by such a duly verified list. The Register in Chancery, if so ordered by the Court, shall give notice of the time and place fixed for the hearing of such petition by registered or certified mail to the surviving or resulting corporation and to the stockholders shown on the list at the addresses therein stated. Such notice shall also be given by 1 or more publications at least 1 week before the day of the hearing, in a newspaper of general circulation published in the City of Wilmington, Delaware or such publication as the Court deems advisable. The forms of the notices by mail and by publication shall be approved by the Court, and the costs thereof shall be borne by the surviving or resulting corporation.

        (g) At the hearing on such petition, the Court shall determine the stockholders who have complied with this section and who have become entitled to appraisal rights. The Court may require the stockholders who have demanded an appraisal for their shares and who hold stock represented by certificates to submit their certificates of stock to the Register in Chancery for notation thereon of the pendency of the appraisal proceedings; and if any stockholder fails to comply with such direction, the Court may dismiss the proceedings as to such stockholder.

        (h) After the Court determines the stockholders entitled to an appraisal, the appraisal proceeding shall be conducted in accordance with the rules of the Court of Chancery, including any rules specifically governing appraisal proceedings. Through such proceeding the Court shall determine the fair value of the shares exclusive of any element of value arising from the accomplishment or expectation of the merger or consolidation, together with interest, if any, to be paid upon the amount determined to be the fair value. In determining such fair value, the Court shall take into account all relevant factors. Unless the Court in its discretion determines otherwise for good cause shown, interest

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from the effective date of the merger through the date of payment of the judgment shall be compounded quarterly and shall accrue at 5% over the Federal Reserve discount rate (including any surcharge) as established from time to time during the period between the effective date of the merger and the date of payment of the judgment. Upon application by the surviving or resulting corporation or by any stockholder entitled to participate in the appraisal proceeding, the Court may, in its discretion, proceed to trial upon the appraisal prior to the final determination of the stockholders entitled to an appraisal. Any stockholder whose name appears on the list filed by the surviving or resulting corporation pursuant to subsection (f) of this section and who has submitted such stockholder's certificates of stock to the Register in Chancery, if such is required, may participate fully in all proceedings until it is finally determined that such stockholder is not entitled to appraisal rights under this section.

        (i) The Court shall direct the payment of the fair value of the shares, together with interest, if any, by the surviving or resulting corporation to the stockholders entitled thereto. Payment shall be so made to each such stockholder, in the case of holders of uncertificated stock forthwith, and the case of holders of shares represented by certificates upon the surrender to the corporation of the certificates representing such stock. The Court's decree may be enforced as other decrees in the Court of Chancery may be enforced, whether such surviving or resulting corporation be a corporation of this State or of any state.

        (j) The costs of the proceeding may be determined by the Court and taxed upon the parties as the Court deems equitable in the circumstances. Upon application of a stockholder, the Court may order all or a portion of the expenses incurred by any stockholder in connection with the appraisal proceeding, including, without limitation, reasonable attorney's fees and the fees and expenses of experts, to be charged pro rata against the value of all the shares entitled to an appraisal.

        (k) From and after the effective date of the merger or consolidation, no stockholder who has demanded appraisal rights as provided in subsection (d) of this section shall be entitled to vote such stock for any purpose or to receive payment of dividends or other distributions on the stock (except dividends or other distributions payable to stockholders of record at a date which is prior to the effective date of the merger or consolidation); provided, however, that if no petition for an appraisal shall be filed within the time provided in subsection (e) of this section, or if such stockholder shall deliver to the surviving or resulting corporation a written withdrawal of such stockholder's demand for an appraisal and an acceptance of the merger or consolidation, either within 60 days after the effective date of the merger or consolidation as provided in subsection (e) of this section or thereafter with the written approval of the corporation, then the right of such stockholder to an appraisal shall cease. Notwithstanding the foregoing, no appraisal proceeding in the Court of Chancery shall be dismissed as to any stockholder without the approval of the Court, and such approval may be conditioned upon such terms as the Court deems just; provided, however that this provision shall not affect the right of any stockholder who has not commenced an appraisal proceeding or joined that proceeding as a named party to withdraw such stockholder's demand for appraisal and to accept the terms offered upon the merger or consolidation within 60 days after the effective date of the merger or consolidation, as set forth in subsection (e) of this section.

        (l) The shares of the surviving or resulting corporation to which the shares of such objecting stockholders would have been converted had they assented to the merger or consolidation shall have the status of authorized and unissued shares of the surviving or resulting corporation.

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PART II
Information Not Required in Joint Proxy Statement/Prospectus

Item 20. Indemnification of Directors and Officers

        Under section 145 of the General Corporation Law of the State of Delaware, Inovio has broad powers to indemnify its directors and officers against liabilities they may incur in such capacities, including liabilities under the Securities Act of 1933, as amended (the "Securities Act"). Inovio's Bylaws also provide for mandatory indemnification of its directors and executive officers, and permissive indemnification of its employees and agents, to the fullest extent permissible under Delaware law.

        Inovio's Certificate of Incorporation provides that the liability of its directors for monetary damages shall be eliminated to the fullest extent permissible under Delaware law. Pursuant to Delaware law, this includes elimination of liability for monetary damages for breach of the directors' fiduciary duty of care to Inovio and its Stockholders. These provisions do not eliminate the directors' duty of care and, in appropriate circumstances, equitable remedies such as injunctive or other forms of non-monetary relief will remain available under Delaware law. In addition, each director will continue to be subject to liability for breach of the director's duty of loyalty to Inovio, for acts or omissions not in good faith or involving intentional misconduct, for knowing violations of law, for any transaction from which the director derived an improper personal benefit, and for payment of dividends or approval of stock repurchases or redemptions that are unlawful under Delaware law. The provision also does not affect a director's responsibilities under any other laws, such as the federal securities laws or state or federal environmental laws.

        Inovio has obtained a policy of directors' and officers' liability insurance that insures Inovio's directors and officers against the cost of defense, settlement or payment of a judgment under certain circumstances.

        Insofar as indemnification for liabilities arising under the Securities Act may be permitted to directors, officers or persons controlling the registrant pursuant to the foregoing provisions, the registrant has been informed that in the opinion of the Securities and Exchange Commission such indemnification is against public policy as expressed in the Act and is therefore unenforceable.

Item 21. Exhibits and Financial Statement Schedules

    (a)
    Exhibits

      See Exhibit Index, which is incorporated by reference in this item.

    (b)
    Financial Statement Schedule

      No financial statement schedules are required to be filed herewith.

    (c)
    Reports, Opinions or Appraisals

      The opinion of Oppenheimer & Co. Inc. is attached as Annex B to the joint proxy statement/prospectus included as part of this registration statement.

Item 22. Undertakings.

        The undersigned registrant hereby undertakes:

(1)
To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement:

(i)
To include any prospectus required by section 10(a)(3) of the Securities Act;

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    (ii)
    To reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in the registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price represent no more than a 20 percent change in the maximum aggregate offering price set forth in the "Calculation of Registration Fee" table in the effective registration statement; and

    (iii)
    To include any material information with respect to the plan of distribution not previously disclosed in the registration statement or any material change to such information in the registration statement.

(2)
That, for the purpose of determining any liability under the Securities Act, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.

(3)
To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.

(4)
The undersigned registrant hereby undertakes that, for purposes of determining any liability under the Securities Act, each filing of the registrant's annual report pursuant to section 13(a) or section 15(d) of the Securities Exchange Act of 1934 (and, where applicable, each filing of an employee benefit plan's annual report pursuant to section 15(d) of the Securities Exchange Act of 1934) that is incorporated by reference in the registration statement and each post-effective amendment hereto shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.

(5)
That prior to any public reoffering of the securities registered hereunder through use of a prospectus which is a part of this registration statement, by any person or party who is deemed to be an underwriter within the meaning of Rule 145(c), the issuer undertakes that such reoffering prospectus will contain the information called for by the applicable registration form with respect to reofferings by persons who may be deemed underwriters, in addition to the information called for by the other Items of the applicable form.

(6)
That every prospectus (i) that is filed pursuant to paragraph (5) immediately preceding, or (ii) that purports to meet the requirements of Section 10(a)(3) of the Securities Act, and is used in connection with an offering of securities subject to Rule 415, will be filed as a part of an amendment to the registration statement and will not be used until such amendment is effective, and that, for purposes of determining any liability under the Securities Act, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.

(7)
Insofar as indemnification for liabilities arising under the Securities Act may be permitted to directors, officers and controlling persons of the registrant pursuant to the foregoing provisions, or otherwise, the registrant has been advised that in the opinion of the Securities and Exchange Commission such indemnification is against public policy as expressed in the Securities Act and is, therefore, unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or

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    controlling person of the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered, the registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by it is against public policy as expressed in the Securities Act and will be governed by the final adjudication of such issue.

(8)
To respond to requests for information that is incorporated by reference into the prospectus pursuant to Items 4, 10(b), 11 or 13 of this Form, within one business day of receipt of such request, and to send the incorporated documents by first class mail or other equally prompt means. This includes information contained in documents filed subsequent to the effective date of the registration statement through the date of responding to the request.

(9)
To supply by means of a post-effective amendment all information concerning a transaction, and the company being acquired involved therein, that was not the subject of and included in the registration statement when it became effective.

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SIGNATURES

        Pursuant to the requirements of the Securities Act, the registrant has duly caused this Amendment No. 1 to the registration statement to be signed on its behalf by the undersigned, thereunto duly authorized, in the City of San Diego, State of California on January 23, 2009.

    Inovio Biomedical Corporation

 

 

By:

 

/s/ AVTAR DHILLON

Avtar Dhillon, M.D.
President and Chief Executive Officer
(Principal Executive Officer)

        Pursuant to the requirements of the Securities Act of 1933, this Amendment No. 1 to the registration statement has been signed by the following persons in the capacities and on the dates indicated.

Signature   Title   Date  

 

 

 

 

 

 

 
/s/ Avtar Dhillon

Avtar Dhillon
  President and Chief Executive Officer
(Principal Executive Officer), Director
    January 23, 2009  

/s/ Peter Kies

Peter Kies

 

Chief Financial Officer (Principal Accounting Officer and Principal Financial Officer)

 

 

January 23, 2009

 

*

James L. Heppell

 

Director

 

 

January 23, 2009

 

*

Riaz Bandali

 

Director

 

 

January 23, 2009

 

*
Tazdin Esmail

 

Director

 

 

January 23, 2009

 

*

Simon X. Benito

 

Director

 

 

January 23, 2009

 

*

Robert W. Rieder

 

Director

 

 

January 23, 2009

 

II-4


Signature   Title   Date  

 

 

 

 

 

 

 
*

Stephen Rietiker
  Director     January 23, 2009  

*

Patrick Gan

 

Director

 

 

January 23, 2009

 

*

Chin-Cheong Chong

 

Director

 

 

January 23, 2009

 


 

 

 

 

 

 

 

 

 

*By:

  /s/ AVTAR DHILLON

Avtar Dhillon, M.D.
Attorney- in- fact
        January 23, 2009  

II-5



EXHIBIT INDEX

Exhibit
 
Description
2.1 #   Amended and Restated Agreement and Plan of Merger By and Among Inovio Biomedical Corporation, Inovio Acquisition, LLC, and VGX Pharmaceuticals, Inc. dated December 5, 2008 (included as Annex A in the joint proxy statement/prospectus within this registration statement).
3.1(a)   Amended and Restated Certificate of Incorporation (incorporated by reference to Exhibit 3.1 of the registrant's Registration Statement on Form S-3 (File No. 333-108752) filed on September 12, 2003).
(b)   Certificate of Amendment to Amended and Restated Certificate of Incorporation as filed with the Delaware Secretary of State on September 10, 2004 (incorporated by reference to Exhibit 3.1 of the registrant's Current Report on Form 8-K filed September 16, 2004).
(c)   Certificate of Amendment to the Amended and Restated Certificate of Incorporation as filed with the Delaware Secretary of State on March 31, 2005 (incorporated by reference to Exhibit 3.1 of the registrant's Current Report on Form 8-K filed on April 4, 2005).
3.2(a)**   Certificate of Incorporation of Inovio Acquisition Corporation dated June 23, 2008.
(b)**   Certificate of Conversion of Inovio Acquisition Corporation to Inovio Acquisition, LLC dated October 31, 2008.
(c)**   Certificate of Formation of Inovio Acquisition, LLC dated October 31, 2008.
3.3(a)   Certificate of Designations, Rights and Preferences of Series C Convertible Preferred Stock of Registrant (incorporated by reference to Exhibit 3.3 of the registrant's Registration Statement on Form S-3 filed on June 21, 2004).
(b)   Certificate of Decrease of Shares of Series C Cumulative Convertible Preferred Stock of Registrant (incorporated by reference to Exhibit 3.4 of the registrant's Registration Statement on Form S-3 filed on June 21, 2004).
3.4   Amended and Restated Bylaws of Inovio Biomedical Corporation, as amended through November 30, 2007 (incorporated by reference to Exhibit 3.2 of the registrant's Form 8-K filed on December 6, 2007).
3.5**   Operating Agreement of Inovio Acquisition, LLC, dated October 31, 2008.
4.1   Amended 2000 Stock Option Plan, as amended by the Board of Directors through March 6, 2006 with approvals by Stockholders through May 5, 2006 (incorporated by reference to Exhibit 4.1 of the registrant's Registration Statement on Form S-8 filed on July 28, 2006).
4.2 +   Forms of Incentive and Nonstatutory Stock Option Agreements used in connection with the 2000 Stock Option Plan (incorporated by reference to Exhibit 10.7 of the registrant's Registration Statement on Form S-4/A (File No. 333-58168) filed on April 5, 2001).
4.3†   Warrant to Purchase Common Stock, dated September 15, 2000 by and between the Registrant and the University of South Florida Research Foundation (incorporated by reference to Exhibit 10.6 of the registrant's Form 10-Q filed on November 9, 2000).
4.4†   Warrant to Purchase Common Stock, dated September 15, 2000 by and between the Registrant and Dr. Richard Gilbert (incorporated by reference to Exhibit 10.7 of the registrant's Form 10-Q filed on November 9, 2000).
4.5†   Warrant to Purchase Common Stock, dated September 15, 2000 by and between the Registrant and Dr. Richard Heller (incorporated by reference to Exhibit 10.8 of the registrant's Form 10-Q filed on November 9, 2000).

Exhibit
 
Description
4.6†   Warrant to Purchase Common Stock, dated September 15, 2000 by and between the Registrant and Dr. Mark Jaroszeski (incorporated by reference to Exhibit 10.9 of the registrant's Form 10-Q filed on November 9, 2000).
4.7   Investors Rights Agreement, dated July 14, 2003, between the Registrant and the Purchasers listed on Schedule 1 thereto (incorporated by reference to Exhibit 4.2 of the registrant's Registration Statement on Form S-3 (File No. 333-108752) filed on September 12, 2003).
4.8   Specimen Common Stock certificate (incorporated by reference to Exhibit 4.8 of the registrant's Registration Statement on Form S-3 (File No. 333-108752) filed on September 12, 2003).
4.9   Investor Rights Agreement dated as of May 10, 2004 by and between the registrant and the purchasers indicated on the schedule thereto (incorporated by reference to Exhibit 4.2 of the registrant's Registration Statement on Form S-3 filed on June 21, 2004).
4.10   Form of Series C Common Stock Purchase Warrant dated as of May 10, 2004 by and between the registrant and the purchasers indicated on the schedule thereto (incorporated by reference to Exhibit 4.3 of the registrant's Registration Statement on Form S-3 filed on June 21, 2004).
4.11   Registration Rights Agreement dated December 30, 2005, by and among the registrant and the investors named on the signature pages thereto (incorporated by reference to Exhibit 99.3 to registrant's Form 8-K filed with the Securities and Exchange Commission on January 6, 2006).
4.12   Form of Common Stock Purchase Warrant dated as of September 15, 2006 by and between the registrant and each of the purchasers listed on Schedule 1 to the Securities Purchase Agreement (Exhibit 10.23 herein) (incorporated by reference to Exhibit 4.3 of the registrant's Current Report on Form 8-K filed on September 20, 2006).
4.13   Registration Rights Agreement dated as of September 15, 2006 by and among registrant and certain investors indicated on a schedule thereto (incorporated by reference to Exhibit 10.5 of the registrant's Quarterly Report on Form 10-Q filed on November 9, 2006).
4.14   Form of Common Stock Purchase Warrant to be used by and between the registrant and each of the purchasers listed on Schedule 1 to the Securities Purchase and Exchange Agreement (Exhibit 10.25 herein) (incorporated by reference to Exhibit 4.24 of the registrant's Annual Report on Form 10-K filed on March 16, 2007).
4.15 +   First Amended and Restated Inovio Biomedical Corporation 2007 Omnibus Incentive Plan (incorporated by reference to Exhibit 4.2 of the registrant's Registration Statement on Form S-8 filed on May 9, 2008).
4.16 +   Form of Restricted Stock Award Grants under the 2007 Omnibus Stock Incentive Plan (incorporated by reference to Exhibit 4.3 to the Registrant's Registration Statement on Form S-8 filed on May 14, 2007).
4.17 +   Form of Incentive and Non-Qualified Stock Option Grants under the 2007 Omnibus Stock Incentive Plan (incorporated by reference to Exhibit 4.4 to the Registrant's Registration Statement on Form S-8 filed with the Securities and Exchange Commission on May 14, 2007).
4.18**   Form of Voting Trust Agreement, by and between certain stockholders listed on Schedule I thereto and the Trustees identified therein, to be executed and effective concurrent with the closing of the Merger.
5.1 *   Opinion of K&L Gates LLP.

Exhibit
 
Description
10.1   Lease Agreement by and between the registrant and Nexus Sorrento Glen LLC dated August 26, 1999 (incorporated by reference to Exhibit 10.15 of the registrant's Registration Statement on Form S-1, as amended (File No. 333-88427), filed on October 5, 1999).
10.2†   License Agreement dated September 20, 2000 by and between the registrant and the University of South Florida Research Foundation, Inc. (incorporated by reference to Exhibit 10.5 of the registrant's Form 10-Q filed on November 9, 2000).
10.3   Asset Purchase Agreement by and among the Registrant, Genetronics, Inc., a subsidiary of the Registrant, and Harvard Bioscience, Inc. dated December 24, 2002 (incorporated by reference to Exhibit A to the registrant's Definitive Proxy Statement filed on January 7, 2003).
10.4   Preferred Stock and Warrant Purchase Agreement dated as of May 10, 2004 by and between the registrant and the purchasers indicated on the schedule thereto (incorporated by reference to Exhibit 4.1 of the registrant's Registration Statement on Form S-3 filed on June 21, 2004).
10.5†   Non-Exclusive License and Research Collaboration Agreement dated as of May 21, 2004 by and among the registrant and Merck & Co., Inc. and Genetronics, Inc., a subsidiary of the registrant (incorporated by reference to Exhibit 10.1 to the Quarterly Report on Form 10-Q filed on August 13, 2004).
10.6   Lease Agreement by and between the registrant and Sorrento Centre Tenancy in Common dated November 29, 2004 (incorporated by reference to Exhibit 10.16 of the registrant's Annual Report of Form 10-K for the year ended December 31, 2004, filed on March 15, 2005).
10.7   Lease Amendment #3 by and between the registrant and Nexus Sorrento Glen LLC dated January 21, 2005 (incorporated by reference to Exhibit 10.17 of the registrant's Annual Report of Form 10-K for the year ended December 31, 2004, filed on March 15, 2005).
10.8   Stock Purchase Agreement dated January 25, 2005 by and among the registrant, Inovio AS and the Shareholders of Inovio AS (incorporated by reference to Exhibit 10.1 to the Current Report on Form 8-K filed on January 31, 2005).
10.9   Securities Purchase Agreement dated as of December 16, 2005, among registrant and each purchaser identified on the signature pages thereto (incorporated by reference to Exhibit 99.1 of the registrant's Report of Form 8-K, filed on January 6, 2006).
10.10   License Agreement dated September 15, 2006 between registrant and Inovio Asia Pte. Ltd. (incorporated by referenced to Exhibit 10.1 to registrant's Quarterly Report on Form 10-Q filed on November 9, 2006).
10.11   Securities Purchase Agreement dated September 15, 2006 between registrant and purchasers named therein (incorporated by reference to Exhibit 4.1 of the registrant's Current Report on Form 8-K filed on September 20, 2006).
10.12   Amendment to Securities Purchase Agreement, amending the Securities Purchase Agreement filed as Exhibit 10.27 (incorporated by reference to Exhibit 4.3 of the registrant's Current Report on Form 8-K filed on October 16, 2006).
10.13   Securities Purchase and Exchange Agreement between registrant and Inovio Asia Pte. Ltd. and the purchasers named therein, dated September 15, 2006 (incorporated by referenced to Exhibit 10.2 to registrant's Quarterly Report on Form 10-Q filed on November 9, 2006).
10.14   Preferred Exchange Agreement dated September 15, 2006 between registrant and certain holders of Series C Preferred Stock (incorporated by referenced to Exhibit 4.4 of the registrant's Registration Statement on Form S-3, filed January 19, 2007).

Exhibit
 
Description
10.15   Securities Purchase Agreement dated May 14, 2007 relating to the Direct Financing between registrant and purchasers named therein (incorporated by reference to Exhibit 4.1 of the registrant's Current Report on Form 8-K, filed May 16, 2007).
10.16   Letter Agreement Dated August 3, 2007 between Registrant and Asia Life Sciences Venture Consulting Inc. (incorporated by reference to Exhibit 4.1 of the registrant's Current Report on Form 8-K filed August 6, 2007).
10.17   Form of Warrant to Purchase Common Stock (incorporated by reference to Exhibit 4.2 of the registrant's Current Report on Form 8-K filed August 6, 2007).
10.18 +   Employment Agreement dated August 31, 2007 by and between the registrant and Dr. Michael Fons (incorporated by reference to Exhibit 99.2 of the registrant's Current Report on Form 8-K/A filed September 10, 2007).
10.19 +   Employment Agreement for Punit Dhillon dated March 12, 2008 (incorporated by reference to Exhibit 99.2 of the registrant's Current Report on Form 8-K/A, filed March 14, 2008).
10.20 +   Consulting Agreement dated May 3, 2008 by and between Dietmar Rabussay and Genetronics, Inc. (incorporated by reference to Exhibit 10.1 of the registrant's Current Report on Form 8-K, filed May 7, 2008).
10.21 +   Addendum to P. Kies Employment Agreement, dated July 2, 2008 (incorporated by reference to Exhibit 10.1 of the registrant's Current Report on Form 8-K, filed July 8, 2008).
10.22 +   Form of Employment Agreement by and between the registrant and Dr. Michael Fons, for use effective only upon closing of the Merger (incorporated by reference to Exhibit 10.22 as filed with the registrant's registration statement on Form S-4 (File No. 333-156035) on December 10, 2008).
10.23 +   Form of Employment Agreement by and between the registrant and Punit Dhillon, for use effective only upon closing of the Merger (incorporated by reference to Exhibit 10.23 as filed with the registrant's registration statement on Form S-4 (File No. 333-156035) on December 10, 2008).
10.24 +   Form of Employment Agreement by and between the registrant and Peter Kies, effective only upon closing of the Merger (incorporated by reference to Exhibit 10.24 as filed with the registrant's registration statement on Form S-4 (File No. 333-156035) on December 10, 2008).
10.25 +   Form of Employment Agreement by and between the registrant and Dr. Avtar Dhillon, for use effective only upon closing of the Merger (incorporated by reference to Exhibit 10.25 as filed with the registrant's registration statement on Form S-4 (File No. 333-156035) on December 10, 2008).
10.26†   License Agreement dated June 26, 2000 by and among Baylor College of Medicine, Valentis, Inc. and Applied Veterinary Systems, Inc., as assigned to VGX Pharmaceuticals, Inc.
10.27†   License Agreement dated January 25, 2001 by and between Baylor College of Medicine and Applied Veterinary Systems, Inc., as assigned to VGX Pharmaceuticals, Inc., as amended by First Amendment dated April 17, 2002, Second Amendment dated May 29, 2002, Third Amendment dated March 5, 2002, Fourth Amendment dated April 14, 2004 and Fifth Amendment dated February 15, 2007.
10.28 +   Employment Agreement dated November 14, 2001 by and between Ruxandra Draghia-Akli, Ph.D. and ADViSYS, as assigned to VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement dated September 2, 2008.

Exhibit
 
Description
10.29†   License Agreement dated November 5, 2001 by and between The Trustees of the University of Pennsylvania and VGX Pharmaceuticals, Inc., as amended by First Amendment dated August 15, 2005.
10.30   Agreement of Lease dated January 21, 2005 by and between 450 Sentry Parkway Associates and VGX Pharmaceuticals, Inc.; Addendum confirming lease term dated June 16, 2005.
10.31†   R&D Alliance Agreement dated December 19, 2005 by and between Ganial Immunotherapeutics, Inc. and VGX Pharmaceuticals, Inc.
10.32†   Asset Purchase Agreement dated February 21, 2007 by and among Ronald O. Bergan, Mary Alice Bergan, and VGX Pharmaceuticals, Inc.
10.33†   Exclusive License Agreement dated April 18, 2007 by and between Dow Global Technologies, Inc. and VGX Pharmaceuticals, Inc.
10.34†   License Agreement dated May 9, 2007 by and between Baylor University and VGX Pharmaceuticals, Inc.
10.35†   R&D Collaboration and License Agreement dated June 27, 2007 by and between VGX International, Inc. and VGX Pharmaceuticals, Inc.
10.36†   Non-Exclusive License Agreement dated September 1, 2007 by and between VGX Animal Health, Inc. and VGX Pharmaceuticals, Inc.
10.37†   License Agreement dated September 1, 2007 by and between VGX Animal Health, Inc. and VGX Pharmaceuticals, Inc.
10.38   Assignment of Contingent Payments Agreement dated October 20, 2007 by and among Ronald O. Bergan, Mary Alice Bergan, VGX Animal Health, Inc., and VGX Pharmaceuticals, Inc.
10.39†   R&D Collaboration and License Agreement dated December 18, 2006 by and between VGX International, Inc. and VGX Pharmaceuticals, Inc., as amended by First Amendment dated October, 31, 2007 and as amended by Second Amendment dated August 4, 2008.
10.40 +   Employment Agreement dated November 1, 2007 by and between Niranjan Sardesai, Ph.D. and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement dated August 20, 2008 and Second Amendment to Employment Agreement dated October 1, 2008.
10.41   Lease Agreement dated August 20, 2001 by and between Woodlands VTO 2000 Land, L.P. and Applied Veterinary Systems, Inc., as assigned to VGX Pharmaceuticals, Inc. and as amended by First Amendment to Lease Agreement dated November 12, 2007.
10.42†   Sales and Marketing Agreement dated February 28, 2008 by and between VGX International and VGX Pharmaceuticals, Inc.
10.43 +   Employment Agreement dated March 31, 2008 by and between J. Joseph Kim, Ph.D. and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement dated March 31, 2008.
10.44†   CELLECTRA™ Device License Agreement dated April 16, 2008 by and between VGX International and VGX Pharmaceuticals, Inc.
10.45 +   Employment Agreement dated December 17, 2005 by and between Kevin Rassas and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement Extension dated August 20, 2008.
10.46 +   Employment Agreement dated August 1, 2005 by and between C. Jo White, M.D. and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement Extension dated August 20, 2008.

Exhibit
 
Description
10.47 +   Employment Agreement dated May 1, 2005 by and between Bryan ByongJin Kim and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement Extension dated May 1, 2008.
10.48   Asset Purchase Agreement dated June 10, 2008 by and among VGXI, Inc. and VGX Pharmaceuticals, Inc.
10.49   Sublease Agreement dated June 10, 2008 by and between VGXI, Inc. and VGX Pharmaceuticals, Inc..
10.50†   Patent License Agreement dated April 27, 2007 by and between The Trustees of the University of Pennsylvania and VGX Pharmaceuticals, Inc., as amended by First Amendment dated June 12, 2008.
10.51 +   Employment Agreement dated October 1, 2005 by and between Gene J. Kim and VGX Pharmaceuticals, Inc., as amended by First Amendment to Employment Agreement Extension dated August 20, 2008.
10.52   Form of Note Purchase Agreement for Notes issued by VGX Pharmaceuticals, Inc. from October 2005 until June 2008.
10.53   Form of Convertible Note for notes issued by VGX Pharmaceuticals, Inc. from October 2005 until June 2008.
10.54   Note Amendment dated January 19, 2008 by and between DongKook Pharm Co., Ltd. and VGX Pharmaceuticals, Inc.
10.55   Note Amendment dated June 11, 2008 by and between Huvitz Co., Ltd. and VGX Pharmaceuticals, Inc.
10.56   [Reserved.]
10.57   Form of Note Assignment utilized by VGX Pharmaceuticals, Inc. in June and July 2008.
10.58   Form of Allonge utilized by VGX Pharmaceuticals, Inc. in June and July 2008.
10.59   Form of Note Purchase Agreement for Notes issued by VGX Pharmaceuticals, Inc. used in November and December 2008.
10.60   [Reserved.]
10.61**   Form of VGX Stockholder Voting Agreement.
10.62 +   2001 Equity Compensation Plan for VGX Pharmaceuticals, Inc., as amended.
10.63 +   2007 Equity Compensation Plan for VGX Animal Health, Inc.
10.64   Form of Allonge utilized by VGX Pharmaceuticals, Inc. in November 2008.
10.65†   License Agreement dated November 9, 2006 by and between Genetronics, Inc. and VGX Pharmaceuticals, Inc.
10.66   Memorandum of NIH Research Grant Agreement by and between National Institute of Allergy and Infectious Diseases and VGX Pharmaceuticals, Inc.
10.67   Form of Warrant to Purchase Common Stock issued by VGX Pharmaceuticals, Inc. since 2003.
10.68   Form of Warrant Purchase Agreement for Warrants to Purchase Common Stock issued by VGX Pharmaceuticals, Inc. since 2003.
14.1   Inovio Biomedical Corporation Code of Ethics for Senior Officers (incorporated by reference to Exhibit 14.1 of the registrant's Annual Report on Form 10-K for the year ended December 31, 2004, filed on March 15, 2005).
21.1**   Subsidiaries of the registrant.

Exhibit
 
Description
23.1 *   Consent of K&L Gates LLP (Included in Exhibits 5.1).
23.2 *   Consent of Duane Morris LLP.
23.3   Consent of Independent Registered Public Accounting Firm.
23.4   Consent of Independent Auditors.
24.1**   Power of Attorney.
99.1**   Consent of Oppenheimer & Co. Inc.
99.2**   Consent of Needham & Company, LLC.
99.3**   Consents of persons named as directors for post-Merger company.

#
The registrant hereby agrees to supplementally furnish the staff, on a confidential basis, a copy of any omitted schedule upon the staff's request.

+
Designates management contract, compensatory plan or arrangement.

The company has applied, or will apply for items to be filed by amendment, with the Secretary of the Securities and Exchange Commission for confidential treatment of certain information pursuant to Rule 24b-2 of the Securities Exchange Act of 1934. The company has filed, or will file for items to be filed by amendment, separately with its application a copy of the exhibit including all confidential portions, which may be made available for public inspection pending the Securities and Exchange Commission's review of the application in accordance with Rule 24b-2.

*
To be filed by amendment to this registration statement.

**
Previously filed with registrant's initial registration statement on Form S-4 on December 10, 2008.



QuickLinks

CALCULATION OF REGISTRATION FEE
PROPOSED MERGER—YOUR VOTE IS VERY IMPORTANT
Table of Contents
ADDITIONAL INFORMATION
ABOUT THIS JOINT PROXY STATEMENT/PROSPECTUS
QUESTIONS AND ANSWERS ABOUT THE TRANSACTION AND THE MEETINGS
SUMMARY OF THE JOINT PROXY STATEMENT/PROSPECTUS
SELECTED SUMMARY HISTORICAL AND PRO FORMA COMBINED FINANCIAL DATA
COMPARATIVE STOCK PRICE AND DIVIDEND INFORMATION
CAUTIONARY NOTE REGARDING FORWARD LOOKING STATEMENTS
RISK FACTORS
THE TRANSACTION
CERTAIN MATERIAL U.S. FEDERAL INCOME TAX CONSEQUENCES OF THE MERGER
THE ACQUISITION AGREEMENT
OTHER AGREEMENTS RELATED TO THE TRANSACTION
INFORMATION ABOUT THE COMPANIES
SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND MANAGEMENT
QUANTITATIVE AND QUALITATIVE DISCLOSURE ABOUT MARKET RISKS
CAPITAL STRUCTURE OF INOVIO
COMPARISON OF RIGHTS OF HOLDERS OF INOVIO COMMON STOCK AND VGX COMMON STOCK
SPECIAL MEETING OF INOVIO STOCKHOLDERS
SPECIAL MEETING OF VGX STOCKHOLDERS
LEGAL MATTERS
EXPERTS
WHERE YOU CAN FIND MORE INFORMATION ABOUT INOVIO
INFORMATION ON INOVIO'S WEBSITE
INFORMATION ON VGX'S WEBSITE
INOVIO BIOMEDICAL CORPORATION Index to Consolidated Financial Statements
Report of Independent Registered Public Accounting Firm
Inovio Biomedical Corporation CONSOLIDATED BALANCE SHEETS
Inovio Biomedical Corporation CONSOLIDATED STATEMENTS OF OPERATIONS
Inovio Biomedical Corporation CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY
Inovio Biomedical Corporation CONSOLIDATED STATEMENTS OF CASH FLOWS
INOVIO BIOMEDICAL CORPORATION NOTES TO THE CONSOLIDATED FINANCIAL STATEMENTS
INOVIO BIOMEDICAL CORPORATION CONDENSED CONSOLIDATED BALANCE SHEETS
INOVIO BIOMEDICAL CORPORATION CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
INOVIO BIOMEDICAL CORPORATION CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited)
INOVIO BIOMEDICAL CORPORATION NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Unaudited)
VGX Pharmaceuticals, Inc. (A Development-Stage Company) Consolidated Financial Statements YEARS ENDED DECEMBER 31, 2007 AND 2006 AND THE PERIOD FROM DECEMBER 12, 2000 (INCEPTION) THROUGH DECEMBER 31, 2007
Contents
Report of Independent Auditors
VGX Pharmaceuticals, Inc. (A Development-Stage Company) Consolidated Balance Sheets
VGX Pharmaceuticals, Inc. (A Development-Stage Company) Consolidated Statements of Operations
VGX Pharmaceuticals, Inc. (A Development-Stage Company) Consolidated Statements of Cash Flows
VGX Pharmaceuticals, Inc. (A Development-Stage Company) Notes to Consolidated Financial Statements December 31, 2007
VGX PHARMACEUTICALS, INC. (A Development-Stage Company) Consolidated Financial Statements For the Period Ended September 30, 2008
VGX PHARMACEUTICALS, INC. (A Development-Stage Company) CONSOLIDATED BALANCE SHEETS
VGX PHARMACEUTICALS, INC. (A Development-Stage Company) CONSOLIDATED STATEMENTS OF OPERATIONS (Unaudited)
VGX PHARMACEUTICALS, INC. (A Development-Stage Company) CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited)
VGX PHARMACEUTICALS, INC. (A Development-Stage Company) NOTES TO CONSOLIDATED FINANCIAL STATEMENTS (Unaudited)
INDEX TO UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS
INOVIO BIOMEDICAL CORPORATION VGX PHARMACEUTICALS, INC. UNAUDITED PRO FORMA CONDENSED COMBINED FINANCIAL STATEMENTS
Inovio Biomedical Corporation Unaudited Pro Forma Condensed Balance Sheet As of September 30, 2008
Inovio Biomedical Corporation Unaudited Pro Forma Condensed Combined Statement of Operations For the Year Ended December 31, 2007
Inovio Biomedical Corporation Unaudited Pro Forma Condensed Combined Statement of Operations For the Nine Months Ended September 30, 2008
INOVIO BIOMEDICAL CORPORATION NOTES TO UNAUDITED PRO FORMA FINANCIAL STATEMENTS
ANNEX A
ARTICLE III REPRESENTATIONS AND WARRANTIES OF INOVIO AND SUBMERGER
ARTICLE IV CONDUCT PRIOR TO THE EFFECTIVE TIME
ARTICLE V ADDITIONAL AGREEMENTS
ANNEX B
ANNEX D
ANNEX E SECTION 262 OF THE GENERAL CORPORATION LAW OF THE STATE OF DELAWARE
PART II Information Not Required in Joint Proxy Statement/Prospectus
SIGNATURES
EXHIBIT INDEX

EXHIBIT 10.26

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

BAYLOR COLLEGE OF MEDICINE

APPLIED VETERINARY SYSTEMS, INC.

VALENTIS, INC.

LICENSE AGREEMENT

 

This License Agreement (this “Agreement”) is made and entered into on this 26 th  day of June, 2000 the (“Effective Date”), by and among Baylor College of Medicine (“BAYLOR”), a Texas non-profit corporation having its principal place of business at One Baylor Plaza, Houston, Texas 77030, Applied Veterinary Systems, Inc., a Delaware corporation having its principal office at 1709 Dryden, Suite 901, Houston, Texas 77030 (hereinafter referred to as “AVS”) and Valentis, Inc., a Delaware corporation having its principal place of business at 863A Mitten Road, Burlingame, California 94010 (hereinafter referred to as “VLTS”).

 

WITNESSETH:

 

WHEREAS, BAYLOR, and VLTS are co-owners of the Jointly Owned Patent Rights and Joint Technology Rights as defined below; and

 

WHEREAS, VLTS is successor in interest to GeneMedicine; and

 

WHEREAS, VLTS has rights (with rights to sublicense) pursuant to the First Amendment and Restatement of License Agreement dated March 7, 1994 and effective September 16, 1992 between BAYLOR and GeneMedicine to the Sublicensed Patent Rights and Sublicensed Technology Rights as defined below (the “BAYLOR/VLTS Agreement”); and

 

WHEREAS, VLTS owns individually certain rights to the VLTS Patent Rights, VLTS Technology Rights and VLTS Improvements, as defined below, which AVS desires to license; and

 

WHEREAS, BAYLOR, and VLTS are willing to grant to AVS and AVS desires to obtain worldwide, royalty-bearing licenses to employ the Jointly Owned Patent Rights, Joint Technology Rights, Sublicensed Patent Rights, Sublicensed Technology Rights, VLTS Patent Rights, VLTS Technology Rights, VLTS Improvements and Baylor Improvements licensed in this Agreement and to make, use, sell, have made and otherwise market and commercialize Licensed Products and VLTS Licensed Products as defined below; and

 

WHEREAS, BAYLOR, and VLTS sometimes negotiate licenses for the rights to market and commercialize the technology they develop to third parties in exchange for the receipt of equity (such as stock or partnership interests) and accept a royalty which is reduced from the royalty which they would receive were no such equity negotiated for and received.

 

NOW, THEREFORE, in consideration of the mutual promises and obligations hereinafter set forth and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties hereto stipulate and agree as follows:

 



 

ARTICLE 1

DEFINITIONS

 

1.1                            “Applicable Laws” shall mean all local, state, federal and foreign governmental laws, orders, rules, decrees or regulations.

 

1.2                            “AVS Common Stock” is as defined in Section 3.7.

 

1.3                            “AVS New Technology” shall mean any technology reduced to practice by AVS that involves the delivery of genes or gene products into a cell.

 

1.4                            “AVS Option” is as defined in Section 5.2.

 

1.5                            “AVS VLTS Improvements” shall mean any modifications, variations and improvements to the VLTS Patent Rights, whether patentable or not, that are reduced to practice by AVS and which, if unlicensed, would infringe one or more claims of the VLTS Patent Rights.

 

1.6                            “Baylor Founders” shall mean those individuals listed in Schedule 1.6 .

 

1.7                            “Baylor Improvements” shall mean any modifications, variations and improvements to the Joint Technology Rights, whether patentable or not, that, during the year between the Effective Date and the first anniversary of the Effective Date, are (i) conceived or reduced to practice, (ii) are owned by BAYLOR or become property of BAYLOR and (iii) arise out of work performed in a laboratory at BAYLOR that is under the direct supervision of the Baylor Founders.

 

1.8                            “BAYLOR/VLTS Agreement” is as defined in the third Whereas clause.

 

1.9                            “Confidential Information” shall mean any proprietary and secret ideas, proprietary technical information, know-how and proprietary commercial information or other similar proprietary information.

 

1.10                      “Field of Interest” shall mean the use of genes within the Growth Hormone Axis (as defined below) for therapeutic and growth applications in livestock and companion animals.

 

1.11                      “First Commercial Sale” shall mean the first sale of a Licensed Product or VLTS Licensed Product, as the case may be, to a third party for commercial use (i.e. not for review, evaluation or testing of the Licensed Product or VLTS Licensed Product).

 

1.12                      “Funded Technology” is as defined in Section 8.1.

 

1.13                      “Growth Hormone Axis” for the purposes of this Agreement, shall mean a gene and the corresponding gene product that directly affects growth by influence of a growth hormone or an upstream or downstream effector of GHRH, GH, IGF-I, somatostatin or CCK.

 

1.14                      “Indemnified Parties” is as defined in Section 6.6.

 

1.15             “Joint Technology Rights” shall mean all technology, plasmids, biological materials, compounds, know-how, methods, documents, materials, tests and confidential information related to the

 

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technology, in each case owned or controlled by BAYLOR and/or VLTS, as of the Effective Date, used in the practice of the Jointly Owned Patent Rights .

 

1.16                            “Jointly Owned Patent Rights” shall mean the United States Patent Application entitled “Growth Hormone Releasing Hormone Expression System and Methods of Use, Including Use in Animals” US Patent Application Serial No. 09/122,171, filed July 24, 1998, (owned jointly by VLTS and BAYLOR) and any and all divisions, reissues, re-examinations, renewals, continuations, and extensions thereof, any United States patent which issues from any such pending applications and all other counterpart, pending or issued patents in all other countries.

 

1.17                            “Licensed Product” shall mean any product or service that is made, used, imported, marketed or sold using all or any part of the Licensed Subject Matter in the Field of Interest.

 

1.18                      “Licensed Subject Matter” shall mean (i) Jointly Owned Patent Rights, (ii) Sublicensed Patent Rights, (iii) Joint Technology Rights, (iv) Sublicensed Technology Rights and (v) Baylor Improvements.

 

1.19                            “Net Sales” shall mean all monies and equivalent goods and services actually received by AVS or its sublicensees from the manufacture, use, sale, lease or other commercial exploitation of Licensed Products less the following:

 

(a)                                   any credits or refunds actually granted to customers for the return of Licensed Products that were previously sold;

 

(b)                                  any separately identified sales, use, excise or similar taxes and custom duties or other governmental charges imposed upon the importation or sales of Licensed Products or except for taxes on income;

 

(c)                                   any separately identified charges for transportation, packing, insurance, shipping or handling which are directly associated with sales of Licensed Products; and

 

(d)                                  in the event that AVS is required to pay a royalty to an unrelated third party in order to make, use or sell a Licensed Product, such amounts actually paid to such third party; provided, however, in no event shall the reduction due to royalties paid to other parties exceed ****** of the “Net Sales” amount as calculated prior to such reduction.

 

If Licensed Products are sold in combination with other products or as part of a product then the Net Sales for such combined products shall be the price paid by the third party purchaser for the combined product times a fraction the numerator of which is the cost of producing the License Product and the denominator of which is the cost of producing the entire combined product.

 

Notwithstanding the foregoing, Net Sales shall not include monies and equivalent goods and services (“Payments”) received from a sponsor for research and development programs for development, including testing, of new vector or gene delivery technologies,  new products, or refinements to AVS’ existing methodologies to deliver the GHRH gene; provided, however, Net Sales shall include Payments for any research and development programs if the product or results of such research and development programs can be or is manufactured, used, sold, leased or otherwise commercially exploited by any sponsor of such research and development programs without making additional Payments or if any additional Payments are below the fair market value of such product or services.

 

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1.20             “Sublicensed Patent Rights” shall mean the rights of VLTS to:

 

(a)  US Patent Application entitled “Method for the Identification of Synthetic Cell or Tissue-Specific Transcriptional Regulatory Regions” US Patent Application Serial No. 60/052,403, filed July 14, 1997;

 

(b)  US Patent entitled “Myogenic Vector Systems” US Patent No. 5,298,422; issued March 29, 1994; and

 

(c)  and any and all divisions, reissues, re-examinations, renewals, continuations, and extensions thereof, any United States patent which issues from any such pending applications and all other counterpart, pending or issued patents in all other countries.

 

1.21             “Sublicensed Technology Rights” shall mean all technology, plasmids, biological materials, compounds, know-how, methods, documents, materials, tests and confidential information related to the technology, owned or controlled by BAYLOR or VLTS, as of the Effective Date, used in the practice of the Sublicensed Patent Rights.

 

1.22                      “VLTS Improvements” shall mean any modifications, variations and improvements of the VLTS Patent Rights, whether patentable or not, that are reduced to practice by VLTS and which, if unlicensed, would infringe one or more claims of the VLTS Patent Rights.

 

1.23                      “VLTS Licensed Product” shall mean any product or service that is made, used, marketed or sold using all or any part of the VLTS Licensed Subject Matter in the Field of Interest; provided, however, if a product or service is a “Licensed Product” as defined in Section 1.17 above, the product or service shall not be a “VLTS Licensed Product.”

 

1.24                      “VLTS Licensed Subject Matter” shall mean (i) VLTS Patent Rights (ii) VLTS Technology Rights and (iii) VLTS Improvements.

 

1.25                      “VLTS Net Sales” shall have the same meaning as “Net Sales” except that all references therein to “Licensed Product” shall be deemed to refer to “VLTS Licensed Products.”

 

1.26                      “VLTS Option” is as defined in Section 5.1.

 

1.27             “VLTS Patent Rights” shall mean US Patent entitled “Formulated Nucleic Acid Composition and the Method of Administering the Same” US Patent No. 6,040,295; issued March 21, 2000 (“the PVP Patent”), and any and all divisions, reissues, re-examinations, renewals, continuations, and extensions thereof, any United States patent which issues from any such pending applications and all other counterpart, pending or issued patents in all other countries.

 

1.28                      “VLTS  Technology Rights” shall mean all technology, plasmids, biological materials, compounds, know-how, methods, documents, materials, tests and confidential information related to the technology, in each case owned or controlled by VLTS, as of the Effective Date, used in the practice of the VLTS Patent Rights.

 

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ARTICLE 2

GRANT OF LICENSES

 

2.1                                  License to Jointly Owned Patent Rights and Joint Technology Rights .  Subject to all of the terms and conditions of this Agreement, effective as of the Effective Date, BAYLOR and VLTS each hereby grant to AVS a royalty-bearing, worldwide, exclusive license in the Field of Interest to the Jointly Owned Patent Rights and the Joint Technology Rights with rights to develop, make and have made, use, sell, market, import, distribute and otherwise commercially exploit Licensed Products.

 

2.2                                  License to Sublicensed Patent Rights and Sublicensed Technology Rights .  Subject to all of the terms and conditions of this Agreement, effective as of the Effective Date, VLTS hereby grants to AVS a royalty-bearing, worldwide, exclusive sublicense in the Field of Interest to the Sublicensed Patent Rights, and the Sublicensed Technology Rights, with rights to develop, make and have made, use, sell, market, import, distribute and otherwise commercially exploit Licensed Products.

 

2.3                                  License to VLTS Patents, VLTS Technology and VLTS Improvements . Subject to all of the terms and conditions of this Agreement, effective as of the Effective Date, VLTS hereby grants to AVS a royalty-bearing, worldwide, nonexclusive license in the Field of Interest to the VLTS Patent Rights, VLTS Technology Rights and VLTS Improvements with rights to develop, make and have made, use, sell, market, import, distribute and otherwise commercially exploit VLTS Licensed Products; provided that VLTS does not need to notify AVS of any VLTS Improvements.

 

2.4                                  License to Baylor Improvements .  Subject to all of the terms and conditions of this Agreement, effective as of the Effective Date, BAYLOR hereby grants to AVS a royalty-bearing, worldwide, exclusive license in the Field of Interest to the Baylor Improvements with rights to develop, make and have made, use, sell, market, import, distribute and otherwise commercially exploit Licensed Products.

 

2.5                            AVS VLTS Improvements .  Subject to all of the terms and conditions of this Agreement, effective as of the Effective Date, AVS grants to VLTS a royalty-free, exclusive, worldwide license outside the Field of Interest to make, have made, use and sell AVS VLTS Improvements.  VLTS shall not have the right to make, have made, use or sell AVS VLTS Improvements in the Field of Interest.

 

2.6                                  Rights Reserved by BAYLOR .  The grants in Sections 2.1, 2.2 and 2.4 shall be further subject to, restricted by and non-exclusive with respect to:

 

(a)                                   the use of the Licensed Subject Matter by BAYLOR for non-commercial research, patient care, teaching and other educationally related purposes;

 

(b)                                  any non-exclusive license to the Licensed Subject Matter that BAYLOR is required by law or regulation to grant to the United States of America or to a foreign state pursuant to an existing or future treaty with the United States of America; and

 

(c)                                   the use of the Joint Technology Rights and Jointly Owned Patent Rights by the Baylor Founders for non-commercial research purposes at academic or research institutions.

 

2.7                                  Right to Sublicense .  Subject to all the terms and conditions of this Agreement, effective as of the Effective Date, BAYLOR and VLTS each hereby grant to AVS the right to enter an agreement or agreements to sublicense the license and rights granted in Sections 2.1, 2.2 and 2.4 hereof.

 

All sublicenses granted by AVS of its rights hereunder shall be subject to the terms of this Agreement.  AVS shall be responsible for its sublicensees and shall not grant any rights which are inconsistent with the rights granted to and obligations of AVS hereunder.  Any act or omission of a

 

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sublicensee which would be a breach of this Agreement if performed by AVS shall be deemed to be a breach by AVS of this Agreement.  If after receiving notice of a sublicensee’s breach from BAYLOR or VLTS, AVS fails to take appropriate action to require such sublicensee to remedy the breach related to such act or omission, including termination of the sublicense, BAYLOR or VLTS may terminate the applicable license granted herein.  Each sublicense agreement granted by AVS shall include an audit right by BAYLOR and/or VLTS of the same scope as provided in Article 4 hereof with respect to AVS.  No such sublicense agreement shall contain any provision which would cause it to extend beyond the term of this Agreement.  AVS shall give BAYLOR and VLTS prompt notification of the identity and address of each sublicensee with whom it concludes a sublicense agreement and shall supply BAYLOR and VLTS with a copy of each such sublicense agreement.

 

ARTICLE 3

CONSIDERATION

 

3.1                                  Royalty to BAYLOR .  As part of the consideration for BAYLOR’s grant of the licenses specified in Article 2, AVS agrees to pay BAYLOR a royalty of ****** of Net Sales.

 

3.2                                  Royalty to VLTS . As part of the consideration for VLTS’ grant of the licenses and sublicense specified in Article 2, AVS agrees to pay VLTS a royalty of ****** of Net Sales.

 

3.3                                  Royalty to VLTS For VLTS Licensed Products . As part of the consideration for the grant of the licenses specified in Article 2, AVS agrees to pay VLTS a royalty of ****** of VLTS Net Sales.

 

3.4                                  Royalty Reduction If No Patent .  In the event that a sale of a Licensed Product is not covered by patent rights within the Jointly Owned Patent Rights or Sublicensed Patent Rights during the term of this Agreement, the royalty owed hereunder pursuant to each of Sections 3.1 and 3.2 shall be reduced by ******.  Provided, however, if in such case the Licensed Products includes only Joint Technology Rights or Sublicensed Technology Rights that have been publicly disclosed by BAYLOR pursuant to Section 7.7(f), AVS shall not be obligated to pay any royalties on such Licensed Products.

 

3.5                                  Exceptions to VLTS Royalty Obligations .  VLTS shall not be obligated to pay BAYLOR a royalty pursuant to the BAYLOR/VLTS Agreement, on revenues received by VLTS from AVS under the licenses granted in herein.

 

3.6                                  Stock Consideration to BAYLOR .  If BAYLOR had not received the equity interest in AVS in the form of stock as described below, BAYLOR would have insisted upon and received a greater royalty and, in consideration and in exchange for (i) property constituting good and valuable consideration, including, but not limited to, the Licensed Subject Matter, and (ii) the reduced royalty consideration provided in Section 3.1, the receipt and sufficiency of which are hereby acknowledged by the parties hereto, AVS has issued to BAYLOR for itself and on behalf of the persons and entities listed on Schedule 3.6 , an aggregate of 633,333 shares of AVS common stock, $.001 par value (the “AVS Common Stock”) as indicated on Schedule 3.6.

 

3.7                                  Stock Consideration to VLTS .  In partial consideration of the license and sublicenses received from VLTS, AVS has issued to VLTS 316,667 shares of the AVS Common Stock in accordance with the Stock Issuance Agreement in Schedule 3.7.

 

3.8                                  Payment of BAYLOR Patent Costs.   AVS shall pay all unreimbursed costs incurred by BAYLOR prior to the Effective Date incident to the filing of the Jointly Owned Patent Rights.

 

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3.9                                  No Other Royalty or Stock Consideration .  AVS shall not have any obligation to pay any other royalties or issue any other stock, other than as provided in this Article 3, in consideration of the licenses granted herein.

 

ARTICLE 4

ACCOUNTING AND RECORDS

 

4.1                                  Royalty Payment .  At the close of each quarter of AVS’ fiscal year, the Net Sales and VLTS Net Sales for the quarter shall be computed, and the royalties earned thereon shall be paid to BAYLOR and VLTS within sixty (60) days after the close of the quarter.  In the event that any payment due hereunder is not made when due, the payment shall accrue interest beginning on the tenth (10 th ) day following the due date thereof, calculated at the annual rate of the sum of (a) ****** plus (b) the prime interest rate quoted by The Wall Street Journal on the date said payment is due, the interest being compounded on the last day of each calendar quarter, provided, however, that in no event shall said annual interest rate exceed the maximum legal interest rate for corporations.  Each such royalty payment when made shall be accompanied by all interest so accrued.  Said interest and the payment and acceptance thereof shall not negate or waive the right of BAYLOR or VLTS to seek any other remedy, legal or equitable, to which it may be entitled because of the delinquency of any payment.

 

4.2                                  Royalty Report .  With each royalty payment, AVS shall furnish to BAYLOR and VLTS a written accounting report relating to the quarter stating the Net Sales, and for VLTS also the VLTS Net Sales, royalties due and royalties paid.

 

4.3                                  Written Records .  AVS agrees to keep and maintain and to require all of its sublicensees to keep and maintain written records with respect to its operations pursuant to this Agreement in sufficient detail to enable BAYLOR and VLTS or its designated accountants to compute the amount of royalties payable to BAYLOR and VLTS and further agrees to permit the records to be examined from time to time, on reasonable notice during normal business hours to the extent necessary to verify the amount of royalties due hereunder.  BAYLOR and/or VLTS shall pay the costs of the examination unless a discrepancy of greater than five percent (5%) in royalties due is present, in which case AVS shall reimburse BAYLOR and/or VLTS for the examination expenses.  All the records shall be kept for four (4) years after the royalty period to which the records relate.

 

4.4                                  Payment in U.S. Dollars .  All payments shall be paid in United States dollars, without deduction of exchange, collection or other charges, to BAYLOR and VLTS by check, or to the account of BAYLOR and VLTS at such bank as BAYLOR or VLTS may from time to time designate by notice to AVS.  All royalty payments shall be converted from the currency of the country of sale to United States dollars using the exchange rate quoted by The Wall Street Journal on the last business day of the period for which the royalty is paid.

 

4.5                                  Foreign Restrictions On Payment .  If governmental regulations prevent remittance from any foreign country of any amounts due in respect of Net Sales or VLTS Net Sales in that country in United States  Dollars, AVS shall so notify BAYLOR and VLTS in writing and, subject to the remainder of this Section 4.5, any obligation under this Agreement to make payments in respect of Net Sales in that country shall be suspended (but the amounts due but not paid shall continue to accrue) without interest until such remittances are possible; provided, however, that notwithstanding the foregoing BAYLOR and/or VLTS shall have the right, at any time and from time to time, upon written notice to AVS, to direct AVS either to pay such funds in any such country in the local currency or to liquidate such currency at available rates and pay the liquidated amounts to BAYLOR and/or VLTS.  Any such payment by AVS in accordance herewith shall be deemed to be payment in full of the amounts so paid or

 

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liquidated, and AVS shall have no further liability to BAYLOR or VLTS for any action taken in accordance with BAYLOR and/or VLTS’ instructions pursuant to this Section 4.5.

 

4.6                                  Payment Addresses.   All payments and reports shall be sent to the addresses listed in Section 15.1.

 

ARTICLE 5

OPTION TO AVS TECHNOLOGIES

 

5.1                                  New Technology Option .  AVS hereby grants to VLTS an option to negotiate a non-exclusive, royalty bearing, worldwide license to make, have made, use and sell the AVS New Technology (the “VLTS Option”) in the field of human therapeutics.  The VLTS Option shall expire twenty-four (24) months after the Effective Date.

 

5.2                                  Gene Switch Technology .  VLTS hereby grants to AVS an option to negotiate a non-exclusive, royalty bearing, worldwide license to make, have made, use and sell VLTS’ proprietary “GeneSwitch technology” (the “AVS Option”) for the use of genes within the Growth Hormone Axis in the Field of Interest.  The AVS Option shall expire twenty-four (24) months after the Effective Date.

 

5.3                                  Option Exercise Procedures .  To exercise either of the options in Sections 5.1 and 5.2, the option holder must give written notice to the party granting the option prior to the option’s expiration.  Upon such exercise the parties shall diligently and in good faith negotiate the terms of the license.  The terms shall include a commercially reasonable royalty and such other terms as are customarily included in such a license.

 

ARTICLE 6

WARRANTIES, REPRESENTATIONS, INDEMNITY AND INSURANCE

 

6.1                                  BAYLOR and VLTS Representations .

 

(a)  BAYLOR hereby represents and warrants that, (i) it is the owner of or has the right to license the Licensed Subject Matter, existing as of the Effective Date; (ii) it has the right to license the Licensed Subject Matter as contemplated herein; and (iii) other than the grants set forth herein, including, without limitation, for or to the United States of America, or for or to a foreign state, it has not encumbered, restricted, transferred or otherwise burdened its rights to the Licensed Subject Matter in the Field of Interest; and

 

(b)  VLTS hereby represents and warrants that, (i) it is the owner of or has the right to license the Licensed Subject Matter and the VLTS Licensed Subject Matter, existing as of the Effective Date; (ii) it has the right to license the Licensed Subject Matter and the VLTS Licensed Subject Matter as contemplated herein; and (iii) it has not encumbered, restricted, transferred or otherwise burdened its rights to the Licensed Subject Matter and the VLTS Licensed Subject Matter in the Field of Interest.

 

6.2                                  DISCLAIMER OF WARRANTY.  WITH THE EXCEPTION OF SECTION 6.1, BAYLOR AND VLTS EACH MAKE NO WARRANTIES OR REPRESENTATIONS, EXPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, WARRANTIES OF FITNESS OR MERCHANTABILITY, REGARDING OR WITH RESPECT TO THE LICENSED SUBJECT MATTER, THE VLTS LICENSED SUBJECT MATTER, LICENSED PRODUCTS, VLTS LICENSED PRODUCTS OR OTHER RIGHTS TRANSFERRED HEREUNDER.  BAYLOR AND VLTS EACH MAKE NO WARRANTIES OR REPRESENTATIONS, EXPRESS OR IMPLIED, OF THE

 

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PATENTABILITY, USE OR OTHER APPLICATION OF THE LICENSED SUBJECT MATTER, THE VLTS LICENSED SUBJECT MATTER, LICENSED PRODUCTS, VLTS LICENSED PRODUCTS OR OTHER RIGHTS TRANSFERRED HEREUNDER IN THE FIELD OF INTEREST OR OF THE VALIDITY OR ENFORCEABILITY OF ANY PATENTS ISSUING THEREUPON, IF ANY, OR THAT THE LICENSED SUBJECT MATTER, THE VLTS LICENSED SUBJECT MATTER, LICENSED PRODUCTS, VLTS LICENSED PRODUCTS OR OTHER RIGHTS TRANSFERRED HEREUNDER ARE OR SHALL BE FREE FROM INFRINGEMENT OF ANY PATENT OR OTHER RIGHTS OF THIRD PARTIES.  BAYLOR AND VLTS EACH MAKE NO WARRANTIES OR REPRESENTATIONS, EXPRESS OR IMPLIED, AS TO THE LIKELIHOOD OF THE SUCCESS OF ANY RESEARCH, DEVELOPMENT, TESTING, MARKETING OR OTHER UTILIZATION OF THE LICENSED SUBJECT MATTER, THE VLTS LICENSED SUBJECT MATTER, LICENSED PRODUCTS, VLTS LICENSED PRODUCTS OR OTHER RIGHTS TRANSFERRED HEREUNDER.

 

6.3                                  AVS Representations .  AVS hereby represents and warrants that:

 

(a)  it is a corporation duly organized and in good standing under the laws of the State of Delaware;

 

(b)  it is qualified to do business and in good standing in the State of Texas and elsewhere as the nature of its business and properties so require;

 

(c)                                   the execution, delivery and performance of this Agreement by AVS and the consideration provided for herein has been duly authorized by all necessary corporate action;

 

(d)                                  it has the full power and authority to enter into and carryout its obligations under this Agreement; and

 

(e)                                   the AVS Common Stock to be issued pursuant to this Agreement has been duly authorized and upon issuance, pursuant to the terms hereof and for the consideration herein set forth, will be validly issued, fully paid and non-assessable.

 

6.4                                  Indemnification by VLTS .  VLTS agrees to indemnify and hold AVS and its officers, employees, agents and representatives, harmless from any liabilities, costs and expenses (including attorneys’ fees and expenses), obligations or causes of action arising out of or related to any breach of the representations and warranties made by VLTS herein.

 

6.5                                  Indemnification by AVS Regarding Representations .  AVS agrees to indemnify and hold BAYLOR and VLTS and each of their respective officers, trustees, faculty, employees, agents and representatives, harmless from any liabilities, costs and expenses (including attorneys’ fees and expenses), obligations or causes of action arising out of or related to any breach of the representations and warranties made by AVS herein.

 

6.6                                  Indemnification by AVS Regarding Licensed Products .

 

(a)                                   AVS agrees to protect, defend, indemnify and hold BAYLOR, each of the entities with which it is or will be in the future affiliated with respect to the invention or development of Licensed Subject Matter or VLTS Licensed Subject Matter and each of BAYLOR’s officers, directors, trustees, faculty, employees, agents and representatives (“Baylor Indemnified Parties”) harmless from and against, and to pay any and all losses, liabilities, claims, demands, causes of action, lawsuits, or other proceedings (whether in contract, tort, strict liability or otherwise), fines, assessments, damages or any other amounts

 

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of whatever nature that any of the Baylor Indemnified Parties may sustain or incur, including all attorneys’ fees and court costs, as a consequence of any third party’s (including, but not limited to, AVS’ officers, directors, employees, agents, consultants, representatives or servants) claims and demands arising from any use, testing, operation, sale or manufacture, by AVS or its sublicensees, of the Licensed Subject Matter, VLTS Licensed Subject Matter, the Licensed Products, the VLTS Licensed Products or products derived therefrom, except as to the extent such claims, causes of action, law suits or other proceedings and the costs (including attorneys’ fees) related thereto arise from the gross negligence or intentional misconduct of any of the Baylor Indemnified Parties.

 

(b)                                  AVS agrees to protect, defend, indemnify and hold VLTS and each of VLTS’ officers, directors, trustees, faculty, employees, agents and representatives (“VLTS Indemnified Parties”) harmless from and against, and to pay any and all losses, liabilities, claims, demands, causes of action, lawsuits, or other proceedings (whether in contract, tort, strict liability or otherwise), fines, assessments, damages or any other amounts of whatever nature that any of the VLTS Indemnified Parties may sustain or incur, including all attorneys’ fees and court costs, as a consequence of any third party’s (including, but not limited to, AVS’ officers, directors, employees, agents, consultants, representatives or servants) claims and demands arising from any use, testing, operation, sale or manufacture, by AVS or its sublicensees, of the Licensed Subject Matter, VLTS Licensed Subject Matter, the Licensed Products, the VLTS Licensed Products or products derived therefrom, except as to the extent such claims, causes of action, law suits or other proceedings and the costs (including attorneys’ fees) related thereto arise from the gross negligence or intentional misconduct of any of the VLTS Indemnified Parties.

 

6.7                                  Indemnification Procedures .

 

(a)                                   A Baylor Indemnified Party or VLTS Indemnified Party will promptly notify AVS in writing of notice of any claims or the commencement of any action, if a claim in respect thereof is to be made against AVS under Section 6.6.  The Baylor Indemnified Party’s or VLTS Indemnified Party’s failure to notify AVS will not relieve AVS from any liability to such Baylor Indemnified Party or VLTS Indemnified Party other than any liability directly resulting from the delay. After receiving notice of said action, AVS is entitled to participate in the defense therein, and may elect to assume the defense thereof by promptly notifying the Baylor Indemnified Party and VLTS Indemnified Party in writing and by selecting counsel reasonably satisfactory to such Baylor Indemnified Party and VLTS Indemnified Party.  After the Baylor Indemnified Party and VLTS Indemnified Party has received notice of AVS’ election to assume the defense of said action and has approved AVS’ counsel, AVS will not be liable to such Baylor Indemnified Party and VLTS Indemnified Party under Section 6.6 for any legal or other expenses subsequently incurred by the Baylor Indemnified Party or VLTS Indemnified Party in connection with the defense thereof unless (i) such Baylor Indemnified Party or VLTS Indemnified Party in any action has reasonably concluded that there may be legal defenses available to it that are different from or additional to those available to AVS, in which case such Baylor Indemnified Party or VLTS Indemnified Party shall have the right to select separate counsel to assume said legal defenses and to otherwise participate in the defense of said action on behalf of such Baylor Indemnified Party or VLTS Indemnified Party, (ii) AVS shall not have employed counsel reasonably satisfactory to the Baylor Indemnified Party or VLTS Indemnified Party to represent such Baylor Indemnified Party or VLTS Indemnified Party within a reasonable time after notice of commencement of the action or (iii) AVS has authorized the employment of counsel for such Baylor Indemnified Party or VLTS Indemnified Party at the expense of AVS.

 

(b)                                  Neither a Baylor Indemnified Party nor VLTS Indemnified Party nor AVS shall settle any action covered by Section 6.6 without first obtaining the consent of the other parties, which consent will not be unreasonably withheld.

 

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(c)                                   Each Party’s indemnity obligations under this Agreement shall survive the termination of this Agreement, regardless of how this Agreement is terminated.

 

6.8                                  Insurance.   AVS shall, for so long as AVS manufactures, uses or sells any Licensed Products or VLTS Licensed Products, maintain in full force and effect policies of (i) worker’s compensation insurance within statutory limits, (ii) employers’ liability insurance with limits of not less than one million dollars ($1,000,000) per occurrence, (iii) general liability insurance (with Broad Form General Liability endorsement) with limits of not less than one million dollars ($1,000,000) per occurrence with an annual aggregate of two million dollars ($2,000,000) and (iv) at the appropriate time, products liability insurance, with limits of not less than one million dollars ($1,000,000) per occurrence with an annual aggregate of five million dollars ($5,000,000).  Such coverage(s) shall be purchased from a carrier or carriers reasonably deemed acceptable to BAYLOR and shall name BAYLOR as an additional insured.  Upon request by BAYLOR and VLTS, AVS shall provide to BAYLOR and VLTS, as the case may be, copies of said policies of insurance.

 

6.9                                  AVS Acknowledgment .  AVS understands that there is no assurance that any patents included in the Jointly Owned Patent Rights, Sublicensed Patent Rights or the VLTS Patent Rights or any patent application subsequently filed on the Licensed Subject Matter or VLTS Licensed Subject Matter will actually be issued or, if issued, will be held not invalid by a court of competent jurisdiction.

 

ARTICLE 7

PROTECTION OF PROPERTY RIGHTS

 

7.1                                  VLTS Determination to File .  VLTS shall decide whether to file United States and foreign patent applications, continue prosecution of any patent applications or to maintain any patent application or patent regarding the VLTS Licensed Subject Matter or Licensed Subject Matter; provided that such Licensed Subject Matter does not include Baylor Improvements.  VLTS will notify AVS of its decisions regarding the patent applications and patents.

 

7.2                                  BAYLOR Determination to File.   In cases where Licensed Subject Matter includes Baylor Improvements, BAYLOR shall decide whether to file United States and foreign patent applications, continue prosecution of any patent applications or to maintain any patent application or patent regarding such Licensed Subject Matter.  BAYLOR will notify AVS of its decisions regarding such patent applications and patents.

 

7.2                                  Patent Costs .  VLTS and AVS (in the case of Baylor Improvements) agree to pay all costs, incident to the United States and foreign applications, patents and like protection that it elects to pursue at its sole discretion, including all costs incurred for filing, prosecution, issuance and maintenance fees as well as any costs incurred in filing continuations, continuations in-part, divisionals or related applications and any re-examination or reissue proceedings.

 

7.3                                  AVS and BAYLOR Right to Assume Filing .  For the Licensed Subject Matter that does not contain Baylor Improvements, if VLTS decides not to continue prosecution of a patent application to issuance or maintain any United States or foreign patent application or patent on technology within such Licensed Subject Matter, VLTS shall timely notify AVS in writing in order that AVS may file United States and appropriate foreign applications and continue prosecution or maintenance of such patent applications at its own expense.  Notwithstanding AVS’ assumption of the patent prosecution or maintenance, VLTS retains the right to practice the invention that is the subject of the applicable patent.  If AVS also decides not to continue prosecution of a patent application to issuance or maintain any

 

11



 

United States or foreign patent application or patent within such Licensed Subject Matter, AVS shall timely notify BAYLOR in writing in order that BAYLOR may file United States and foreign applications and continue prosecution or maintenance of such patent applications at its own expense.  Whether or not AVS decides to assume the prosecution of any application, AVS shall retain right to use the rights licensed hereunder subject to the terms hereof.

 

7.4                                  AVS Right to Assume Filing .  In those cases that Licensed Subject Matter includes Baylor Improvements, if BAYLOR decides not to continue prosecution of a patent application to issuance or maintain any United States or foreign patent application or patent on technology within such Licensed Subject Matter, BAYLOR shall timely notify AVS in writing in order that AVS may file United States and appropriate foreign applications and continue prosecution or maintenance of such patent applications at its own expense.  Whether or not AVS decides to assume the prosecution of any application, AVS shall retain right to use the rights licensed hereunder subject to the terms hereof.

 

7.5                                  Information Regarding Filings .  (i) VLTS agrees to keep AVS and BAYLOR fully informed, at VLTS’ expense, of prosecutions of Licensed Subject Matter that does not contain Baylor Improvements pursuant to this Article 7 including submitting to AVS and BAYLOR copies of all official actions and responses thereto; provided, however, AVS and BAYLOR shall be responsible for any of their expenses including attorneys’ fees that AVS or BAYLOR incurs in reviewing and commenting on the information AVS or BAYLOR receives from VLTS.  As per Section 7.3, VLTS shall notify AVS and BAYLOR regarding any abandonment of the prosecution of the patents and (ii) in those cases that Licensed Subject Matter includes Baylor Improvements, BAYLOR agrees to keep AVS fully informed, at AVS’ expense, of prosecutions of such Licensed Subject Matter pursuant to this Article 7 including submitting to AVS copies of all official actions and responses thereto.  As per Section 7.4, BAYLOR shall notify AVS regarding any abandonment of the prosecution of such patents.

 

7.6                                  Cooperation .  AVS, VLTS and BAYLOR agree to reasonably cooperate with the other parties to whatever extent is reasonably necessary to procure patent protection of any rights, including fully agreeing to execute any and all documents to provide AVS the full benefit of the licenses granted herein.

 

7.7                                  Confidentiality .  Each party shall use its best efforts to maintain and assure the confidentiality of the Confidential Information disclosed to it by the other parties; provided, however, none of the parties shall have an obligation of confidentiality with respect to Confidential Information that:

 

(a)                                   at the time of its disclosure or thereafter is disclosed in a publicly available document through no fault of the receiving party;

 

(b)                                  at the time of its disclosure is, or thereafter becomes without fault of the receiving party, part of the public domain;

 

(c)                                   was in the possession of the receiving party prior to disclosure by the disclosing party hereunder, except if received in conjunction with the transactions contemplated under this Agreement, and was not acquired directly or indirectly from any third party under obligation of confidentiality to the disclosing party;

 

(d)                                  subsequent to its disclosure, is obtained from a third party not subject to a contractual or fiduciary obligation for confidentiality to the disclosing party;

 

12



 

(e)                                   is required by court or governmental order, law or regulation to be disclosed; or

 

(f)                                     if BAYLOR Confidential Information is disclosed pursuant to any research grant relating to the Licensed Subject Matter from a non-commercial granting entity, such as grants from the United States Department of Health and Human Services and other governmental and private non-profit agencies; provided, however, that AVS be notified of the terms of such research grant applications within sixty (60) days after submission of such research grant.

 

7.7                                  Permitted Disclosure .  Notwithstanding the foregoing, the parties understand and agree that AVS may, to the extent it deems necessary or appropriate, disclose the Licensed Subject Matter and VLTS Licensed Subject Matter to potential licensees, purchasers, investors, joint ventures and the like, but AVS agrees to make such disclosures subject to a satisfactory confidentiality agreement.

 

ARTICLE 8

RIGHTS IN ADDITIONAL RESEARCH

 

8.1                                  The parties acknowledge that AVS may support research on the Licensed Subject Matter in laboratories and facilities at BAYLOR that are under the direct personal supervision of the Baylor Founders and that said research may result in discoveries or inventions (“Funded Technology”) that are not included within the definition of Licensed Subject Matter transferred by this Agreement.  Nothing in this Agreement shall be deemed to allocate rights or ownership of any Funded Technology, and any rights to Funded Technology shall be determined by a separate written agreement.

 

ARTICLE 9

INFRINGEMENT

 

                                                9.1                                  Notice and Right To Bring Suit .  Each party shall promptly inform the other of any suspected infringement of any  Licensed Subject Matter rights or misuse, misappropriation, theft or breach of confidence of other Licensed Subject Matter licensed hereunder in the Field of Interest by a third party.  With respect to such activities as are suspected, VLTS shall have the right, but not the obligation, to institute an action for infringement, misuse, misappropriation, theft or breach of confidence of the proprietary rights against such third party.  If VLTS fails to bring such action proceedings within a period of three (3) months after receiving notice or otherwise having knowledge of such infringement, then AVS shall have the right, but not the obligation, to prosecute at its own expense any such claim. If AVS fails to bring such action  within a period of three (3) months after receiving notice or otherwise having knowledge of such infringement, then BAYLOR shall have the right, but not the obligation, to prosecute at its own expense any such claim.  Should any of BAYLOR, VLTS or AVS commence suit under the provisions of this Article 9 and thereafter elect to abandon the same, it shall give timely notice to the other parties who may, if they so desire, continue prosecution of such suit.  All recoveries, whether by judgment, award, decree or settlements, from infringement or misuse of Licensed Subject Matter shall be apportioned as follows: the party bringing the suit shall first recover an amount equal to two (2) times the costs and expenses incurred by such party directly related to the prosecution of such action.  The remainder, if concerning Licensed Subject Matter, shall be divided equally among AVS, VLTS and BAYLOR.  Each party agrees to cooperate with any party bringing suit, at the expense of the party bringing suit, including being joined as a party to such suit if necessary to prosecute such action; provided, however that BAYLOR shall have the right, but not the obligation, to join in such an action.  No party shall settle any action under this Section 9.1 without the consent of BAYLOR and VLTS, such consent not to be unreasonably withheld, where such settlement may affect patent validity, enforceability, infringement or interpretation.

 

13



 

9.2                                  Disclaimer of Liability .  Neither BAYLOR nor VLTS shall be liable for any losses incurred as the result of an action for infringement brought against AVS as the result of AVS’ exercise of any right granted under this Agreement.

 

9.3                                  Enforcement of VLTS Licensed Subject Matter.   VLTS shall have no obligation to prosecute or enforce any patent rights or any misuse, misappropriation or theft of breach of confidence claims with respect to VLTS Licensed Subject Matter.  All such enforcement or prosecution activities shall be within VLTS’ sole discretion.

 

ARTICLE 10

INDEPENDENT CONTRACTOR STATUS

 

10.1  The parties hereby acknowledge and agree that each is an independent contractor and that none of the parties shall be considered to be the agent, representative, master or servant of the other party for any purpose whatsoever, and that none of the parties has any authority to enter into a contract, to assume any obligation or to give warranties or representations on behalf of the other party. Nothing in this relationship shall be construed to create a relationship of joint ventures, partnerships, fiduciary or other similar relationships among the parties.

 

ARTICLE 11

TERM AND TERMINATION

 

11.1                            Term .  Unless sooner terminated as otherwise provided herein, the licenses granted herein pursuant to Article 2 shall terminate on the later of (i) the date of expiration of the last of the Jointly Owned Patent Rights, Sublicensed Patent Rights or VLTS Patent Rights licensed hereunder to expire and (ii) in the event no patents included within the Licensed Subject Matter or VLTS Licensed Subject Matter issue, the first date following the twelfth (12 th ) anniversary of the First Commercial Sale.

 

11.2                            Automatic Termination .  This Agreement shall be terminated automatically in any one or more of the following circumstances:

 

(a)                                   the assets of AVS are seized or attached, in conjunction with any action against them by any third party, and such seizure or attachment is not abated within ninety (90) days;

 

(b)                                  AVS is dissolved, or a sale of all or substantially all of the assets of AVS pursuant to a liquidation not approved in writing by BAYLOR and VLTS is made; or

 

(c)                                   a breach of Section 13.1 or Section 13.2.

 

11.3                            Termination Upon Breach .  Each of BAYLOR and VLTS may terminate this Agreement with respect to their respective grants hereunder if AVS fails to perform any of its material obligations under this Agreement and fails to remedy the default within thirty (30) days after being given written notice of the specific failure or default and termination by BAYLOR or VLTS; however, if the default is susceptible of being cured but the cure cannot be reasonably completed within the thirty-day (30-day) period, this Agreement may only be terminated if AVS fails to promptly commence and thereafter diligently prosecute actions to cure the default.

 

11.4                            Termination Upon Failure to Obtain Financing .  Each of BAYLOR and VLTS may terminate this Agreement with respect to their respective grants hereunder if AVS fails to secure, in the

 

14



 

aggregate, at least two million five hundred thousand dollars ($2,500,000) in financing within two (2) years of the Effective Date.

 

11.5                            AVS Right to Terminate .  AVS, upon  one hundred eighty (180) days prior written notice to BAYLOR and VLTS, may terminate this Agreement with respect to any of their respective grants hereunder with or without cause.

 

11.6                            Effect of Termination . If this Agreement is terminated pursuant to Sections 11.2, 11.3 or 11.4, then:

 

(a)                                   any and all rights in and to the Licensed Subject Matter shall revert to BAYLOR and VLTS in the case of Jointly Owned Patent Rights, to VLTS in the case of Sublicensed Patent Rights or to BAYLOR in the case of Baylor Improvements;

 

(b)                                  any and all rights in and to the VLTS Licensed Subject Matter shall revert to VLTS;

 

(c)                                   all grants and licenses made by BAYLOR and VLTS to AVS pursuant to this Agreement shall automatically terminate;

 

(d)                                  AVS will deliver to BAYLOR and VLTS, as the case may be, within ten (10) days of termination all copies in its possession or control of all documents and other tangible information that contain the Licensed Subject Matter and/or VLTS Licensed Subject Matter;

 

(e)                                   AVS agrees to execute all instruments as BAYLOR may reasonably request that are necessary to reinvest any licensed rights in BAYLOR;

 

(f)                                     AVS, subject to Article 7, shall have an obligation to maintain the confidentiality of all Licensed Subject Matter and VLTS Licensed Subject Matter;

 

(g)                                  AVS shall have thirty (30) days to complete the manufacture and ninety (90) days to complete the sale or license of any Licensed Products and VLTS Licensed Products in stock or in the course of manufacture at the time of termination, all subject, however, to payments of royalty and accounting as provided herein, even if such royalty obligations arise from transactions subsequent to the effective date of termination.

 

11.7                            Obligation to Pay Accrued Royalties .  AVS’ obligation to pay royalties accruing before the termination date, keep records and allow a final audit shall survive termination.

 

11.8                            Stock Remains Outstanding .  The AVS Common Stock issued or other consideration paid pursuant to this Agreement or the ownership thereof shall not be affected by any termination hereof, regardless of the reason for, or the timing of, such termination.

 

11.9                            Survival of Accrued Liabilities .  Except as expressly provided herein, no party hereunder shall be discharged or relieved from any liability or obligation existing prior to such termination.

 

11.10                      Survival of Sublicenses.   In the event that the license granted to AVS under this Agreement is terminated, any granted sublicenses shall remain in full force and effect as direct license from BAYLOR and VLTS to each sublicensee(s); provide, however, that such sublicensee(s) agree to abide by all of the terms of this Agreement.

 

15



 

ARTICLE 12

GOVERNMENTAL COMPLIANCE

 

12.1                            Compliance With Laws .  AVS shall at all times during the term of this Agreement and for so long as it shall sell Licensed Products or VLTS Licensed Products comply and cause its sublicensees to comply with all Applicable Laws that may control the import, export, manufacture, use, sale, marketing, distribution and other commercial exploitation of Licensed Products, VLTS Licensed Products or any other activity undertaken pursuant to this Agreement.

 

12.2                            Required Letter of Assurance .  AVS understands and agrees that before BAYLOR and VLTS shall be required to perform any obligation hereunder that shall be subject to Applicable Laws, AVS shall first provide BAYLOR and VLTS with any letter of assurance or other certification that may be required to comply with the Applicable Laws of any agency or instrumentality having jurisdiction. For example and not by limitation, this includes United States import and export regulations, Food & Drug Administration regulations, Department of Agriculture regulations, environmental regulations and recombinant DNA regulations.

 

12.3                            Further Acts .  Each party shall reasonably assist the other, execute any required documentation and take such other action as may be reasonably necessary to allow a party to perform its obligations under this Agreement in accordance with all Applicable Laws.

 

12.4                            Failure to Obtain Governmental Approvals .  Inability or failure, if any, of AVS to secure any necessary government license or approval shall not entitle AVS to terminate this Agreement or to obtain any form of relief, credit, rebate or recovery from BAYLOR or VLTS.

 

12.5                            Compliance Costs .  AVS shall be responsible for any and all expenses, costs, fees, duties or taxes necessary to comply with government orders, formalities, rules, regulations and laws.

 

ARTICLE 13

ASSIGNMENT AND LICENSING

 

13.1                            Assignment .  AVS may not assign or attempt to assign any rights under this Agreement, except in connection with the sale of substantially all of its assets, without the prior written consent of both BAYLOR and VLTS, which consent shall not be unreasonably withheld.

 

13.2                            License .  Except as expressly permitted by the Agreement, AVS may not license or attempt to license any rights under this Agreement without the prior written consent of both BAYLOR and VLTS, which consent shall not be unreasonably withhold.

 

13.3                            Preexisting Agreements.   This Agreement shall not supersede any preexisting agreement BAYLOR and VLTS have with a third party in the event that this Agreement is assigned by AVS to that third party, even if BAYLOR and VLTS have consented to the assignment.

 

ARTICLE 14

PUBLICITY

 

14.1                            No party shall use the name, logotypes or symbols of the other parties or the name of any employee, faculty, staff, director, trustee, officer, affiliate or associate of the other parties for publication or advertising purposes, except with the written consent of the applicable party.

 

16



 

ARTICLE 15

ADDRESSES

 

15.1                            Payments.

 

(a)                                   All payments to BAYLOR shall be made payable to “Baylor College of Medicine” and all payments and reports to BAYLOR shall be sent to the address below:

 

BAYLOR Tax ID #: 74-1613878

Director, Office of Technology Administration

Baylor College of Medicine

1709 Dryden Road, Suite 901

Houston, TX  77030

 

(b)                                  All payments to VLTS shall be made payable to “Valentis, Inc.” and all payments and reports to VLTS shall be sent to the address below:

 

Valentis, Inc.

863A Mitten Road

Burlingame, CA  94010

 

15.2                            Notices.   All notices or other communication pursuant to this Agreement shall be sufficiently made or given on the date of mailing if sent to such party by United States Postal Service certified mail, return receipt requested, postage prepaid, or via overnight courier, addressed to it at its address below or as it shall designate by written notice given to the other party:

 

In the case of BAYLOR:

 

With a copy to:

Senior Vice President & General Counsel

 

Director, Office of Technology Administration

Baylor College of Medicine

 

Baylor College of Medicine

One Baylor Plaza

 

1709 Dryden Road, Suite 901

Houston, TX 77030

 

Houston, TX 77030

 

 

 

In the case of VLTS:

 

 

Legal Department

 

 

Valentis, Inc.

 

 

863A Mitten Road

 

 

Burlingame, CA 94010

 

 

 

 

 

In the case of AVS:

 

 

President

 

 

Applied Veterinary Systems, Inc.

 

 

1709 Dryden Road, Suite 901

 

 

Houston, TX 77030

 

 

 

ARTICLE 16

MISCELLANEOUS

 

16.1                            Further Acts .  Without further consideration, BAYLOR and VLTS each hereby agree to execute and deliver, and BAYLOR agrees to cause its officers, trustees, employees, and agents to execute and deliver, such other instruments, and to take such other action as AVS hereunder may reasonably

 

17



 

request to more effectively convey and transfer to and vest in AVS, and to put AVS in possession of, the rights granted hereunder, and to assist AVS in the recordation of same as necessary, all in such form and substance as AVS may reasonably request and at AVS’ expense.

 

16.2                            Binding On Successors .  This Agreement shall be binding upon and shall inure to the benefit of the legal representatives, administrators, successors, permitted assigns and licensees of the parties hereto.

 

16.3                            Governing Law .  This Agreement shall be deemed to be subject to, and have been made under, and shall be construed and interpreted in accordance with the laws of the State of Texas. This Agreement is expressly acknowledged to be subject to all federal laws including but not limited to the Export Administration Act of the United States of America. No conflict-of-laws rule or law that might refer such construction and interpretation to the laws of another state, republic, or country shall be considered.

 

16.4                            Consent to Jurisdiction .  This Agreement is performable in part in Harris County, Texas, and the parties mutually agree that personal jurisdiction and venue shall be proper in the state and federal courts situated in Harris County, Texas, and agree that any litigated dispute will be conducted solely in such courts.

 

16.5                            Severability .  If any word, sentence, paragraph or clause or combination thereof of this Agreement is found, by a court or executive body with judicial powers having jurisdiction over this Agreement or any of its parties hereto, in a final unappealed order to be in violation of any law, rule or regulation in any country or community or association of countries, such words, sentences, paragraphs or clauses or combination shall be inoperative in such country or community or association of countries, and the remainder of this Agreement shall remain binding upon the parties hereto.

 

16.6                            Entire Agreement .  The terms and conditions herein contained, including all the schedules hereto, and all the agreements referenced herein, or contemplated by any of such agreements constitute the entire agreement between the parties and supersede all previous communications whether oral or written between the parties hereto with respect to the Licensed Subject Matter and VLTS Licensed Subject Matter hereof, and no previous agreement or understanding varying or extending the same shall be binding upon any of the  parties hereto.

 

16.7                            No Waiver .  The parties covenant and agree that if a party fails or neglects for any reason to take advantage of any of the terms herein or if a party, having the right to declare this Agreement terminated, shall fail to do so, any such failure or neglect by such party shall not be a waiver or be deemed or be construed to be a waiver of any cause for the termination of this Agreement subsequently arising, or as a waiver of any of the terms, covenants or conditions of this Agreement or of the performance thereof.  None of the terms, covenants and conditions of this Agreement may be waived by a party except by its written consent.

 

16.8                            Survival .  The provisions, rights and obligations set forth in Articles 1, 3, 4, 5, 6, 7, 8, 9, 10, 12, 13, 14, 15 and 16, and Sections 2.1, 2.2 and 2.3 (insofar as Section 2.1, 2.2 and 2.3 pertain to Licensed Products or VLTS Licensed Products), and 11.6, along with any other obligations and rights that by their terms survive termination, shall survive the termination of this Agreement.

 

16.9                            Amendment .  No amendment or modification to this Agreement shall be effective unless it is in writing and signed by duly authorized representatives of both parties.

 

18



 

16.10                      Construction .  The parties acknowledge that each party has received and reviewed this Agreement and that normal rules of construction to the effect that any ambiguities are to be resolved against the drafting party shall not be employed in the interpretation of this Agreement or any amendments or exhibits thereto.

 

19



 

IN WITNESS WHEREOF, the Parties hereto have executed and delivered this Agreement in multiple originals by their duly authorized officers and representatives on the respective dates shown below, but effective as of the Effective Date.

 

 

BAYLOR COLLEGE OF MEDICINE

APPLIED VETERINARY SYSTEMS, INC.

 

 

 

 

Name:

/s/ W. Dalton Tomlin

 

Name:

/s/ William A. McMinn

 

W. Dalton Tomlin

 

 

William A. McMinn

 

 

 

 

 

Title:

Senior Vice President &

 

Title:

Vice President

 

General Counsel

 

 

 

 

 

 

 

 

 

 

 

 

 

VALENTIS, INC.

 

 

 

 

 

 

 

 

Name:

/s/ Margaret M. Snowden

 

 

 

 

 

 

 

 

 

 

 

 

 

Title:

VP, Intellectual Property & Legal Affairs

 

 

 

 

 

 

 

 

 

 

 

 

 

Date:

07/14/00

 

 

 

 

 

 

 

 

 

 

 

5/16/00

VLTS

OTA 98-24, 98-25, 98-36

 

 

 

20


 

Schedule 1.6

 

BAYLOR FOUNDERS

 

1.                                        Robert Schwartz

 

2.                                        Bert W. O’Malley

 

3.                                        Ruxandra Draghia-Akli

 

4.                                        Xuyang Li

 

1



 

Schedule 3.6

 

DISTRIBUTION OF SHARES OF COMMON STOCK

 

NAME

 

NUMBER OF COMPANY SHARES ISSUED

 

 

 

 

 

Baylor College of Medicine

 

329,999

 

 

 

 

 

Robert Schwartz

 

146,878

 

 

 

 

 

Bert W. O’Malley

 

123,872

 

 

 

 

 

Ruxandra Draghia-Akli

 

30,084

 

 

 

 

 

Xuyang Li

 

2,500

 

 

1




EXHIBIT 10.27

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

BAYLOR COLLEGE OF MEDICINE

 

APPLIED VETERINARY SYSTEMS, INC.

 

LICENSE AGREEMENT

 

This License Agreement (this “Agreement”) is made and entered into on this 25th day of January, 2001 (the “Agreement Date”), by and between Baylor College of Medicine (hereinafter called “BAYLOR”), a Texas non-profit corporation having its principal place of business at One Baylor Plaza, Houston, Texas 77030, and Applied Veterinary Systems, a corporation organized under the laws of Delaware and having a principal place of business at 1709 Dryden Road, Suite 901, Houston, Texas 77030 and its Affiliates (hereinafter, collectively referred to as “AVS”).

 

WITNESSETH:

 

WHEREAS, BAYLOR, AVS AND Valentis, Inc. have entered into a License Agreement dated June 26, 2000 (the “First License Agreement”) pursuant to which AVS has licensed from BAYLOR, and Valentis certain rights to the technology described therein;

 

WHEREAS, BAYLOR, by virtue of its relationship with its faculty, staff and students, and conveyances with the individuals listed on Schedule 1, and under and pursuant to the terms and provisions of its Policy on Inventions and Patents (the “Baylor Patent Policy”), is the owner of certain right, title and interest in and to the Licensed Subject Matter (as defined below); and

 

WHEREAS, AVS, as per Article 5.2 of that certain Sponsored Research Agreement between BAYLOR and AVS (dated January 14, 1998), had an option to acquire an exclusive license to the Licensed Subject Matter with said option period extended to June 1, 2000 via three Amendments to the Sponsored Research Agreement; and

 

WHEREAS, AVS indicated its intention to exercise the option and acquire an exclusive license to the Licensed Subject Matter; and

 

WHEREAS, BAYLOR desires to grant to AVS and AVS desires to obtain an exclusive worldwide license to employ the Licensed Subject Matter and to make, use, sell, have made and otherwise market and commercialize Licensed Products and Licensed Patented Products; and

 

WHEREAS, BAYLOR sometimes negotiates licenses for the rights to market and commercialize the technology it develops to third parties in exchange for the receipt of equity (such as stock or partnership interests) and accepts a royalty which is reduced from the royalty which it would receive were no such equity negotiated for and received.

 

NOW, THEREFORE, in consideration of the mutual promises and obligations hereinafter set forth and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereto stipulate and agree as follows:

 



 

ARTICLE 1

 

DEFINITIONS

 

1.1           “Affiliate” shall mean any corporation, partnership, joint venture or other entity of which the common stock or other equity ownership thereof is twenty five percent (25%) or more owned by AVS or BAYLOR.

 

1.2           “Baylor Patent Policy” is as defined in the first Whereas clause.

 

1.3           “Common Stock” is as defined in Paragraph 3.4.

 

1.4           “Confidential Information” shall mean any proprietary and secret ideas, proprietary technical information, know-how and proprietary commercial information or other similar proprietary information.

 

1.5           “First Commercial Sale” shall mean the first sale of a Licensed Product to an independent third party for commercial use (i.e. not for review, evaluation, or testing of the Licensed Product).

 

1.6           “Funded Technology” is as defined in Paragraph 7.1.

 

1.7           “Indemnified Parties” is as defined in Paragraph 5.4.

 

1.8           “Licensed Product” shall mean any product or service that is made, used, imported, marketed, or sold using all or any part of the Licensed Subject Matter.

 

1.9           “Licensed Products Net Sales” shall mean that portion of Net Sales related to Licensed Products.

 

1.10         “Licensed Subject Matter” shall mean and include the Patent Rights, together with all improvements, technology, plasmids, biological materials, compounds, know-how, methods, documents, materials, tests, and confidential information, whether or not patentable, in each case that are related to, or pertain to, the Patent Rights and are currently, or prior to the first anniversary of the Effective Date become, (i) owned by BAYLOR and arise out of work performed in a laboratory at BAYLOR that is under the direct supervision of the Baylor Founders or (ii) developed in a laboratory at BAYLOR that is under direct supervision of the Baylor Founders. Licensed Subject Matter shall not include know-how, discoveries and inventions developed in laboratories at BAYLOR not under the direct supervision of the Baylor Founders.

 

1.11         “Net Sales” shall mean all monies and equivalent goods and services actually received by AVS or its sublicensees from the manufacture, use, sale, lease, or other commercial exploitation of Licensed Products less the following:

 



 

(a)           any credits or refunds actually granted to customers for the return of Licensed Products that were previously sold;

 

(b)           any separately identified sales, use, excise or similar taxes and custom duties or other governmental charges imposed upon the importation or sales of Licensed Products, except for taxes on income;

 

(c)           any separately identified charges for transportation, packing, insurance, shipping, or handling which are directly associated with sales of Licensed Products; and

 

(d)                                  in the event that AVS is required to pay a royalty to an unrelated third party in order to make, use, or sell a Licensed Product, such amounts actually paid to such third party; provided, however, in no event shall the reduction due to royalties paid to other parties exceed ****** of the “Net Sales” amount as calculated prior to such reduction.

 

If Licensed Products are sold in combination with other products or as part of a product then the Net Sales for such combined products shall be the price paid by the third party purchaser for the combined product times a fraction the numerator of which is the cost of producing the Licensed Product and the denominator of which is the cost of producing the entire combined product.

 

Notwithstanding the foregoing, Net Sales shall not include monies and equivalent goods and services (“Payments”) received from a sponsor for research and development programs for development, including testing, of new vector or gene delivery technologies, new products, or refinement, to AVS’ existing methodologies to deliver the GHRH gene; provided, however, Net Sales shall include Payments for any research and development programs if the product or results of such research and development programs can be or is manufactured, used, sold, leased or otherwise commercially exploited by any sponsor of such research and’ development programs without making additional Payments or if any additional Payments are below the fair market value of such products or services.

 

1.12  “Patent Rights” shall mean (i) the United States Patent Application ****** , and (ii) the United States Patent Application ******, and all corresponding foreign patent applications and any and all divisions, reissues, re-examinations, renewals, continuations, claims of continuation-in-part applications and patents issued therefrom directed to subject matter specifically described in the aforementioned patents or foreign applications, and extensions thereof, and all other counterpart applications in all other countries and patents, inventor’s certificates, utility models and the like issuing therefrom, which list shall be amended and updated from time to time.

 



 

1.13         “Party” shall mean either AVS or BAYLOR, and “The Parties” shall mean AVS and BAYLOR.

 

1.14         “Sponsored Research Agreement” shall mean the research agreement between AVS and BAYLOR, having an effective date of January 14, 1998. The Option period in the original agreement was extended to June I, 2000 via three Amendments to the Sponsored Research Agreement. The Sponsored Research Agreement and Amendments thereto are attached to this Agreement as Schedule 1.14.

 

1.15         “Sublicensing Revenue” shall mean all (i) cash, (ii) sublicensing fees and (iii) all other payments and the cash equivalent thereof, which are paid to AVS by the sublicensees of its rights hereunder, other than research and development money paid to AVS to conduct research.

 

1.16         “Valid Claim” shall mean a pending or issued claim of an unexpired patent included within the Patent Rights claiming an invention, which has not been revoked or held unenforceable or invalid by a decision of a court or other governmental agency of competent jurisdiction, unappealable or unappealed within the time allowed for appeal, and which has not been disclaimed, denied or admitted to be invalid or unenforceable through reissue, disclaimer or otherwise.

 

ARTICLE 2

 

GRANT OF EXCLUSIVE LICENSE

 

2.1           Grant of License. Subject to the reservations of rights set forth in Paragraph 2.2 and effective as of the Agreement Date and continuing through the term of this Agreement, BAYLOR hereby grants to AVS an exclusive, worldwide right and license with rights to sublicense the Licensed Subject Matter with rights to use, develop, make, have made, market, sell, offer to sell and otherwise commercially exploit Licensed Products.

 

2.2           Rights Reserved by Baylor . The grant in Paragraph 2.1 shall be further subject to, restricted by and non-exclusive with respect to:

 

(a)           the use of the Licensed Subject Matter by BAYLOR for non-commercial research, patient care, teaching and other educationally related purposes;

 

(b)           the use of the Licensed Subject Matter by the Baylor Founders for noncommercial research purposes at academic or research institutions; and

 

(c)           any non exclusive license of the Licensed Subject Matter that BAYLOR is required by law or regulation to grant to the United States of America or to a foreign state pursuant to an existing or future treaty with the United States of America.

 

2.3           Right to Sublicense . Subject to all the terms and conditions of this Agreement, effective as of the Effective Date, BAYLOR grants to AVS the right to enter into an agreement or agreements to sublicense the license and rights granted in Section 2.1 hereof.

 



 

All sublicenses granted by AVS of its rights hereunder shall be subject to the terms of his Agreement. AVS shall be responsible for its sublicensees and shall not grant any rights which are inconsistent with the rights granted to and obligations of AVS hereunder. Any act or omission of   sublicensee which would be a breach of this Agreement if performed by AVS shall be deemed to be a breach by AVS of this Agreement. If after receiving notice of a sublicensee’s breach from BAYLOR, AVS fails to take appropriate action to require such sublicensee to remedy the breach related to such act or omission, including termination of the sublicense, BAYLOR may terminate the applicable license granted herein. Each sublicense agreement granted by AVS shall include an audit right by BAYLOR of the same scope as provided in Article 4 hereof with respect to AVS. No such sublicense agreement shall contain any provision which would cause it to extend beyond the term of this Agreement. AVS shall give BAYLOR prompt notification of the identity and address of each sublicensee with whom it concludes a sublicense agreement and shall supply BAYLOR with a copy of each such sublicense agreement.

 

ARTICLE 3

 

CONSIDERATION

 

3.1           Royalty to BAYLOR . In consideration of the grant of the exclusive licenses specified in Paragraph 2.1, and in adherence to Article 5.2 (e) of the Sponsored Research Agreement, AVS agrees to pay BAYLQR a royalty of ****** of Net Sales of Licensed Products.

 

3.2           Royalty Reduction if No Patent . In the event that a sale of a Licensed Product is not covered by patent rights within the Patent Rights during the term of this agreement, the royalty owed hereunder pursuant to section 3.1 shall be reduced to ****** of Net Sales of Licensed Products; provided, however, if in such case the Licensed Products include only Technology Rights that have been publicly disclosed by BAYLOR pursuant to Section 6.7 (f), AVS shall not be obligated to pay royalties on such licensed products.

 

3.3           Maximum Royalty . Notwithstanding anything contained herein, or in the First License Agreement or any other agreement ‘between BAYLOR and AVS, if any product that is a Licensed Product would otherwise entitle BAYLOR to a royalty under this Agreement and under the First License Agreement and/or any other license between BAYLOR and AVS, in no event will the maximum combined royalty to be paid under all agreements between BAYLOR and AVS exceed ******.

 

3.4           Stock Consideration to BAYLOR . Since, but for the equity received hereunder, BAYLOR would have insisted upon and received a greater royalty and, in consideration and in exchange for (i) property constituting good and valuable consideration, including, but not limited to, the Technology, and (ii) the reduced royalty consideration provided in Paragraphs 3.1 and 3.2, the receipt and sufficiency of which are hereby acknowledged by the Parties hereto, AVS shall issue to BAYLOR upon execution of the Agreement, 100,000 shares of its common stock, $0.01  par value (the “Common Stock”).

 



 

3.4.1        AVS may repurchase, on a pro-rated basis, from BAYLOR and the Baylor inventors (as listed in Schedule 1), Twenty-Five Thousand (25,000) of the shares of Common Stock issued hereunder at a price of $0.01 per share if a patent claiming priority to the U.S. Patent Application 09/624,268 entitled “Super-Active Porcine Growth Hormone Releasing Hormone Analog”, is not issued within six (6) years of the Effective Date. The issuance or receipt of notice of allowance of any divisional application, continuation-in-part application, continuation application, reissue, re-examination, or renewal claiming priority to U.S. Patent Application 09/624,268 or any corresponding foreign patent application shall completely satisfy the requirement for an issued patent and shall terminate the repurchase provision. lf AVS exercises the repurchase provision, any and all rights associated with the Patent Rights shall immediately revert to Baylor, with the exception of claims of continuation-in-part applications that are developed by AVS and not disclosed in the original patent applications licensed to the company.

 

3.4.2        AVS may repurchase, on a pro-rated basis, from BAYLOR and the Baylor inventors (as listed in Schedule 1), Twenty-Five Thousand (25,000) of the shares of Common Stock issued hereunder at a price of $0.01 per share if a patent claiming priority to the U.S. Patent Application entitled “Increasing Growth In Offspring through Administration of Growth Hormone Releasing Hormone to Pregnant Mothers,” filed December 13, 2000, is not issued within six (6) years of the Effective Date. The issuance or receipt of notice of allowance of any divisional application, continuation-in-part application, continuation application, reissue, re-examination, or renewal claiming priority the U.S. Patent Application entitled “Increasing Growth in Offspring through Administration of Growth Hormone to Pregnant Mothers” or any corresponding foreign patent application shall completely satisfy’ the requirement for an issued patent and shall terminate the repurchase provision. If AVS exercises the repurchase provision, any and all rights associated with the Patent Rights shall immediately revert to Baylor, with the exception of claims of continuation-in-part applications that are developed by AVS and not disclosed in the original patent applications licensed to the company.

 

3.4.3        The Company shall exercise its repurchase rights only after meeting with BAYLOR to discuss the state of prosecution of the Patent Rights, then by giving written notice of exercise and delivering the repurchase price to BAYLOR within six (6) months of the seventh anniversary of the Effective Date.

 

3.4.4        The repurchase provisions of articles 3.4.1 and 3.4.2 shall terminate upon the initial public offering of common stock or upon the sale or disposition of all or substantially all of the assets of AVS pursuant to a liquidation not approved in writing by BAYLOR.

 

3.4.5         The stock certificates issued by AVS pursuant to this agreement shall contain a legend referencing the repurchase provision. Upon termination of the repurchase provisions by patent issuance or notice of allowance (as specified in articles 3.4.1 and 3.4.2) or by a liquidity event (as specified in article 3.4.4), AVS will reissue stock certificates that no longer bear a legend referencing the repurchase provision.

 



 

3.5           Common Stock Issuance. The Common Stock shall be divided and issued as described in Schedule 1.

 

3.6           Patent Costs. AVS shall pay all unreimbursed costs incurred by BAYLOR prior to the Agreement Date incident to the filing of the United States patents and corresponding foreign patent applications listed in Section 1.12.

 

ARTICLE 4

 

ACCOUNTING AND RECORDS

 

4.1           Royalty Payment . At the close of each quarter of AVS’ fiscal year, the Net Sales for said quarter shall be computed, and the royalties earned thereon shall be paid to BAYLOR within sixty (60) days after the close of said quarter. In the event that any payment due hereunder is not made when due, the payment shall accrue interest beginning on the tenth day following the due date thereof, calculated at the annual rate of the sum of (a)  ****** plus (b) the prime interest rate quoted by The Wall Street Journal on the date said payment is due, the interest being compounded on the last day of each calendar quarter, provided, however, that in no event shall said annual interest rate exceed the maximum legal interest rate for corporations. Each such royalty payment when made shall be accompanied by all interest so accrued. Said interest and the payment and acceptance thereof shall not negate or waive the right of BAYLOR to seek any other remedy, legal or equitable, to which it may be entitled because of the delinquency of any payment.

 

4.2           Payment in U.S. Dollars . All payments due hereunder are expressed in and shall be paid in United States of America currency, without deduction of exchange, collection or other charges, to BAYLOR by check, or to the account of BAYLOR at such bank as BAYLOR may from time to time designate by notice to AVS.

 

4.3           Foreign Restrictions On Payment . If governmental regulations prevent remittance from any foreign country of any amounts due in respect of Net Sales in that country in United States Dollars, AVS shall so notify BAYLOR in writing and, subject to the remainder of this Section 4.3, any obligation under this Agreement to make payments in respect of Net Sales in that country shall be suspended (but the amounts due but not paid shall continue to accrue) without interest until such remittances are possible; provided, however, that notwithstanding the foregoing BAYLOR shall have the right, at any time and from time to time, upon written notice to AVS, to direct AVS either to pay such funds in any such country in the local currency or to liquidate such currency at available rates and pay the liquidated amounts to BAYLOR. Any such payment by AVS in accordance herewith shall be deemed to be payment in full of the amounts so paid or liquidated, and AVS shall have no further liability to BAYLOR for any action taken in accordance with BAYLOR’s instructions pursuant to this Section 4.3.

 

4.4           Royalty Report . With each royalty payment, AVS shall furnish to BAYLOR a written accounting report related to said quarter stating the Net Sales, royalties due and royalties paid.

 



 

4.5           Written Records . AVS agrees to keep and maintain and to require all of its sublicensees to keep and maintain written records with respect to its operations pursuant to this Agreement in sufficient detail to enable BAYLOR or its designated accountants to compute the amount of royalties payable to BAYLOR and further agrees to permit the records to be examined from time to time, on reasonable notice during normal business hours to the extent necessary to verify the amount of royalties due hereunder. BAYLOR shall pay the costs of the examination unless a discrepancy of greater than five percent (5%) in royalties due is present, in which case AVS shall reimburse BAYLOR for the examination expenses. All the records shall be kept for four (4) years after the royalty period to which the records relate.

 

4.6           Due Diligence . Once per calendar year on the anniversary of the Agreement Date and thereafter throughout the term of this Agreement, or at such time as an annual report to shareholders is delivered, AVS shall deliver to BAYLOR a written annual report as to: (i) the efforts and accomplishments of AVS and each of its sublicensees during the preceding year in developing and commercializing’ Licensed Products in every country in which it or its sublicensees shall have developed and/or sold Licensed Products; (ii) the status of scientific trials, if any, on Licensed Products; (iii) the activities of AVS, if any, with respect to the filing, prosecution, obtaining, and maintenance of patents in the United States and any foreign countries in which such protection has been sought on the Patent Rights, as provided in Article 6; and (iv) the obtaining of regulatory approvals in the United States and foreign countries for the advertising, use and sale of Licensed Products.

 

4.7           Reports and Payments Address . All payments and reports shall be sent to the address listed in Paragraph 14.1.

 

ARTICLE 5

 

WARRANTIES, REPRESENTATIONS, INDEMNITY AND INSURANCE

 

5.1           (a)  BAYLOR Representations . BAYLOR hereby represents and warrants that, (i) It is the owner of or has the right to license the Licensed Subject Matter, existing as of the  effective Date; (ii) it has the right to license the Licensed Subject Matter as contemplated herein; and (iii) other than the grants set forth herein, including, without limitation, for or to the United States of America, or for or to a foreign state, it has not encumbered, restricted; transferred or otherwise burdened the Licensed Subject Matter.

 

(b)  DISCLAIMER OF WARRANTY. WITH THE EXCEPTION OF PARAGRAPH 5.I(a), BAYLOR MAKES NO WARRANTIES OR REPRESENTATIONS. EXPRESS OR IMPLIED. INCLUDING. BUT NOT LIMITED TO, WARRANTIES OF FITNESS ORMERCHANTABILITY. REGARDING OR WITH RESPECT TO THE LICENSED SUBJECT  MATTER OR LICENSED PRODUCTS. AND BAYLOR MAKES NO WARRANTIES OR REPRESENTATIONS. EXPRESS OR IMPLIED, OF THE PATENTABILITY. USE OR OTHER APPLICATION OF THE LICENSED SUBJECT MATTER OR LICENSED PRODUCTS OR OF THE ENFORCEABILITY OF ANY

 



 

PATENTS ISSUING THEREUPON. IF ANY, OR THAT THE LICENSED SUBJECT MATTER OR LICENSED PRODUCTS ARE OR SI-IALL BE FREE FROM INFRINGEMENT OF ANY PATENT OR OTHER RIGHTS OF THIRD PARTIES AND BAYLOR MAKES NO WARRANTIES OR REPRESENTATIONS. EXPRESS OR IMPLIED. AS TO THE LIKELIHOOD OF THE SUCCESS OF ANY RESEARCH. DEVELOPMENT, TESTING, MARKETING OR OTHER UTILIZATION OF THE TECHNOLOGY.

 

5.2           AVS Representations . AVS hereby represents and warrants that:

 

(a)           it is a corporation duly organized and in good standing under the laws of  the State of Delaware;

 

(b)           it is qualified to do business and in good standing in the State of Texas and elsewhere as the nature of its business and properties so require;

 

(c)           the execution, delivery and performance of this Agreement by AVS and the consideration provided for herein has been duly authorized by all necessary corporate action;

 

(d)           it has the full power and authority to enter into and carry out its obligations under this Agreement; and

 

(e)           the Common Stock to be issued pursuant to this Agreement has been duly authorized and upon issuance, pursuant to the terms hereof and for the consideration herein set forth, will be validly issued, fully paid and non-assessable.

 

5.3           Indemnification by AVS Regarding Representations . AVS agrees to indemnify BAYLOR and each of its respective officers, trustees, faculty, employees, agents, and representatives, harmless from any liabilities, costs, and expenses (including attorney’s fees and expenses), obligations or causes of action arising out of or related to any breach of the representations and warranties made by AVS herein.

 

5.4           Indemnification by AVS Regarding Licensed Products . AVS agrees to protect, defend. Indemnify and hold BAYLOR. Each of the entities with which it is or will be in the future affiliated with respect to the invention or development of the Licensed Subject Matter. And each of BAYLOR’s, officers, trustees. Faculty, employees, agents, representatives, and each of them (“the Indemnified Parties”) harmless from and against. and to pay any and all losses, liabilities, claims, demands. Causes of action. Lawsuits. or other proceedings (whether in contract, tort strict liability or otherwise), fines, assessments, damages or any other amounts of whatever nature that any of the Indemnified Parties may sustain or incur. Including all reasonable attorneys’ fees and court costs, as a consequence of any third party’s (including, but not limited to, AVS’ officers, directors, employees, agents, consultants, representatives or servants) claims and demands arising from the use, testing, operation, sale or manufacture of the Licensed Subject Matter, or the Licensed Products by AVS or its sublicensees, except as to the extent such claims, causes of action, lawsuits or other proceedings and the costs (including attorney’s fees) related thereto arise from the cross negligence or intentional misconduct of any of the Indemnified Parties.

 



 

5.5           Indemnification Procedures . BAYLOR will promptly notify AVS in writing of notice of any claims or the commencement of any action, if a claim in respect thereof is to be made under Paragraph 5.4. BAYLOR’s failure to notify AVS will not relieve AVS from any liability to BAYLOR except to the extent any BAYLOR delay in notifying AVS causes such damages. After receiving notice of said action, AVS is entitled to participate in the defense therein, and may elect to assume the defense thereof by promptly notifying the Indemnified Party in writing and by selecting counsel reasonably satisfactory to such Indemnified Party. After BAYLOR has received notice of AVS’ election to assume the defense of said action and has approved AVS’ counsel, AVS will not be liable to BAYLOR under Paragraph 5.4 for any legal or other expenses subsequently incurred by BAYLOR in connection with the defense thereof unless (i) BAYLOR has reasonably concluded that there may be legal defenses available to it that are different from or additional to those available to AVS, in which case such BAYLOR shall have the right to select separate counsel to assume said legal defenses and to otherwise participate in the defense of said action on behalf of BAYLOR, (ii) AVS shall not have employed counsel reasonably satisfactory to BAYLOR to represent BAYLOR within a reasonable time after notice of commencement of the action or (iii) AVS has authorized the employment of counsel for BAYLOR at the expense of AVS.

 

(a)           Neither BAYLOR nor AVS shall settle any action covered by Paragraph 5.4 without first obtaining the consent of the other Party, which consent will not be unreasonably withheld.

 

(b)           AVS’ indemnity obligations under this Agreement shall survive the termination of this Agreement, regardless of how this Agreement is terminated.

 

5.6           Insurance . AVS shall, for so long as AVS manufactures, uses or sells any Licensed Product(s), maintain in full force and effect policies of (i) worker’s compensation insurance within statutory limits, (ii) employers’ liability insurance with limits of not less than one million dollars ($1,000,000) per occurrence, (iii) general liability insurance (with Broad Form General Liability endorsement) with limits of not less than one million dollars ($1,000,000) per occurrence with an annual aggregate of two million dollars ($2,000,000) and, upon the introduction of Licensed Product(s), (iv) products liability insurance with limits of not less than one million dollars ($1,000,000) per occurrence with an annual aggregate of five million dollars ($5,000000). Such coverage(s) shall be purchased from a carrier or carriers reasonably deemed acceptable to BAYLOR and shall name BAYLOR as an additional insured. Upon request by BAYLOR, AVS shall provide to BAYLOR copies of said policies of insurance.

 

5.7           AVS Acknowledgement . AVS understands that there is no assurance that any patents included in the Patent Rights, or any patent application subsequently filed on the Licensed Subject Matter will actually be issued, or if issued, will be held not invalid by a court of competent jurisdiction.

 


 

ARTICLE 6

 

PROTECTION OF PROPERTY RIGHTS

 

6.1                                  Patent Costs .

 

(a)                                   As stated in Paragraph 3.6, AVS shall pay all costs incurred prior to the       Effective Date incident to the filing of the United States Patent Applications and corresponding foreign patent applications listed in Article 1.12.

 

(b)                                  During the term of this Agreement, AVS agrees to pay all costs reasonably incurred by it after the Effective Date incident to the United States and foreign applications, patents and like protection, including all costs incurred for filing, prosecution, issuance and maintenance fees as well as any costs reasonably incurred in filing continuations, continuations-in-part, divisionals or related applications and any reexamination or reissue proceedings.

 

6.2                                  Patent Prosecution Responsibility . From the Effective Date and for the term of this Agreement, AVS shall have primary responsibility for deciding whether to file United States and foreign patent applications, continue prosecution of any patent applications or maintain any patent application or patent regarding the Licensed Subject Matter hereunder, except that BAYLOR may assume responsibility at its sole expense for pursuing any protection which AVS declines to prosecute pursuant to Paragraph 6.4 of this Agreement.

 

6.3                                  Patent Prosecution Due Diligence . During the term of this Agreement, AVS agrees to prosecute with good faith and due diligence all such patent applications and to take all actions reasonably necessary to maintain and enforce the patents and proprietary rights in and to the Licensed Subject Matter.

 

6.4                                  Baylor Right to Assume Filing . During the term of this Agreement, in the event that AVS decides not to file any or all United States and foreign applications or to continue prosecution of a patent application to issuance or maintain any United States or foreign patent application or patent, AVS shall timely notify BAYLOR in writing in order that BAYLOR may file said United States and foreign applications and continue said prosecution or maintenance of such patent applications at its own expense. Notwithstanding AVS’ election to not file for any patent or to not continue prosecution of any application, AVS shall retain the right to use the rights licensed hereunder, subject to the terms hereof. If AVS fails to notify BAYLOR in sufficient time for BAYLOR to assume the cost, AVS shall be considered in default of this Agreement.

 

6.5                                  Information Regarding Filings . During the term of this Agreement AVS shall instruct counsel for AVS to keep BAYLOR reasonably informed, at AVS’ expense, of prosecutions pursuant to this Article 6 including submitting to BAYLOR copies of all official actions and responses thereto. As per Paragraph 6.4, AVS shall consult BAYLOR prior to any abandonment of the prosecution of the patents.

 

6.6                                  Cooperation . BAYLOR agrees to cooperate with AVS to whatever extent is necessary to procure patent protection of any rights, including fully agreeing to execute any and all documents to give AVS the full benefit of the licenses granted herein.

 



 

6.7                                  Confidentiality . Each Party shall use its best efforts to maintain and assure the confidentiality of the Confidential Information disclosed to it by the other Party hereto; provided, however, neither Party shall have an obligation of confidentiality with respect to Confidential Information that:

 

(a)                                   at the time of its disclosure or thereafter is disclosed in a publicly available document through no fault of the receiving Party;

 

(b)                                  at the time of its disclosure is, or thereafter becomes without fault of the receiving Party, part of the public domain;

 

(c)                                   was in the possession of the receiving Party prior to disclosure by the disclosing Party hereunder and was not acquired directly or indirectly from any third party under obligation of confidentiality to the disclosing Party;

 

(d)                                  subsequent to its disclosure, is obtained from a third party not subject to a contractual or fiduciary obligation for confidentiality to the disclosing Party;

 

(e)                                   is required by county or governmental order, law or regulation to be disclosed; or

 

(f)                                     is disclosed pursuant to any research grant relating to the Licensed Subject Matter from a non-commercial granting entity, such as grants from the United States Department of Health and Human Services and other governmental and private non-profit agencies; provided, however, that AVS be notified of the terms of such research grant applications.

 

6.8                                  Permitted Disclosure. Notwithstanding the foregoing, the Parties understand and agree that AVS may, to the extent it deems necessary or appropriate, disclose the Licensed Subject Matter to potential licensees, purchasers, investors, joint venturers and the like, but AVS agrees to make such disclosures subject to a satisfactory confidentiality agreement.

 

ARTICLE 7

 

RIGHTS IN ADDITIONAL RESEARCH

 

7.1                                  The Parties acknowledge that AVS may support research on the Licensed Subject Matter in laboratories and facilities at BAYLOR that are under the direct personal supervision of the Baylor Founders and that said research may result in discoveries or inventions (“Funded Technology”) that are not included within the definition of Licensed Subject Matter transferred by this Agreement. Nothing in this Agreement shall be deemed to allocate rights or ownership of any Funded Technology, and any rights to Funded Technology shall be determined by a separate written agreement.

 



 

ARTICLES 8

 

INFRINGEMENT

 

8.1                                  Notice and Right to Bring Suit . Each Party shall promptly inform the other of any suspected infringement of any licensed Patent Rights or misuse, misappropriation, theft or breach of confidence of other proprietary rights in the Licensed Subject Matter by a third party, and with respect to such activities as are suspected, BAYLOR and AVS each shall have the right to institute an action for infringement, misuse, misappropriation, theft or breach of confidence of the proprietary rights against such third party in accordance with the following:

 

(a)                                   If BAYLOR and AVS agree to institute suit jointly, the suit shall be brought in both their names and all of the out-of-pocket costs and legal fees relative to such procedures shall be borne by AVS. AVS shall exercise control over such action; provided, however, that BAYLOR may, if it so desires, be represented by counsel of its own selection and at its own cost.

 

(b)                                  If BAYLOR or AVS, as the case may be, decides not to take action, then the other Party may do so in its own name and at its own cost.

 

(c)                                   Should either BAYLOR or AVS commence suit under the provisions of this Article 8 and thereafter elect to abandon the same, it shall give timely notice to the other Party who may, if it so desires, continue prosecution of such suit at such continuing Party’s sole expense.

 

(d)                                  All recoveries, whether by judgment, award, decree or settlements, from infringement or misuse of the Licensed Subject Matter shall belong first to the Party or Parties paying the costs of the suit, in such amount, then to AVS subject to any royalties due BAYLOR. All recoveries, whether by judgment, award, decree or settlement that result from recovery for technologies owned by BAYLOR and not licensed to AVS, shall belong to BAYLOR and those that result from recovery for technologies not issued by BAYLOR shall belong to AVS.

 

8.2                                  Consent . Neither BAYLOR nor AVS shall settle any action covered by this Article 8 without first obtaining the consent of the other Party, which consent will not be unreasonably withheld.

 

8.3                                  Disclaimer of Liability . BAYLOR shall not be liable for any losses incurred as the result of an action for infringement brought against AVS as the result of AVS’ exercise of any right granted under this Agreement. The decision to defend or not defend shall be in AVS’ sole discretion.

 



 

ARTICLE 9

 

INDEPENDENT CONTRACTOR STATUS

 

9.1                                  The Parties hereby acknowledge and agree that each is an independent contractor and that neither Party shall be considered to be the agent, representative, master or servant of the other party for any purpose whatsoever, and that neither Party has any authority to enter into a contract, to assume any obligation or to give warranties or representations on behalf of the other Party. Nothing in this relationship shall be construed to create a relationship of joint ventures, partnerships, fiduciary or other similar relationships between the Parties.

 

ARTICLE 10

 

TERM AND TERMINATION

 

10.1                            Term . Unless sooner terminated as otherwise provided herein, the license to employ Patent Rights granted herein as part of Article 2 shall terminate on the later of (i) the date of expiration of the last of the Patent Rights to expire and (ii) in the event no patents included within the Patent Rights issue, the first date following the twelfth (12th) anniversary of the First Commercial Sale.

 

10.2                            Automatic Termination . This Agreement shall be terminated automatically in any one or more of the following circumstances:

 

(a)                                   the assets of AVS are seized or attached, in conjunction with any action   against them by any third party, and such seizure or attachment is not abated within ninety (90) days;

 

(b)                                  AVS is dissolved, or a sale of all or substantially all of the assets of AVS pursuant to a liquidation not approved in writing by BAYLOR is made;

 

(c)                                   a breach of Section 12.1 or 12.2.

 

10.3                            Termination Upon Breach . BAYLOR may terminate this Agreement if AVS fails to perform any of its obligations under this Agreement and fails to remedy said breach within thirty (30) days after being given written notice of the specific failure or default and termination by BAYLOR; however, if the default is susceptible of being cured but the cure cannot be reasonably completed within the thirty-day (30-day) period, this Agreement may only be terminated if AVS fails to promptly commence and thereafter diligently prosecute actions to cure the default.

 

10.4                            AVS Right to Terminate . AVS, upon one hundred eighty (180) days prior written notice to BAYLOR, may terminate this Agreement with or without cause.

 



 

10.5                            Effect of Termination . In the event that this Agreement is terminated for whatever reason:

 

(a)                                   any and all rights in and to the Licensed Subject Matter shall revert to BAYLOR;

 

(b)                                  all grants and licenses made by BAYLOR to AVS pursuant to this Agreement shall automatically terminate;

 

(c)                                   AVS will deliver to BAYLOR within ten (10) days of terminate all copies in its possession or control of all documents and other tangible information that contain the Licensed Subject Matter;

 

(d)                                  AVS agrees to execute all instruments as BAYLOR may reasonably request that are necessary to reinvest any licensed lights in BAYLOR;

 

(e)                                   AVS, subject to Article 6.8, shall have an obligation to maintain the confidentiality of all Licensed Subject Matter;

 

(f)                                     AVS will not use any Confidential Information owned by BAYLOR regarding non-patented Licensed Subject Matter for a period of five (5) years after termination of this Agreement; provided, however, AVS shall be entitled to use the non-patented Licensed Subject Matter royalty free after the termination of this Agreement so long as it has paid twelve (12) years of royalties as specified in Article 3 and Paragraph 10.6;

 

(g)                                  AVS shall have thirty (30) days to complete the manufacture and ninety (90) days to complete the sale or license of any Licensed Products in stock or in the course of manufacture at the time of termination, all subject, however, to payments of royalty and accounting as provided herein, even if such royalty obligations arise from transactions subsequent to the effective date of termination;

 

10.6                            Obligation to Pay Accrued Royalties . AVS’ obligation to pay royalties, keep records and allow a final audit shall survive termination;

 

10.7                            Stock Remains Outstanding . The Common Stock issued pursuant to this Agreement or the ownership thereof shall not be affected by any termination hereof, regardless of the reason for, or the timing of, such termination;

 

10.8                            Survival of Accrued Liabilities . Except as expressly provided herein, no Party hereunder shall be discharged or relieved from any liability or obligation existing prior to such termination; and

 

10.9                            Survival of Sublicenses . Upon termination of this License Agreement, BAYLOR agrees to accept as successor to AVS, existing sublicenses in good standing at the date of

 



 

termination; provided that such sublicensees consent in writing to be bound by all the terms and conditions of this Agreement.

 

ARTICLE 11

 

GOVERNMENTAL COMPLIANCE

 

11.1                            Obligation to Comply with Laws . AVS shall at all times during the term of this Agreement and for so long as it shall sell Licensed Products comply and cause its sublicensees to comply with all local, state, federal and foreign formalities, laws, orders, rules, decrees or regulations that may control the import, export, manufacture, use or sale of Licensed Products or any other activity undertaken pursuant to this Agreement.

 

11.2                            Required Letter of Assurance . AVS understands and agrees that before BAYLOR shall be required to perform any obligation hereunder that shall be subject to local, state, federal and foreign formalities, laws, orders, decrees or regulations, AVS shall first provide BAYLOR with any letter of assurance or other certification that may be required to comply with the formalities, laws, decrees, rules, orders or regulations of any agency or instrumentality having jurisdiction. For example and not by limitation, this includes United States import and export regulations, Food & Drug Administration regulations, Department of Agriculture regulations, environmental regulations and recombinant DNA regulations.

 

11.3                            Failure to Obtain Government Approvals . Inability or failure, if any, of AVS to secure any necessary government license or approval shall not entitle AVS to terminate this Agreement or to obtain any form of relief, credit, rebate or recovery from BAYLOR.

 

11.4                            Compliance Costs . During the term of this Agreement, AVS shall be responsible for any and all expenses, costs, fees, duties or taxes reasonably necessary to comply with government orders, formalities, rules, regulations and laws.

 

ARTICLE 12

 

ASSIGNMENT AND LICENSING

 

12.1                            AVS Assignment of Rights . AVS may not assign or attempt to assign any rights under this Agreement, except in connection with the sale of substantially all of its assets, without the prior written consent of BAYLOR, which consent shall not be unreasonably withheld.

 

12.2                            AVS Right to License . Except as expressly permitted by the Agreement, AVS may not license or attempt to license any rights under this Agreement prior to the written consent of BAYLOR, which consent shall not be unreasonably withheld.

 



 

12.3                            AVS Sublicensing Rights . All sublicenses granted by AVS of its rights hereunder shall be subject to the terms of this Agreement, as per Article 2.3.

 

12.4                            Preexisting Agreements . This Agreement shall not supersede any preexisting agreement BAYLOR has with a third party in the event that this Agreement is assigned by AVS to that third party, even if BAYLOR has consented to the assignment.

 

12.5                            BAYLOR Assignment of Rights . BAYLOR may assign its rights hereunder, including the right to receive the consideration (equity and monetary) for the licenses herein granted, to its Affiliates, or to such other parties as may be entitled to receive or exercise same under the Baylor Patent Policy.

 

ARTICLE 13

 

PUBLICITY

 

13.1                            Use of Name . Neither Party shall use the name, logotypes or symbols of the other Party or the name of any emploY’1e, faculty, staff, affiliate or associate of the other Party for publication or advertising pUf1Joses, except with the written consent of the other Party.

 

ARTICLE 14

 

ADDRESSES

 

14.1                            All payments shall be made payable to “Baylor College of Medicine” and all payments and reports shall be sent to the address below:

 

 

BAYLOR Tax ID #: 74-1613878

 

 

 

 

 

Director, Office of Technology Administration

 

 

Baylor College of Medicine

 

 

One Baylor Plaza, BCMD 600D

 

 

Houston, TX 77030

 

 

14.2                            All notices or other communication pursuant to this Agreement shall be sufficiently made or given on the date of mailing if sent to such Party by United States Postal Service certified mail, return receipt requested, postage prepaid, or via overnight courier, addressed to it at its address below or as it shall designate by written notice given to the other Party:

 

 

In the case of BAYLOR:

 

 

Senior Vice President & General Counsel

 

 

Baylor College of Medicine

 

 

One Baylor Plaza

 

 

Houston, TX 77030

 

 



 

In the case of AVS:

 

 

Douglas Kern, D.V.M.

 

 

Applied Veterinary Systems, Inc.

 

 

c/o

 

 

BCM Technologies, Inc.

 

 

1709 Dryden Road, Suite 901

 

 

Houston, TX 77030

 

 

With a copy to:

 

Director, Office of Technology Administration

Baylor College of Medicine

One Baylor Plaza, BCMD 600D

Houston, TX 77030

 

ARTICLE 15

 

MISCELLANEOUS

 

15.1                            Further Acts . Without further consideration, BAYLOR hereby agrees to execute and deliver, and BAYLOR agrees to cause its officers, trustees, employees, and agents to execute and deliver, such other instruments, and to take such other action as AVS hereunder may reasonably request to more effectively convey and transfer to and vest in AVS, and to put AVS in possession of, the rights granted hereunder, and to assist AVS in the recordation of same as necessary, all in such form and substance as AVS may reasonably request and at AVS’ expense.

 

15.2                            Binding on Successors . This Agreement shall be binding upon and shall inure to the benefit of the legal representatives, administrators, successors, permitted assigns and licensees of the Parties hereto.

 

15.3                            Governing Law . This Agreement shall be deemed to have been made under, and shall be construed and interpreted in accordance with the laws of the State of Texas. This Agreement is expressly acknowledged to be subject to the Export Administration Act of the United States of America. No conflict-of-laws rule or law that might refer such construction and interpretation to the laws of another state, republic, or country shall be considered.

 

15.4                            Consent to Jurisdiction . This Agreement is performable in part in, Harris County, Texas, and the Parties mutually agree that personal jurisdiction and venue shall be proper in the state and federal courts situated in Harris County, Texas, and agree that any litigated dispute will be conducted solely in such courts.

 



 

15.5                            Severability . The Parties hereby agree that neither Party intends to violate any public policy, statutory or common law, rule, regulation, treaty or decision of any government agency or executive body thereof of any country or community or association of countries, and that if any word, sentence, paragraph or clause or combination thereof of this Agreement is found, by a court or executive body with judicial powers having jurisdiction oyer this Agreement or any of the Parties hereto, in a final, unappeasable order to be in violation of any such provision in any country or community or association of countries, such words, sentences, paragraphs or clauses or combination shall be inoperative in such country or community or association of countries, and the remainder of this Agreement shall remain binding upon the Parties hereto,

 

15.6                            Entire Agreement . The terms and conditions herein contained, including all the schedules hereto, and all the agreements referenced herein, or contemplated by any of such agreements constitute the entire agreement between the parties and supersede all previous communications whether oral or written between the parties hereto with respect to the Licensed Subject Matter, and no previous agreement or understanding varying or extending the same shall be binding upon any of the Parties hereto.

 

15.7                            No Waiver . The Parties covenant and agree that if either Party fails or neglects for any reason to take advantage of any of the terms provided for the termination of this Agreement or if either Party, having the right to declare this Agreement terminated, shall fail to do so, any such failure or neglect by either Party shall not be a waiver or be deemed or be construed to be a waiver of any cause for the termination of this Agreement subsequently arising, or as a waiver of any of the terms, covenants or conditions of this Agreement or of the performance thereof. None of the terms, covenants and conditions of this Agreement may be waived by either Party except by its written consent.

 

15.8                            Survival . The provisions, rights and obligations set forth in Articles 1, 3, 4, 5, 6, 7, 8, 9, 11, 12, 13, 14 and 15, and Paragraphs 2.1 (insofar as Paragraph 2.1 pertains to Licensed Products), 10.5, 10.6, 10.8, and 10.9 along with any other obligations that by their terms survive termination, shall survive the termination of this Agreement.

 

15.9                            Amendment . No amendment or modification to this Agreement shall be effective unless it is in writing and signed by duly authorized representatives of both Parties.

 

15.10                      Construction . The Parties acknowledge that each Party has received and reviewed this Agreement and that normal rules of construction to the effect that any ambiguities are to be resolved against the drafting Party shall not be employed in the interpretation of this Agreement or any amendments or exhibits thereto.

 

In Witness Whereof, the Parties hereto have executed and delivered this Agreement in multiple originals by their duly authorized officers and representatives on the respective dates shown below, but effective as of the Agreement Date.

 



 

IN WITNESS WHEREOF, the Parties hereto have executed and delivered this Agreement in multiple originals by their duly authorized officers and representatives on the respective dates shown below, but effective as of the Effective Date.

 

 

APPLIED VETERINARY SYSTEMS, INC.

 

BAYLOR COLLEGE OF MEDICINE

 

 

 

 

 

 

 

 

Name:

/s/ William A. McMinn

 

Name:

/s/ W. Dalton Tomlin

 

 

 

 

 

William A. McMinn

 

 

W. Dalton Tomlin

 

 

 

 

 

 

 

 

Title:

Vice President

 

Title:

Senior Vice President &

 

 

 

 

 

 

 

 

General Counsel

 

 

 

 

Date:

01/25/01

 

Date:

01/17/01

 



 

Schedule 1: Distribution of AVS Common Stock

 

Party

 

Number of AVS Shares Issued

 

Baylor College of Medicine

 

57,500

 

Robert J. Schwartz, Ph.D.

 

17,709

 

Ruxandra Draghia-Akli, Ph.D.

 

17,709

 

Roy G. Smith, Ph.D.

 

7, 083

 

 




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EXHIBIT 10.28

EMPLOYMENT AGREEMENT

        THIS EMPLOYMENT AGREEMENT (the "Agreement") is made effective the 14 th day of November, 2001 between ADViSYS, Inc. ("ADViSYS"), a Delaware corporation, with its place of business at 2700 Research Forest Drive, Suite 180, The Woodlands, Texas, 77381and Ruxandra Draghia-Akli ("Employee") whose residence address is 5215 Starkridge Drive, Houston, Texas, 77035.

        WHEREAS, ADViSYS is a Delaware corporation and is engaged in the research and marketing of services relating to animals and animal care; and

        WHEREAS, ADViSYS is a start-up company, with a limited number of employees, with limited resources and without any assurances of its ability to raise additional funds; and

        WHEREAS, ADViSYS does not have any existing products and is engaged in a high risk research program to develop one or more commercial products, and ADViSYS cannot assure Employee of the successful development of any product; and

        WHEREAS, ADViSYS has its principal place of business at Houston, Texas; and

        WHEREAS, ADViSYS wishes to retain the services of Employee, and Employee wishes to be employed by ADViSYS in the capacity and under the terms and conditions as set forth in this Agreement; and

        WHEREAS, this Agreement represents the employment terms, conditions and agreements reached between the parties.

        NOW THEREFORE, in consideration of the mutual covenants hereinafter set forth, it is hereby agreed between the parties as follows:

1.     Employment Period.     ADViSYS agrees to employ Employee and Employee agrees to be employed by ADViSYS on the terms and conditions herein. This Agreement will have a term commencing on February 1, 2002 and will be terminable as provided in Section 4 herein.

2.     Position.     

2.1     Position and Duties.    During the employment period, Employee shall serve as Research Team Leader of ADViSYS under the President of ADViSYS, with such duties and responsibilities that are customarily assigned to such position and such other duties and responsibilities as may be from time to time assigned to him by the President of ADViSYS.

2.2     Time.    During the employment period, and excluding any periods of vacation and sick leave to which Employee is entitled, Employee shall devote all of his business time and attention to the business and affairs of ADViSYS. Employee shall use his best efforts to carry out such responsibilities. Employee understands that ADViSYS is a start-up company with limited resources and consequently Employee may be required to devote time significantly in excess of normal business hours to his obligations hereunder. Employee may not serve as a consultant to, or on any board of, any other company or engage actively in any other business without the consent of the Board of Directors, which it may withhold in its sole discretion.

2.3     Annual Review.    At the end of each year during the employment period, the President shall review and evaluate Employee's performance.

3.     Compensation and Benefits.     

3.1     Base Salary.    ADViSYS will pay Employee at a rate of Twelve Thousand Nine Hundred Seventeen Dollars ($12,917) per month. Any increases in Employee's monthly base compensation will be subject to the mutual agreement of ADViSYS and Employee, which agreement either party may withhold in their sole discretion.


3.2     Incentive Compensation.    As incentive compensation, ADViSYS will grant Employee an option to acquire 130,000 shares of ADViSYS common stock at the purchase price of $1.00 per share pursuant to the terms of the Option Agreement executed concurrently herewith.

3.3     Benefits.    Employee shall receive the following:

        (1)   Reimbursement of all usual, customary and normal business expenses reasonably incurred by Employee in the performance of his duties.

        (2)   Automobile expense reimbursement for Employee's business travel using his vehicle at the rates established by the Internal Revenue Service from time to time for such reimbursement.

        (3)   Three weeks paid vacation per year, or as otherwise agreed in writing between Employee and ADViSYS.

        (4)   Medical health insurance as provided generally to employees in ADViSYS' company policies and procedures

        (5)   Retirement benefits as provided generally to employees in ADViSYS' company policies and procedures

        (6)   Any additional benefits provided generally to employees in ADViSYS' company policies and procedures, as may be applicable from time to time to Employee.

        (7)   Any additional benefits provided to all employees with the same supervisory responsibilities as Employee.

4.     Termination.     

4.1     Death.    Employee's employment hereunder shall terminate upon his death.

4.2     At Will Employee Termination Without Cause.    Employee agrees that he is an employee terminable "at will" and that ADViSYS may terminate Employee for any reason or no reason, at any time, including during a period of disability, by giving Employee written notice of termination, subject to the terms of Section 5.1 hereof. Employee may terminate this Agreement at any time by giving ADViSYS thirty (30) days advance written notice. Termination of this Agreement will not terminate Employee's obligations under the Proprietary Information, Assignment of Inventions and Noncompetition Agreement which by their terms survive termination of employment.

5.     Compensation Upon Termination.     

5.1     Termination By ADViSYS Without Cause.    If Employee's employment is terminated by ADViSYS without "Cause" as defined below, then so long as Employee complies with the terms of this Agreement and the Proprietary Information, Assignment of Inventions and Noncompetition Agreement dated the date hereof, ADViSYS shall until six months after the date of termination (l) continue to pay to Employee his then current salary, on the usual schedule for payment of the salary, and (2) pay Employee monthly an amount equal to the amount contributed by ADViSYS for his health insurance for the month prior to termination. Provided, however, that payments so made to Employee shall be reduced by the sum of the amounts, if any, payable to Employee at or prior to the time of any such payment under any disability benefit plans of ADViSYS.

        Employee agrees that the receipt of all of the salary payments and benefits under this Section 5.1 shall constitute and act as liquidated damages and not as a penalty and as the exclusive remedy for any such termination.

5.2     Termination for Cause.    Upon termination for "Cause," Employee shall not be entitled to any payments, other than unpaid salary for past services. "Cause" shall mean:

        (l)    conviction of, or a plea of non contendere to a charge of, the commission of a felony; or

        (2)   willful and continuing failure to substantially perform his duties hereunder after demand for substantial performance is delivered by ADViSYS in writing that specifically identifies the manner in



which ADViSYS believes Employee has not substantially performed his duties and Employee does not remedy such failure within ten (10) days following receipt of such written notice;

        (3)   commission of fraud by Employee against ADViSYS, its affiliates or customers, including any misrepresentation on Employee's resume or regarding the terms of separation from any prior employer;

        (4)   misappropriation of any funds or property of ADViSYS by Employee;

        (5)   breach of any provision of this Agreement or of the Proprietary Information, Assignment of Inventions and Noncompetition Agreement dated the date hereof between ADViSYS and Employee;

        (6)   grossly negligent or intentional commission of any act that results in, or Employee's failure to act so as to prevent, material injury to the business of ADViSYS, or

        (7)   engagement (including investment in a nonpublic company), without the written approval of the Board of Directors of ADViSYS, in any activity which competes with the business of ADViSYS.

6.     Other Agreements.     

6.1     Proprietary Information.    Inventions and Noncompetition Agreement. Employee shall execute and comply with the Proprietary Information, Assignment of Inventions and Noncompetition Agreement in the form attached as Exhibit A hereto and incorporated herein by reference. Employee acknowledges that the terms of such Proprietary Information, Assignment of Inventions and Noncompetition Agreement are agreed to in consideration of ADViSYS's agreement to employ Employee and the consideration set out in this Agreement.

6.2     Standstill Agreements.    So long as Employee is employed by ADViSYS or receives payments pursuant to Section 5.1 above, Employee agrees that he will sign any lock-up letters, standstill agreements, or other similar documentation required by an underwriter in connection with an offering of securities by ADViSYS. Such agreements shall be on terms substantially the same as those applicable to other officers or directors of ADViSYS. Failure to take any such action shall cause Employee to forfeit any further rights to the salary continuation payments in Section 5.1. In addition, Employee agrees that in such event ADViSYS can seek and obtain specific performance of such covenant, including any injunction requiring execution thereof, and Employee hereby appoints the then current president of ADViSYS to sign any such documents on his behalf.

7.     Assignment and Successors.     

7.1     No Assignment By Employee.    This Agreement is personal to Employee and shall not be assignable by Employee. This Agreement shall inure to the benefit of and be enforceable by Employee's legal representatives.

7.2     Assignment by ADViSYS.    This Agreement shall inure to the benefit of and be binding upon ADViSYS and its successors and assigns.

8.     Miscellaneous.     

8.1     Arbitration.    Except with respect to injunctive relief which may be sought by the parties if the necessary legal and equitable requirements under applicable law are met pending the institution of proceedings in accordance with this paragraph, the parties agree to resolve any and all claims or controversies arising out of or relating to this Agreement, Employee's employment and/or termination of employment with ADViSYS, including but not limited to claims for breach of contract, misappropriation of trade secrets, defamation or other torts, wrongful termination of employment, and claims under Title VII of the Civil Rights Act, the Americans with Disabilities Act, the Age Discrimination in Employment Act, the Family Medical Leave Act, the Equal Pay Act, the Texas Commission on Human Rights Act, retaliatory discharge under the Texas Worker's Compensation Act, the Texas Pay Day Act, and any similar state law or local ordinance by binding arbitration under the Federal Arbitration Act before one arbitrator in the city of Houston, State of Texas, administered by the American Arbitration Association ("AAA") under its National Rules for the Resolution of Employment Disputes. The arbitrator shall have at least 10 years of experience in labor relations and



employment agreements. If the parties cannot agree upon an arbitrator within three weeks of the commencement of arbitration, the arbitrator shall be appointed by AAA. The parties further agree that the work of Employee involves interstate commerce, the award rendered by the arbitrator is final and binding, and judgment thereon may be entered in any court having jurisdiction thereof. The arbitrator shall deliver to the parties a written decision describing in detail the basis for each of his decisions. The fees and expenses of the arbitrator shall be equally shared by the parties unless Employee can establish that paying his share of the costs would preclude him from enforcing his rights under this Agreement. The invalidity or unenforceability of any provision of this paragraph shall not affect the validity or enforceability of any other provision of this Agreement which shall remain in full force and effect. Nothing in this paragraph shall limit the remedies available to a party asserting a claim pursuant to the statutes listed herein.

8.2     Damage Limitation.    In no event shall either party be entitled to exemplary, punitive, consequential, indirect or similar damages from the other party except as may be permitted pursuant to any of the statutes or ordinances referred to in Section 8.1.

8.3     Notice.    All notices and other communications under this Agreement shall be in writing and sent to the addresses as provided on the signature page hereto. Notice shall be deemed given and effective on the earlier of five (5) days after the deposit in the U.S. mail of a writing addressed as above and sent first-class mail, certified, return receipt requested, or when actually received. Either party may change the address for notice by notifying the other party of such change in accordance with this paragraph.

8.4     Governing Law.    This agreement shall in all respects be construed according to the laws of the State of Texas without regard to its conflicts of law provisions.

8.5     Counsel.    Each party hereto acknowledges that they have obtained the advice of their own counsel in connection with this Agreement and the agreements referenced herein.

8.6     Severability and Headings.    The invalidity or unenforceability of any provision of this Agreement shall not affect the validity or enforceability of any other provision of this Agreement. If any provision of this Agreement shall be held invalid or unenforceable in part, the remaining portion of such provision, together with allover provisions of this Agreement, shall remain valid and enforceable and continue in full force and effect to the fullest extent consistent with law. The paragraph headings herein are for reference purposes only and are not intended in any way to describe, interpret, define or limit the extent or intent of the Agreement or of any part hereof.

8.7     No Waiver.    The failure of a party to insist upon strict compliance with any provision of, or to assert any right under, this Agreement shall not be deemed to be a waiver of such provision or right, or of any other provision of or right under this Agreement.

8.8     Entire Agreement.    The parties acknowledge that this Agreement supersedes any other agreement, written or oral, between them concerning the subject matter hereof.

8.9     Amendment.    This Agreement may be amended only in writing signed by both parties.

8.10     Counterparts.    This Agreement and amendments may be executed in counterparts, each of which shall be deemed an original and such counterparts shall constitute but one and the same instrument.


        IN WITNESS WHEREOF the parties hereto Agreement as of the date written above.

ADViSYS, INC.   EMPLOYEE

By

 

/s/ Douglas R. Kern

Douglas R. Kern
President

 

/s/ Ruxandra Draghia-Akli

Ruxandra Draghia-Akli

Address for Notices:
2700 Research Forest Drive
Suite 180
The Woodlands, TX 77381

 

Address for Notices:
5215 Starkridge Drive
Houston. TX 77035

With a copy of all notices to:
Michael C. Blaney
Vinson & Elkins LLP
1001 Fannin St, Suite 2300
Houston, TX 77002

 

 

FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
NOVEMBER 14, 2001

        This is the First Amendment ("Amendment") to the Employment Agreement between ADViSYS, Inc. ("ADVISYS") and Ruxandra Draghia-Akli ("Executive") dated as of 2 day of September, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated November 14, 2001 between ADViSYS and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Dr. Ruxandra Draghia-Akli
5215 Starkridge Drive
Houston, Texas 77035
Telephone: 713-557-5434
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Ruxandra Draghia-Akli

Ruxandra Draghia-Akli
Vice President, Research
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

September 2, 2008


 

Date:

 

September 2, 2008



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EXHIBIT 10.29

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

LICENSE AGREEMENT

 

 

BETWEEN

 

 

VIRAL GENOMIX, INC.

 

(COMPANY)

 

 

AND

 

 

THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA

 

(PENN)

 



 

TABLE OF CONTENTS

 

 

 

Page

 

 

 

1.

DEFINITIONS

1

 

 

 

2.

LICENSE GRANT

4

 

 

 

3.

FEES AND ROYALTIES

5

 

 

 

4.

CONFIDENTIALITY

10

 

 

 

5.

TERM AND TERMINATION

11

 

 

 

6.

PATENT MAINTENANCE and REIMBURSEMENT

14

 

 

 

7.

INFRINGEMENT AND LITIGATION

14

 

 

 

8.

REPRESENTATIONS AND WARRANTIES OF PENN; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

15

 

 

 

9.

USE OF PENN’S NAME

17

 

 

 

10.

ADDITIONAL PROVISIONS

18

 

1



 

LICENSE AGREEMENT

 

This License Agreement (“AGREEMENT”) is between The Trustees of the University of Pennsylvania (“PENN”), a Pennsylvania nonprofit corporation, with offices located at 3700 Market Street, Suite 300, Philadelphia, Pennsylvania 19104-3147, and Viral Genomix, Inc., a corporation organized and existing under the laws of the State of Delaware (“COMPANY”), having a place of business at 3600 Market Street, Suite 100, Philadelphia, PA 19104-2642.

 

BACKGROUND

 

A. PENN controls certain intellectual property developed by Dr. David B. Weiner (“Dr. Weiner”) of PENN’s School of Medicine related to pathogenic viral proteins which control host cell functions;

 

B. PENN (and in the case of U.S. Patent #5,874,225, PENN and the Wistar Institute) controls United States letters patent and patent applications listed in Attachment 1 to this AGREEMENT, and foreign counterparts thereof, all relating to pathogenic viral proteins which control host cell functions;

 

C. COMPANY may fund further research in the laboratory of Dr. Weiner relating to pathogenic viral proteins which control host cell functions under a separate sponsored research agreement between PENN and COMPANY (“SPONSORED RESEARCH AGREEMENT”);

 

D. COMPANY desires to obtain the exclusive right and license to use and exploit PENN’s rights to intellectual property developed by Dr. Weiner described in Attachment 1 relating to pathogenic viral proteins which control host cell functions, in accordance with the DEVELOPMENT PLAN (as defined below); and

 

E. PENN has determined that the exploitation hereunder of intellectual property developed by Dr. Weiner relating to pathogenic viral proteins which control host cell functions is in the best interest of PENN and is consistent with its educational and research missions and goals.

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties agree as follows:

 

1.              DEFINITIONS

 

1.1   AFFILIATE means any legal entity directly or indirectly controlling, controlled by or under common control with COMPANY that has executed (a) this AGREEMENT, or (b) a written joinder agreement, in a form reasonably satisfactory to PENN, agreeing to be bound by all of the terms and conditions of this AGREEMENT, as if such AFFILIATE were an original party to this AGREEMENT.  For purposes of this AGREEMENT, “control” means the direct or indirect ownership of more than fifty percent (50%) of the outstanding voting securities of a legal entity, and/or the right to receive more than fifty

 

1



 

percent (50%) of the profits or earnings of a legal entity, and/or the right to control the policy decisions of a legal entity.

 

1.2   CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.3   CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.4   DEVELOPMENT PLAN means the plan, as it may be amended from time to time, for the development and/or marketing of the PENN LICENSED PRODUCTS that demonstrates COMPANY’s commitment to bring the PENN PATENT RIGHTS to practical application.  The initial DEVELOPMENT PLAN will be attached hereto, as Attachment 2, within 60 days of the EFFECTIVE DATE.

 

1.5   EFFECTIVE DATE means the date on which COMPANY and PENN have both fully executed this AGREEMENT.

 

1.6   FAIR MARKET VALUE means the cash consideration which COMPANY or a sublicensee thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.7   IND APPLICATION means an Investigational New Drug Application filed with the United States Food & Drug Administration prior to administration of a pharmaceutical product to humans.

 

1.8   KNOWLEDGE means, with respect to any representation or warranty of PENN, the actual knowledge of any employee or agent of PENN’s Center for Technology Transfer.

 

1.9   NDA means an New Drug Application filed with the United States Food & Drug Administration prior to sale of a pharmaceutical product to humans.

 

1.10 NET SALES means the gross amount invoiced for SALES, less qualifying costs directly attributable to such SALES and actually identified on the invoice and borne by COMPANY or its sublicensee(s).  Such qualifying costs shall be limited to the following:

 

1.10.1      Discounts and rebates, in amounts customary in the trade, for quantity purchases, prompt payments, for wholesalers and distributors;

 

1.10.2      Credits, allowances and/or refunds, not exceeding the original invoice amount, for rejections, claims and/or returns;

 

1.10.3      Prepaid outbound transportation expenses and transportation insurance premiums;

 

1.10.4      Sales and use taxes, tariffs, duties, surcharges and other fees imposed by a governmental agency; and

 

2



 

1.10.5      Retroactive price reductions actually applied in an invoice.

 

NET SALES of a commercial product comprising one or more PENN LICENSED PRODUCTS and one or more other active ingredients (a “COMBINATION PRODUCT”) shall be calculated as set forth above, subject to the provisions of Section 3.1.6.

 

1.11 PENN LICENSED PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale by COMPANY and/or any sublicensee(s) of COMPANY to unrelated third parties which (1) in the absence of this AGREEMENT would infringe at least one claim of PENN PATENT RIGHTS, or (2) use a process and/or machine covered by at least one claim of PENN PATENT RIGHTS.

 

1.12 PENN PATENT RIGHTS means all of PENN’s interest in the rights represented by or issuing from (including all claims referenced within) those United States patents and patent applications listed in Attachment 1, including, in each case, any continuations, continuations-in-part (only to the extent that the subject matter of the first patent application is continued in the second patent application, and expressly excluding any claims directed to new subject matter not included in the first application), divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.13 PHASE II CLINICAL TRIALS means a clinical study comprising patients with the disease or condition of interest, to whom a PENN LICENSED PRODUCT is administered in order to preliminarily assess the effectiveness of the product for the intended indication, the optimal dose thereof and regimen therefor, and the side effects associated with the product.

 

1.14 PHASE III CLINICAL TRIALS means a series of expanded controlled and uncontrolled, pivotal, multi-center (generally) clinical studies, after adequate completion of preliminary efficacy and dose-ranging studies, and after safety data has been established for a PENN LICENSED PRODUCT, comprising patients with the disease or condition of interest, to whom the PENN LICENSED PRODUCT is administered in order to obtain sufficient efficacy and safety data (and better understand drug-related adverse effects) to support regulatory submissions and labeling of the PENN LICENSED PRODUCT.

 

1.15 SALE means any bona fide transaction for which consideration is received or expected for the sale, use, lease, transfer or other disposition of PENN LICENSED PRODUCT(S) to an unrelated third party.  A SALE of PENN LICENSED PRODUCT(S) shall be deemed completed at the time COMPANY or its sublicensee invoices, ships or receives payment for such PENN LICENSED PRODUCT(S), whichever occurs first.

 

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2.              LICENSE GRANT

 

2.1   Subject to the terms and conditions of this AGREEMENT, PENN grants to COMPANY for the term of this AGREEMENT an exclusive (with respect to PENN’s rights), world-wide right and license, with the right to grant sublicenses, to make, have made, use, import, sell and offer for sale PENN LICENSED PRODUCT(S).  No other rights or licenses are granted by either party hereunder.  Intellectual property created or conceived during the performance of the SPONSORED RESEARCH AGREEMENT, if any, shall be governed by the SPONSORED RESEARCH AGREEMENT, and not this AGREEMENT.

 

2.2   This license grant is exclusive with respect to PENN’s rights, except that PENN may use and permit other nonprofit organizations to use the PENN PATENT RIGHTS for educational and research purposes and not for sale or offer of sale.

 

2.3   COMPANY acknowledges that pursuant to Public Laws 96-517, 97-256 and 98-620, codified at 35 U.S.C. 200-212, the United States government retains certain rights in intellectual property funded in whole or part under any contract, grant or similar agreement with a Federal agency.  Pursuant to these laws, the government may impose certain requirements regarding such intellectual property, including but not limited to the requirement that products resulting from such intellectual property sold in the United States shall be substantially manufactured in the United States.  This license grant is expressly subject to all applicable United States government rights as provided in the above-mentioned laws and any regulations issued under those laws, as those laws or regulations may be amended from time to time.

 

2.4   The right to sublicense granted to COMPANY under this AGREEMENT is subject to the following conditions:

 

2.4.1        COMPANY may sublicense the rights granted in this AGREEMENT by written sublicense agreement, in a form reasonably acceptable to PENN, which form shall, unless otherwise agreed to by PENN, (a) prohibit the sublicensee from further sublicensing to more than one additional sublicensee in any jurisdiction, and (b) require that the sublicensee be subject to the terms and conditions of the license granted to COMPANY under this AGREEMENT;

 

2.4.2        Within thirty (30) days after COMPANY enters into any sublicense, COMPANY shall deliver to PENN a complete copy of the sublicense written in the English language (PENN’s receipt of the sublicense shall not constitute an approval of the sublicense or a waiver of any of PENN’s rights or COMPANY’s obligations under this AGREEMENT);

 

2.4.3        In the event of a Default under Section 3.1 hereof, all payments then or thereafter due to COMPANY from its sublicensees shall, upon notice from PENN to COMPANY and any such sublicensees, become owed directly to PENN for the account of COMPANY; provided , however , that PENN shall promptly remit to COMPANY the amount by which such payments in the aggregate exceed the amounts owed by COMPANY to PENN; and

 

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2.4.4        Even if COMPANY enters into sublicenses, COMPANY remains primarily liable to PENN for all of COMPANY’s duties and obligations contained in this AGREEMENT, and any act or omission of a sublicensee which would be a breach of this AGREEMENT if performed by COMPANY shall be deemed to be a breach by COMPANY of this AGREEMENT.

 

3.              FEES AND ROYALTIES

 

3.1   License Initiation Fee and Royalties

 

3.1.1        In partial consideration for the exclusive license granted to COMPANY, COMPANY shall issue to PENN within thirty (30) days of the EFFECTIVE DATE such number of shares of COMPANY Common Stock, par value $.0001 per share (“Common Stock”), as will cause PENN to own shares of Common Stock representing twenty percent  (20.0%) of the outstanding shares of the capital stock of COMPANY on a fully-diluted basis, assuming the exercise, conversion and/or exchange of all outstanding securities of COMPANY for or into shares of Common Stock, all on the terms and conditions as set forth in a stock purchase agreement, negotiated in good faith, between COMPANY and PENN (“STOCK PURCHASE AGREEMENT”) in substantially the form  attached as Attachment 3.

 

3.1.2        Until COMPANY has achieved a capitalization of Three million dollars ($3,000,000), COMPANY shall issue to PENN, at no additional consideration, from time to time, such number of additional shares of Common Stock (collectively, the “Additional Purchased Shares”) as will cause PENN to continue to hold shares of Common Stock representing twenty percent  (20.0%) of the outstanding capital stock of COMPANY on a fully-diluted basis, assuming the exercise, conversion and/or exchange of all outstanding securities of COMPANY for or into shares of Common Stock, all on the terms and conditions as set forth in the STOCK PURCHASE AGREEMENT.  Each transfer to PENN of any Additional Purchased Shares shall occur at a time and place as mutually agreed and COMPANY shall deliver to PENN within thirty (30) days of the increase of shares a stock certificate or certificates representing such Additional Purchased Shares.

 

3.1.3        In further consideration of the exclusive license granted to COMPANY, COMPANY shall pay to PENN, on a quarterly basis, a royalty of ****** of the NET SALES of each PENN LICENSED PRODUCT which is sold by COMPANY and any sublicensee(s), agent(s), and/or independent contractor(s) of COMPANY.  In determining the earned royalty payment, if any, to be made by COMPANY at the end of any CALENDAR QUARTER following first SALE of a PENN LICENSED PRODUCT, one-quarter of the minimum royalty paid at the beginning of the CALENDAR YEAR with respect to such PENN LICENSED PRODUCT shall be subtracted from the earned royalties otherwise payable for the CALENDAR QUARTER, and COMPANY shall owe only the difference, if any.

 

5



 

Such royalty payments shall terminate on a product-by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first SALE of such PENN LICENSED PRODUCT in such country, and (b) in any country in which patent rights exist for any PENN LICENSED PRODUCT, the date of expiration of the last-to-expire patent in such country, within the definition of PENN PATENT RIGHTS, with a valid claim covering the PENN LICENSED PRODUCT.

 

3.1.4        Within thirty (30) days after the end of each of the periods specified below, the COMPANY shall pay to PENN the specified percentage of any sublicense initiation fee and any other non-royalty payment(s), including those resulting from co-marketing, strategic alliance, joint venture and other similar arrangement(s), actually received during such period by COMPANY from a sublicensee resulting from activities with PENN LICENSED PRODUCT(S).  Any non-cash consideration received by COMPANY from such sublicensee shall be valued at its FAIR MARKET VALUE as of the date of receipt by COMPANY.

 

Period

 

Percentage

 

 

 

 

 

EFFECTIVE DATE to 12 months after the EFFECTIVE DATE

 

******

 

 

 

 

 

12 months and one day after EFFECTIVE DATE to 24 months after the EFFECTIVE DATE

 

******

 

 

 

 

 

24 months and one day after EFFECTIVE DATE to 36 months after the EFFECTIVE DATE

 

******

 

 

 

 

 

36 months and one day after the EFFECTIVE DATE and thereafter

 

******

 

 

3.1.5        Monies paid to COMPANY to fund research and development or clinical studies, or paid in the form of loans to, or as an equity investment in, COMPANY are not subject to any payment to PENN, except to the extent and only the extent such monies are paid to COMPANY as a substitute, wholly or in part, for a royalty on SALES of PENN LICENSED PRODUCTS or for license initiation, maintenance or other related fees and payments covered by this AGREEMENT.

 

3.1.6        In the event one or more PENN LICENSED PRODUCTS are sold in a COMBINATION PRODUCT, the amount of royalties and sublicense revenues paid to PENN pursuant to this Section 3.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the PENN LICENSED PRODUCT(S).

 

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3.2   Diligence and Milestone Fees

 

3.2.1        COMPANY shall use commercially-reasonable efforts to develop for SALE and to market PENN LICENSED PRODUCTS in a manner consistent with the DEVELOPMENT PLAN.

 

3.2.2        COMPANY shall provide PENN on each June 1 and December 1 for six years after the EFFECTIVE DATE (but excluding the December 1 first succeeding the EFFECTIVE DATE), written progress reports, setting forth in such detail as PENN may reasonably request, the progress of the development, evaluation, testing and commercialization of each PENN LICENSED PRODUCT.  After the date that is six years after the EFFECTIVE DATE, COMPANY shall provide PENN the foregoing written progress reports annually on May 1 of each year. PENN is entitled to only one copy of any such progress report, and shall distribute such progress report only to such persons as may reasonably require such report in order for PENN to fulfill its obligations, or enforce its rights, under this AGREEMENT.  COMPANY shall also notify PENN in writing within thirty (30) days of the first SALE of each PENN LICENSED PRODUCT.

 

3.2.3        COMPANY shall provide PENN with a written, current DEVELOPMENT PLAN once every six months, beginning upon attachment of the initial DEVELOPMENT PLAN, as provided in Section 1.4

 

3.2.4        COMPANY shall pay to PENN annual due diligence fees in the following amounts, payable on each anniversary of the EFFECTIVE DATE until, and only until, the first SALE as follows: first anniversary, $250,000; second anniversary, $500,000; third anniversary, $750,000; fourth and successive anniversaries, $1,000,000.  In addition, all monies spent directly for development of PENN LICENSED PRODUCTS by COMPANY, its subsidiaries, sublicensees, business partners and independent contractors in any given year shall be applied as a credit against the due diligence fees due at the end of that year.  Any part of such due diligence fees not wholly satisfied by such credits must be paid by check on the date due.

 

3.2.5        The following milestone payments are payable by COMPANY to PENN within sixty (60) days after the achievement of the respective milestone event:

 

Event

 

Amount

 

 

 

 

 

Filing of an IND APPLICATION for the first PENN LICENSED PRODUCT

 

$

250,000

 

 

 

 

 

Enrollment of the first patient in PHASE II CLINICAL TRIALS for the first PENN LICENSED PRODUCT

 

$

500,000

 

 

 

 

 

Enrollment of the first patient in PHASE III CLINICAL TRIALS for the first PENN LICENSED PRODUCT

 

$

750,000

 

 

 

 

 

Filing an NDA for the first PENN LICENSED PRODUCT

 

$

500,000

 

 

 

 

 

First anniversary of such filing

 

$

500,000

 

 

 

 

 

Receipt of an NDA approval letter for the first PENN LICENSED PRODUCT

 

$

1,500,000

 

 

 

 

 

First anniversary of such receipt

 

$

1,500,000

 

 

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3.3   Minimum Royalties

 

3.3.1        COMPANY shall pay to PENN a non-refundable minimum royalty for each PENN LICENSED PRODUCT sold during the following periods, in the corresponding amounts:

 

Period

 

Due Date

 

Minimum
Royalty

 

 

 

 

 

 

 

First CALENDAR YEAR following the first SALE of such PENN LICENSED PRODUCT

 

January 1 st  of the first CALENDAR YEAR

 

******

 

 

 

 

 

 

 

Second CALENDAR YEAR following the first SALE of such PENN LICENSED PRODUCT

 

January 1 st  of the second CALENDAR YEAR

 

******

 

 

 

 

 

 

 

Third CALENDAR YEAR following the first SALE of such PENN LICENSED PRODUCT

 

January 1 st  of the third CALENDAR YEAR

 

******

 

 

 

 

 

 

 

Fourth and successive CALENDAR YEARS following the first SALE of such PENN LICENSED PRODUCT

 

January 1 st  of the fourth and successive CALENDAR YEARS, respectively

 

******

 

 

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3.4   Reports and Records

 

3.4.1        COMPANY shall deliver to PENN within forty-five (45) days after the end of each CALENDAR QUARTER following the first SALE, a written report, certified by the chief financial officer or treasurer of COMPANY (or an officer of COMPANY charged with the duties typically entrusted to the chief financial officer or treasurer of a Delaware corporation), setting forth the calculation of the royalties due to PENN under Section 3.1.3 hereof for such CALENDAR QUARTER, including, without limitation:

 

3.4.1.1             Gross consideration for SALES of PENN LICENSED PRODUCTS, including all amounts invoiced, billed or received;

 

3.4.1.2             NET SALES of PENN LICENSED PRODUCTS listed by country;

 

3.4.1.3             Monies spent directly for development of PENN LICENSED PRODUCTS by COMPANY, its subsidiaries, sublicensees, business partners and independent contractors in any given year to be applied as a credit against the due diligence fees in Section 3.2.4;

 

3.4.1.4             Royalties owed to PENN, listed by category, including, without limitation, earned, sublicensee-derived, and minimum royalty categories; and

 

3.4.1.5             Minimum royalty amounts credited against earned royalty payments.

 

3.4.2        COMPANY shall pay the royalties due under Section 3.1.3 within forty-five (45) days following the last day of each CALENDAR QUARTER in which the royalties accrue.  With royalties, COMPANY shall send the report described in Section 3.4.1.

 

3.4.3        COMPANY shall maintain, and cause its sublicensees to maintain, complete and accurate books and records which enable the royalties payable under this AGREEMENT to be verified.  The records for each CALENDAR QUARTER shall be maintained for three years after the submission of the report covering such period, under Section 3.4.  Upon reasonable prior notice to COMPANY, COMPANY shall provide PENN (or an independent, certified public accounting firm selected by PENN and reasonably acceptable to COMPANY) with access, during normal business hours, to all books and records relating to the SALES of PENN LICENSED PRODUCTS by COMPANY and its sublicensees to conduct a review or audit of those books and records solely for purposes of verifying royalties paid or due under this AGREEMENT.  Access to COMPANY’s and sublicensee’s books and records for the applicable period(s) shall be available at least once each CALENDAR YEAR, during normal business hours, during the term of this AGREEMENT and for three years after the expiration or termination of this AGREEMENT.  If the audit is performed by an independent, certified public accounting firm selected by PENN and reasonably

 

9


 

acceptable to COMPANY and such auditor determines that COMPANY has underpaid royalties by five percent (5%) or more, then COMPANY shall pay the costs and expenses of PENN and its accountants in connection with their review or audit, in addition to such underpayment.

 

3.4.4                         PENN is entitled to only one copy of any reports under this Section 3.4, and shall distribute such reports or audit results only to such persons as may reasonably require such reports or audit results in order for PENN to fulfill its obligations, or enforce its rights, under this AGREEMENT.

 

3.5          Currency, Payment Method.

 

3.5.1                         All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to PENN under this AGREEMENT shall be made in United States dollars by check payable to “The Trustees of the University of Pennsylvania.”  If COMPANY receives revenues from SALES of PENN LICENSED PRODUCTS in currency other than United States dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

3.5.2                         Amounts that are not paid when due shall accrue interest from the due date until paid, at a rate equal to one and one-half percent (1.5%) per month (or maximum allowed by law, if less).

 

3.5.3                         COMPANY shall pay all reasonable documented out-of-pocket expenses of PENN incurred prior to November 1, 2001, including legal fees and expenses, in connection with the negotiation of this AGREEMENT, the STOCK PURCHASE AGREEMENT; provided, however, that the total amount of such out-of-pocket expenses shall not exceed $5,000.  COMPANY shall pay such expenses directly, within thirty (30) days of presentment of invoices by PENN.  In the event that COMPANY requests PENN to enter into additional agreements or amendments related to the above documents, PENN and COMPANY shall agree upon appropriate reimbursement before PENN incurs any out-of-pocket expenses.

 

4.                                        CONFIDENTIALITY

 

4.1          CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and

 

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marked confidential or, if oral, should be reduced to writing within two weeks of disclosure and marked confidential.

 

4.2          Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party for the term of this Agreement and for five (5) years thereafter.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this AGREEMENT.  The foregoing obligation shall not apply to:

 

4.2.1                         information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless received subject to non-disclosure and non-use obligations, or independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records;

 

4.2.2                         information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure;

 

4.2.3                         information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

4.2.4                         information which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

4.3          PENN shall not be obligated to maintain any CONFIDENTIAL INFORMATION of COMPANY except for the reports required in Sections 3.2.2, 3.2.3 and 3.4.  PENN shall use reasonable efforts not to disclose those reports to any third party (subject to the exceptions of Section 4.2).  PENN bears no institutional responsibility for maintaining the confidentiality of any other CONFIDENTIAL INFORMATION of COMPANY.

 

5.                                        TERM AND TERMINATION

 

5.1          This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the later of: (a) expiration of the last-to-expire or become abandoned of the PENN PATENT RIGHTS; or (b) twenty-five (25) years after the EFFECTIVE DATE.

 

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5.2          COMPANY may terminate this Agreement (a) upon ten (10)-days written notice to PENN, if PENN is more than sixty (60) days late in paying any amounts payable to COMPANY under Section 2.4.3, or if PENN breaches this AGREEMENT and does not cure the breach within sixty (60) days after written notice of breach; (b) upon thirty (30)-days written notice to PENN, if the sale or other exploitation of the PENN LICENSED PRODUCT(s) becomes technologically or commercially unfeasible; or (c) upon thirty (30)-days written notice to PENN, and by doing all of the following:

 

5.2.1                         ceasing to make, have made, use, import, sell and offer for sale all PENN LICENSED PRODUCTS; and

 

5.2.2                         terminating all sublicenses relating to PENN LICENSED PRODUCTS, and causing all sublicensees to cease making, having made, using, importing, selling and offering for sale all PENN LICENSED PRODUCTS; and

 

5.2.3                         paying all monies owed to PENN under this AGREEMENT.

 

5.3          PENN may terminate this AGREEMENT, upon ten (10)-days written notice to COMPANY, if any of the following events of default (“Default”) occur:

 

5.3.1                         COMPANY is more than sixty (60) days late in paying to PENN royalties, expenses or any other monies due under this AGREEMENT and COMPANY does not immediately pay PENN in full any amounts due upon demand; or

 

5.3.2                         COMPANY experiences a Trigger Event (defined below);

 

5.3.3                         COMPANY materially breaches this AGREEMENT and does not cure the material breach within sixty (60) days after written notice such material of the breach.

 

5.4          “Trigger Event” means any of the following:

 

5.4.1                         An event of default by COMPANY under the STOCK PURCHASE AGREEMENT or the SPONSORED RESEARCH AGREEMENT (if any);

 

5.4.2                         If COMPANY:

 

5.4.2.1                          becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

5.4.2.2                          is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

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5.4.2.3                          makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

5.4.3                         If proceedings under any United States law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by COMPANY;

 

5.4.4                         If any order for relief is entered relating to any of the proceedings described in Sections 5.4.2 or 5.4.3;

 

5.4.5                         If COMPANY shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

5.4.6                         If COMPANY shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 5.4.2, 5.4.3, 5.4.4, or 5.4.5.

 

5.5          The provisions of Sections 5.3 and 5.4 shall apply to a Default of, or a Trigger Event experienced by, any sublicensee of COMPANY’s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the sublicensee causes COMPANY to fail to meet its diligence obligations under Section 3.2.

 

5.6          In the event of a termination under Section 5.1 or 5.3, all duties of PENN (other than under Sections 2.4.3 or 5.10) and all rights (but not duties) of COMPANY (other than under Section 2.4.3 or 5.10) under this AGREEMENT immediately terminate without the necessity of any action being taken either by PENN or by COMPANY, provided, however, that in no event shall the foregoing be construed to obligate COMPANY to pay any amounts accruing under Sections 3.1 or 3.3 after the date of termination except under Section 5.9.  Upon and after any termination of this AGREEMENT, COMPANY and any sublicensee thereof shall refrain from further manufacture, sale, marketing, importation and/or distribution of PENN LICENSED PRODUCT(s).

 

5.7          Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

5.8          Upon termination of this AGREEMENT, COMPANY shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed PENN LICENSED PRODUCT(s) on hand, under the control of COMPANY or sublicensee(s) thereof; and (b) such PENN LICENSED PRODUCT(s) as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be reduced to writing.  COMPANY shall deliver copies of such written inventories, verified

 

13



 

by an officer of COMPANY, forthwith to PENN.  PENN shall have 45 days after receipt of such verified inventories within which to challenge the inventory and request an audit thereof.  Upon five (5)-days written notice to COMPANY, PENN and its agents shall be given access during normal business hours to the premises of COMPANY, and/or sublicensees thereof for the purpose of conducting an audit.  Upon the termination of this AGREEMENT, COMPANY shall at its own expense forthwith remove, efface or destroy all references to PENN from all advertising or other materials used in the promotion of COMPANY’s business or the business of any sublicensee of COMPANY and COMPANY and any sublicensee thereof shall not thereafter represent in any manner that it has rights in or to the PENN PATENT RIGHTS or PENN LICENSED PRODUCT(s).

 

5.9          Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 5.3.1 or 5.3.2, COMPANY shall have a period of six (6) months to sell off its inventory of PENN LICENSED PRODUCT(s) existing on the date of termination of this AGREEMENT and shall pay royalties to PENN with respect to such PENN LICENSED PRODUCT(s) within thirty (30) days following the expiration of such six-month period.

 

5.10  Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Articles 4, 5, 8, 9 and 10 shall survive such termination.

 

6.                                        PATENT MAINTENANCE AND REIMBURSEMENT

 

6.1          PENN and COMPANY shall jointly control, prosecute and maintain the PENN PATENT RIGHTS during the term of this AGREEMENT pursuant to the terms of a Client and Billing Agreement to be (the “BILLING AGREEMENT”) appended hereto as Attachment 4 and to be entered into promptly after the EFFECTIVE DATE hereof by COMPANY, PENN and the law firm party thereto.

 

6.2          Unless otherwise indicated in the Client and Billing Agreement, COMPANY shall reimburse PENN for all reasonable documented attorneys fees, expenses, official fees and other charges incident to the preparation, prosecution and maintenance of PENN PATENT RIGHTS incurred by PENN after the EFFECTIVE DATE within thirty (30) days after COMPANY’S receipt of invoices for such fees, expenses and charges.

 

6.3          Effective on the earlier of the date on which COMPANY has raised equity investment capital of one million dollars ($1,000,000) or June 30, 2002, COMPANY shall promptly reimburse PENN for all documented attorneys fees, expenses, official fees and other charges incident to the preparation, prosecution, and maintenance of PENN PATENT RIGHTS incurred by PENN (either directly or by way of invoice from a third party) prior to the EFFECTIVE DATE and not previously reimbursed to PENN by COMPANY or a third party.

 

7.                                        INFRINGEMENT AND LITIGATION

 

7.1          PENN and COMPANY are responsible for notifying each other promptly of any known or suspected infringement of PENN PATENT RIGHTS, which may come to their

 

14



 

attention after the EFFECTIVE DATE.  PENN and COMPANY shall consult one another in a timely manner concerning an appropriate response to the infringement.

 

7.2          COMPANY may prosecute such infringement at its own expense.  COMPANY shall not settle or compromise any such suit in a manner that imposes any obligations or restrictions on PENN or grants any rights to the PENN PATENT RIGHTS, without PENN’s prior written permission.  Financial recoveries from any such litigation will first be applied to reimburse COMPANY for its litigation expenditures with additional recoveries being paid to COMPANY, subject to lost royalty due PENN based on such infringement.

 

7.3          COMPANY’s rights under Section 7.2 are subject to the continuing right of PENN to intervene at PENN’s own expense and join COMPANY in any claim or suit for infringement of the PENN PATENT RIGHTS.  Any consideration received by PENN or COMPANY in settlement of any claim or suit shall be shared between PENN and COMPANY in proportion with each party’s share of the litigation expenses reasonably incurred in such infringement action.

 

7.4          If COMPANY fails to prosecute any material infringement of PENN PATENT RIGHTS, PENN may prosecute such material infringement at its own expense.  In such event, financial recoveries will be entirely retained by PENN.

 

7.5          In any action to enforce any of the PENN PATENT RIGHTS, either party, at the request and reasonable expense of the other party, shall cooperate to the fullest extent reasonably possible.  This provision shall not be construed to require either party to undertake any activities, including legal discovery, at the request of any third party except as may be required by lawful process of a court of competent jurisdiction.

 

8.                                        REPRESENTATIONS AND WARRANTIES OF PENN; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

8.1          PENN represents and warrants to COMPANY that to its KNOWLEDGE as of the date hereof:

 

8.1.1                         PENN has the full authority to execute and deliver this AGREEMENT.

 

8.1.2                         No material claim by any third party contesting the validity, enforceability, licensability, use or ownership of any of such PENN PATENT RIGHTS has been made, is currently outstanding or is threatened against PENN.

 

8.1.3                         No loss or expiration of any part of the PENN PATENT RIGHTS is currently pending.

 

8.2          EXCEPT AS SET FORTH IN SECTION 8.1, THE PENN PATENT RIGHTS,  PENN LICENSED PRODUCTS AND ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT ARE PROVIDED ON AN “AS IS” BASIS AND PENN MAKES NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED,

 

15



 

WITH RESPECT THERETO.  BY WAY OF EXAMPLE, BUT NOT OF LIMITATION, PENN MAKES NO REPRESENTATIONS OR WARRANTIES (i) OF COMMERCIAL UTILITY; (ii) OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE; OR (iii) THAT THE USE OF THE PENN PATENT RIGHTS, PENN LICENSED PRODUCTS OR ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADE SECRET OR TRADEMARK OR OTHER PROPRIETARY RIGHTS OF OTHERS.  PENN SHALL NOT BE LIABLE TO COMPANY, COMPANY’S SUCCESSORS OR ASSIGNS OR ANY THIRD PARTY WITH RESPECT TO: ANY CLAIM ARISING FROM USE OF THE PENN PATENT RIGHTS, PENN LICENSED PRODUCTS AND ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT OR FROM THE MANUFACTURE, USE OR SALE OF PENN LICENSED PRODUCTS; OR ANY CLAIM FOR LOSS OF PROFITS, LOSS OR INTERRUPTION OF BUSINESS, OR FOR INDIRECT, SPECIAL OR CONSEQUENTIAL DAMAGES OF ANY KIND.

 

8.3          COMPANY shall defend, indemnify and hold harmless PENN, its trustees, officers, agents and employees (individually, an “Indemnified Party”, and collectively, the “Indemnified Parties”), from and against any and all liability, loss, damage, action, claim or expense suffered or incurred by the Indemnified Parties (including attorney’s fees and expenses) (individually, a “Liability”, and collectively, the “Liabilities”) that results from or arises out of:  (a) the development, use, manufacture, promotion, sale or other disposition of any PENN PATENT RIGHTS or PENN LICENSED PRODUCTS by COMPANY, its assignees, sublicensees, vendors or other third parties; (b) any breach by COMPANY of this AGREEMENT; and (c) the enforcement by an Indemnified Party of this Section.  Without limiting the foregoing, COMPANY shall defend, indemnify and hold harmless the Indemnified Parties from and against any Liabilities resulting from:

 

8.3.1                         any product liability or other claim of any kind related to the use by a third party of a PENN LICENSED PRODUCT that was manufactured, sold or otherwise disposed by COMPANY, its assignees, sublicensees, or agents, other than such Liabilities arising from or related to the inaccuracy of any representation or warranty of PENN in Section 8.1 of this AGREEMENT; and

 

8.3.2                         a claim by a third party that the PENN PATENT RIGHTS or the design, composition, manufacture, use, sale, or other disposition of any PENN LICENSED PRODUCT infringes or violates any patent, copyright, trademark or other intellectual property rights of such third party, except to the extent that any such claim may relate to the inaccuracy of any representation or warranty in Section 8.1; and

 

8.3.3                         clinical trials or studies conducted by or on behalf of COMPANY and/or its sublicensees relating to the PENN LICENSED PRODUCTS, including, without limitation, any claim by or on behalf of a human subject of any such clinical trial or study.

 

16



 

8.4          COMPANY is not permitted to settle or compromise any claim or action giving rise to Liabilities in a manner that imposes any restrictions or obligations on PENN or grants any rights to the PENN PATENT RIGHTS or PENN LICENSED PRODUCTS without PENN’s prior written consent.  If COMPANY fails or declines to assume the defense of any such claim or action within thirty (30) days after notice thereof, PENN may assume the defense of such claim or action for the account and at the risk of COMPANY, and any Liabilities related thereto shall be conclusively deemed a liability of COMPANY.  The indemnification rights of the parties or any other Indemnified Party contained herein are in addition to all other rights which the parties or such Indemnified Party may have at law or in equity or otherwise.

 

8.5          Insurance

 

8.5.1                         COMPANY shall procure and maintain a policy or policies of comprehensive general liability insurance, including broad form and contractual liability, in a minimum amount of $2,000,000 combined single limit per occurrence and in the aggregate, as respects personal injury, bodily injury and property damage arising out of COMPANY’s performance under this AGREEMENT.

 

8.5.2                         COMPANY shall, upon commencement of clinical trials involving PENN LICENSED PRODUCTS, procure and maintain a policy or policies of product liability insurance in a minimum amount of $3,000,000 combined single limit per occurrence and in the aggregate as respects bodily injury and property damage arising out of COMPANY’s performance of this AGREEMENT.

 

8.5.3                         The policy or policies of insurance described in this Section 8.5 shall be issued by a recognized insurance carrier with an A.M. Best rating of “A” or better and shall name PENN as an additional insured with respect to COMPANY’s performance of this AGREEMENT.  COMPANY shall provide PENN with certificates evidencing the insurance coverage required herein and all subsequent renewals thereof.  Such certificates shall provide that COMPANY’s insurance carrier(s) notify PENN in writing at least 30 days prior to cancellation or material change in coverage.

 

8.6          PENN may periodically review the adequacy of the minimum limits of liability insurance specified in Section 8.5 and PENN reserves the right to require COMPANY to adjust the liability insurance coverages. The specified minimum insurance amounts do not constitute a limitation on COMPANY’s obligation to indemnify PENN under this AGREEMENT.

 

9.                                        USE OF PENN’S NAME

 

9.1          COMPANY and its employees and agents shall not use and COMPANY shall not permit its sublicensees to use PENN’s name or any adaptation thereof, or any PENN seal, logotype, trademark, or service mark, or the name, mark, or logotype of any PENN representative or organization in any way without the prior written consent of PENN.

 

17



 

10.                                  ADDITIONAL PROVISIONS

 

10.1                  Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between PENN and COMPANY, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

10.2                  COMPANY is not permitted to assign this AGREEMENT or any part of it to any person or entity other than an AFFILIATE of COMPANY, either directly or by operation of law, without the prior written consent of PENN in its sole discretion.  Any prohibited assignment of this AGREEMENT or the rights hereunder shall be null and void.  No assignment relieves COMPANY of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

10.3                  A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

10.4                  Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by public courier (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for PENN:

with a copy to:

 

 

University of Pennsylvania

Office of General Counsel

Center for Technology Transfer

University of Pennsylvania

3700 Market Street, Suite 300

133 South 36 th  Street, Suite 300

Philadelphia, PA 19104-3147

Philadelphia, PA 19104-3246

Attention: Managing Director

Attention: General Counsel

 

 

If for COMPANY:

with a copy to:

 

 

Viral Genomix, Inc.

Morgan, Lewis & Bockius LLP

3600 Market Street, Suite 100

1701 Market Street

Philadelphia, PA 19104-2642

Philadelphia, PA 19103-2921

Attention: Chief Executive Officer

Attention:Gary Smith

 

Either party may change its official address upon written notice to the other party.

 

10.5                  This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive

 

18



 

jurisdiction of and venue in the courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.

 

10.6                  PENN and COMPANY shall not discriminate against any employee or applicant for employment because of race, color, sex, sexual or affectional preference, age, religion, national or ethnic origin, handicap, or because he or she is a disabled veteran or a veteran of the Vietnam Era.

 

10.7                  COMPANY shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.  The transfer of certain technical data and commodities may require a license from the cognizant agency of the United States Government and/or written assurances by COMPANY that COMPANY shall not export data or commodities to certain foreign countries without prior approval of such agency.  PENN neither represents that a license is not required nor that, if required, it will issue.

 

10.8                  If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

10.9                  This AGREEMENT, the STOCK PURCHASE AGREEMENT, and the CLIENT BILLING AGREEMENT embody the entire agreement and understanding among the parties hereto and thereto and supersede all prior agreements and understandings relating to the subject matter.  This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.  The EXCLUSIVE NEGOTIATION AGREEMENT, effective as of May 1, 2001, by and between PENN and COMPANY is hereby terminated as of the EFFECTIVE DATE referenced above, and shall be of no further force or effect.

 

19


 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

THE TRUSTEES OF THE UNIVERSITY

 

 

OF PENNSYLVANIA

 

VIRAL GENOMIX, INC.

 

 

 

 

 

 

By:

 /s/ Louis P. Berneman

 

By:

 /s/ J. Joseph Kim

 

 

 

Name:

 Louis P. Berneman

 

Name:

 J. Joseph Kim

 

 

 

Title:

 Managing Director, CTT

 

Title:

 CEO/President

 

 

 

Date:

 11/5/01

 

Date:

  Nov 5, 2001

 

 

20



 

First Amendment

to the License Agreement between

Viral Genomix, Inc.

and

The Trustees of the University of Pennsylvania

 

This First Amendment (this “AMENDMENT A”) to the License Agreement between Viral Genomix, Inc. (“COMPANY”) and The Trustees of the University of Pennsylvania (“PENN”) is made effective by the parties on August 15, 2005 (the “AMENDMENT A EFFECTIVE DATE”).

 

RECITALS

 

WHEREAS, PENN and COMPANY entered into a License Agreement (the “AGREEMENT”) effective as of November 5, 2001.  Pursuant to the terms and conditions of the AGREEMENT, PENN granted to COMPANY an exclusive, worldwide right and license, with the right to grant sublicenses, to make, have made, use and sell PENN LICENSED PRODUCT(S).  In consideration of this exclusive license granted, COMPANY issued to PENN stock of COMPANY, and agreed to pay to PENN royalties based on the NET SALES of PENN LICENSED PRODUCTS.

 

WHEREAS PENN and COMPANY desire to amend certain provisions of the AGREEMENT.

 

NOW, THEREFORE, the parties agree as follows:

 

1.                                        Unless otherwise defined in this AMENDMENT A, all capitalized terms shall have the same meaning as set forth in the AGREEMENT.

 

2.                                        As of the AMENDMENT A EFFECTIVE DATE, Section 3.1.3 of the AGREEMENT is superceded with a new Section 3.1.3 to read in full as follows:

 

3.1.3                         In further consideration of the exclusive license granted to COMPANY, COMPANY shall pay to PENN, on a quarterly basis, a royalty on the NET SALES of each PENN LICENSED PRODUCT which is sold by COMPANY and any sublicensee(s), agent(s), and/or independent contractor(s) of COMPANY.  If the PENN LICENSED PRODUCT is Mifepristone for the treatment and/or prevention of HIV , then COMPANY shall pay to PENN a royalty of ****** on the NET SALES of such PENN LICENSED PRODUCT.  COMPANY shall pay to PENN a royalty of ****** on the NET SALES of all other PENN LICENSED PRODUCTS.  In determining the earned royalty payment, if any, to be made by COMPANY at the end of any CALENDAR QUARTER following first SALE of a PENN LICENSED PRODUCT, one-quarter of the minimum royalty paid at the beginning of the CALENDAR YEAR with respect to such PENN LICENSED PRODUCT shall be subtracted from the earned royalties otherwise payable for the CALENDAR QUARTER, and COMPANY shall owe the difference, if any.  Such royalty payments shall terminate on a product-by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first

 



 

SALE of such PENN LICENSED PRODUCT in such country, and (b) in any country in which patent rights exist for any PENN LICENSED PRODUCT, the date of expiration of the last-to-expire patent in such country, within the definition of PENN PATENT RIGHTS, with a valid claim covering the PENN LICENSED PRODUCT.

 

3.                                        As of the AMENDMENT A EFFECTIVE DATE, Section 3.2.5 of the AGREEMENT is superceded with a new Section 3.2.5 to read in full as follows:

 

3.2.5                         The following milestone payments are payable by COMPANY to PENN within sixty (60) days after the achievement of the respective milestone event:

 

Event

 

Amount

 

 

 

 

 

Filing of an IND APPLICATION for the first PENN LICENSED PRODUCT

 

$

250,000

 

 

 

 

 

 

Enrollment of the first patient in PHASE III CLINICAL TRIALS for the first PENN LICENSED PRODUCT

 

$

500,000

 

 

 

 

 

 

Filing of an NDA for the first PENN LICENSED PRODUCT

 

$

500,000

 

 

 

 

 

 

First anniversary of such filing

 

$

500,000

 

 

 

 

 

 

Receipt of an NDA approval letter for the first PENN LICENSED PRODUCT

 

$

1,500,000

 

 

 

 

 

 

First anniversary of such receipt

 

$

1,500,000

 

 

4.                                        As of the AMENDMENT A EFFECTIVE DATE, Section 10.4 of the AGREEMENT is superceded with a new Section 10.4 to read in full as follows:

 

10.4                            Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by public courier (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for PENN:

with a copy to:

 

 

University of Pennsylvania

Office of General Counsel

Center for Technology Transfer

University of Pennsylvania

3160 Chestnut Street, Suite 200

133 South 36 th  Street, Suite 300

Philadelphia, PA 19104-6283

Philadelphia, PA 19104-3246

Attention: Managing Director

Attention: General Counsel

 



 

If for COMPANY:

with a copy to:

 

 

V iral Genomix, Inc.

Duane Morris LLP

450 Sentry Parkway

One Liberty Place

Blue Bell, PA 19422

Philadelphia, PA 19103- 7396

Attention:  Chief Executive Officer

Attention:  Kathleen M. Shay

 

Either party may change its official address upon written notice to the other party.

 

5. As of the AMENDMENT A EFFECTIVE DATE, Section 10.9 of the AGREEMENT is superceded with a new Section 10.9 to read in full as follows:

 

10.9                            This AGREEMENT, AMENDMENT A, the STOCK PURCHASE AGREEMENT, and the CLIENT BILLING AGREEMENT embody the entire agreement and understanding among the parties hereto and thereto and supersede all prior agreements and understandings related to the subject matter.  This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.  The EXCLUSIVE NEGOTIATION AGREEMENT, effective as of May 1, 2001, by and between PENN and COMPANY is hereby terminated as of the EFFECTIVE DATE referenced above, and shall be of no further force or effect.

 

IN WITNESS THEREOF, the parties have executed this AMENDMENT A through their duly authorized representatives as set forth below, and this AMENDMENT A shall be attached to, and shall become a part of, the AGREEMENT between the parties.

 

 

THE TRUSTEES OF THE

 

VGX PHARMACEUTICALS, INC.

UNIVERSITY OF PENNSYLVANIA

 

 

 

 

 

 

 

 

By:

    /s/ Perry B. Molinoff

 

By:

    /s/ J. Joseph Kim

Perry B. Molinoff, M.D.

 

J. Joseph Kim, Ph.D.

Vice Provost for Research

 

President & Chief Executive Officer

 

 

 

Date:

    11 OCT 2005

 

Date:

    8/4/05

 




Exhibit 10.30

 

AGREEMENT OF LEASE

between

450 SENTRY PARKWAY ASSOCIATES

a Pennsylvania limited partnership,

acting by and through its General Partner,

AK Real Estate Corp. , Landlord

and

VIRAL GENOMIX, INC. d/b/a

VGX PHARMACEUTICALS , Tenant

 

1.

Reference Data

3

2.

Demise

4

3.

Construction by Landlord

5

4.

Term

6

5.

Holding Over

6

6.

Base Rent and Additional Rent

6

7.

Security Deposit

8

8.

Landlord’s Services

8

9.

No Other Services by Landlord

10

10.

Insurance

10

11.

Casualty

12

12.

Condemnation

12

13.

Tenant’s Fixtures

13

14.

Alterations

13

15.

Mechanics’ Liens

14

16.

Use of Premises

14

17.

Rules and Regulations

15

18.

Governmental Regulations

15

19.

Signs

15

20.

Landlord’s Entry

16

21.

Indemnification

16

22.

Curing Tenant’s Defaults

16

23.

Default

17

24.

Quiet Enjoyment

21

25.

Assignment and Subletting

21

26.

Subordination

22

27.

Tenant’s Certificates

23

28.

Acceptance; Surrender

23

 

1



 

29.

Option to Renew

24

30.

Notices

24

31.

Broker

24

32.

Definition of Parties

24

33.

Entire Agreement; Interpretation

25

34.

Waiver of Jury Trial

25

 

2



 

AGREEMENT OF LEASE made this 21 st  day of January, 2005, by and between 450 SENTRY PARKWAY ASSOCIATES, a Pennsylvania limited partnership, acting by and through its General Partner, AK Real Estate Corp . ( “Landlord” ), party of the first part, and VIRAL GENOMIX, INC. d/b/a VGX PHARMACEUTICALS , a Delaware corporation, ( “Tenant” ), party of the second part.

 

WITNESSETH THAT , for and in consideration of the rents, covenants and agreements herein contained and intending to be legally bound hereby, the parties hereto covenant and agree as follows:

 

1.                                        Reference Data .  As used in this Lease, the following terms shall be defined as indicated and refer to the data set forth in this Section 1.

 

LANDLORD’S ADDRESS:

550 Township Line Road, Suite 500

 

Blue Bell, PA 19422

 

FAX (610) 825-6858

 

E-mail: jim@kilduffco.com, cc: patp@kilduffco.com

 

 

TENANT’S ADDRESS:

3701 Market Street, 4 th  Floor

 

Philadelphia, PA 19104

 

FAX (215) 966-6101

 

E-mail: shine@vgxp.com

 

 

 

After the Commencement Date, at the Premises.

 

PREMISES:

that 7,050 SF + rentable square foot portion (“Premises”) of the first floor of the 37,417 square foot building (“Building”) owned by Landlord on a parcel of land containing approximately 5 acres (the “Land”) located at 450 Sentry Parkway, Blue Bell, Whitpain Township, Montgomery County, Pennsylvania (the “ Land ”), as further identified in Exhibits “A” and “B” attached hereto and made a part hereof.  The Building and the Land are hereinafter collectively referred to as the “Property” .

 

TERM:

Five (5) years, unless sooner terminated, as herein provided.

 

SCHEDULED COMMENCEMENT DATE:                                                                  March 15, 2005

 

3



 

BASE RENT:

Year 1 $ 95,000

($ 7,916.67 per month)

 

Year 2 $125,000

($10,416.67 per month)

 

Year 3 $150,000

($12,500.00 per month)

 

Year 4 $155,000

($12,916.67 per month)

 

Year 5 $160,000

($13,333.33 per month)

 

The first monthly installment shall be paid upon the signing of this Lease.

 

LEASE YEAR:

Any twelve month period beginning on the Commencement Date or any anniversary thereof.

 

ADDITIONAL RENT:

 

Sums not including Base Rent which Tenant is obligated to pay to Landlord from time to time pursuant to the terms of this Lease.

 

 

 

SECURITY DEPOSIT:

 

$24,000.00

 

 

 

PERMITTED USES:

 

Tenant shall use and occupy the Premises for general office and laboratory uses and for no other purpose.

 

TENANT’S PROPORTIONATE SHARE:18.84% (determined by dividing the area of the Premises by the area of the Building).  For purposes of determining electric usage, Tenant’s Proportionate Share shall be determined by multiplying the electric bill by a fraction, the numerator of which is 7,050 and the denominator of which is the occupied area of the 25,417 square foot two-story section of the Building.  Tenant’s Proportionate Share of gas usage shall be determined by multiplying the first floor gas bill by a fraction, the numerator of which is 7,050 and the denominator of which is the occupied area of the 12,450 square foot first floor of the two-story section of the building.

 

2.                                        Demise .

 

Landlord hereby demises and lets to Tenant and Tenant hereby hires and leases from Landlord the Premises, TOGETHER WITH, appurtenant to the Premises, the right to use in common with Landlord and other tenants, occupants and visitors to

 

4



 

the Building, the common driveways, parking lots, walkways and sidewalks on the Land and the lobbies, hallways, rest rooms, and other common facilities in the Building, for the Term and upon the conditions and limitations set forth herein.  This Lease shall not be binding upon Landlord unless Landlord’s mortgagee shall have approved this Lease within thirty (30) days from the date hereof.

 

3.                                        Construction by Landlord .

 

A.                                    Landlord shall repaint and carpet the Premises and construct and do such other work (collectively, the “Landlord’s Work”) in substantial conformity with Scheme 2 on the sketch plan attached hereto as Exhibit “C”, which has been initialed by the parties and which is incorporated herein by reference.

 

B.                                      If Landlord deems any changes, additions or alterations in the Space Plan necessary in connection with the construction of the Premises, such /changes, additions or alterations shall be submitted to Tenant for approval, which approval shall not be unreasonably withheld or delayed and shall be deemed to be given if not disapproved in writing within seven (7) days after Landlord’s submission of the same to Tenant.  Any dispute as to the content of such changes, additions or alterations may, at the option of either party hereto, be conclusively determined by the independent architect or engineer retained by Landlord for the construction of the Building.

 

C.                                      The Premises shall be substantially completed on or before the Scheduled Commencement Date, provided that the Scheduled Commencement Date shall be extended for the time equivalent to any time lost by Landlord due to strikes, labor disputes, governmental restrictions or limitations, scarcity of or inability to obtain labor or materials, accidents, fire or other casualties, weather conditions, current Tenant’s failure to vacate when anticipated, or any cause similar to or dissimilar to the foregoing beyond the reasonable control of Landlord.  All the aforesaid work shall be done in compliance with applicable laws and lawful ordinances.

 

D.                                     Landlord will remove any furniture that Tenant does not use.

 

5



 

E.                                       Landlord shall be responsible to make any repairs necessitated by defective workmanship or materials in the aforesaid work, provided that such defect appears and Tenant gives Landlord written notice thereof during the first 365 days of the Term.

 

4.                                        Term .  The Term shall commence on the earlier of (the “Commencement Date” ):  (a) the date when Tenant, with Landlord’s consent, assumes possession of the Premises or any part thereof, or (b) the fifth consecutive business day following Landlord’s notice to Tenant that the Premises are substantially completed (provided that the Premises are, in fact, substantially completed).  The Premises shall be substantially completed when the construction work and other items of work for which Landlord is responsible under Section 3 hereof have been completed to the extent that the Premises may be fully occupied by Tenant for its Permitted Uses, subject only to completion of minor finishing and adjustment of equipment.  If Commencement Date shall fall on a day other than the first day of a calendar month, the Term shall be increased by the number of days remaining in such calendar month.  The commencement and expiration dates of the Term, when determined as above provided, shall be confirmed by an addendum to this Lease.

 

5.                                        Holding Over .  This Lease shall expire absolutely and without notice on the last day of the Term, provided that if Tenant, with the prior written consent of Landlord, retains possession of the Premises or any part thereof after the termination of this Lease by expiration of the Term or otherwise, a month-to-month tenancy shall be deemed to exist, and Tenant shall continue to pay the Base Rent and Additional Rent due hereunder.  If such holding over exists without Landlord’s prior written consent, Tenant shall pay Landlord, as partial compensation for such unlawful retention, an amount calculated on a per diem basis for each day of such continued unlawful retention, equal to 200% of the Base Rent for the time Tenant thus remains in possession.  Such payments for unlawful retention shall not limit any rights or remedies of Landlord resulting by reason of the wrongful holding over by Tenant or create any right in Tenant to continue in possession of the Premises.

 

6.                                        Base Rent and Additional Rent .

 

A.                                    Tenant shall pay to Landlord during the Term the Base Rent, without notice or demand, in the monthly installments specified in Section 1, in advance on the first day of each calendar month of the Term, at Landlord’s principal office as

 

6



 

indicated in Section 1 above.  The first month’s installment of Base Rent shall be payable upon the execution of this Lease.  If the Term commences other than on the first day of a calendar month, then the installment of Base Rent for the first calendar month of the Term shall be adjusted proportionately, and the aforesaid first installment paid by Tenant upon the execution of this Lease shall be initially applied to the first partial month of the Term, and the balance to the next month.

 

B.                                      Within ninety (90) days of the end of each calendar year, Landlord shall determine its costs for the services provided in accordance with Section 8 hereof for the preceding calendar year (“Annual Operating Expenses”) and shall provide Tenant with a copy of such statement.  The Annual Operating Expenses so determined for the 2005 calendar year shall constitute the “Base Year Operating Expenses”.  Should Landlord’s Annual Operating Expenses for any successive calendar year during the Term of this Lease exceed its Base Year Operating Expenses, Tenant shall pay to Landlord, as Additional Rent, upon receipt of Landlord’s statement, its proportionate share of such excess.

 

C.                                      Base Rent, Additional Rent and all other sums payable by Tenant to Landlord hereunder shall be paid, without set-off or deduction, in lawful currency of the United States of America to Landlord at the address set forth in Section 1 hereof, or at such other address as Landlord may from time to time designate in writing to Tenant.  In order to partially compensate Landlord for the extra expense incurred in the handling of delinquent payments, Tenant agrees to pay Landlord a late charge equal to the product obtained by multiplying each installment of Base Rent or Additional Rent not paid by its due date by five percent (5%) (the “Default Rate” ).

 

D.                                     Notwithstanding the foregoing, “Operating Expenses” shall not include expenditures for any of the following:

 

(i)                                      The costs for alterations or additions which are considered capital improvements or replacements under generally accepted accounting principles,

 

Repairs or other work occasioned by fire, windstorm or other insured casualty or hazard, to the extent that Landlord shall receive proceeds of such insurance,

 

Repairs for which Landlord is responsible pursuant to Section 11 below, and work for which Landlord is responsible under Section 3 above,

 

Repairs or rebuilding necessitated by condemnation,

 

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Depreciation and amortization of the Building,

 

The salaries and benefits of executive officers of Landlord, if any,

 

Net income, franchise or capital stock taxes payable by Landlord,

 

Interest on debt or amortization or principal on any mortgage or other obligations of Landlord.

 

Items of Operating Expense which are not exclusively incurred with respect to the Building by reason of the nature of the items or otherwise shall be equitably allocated by Landlord among the buildings to which the same relate or for whose benefit the same have been incurred, and only the portion allocated to the building shall be included in calculating the Operating Expense for the Building.

 

7.                                        Security Deposit .  Upon the date hereof Tenant shall pay to Landlord a security deposit in the amount set forth in Section 1 hereof which Landlord will hold as security for the faithful performance by Tenant of all its covenants and agreements under this Lease, but in no event shall Landlord be obliged to apply same to rents or other charges in arrears or damages for Tenant’s default hereunder, but Landlord may so apply the security deposit at its option.  Landlord’s right to possession of the Premises for Tenant’s default or any other reason shall not be affected by the fact that Landlord holds said security deposit.  The security deposit, if not so applied by Landlord, shall be returned to Tenant within sixty (60) days after this Lease terminates, provided that Tenant shall have vacated the Premises and delivered the same to Landlord, as herein provided.  In the event of any transfer of Landlord’s interest in the Premises, Landlord shall have the right to transfer its interest in the security deposit, whereupon Landlord shall be released of all liability with respect to such security deposit, and Tenant shall look solely to such transferee for the return of the same.

 

8.                                        Landlord’s Services .  So long as Tenant is not in default hereunder, Landlord shall:

 

A.                                    Arrange for all required utility services to the Premises; provided , however , that Landlord shall not be liable to Tenant for any loss or damage arising from interruption in such utility services.  It is expressly understood and agreed by the parties hereto that Tenant shall be responsible for payment of the cost of all gas and electricity

 

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consumed on the Premises.

 

B.                                      Clean or cause the Premises and Building to be kept clean to the standards of a first-class suburban office building, provided the same are kept in order by Tenant.

 

C.                                      Pay all real estate taxes and other taxes or charges levied in lieu of such taxes, general and special public assessments, charges imposed by any governmental authority pursuant to anti-pollution or environmental legislation, taxes on the rentals of the Building or the use, occupancy or renting of space therein.

 

D.                                     Pay all premiums and fees for fire and extended coverage insurance, insurance against loss of rentals for space in the Building and public liability insurance.

 

E.                                       Pay all water and sewer service charges, electricity, heat and other utility charges not separately metered to tenants in the Building.

 

F.                                       Provide for snow and trash removal and maintenance and repair of parking lots and sidewalks, lawn and general grounds upkeep, and the costs of all labor, material and supplies incidental thereto.

 

G.                                      Make all repairs necessary to maintain the plumbing and electrical systems, windows, floors (excluding carpeting),  roof, common areas and all other items which constitute a part of the Premises and the Building and are installed or furnished by Landlord, except repairs to Tenant’s trade fixtures and property and installations which Tenant is obligated to make or which were performed by Landlord at Tenant’s request; provided , however , that Landlord shall not be obligated for any of such repairs until the expiration of a reasonable period of time after written notice from Tenant that such repair is needed.  In no event shall Landlord by obligated under this paragraph to repair any damage caused by any act, omission or negligence of Tenant or its employees, agents, invitees, licensees, subtenants, or contractors.

 

Tenant shall keep clean and otherwise take good care of the Premises and the fixtures and appurtenances therein.  Tenant shall, at its sole cost and expense, repair and replace all damage or injury to the Premises and the Building and to fixtures

 

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and equipment caused by Tenant or its employees, agents, invitees, licensees, subtenants, or contractors, or as the result of all of any of them moving in or out of the Building or by installation or removal of furniture, fixtures or other property, which repairs and replacements shall be in quality and class equal to the original work or installations.  If Tenant fails to make such repairs or replacements, the same may be made by Landlord and such expense shall be collectible as Additional Rent and paid by Tenant within fifteen (15) days after rendition of a bill therefor.

 

Landlord shall not be liable by reason of any injury to or interference with Tenant’s business arising from the making of any repairs, alterations, additions or improvements in or to the Premises or the Building or to any appurtenances or equipment therein.  Except as expressly provided in Sections 11 and 12 hereof, there shall be no abatement of rent because of such repairs, alterations, additions or improvements.

 

9.                                        No Other Services by Landlord .

 

Landlord shall not be required to render any services to Tenant or to make any repairs or replacements to the Premises, except as provided in Sections 3, 8, 11 and 12 hereof.

 

10.                                  Insurance .

 

A.                                    Tenant, at Tenant’s expense, shall maintain in effect throughout the Term, through insurance carriers reasonably satisfactory to Landlord, insurance against claims for personal injury (including death) and property damage, under a policy of general public liability insurance, in amounts not less than $1,000,000 combined single limit in respect of bodily injury (including death) and $100,000 for property damage.  The insurance policy shall name both Landlord and Tenant as insured parties.

 

B.                                      Tenant shall, at its own expense, maintain fire and comprehensive casualty insurance of adequate amounts with respect to its own fixtures, merchandise, equipment and other property contained in the Premises, it being understood that all merchandise, furniture, fixtures, effects and property of every kind of Tenant which may be in the Premises, or the Building or on the Land shall be at the sole risk and hazard of Tenant.

 

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C.                                      Prior to the commencement of the Term, Tenant shall provide Landlord with certificates of the insurance policies herein required of Tenant.  All policies shall provide that coverage thereunder may not be reduced or terminated without at least thirty (30) days prior written notice to Landlord.  Tenant shall furnish to Landlord throughout the Term replacement certificates at least thirty (30) days prior to the expiration date of the then current policies and, upon request of Landlord, shall supply to Landlord copies of all policies herein required of Tenant.

 

D.                                     Landlord shall maintain and keep in effect throughout the Term of this Lease insurance against loss or damage to the building by fire and such other casualties as may be included within either fire and extended coverage insurance or all-risk insurance and such other insurance as Landlord may desire or as may reasonably be required from time to time by any mortgagee.

 

E.                                       Each of the parties hereto hereby releases the other from liability for injury, loss or damage which may be inflicted upon the property of such party, even if such liability results from the negligence of the other party; provided , however , that this release shall be effective only (i) during such time as the applicable insurance policy carried by such party names the other party as a co-insured or contains a clause to the effect that this release shall not affect said policy or the right of the insured to recover thereunder, and (ii) to the extent of the coverage of such policy.  If any policy does not permit such a waiver, and if the party to benefit therefrom requests that such a waiver be obtained, the other party agrees to obtain an endorsement to its insurance policies permitting such waiver of subrogation, if available, and if an additional premium is charged for such waiver, the party benefiting therefrom shall pay same promptly upon being billed therefor.

 

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11.                                  Casualty .

 

A.                                    If the Premises shall be damaged or destroyed by fire or other casualty, Tenant shall promptly notify Landlord, and Landlord shall repair the damaged portions of the Premises (but not any of the Tenant’s property therein or improvements or alterations made by the Tenant), except that if, in Landlord’s reasonable judgment, the damage would require more than sixty days work to repair, or if the insurance proceeds (excluding rent insurance) which Landlord anticipates receiving must be applied to repay any mortgages encumbering the Building or are otherwise inadequate to pay the cost of such repair, then Landlord shall have the right to terminate this Lease by so notifying Tenant, which notice shall specify a termination date not less than fifteen (15) days after its transmission.  If Landlord is so required to repair, the work shall be commenced promptly and completed with due diligence, taking into account the time required by Landlord to effect a settlement with, and procure insurance proceeds from, the insurer, except for delays due to governmental regulation, scarcity of or inability to obtain labor or materials, or causes beyond Landlord’s reasonable control.

 

B.                                      During the period when Tenant shall be deprived of possession of the Premises by reason of such damage, Tenant’s obligation to pay Base Rent under Section 6 shall abate as of the date of the casualty in the proportion which the damaged area of the Premises bears to the entire Premises.

 

C.                                      If Landlord does not restore the Premises or the affected portion to tenantability within one hundred eighty (180) days after such casualty (provided that the nature of the damage is such that it reasonably could be repaired within one hundred eighty [180] days after commencement of work), or so commences restoration and pursues the same with due diligence if restoration cannot be completed within such one hundred eighty (180) days, Tenant may then terminate this Lease, retroactive to the date of casualty; provided , however , such one hundred eighty (180) day period shall be extended by causes delaying the work of restoration which are beyond Landlord’s reasonable control.

 

12.                                  Condemnation .

 

A.                                    If all or a substantial portion of the Premises is taken through the exercise of the power of eminent domain, this Lease shall terminate on the date when possession of the Premises is required by the condemning authority.  If only part of the

 

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Premises is taken, then (i) if the condemnation award is insufficient to restore the remaining portion of the Premises or if such award must be applied to repay any mortgages encumbering the Premises, or (ii) if a substantial portion of the Premises is so taken, and it is commercially impossible for Tenant to continue its business within the Premises, then Landlord in the case of (i) above and Tenant in the case of (ii) above shall have the right to terminate this Lease on the date when the condemned portion of the Premises is required to be delivered to the condemning authority, which right shall be exercisable by the exercising party so notifying the other party no later than thirty (30) days prior to such date.

 

B.                                      If this Lease is not so terminated after a partial condemnation, then after the date when the condemned portion of the Premises is delivered to the condemnor, the Base Rent shall be reduced effective as of the date of delivery in the proportion which the condemned area bears to the entire area of the Premises.

 

C.                                      Tenant shall have the right to claim against the condemnor only for removal and moving expenses and business dislocation damages which may be separately payable to tenants in general under Pennsylvania law, provided such payment does not reduce the award otherwise payable to Landlord.  Subject to the foregoing, Tenant hereby waives all claims against Landlord with respect to a condemnation, and hereby assigns to Landlord all claims against the condemnor including, without limitation, all claims for leasehold damages and diminution in the value of Tenant’s leasehold estate.

 

13.                                  Tenant’s Fixtures .  Tenant shall have the right to install trade fixtures, machinery and equipment (excluding alterations, improvements and additions which are governed by Section 14) required by Tenant or used by it in its business, provided that same do not impair the structural strength of the Building and further provided that such trade fixtures, machinery and equipment shall be limited to items normally used in an office/warehouse building.  Tenant shall remove all such trade fixtures, machinery and equipment prior to the end of the Term, and Tenant shall repair and restore any damage to the Premises caused by such installation or removal.

 

14.                                  Alterations .  Tenant shall not, without on each occasion first obtaining Landlord’s prior written consent, make any alterations, improvements or additions to the Premises, except that Tenant may, without the consent of Landlord but with prior written notice to Landlord, make minor improvements to the interior of the Premises provided that they do not impair the structural strength, operation or value of the Premises.

 

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Tenant agrees to pay for such alterations, etc. and to indemnify, save and hold Landlord harmless from any cost, expense or liens arising in connection therewith.  All alterations, improvements and additions, except for minor alterations and improvements as aforesaid, upon completion of construction thereof, shall become part of the Premises and the property of Landlord without payment therefor by Landlord and shall be surrendered to Landlord at the end of the Term; provided , however , if so notified by Landlord at the time Tenant requests Landlord’s consent to such alterations, etc., Tenant shall, prior to the end of the Term, remove all such alterations and improvements, or the parts thereof specified by Landlord, from the Premises and shall repair all damage caused by installation and removal.  For purposes of this Section 14, “minor improvements” shall be defined as those improvements costing no more than $5,000.  Landlord acknowledges that Tenant will be setting up a laboratory in the Premises and Landlord shall consent to such improvements.

 

15.                                  Mechanics’ Liens .  Tenant shall not, in the making of any repairs or alterations pursuant to the provisions of Section 14 hereof, suffer or permit any mechanic’s, laborer’s or materialman’s lien to be filed against the Premises or any part thereof by reason of labor or materials supplied or claimed to have been supplied to Tenant; and if any such lien shall be filed, Tenant, within thirty days after notice of filing, shall cause it to be discharged of record (by payment, payment into court or bonding).

 

16.                                  Use of Premises .

 

A.  Tenant shall not commit or suffer any waste upon the Premises, or any nuisance or any other act which may disturb the quiet enjoyment of any other tenant in the Building.

 

B.  Tenant shall not dispose of, store, deposit, bury, dump, spill, leak, place, release or inject in the Building or on the Land any Hazardous Waste (as hereinafter defined) in any manner which would violate any of the Environmental Statutes (as hereinafter defined).  For purposes of this Lease, the term “Environmental Statutes” shall mean all federal, state or local laws, ordinances, rules, regulations or policies, now or hereafter existing, which govern or otherwise relate to the use, storage, treatment, transportation, manufacture, refinement, handling, production or disposal of any hazardous waste as defined in the Comprehensive Environmental Response, Compensation and Liability Act (42 U.S.C. 9, 601 et seq.) ( “CERCLA” ) or

 

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any other applicable federal, state or local statute.  For purposes of this Agreement, the term “Hazardous Waste” shall mean any flammable substance, explosive, radio active material, hazardous material, hazardous waste, toxic substance, pollutant, pollution or any related materials or substances specified in any of the Environmental Statutes, including, but not limited to, asbestos, PCBs and any “hazardous substance” as defined in CERCLA.

 

17.                                  Rules and Regulations .  Tenant covenants and agrees that Tenant, its employees, agents, invitees, licensees and other visitors, shall observe faithfully, and comply strictly with, such reasonable Rules and Regulations as Landlord or Landlord’s agents may, after notice to Tenant, from time to time adopt with respect to the Building.

 

18.                                  Governmental Regulations .  Tenant shall throughout the term of this Lease, at Tenant’s sole cost and expense, promptly comply with all laws and ordinances and notices, orders, rules, regulations and requirements of all federal, state and municipal governments and appropriate departments, commissions, boards and officers thereof, and notices, orders, rules and regulations of the National Board of Fire Underwriters, or any other body now or hereafter constituted exercising similar functions, relating to the Premises, exterior as well as interior, foreseen or unforeseen, ordinary as well as extraordinary, or to the use or manner of use of the Premises, or to the fixtures and equipment thereof.  Without limiting the generality of the foregoing, Tenant shall keep in force at all times all licenses, consents and permits necessary for the lawful use of the Premises for the purposes herein provided and Tenant shall pay all personal property taxes, income taxes, license fees, and other taxes which are or may be assessed, levied or imposed upon Tenant in connection with Tenant’s operation of its business upon the Premises.  Tenant shall likewise observe and comply with the requirements of all policies of public liability, fire and other policies of insurance at any time in force with respect to the Premises.

 

19.                                  Signs .  Except for signs which are located wholly within the interior of the Premises and which are not visible from the exterior of the Building, no signs shall be placed, erected or maintained at any place upon the Premises or the Building without the prior written consent of Landlord as to the size, location, content and illumination thereof.  Tenant shall have the right to use two-thirds of the area of the existing “Health Advocate” sign currently installed on the Land, substituting its own name thereon, so long as Whitpain Township shall permit Tenant’s use of the sign. Upon submission of its artwork to Landlord, Landlord shall endeavor to secure the required permit from Whitpain Township and, if approved and granted, shall have the new sign faces fabricated and installed by its vendor.  Any permitted signs shall be maintained by Tenant in good condition during the Term, and Tenant shall remove the same at the

 

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expiration or earlier termination of this Lease, repairing any damage caused by the installation and/or removal.

 

20.                                  Landlord’s Entry .  Landlord and its agents, contractors and invitees shall have the right to enter the Premises at all reasonable times to inspect the same, to exhibit same to prospective purchasers, tenants and mortgagees, and to make any necessary repairs thereto.  Landlord agrees not to unreasonably interfere with Tenant’s business operations in the Premises during such entry.  Landlord shall not be liable in any manner to Tenant by reason of such entry or the performance of repair work in the Premises and the obligations of Tenant hereunder shall not thereby be affected.

 

21.                                  Indemnification .

 

A.  The parties hereto shall each indemnify the other from and against any and all losses, costs (including reasonable counsel fees), claims, suits, actions and causes of action, whether legal or equitable, sustained or arising by reason of the indemnifying party’s default in any of its obligations hereunder, or of the fault or neglect of the indemnifying party or of the failure by the indemnifying party or any of its officers, agents, employees or invitees to fulfill any duty toward the public, or any person or persons whomsoever, which the indemnifying party, by reason of its occupancy or use of the Premises, may owe.

 

B.  Tenant shall protect, indemnify and save Landlord harmless from and against any and all liability, laws, damage, cost or expense that Landlord may suffer or incur as a result of any claims, demands, damages, losses, liabilities, costs, charges, suits, orders, judgments or adjudications asserted, assessed, filed or entered against Landlord by any third party, including any governmental authority, arising from the alleged deposit, storage, disposal, burial, dumping, injecting, spilling, leaking or other use, placement or release in, on or affecting the Building or the Land of a Hazardous Waste or otherwise arising from any other alleged violation of any of the Environmental Statutes, including, but not limited to, liability for costs and expenses of abatement, correction or clean-up, fines, damages, response costs or penalties, or liability for personal injury or property damage.

 

22.                                  Curing Tenant’s Defaults .  If Tenant shall default in performing any of its obligations hereunder, Landlord may (but shall not be so obliged), in addition to Landlord’s other rights and remedies and without waiver of such default, cure such default on behalf of Tenant, thereby entering and possessing the Premises if deemed

 

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necessary by Landlord, provided that Landlord shall have first given Tenant written notice of such default and Tenant shall have failed within fifteen (15) days following said written notice to cure or diligently to pursue the cure of said default (which notice and opportunity to cure shall not be required in case of emergency).  Tenant, upon demand of Landlord, shall reimburse Landlord for all costs (including reasonable counsel fees) incurred by Landlord with respect to such default, and, if Landlord so elects, Landlord’s efforts to cure the same, which costs shall be deemed Additional Rent hereunder.

 

23.                                  Default .

 

A.                                    If

 

(i)                                      Tenant fails to pay any installment of Base Rent when due and such failure continues for a period of five (5) days after notice by or on behalf of Landlord; provided , however , that Landlord need not give any such notice, and Tenant shall not be entitled to any such period of grace, more than twice in any twelve (12) month period,

 

(ii)                                   Tenant fails to pay any Additional Rent when due and such failure continues for a period of ten (10) days after written notice from Landlord,

 

(iii)                                Tenant abandons the Premises,

 

(iv)                               Tenant fails to observe or perform any of Tenant’s other obligations herein contained and such failure continues for more than fifteen (15) days after written notice from Landlord,

 

(v)                                  Tenant makes an assignment for the benefit of creditors,

 

(vi)                               Tenant commits an act of bankruptcy or files a petition or commences any proceeding under any bankruptcy or insolvency law,

 

(vii)                            a petition is filed or any proceeding is commenced against Tenant under any bankruptcy or insolvency law and is not dismissed within thirty (30) days,

 

(viii)                         Tenant is adjudicated a bankrupt,

 

(ix)                                 a receiver or other official is appointed for Tenant or for a substantial part of Tenant’s assets or for Tenant’s interests in this Lease, or

 

(x)                                    any attachment or execution is filed or levied against a

 

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substantial part of Tenant’s assets or Tenant’s interests in this Lease or any of Tenant’s property in the Premises, then, in any such event, an Event of Default shall be deemed to exist and Tenant shall be in default hereunder, and, at the option of Landlord:

 

a)                                       the balance of the Base Rent and all Additional Rent and all other sums to which Landlord is entitled hereunder shall be deemed to be due, payable and in arrears, as if payable in advance hereunder; or

 

b)                                      this Lease and the Term shall, without waiver of Landlord’s other rights and remedies, terminate without any right of Tenant to save the forfeiture.

 

Any acceleration of the rent by Landlord shall not constitute a waiver of any right or remedy of Landlord, and if Tenant shall fail to pay the accelerated rent upon Landlord’s demand, then Landlord may thereafter terminate this Lease, as aforesaid.  Immediately upon such termination by Landlord, Landlord shall have the right to recover possession of the Premises with or without legal process, breaking locks and replacing locks, and removing Tenant’s and any third party’s property therefrom, and making any disposition thereof as Landlord may deem commercially reasonable.

 

B.                                      Unless and until Landlord shall have terminated this Lease under subsection 23.A above, Tenant shall remain fully liable and responsible to perform all of the covenants and to observe all of the conditions of this Lease throughout the remainder of the Term; and, in addition, Tenant shall pay to Landlord, upon demand and as Additional Rent, the total sum of all costs, losses and expenses, including reasonable counsel fees, as Landlord incurs, directly or indirectly, because of any Event of Default having occurred.

 

At any time or from time to time after the repossession of the Premises or any part thereof, pursuant to subsection 23.A., whether or not the Term shall have been terminated pursuant to subsection 23.A., Landlord shall attempt to relet all or any part of the Premises for the account of Tenant for such term or terms (which may be greater or less than the period which would otherwise have constituted the balance of the Lease Term) and on such conditions (which may include concessions or free rent) and for such uses as Landlord, in its absolute discretion, may determine, but Landlord shall have no obligation to rent the Premises so long as Landlord (or any related entity) has other comparable vacant space available for leasing in the general geographical area of the Premises.  Upon each such reletting all rents received by Landlord from such reletting shall be applied: first, to the payment of any indebtedness other than rent due hereunder from Tenant to Landlord; second, to the payment of any costs and expenses of such reletting, including brokerage fees and attorney’s fees and all costs of such alterations and repairs; third, to the payment of rent due and unpaid hereunder; and the

 

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residue, if any, shall be held by Landlord and applied in payment of future rent as it may become due and payable hereunder.  If such rentals received from such reletting during any month shall be less than that to be paid during that month by Tenant hereunder, Tenant shall pay any such deficiency to Landlord.  Such deficiency shall be calculated and paid monthly.

 

The damages which Landlord shall be entitled to recover from Tenant in such case shall be the sum of:

 

i)                                          all Base Rent and Additional Rent accrued and unpaid as of the termination date;

 

ii)                                       a) all costs and expenses incurred by Landlord in recovering possession of the Premises, including removal and storage of Tenant’s property, improvements and alterations therefrom,

 

b)  the costs and expenses of restoring the Premises to the condition in which the same were to have been surrendered by Tenant as of the expiration of the Term, or, in lieu thereof, the costs and expenses of remodeling or altering the Premises or any part for reletting the same,

 

c)  the costs of reletting (exclusive of those covered by the foregoing b) including brokerage fees and reasonable counsel fees, and

 

d)  general overhead and advertising expenses not in excess of one percent (1%) of the total Base Rent otherwise to be paid by Tenant over the remainder of the Term, for each month or part thereof between the date of termination and the reletting of the entire Premises; AND

 

iii)                                    all Base Rent and other charges (including Additional Rent when the same can be determined) otherwise payable by Tenant over the remainder of the Term:

 

—LESS—

 

iv)                                   all rent, including Additional Rent to the extent that the same would have been payable by Tenant, as Landlord may receive from other tenant(s) by reason of the leasing of the Premises or part thereof during or attributable to any period falling within the otherwise remainder of the Term.

 

The damage sums payable by Tenant under the preceding

 

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provisions of this subsection 23.B. shall be payable on demand from time to time as the amounts are determined; and if from Landlord’s subsequent receipt of rent as aforesaid from reletting, there be any excess payment(s) by Tenant by reason of the crediting of such rent thereafter received, the excess payment(s) shall be refunded by Landlord to Tenant, without interest.

 

Any sums payable by Tenant hereunder which are not paid within ten (10) days after the same shall be due shall bear interest from that day until paid at the rate of two percent (2%) over the then “prime rate” being charged by Harleysville National Bank & Trust Company for ninety (90) day loans to major corporate borrowers (unless such rate be usurious as applied to Tenant, in which case the highest permitted legal rate shall apply).

 

C.                                      FOR THE PURPOSE OF PROCURING POSSESSION OF THE PREMISES WHEN THE TERM SHALL END BY EXPIRATION OR BY TERMINATION THEREOF ON ACCOUNT OF TENANT’S DEFAULT, TENANT HEREBY AUTHORIZES AND EMPOWERS ANY ATTORNEY OF ANY COURT OF RECORD IN THE COMMONWEALTH OF PENNSYLVANIA OR ELSEWHERE, AS ATTORNEY FOR TENANT AND ALL PERSONS CLAIMING UNDER OR THROUGH TENANT, TO SIGN AN AGREEMENT FOR ENTERING IN ANY COMPETENT COURT AN ACTION IN EJECTMENT FOR POSSESSION OF THE PREMISES AND TO APPEAR FOR AND CONFESS JUDGMENT AGAINST TENANT, AND AGAINST ALL PERSONS CLAIMING UNDER OR THROUGH TENANT, FOR THE RECOVERY BY LANDLORD OF POSSESSION OF THE SAME, WITHOUT ANY STAY OF EXECUTION, FOR WHICH THIS LEASE, OR A COPY THEREOF VERIFIED BY AFFIDAVIT, SHALL BE A SUFFICIENT WARRANT; AND THEREUPON A WRIT OF POSSESSION MAY BE ISSUED FORTHWITH, WITHOUT ANY PRIOR WRIT OR PROCEEDING WHATSOEVER.  TENANT HEREBY RELEASES LANDLORD FROM ALL ERRORS AND DEFECTS WHATSOEVER IN ENTERING SUCH ACTION AND JUDGMENT AND IN CAUSING SUCH WRIT OR WRITS TO BE ISSUED, AND HEREBY AGREES THAT NO WRIT OF ERROR, APPEAL, PETITION TO OPEN OR STRIKE OFF JUDGMENT, OR OTHER OBJECTION SHALL BE FILED OR MADE WITH RESPECT THERETO.  IF FOR ANY REASON AFTER SUCH ACTION HAS BEEN COMMENCED THE SAME SHALL BE DISCONTINUED OR POSSESSION OF THE PREMISES SHALL REMAIN IN OR BE RESTORED TO TENANT, LANDLORD SHALL HAVE THE RIGHT FOR THE SAME DEFAULT OR ANY SUBSEQUENT DEFAULT TO BRING ONE OR MORE FURTHER ACTIONS AS ABOVE PROVIDED TO RECOVER POSSESSION OF THE PREMISES.

 

D.                                     TENANT, BEING FULLY AWARE OF THE RIGHT TO NOTICE AND A HEARING CONCERNING THE VALIDITY OF ANY AND ALL CLAIMS THAT MAY BE ASSERTED AGAINST TENANT BY LANDLORD BEFORE A JUDGMENT

 

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CAN BE ENTERED HEREUNDER OR BEFORE EXECUTION MAY BE LEVIED ON SUCH JUDGMENT, HEREBY WAIVES THESE RIGHTS AND AGREES AND CONSENTS TO JUDGMENT BEING ENTERED BY CONFESSION IN ACCORDANCE WITH THE TERMS HEREOF AND EXECUTION BEING LEVIED ON SUCH JUDGMENT, IN EACH CASE WITHOUT FIRST BEING GIVEN NOTICE AND THE OPPORTUNITY TO BE HEARD ON THE VALIDITY OF THE CLAIM OR CLAIMS UPON WHICH SUCH JUDGMENT IS ENTERED.

 

E.              No act or forbearance by Landlord shall be deemed a waiver or election of any right or remedy by Landlord with respect to Tenant’s obligations hereunder, unless and to the extent that Landlord shall execute and deliver to Tenant a written instrument to such effect, and any such written waiver by Landlord shall not constitute a waiver or relinquishment for the future of any obligation of Tenant.  Landlord’s acceptance of any payment from Tenant (regardless of any endorsement on any check or any writing accompanying such payment) may be applied by Landlord to Tenant’s obligations then due hereunder, in any priority as Landlord may elect, and such acceptance by Landlord shall not operate as an accord and satisfaction or constitute a waiver of any right or remedy of Landlord with regard to Tenant’s obligations hereunder.

 

24.            Quiet Enjoyment .  Landlord covenants and agrees with Tenant that upon Tenant’s paying rent and observing and performing all the terms, covenants and conditions on Tenant’s part to be observed and performed, Tenant may peacefully and quietly enjoy the Premises free from any interference by Landlord or anybody claiming rights by, through or under Landlord.

 

25.            Assignment and Subletting .  Tenant shall not assign, pledge, mortgage or otherwise transfer or encumber this Lease, nor sublet all or any part of the Premises or permit the same to be occupied or used by anyone other than Tenant or its employees or any subsidiary, parent or affiliated company of Tenant without Landlord’s prior written approval, which Landlord agrees not unreasonably to withhold.  It will not be unreasonable for Landlord to withhold consent if the reputation, financial responsibility, or business of a proposed assignee or subtenant is unsatisfactory to Landlord.

 

Tenant’s request for approval shall be in writing and contain the name, address and description of the business of the proposed assignee or subtenant, its most recent financial statement and other evidence of financial responsibility, its intended use of the Premises, and the terms and conditions of the proposed assignment or subletting.

 

21



 

Within fifteen (15) days from receipt of such request, Landlord shall either:

 

A.             grant or refuse consent; or

 

B.             elect to require Tenant

 

i)               to execute an assignment or lease or sublease of Tenant’s interest hereunder to Landlord or its designee upon the same terms and conditions as are contained herein, together with an assignment of Tenant’s interest as sublessor in any such proposed sublease, or

 

ii)              Deleted.

 

Each assignee or sublessee of Tenant’s interest hereunder shall assume and be deemed to have assumed this Lease and shall be and remain liable jointly and severally with Tenant for all payments and for the due performance of all terms, covenants, conditions and provisions herein contained on Tenant’s part to be observed and performed.  No assignment shall be binding upon Landlord unless the assignee shall deliver to Landlord an instrument in recordable form containing a covenant or assumption by the assignee, but the failure or refusal of an assignee to execute the same shall not release assignee from its liability as set forth herein.

 

Any assignment or subletting shall terminate any right in Tenant (as may otherwise be provided for herein) to renew or extend the Term of this Lease or any right of expansion to new or additional space, and shall likewise terminate and render void and of no effect any prior exercise of any of the rights enumerated above (except and only to the extent that a renewal term is then in effect).

 

Any consent by Landlord hereunder shall not constitute a waiver of strict future compliance by Tenant of the provisions of this Section 25 or a release of Tenant from the full performance by Tenant of any of the terms, covenants, provisions or conditions in this Lease contained.

 

26.            Subordination .  This Lease is and shall be subject and subordinate at all

 

22



 

times to all mortgages and other encumbrances now or hereafter placed upon the Premises without the necessity of any further instrument or act on the part of Tenant to effectuate such subordination.  Tenant shall from time to time execute and deliver within ten (10) days following the request of Landlord or Landlord’s mortgagee, grantee or lessor, recordable instruments evidencing such subordination and Tenant’s agreement to attorn to the holder of such prior right.  Notwithstanding the foregoing, any mortgagee may, at any time, subordinate its mortgage to this Lease, without Tenant’s consent, by notice in writing to Tenant, whereupon this Lease shall be deemed prior to such mortgage without regard to their respective dates.

 

Landlord agrees to use reasonable efforts to obtain a non-disturbance agreement from the holder of any mortgage or other encumbrance now or hereafter placed upon the Premises.  Tenant acknowledges that any such agreement will be prepared on the lender’s standard form, may require Tenant to confirm the subordination of this Lease and may require Tenant to agree to attorn to the holder of such mortgage or other encumbrance.  In the event Landlord is unable to obtain a non-disturbance agreement despite using reasonable efforts, such failure shall not affect the effectiveness of this Lease or diminish in any way Tenant’s obligations hereunder.

 

27.            Tenant’s Certificates .  Tenant shall, from time to time, within fifteen (15) days after Landlord’s request, execute and deliver to Landlord a recordable written instrument(s) certifying that this Lease is unmodified and in full effect (or if there have been modifications, that it is in effect as modified), and the dates to which rental charges have been prepaid by Tenant, if any, and whether or not Landlord is in default of any of its obligations hereunder.  Tenant agrees that such statement may be relied upon by any mortgagee, purchaser or assignee of Landlord’s interest in this Lease or the Premises.

 

28.            Acceptance; Surrender .  By entry and possession of the Premises, Tenant hereby acknowledges that Tenant has examined the Premises and accepts the same as being in the condition called for by this Lease.  Tenant shall, at the end of the Term, promptly surrender the Premises in good order and condition and in conformity with the applicable provisions of this Lease, excepting only reasonable wear and tear and damage by fire or other insured casualty.

 

23



 

29.            Option to Renew .  Tenant shall have one (1) option to extend this Agreement of Lease for an additional period of five (5) years, at Tenant’s option, following the conclusion of the original Term hereof, provided that Tenant is not in default either at the time Tenant exercises the option or at the conclusion of the original Term.  Tenant may exercise such option by providing Landlord with written notice of its intention to exercise its option to renew not less than six (6) months prior to the expiration of the original Term, and thereupon this Agreement of Lease shall be extended for the additional term.  The terms, covenants and conditions set forth herein shall continue to govern the relationship between Landlord and Tenant during any extended period and the annual Base Rent payable during such renewal term shall be the then fair market rental for leases in the Building.  In no event, however, shall the annual Base Rent payable during the renewal term be less than the annual Base Rent payable during the last Lease Year of the original Term.

 

30.            Notices .  All notices, requests and consents herein required or permitted from either party to the other shall be in writing and shall be sent by personal delivery, nationally-recognized courier guaranteeing overnight delivery, facsimile (with receipt confirmed), e-mail with evidence of receipt and delivery of a copy of the notice by first class mail, or by mailing the same by registered or certified mail, postage prepaid, return receipt requested, addressed to Landlord at its address aforesaid, with a copy to any mortgagee designated by Landlord, or, as the case may be, addressed to Tenant at its address aforesaid, or to such other address as the party to receive same may designate by notice to the other.  All such notices, requests and other communications shall be deemed to have been sufficiently given for all purposes on the date of personal delivery, upon confirmation of receipt of facsimile, on the day after the date of deposit with a courier guaranteeing overnight delivery, or if deposited in the United States mail, the date when the notice is either received or rejected by the addressee.

 

31.            Broker .  Tenant represents and warrants to Landlord that all of Tenant’s dealings in regard to the Premises have been solely with Landlord, Skyline Commercial Real Estate and The Windsor Realty Group and that no other broker, agent or party has shown the Premises to Tenant or negotiated with Tenant in regard thereto.

 

32.            Definition of Parties .  The word “Landlord” is used herein to include the Landlord named above and any subsequent person who succeeds to the rights of Landlord herein, each of whom shall have the same rights and remedies as he would have had had he originally signed this Lease as Landlord, but neither Landlord nor any such person shall have any liability hereunder after he ceases to hold a fee or

 

24



 

leasehold interest in the Premises, except for obligations which may have theretofore accrued; and in all events, Tenant shall look solely to the Premises and rent derived therefrom for enforcement of any obligation hereunder or by law assumed or enforceable against Landlord or such other person.  The word “Tenant” is used herein to include the party named above as Tenant as well as its or their respective heirs, personal representatives, successors and assigns, each of whom shall be under the same obligations, liabilities and disabilities and have only such rights, privileges and powers as he would have possessed had he originally signed this Lease as Tenant.

 

33.            Entire Agreement; Interpretation .  This Lease constitutes the entire agreement between the parties hereto with respect to the Premises and there are no other agreements or understandings.  This Lease shall not be modified except by written instrument executed by both parties.  The captions used herein are for convenience only, and are not part of the Lease.  This Lease shall be construed in accordance with the laws of the Commonwealth of Pennsylvania.

 

34.            Waiver of Jury Trial .  LANDLORD AND TENANT EACH HEREBY WAIVE ANY AND ALL RIGHTS EITHER MAY HAVE TO A JURY TRIAL IN CONNECTION WITH ANY LITIGATION COMMENCED BY OR AGAINST ANY OF THE PARTIES TO THIS LEASE WITH RESPECT TO RIGHTS AND OBLIGATIONS OF THE PARTIES HERETO UNDER THIS LEASE.

 

25



 

IN WITNESS WHEREOF, the parties hereto have executed this Lease, under seal, as of the day and year first above written.

 

 

450 SENTRY PARKWAY ASSOCIATES
a Pennsylvania limited partnership
BY:  AK Real Estate Corp.

 

           General Partner

 

LANDLORD

 

 

 

 

 

 

WITNESS:

/s/ R. Scott Pierson

 

 

 

BY:

/s/ James Kilduff

 

 

 

 

President

 

 

 

 

 

 

(CORPORATE SEAL)

 

VIRAL GENOMIX, INC.

 

 

VGX PHARMACEUTICALS

TENANT

 

 

 

 

 

 

ATTEST: 

/s/ Ernest E. Shin

 

BY:

 

/s/ J. Joseph Kim

 



 

ADDENDUM CONFIRMING LEASE TERM

 

THIS ADDENDUM dated as of the 16th day of June, 2005, by and between 450 Sentry Parkway Associates (“Landlord”) and Viral Genomix, Inc. d/b/a VGX Pharmaceuticals (“Tenant”).

 

WITNESSETH THAT :

 

Landlord and Tenant entered into an Agreement of Lease dated January 21, 2005 (the “Lease”), for premises in the building located at 450 Sentry Parkway, Blue Bell, Whitpain Township, Montgomery County, Pennsylvania (the “Premises”).

 

NOW, THEREFORE, the parties hereto, intending to be legally bound hereby, agree as follows:

 

The Term of the Lease commenced on May 1, 2005 and shall expire on April 30, 2010.

 

Tenant’s obligation to pay Base Rent pursuant to Section 6 of the Lease  commenced on May 1, 2005.

 

Landlord has completed all improvements to the Premises as required pursuant to Section 3 of the Lease.

 

IN WITNESS WHEREOF, the parties hereto have caused this Addendum to be executed the day and year first above written.

 

 

450 Sentry Parkway Associates

Landlord

 

By: AK Real Estate Corp., General Partner

 

 

 

BY:

 

/s/ James A. Kilduff

 

 

 

James A. Kilduff, President

 

 

 

Viral Genomix, Inc.

 

d/b/a VGX Pharmaceuticals

Tenant

 

 

 

 

 

BY:

 

/s/ Ernest Shin

 




EXHIBIT 10.31

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

R&D ALLIANCE AGREEMENT

 

 

BETWEEN

 

 

GANIAL IMMUNOTHERAPEUTICS, INC.

 

(“GIT”)

 

 

AND

 

 

VIRAL GENOMIX, INC.

 

(VGX)

 



 

TABLE OF CONTENTS

 

 

 

Page

 

 

 

1.

DEFINITIONS

1

 

 

 

2.

R&D GRANT

3

 

 

 

3.

FEES AND ROYALTIES

3

 

 

 

4.

CONFIDENTIALITY

5

 

 

 

5.

TERM AND TERMINATION

6

 

 

 

6.

REPRESENTATIONS AND WARRANTIES OF GIT; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

8

 

 

 

7.

USE OF GIT’S AND VGX’S NAME

10

 

 

 

8.

ADDITIONAL PROVISIONS

10

 

1



 

R&D ALLIANCE AGREEMENT

 

This R&D Agreement (“AGREEMENT”) is between Viral Genomix, Inc. (“VGX”), a Delaware corporation, with offices located at 450 Sentry Parkway East, Blue Bell, Pennsylvania 19422, and GANIAL IMMUNOTHERAPEUTICS, INC (“GIT”), a Delaware corporation, having a place of business at 24 High Street, Locust Valley, NY 11560.

 

BACKGROUND

 

A. GIT controls certain intellectual property related to GIT027 (3-phenyl-4,5-dihydro-5-isoxazoleacetic acid) (hereinafter referred to as “GIT027”) as drugs for treating all and any disease indications in humans and animals, not limited to listed in Attachment I;

 

B. VGX desires to obtain EXCLUSIVE, WORLDWIDE rights to conduct research and development activities and to market GIT027 for all indications;

 

C. GIT will also grant VGX future rights, but not an obligation to attain additional derivative compounds/technology of GIT027 from GIT on the same terms as those of GIT027.

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties agree as follows:

 

1.              DEFINITIONS

 

1.1    AFFILIATE of VGX means any legal entity directly or indirectly controlling, controlled by or under common control with VGX that has executed (a) this AGREEMENT, or (b) a written joinder agreement, in a form reasonably satisfactory to GIT, agreeing to be bound by all of the terms and conditions of this AGREEMENT, as if such AFFILIATE of VGX were an original party to this AGREEMENT.  For purposes of this AGREEMENT, “control” means the direct or indirect ownership of more than fifty percent (50%) of the outstanding voting securities of a legal entity, and/or the right to receive more than fifty percent (50%) of the profits or earnings of a legal entity, and/or the right to control the policy decisions of a legal entity.

 

1.2    AFFILIATE OF GIT means any legal entity directly or indirectly controlling, controlled by or under the common control with GIT that has executed (a) this AGREEMENT, or (b) a written joinder agreement, in a form reasonably satisfactory to VGX, agreeing to be bound by all of the terms and conditions of this AGREEMENT, as if such AFFILIATE of GIT were an original party to this AGREEMENT.  For purposes of this AGREEMENT, “control” means the direct or indirect ownership of more than fifty percent (50%) of the outstanding voting securities of a legal entity, and/or the right to receive more than fifty percent (50%) of the profits or earnings of a legal entity, and/or the right to control the policy decisions of a legal entity.

 

1



 

1.3    CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.4    CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.5    EFFECTIVE DATE means the date on which VGX and GIT have both fully executed this AGREEMENT.

 

1.6    FAIR MARKET VALUE means the cash consideration which VGX thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.7    NET SALES is defined as the gross amount of monies or cash equivalent or other consideration which is paid by unrelated third parties to VGX for GIT027 by sale or other mode of transfer, less all qualifying costs directly attributable to such sales, which are made, made for, used or sold by VGX, its agents, employees and/or independent contractors.

 

NET SALES of a commercial product comprising one or more GIT R&D PRODUCTS and one or more other active ingredients (a “COMBINATION PRODUCT”) shall be calculated as set forth above, subject to the provisions of Section 3.1.3.

 

1.8    GIT R&D PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale by VGX for each indication and/or any affiliate(s) of VGX to unrelated third parties which (1) in the absence of this AGREEMENT would infringe at least one claim of GIT PATENT RIGHTS described in patents listed in Attachment I, or (2) use a process and/or machine covered by at least one claim of GIT PATENT RIGHTS described in patents listed in Attachment I.

 

1.9    PHASE III CLINICAL TRIALS means a series of expanded controlled and uncontrolled, pivotal, multi-center (generally) clinical studies, after adequate completion of preliminary efficacy and dose-ranging studies, and after safety data has been established for a GIT R&D PRODUCT, comprising patients with the disease or condition of interest, to whom the GIT R&D PRODUCT is administered in order to obtain sufficient efficacy and safety data (and better understand drug-related adverse effects) to support regulatory submissions and labeling of the GIT R&D PRODUCT.

 

1.10 SALE means any bona fide transaction for which consideration payment is received or expected for the sale, use, lease, transfer or other disposition of GIT R&D PRODUCT(S) to an unrelated third party.  A SALE of GIT R&D PRODUCT (S) shall be deemed completed at the time VGX or its affiliate receives payment for such GIT R&D PRODUCT (S).

 

1.11 GIT PATENT RIGHTS means all of GIT’s interest in the rights represented by or issuing from (including all claims referenced within) those patent applications listed in

 

2



 

ATTACHMENT I and all future interests in such rights anywhere in the world of the GIT027 intellectual property.

 

2.              R&D GRANT

 

Subject to the terms and conditions of this AGREEMENT, GIT grants to VGX for the term of this AGREEMENT EXCLUSIVE WORLD-WIDE rights to research, develop and market GIT R&D PRODUCTS. VGX has the rights to freely choose any and/or all of the product types. No other rights are granted by either party hereunder.  This agreement shall not impair VGX’s freedom (without any restriction or any obligation to GIT) to research, develop, and market products that do not infringe GIT PATENT RIGHTS.

 

2.1    , GIT shall deliver GIT027 (3-phenyl-4,5-dihydro-5-isoxazoleacetic acid) (GIT027) necessary for the production or intended for production of GIT R&D PRODUCTS upon VGX’s request. GIT shall provide technical assistance/expertise to, share pre-clinical testing data, and clinical results with VGX for product development and clinical development. GIT shall also provide relevant documentation, including the history and generation of GIT027, established assay protocols, summary for pre-clinical testing procedures and results, and to assist VGX’s regulatory filing.   GIT will provide technical assistance and expertise related to the production and development of GIT027 at a mutually agreed timeline.

 

3.              FEES AND ROYALTIES

 

3.1    Fees and Royalties .

 

3.1.1         VGX shall pay to GIT within thirty days (30) days of the EFFECTIVE DATE a payment of ****** in cash, certified funds, or by wire transfer .

 

3.1.2         VGX shall pay GIT an additional ****** issuing ****** of VGX common stock (par value $.0001 per share) to GIT or its assignees within thirty (30) days of the EFFECTIVE DATE.

 

3.1.3         Within first 5 years from the Effective Date, VGX also agrees to provide an amount equal to ****** of total funds from EACH funded government grant directly received by VGX involving research and development of GIT027.  The amount provided to GIT per EACH funded grant shall not exceed a total of ******.

 

3.1.4         In further consideration of the exclusive worldwide R&D granted to VGX, VGX shall pay to GIT, on a quarterly basis, a royalty of ****** of the NET SALES of each GIT R&D PRODUCT, which is sold by VGX and any affiliate(s), agent(s), and/or independent contractor(s) of VGX. Such royalty payments shall terminate on a product-by-product basis upon the date, which is ten (10) years after the date of the first SALE of such GIT R&D PRODUCT but not to exceed the date when effective patent protection on individual product is lost in each respective country.

 

3



 

3.1.5         In the event one or more GIT R&D PRODUCTS are sold in a COMBINATION PRODUCT, the amount of royalties and affiliate(s) revenues paid to GIT pursuant to this Section 3.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the GIT R&D PRODUCT(S).

 

3.2    Diligence and Milestone Fees.

 

3.2.1         VGX shall use commercially reasonable efforts to develop for SALE and to market GIT R&D PRODUCTS as drugs for treating all and any disease indications in humans and animals.

 

3.2.2         The following R&D milestone payments are payable by VGX to GIT within sixty (60) days after the achievement of the respective milestone event:

 

Due Date

 

Payment

Upon completion of patient accrual for the initial Phase II clinical trial for GIT027 in the United States for the FIRST disease indication

 

$

50,000

Upon completion of patient accrual for Phase III clinical trial for GIT027 in the United States for the FIRST disease indication

 

$

250,000

Upon NDA approval for GIT027 for EACH disease indication

 

$

2,000,000

 

3.3    Option to Purchase Rights.

 

3.3.1         Within first 7 years from the Effective Date, VGX shall have the option to purchase all of GIT’s worldwide rights to GIT027 for ******. VGX shall provide thirty (30) days written notice of its intention to purchase such rights any time during the first ****** years. The payment for worldwide rights for GIT027 shall be made forty five (45) days after VGX notifies GIT of its intention to purchase such rights and no further payment of any kind, including but not limited to any royalty payments, milestone payments, etc. under this Agreement shall be due to GIT upon completion of such purchase. In addition, if VGX or its Affiliates fails

 

4



 

to lead GIT027 to Phase I Human Clinical trial study in the United States within five (5) years from the effective date, VGX will return the rights to develop GIT027 back to GIT. In such case, all further obligations of VGX to GIT will be terminated.

 

3.4    Currency, Payment Method.

 

3.4.1         All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to GIT under this AGREEMENT shall be made in United States dollars by check or wire-transfer.  If VGX receives revenues from SALES of GIT R&D PRODUCTS in currency other than United States dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

4.              CONFIDENTIALITY

 

4.1    CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and marked confidential or, if oral, should be reduced to writing within thirty (30) days of disclosure and marked confidential.

 

4.2    Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party during the term of this Agreement and for five (5) years after the date of termination of this Agreement.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this Agreement.  The foregoing obligation shall not apply to:

 

4.2.1         information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records;

 

4.2.2         information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure;

 

5



 

4.2.3         information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

4.2.4         information, which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

Note: Confidential information shall not be disclosed to third party and this rule shall apply to both VGX and GIT. This is particularly true for process development data.

 

5.              TERM AND TERMINATION

 

5.1    This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the earlier of: (a) expiration of the last-to-expire or become abandoned of the GIT PATENT RIGHTS in United States; or (b) twenty (20) years after the EFFECTIVE DATE.

 

5.2    VGX may terminate this Agreement (a) upon thirty (30) days written notice to GIT, if the sale or other exploitation of the GIT R&D PRODUCT(s) becomes technologically or commercially unfeasible; or (b) upon thirty (30)-days written notice to GIT, and by doing all of the following:

 

5.2.1                         ceasing to make, have made, use, import, sell and offer for sale all GIT R&D PRODUCTS; and

 

5.2.2         paying all monies owed to GIT up to the date of the termination excluding any future obligation under this AGREEMENT.

 

5.3    GIT may terminate this AGREEMENT, upon thirty (30)-days written notice to VGX, if any of the following events of default (“Default”) occur:

 

5.3.1         VGX is more than sixty (60) days late in paying to GIT royalties, expenses or any other monies due under this AGREEMENT and VGX does not immediately pay GIT in full any amounts due upon demand; or

 

5.3.2         VGX experiences a Trigger Event (defined below);

 

5.3.3         VGX materially breaches this AGREEMENT and does not cure the material breach within sixty (60) days after the receipt of the written notice of such breach.

 

6



 

5.4    “Trigger Event” means any of the following:

 

5.4.1         If VGX:

 

5.4.1.1              becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

5.4.1.2              is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

5.4.1.3              makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

5.4.2         If proceedings under any International law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VGX;

 

5.4.3         If any order for relief is entered relating to any of the proceedings described in Sections 5.4.2 ;

 

5.4.4         If VGX shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

5.4.5         If VGX shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 5.4.2, 5.4.3, 5.4.4.

 

5.5    The provisions of Sections 5.3 and 5.4 shall apply to a Default of, or a Trigger Event experienced by, any affiliate(s) of VGX’s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the affiliate(s) causes VGX to fail to meet its diligence obligations under Section 3.2.

 

5.6    In the event of a termination under Section 5.1 or 5.3, all duties of GIT (other than under Sections 5.11) and all rights (but not duties) of VGX (other than under Section 5.11) under this AGREEMENT immediately terminate without the necessity of any action being taken either by GIT or by VGX, provided, however, that in no event shall the foregoing be construed to obligate VGX to pay any amounts accruing under Sections 3.1  after the date of termination except under Section 5.10.  Upon and after any termination of this AGREEMENT, the rights covered by this agreement for VGX and any affiliate thereof to manufacture, sale, marketing, importation and/or distribution of GIT

 

7



 

R&DPRODUCT(s) shall terminate on the same date of the termination of the agreement, except otherwise specified in this agreement or agreed upon by both parties.

 

5.7    Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

5.8    Upon termination of this AGREEMENT under section 5.2 and 5.3, VGX shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed GIT R&D PRODUCT(s) on hand, under the control of VGX or affiliate(s) thereof; and (b) such GIT R&D PRODUCT(s) as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be reduced to writing.  VGX shall deliver copies of such written inventories, verified by an officer of VGX, forthwith to GIT.  GIT shall have forty five (45) days after receipt of such verified inventories within which to challenge the inventory and request an audit thereof.

 

5.9    Upon termination of this agreement under section 5.1, VGX shall pay all monies owe to GIT up to the date of the termination.

 

5.10 Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 5.3.1 or 5.3.2, VGX shall have a period of six (6) months to sell off its inventory of GIT R&D PRODUCT(s) existing on the date of termination of this AGREEMENT and shall pay royalties to GIT with respect to such GIT R&D PRODUCT(s) within thirty (30) days following the expiration of such six-month period.

 

5.11 Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Articles 4, 5, 6, 7 and 8 shall survive such termination.

 

6.                                        REPRESENTATIONS AND WARRANTIES OF GIT AND VGX; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

6.1    GIT represents and warrants to VGX that:

 

6.1.1         GIT has the full authority to execute and deliver this AGREEMENT.

 

6.1.2         No material claim by any third party contesting the validity, enforceability, collaborations, use or ownership of any of such GIT PATENT RIGHTS has been made, is currently outstanding or is threatened against GIT.

 

8



 

6.2    GIT and VGX will work together to file the patents and/or patent applications listed in ATTACHMENT I before the deadline permitted by the international and US patent laws.

 

6.3    GIT shall defend and indemnify and hold VGX (and its Affiliates, and their respective officers, directors and employees) harmless against any and all Losses, arising out of, relating to, based on, or caused by (A) the breach by GIT of any representation or warranty contained in this Agreement, (B) a claim that the formulation or manufacture of the GIT027 by GIT for VGX or other activities of GIT under this Agreement infringe on the patent or other intellectual property rights of a third party, (C) any governmental or regulatory action arising out of GIT, or (D) any negligence or intentional misconduct by GIT in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated in any substantial respect by the negligent acts of or failure to act by VGX or its Affiliates.  VGX will promptly notify GIT of any such Losses which come to VGX’s attention, but failure to do so will not relieve GIT of its indemnification obligations under this Section 6.3 except to the extent any such delay results in a material prejudice to GIT.  Notwithstanding anything to the contrary in this Agreement, GIT shall not be liable for any Losses to the extent that the Losses suffered by VGX (and its Affiliates, and their respective officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.4    VGX shall defend and indemnify and hold GIT (and its Affiliates, and their respective officers, directors and employees) harmless against any Losses, arising out of, relating to, based on, or caused by (A) the breach by VGX of any representation or warranty contained in this Agreement or (B) any negligence or intentional misconduct by VGX in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated by the negligent acts of or failure to act by GIT or its Affiliates.  GIT will promptly notify VGX of any such Losses which come to GIT’s attention, but failure to do so will not relieve VGX of its indemnification obligations under this Section 6.4 except to the extent any such delay results in a material prejudice to VGX.  Notwithstanding anything to the contrary in this Agreement, VGX shall not be liable for any Losses where the Losses suffered by GIT (and its Affiliates, and their respective officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.5    There are no pending or threatened suits, claims, or actions of any type whatsoever against GIT with respect to the GIT027.

 

6.6    All necessary corporate authorizations, consents and approvals which are necessary or required for GIT to enter into this Agreement have been duly obtained;

 

6.7    To the best of its knowledge, the entering into of this Agreement by GIT will not (i) violate any Applicable Law or(ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination,

 

9


 

cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of GIT, under its organizational documents, as amended to date, or any material note, indenture, mortgage, le ase, agreement, contract, purchase order or other instrument, document or agreement to which GIT is a party or by which it or any of its properties or assets is bound or affected.

 

7.           USE OF GIT’S AND VGX’S NAME

 

7.1   VGX and its employees and agents shall not use and VGX shall not permit its affiliate(s) to use GIT’s name or any adaptation thereof, or any GIT seal, logotype, trademark, or service mark, or the name, mark, or logotype of any GIT representative or organization in any way without the prior written consent of GIT. However, GIT shall not unreasonably withhold such written consent.

 

7.2   GIT and its employees and agents shall not use and GIT shall not permit its affiliate(s) to use the VGX’s name or any adaptation thereof, or any VGX seal, logotype, trademark, or service mark, or the name, mark, or logotype of any VGX representative or organization in any way without the prior written consent of the VGX. However, VGX shall not unreasonably withhold such written consent.

 

8.           ADDITIONAL PROVISIONS

 

8.1   Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between GIT and VGX, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

8.2   From EFFECTIVE DATE, VGX will pay all fees charged by the patent office (including application fees and maintenance fees for patents listed in Attachment I and future patents selected by VGX according to section 3.1.4) and by patent application agencies (including translation fees, agency fees, and lawyer fees for patents listed in Attachment I and future patents selected by VGX according to section 3.1.4) if these expenses incurred after the effective date of the agreement. VGX shall control, prosecute and maintain the patent rights related to this AGREEMENT.

 

8.3   VGX is permitted to assign this AGREEMENT or any part of it to any person or entity, either directly or by operation of law, without the prior written consent of GIT in its sole discretion.  VGX has the rights to contract out the manufacturing of the products covered in this agreement and rights to establish collaboration, development, and marketing partnership with a third party. In case any products covered in this agreement is sold by a marketing partnership, VGX shall have the responsibility to pay royalty that is calculated on the bases of the combined net sales of VGX and its marketing partners. No assignment relieves VGX of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

10



 

8.4   A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

8.5   Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by public courier (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGX:

 

Viral Genomix, Inc.

VGX Pharmaceuticals

450 Sentry Parkway East

Blue Bell, PA 19422

Attention: Chief Executive Officer

 

If for GIT:

 

Ganial Immunotherapeutics, Inc.

24 High Street

Locust Valley, NY 11560

Attention: Chief Executive Officer

 

Either party may change its official address upon written notice to the other party.

 

8.6   This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.

 

11



 

8.7   VGX shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.

 

8.8   If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

8.9   This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

[SIGNATURE PAGE FOLLOWS]

 

12



 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

GANIAL IMMUNOTHERAPEUTICS, INC.

VIRAL GENOMIX, INC.

 

 

 

 

 

 

 

 

 

By:

      /s/ Ferdinando Nicoletti

 

By:

       /s/ J. Joseph Kim

 

 

 

 

 

Name:

 Dr. Ferdinando Nicoletti

 

Name:

J. Joseph Kim, Ph.D.

 

 

 

 

 

Title:

    President and CEO

 

Title:

      President and CEO

 

 

 

 

 

Date:

   December 19,2005

 

Date:

    December 19, 2005

 

13




EXHIBIT 10.32

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

 

 

 

 

 

 

ASSET PURCHASE AGREEMENT

 

 

 

 

 

by and among

 

 

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

ADViSYS INC.,

 

 

 

 

 

RONALD O. BERGAN

 

 

 

 

 

and

 

 

 

 

 

MARY ALICE BERGAN

 

 

 

 

 

 

 

 

Dated February 21, 2007

 

 



 

TABLE OF CONTENTS

 

 

Page

 

 

ARTICLE I PURCHASE AND SALE

1

 

 

1.1

Purchased Assets

1

1.2

Excluded Assets

2

1.3

Assumption of Liabilities

3

1.4

Retained Liabilities

3

 

 

 

ARTICLE II PURCHASE PRICE

4

 

 

2.1

Purchase Price

4

2.2

Allocation of the Purchase Price

6

 

 

 

ARTICLE III CLOSING; DELIVERIES

6

 

 

3.1

Closing

6

3.2

Deliveries by the Purchaser

6

3.3

Deliveries by the Company

7

3.4

Deliveries by the Stockholders

7

 

 

 

ARTICLE IV REPRESENTATIONS AND WARRANTIES OF THE COMPANY AND THE STOCKHOLDERS

7

 

 

4.1

Authority; Enforceability

7

4.2

Consents; Non-Contravention

7

4.3

Subsidiaries

8

4.4

Organization

8

4.5

Capitalization

8

4.6

Books and Records; Financial Statements

8

4.7

No Undisclosed Liabilities

9

4.8

Compliance with Laws

9

4.9

Litigation

10

4.10

Absence of Certain Changes or Events

11

4.11

Title to Assets

11

4.12

Inventory; Accounts Receivable

12

4.13

Intellectual Property

12

4.14

Company Contracts

13

4.15

Environmental Matters

13

4.16

Employee Matters

14

4.17

Employee Benefit Matters

15

4.18

Taxes

16

4.19

Transactions with Related Persons

16

4.20

Insurance

17

4.21

Customers and Suppliers

17

4.22

Product Liability and Product Warranty

17

 

i



 

4.23

Brokers

17

4.24

Disclosure

18

 

 

 

ARTICLE V REPRESENTATIONS AND WARRANTIES OF THE STOCKHOLDERS

18

 

 

5.1

Authority; Enforceability

18

5.2

Consents; Non-Contravention

18

5.3

Brokers

18

5.4

Litigation

19

 

 

 

ARTICLE VI REPRESENTATIONS AND WARRANTIES OF THE PURCHASER

19

 

 

6.1

Authority; Enforceability

19

6.2

Consents; Non-Contravention

19

6.3

Brokers

20

6.4

Litigation

20

 

 

 

ARTICLE VII COVENANTS OF THE COMPANY AND THE STOCKHOLDERS

20

 

 

7.1

Fulfillment of Agreements

20

7.2

Further Assurances

20

7.3

Confidentiality

20

7.4

Books and Records

21

7.5

Conduct of Business

21

7.6

Access

22

7.7

Insurance

22

7.8

Exclusivity

22

7.9

Tax Matters

22

7.10

Change of Name

22

7.11

Guarantee

23

7.12

Release

23

7.13

Noncompetition, Nonsolicitation and Nondisparagement

23

7.14

Liquidation and Dissolution Documents

24

 

 

 

ARTICLE VIII COVENANTS OF THE PURCHASER

24

 

 

8.1

Fulfillment of Agreements

24

8.2

Further Assurances

25

8.3

Confidentiality

25

8.4

Books and Records

25

8.5

Arrangement with Administaff and Other Employee Matters

25

8.6

Recent Financials

26

8.7

Services of Dr. Kern

26

(a)

Guarantee Obligations

26

 

 

 

ARTICLE IX CONDITIONS TO THE PURCHASER’S OBLIGATIONS

26

 

 

9.1

Representations and Warranties True and Correct

26

 

ii



 

9.2

Covenants and Agreements Performed

26

9.3

Company Closing Certificate

26

9.4

Stockholders Closing Certificate

27

9.5

No Prohibition

27

9.6

Consents

27

9.7

Assignment

27

9.8

Intellectual Property Assignments

27

9.9

Subscription Agreement

27

 

 

 

ARTICLE X CONDITIONS TO THE STOCKHOLDERS’ AND THE COMPANY’S OBLIGATIONS

27

 

 

10.1

Representations and Warranties True and Correct

27

10.2

Covenants and Agreements Performed

27

10.3

Purchaser Closing Certificate

27

10.4

No Prohibition

28

10.5

Consents

28

10.6

Payment of Closing Payment

28

10.7

Assignment

28

 

 

 

ARTICLE XI TERMINATION PRIOR TO CLOSING; REORGANIZATION

28

 

 

11.1

Termination

28

11.2

Effect on Obligations

28

 

 

 

ARTICLE XII SURVIVAL; INDEMNIFICATION AND OFFSET

28

 

 

12.1

Survival; Knowledge of Breach

28

12.2

Indemnification

29

12.3

Limitations

30

12.4

Notice of Indemnity Claims

31

12.5

Third-Party Claims

31

12.6

Settlement of Indemnity Claims

32

12.7

Right of Setoff

32

12.8

Exclusive Remedy

32

 

 

 

ARTICLE XIII MISCELLANEOUS

33

 

 

13.1

Entire Agreement

33

13.2

Successors and Assigns

33

13.3

Headings

33

13.4

Amendment; Modification and Waiver

33

13.5

Expenses

33

13.6

Notices

33

13.7

Governing Law

35

13.8

No Third Party Beneficiaries

35

13.9

Counterparts

35

13.10

Drafting of Agreement

35

 

iii



 

13.11

Savings Clause

35

13.12

Injunctive Relief

35

 

 

 

ARTICLE XIV CERTAIN DEFINITIONS

35

 

 

14.1

“Administaff”

35

14.2

“Administaff Agreement”

36

14.3

“Affiliate”

36

14.4

“Ancillary Agreements”

36

14.5

“Business Day”

36

14.6

“Claim”

36

14.7

“Code”

36

14.8

“Company Contract”

36

14.9

“Contract”

36

14.10

“EKD

36

14.11

“Encumbrances”

36

14.12

“Environment”

36

14.13

“Environmental Claim”

36

14.14

“Environmental Law”

36

14.15

“ERISA”

36

14.16

“FD&C Act”

37

14.17

“FDA”

37

14.18

“GAAP”

37

14.19

“GHRH

37

14.20

“Governing Documents”

37

14.21

“Governmental Authority”

37

14.22

“Governmental Authorization”

37

14.23

“Hazardous Substance”

37

14.24

“Intellectual Property”

37

14.25

“IRS”

38

14.26

“Knowledge of the Company”

38

14.27

“Legal Requirement”

38

14.28

“Losses”

38

14.29

“Liabilities”

38

14.30

“Material Adverse Effect”

39

14.31

“Order”

39

14.32

“Permitted Encumbrances”

39

14.33

“Person”

39

14.34

“Proceeding”

39

14.35

“Restricted Business

39

14.36

“Schedules”

39

14.37

“Securities”

39

14.38

“Straddle Period”

39

14.39

“Tax”

39

14.40

“Taxing Authority”

40

14.41

“Tax Return”

40

 

iv



 

Exhibits

 

 

 

Exhibit A

Purchase Price Allocation

Exhibit B

Assignment and Assumption Agreement

Exhibit C

IP Assignment

Exhibit D

Subscription Agreement

 

 

Schedules

 

 

 

Schedule 1.1(f)

Assigned Contracts

Schedule 4.2

Consents

Schedule 4.3

Subsidiaries

Schedule 4.4

Foreign Qualifications

Schedule 4.5

Capitalization

Schedule 4.8

Governmental Authorizations

Schedule 4.10

Absence of Changes

Schedule 4.13

Intellectual Property

Schedule 4.15

Environmental Matters

Schedule 4.16

Employee Matters

Schedule 4.18

Employee Benefits Matters

Schedule 4.19

Related Party Transactions

Schedule 4.20

Insurance Policies

Schedule 4.21

Customers and Suppliers

Schedule 4.22

Warranty Policies

Schedule 5.2

Consents

Schedule 6.2

Consents

Schedule 8.5

Excluded Employees

 

v



 

DEFINED TERMS

 

Page

 

Administaff

35

Administaff Agreement

36

Affiliate

36

Agreement

1

Ancillary Agreements

36

Assigned Contracts

2

Assigned Governmental Authorizations

2

Assignment

27

Assumed Liabilities

3

Balance Sheets

8

Business

1

Business Day

36

Cash Portion

4

Claim

36

Claim Notice

31

Closing

6

Closing Date

6

Code

36

Company

1

Company Closing Certificate

26

Company Confidential Information

20

Company Contract

36

Company Financial Statements

9

Company Indemnitees

30

Company Indemnitors

29

Company Parties

21

Company Threshold

30

Contract

36

Defense Notice

32

Drop Dead Date

28

EKD

36

Employee Benefit Plans

15

Employees

25

Encumbrances

36

Environment

36

Environmental Claim

36

Environmental Law

36

ERISA

36

Excluded Assets

2

Extended Survival Period

29

FD&C Act

37

FDA

37

Form 8594

6

GAAP

37

GHRH

37

Governing Documents

37

Governmental Authority

37

 

vi



 

Governmental Authorization

37

Hazardous Substance

37

Indemnified Party

31

Indemnifying Party

31

Indemnity Claim

31

Intellectual Property

37

Interim Balance Sheet

8

Inventories

1

IP Assignment

27

IRS

38

Knowledge

38

Legal Requirement

38

Liabilities

38

Losses

38

Material Adverse Effect

39

Obligations

23

Order

39

Permitted Encumbrances

39

Person

39

Proceeding

39

Purchase Price

4

Purchased Assets

1

Purchaser

1

Purchaser Closing Certificate

27

Purchaser Indemnitees

29

Purchaser Parties

25

Related Person

16

Released Parties

23

Releasors

23

Restricted Business

39

Restricted Period

23

Restrictive Parties

23

Retained Liabilities

3

Schedules

39

Securities

39

Software

38

Stock Portion

4

Stockholders

1

Stockholders Closing Certificate

27

Straddle Period

39

Survival Period

29

Tax

39

Tax Return

40

Taxes

39

Taxing Authority

40

Third Party Claim

31

Transaction

22

 

vii



 

ASSET PURCHASE AGREEMENT

 

THIS ASSET PURCHASE AGREEMENT (this “ Agreement ”) is made and entered into as of February 21, 2007, by and among VGX Pharmaceuticals, Inc. (the “ Purchaser ”), ADViSYS Inc. (the “ Company ”), a Delaware corporation, and Ronald O. Bergan and Mary Alice Bergan (Mr. and Ms. Bergan together, the “ Stockholders ”).

 

RECITALS:

 

WHEREAS, the Company is engaged in the business of (a) developing, marketing, manufacturing, distributing or otherwise commercializing (i) veterinary applications of GHRH technology and (ii) EKDs for the delivery of plasmids into tissue, (b) performing contract services, which services include process development, quality control, quality assurance and validation services, as well as the manufacture of plasmid-based biopharmaceuticals and (c) performing contract research services (clauses (a) through (c), the “ Business ”);

 

WHEREAS, the Purchaser wishes to purchase, and the Company wishes to sell, substantially all of the assets of the Business, subject to certain liabilities of the Business, upon the terms and subject to the conditions set forth herein; and

 

WHEREAS, the Stockholders are the principal stockholders of the Company and, as a result thereof, will receive substantial benefits in connection with the transactions contemplated hereby.

 

NOW , THEREFORE, for good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, and intending to be legally bound hereby, the parties hereto hereby agree as follows:

 

ARTICLE I

PURCHASE AND SALE

 

1.1                                  Purchased Assets .  At the Closing, the Company shall sell, transfer, convey and deliver to the Purchaser, free and clear of all Encumbrances other than Permitted Encumbrances, all of the Company’s right, title and interest in and to all of the assets and properties of every kind and description, tangible and intangible, that are used in or related to the Business, wherever located (such transferred assets and properties, the “ Purchased Assets ”).  The Purchased Assets shall include the following:

 

(a)                                   All cash and cash equivalents of the Company less an amount equal to the sum of $10,000 (representing amounts retained by the Company to pay liquidation expenses) and the amount of the Excluded Accounts;

 

(b)                                  All accounts receivable of the Company;

 

(c)                                   All inventories of raw materials, work-in-process, finished goods and other supplies of the Company (the “ Inventories ”);

 

1



 

(d)                                  All equipment, machinery, furniture, fixtures and other tangible assets of the Company;

 

(e)                                   The Company Contracts set forth on Schedule 1.1(f)  (such Company Contracts, the “ Assigned Contracts ”);

 

(f)                                     All transferable Governmental Authorizations of the Company (the “ Assigned Governmental Authorizations ”);

 

(g)                                  All of the Company’s Intellectual Property;

 

(h)                                  All telephone numbers, facsimile numbers and email addresses used in the Business;

 

(i)                                      All goodwill and going concern value of the Business;

 

(j)                                      All Claims of the Company against any Person to the extent relating to the Purchased Assets or Assumed Liabilities;

 

(k)                                   All advertising materials, marketing plans, catalogues, brochures, promotional material and cost and pricing information of the Company; and

 

(l)                                      All data, records, books, ledgers, files, reports and plans maintained by the Company in connection with the Business.

 

1.2                                  Excluded Assets .  Notwithstanding anything to the contrary contained in Section 1.1 above, the Purchased Assets shall not include the following assets and properties (such assets and properties, the “ Excluded Assets ”):

 

(a)                                   All shares of capital stock of the Company held in treasury;

 

(b)                                  Cash in an amount equal to the sum of $10,000 (representing amounts retained by the Company to pay liquidation expenses) and the amount of the Excluded Accounts;

 

(c)                                   All rights of the Company under this Agreement and the Ancillary Agreements;

 

(d)                                  The minute books, stock ledgers, Stockholders lists, similar corporate records and corporate seals of the Company;

 

(e)                                   The Company’s rights under the Employee Benefit Plans;

 

(f)                                     The Company’s ownership interest in any Person listed on Schedule 4.3 hereto;

 

(g)                                  All Company Contracts other than the Assigned Contracts;

 

(h)                                  All Assigned Governmental Authorizations of the Company other than the Assigned Governmental Authorizations; and

 

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(i)             All Claims of the Company against any Person to the extent relating to an Excluded Asset or a Retained Liability.

 

1.3            Assumption of Liabilities . At the Closing, the Company shall assign to the Purchaser, and the Purchaser shall assume and agree to pay, perform and discharge, from and after the Closing, only the following Liabilities of the Company (all such Liabilities, the “ Assumed Liabilities ”):

 

(a)            Any account payable (other than in respect of amounts owed to Vinson & Elkins, legal counsel to the Company, and amounts owed to Jackson Walker, patent counsel to the Company, in connection with the transactions contemplated hereby (the “Excluded Payables”)) either (i) reflected on the Interim Balance Sheet or (ii) incurred after the date of the Interim Balance Sheet in the ordinary course of business that, in the case of either of clause (i) or clause (ii), remains unpaid at and is not delinquent immediately prior to the Closing;

 

(b)            Any Liability arising after the occurrence of the Closing under the Assigned Contracts (other than any Liability under the Assigned Contracts arising out of or relating to a breach or violation of, or non-compliance with, any of the covenants, obligations, representations, warranties or other provisions of any such Assigned Contract that relates to periods prior to the occurrence of the Closing or to the extent that such Liability would constitute a breach or violation of, or non-compliance with, any covenant, obligations, representation, warranty or other provision of this Agreement or any Ancillary Agreement); and

 

(c)            Any Liability arising after the occurrence of the Closing under the Assigned Governmental Authorizations (other than any Liability under the Assigned Governmental Authorizations arising out of or relating to a breach or violation of, or non-compliance with, any of the Company’s obligations under any such Assigned Governmental Authorization that relates to periods prior to the occurrence of the Closing or to the extent that such Liability would constitute a breach or violation of, or non-compliance with, any covenant, obligation, representation, warranty or other provision of this Agreement or any Ancillary Agreement).

 

1.4            Retained Liabilities . The Retained Liabilities shall not be assumed by the Purchaser, and shall remain the sole responsibility of, and shall be retained, paid, performed and discharged solely by, the Company. “ Retained Liabilities ” shall mean every Liability of the Company other than the Assumed Liabilities, including:

 

(a)            Any Liability under (i) any Company Contract that does not constitute an Assigned Contract; (ii) any Governmental Authorization that does not constitute an Assigned Governmental Authorization; (iii) any Assigned Contract to the extent not assumed pursuant to Section 1.3(b)  hereof or (iv) any Assigned Governmental Authorization to the extent not assumed pursuant to Section 1.3(c)  hereof;

 

(b)            Any Liability of the Company arising under, or relating to the execution, delivery or consummation of, this Agreement and the Ancillary Agreements and the transactions contemplated hereby and thereby;

 

(c)            Any Liability under or with respect to the insurance plans of the Company or the Employee Benefit Plans;

 

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(d)            Any Liability of the Company relating to, arising out of or incurred in connection with the Retained Assets;

 

(e)            Any Liability for the Excluded Accounts; and

 

(f)             Any Liability for amounts due in respect of any Taxes imposed with respect to any taxable period of the Company or relating to, arising out of or incurred in connection with the operations of the Company or the ownership of the Purchased Assets, including any Taxes asserted against the Company or the Purchased Assets by reason of its or their inclusion in any consolidated, combined or unitary Tax Return.

 

ARTICLE II

PURCHASE PRICE

 

2.1            Purchase Price .

 

(a)            The consideration payable to the Company for the purchase of the Purchased Assets (the “ Purchase Price ”) shall be:

 

(i)             Cash in an amount equal to $2,211,365.25 (the “ Cash Portion ”), to be delivered to the Company at the Closing;

 

(ii)            924,219 shares (as adjusted for stock splits, stock dividends, stock combinations, recapitalizations and similar events) of the Common Stock of the Purchaser (the “ Stock Portion ”), to be delivered to the Company at the Closing;

 

(iii)           The assumption by the Purchaser of the Assumed Liabilities at the Closing;

 

(iv)           200,000 shares (as adjusted for stock splits, stock dividends, stock combinations, recapitalizations and similar events) of the Common Stock of the Purchaser, to be issued to Company within 15 Business Days after the issuance of approvals from all applicable Governmental Authorities, required to market in Australia a porcine GHRH that constitutes a Purchased Asset or is derived or developed from proprietary technology that constitutes a Purchased Asset;

 

(v)            ****** shares (as adjusted for stock splits, stock dividends, stock combinations, recapitalizations and similar events) of the Common Stock of the Purchaser, to be issued to the Company within 15 Business Days after the first use by the Purchaser of an EKD that constitutes a Purchased Asset or is derived or developed from proprietary technology that constitutes a Purchased Asset on a human subject in a clinical trial conducted anywhere in the United States of America or the European Union in accordance with applicable Legal Requirements governing such clinical trials;

 

(vi)           ****** shares (as adjusted for stock splits, stock dividends, stock combinations, recapitalizations and similar events) of the Common Stock of the Purchaser, to be issued to the Company within 15 Business Days after (A) the first license granted by the Purchaser to any Person for the use of any EKD that constitutes a Purchased Asset or is derived

 

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or developed from proprietary technology that constitutes a Purchased Asset and (B) the use by the licensee of the licensed technology on a human subject in a clinical trial conducted anywhere in the United States of America or the European Union in accordance with applicable Legal Requirements governing such clinical trials;

 

(vii)          The following contingent payments, if any:

 

(A)           An amount equal to ****** of all upfront and milestone payments, net of all Excluded Proceeds, received by or on behalf of the Purchaser from the Closing Date until the fifth anniversary thereof in respect of any license granted by the Purchaser to any other Person to manufacture, produce, distribute, market or otherwise commercialize, for any application, any EKD or GHRH technology or product that constitutes a Purchased Asset or is derived or developed from proprietary technology that constitutes a Purchased Asset; and
 
(B)            An amount equal to ****** of all royalties received by or on behalf of the Purchaser from the Closing Date until the 10th anniversary thereof to the extent received on account of sales of products under any license granted by the Purchaser to any other Person to manufacture, produce, distribute, market or otherwise commercialize, for any non-human application, any GHRH technology or product that constitutes a Purchased Asset or is derived or developed from proprietary technology that constitutes a Purchased Asset.
 

(b)            Each obligation to issue shares of the Purchaser’s Common Stock issuable pursuant to Sections 2.1(a)(iv) through (vi) above shall be contingent upon the Company executing and delivering such subscription documents and other Contracts with respect to such shares as the Purchaser shall reasonably request.

 

(c)            All amounts payable pursuant to Section 2.1(a)(vii)  above shall be paid by certified or cashier’s check, or by wire transfer of immediately available funds to an account designated by the Company from time to time or such other method as the Purchaser and the Company shall agree, or, with respect to non-cash consideration, in such manner as the Purchaser shall in good faith determine, within 15 Business Days after the end of each calendar quarter in respect of all payments received by the Purchaser in such calendar quarter.

 

(d)            For purposes of calculating any payment required to be made pursuant to Section 2.1(a)(vii)  above:

 

(i)             Non-cash consideration that is received by or on behalf of the Purchaser shall be valued at the fair market value thereof, as determined in good faith by the Purchaser; and

 

(ii)            If any cash payment received by or on behalf of the Purchaser is not an amount in U.S. dollars, the payment shall be calculated by including the fair market value in U.S. dollars of any such payment received as of the date received by the Purchaser, as determined in good faith by the Purchaser.

 

(e)            As used herein, “ Excluded Proceeds ” means all proceeds reasonably and fairly attributable to bona fide (i) debt financing; (ii) equity (and conditional equity, such as warrants, convertible debt and the like) investments in the Purchaser at fair market value; (iii) reimbursements of patent prosecution costs and patent maintenance expenses; (iv) 

 

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reimbursement for the cost of research and/or development services provided on the basis of full-time equivalent efforts of personnel not in excess of commercially reasonable full-time equivalent rates, (v) any amount on which payments have been paid under Section 2.1(a)(vii)(B)  hereof.

 

2.2            Allocation of the Purchase Price . At least 30 days before the required due date of Form 8594 under Section 1060 of the Code (or any successor form or successor provision of any future Tax law) (“ Form 8594 ”), the Purchaser, the Stockholders and the Company shall agree upon an allocation of the Purchase Price, which shall be allocated among the Purchased Assets in accordance with the requirements of such Section 1060, using the unconsolidated assets of the Company. The Purchaser and the Company shall each report the federal, state and local income and other Tax consequences of the transactions contemplated by this Agreement in a manner consistent with such allocation, including the preparation and filing of Form 8594 with their respective federal income Tax returns for the taxable year that includes the Closing Date, and neither the Purchaser, the Stockholders, nor the Company shall take any position or other action inconsistent with such allocation unless otherwise required by applicable Legal Requirements. In the event that the agreed upon allocation is disputed by any Governmental Authority, the party receiving notice of such dispute shall promptly notify and consult with the other parties hereto concerning resolution of such dispute, and shall keep such other parties apprised of the status of such dispute and the resolution thereof.

 

ARTICLE III

CLOSING; DELIVERIES

 

3.1            Closing . The consummation of the purchase and sale of the Purchased Assets and the assignment and assumption of the Assumed Liabilities (the “ Closing ”) shall take place at 10:00 a.m. (Philadelphia time) on the second Business Day after the satisfaction or waiver of the conditions (excluding conditions that, by their terms, cannot be satisfied until the Closing Date) set forth in Articles X and XI hereof (the “ Closing Date ”), unless another time or date is agreed to by the parties hereto. The Closing shall be held at the offices of Duane Morris LLP, 30 South 17th Street, Philadelphia, PA  19103, unless another place is agreed to by the parties hereto.

 

3.2            Deliveries by the Purchaser . At the Closing, the Purchaser shall deliver or cause to be delivered the following to the Company:

 

(a)            The Cash Portion, by wire transfer of immediately available funds to an account designated by the Company at least two Business Days prior to the Closing Date;

 

(b)            A certificate representing the Stock Portion, issued by the Purchaser in favor of the Company;

 

(c)            The Purchaser Closing Certificate and the Ancillary Agreements required to be executed by the Purchaser pursuant to Article X hereof, executed by the Purchaser; and

 

(d)            Such other Contracts, certificates and documents as shall be contemplated hereby or as shall be reasonably requested by the Stockholders or the Company.

 

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3.3            Deliveries by the Company . At the Closing, the Company shall deliver or cause to be delivered the following to the Purchaser:

 

(b)            The Company Closing Certificate and the Ancillary Agreements required to be executed by the Company pursuant to Article IX hereof, executed by the Company; and

 

(c)            Such other Contracts, consents, certificates and documents as shall be contemplated hereby or as shall be reasonably requested by the Purchaser.

 

3.4            Deliveries by the Stockholders . At the Closing, the Stockholders shall deliver or cause to be delivered the following to the Purchaser:

 

(a)            The Stockholders Closing Certificate and the Ancillary Agreements required to be executed by the Stockholders pursuant to Article IX hereof, executed by the Stockholders; and

 

(b)            Such other Contracts, consents, certificates and documents as shall be contemplated hereby or as shall be reasonably requested by the Purchaser.

 

ARTICLE IV

REPRESENTATIONS AND WARRANTIES OF THE COMPANY AND THE STOCKHOLDERS

 

The Company and the Stockholders hereby jointly and severally represent and warrant to the Purchaser as follows:

 

4.1            Authority; Enforceability . The execution, delivery and performance by the Company of this Agreement and each Ancillary Agreement to which it is a party, and the consummation of the transactions contemplated hereby and thereby, have been duly authorized by all necessary action on the part of the Company (including Board of Directors and stockholder approval).  This Agreement has been, and each Ancillary Agreement to which the Company is a party will be, duly and validly executed and delivered by the Company and constitutes, and will constitute, the valid and binding obligation of the Company, enforceable against it in accordance with its respective terms, except (a) as limited by Legal Requirements of general application relating to bankruptcy, insolvency and relief of debtors or (b) as limited by Legal Requirements governing specific performance, injunctive relief or other equitable remedies and by general principles of equity. The Company has the requisite power and authority to execute and deliver this Agreement and each Ancillary Agreement to which it is a party and to consummate the transactions contemplated hereby and thereby.

 

4.2            Consents; Non-Contravention .

 

(a)            Except as set forth on Schedule 4.2 , no consent, approval, authorization, exemption or waiver of, or notice or filing with, any Person is required to be obtained, given or made, as applicable, by the Company in connection with the execution, delivery and performance by the Company of this Agreement or any Ancillary Agreement to which it is a party, or to consummate the transactions contemplated hereby and thereby.

 

(b)            Except as set forth on Schedule 4.2 , the execution, delivery and performance by the Company of this Agreement and each Ancillary Agreement to which it is a party or by which

 

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it is bound and the consummation of the transactions contemplated hereby and thereby does not and will not, with or without the giving of notice or the lapse of time or both, (i) contravene, conflict with or violate any Legal Requirement to which the Company is subject; (ii) contravene, conflict with or violate any Order applicable to the Company; (iii) contravene, conflict with or violate any provision of the Governing Documents of the Company; (iv) contravene, conflict with, violate, result in a breach of, constitute a default under, result in or permit the termination or amendment of any provision of, or result in or permit the acceleration of the maturity or cancellation of performance of any obligation under, any Company Contract or (v) result in the creation or imposition of any Encumbrance upon any of the Purchased Assets or give to any other Person any interests or rights therein, other than, in both cases, Permitted Encumbrances.

 

4.3            Subsidiaries . Except as described on Schedule 4.3 , the Company does not own or control (as defined in Section 14.3 hereof), directly or indirectly, any Securities of or other investment in any other Person, or has any joint venture or similar arrangement with any other Person. Except as set forth on Schedule 4.3 , no Person listed on Schedule 4.3 pursuant to the foregoing sentence conducts any business, or owns or otherwise has any rights to any assets or properties necessary for the conduct by the Company of its business.

 

4.4            Organization . The Company is a corporation duly organized, validly existing and in good standing under the laws of the State of Delaware, and has all requisite power and authority to carry on the Business and to own, lease and/or use the Purchased Assets. The Company is duly qualified to do business and is in good standing as a foreign corporation in all jurisdictions listed on Schedule 4.4 hereto, which are the only jurisdictions where the nature of its assets and properties or the Business makes such qualification necessary.

 

4.5            Capitalization . The authorized Securities of the Company on the date hereof are as set forth on Schedule 4.5 hereto. Schedule 4.5 hereto sets forth the holder of each Security of the Company and the number and type of Securities owned by each such holder. The outstanding shares of the Company’s capital stock have been duly and validly authorized and issued, are fully paid and nonassessable, and were issued in accordance with all Legal Requirements, or pursuant to valid exemptions therefrom. Except as set forth on Schedule 4.5 hereto, there are no Contracts to which the Company is a party or is bound or, to the Company’s and the Stockholders’ Knowledge, any holder of its Securities is a party or is bound, relating to any Securities of the Company. Except as set forth on Schedule 4.5 , there are no preemptive rights, rights of first refusal, put or call rights or obligations, or anti-dilution rights with respect to the issuance, sale or redemption of the Company’s Securities.

 

4.6            Books and Records; Financial Statements . The minute books and stock record books of the Company are complete and correct. All books and records of the Company have been maintained in accordance with an adequate system of internal controls. The (a) unaudited consolidated balance sheets of the Company as at December 31, 2005 and December 31, 2004, together with the notes thereto (the “ Balance Sheets ”) and the related unaudited consolidated Statements of Cash Flows and Income Statements for the fiscal years then ended, together with the notes thereto and (b) unaudited balance sheet of the Company as at November 30, 2006, together with the notes thereto (the “ Interim Balance Sheet ”) and the related unaudited consolidated Statements of Cash Flows and Income Statements of the Company for the period then ended, together with the notes thereto (all of the foregoing in clauses (a) and (b) of this

 

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Section 4.6 , the “ Company Financial Statements ”):  (i) are true and correct in all material respects; (ii) were prepared in accordance with GAAP and, in the case of the interim Company Financial Statements, on a basis consistent with the December 31, 2005 Company Financial Statements (except that the Company Financial Statements may not contain all footnotes required by GAAP and normal recurring year-end adjustments, the effect of which, individually or in the aggregate, would not be material to the Company); (iii) fairly and accurately present in all material respects the financial position, changes in stockholders equity, results of operations and cash flows of the Company as of such dates and for the periods then ended and (iv) represent only actual, bona fide transactions.

 

4.7            No Undisclosed Liabilities . The Company does not have any Liability that is not reflected or reserved against the Balance Sheet or the Interim Balance Sheet except (a) for those which are not required by GAAP to be included on either such Balance Sheet, and (b) current Liabilities incurred in the ordinary course of business subsequent to November 30, 2006 which, individually or in the aggregate, are not material to the Company.

 

4.8            Compliance with Laws .

 

(a)            The Company is, and since December 31, 2003 has been, in material compliance with all Legal Requirements applicable to it or to the conduct of the business and, since December 31, 2003, the Company has not received any notice of an actual, possible or alleged violation of any such Legal Requirement. To the Knowledge of the Company, no event has occurred or circumstance exists that (with or without notice or lapse of time or both) may constitute or result in a violation by Company of, or a failure by the Company to comply with, any Legal Requirement.

 

(b)            Set forth on Schedule 4.8 are all Governmental Authorizations. Each Governmental Authorization is in full force and effect in favor of the Company and the Company is, and since December 31, 2003 has been, in compliance with each Governmental Authorization. No event has occurred or circumstance exists that (with or without notice or lapse of time or both) may constitute or result in (i) a violation by the Company of, or failure by the Company to comply with, any Governmental Authorization or (ii) the revocation, suspension or termination of any Governmental Authorization. The Company has not received, at any time since December 31, 2003, any notice of any actual, possible or alleged violation of any Governmental Authorization.

 

(c)            Except as set forth on Schedule 4.8 :

 

(i)             The Company has not sold any products prior to receiving any required or necessary approvals or consents from any Governmental Authority, including the FDA under the FD&C Act, or any equivalent Governmental Authority in any other jurisdiction. The Company has not received any written notice of, and neither the Company nor any Stockholder has any Knowledge of, any citations, decisions, product recalls, medical device reports, information requests, Warning Letters, Untitled Letters or Section 305 notices from the FDA or similar Proceedings instituted by the FDA or any equivalent Governmental Authority in any other jurisdiction.

 

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(ii)            All preclinical tests and clinical trials conducted by or on behalf of the Company were and, if still pending, are, being conducted in all material respects in accordance with protocols filed with the applicable Governmental Authorities for each such preclinical test and clinical trial, as the case may be, and in compliance in all material respects with all applicable Legal Requirements. The Company has provided Purchaser with access to all the studies it has conducted.

 

(iii)           The Company has complied in all material respects with all applicable Legal Requirements with respect to the design, manufacture, labeling, testing and inspection of all of the Company’s products and the operation of manufacturing facilities promulgated by the FDA or any equivalent Governmental Authority in any other jurisdiction.

 

(iv)           To the Knowledge of the Company and the Stockholders, there is no adverse Claim or Proceeding relating to any FDA regulatory matter that is pending or threatened against the Company or any of its officers or directors, nor is there any violation of the FD&C Act by the Company that would cause the Company not to be in compliance in all material respects with the FD&C Act.

 

(v)            The Company has not engaged in any activities requiring (i) premarket approval applications or premarket notification (510(k)) clearances from the FDA or (ii) investigational device exemptions or investigational new drug applications from the FDA for any clinical studies of its investigational devices or drugs. To the extent that the Company has filed any such applications or notifications, such applications and notifications, and all other regulatory filings made by the Company with respect to its Products were, at the time of filing, true, complete and accurate in all material respects.

 

4.9            Litigation .

 

(a)            There is no (i) outstanding Order or Proceeding pending or, to the Knowledge of the Stockholders and the Company, threatened, against or affecting the Company, the Business, the Purchased Assets or the Assumed Liabilities except, in each of the foregoing cases, for any such matter that would not have a Material Adverse Effect or would not reasonably be expected to affect (i) the validity or enforceability of this Agreement or any Ancillary Agreement; (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements or (iii) the compliance by the Company or the Stockholders with the terms of this Agreement or any Ancillary Agreement to which any of them is a party or by which any of them is bound.

 

(b)            To the Knowledge of the Company and the Stockholders, there is no outstanding Order or Proceeding pending or threatened against or affecting any of the Company’s officers, directors or employees, the enforcement of or compliance with which, in either of the foregoing cases, would have a Material Adverse Effect or would reasonably be expected to affect (i) the validity or enforceability of this Agreement or the Ancillary Agreements; (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements or (iii) the compliance by the Company or either Stockholders with the terms of this Agreement or any Ancillary Agreement to which any of them is a party or by which any of them is bound.

 

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4.10          Absence of Certain Changes or Events . Except as set forth on Schedule 4.10 , since July 1, 2006, the Company has conducted its business only in the ordinary course consistent with past practice and there has been no Material Adverse Effect. Without limiting the foregoing, except as set forth on Schedule 4.10 , since December 31, 2006, there has not been any:

 

(a)            Grant of any increase in the salary or other compensation payable to, or any advance (excluding advances for ordinary business expenses consistent with past practice) or loan to, any officer, director or employee of the Company, or any material change in any other benefits to which any of the officers and employees of the Company may be entitled, or any other payment to or on behalf of any officer, director or employee of the Company other than payment of salary or reimbursement for reasonable expenses in the ordinary course of business consistent with past practice;

 

(b)            Resignation or termination of employment of any officer or key employee of the Company;

 

(c)            Change or, to the Company’s Knowledge, threatened change, in the Company’s relations with, or any loss or, to the Company’s Knowledge, threatened loss of, any of the suppliers, vendors, distributors, clients or customers that are material to the Business;

 

(d)            Sale or other disposition or transfer of the Company’s assets or properties, except for sales of inventory in the ordinary course of business consistent with past practice;

 

(e)            Change in any method of keeping the Company’s books of account or accounting practices, including any change or modification to its existing credit, collection or payment policies, procedures or practices;

 

(f)             Damage or destruction of, or loss to, any of the Company’s material assets or properties, whether covered by insurance or not;

 

(g)            Waiver or release of any material Claim of the Company;

 

(h)            Amendment or other change to any Company Contract or Governing Document of the Company, except as otherwise set forth on Schedule 1.1(f)  hereto;

 

(i)             Dividend, distribution or other payment to any holder of the Company’s Securities (other than as an employee of the Company in accordance with the Company’s policies); or

 

(j)             Agreement or commitment by the Stockholders or the Company to do any of the foregoing.

 

4.11          Title to Assets . The Company has good and marketable title to all of the Purchased Assets and, in the case of leased Purchased Assets, to its leasehold interests, free and clear of all Encumbrances, except for Permitted Encumbrances. The Purchased Assets constitute all of the assets and properties necessary to operate the Business after the Closing in substantially the same manner as it is conducted prior to the Closing. Except as set forth on Schedule 4.11 ,

 

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the Company does not own or lease, nor has it ever owned or leased, any interest in any real property.

 

4.12          Inventory; Accounts Receivable .

 

(a)            All Inventories are usable and, with respect to finished goods, saleable by the Company in the ordinary course of business, except for obsolete items and items of below-standard quality, which have been written off or written down to net realizable value in the Balance Sheets or the Interim Balance Sheet. The Inventories are not excessive, and are reasonable based on the operations of the Company.

 

(b)            All of the accounts and notes receivable of the Company represent amounts receivable for merchandise actually delivered or services actually provided (or, in the case of non-trade accounts or notes represent amounts receivable in respect of other bona-fide business transactions), have arisen in the ordinary course of the Company’s business, are not subject to any defenses, counterclaims or offsets and have been billed and are generally due within 30 days of billing. All such receivables are fully collectible in the normal and ordinary course of business, except to the extent of a reserve in an amount not in excess of the reserve for doubtful accounts reflected on the Balance Sheet or the Interim Balance Sheet.

 

4.13          Intellectual Property .

 

(a)            The patents included in the Company’s Intellectual Property owned by or licensed to the Company is set forth on Schedule 4.13 hereto. All of the Company’s Intellectual Property is owned by the Company or is validly licensed for use by the Company. Except as disclosed on Schedule 4.13 , (i) the Company has all necessary rights to use its Intellectual Property in its operation of the Business as currently operated; (ii) all Patents and registrations owned by or licensed to the Company and applications to Governmental Authorities in respect of such Intellectual Property are valid and in full force and effect and, to the extent applicable, all annuities, Taxes, renewal fees and other maintenance fees in respect of such have been duly and promptly paid; (iii) except as disclosed in the Schedules, the Company has not granted any license or other permission to use, exploit, transfer or assert Claims in the Intellectual Property; (iv) to the Knowledge of the Company, the Company’s Intellectual Property is not being infringed, misappropriated or otherwise violated by any other Person and (v) to the Knowledge of the Company, no Person other than the Company has any right to, or intends to allege that such Person has any right to, any of the Company’s Intellectual Property other than pursuant to licenses and other agreements listed in the Schedules. Each assignment of registered Intellectual Property assigned to the Company has been recorded with the relevant Governmental Authority. The Company has not received any notice asserting that the Company’s Intellectual Property is infringing on any rights of any other Person. The Company’s Intellectual Property is not subject to any obligation to make payment, or the obligation to grant rights, to any Person in exchange, except (i) as otherwise set forth in the Schedules and (ii) license fees due in connection with any commercial off-the-shelf Software. Except as set forth on the Schedules, the Company is not bound by, or party to, any Contract that would prevent, prohibit or otherwise interfere with the ability of the Company to utilize its Intellectual Property. No Claim is pending or, to the Knowledge of the Company and the Stockholders, has been threatened, challenging the Company’s ownership of, rights in or use of any of its Intellectual Property or alleging any

 

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infringement, misappropriation or violation of any other Person’s Intellectual Property, either by the Company’s Intellectual Property or by the sale of any products or services by the Company.

 

(b)                                  Each former and current director, officer, manager, employee, agent, researcher, consultant, contractor or other Person who has contributed to or participated in the creation and development of any of the Company’s Intellectual Property on behalf of the Company has either (i) been party to a “work-made-for-hire” arrangement or Contract that has accorded the Company ownership of all of such Person’s rights in such Intellectual Property or (ii) executed a written assignment that assigns to the Company all of such Person’s rights to any inventions, improvements, discoveries or information developed or discovered by such Person in connection with providing services to the Company or otherwise using the Company’s assets or properties.  Each former and current director, officer, manager, employee, agent, researcher, consultant, contractor or third party who has had or has access to, contributed to or participated in the creation and/or development of any of the Company’s Intellectual Property has executed a confidentiality and nondisclosure agreement that protects the confidentiality of such Intellectual Property in favor of the Company and prohibits such party from using such Intellectual Property other than for the benefit of the Company.

 

4.14                            Company Contracts .  Each Company Contract is valid, binding and enforceable against the Company, and, to the Company’s Knowledge, the other parties thereto, in accordance with its terms, and is in full force and effect.  No event or condition has occurred or become Known to the Company or is alleged to have occurred that constitutes or (with notice or the passage of time or both) would constitute a default by the Company or a basis of force majeure or other Claim of any other party thereto of excusable delay, termination, nonperformance or accelerated or increased rights.  To the Knowledge of the Company, no event or condition has occurred or exists or is alleged to have occurred or to exist that constitutes or (with notice or the passage of time or both) would constitute a default by any Person (other than the Company) or a basis of force majeure or other Claim of the Company of excusable delay, termination, nonperformance or accelerated or increased rights.

 

4.15                            Environmental Matters .

 

(a)                                   Schedule 4.15 sets forth a list of all reports, studies, analyses, tests, monitoring results, notices, memoranda or other documents possessed by the Company pertaining compliance or non-compliance with Environmental Laws.

 

(b)                                  Except as set forth on Schedule 4.15 :

 

(i)                                      The operations of the Company, including the use, handling, manufacture, treatment, processing, storage, generation, release, discharge and disposal of Hazardous Substances, are, and have at all times been, in material compliance with all Environmental Laws;

 

(ii)                                   The Company has obtained all Governmental Authorizations required under applicable Environmental Laws, and the operations of all the Company are, and have at all times been, in material compliance with the terms and conditions of any such required Governmental Authorizations;

 

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(iii)                                There are no pending or, to the Knowledge of the Company, threatened Environmental Claims against the Company, and to the Knowledge of the Company there is no basis on which to expect any Environmental Claim to be made against the Company;

 

(iv)                               The Company does not own or operate, or has it ever owned or operated, any underground storage tanks; and

 

(v)                                  There has been no actual, alleged or threatened release (as defined in 42 U.S.C. Section 9601) of any Hazardous Substance(s) at or from any real properly currently or formerly operated or leased by the Company, nor are any Hazardous Substances present on, in or under any such real property, except for such Hazardous Substances as are used in the ordinary course of business as it is now conducted at such real property and in compliance with all applicable Environmental Laws.

 

4.16                            Employee Matters .

 

(a)                                   Set forth on Schedule 4.16 is a list of each employee of the Company (which, for purposes hereof, shall include all individuals performing services for the Company who are co-employed by the Company and Administaff under the Administaff Agreement), including such employee’s job title, current compensation paid or payable, accrued vacation, sick and personal time and service credited for purposes of vesting and eligibility for severance pay or participating in any Employee Benefit Plan.  Except as disclosed on Schedule 4.16 , the employment of each employee of the Company is terminable at will and no employee of the Company has been granted the right to continued employment or by the Company or to any severance or other material compensation following termination of employment with the Company.  To the Company’s Knowledge, no employee of the Company, nor any consultant with whom the Company has contracted, is in violation of any Order to which such Person is subject or any material term of any employment Contract, proprietary information Contract or any other Contract relating to the right of any such Person to be employed by, or to contract with, the Company; and to the Company’s Knowledge, the continued retention by the Company of any such Person will not result in any such violation.

 

(b)                                  Except as set forth on Schedule 4.16 , each officer and employee of the Company is devoting substantially all of such Person’s business time to the conduct of the business of the Company.  Except as set forth on Schedule 4.16 , to the Stockholders’ and the Company’s Knowledge, no officer or employee of the Company is planning to work less than full time with the Company.

 

(c)                                   No employee of the Company is or, since December 31, 2003, has been:  (i) a party to or otherwise bound by any collective bargaining Contract; (ii) a party to, involved in or, to the Knowledge of the Stockholders and the Company, threatened by, any labor dispute, union organizing drive or unfair labor practice charge; (iii) engaged in any unfair labor practices or (iv) participated in any general work stoppage or slowdown.

 

(d)                                  Except as disclosed on Schedule 4.16 , there are no outstanding material Claims against the Company asserted by or on behalf of any present or former employee or job applicant.  The Company has not received any notice from any Person asserting any Claim

 

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against the Company relating to discrimination, breach of Contract, occupational safety in employment, wage and hour violations, the National Labor Relations Act or employment practices in relation to the Business, whether or not such Claim would be covered by employment practices liability insurance coverage.

 

(e)                                   Except as disclosed on Schedule 4.16 , there are no outstanding material Claims either asserted by or against the Company for breach of the Administaff Agreement or for indemnification or arbitration under the Administaff Agreement.  The Company has not committed any act of default under Article IX of the Administaff Agreement nor breached any representation or warranty under Article XI of the Administaff Agreement.  To the Stockholders’ and the Company’s Knowledge, the Company is in full compliance with the Texas Staff Leasing Services Act, Texas Labor Code, Chapter 91.

 

4.17                            Employee Benefit Matters .

 

(a)                                   Schedule 4.17 lists all qualified pension or profit sharing plans, deferred compensation, bonus, group insurance contract or any other incentive, welfare or agreement, commitment, arrangement or employee benefit plan (as defined in Section 3(3) of ERISA) maintained by each the Company, or to which the Company has been or is required to contribute or any Administaff Employee Benefit Plan that the Company employees participate in or are covered under (hereinafter “ Employee Benefit Plans ”).  The Company has provided or made available to the Purchaser a complete copy of each Employee Benefit Plan as well as, if applicable, a complete copy of each trust or other funding arrangement, each summary plan description and summary of material modifications, the most recent determination letter received by the Company from the IRS and the most recent Form 5500 annual report filed for each applicable Employee Benefit Plan.

 

(b)                                  The Company has never maintained, contributed to or had any obligation under any defined benefit pension plan, including any multiemployer pension benefit plan (as defined in Section 4(37) of ERISA).

 

(c)                                   The Company’s Employee Benefit Plans have been maintained, operated and administered, in all material respects, in compliance with its terms and any related documents and Contracts and the applicable provisions of ERISA, the Code and other applicable Legal Requirements, except in any case in which such the Company’s Employee Benefit Plan is currently required to comply with a provision of ERISA or of the Code, but is not yet required to be amended to reflect such provision, it has been administered in all material respects in accordance with such provision of ERISA or the Code.

 

(d)                                  With respect to each of the Company’s Employee Benefit Plans, there are no pending or, to the Knowledge of the Company, threatened, Claims or Proceedings for benefits that have been denied, or any similar Claims or Proceedings that may result in Liability to the Company.

 

(e)                                   No fiduciary, party in interest, or disqualified person with respect to any of the Employee Benefit Plans has engaged in any transaction described in Section 406(a) or 406(b) of

 

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ERISA (and not exempt under Section 408 of ERISA) or in any transaction described in Section 4975 of the Code.

 

(f)                                     Each Employee Benefit Plan complies in all material respects with all applicable Legal Requirements.

 

(g)                                  No Employee Benefit Plan provides, with respect to employees of such the Company, death or medical benefits beyond termination of service or retirement other than (i) coverage mandated by Legal Requirements or (ii) benefits under an Employee Benefit Plan qualified under Section 401(a) of the Code.

 

(h)                                  The Company has made or will accrue prior to the Closing Date all payments and contributions (including insurance premiums) due and payable as of the Closing Date to each of the Company’s Employee Benefit Plan as required to be made under the terms of such Employee Benefit Plan.

 

4.18                            Taxes .  Except as set forth on Schedule 4.18 :

 

(a)                                   (i) All Tax Returns required to be filed by or on behalf of the Company have been duly and timely filed with the appropriate Taxing Authority in all jurisdictions in which such Tax Returns are required to be filed (after giving effect to any valid extensions of time in which to make such filings) and all such Tax Returns are true, complete and correct in all material respects and (ii) all Taxes payable by or on behalf of the Company (whether or not shown on any Tax Return), have been fully and timely paid.  With respect to any period for which Tax Returns have not yet been filed or for which Taxes are not yet due or owing, the Company has made due and sufficient accruals for such Taxes in its financial statements and its books and records.

 

(b)                                  The Company has complied in all material respects with all Legal Requirements relating to the payment and withholding of Taxes and has duly and timely withheld and paid over to the appropriate Taxing Authority all amounts required to be so withheld and paid under all applicable Legal Requirements.

 

(c)                                   No Claim has been made by a Taxing Authority in a jurisdiction where the Company does not file Tax Returns such that it is or may be subject to taxation by that jurisdiction.

 

4.19                            Transactions with Related Persons .  Except as set forth on Schedule 4.19 , no current or former employee, consultant, holder of Securities, officer of director of the Company or any other current or former Affiliate of the Company (each, a “ Related Person ”) has any Liability for borrowed money or any other material Liability to the Company, nor does the Company have any such Liability to any Related Person.  No Related Person holds, directly or indirectly, any Securities in any Person (a) who is an Affiliate of the Company; (b) with whom the Company has a material business relationship or (c) who competes with the Company except, in the case of clause (c), for ownership by a Related Person of less than one percent of the outstanding Securities of a publicly traded company.  No Related Person has a direct or indirect interest in any Company Contract.

 

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4.20                            Insurance .  Set forth on Schedule 4.20 is a list of all policies of insurance to which the Company is a party or under which the Company or any officer or director of the Company is or has been covered at any time since December 31, 2003.  All such policies are outstanding and in full force and effect.  No event or condition has occurred or become Known to the Company or is alleged to have occurred that constitutes (or with notice or the passage of time or both) would constitute, a breach or default of any provision contained in any such policy, nor has there been any failure to give any notice or present in a timely fashion any Claim under any such policy or in the manner or detail required by such policy.  Except as set forth on Schedule 4.20 :  (a) all of such coverages are provided on an “occurrence” (as opposed to “claims made”) basis; (b) there are no outstanding Claims under such policies; (c) there are no premiums or other payments due by the Company under such policies that remain unpaid; (d) since December 31, 2003, no notice of cancellation or non-renewal with respect to, or disallowance of any material Claim under, any such policy has been received by the Company and (e) the Company has not been refused any insurance, nor has any of its coverages been limited by any insurance carrier to which it has applied for insurance or with which it has carried insurance during the last two years.  The amounts of coverage under such policies of insurance are sufficient in amount to allow the Company to repair or replace any of its assets or properties that might be damaged or destroyed, and are sufficient to cover Liabilities to which the Company may reasonably become subject.

 

4.21                            Customers and Suppliers .

 

(a)                                   Schedule 4.21 sets forth the name and address of the ten largest customers of the Company during the twelve-month period ended December 31, 2006 with the amount of sales made to each such customer during such period.

 

(b)                                  Schedule 4.21 sets forth the name and address of the ten largest suppliers of the Company during the 12-month period ended December 31, 2006, with the amount of purchases made from each such supplier during such period.

 

(c)                                   The Company has not received any advance, progress payment or deposit in respect of any sales Contract, and the Company is not a party to or bound by any sales Contract that will result, upon completion or performance thereof, in gross margins materially lower than those normally experienced by the Company for the services or products covered by such sales Contract.  No purchase Contract to which the Company is a party or bound is in excess of the normal, ordinary and usual requirements of the Business or at a price that is materially higher than prevailing market prices for the same item at the time it was ordered.

 

4.22                            Product Liability and Product Warranty Schedule 4.22 sets forth (a) a description of the Company’s warranty policy with respect to products sold or services rendered by the Company and (b) a description of the Company’s product and service liability and product and service warranty experience since December 31, 2003, including any quality-related complaints from customers who, in the aggregate, represented five percent or more of the total sales of the Company during any such year.

 

4.23                            Brokers .  The Company has not retained any broker, finder or investment banking firm or any other Person to act on its behalf in connection with the transactions contemplated by

 

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this Agreement and, to the Company’s and the Stockholders’ Knowledge, no other Person is entitled to receive any brokerage commission, finder’s fee or other similar compensation in connection with the transactions contemplated by this Agreement and the Ancillary Agreements.

 

4.24                            Disclosure .  No representation or warranty by the Stockholders or the Company in this Agreement contains any untrue statement of a material fact or fails to state a fact necessary to make the statements made herein correct.

 

ARTICLE V

REPRESENTATIONS AND WARRANTIES OF THE STOCKHOLDERS

 

Each Stockholder hereby jointly and severally represents and warrants to the Purchaser as follows:

 

5.1                                  Authority; Enforceability .  The execution, delivery and performance by the Stockholders of this Agreement and each Ancillary Agreement to which he or she is a party, and the consummation of the transactions contemplated hereby and thereby, have been duly authorized by all necessary action on the part of the Stockholder.  This Agreement has been, and each Ancillary Agreement to which each Stockholder is a party will be, duly and validly executed and delivered by such Stockholder and constitutes, and will constitute, the valid and binding obligation of such Stockholder, enforceable against him or her in accordance with its respective terms, except (a) as limited by Legal Requirements of general application relating to bankruptcy, insolvency and relief of debtors or (b) as limited by Legal Requirements governing specific performance, injunctive relief or other equitable remedies and by general principles of equity.  The Stockholder has the requisite power and authority to execute and deliver this Agreement and each Ancillary Agreement to which he or she is a party and to consummate the transactions contemplated hereby and thereby.

 

5.2                                  Consents; Non-Contravention .

 

(a)                                   Except as set forth on Schedule 5.2 , no consent, approval, authorization, exemption or waiver of, or notice or filing with, any Person is required to be obtained, given or made, as applicable, by either Stockholder in connection with the execution, delivery and performance by such Stockholder of this Agreement or any Ancillary Agreement to which he or she is a party, or to consummate the transactions contemplated hereby and thereby.

 

(b)                                  Except as set forth on Schedule 5.2 , the execution, delivery and performance by each Stockholder of this Agreement and each Ancillary Agreement to which such Stockholder is a party or by which he or she is bound and the consummation of the transactions contemplated hereby and thereby does not and will not, with or without the giving of notice or the lapse of time or both, (i) contravene, conflict with or violate any Legal Requirement to which either Stockholder is subject or (ii) contravene, conflict with or violate any Order applicable to either Stockholder.

 

5.3                                  Brokers .  Neither Stockholder has retained any broker, finder or investment banking firm to act on his or her behalf in connection with the transactions contemplated by this Agreement and, to the Stockholders’ Knowledge, no other Person is entitled to receive any

 

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brokerage commission, finder’s fee or other similar compensation in connection with the transactions contemplated by this Agreement.

 

5.4                                  Litigation .  There is no (i) outstanding Order or Proceeding pending or, to the Knowledge of the Stockholders, threatened, against or affecting either Stockholder except for any such matter that would not reasonably be expected to affect (i) the validity or enforceability of this Agreement or any Ancillary Agreement; (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements or (iii) the compliance by each Stockholder with the terms of this Agreement or any Ancillary Agreement to which such Stockholder is a party or by which such Stockholder is bound.

 

ARTICLE VI

REPRESENTATIONS AND WARRANTIES OF THE PURCHASER

 

The Purchaser hereby represents and warrants to the Company and the Stockholders as follows:

 

6.1                                  Authority; Enforceability .  The execution, delivery and performance by the Purchaser of this Agreement and each Ancillary Agreement to which it is a party, and the consummation of the transactions contemplated hereby and thereby, have been duly authorized by all necessary action on the part of the Purchaser.  This Agreement has been, and each Ancillary Agreement to which the Purchaser is a party will be, duly and validly executed and delivered by the Purchaser and constitutes, and will constitute, the valid and binding obligation of the Purchaser, enforceable against it in accordance with its respective terms, except (a) as limited by Legal Requirements of general application relating to bankruptcy, insolvency and relief of debtors or (b) as limited by Legal Requirements governing specific performance, injunctive relief or other equitable remedies and by general principles of equity.  The Purchaser has the requisite power and authority to execute and deliver this Agreement and each Ancillary Agreement to which it is a party and to consummate the transactions contemplated hereby and thereby.

 

6.2                                  Consents; Non-Contravention .

 

(a)                                   Except as set forth on Schedule 6.2 , no consent, approval, authorization, exemption or waiver of, or notice or filing with, any Person is required to be obtained, given or made, as applicable, by the Purchaser in connection with the execution, delivery and performance by the Purchaser of this Agreement or any Ancillary Agreement to which it is a party, or to consummate the transactions contemplated hereby and thereby.

 

(b)                                  Except as set forth on Schedule 6.2 , the execution, delivery and performance by the Purchaser of this Agreement and each Ancillary Agreement to which it is a party or by which it is bound and the consummation of the transactions contemplated hereby and thereby does not and will not, with or without the giving of notice or the lapse of time or both, (i) contravene, conflict with or violate any Legal Requirement to which the Purchaser is subject; (ii) contravene, conflict with or violate any Order applicable to the Purchaser or (iii) contravene, conflict with or violate any provision of the Governing Documents of the Purchaser.

 

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6.3                                  Brokers .  The Purchaser has not retained any broker, finder or investment banking firm to act on its behalf in connection with the transactions contemplated by this Agreement and, to the Purchaser’s Knowledge, no other Person is entitled to receive any brokerage commission, finder’s fee or other similar compensation in connection with the transactions contemplated by this Agreement.

 

6.4                                  Litigation .  There is no (i) outstanding Order or Proceeding pending or, to the Knowledge of the Purchaser, threatened, against or affecting the Purchaser except for any such matter that would not reasonably be expected to affect (i) the validity or enforceability of this Agreement or any Ancillary Agreement; (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements or (iii) the compliance by the Purchaser with the terms of this Agreement or any Ancillary Agreement to which the Purchaser is a party or by which the Purchaser is bound.

 

ARTICLE VII

COVENANTS OF THE COMPANY AND THE STOCKHOLDERS

 

7.1                                  Fulfillment of Agreements .  The Stockholders and the Company shall use their respective best commercially reasonable efforts to cause all of the conditions to the obligations of the Purchaser under Article IX to be satisfied on or prior to the Closing.  The Stockholders or the Company, as the case may be, shall promptly notify the Purchaser of any event or fact coming to any of their attention prior to the Closing that causes any of their representations or warranties, covenants or obligations contained herein to be breached or become inaccurate, as the case may be.  The Stockholders shall cause the Company to satisfy and comply with all of its obligations and covenants hereunder and under the Ancillary Agreements.

 

7.2                                  Further Assurances .  At any time or from time to time after the Closing, the Stockholders and the Company shall, at the sole cost and expense of the Purchaser, execute and deliver any further instruments or documents and take all such further action as the Purchaser shall reasonably request to evidence the consummation of the transactions contemplated hereby.  For purposes of the foregoing sentence, such further actions shall include, but not be limited to, executing and filing any documents necessary to memorialize, evidence and reflect the transfer of any and all title, rights, and/or interests that the Company and/or the Stockholders may have in the Intellectual Property, including but not limited to, patent assignments, releases from security interests, any and all other conveyances of any and all rights and/or interests in the Intellectual Property. In addition, after the Closing, the Company and the Stockholders shall cooperate with the Purchaser in its efforts to continue and maintain for the benefit of the Purchaser the business relationships of the Company existing prior to the Closing and relating to the Business and the Company and the Stockholders shall refer to the Purchaser all inquiries relating to the Business that are made to any of them.

 

7.3                                  Confidentiality .

 

(a)                                   The Stockholders and the Company acknowledge that they may have, or may have access to, proprietary or confidential information that is related to the Business (the “ Company Confidential Information ”); provided, however, that Company Confidential Information shall not include any information (i) that is or becomes a matter of public knowledge through no fault of the Stockholders or the Company or (ii) to the extent it relates to the

 

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Excluded Assets or the Retained Liabilities.  The Stockholders, the Company and their respective Affiliates (together, the “ Company Parties ”) shall keep all Company Confidential Information strictly confidential, shall not disclose Company Confidential Information to any other Person and, other than in connection with the operation of the Business in accordance with this Agreement prior to the Closing, and shall not use the Company Confidential Information for any purpose.  Notwithstanding the foregoing, any Company Party may disclose Company Confidential Information to the extent required by any Legal Requirement, in which event such Company Party shall provide the Purchaser with prompt written notice of such requirement, so that the Purchaser may seek an appropriate protective order or other remedy (as to which the Company Parties shall provide reasonable cooperation).

 

(b)                                  Unless otherwise consented to by the Purchaser, the Company Parties shall keep strictly confidential, and shall not disclose to any Person, the terms or existence of this Agreement, the Ancillary Agreements or the transactions contemplated hereby or thereby; provided, however, that the Company Parties may disclose such information to the extent required by any Legal Requirement, in which event the applicable Company Party shall provide the Purchaser with prompt written notice of such requirement, so that the Purchaser may seek an appropriate protective order or other remedy (as to which the Company Parties shall provide reasonable cooperation).

 

(c)                                   The Stockholders and the Company shall be liable for any breach of this Section 7.3 by any of their Affiliates.

 

7.4                                  Books and Records .  From the Closing Date until the fifth anniversary thereof, the Stockholders and the Company shall provide the Purchaser with access to the business records, contracts and other information existing at the Closing Date and relating to the Purchased Assets, the Assumed Liabilities and the conduct of the Business as is reasonably necessary for (a) the preparation for or the prosecution or defense of any Proceeding or investigation; (b) the preparation and filing of any Tax return or election relating the Purchased Assets, the Assumed Liabilities or the conduct of the Business and any audit by any Taxing Authority of any returns of the Purchaser relating thereto and (c) the preparation and filing of any other documents required by any Governmental Authority to be prepared and filed by or on behalf of the Purchaser.  The Purchaser shall reimburse the party from whom any such information and assistance shall be requested for all reasonable out-of-pocket costs and expenses incurred by such party in providing such information and in rendering such assistance.  The access to files, books and records contemplated by this Section 7.4 shall be during normal business hours and upon reasonable notice and shall be subject to such reasonable limitations as the party having custody or control thereof may impose to preserve the confidentiality of information contained therein.

 

7.5                                  Conduct of Business .  Prior to the Closing, except as expressly permitted herein, or unless the Purchaser shall otherwise consent in writing, the Company shall, and the Stockholders shall cause the Company to:  (a) carry on the Business in the ordinary course and in substantially the same manner in which it has been conducted; (b) use its commercially reasonable efforts to preserve intact its present business organization and to keep available the services of its present officers, independent contractors and employees; (c) preserve the goodwill of the customers and suppliers of the Business and others having material business relations with

 

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the Company; (d) perform and discharge its Liabilities in a timely manner; (e) not take any action or omit to take any action, which action or omission would result in a breach or inaccuracy of any representation or warranty contained herein or any breach or noncompliance with any of its agreements or obligations hereunder; (f) not agree or commit to do any of the foregoing referred to in clauses (a) through (e) and (g) promptly advise the Purchaser of any fact, condition, occurrence or change that becomes Known to the Stockholders or the Company that would cause of breach of this Section 7.5 or would have a Material Adverse Effect.  After the Closing, the Company shall continue to operate as an ongoing corporate entity for the purpose of winding up its affairs until all of the Retained Liabilities are discharged in full or adequate provision for contingent Retained Liabilities is made.

 

7.6                                  Access .  Prior to the Closing, the Company and the Stockholders shall provide the Purchaser and advisors and other representatives full access during regular business hours and upon reasonable notice to the Company’s properties, books and records and shall provide to the Purchaser such financial and operating data and other information concerning the Business as the Purchaser shall from time to time reasonably request.

 

7.7                                  Insurance .  The Company shall maintain in full force and effect the policies of insurance listed on Schedule 4.20 , or else shall obtain, prior to the lapse of any such policy, the same coverage with insurers of recognized standing and approved in writing by the Purchaser.

 

7.8                                  Exclusivity .  Neither the Stockholders nor the Company nor any of their respective Affiliates shall, directly or indirectly:  (a) solicit, initiate or participate in any manner in any discussions or negotiations regarding a possible sale or other transfer of equity securities of the Company, or any sale of the Purchased Assets by the Company, or any merger, consolidation or similar transaction involving the Company or its equity securities (any of the foregoing, a “ Transaction ”) with any Person other than the Purchaser; (b) provide any information regarding the Company or any of the Stockholders in connection with a possible Transaction with any Person other than the Purchaser or (c) enter into any Contract with respect to a Transaction with a Person other than the Purchaser; provided, however, that the foregoing shall not be deemed to preclude the Company from sharing information with any of the foregoing Persons in furtherance of a Transaction with the Purchaser.  The Company and the Stockholders shall be liable for any breach of this Section 7.8 by their Affiliates.

 

7.9                                  Tax Matters .

 

(a)                                   The Company shall file timely all Tax Returns required to be filed by it on, prior to or after the Closing Date and shall pay or cause to be paid all Taxes when due; and

 

(b)                                  The Company shall be liable for and shall pay all sales, use, stamp, documentary, filing, recording, transfer or similar fees or taxes or governmental charges or a similar nature levied by any Taxing Authority (including any interest and penalties) in connection with the sale of the Purchased Assets and the assignment of the Assumed Liabilities.

 

7.10                            Change of Name .  From and after the Closing Date, neither the Company nor the Stockholders shall have any right to use the present corporate name of the Company or any trade names or trademarks included in the Purchased Assets (whether or not registered and whether

 

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existing under common law or otherwise).  Within three Business Days after the occurrence of the Closing, the Company shall take all such action as is necessary to change its corporate name.

 

7.11                            Guarantee .  The Stockholders hereby jointly and severally irrevocably and unconditionally guarantee, as primary obligors and not as sureties, the full and prompt payment and performance when due of all obligations of the Company under this Agreement and all of the Ancillary Agreements to which the Company is a party (such obligations, the “ Obligations ”).  This guarantee shall be continuing and irrevocable, and shall be a guarantee of performance and not of collection.  The Stockholders hereby unconditionally waive promptness, diligence, notice of acceptance of this guarantee and any other notice with respect thereto.  The Stockholders shall pay the Purchaser on demand all reasonable fees and costs incurred by or on behalf of the Company in successfully enforcing observance of the obligations of the Stockholders pursuant to this Section 7.11 .

 

7.12                            Release .  Effective immediately after the Closing, the Stockholders, for themselves, their successors and assigns, and all other Persons who may ever claim by, through or under them (together with the Stockholders, the “ Releasors ”), forever remise, release, acquit and discharge the Company, the Purchaser and each of their respective past, present and future Stockholders, directors, officers, Affiliates, employees, agents, successors and assigns and each past, present and future investor, director, officer, Affiliate, employee, agent, successor, assign, heir, executor and administrator of each of all such Persons, as applicable (together, the “ Released Parties ”), from any and all Claims and Liabilities of any kind or nature whatsoever arising out of or relating to the conduct of the Business, or any Liabilities that arose (whether or not due and payable on the Closing Date), at any time prior to the occurrence of the Closing, which any Releasor ever had, now has or by which any Releasor hereafter can, shall or may have against any of the Released Parties by reason of anything done, omitted or suffered to be done or omitted by any Person or by reason of any matter, cause, thing or event whatsoever.

 

7.13                            Noncompetition, Nonsolicitation and Nondisparagement .

 

(a)                                   For a period of five years after the Closing Date (the “ Restricted Period ”), neither the Company nor either Stockholder shall, anywhere in the world, directly or indirectly (whether through an Affiliate, by giving direction to any other Person or otherwise), lend its, his or her name to, invest in, own, manage, operate, provide any financial assistance to (or otherwise finance), control, advise, render services to, receive any financial benefit from or guarantee the obligations of, any Person engaged in or planning to become engaged in the Restricted Business.

 

(b)                                  During the Restricted Period, neither the Company nor either Stockholder shall, directly or indirectly (whether through an Affiliate, by giving direction to any other Person or otherwise, and whether for such Person or any other Person), employ, retain, recruit, solicit or otherwise interfere with or attempt to entice away from the Purchaser or any of its Affiliates (the “ Restrictive Parties ”) any Person who (i) at the time of such employment, retention, recruitment, solicitation, interference or enticement is, or has agreed to become, an employee, consultant or other independent contractor of any Restrictive Party or (ii) at any time during the 12-month period preceding such employment, retention, recruitment, solicitation, interference or enticement was an employee, consultant or other independent contractor of any Restrictive Party.

 

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(c)                                   During the Restricted Period, neither the Company nor either Stockholder shall, directly or indirectly, (whether through an Affiliate, by giving direction to any other Person or otherwise, and whether for such Person or any other Person), solicit or otherwise interfere with or attempt to entice away from any Restrictive Party any Person who (i) at the time of such solicitation, interference or enticement is, or has agreed to become, a customer, licensee, licensor or supplier of any Restrictive Party, or is in, or has agreed to enter into, any other material business relationship with any Restrictive Party or (ii) at any time during the 12-month period preceding such solicitation, interference or enticement was a customer, licensee, licensor or supplier of any Restrictive Party or had a material business relationship with any Restrictive Party.

 

(d)                                  Neither the Company nor either Stockholder shall, directly or indirectly (whether through an Affiliate, giving direction to any other Person or otherwise), disparage or criticize any Restrictive Party, the Business (either as formerly conducted by the Company or as conducted by the Purchaser) or the business conducted by any other Restrictive Party, or engage in any other action that is intended to hinder the business relationships of any Restrictive Party.

 

(e)                                   The running of the Restricted Period shall be tolled by any court of competent jurisdiction or arbiter before whom any action is brought to enforce the restrictive covenants set forth in this Section 7.13 during any period of time of the Company’s or either Stockholder’s violation of such covenant, and such period of time of violation shall be added to the end of the Restricted Period for the particular covenant that has been violated, once such violation ceases.

 

(f)                                     Notwithstanding anything to the contrary contained in this Section 7.13 , in no event shall Ronald O. Bergan’s ownership interests in Aldevron LLC, its subsidiary Genovac, and Copernicus Therapeutics, Inc., to the extent that each of them continues to conduct its business as conducted on the date hereof, constitute a breach by the Company or the Stockholders of their obligations under subsections (a) , (b)  or (c)  of this Section 7.13 hereof.

 

7.14                            Liquidation and Dissolution Documents .  In the event that the Company determines to liquidate and dissolve, the Company shall provide the Purchaser with copies of all documentation relating to the liquidation and dissolution and shall not sign, distribute for signature or file any such documents, or take any similar action in furtherance of the liquidation and dissolution, until the form and substance of such documents shall be approved by the Purchaser, such approval not to be unreasonably withheld.

 

ARTICLE VIII

COVENANTS OF THE PURCHASER

 

8.1                                  Fulfillment of Agreements .  The Purchaser shall use best efforts to cause all of the conditions to the obligations of the Stockholders and the Company under Article X to be satisfied on or prior to Closing.  The Purchaser shall promptly notify the Stockholders and the Company of any event or fact coming to its attention prior to the Closing that causes any of its representations or warranties, covenants or obligations contained herein to be breached or become inaccurate, as the case may be.

 

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8.2                                  Further Assurances .  At any time or from time to time after the Closing, the Purchaser shall, at the sole cost and expense of the Stockholders and the Company, execute and deliver any further instruments or documents and take all such further action as the Stockholders or the Company shall reasonably request to evidence the consummation of the transactions contemplated hereby.

 

8.3                                  Confidentiality .  Unless otherwise consented to by the Stockholders and the Company, the Purchaser and its Affiliates (together, the “ Purchaser Parties ”) shall keep strictly confidential, and shall not disclose to any Person the terms or existence of this Agreement, the Ancillary Agreements or the transactions contemplated hereby or thereby; provided, however, that the Purchaser Parties may disclose such information to the extent required by any Legal Requirement, in which event the applicable Purchaser Party shall provide the Stockholders and the Company with prompt written notice of such requirement, so that the Stockholders and/or the Company may seek an appropriate protective order or other remedy (as to which the Purchaser Parties shall provide reasonable cooperation).  The Purchaser shall be liable for any breach of this Section 8.3 by any of its Affiliates.

 

8.4                                  Books and Records .  From the Closing Date until the fifth anniversary thereof, the Purchaser shall provide the Stockholders and the Company with access to the business records, contracts and other information existing at the Closing Date and relating to the Purchased Assets, the Assumed Liabilities and the conduct of the Business prior to the Closing as is reasonably necessary for (a) the preparation for or the prosecution or defense of any Proceeding or investigation; (b) the preparation and filing of any Tax return or election relating the Purchased Assets, the Assumed Liabilities or the conduct of the Business prior to the Closing and any audit by any Taxing Authority of any returns of the Stockholders or the Company relating thereto and (c) the preparation and filing of any other documents required by any Governmental Authority to be prepared and filed by or on behalf of the Stockholders or the Company.  The party requesting such information and assistance shall reimburse the Purchaser for all reasonable out-of-pocket costs and expenses incurred by the Purchaser in providing such information and in rendering such assistance.  The access to files, books and records contemplated by this Section 8.4 shall be during normal business hours and upon reasonable notice and shall be subject to such reasonable limitations as the Purchaser may impose to preserve the confidentiality of information contained therein.

 

8.5                                  Arrangement with Administaff and Other Employee Matters .  The Purchaser shall offer full-time employment to all employees of the Company as of the date hereof, other than those whose employment was terminated prior to the occurrence of the Closing and those employees of the Company listed on Schedule 8.5 hereto (such employees who are offered employment, the “ Employees ”) upon terms (including with respect to compensation, benefits, vacation and recognition of service time and seniority) substantially similar to (or, at the option of the Purchaser, more favorable to) the Employees as those on which the Employees were employed by the Company as of the date hereof.  Employment of the Employees by the Purchaser will be in accordance with the Purchaser’s employment practices and policies and without a commitment to any particular term.  For purposes of this Section 8.5 , “Employees” shall include those individuals performing services for the Company who are co-employed by the Company and Administaff under the Administaff Agreement, and for purposes of satisfying

 

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its obligations hereunder, the Purchaser may employ such employees in conjunction with Administaff.

 

8.6                                  Recent Financials .  Promptly after the Company’s request therefor, the Purchaser shall provide the Company with copies of the Purchaser’s balance sheets as of December 31, 2006 (unaudited) and December 31, 2005 (audited) and its income statement for the fiscal year ended December 31, 2006 (unaudited), subject to such confidentiality obligations with respect to such information as the Purchaser shall reasonably request.  The Company may provide such information to its option holders and warrant holders, subject to such confidentiality obligations and other terms and conditions as the Purchaser shall reasonably request.

 

8.7                                  Services of Dr. Kern .  During the six-month period following the Closing Date, the Purchaser will permit Douglas Kern and his assistant to devote a reasonable amount of time to assisting with the winding up and liquidation of the Company.  Nothing contained in this Section 8.7 shall be deemed to constitute any obligation of the Company with respect to the continued employment of Dr. Kern or his assistant.

 

8.8                                  Guarantee Obligations .  The Purchaser shall use its commercially reasonable efforts to cause Douglas Kern to be released from his obligations under the guarantee issued by him to Creekstone Woodlands, LLC, the landlord for the Company’s head offices.  The Purchaser hereby assumes Ronald O. Bergan’s obligation to reimburse Dr. Kern for amounts paid by Dr. Kern to Creekstone Woodlands, LLC under the guarantee.

 

ARTICLE IX

CONDITIONS TO THE PURCHASER’S OBLIGATIONS

 

The obligations of the Purchaser to consummate the transactions contemplated hereby at the Closing shall be subject to the satisfaction on or prior to the Closing Date of each of the following conditions:

 

9.1                                  Representations and Warranties True and Correct .  Without giving effect to any disclosure made to the Purchaser pursuant to Sections 7.1 or 7.5 , all of the representations and warranties of the Company and the Stockholders contained in this Agreement shall be true and correct in all material respects (i) on and as of the date of this Agreement and (ii) on and as of the Closing Date, as if made on and as of the Closing Date, except in both cases for representations and warranties that expressly relate to a date other than the date of this Agreement or the Closing Date, as the case may be, which shall continue to be true and correct as of the specified date and except for representations and warranties that contain Material Adverse Effect or other materiality qualifications, which shall be true and correct in all respects).

 

9.2                                  Covenants and Agreements Performed .  The Company and the Stockholders shall have performed or complied with, in all material respects, all covenants and obligations required by this Agreement to be performed or complied with by them prior to or on the Closing Date.

 

9.3                                  Company Closing Certificate .  The Purchaser shall have been furnished with a certificate executed by the Company (the “ Company Closing Certificate ”), dated the Closing Date, certifying that the conditions set forth in Sections 9.1 and 9.2 with respect to the Company have been fulfilled at or prior to the Closing Date.

 

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9.4                                  Stockholders Closing Certificate .   The Purchaser shall have been furnished with a certificate executed by the Stockholders (the “ Stockholders Closing Certificate ”), dated the Closing Date, certifying that the conditions set forth in Sections 9.1 and 9.2 have been fulfilled at or prior to the Closing Date.

 

9.5                                  No Prohibition .  No Legal Requirement or Order shall be in effect, or Proceeding pending or threatened, that restrains or prevents, or would restrain or prevent, the Purchaser from consummating the transactions contemplated hereby or would adversely affect the conduct of the Business substantially in the manner that the Business was being conducted immediately prior to the Closing.

 

9.6                                  Consents .  The Company and/or the Stockholders, as applicable, shall have obtained the consents set forth on Schedules 4.2 and 5.2 , all in forms reasonably acceptable to the Purchaser.

 

9.7                                  Assignment .  The Company shall have executed an Assignment and Assumption Agreement with respect to the Purchased Assets and the Assumed Liabilities substantially in the form of Exhibit B hereto (the “ Assignment ”).

 

9.8                                  Intellectual Property Assignments .  The Company shall have executed one or more Intellectual Property Assignments to transfer the Company Intellectual Property from the Company to the Purchaser, substantially in the form of Exhibit C hereto (the “ IP Assignments ”).

 

9.9                                  Subscription Agreement .  The Company shall have executed the Subscription Agreement substantially in the form of Exhibit D hereto.

 

ARTICLE X

CONDITIONS TO THE STOCKHOLDERS’ AND THE COMPANY’S OBLIGATIONS

 

The obligations of the Stockholders and the Company to consummate the transactions contemplated hereby at the Closing shall be subject to the satisfaction on or prior to the Closing Date of each of the following conditions:

 

10.1                            Representations and Warranties True and Correct .  Without giving effect to any disclosure made to the Stockholders or the Company pursuant to Section 8.1 , all of the representations and warranties of the Purchaser contained in this Agreement shall be true and correct in all material respects (i) on and as of the date of this Agreement and (ii) on and as of the Closing Date, as if made on and as of the Closing Date.

 

10.2                            Covenants and Agreements Performed .  The Purchaser shall have performed or complied with, in all material respects, all covenants and agreements required by this Agreement to be performed or complied with by the Purchaser prior to or on the Closing Date.

 

10.3                            Purchaser Closing Certificate .  The Company and the Stockholders shall have been furnished with a certificate executed by an officer of the Purchaser (the “ Purchaser Closing Certificate ”), dated the Closing Date, certifying that the conditions set forth in Sections 10.1 and 10.2 have been fulfilled at or prior to the Closing Date.

 

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10.4                            No Prohibition .  No Legal Requirement or Order shall be in effect that restrains or prevents, or would restrain or prevent, the Stockholders or the Company from consummating the transactions contemplated hereby.

 

10.5                            Consents .  The Purchaser shall have obtained the consents set forth on Schedule 6.2 in forms reasonably acceptable to the Stockholders and the Company.

 

10.6                            Payment of Closing Payment .  The Purchaser shall have delivered the Cash Portion and the Stock Portion to the Company in the manner set forth in Section 3.1(b) .

 

10.7                            Assignment .  The Purchaser shall have executed the Assignment.

 

ARTICLE XI

TERMINATION PRIOR TO CLOSING; REORGANIZATION

 

11.1                            Termination .  This Agreement may be terminated at any time prior to the Closing:

 

(a)                                   By the written consent of the Purchaser, the Stockholders and the Company;

 

(b)                                  By either the Purchaser, on the one hand, or the Company and the Stockholders, on the other hand, by written notice given to the other, if the Closing shall not occur on or before February 28, 2007 (the “ Drop Dead Date ”) (other than through the failure of the party seeking to terminate this Agreement to comply fully with such party’s covenants or obligations under this Agreement); or

 

(c)                                   By either the Purchaser, on the one hand, or the Company and the Stockholders, on the other hand, by written notice given to the other, if there has been a material breach of any provision of this Agreement by (i) the Company or either Stockholder, in the case of notice from the Purchaser or (ii) the Purchaser, in the case of notice from the Company and the Stockholders, provided, however, that the Person receiving such notice shall have the opportunity to cure any such breach for seven Business Days after the date the notice is provided before any such termination shall be effective.

 

11.2                            Effect on Obligations .  Termination of this Agreement pursuant to Section 11.1 hereof shall terminate all obligations of the parties hereunder, except for their obligations under Article XII hereof and Sections 7.6 and 8.6 hereof; provided, however, that termination pursuant to Section 11.1(c)  hereof by reason of a material breach by any Person of such Person’s obligations hereunder shall not relieve such Person from any Liability arising from or related to such breach under Article XII hereof or otherwise.

 

ARTICLE XII

SURVIVAL; INDEMNIFICATION AND OFFSET

 

12.1                            Survival; Knowledge of Breach .

 

(a)                                   The covenants, agreements, representations and warranties contained herein shall survive the Closing; provided, however, that the representations and warranties contained herein shall survive only until the expiration of the 15-month period following the Closing Date (the

 

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Survival Period ”), and no Claim for Losses resulting from any misrepresentation or breach of warranty shall be brought or made after the Survival Period, except that such 15-month time limitation shall not apply to:

 

(i)                                      Claims for misrepresentations and breaches of warranties with respect to Sections 4.1 , 4.2 , 4.4 , 4.23 , 5.1 , 5.2 , 5.3 , 6.1 , 6.2 and 6.3 and the first sentence of Section 4.11 , which may be asserted without limitation;

 

(ii)                                   Claims for misrepresentations and breaches of warranties with respect to Sections 4.15 , 4.17 and 4.18 , which may be asserted until 60 days after the expiration of the applicable statute of limitations (the “ Extended Survival Period ”); and

 

(iii)                                Claims for misrepresentations and breach of warranties that have been asserted and that are the subject of a written notice from a Company Indemnitee to the Purchaser or from a Purchaser Indemnitee to a Company Indemnitor prior to the expiration of the Survival Period or the Extended Survival Period, as applicable, which notice specifies in reasonable detail the nature of the Claim.

 

(b)                                  The right to indemnification, payment for Losses or other remedy based on representations, warranties, covenants and obligations in this Agreement shall not be affected by any investigation conducted with respect to, or any Knowledge acquired (or capable of being acquired) at any time, whether before or after the execution and delivery of this Agreement or the Closing Date, with respect to the accuracy or inaccuracy or compliance with, any such representation, warranty, covenant or obligation.  The waiver of any condition based on the inaccuracy of any representation or warranty, or on the non-compliance with or breach of any covenant or obligation, shall not affect the right to indemnification, payment for Losses or other remedy based on such representation, warranties, covenants or obligations.

 

12.2                            Indemnification .

 

(a)                                   The Stockholders and the Company (together, the “ Company Indemnitors ”) shall indemnify and defend the Purchaser and each of its directors, officers, employees, agents and other Affiliates and their respective successors and assigns (together, the “ Purchaser Indemnitees ”), and shall hold each of them harmless from and against, all Losses that are incurred or suffered by any of them in connection with, arising out of or resulting from:

 

(i)                                      Any misrepresentation or breach of any warranty made by the Stockholders or the Company in this Agreement or any Ancillary Agreement;

 

(ii)                                   Any breach of any covenant or obligation of any of the Stockholders or the Company in this Agreement or any Ancillary Agreement to which such Person is a party;

 

(iii)                                Any noncompliance with any bulk-transfer provisions of the Uniform Commercial Code (or any similar Legal Requirement) or fraudulent transfer law arising as a result of the transactions contemplated hereby; and

 

(iv)                               Any of the Retained Assets or Retained Liabilities.

 

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(b)                                  The Purchaser shall indemnify the Company, the Stockholders and each of their directors, officers, employees, agents and other Affiliates, as applicable (together, the “ Company Indemnitees ”), and shall hold each of them harmless from and against, all Losses that are incurred or suffered by any of them in connection with, arising out of or resulting from:

 

(i)                                      Any misrepresentation or breach of any warranty made by the Purchaser in this Agreement or any Ancillary Agreement;

 

(ii)                                   Any breach of any covenant or obligation of the Purchaser in this Agreement or any Ancillary Agreement; or

 

(iii)                                Any of the Purchased Assets or Assumed Liabilities.

 

12.3                            Limitations .

 

(a)                                   The Purchaser shall not be entitled to recover under this Article XII for Losses suffered by it under Section 12.2(a)(i)  until the aggregate amount that the Purchaser Indemnitees are entitled to recover in respect of all such claims exceeds $150,000 (the “ Company Threshold ”); provided, that upon such time as such Losses exceed the Company Threshold, the Purchaser Indemnitees shall be entitled to recover in respect of all Losses and; provided, further, that the Company Threshold shall not apply with respect to Losses incurred by the Purchaser Indemnitees arising in respect of claims for misrepresentations and breach of warranties relating to Sections 4.1, 4.2, 4.4, 4.18, 4.23, 5.1, 5.2, 5.3 and the first sentence of Section 4.11 ;provided, however, that.

 

(b)                                  The Company and the Stockholders may satisfy any payment obligation arising under this Article XII by transferring to the appropriate Purchaser Indemnitee shares of the Purchaser’s Common Stock received hereunder on the date that such payment becomes due (such date, the “Payment Date”).  When payment is made by transferring the Purchaser’s Common Stock, the shares shall be valued at their fair market value on the Payment Date.  If the shares are traded on any national exchange or quoted on any Nasdaq market, the shares shall be valued at their closing price on the Payment Date; or if no closing price is reported the average of the closing offering and bid prices on the Payment Date.  If the shares are not traded on a national exchange or quoted on a Nasdaq market, the Purchaser and the Company and/or the Stockholders, as the case may be, shall attempt to agree upon a fair market value as of the Determination Date for the shares within 20 days after the payment is due.  If such parties are not able to agree upon a value within such 20-day period, each such party (for purposes hereof, with the Company and the Stockholders, to the extent applicable, being one party) shall, within five days after the expiration of the 20-day period referred to above, engage an accounting firm or appraiser experienced in valuing shares of private companies (an “Appraiser”), and those two Appraisers shall engage a third Appraiser.  The Purchaser, the Company and Stockholders shall promptly provide all three Appraisers with any information that they request, and the three Appraisers shall attempt to agree in good faith upon a valuation within 60 days after the third Appraiser shall be selected.  If the three Appraisers cannot agree upon a valuation, the value shall be the average of the individual valuations of the Appraisers.  The fees and expenses of each Appraiser appointed by a party hereto shall be borne by the appointing party and the fees and expenses of the third Appraiser appointed shall be shared equally by the parties (for purposes

 

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hereof, the Company and the Stockholders shall be one party).  Notwithstanding anything to the contrary herein, the liability of the Company pursuant to this Article XII shall not exceed the 24,219 shares of Purchaser’s Common Stock and the liability of the Stockholders pursuant to this Article XII shall not exceed 900,000 shares plus any shares or amounts actually received pursuant to Section 2.1(a)(iv)  through 2.1(a)(vii)  hereof, so that once the Company or the Stockholders, as the case may be, have transferred such shares and, in the case of the Stockholders, any such amounts, such party will have no further liability hereunder; provided, however, that with respect to claims for misrepresentations and breach of warranties relating to Sections 4.1, 4.2, 4.4, 4.18, 4.23, 5.1, 5.2, 5.3 and the first sentence of Section 4.11, the maximum liability of the Company shall be increased so as to include an amount equal to the Cash Portion.

 

(c)                                   No limitation or condition of liability provided in this Article XII shall apply to any misrepresentation or breach of warranty contained herein if such misrepresentation or breach of warranty was made willfully or with intent to deceive.  For purposes of calculating the amount of any Losses incurred in connection with any misrepresentation, breach of warranty or nonfulfillment of any covenant or agreement, any disclosures made pursuant to Sections 7.2, 7.6 and 8.2 shall be disregarded.

 

12.4                            Notice of Indemnity Claims .  If any Purchaser Indemnitee or Company Indemnitee entitled to or seeking indemnification hereunder (an “ Indemnified Party ”) (i) determines that any event, occurrence, fact, condition or Claim gives rise, or could reasonably be expected to give rise to, Losses for which such Indemnified Party is or may be entitled to, or may seek, indemnification under this Agreement; (ii) otherwise identifies an event, occurrence, fact, condition or Claim giving rise, or that could reasonably be expected to give rise, to a right of indemnification hereunder in favor of such Indemnified Party or (iii) with respect to any Third Party Claim, becomes aware of the assertion of any Claim or of the commencement of any Proceeding at law or in equity (any of the foregoing, an “ Indemnity Claim ”), such Indemnified Party shall promptly notify the party obligated to provide indemnification or from whom indemnification is being or will be sought (the “ Indemnifying Party ”) in writing of such Indemnity Claim (a “ Claim Notice ”), describing in reasonable detail the facts giving rise to the claim for indemnification under this Agreement and shall include in such Claim Notice the amount or the method of computation of the amount of such Indemnity Claim (if then Known) and a reference to the provision of this Agreement upon which such Indemnity Claim is based; provided, however, that the failure of any Indemnified Party to give timely notice thereof shall not affect any of the Indemnified Party’s rights to indemnification hereunder nor relieve the Indemnifying Party from any of the Indemnified Party’s indemnification obligations hereunder, except to the extent the Indemnifying Party is actually prejudiced by such failure in the Indemnified Party’s defense of the Indemnity Claim.  Any Claim Notice not relating to a Third Party Claim shall specify the nature of the Losses and the estimated amount thereof.

 

12.5                            Third-Party Claims .  Any obligation to provide indemnification hereunder with respect to any Proceeding by or against any Person other than any party hereto, including any Governmental Authority (a “ Third Party Claim ”), shall be subject to the following terms and conditions:

 

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(a)                                   Upon receipt of a Claim Notice in respect of any Third Party Claim that involves (and continues to involve) solely monetary damages, the Indemnifying Party shall be entitled, at its option and its sole cost and expense and upon written notice (the “ Defense Notice ”) to the Indemnified Party within 15 days of its receipt of such Claim Notice, to assume and control the defense, compromise, settlement and investigation of such Third Party Claim, and to employ and engage counsel reasonably acceptable to the Indemnified Party; provided, however, that the Indemnified Party may, at its option, participate in such defense, compromise, settlement and investigation at its sole cost and expense; provided, further, however, that if there exists a conflict of interest between the Indemnified Party, on the one hand, and the Indemnifying Party, on the other hand, or if the Indemnified Party has been advised by counsel that there may be one or more defenses available to it that are different from or additional to those available to the Indemnifying Party, then the Indemnified Party shall be entitled to retain its own counsel at the cost and expense of the Indemnifying Party.

 

(b)                                  If the Indemnifying Party exercises the right to undertake the defense and investigation of any Third Party Claim as provided in Section 12.5(a) , then (i) the Indemnified Party shall provide reasonable cooperation to the Indemnifying Party in such efforts; (ii) the Indemnifying Party shall keep the Indemnified Party reasonably informed of the progress of the defense of any such Third Party Claim and (iii) the Indemnifying Party shall diligently pursue the Third Party Claim.  If the Indemnifying Party fails to undertake the defense and investigation of any such Third Party Claim as provided in Section 12.5(a) , (x) the Indemnified Party against which such Indemnity Claim has been asserted shall have the right to undertake the defense, compromise, settlement and investigation of such Indemnity Claim on behalf of, and at the reasonable cost and expense of and for the account and risk of, the Indemnifying Party; (y) the Indemnifying Party shall cooperate with the Indemnified Party in such efforts and (z) the Indemnified Party shall keep the Indemnifying Party reasonably informed of the progress of the defense of any such Indemnity Claim.

 

12.6                            Settlement of Indemnity Claims .  The Indemnifying Party shall not, without the prior written consent of the Indemnified Party settle or compromise any Indemnity Claim or consent to the entry of any final Judgment that does not include as an unconditional term thereof the delivery by the claimant or plaintiff of a written release or releases from all Liability in respect of such Indemnity Claim of all Indemnified Parties affected by such Indemnity Claim and the sole relief for which are monetary damages that are paid in full by the Indemnifying Party.

 

12.7                            Right of Setoff .  Upon notice to the Company specifying in reasonable detail the basis therefor, the Purchaser may set off any amount to which it is entitled under this Article XIII against amounts otherwise payable to the Company under Section 2.1 hereof.

 

12.8                            Exclusive Remedy . The indemnification provisions of this Article XII shall be the sole and exclusive remedy of each party hereto for any breach of any representation, warranty or pre-closing covenant and each party hereby waives its right to seek any other remedy therefor.  Notwithstanding the foregoing, no party hereto waives such party’s right to bring an action based on fraud or seeking an equitable remedy.

 

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ARTICLE XIII

MISCELLANEOUS

 

13.1         Entire Agreement .  This Agreement together with the Ancillary Agreements and the certificates delivered hereunder constitutes the sole understanding of the parties with respect to the subject matter hereof.

 

13.2         Successors and Assigns .  The terms and conditions of this Agreement shall inure to the benefit of and be binding upon the respective successors and assigns of the parties hereto; provided however, that this Agreement may not be assigned (either by operation of law or otherwise) (a) by either Stockholders or the Company without the prior written consent of the Purchaser or (b) by the Purchaser without the prior written consent of the Stockholders and the Company.  Notwithstanding the foregoing, the Company may assign this Agreement and the Ancillary Agreements to its Stockholders in connection with a liquidation of the Company pursuant to terms and conditions reasonably satisfactory to the Purchaser. Any attempted assignment in violation of this Section 13.2 shall be null and void.

 

13.3         Headings .  The headings of the Articles, Sections, and paragraphs of this Agreement are inserted for convenience only and shall not be deemed to constitute part of this Agreement or to affect the construction hereof.

 

13.4         Amendment; Modification and Waiver .  No amendment, modification, or waiver of the terms of this Agreement shall be binding unless the same shall be in writing and duly executed by all of the parties hereto, except that any terms of this Agreement may be waived in writing at any time by the party that is entitled to the benefits of such waived term.  No single waiver of any term of this Agreement shall be deemed to or shall constitute, absent an express statement otherwise, a continuous waiver of such term or a waiver of any other term hereof.  No delay on the part of any party in exercising any right, power, or privilege hereunder shall operate as a waiver thereof.

 

13.5         Expenses .  Except as otherwise expressly provided herein, each of the parties hereto shall bear the expenses incurred by that party incident to this Agreement and the transactions contemplated hereby, including all fees and disbursements of counsel and accountants retained by such party, whether or not the transactions contemplated hereby shall be consummated.

 

13.6         Notices .  Any notice, request, instruction, or other document to be given hereunder by any party hereto to any other party shall be in writing and shall be given by delivery in person, by electronic facsimile transmission, by a nationally recognized overnight courier or by registered or certified mail, postage prepaid (and shall be deemed given when delivered if delivered by hand, when transmission confirmation is received if sent by facsimile, three days after mailing if mailed, one Business Day after deposited for domestic delivery with a nationally recognized overnight courier service if delivered by overnight courier, and three Business Days after deposited for international delivery with an internationally recognized overnight courier service), as follows:

 

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if to the Company, to:

 

ADViSYS, Inc.

2700 Research Forest Drive, Suite 180

The Woodlands, TX 77381

Attention:  Ronald O. Bergan

Fax No.:  282-296-7333

 

with a copy (which shall not constitute notice) to:

 

Vinson & Elkins LLP

2300 First City Tower

1001 Fannin Street

Houston, TX 77002

Attention:  Michael C. Blaney

Fax No.:  713-615-5487

 

if to Ronald O. Bergan or Mary Alice Bergen, to his or her attention at:

 

3300 North 7th Avenue

Fargo, ND 58108

 

with a copy (which shall not constitute notice) to:

 

Johnson, Rodenberg & Lauinger

107 Roberts Street

P.O. Box 2427

Fargo, ND 58108-2427

Attention:  Bruce D. Johnson

Fax No.:  701-235-6678

 

if to the Purchaser to:

 

VGX Pharmaceuticals, Inc.

450 Sentry Parkway

Blue Bell, PA 19422

Attention:  Kevin Rassas

Fax No.:  267-440-4242

 

with a copy (which shall not constitute notice) to:

 

Duane Morris LLP

30 South 17th Street

Philadelphia, PA 19103

Attention:  Kathleen M. Shay

Fax No.:  215-979-1020

 

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or at such other address for a party as shall be specified by like notice.

 

13.7         Governing Law .  This Agreement shall be construed in accordance with and governed by the laws of the Commonwealth of Pennsylvania applicable to agreements made and to be performed wholly within that jurisdiction.

 

13.8         No Third Party Beneficiaries .  This Agreement is intended and agreed to be solely for the benefit of the parties hereto and their permitted successors and assigns, and no other Person, including any employee of the Company shall be entitled to rely on this Agreement or accrue any Claim pursuant to, under, by, or through this Agreement.

 

13.9         Counterparts .  This Agreement may be executed in one or more counterparts, each of which shall for all purposes be deemed to be an original and all of which shall constitute the same instrument.

 

13.10       Drafting of Agreement .  Each party acknowledges that such party has had the opportunity to participate in the drafting of this Agreement and to review this Agreement with legal counsel of its choice, and there shall be no presumption that ambiguities shall be construed or interpreted against the drafter, and no presumptions made or inferences drawn because of the inclusion of a term not contained in a prior draft or the deletion of a term contained in a prior draft.

 

13.11       Savings Clause .  If any one or more of the terms hereof shall be adjudged, adjudicated, declared or deemed by a Governmental Authority to be invalid, illegal or void or unenforceable in any particular respect, this Agreement shall be construed as if the invalid, illegal, void or unenforceable term or part thereof had never been contained herein, and the remaining portions of this Agreement shall nonetheless continue in full force and effect.  If one or more of the terms, or part thereof, of this Agreement shall, for any reason, be adjudged, adjudicated, declared or deemed by any Governmental Authority to be excessive, then such terms shall be deemed reformed to the maximum limitations permitted by applicable law, and this Agreement shall be construed, by limiting and reducing its terms, so as to be enforceable to the extent compatible with the applicable law.

 

13.12       Injunctive Relief .  The covenants set forth in Sections 7.3 and 7.13 of this Agreement are a reasonable and necessary protection of the legitimate interests of the Purchaser and any failure of Company or either Stockholder to comply with the requirements of such Sections will cause the Purchaser irreparable injury.  The remedy at law for any breach or threatened breach of either such Section will be inadequate and, accordingly, the Purchaser shall, in addition to any other rights and remedies that the Purchaser may have, be entitled to seek an injunction or temporary restraining order to prevent such breach or threatened breach and to enforce specifically such Sections with any court of competent jurisdiction, in addition to any other remedy to which the Purchaser is entitled at law or in equity.

 

ARTICLE XIV

CERTAIN DEFINITIONS

 

14.1         “Administaff” means Administaff Companies II, L.P.

 

35



 

14.2         “Administaff Agreement” means that certain Client Services Agreement entered into between Administaff and the Company on March 17, 2003.

 

14.3         “Affiliate” means, with respect to any Person, any Person directly or indirectly controlling, controlled by or under common control with, such Person.  For the purposes of this definition, “control” (including, with correlative meaning, the terms “controlling,” “controlled by” and “under common control with”) shall mean the possession, directly or indirectly, of the power to direct or cause the direction of management and policies of such Person, whether through the ownership of voting securities, by contract or otherwise.

 

14.4         “Ancillary Agreements” means (a) the Assignment; (b) the IP Assignments; (c) the Subscription Agreement and (d) any other document specifically identified therein as an Ancillary Agreement.

 

14.5         “Business Day” means any day other than a day on which banks in Philadelphia, Pennsylvania are required or authorized to be closed.

 

14.6         “Claim” means any claim, suit, demand, cause of action, chose in action, right of recovery or right of set-off of whatever kind or description asserted by the claimant against any Person.

 

14.7         “Code” means the Internal Revenue Code of 1986, as amended.

 

14.8         “Company Contract” means any Contract to which Company is a party or by which it is bound.

 

14.9         “Contract” means any agreement, purchase order, sales order, contract or similar instrument, arrangement or commitment.

 

14.10       “EKD ” means electrokinetic delivery system.

 

14.11       “Encumbrances” means liens, security interests, pledges, equities, proxies, claims, charges, adverse claims, mortgages, rights of first refusal, preemptive rights, restrictions, encumbrances, easements, covenants, licenses, options or title defects of any kind whatsoever.

 

14.12       “Environment” means soil, surface waters, ground water, land, surface or subsurface strata and ambient air.

 

14.13       “Environmental Claim” shall mean any Claim, Proceeding, Order, directive, summons, complaint or citation asserted, filed or otherwise made by any Governmental Authority relating to Environmental Laws or Hazardous Substances.

 

14.14       “Environmental Law” means all foreign, federal, state and local laws, regulations, rules, codes, ordinances, common law, Orders and consent agreements relating to pollution, Hazardous Substances or the discharge, emission or release of materials into the Environment.

 

14.15       “ERISA” means the Employee Retirement Income Security Act of 1974, as amended.

 

36



 

14.16       “FD&C Act” shall mean the Federal Food, Drug & Cosmetics Act, as amended, or any successor statute, including all regulations promulgated thereunder.

 

14.17       “FDA” shall mean the United States Food and Drug Administration, or any successor agency thereto.

 

14.18       “GAAP” means United States generally accepted accounting principles for financial reporting in the United States, applied on a consistent basis.

 

14.19       “GHRH ” means growth hormone releasing hormone.

 

14.20       “Governing Documents” means, with respect to the Company or the Purchaser, the articles or certificate of incorporation and the bylaws of the applicable corporation; (b) all Security holders’ Contracts, voting Contracts, voting trust Contracts, joint venture Contracts, registration rights Contracts or other Contracts or documents relating to the organization, management or operation of such corporation or relating to the rights, duties and obligations of the Security holders of any such corporation and (c) any amendment or supplement to any of the foregoing.

 

14.21       “Governmental Authority” means any government, court, department, authority, commission, board, bureau, agency or official or other regulatory, administrative authority, whether (in each case) federal, foreign, state or local.

 

14.22       “Governmental Authorization” means any permit, license or other authorization given or otherwise made available by or under the authority of any Governmental Authority or pursuant to any Legal Requirement and required to:  (a) conduct the Business as currently conducted or (b) occupy, maintain, operate or use the Company’s assets or properties as currently maintained, operated or used.

 

14.23       “Hazardous Substance” shall mean any substance which is a “hazardous substance,” “hazardous waste,” “toxic substance,” “toxic waste,” “pollutant,” “contaminant” or words of similar import under any Environmental Law including, without limitation, the Comprehensive Environmental Response, Compensation and Liability Act (42 U.S.C. §9601 et seq. ), the Resource Conservation and Recovery Act (42 U.S.C. §6901 et seq. ), the Federal Water Pollution Control Act (33 U.S.C. §1251 et seq. ), and the Clean Air Act (42 U.S.C. §7401 et seq. ), and including, without limitation, any substance which contains polychlorinated biphenyls or gasoline, diesel fuel or other petroleum hydrocarbons or volatile organic compounds.

 

14.24       “Intellectual Property” means all intellectual property, confidential information, and proprietary information and any improvements, modifications and enhancements thereto, compilations and derivatives thereof, and all licenses related thereto, including, but not limited to, (a) letters patents and patent applications (including all reissuances, continuations, continuations-in-part, revisions, extensions and reexaminations thereof), including, without limitation, regional patents, certificates of invention and utility models, rights of license or otherwise under letters patent, certificates of invention and utility models patent disclosures and inventions (whether or not patentable and whether or not reduced to practice) (“ Patents ”); (b) trademarks, service marks, trade dress, trade names, logos, Internet domain names, brand names, brand marks, fictitious names assumed names and corporate names, together with any

 

37



 

adaptations combinations, derivations and translations thereof and the goodwill of the business associated with and symbolized by such trademarks, service marks, trade dress, trade names and corporate names, in each case whether or not registered; (c) published and unpublished works of authorship and mask works, whether copyrightable or not, including all statutory and common law copyrights associated therewith; in each case, whether or not registered; (d) all registrations, applications, reissues, divisionals, continuations, continuations-in-part, extensions and renewals for any of the terms listed in clauses (a), (b) and (c); (e) trade secrets and confidential business information; (f) websites; (g) all versions of computer programs, whether in source code or object code assembly language, compiler language, machine code, and all other computer instructions, code, and languages embodied in computer software of any nature whatsoever and all error corrections, updates, upgrades, enhancements, translations, modifications, adaptations, further developments, derivative works thereto; (“ Software ”); (h) lists of customers and potential customers (including any lists of electronic mail addresses or other contact information of customers and potential customers); formulae; compositions; know-how; research and development information; manuscripts; drawings; specifications; list of suppliers and service providers; pricing and cost information and records; test reports; manuals; financial, business, sales and marketing information and proposals, research, data, and plans; technical and computer data; databases; documentation; promotional materials and related information and (i) all copies and tangible embodiments thereof, including without limitation, any Software and databases; and other intellectual property, confidential information and proprietary rights, in each case in any medium, including digital, and in any jurisdiction, together with all causes of action, judgment, settlements, claims and demands of any nature related thereto, including the right to prosecute any past infringements or other violations thereof.

 

14.25       “IRS” means the Internal Revenue Service.

 

14.26       “Knowledge of the Company” and words of similar import means (i) for matters addressed in Sections 4.8 , 4.13 and 4.14 hereof, the actual knowledge of Ronald O. Bergan, Douglas R. Kern, Ruxandra Draghia Akli, Henry Hebel and JoAnne Greenwell, after reasonable inquiry with respect to such matters and (ii) for all other matters, the actual knowledge of such individuals.

 

14.27       “Legal Requirement” means any federal, state, local, municipal, foreign, international, multinational or other constitution, law, ordinance, principle of common law, code, regulation, statute or treaty.

 

14.28       “Losses” means any and all losses, Liabilities, damages (including incidental and consequential damages), penalties, obligations, awards, fines, deficiencies, interest, Claims, diminution in value, costs and expenses whatsoever (excluding attorneys’, consultants’ and other professional fees and disbursements) resulting from, arising out of or incident to any matter for which indemnification is provided under this Agreement.

 

14.29       “Liabilities” means with respect to any Person, means any liability or obligation of such Person of any kind, character or description, whether known or unknown, absolute or contingent, accrued or unaccrued, disputed or undisputed, liquidated or unliquidated, secured or unsecured, joint or several, due or to become due, vested or unvested, executory, determined,

 

38



 

determinable or otherwise, and whether or not the same is required to be accrued on the financial statements of such Person.

 

14.30       “Material Adverse Effect” means any circumstance or event that, individually or in the aggregate with any other circumstance or event could reasonably be expected to be, or is, material and adverse to the business, properties, operations, earnings, prospects, condition (financial or otherwise), assets, properties, results of operations or Liabilities of the Company.

 

14.31       “Order” means any award, decision, injunction, judgment, order, ruling, subpoena or verdict entered, issued, made or rendered by any Governmental Authority or any arbitrator.

 

14.32       “Permitted Encumbrances” means (a) liens for Taxes not yet due and payable or (b) minor imperfections of title, none of which, individually or in the aggregate, detracts from the value of the affected assets or properties, or impairs the use of the affected assets or properties or impairs the operation of the Business.

 

14.33       “Person” means an individual, corporation, partnership, association, limited liability company, trust, unincorporated organization, Governmental Authority, other entity or group.  For purposes of this definition, “group” means when two or more persons act as a partnership, limited partnership, syndicate, or other group for the purpose of acquiring, holding, or disposing of Securities of an issuer.

 

14.34       “Proceeding” means any action, arbitration, audit, hearing, investigation, litigation or suit commenced, brought, conducted or heard by or before, or otherwise involving, any Governmental Authority or arbitrator.

 

14.35       “Restricted Business ” means (a) the Business and (b) to the extent not otherwise covered by the definition of “Business”, the business of providing, developing, selling, manufacturing, marketing or otherwise commercializing, as applicable, (i) electroporation services or devices; (ii) EKDs; (iii) constant current devices; (iv) plasmid DNA products; (v) DNA delivery devices; (vi) GHRH (including species-specific GHRH for veterinary applications); (vii) formulation technologies including poly-L-glutamate and (viii) insulin-like growth factor 1 (IGF1) for human and veterinary applications.

 

14.36       “Schedules” means all of the Schedules made a part of this Agreement.

 

14.37       “Securities” with respect to any Person means any equity securities of such Person, including securities convertible into, exchangeable for, or carrying the right to acquire any equity securities of the Person, or subscriptions, warrants, options, rights (including anti-dilution rights), or other arrangements or commitments obligating such Person to issue of any equity securities or any interest therein of such Person.

 

14.38       “Straddle Period” means any complete Tax period that begins before and ends after the Closing Date.

 

14.39       “Tax” means any of the Taxes, where “ Taxes ” means (i) all federal, state, local or foreign taxes, charges, fees, imposts, levies or other assessments, including all income, gross receipts, capital, sales, use, ad valorem, value added, transfer, franchise, profits, inventory,

 

39



 

capital stock, license, withholding, payroll, employment, social security, unemployment, excise, severance, stamp, occupation, property and estimated taxes, customs duties, fees, assessments and charges of any kind whatsoever or (ii) all interest, penalties, fines, additions to tax or additional amounts imposed by any Taxing Authority in connection with any item described in clause (i) and (iii) any transferee liability in respect of any items described in clauses (i) or (ii) payable by reason of Contract, assumption, transferee liability, operation of law, Treasury Regulation Section 1.1502 6(a) (or any predecessor or successor thereof of any analogous or similar provision under any Legal Requirement) or otherwise.

 

14.40       “Taxing Authority” means the IRS and any other Governmental Authority responsible for the administration of any Tax.

 

14.41       “Tax Return” means any return, report or statement required to be filed with respect to any Tax (including any elections, declarations, schedules or attachments thereto, and any amendment thereof) including any information return, claim for refund, amended return or declaration of estimated Tax, and including, where permitted or required, combined, consolidated or unitary returns for any group of entities that includes the Company or any of its Affiliates.

 

[SIGNATURE PAGE FOLLOWS]

 

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IN WITNESS WHEREOF , each of the parties hereto has caused this Agreement to be executed on its behalf as of the date first above written.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

By:

/s/ Joseph Kim

 

Name:

Joseph Kim

 

Title:

President and Chief Executive Officer

 

 

 

 

 

ADVISYS INC.

 

 

 

By:

/s/ Douglas R. Kern

 

Name:

Douglas R. Kern

 

Title:

President and Chief Executive Officer

 

 

 

 

 

/s/ Mary Alice Bergan

 

Mary Alice Bergan

 

 

 

 

 

/s/ Ronald O. Bergan

 

Ronald O. Bergan

 



 

EXHIBIT A

 

Purchase Price Allocation

 


 

EXHIBIT B

 

ASSIGNMENT AND ASSUMPTION AGREEMENT

 

THIS ASSIGNMENT AND ASSUMPTION AGREEMENT (this “Assignment”), dated as of February 21, 2007, between VGX Pharmaceuticals, Inc., a Delaware corporation (the “Assignee”), and ADViSYS, Inc., a Delaware corporation (the “Assignor”).

 

Recitals :

 

WHEREAS, the Assignor, the Assignee, Ronald Bergan and Mary Alice Bergan have entered into an Asset Purchase Agreement dated as of even date herewith (the “Agreement”);

 

WHEREAS, pursuant to the Agreement, the Assignor has agreed to sell, assign, convey, transfer and deliver the Purchased Assets to the Assignee;

 

WHEREAS, pursuant to the Agreement, the Assignee has agreed to assume the Assumed Liabilities; and

 

WHEREAS, capitalized terms used but not otherwise defined herein shall have the meanings ascribed to them in the Agreement.

 

NOW, THEREFORE, in consideration of the foregoing and the respective representations, warranties, covenants and agreements set forth herein, and intending to be legally bound hereby, the parties hereto agree as follows:

 

1.                                        Assignment of Purchased Assets .  The Assignor, for good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, and intending to be legally bound, hereby sells, transfers, conveys and delivers to the Assignee, and the Assignee does hereby accept from the Assignor, all of the right, title and interest of the Assignor in and to all of the Purchased Assets free and clear of all Encumbrances, other than the Permitted Encumbrances.

 

2.                                        Assumption of Liabilities .  The Assignee hereby assumes and agrees to pay, perform and discharge the Assumed Liabilities.

 

3.                                        Modification and Waiver .  No amendment, modification, or alteration of the terms or provisions of this Assignment shall be binding unless the same shall be in writing and duly executed by the parties hereto, except that any of the terms or provisions of this Assignment may be waived in writing at any time by the party that is entitled to the benefits of such waived terms or provisions.  No single waiver of any of the provisions of this Assignment shall be deemed to or shall constitute, absent an express statement otherwise, a continuous waiver of such provision or a waiver of any other provision hereof (whether or not similar).  No delay on the part of any party in exercising any right, power, or privilege hereunder shall operate as a waiver thereof.

 



 

4.                                        Governing Law .  This Agreement shall be construed in accordance with and governed by the laws of the Commonwealth of Pennsylvania applicable to agreements made and to be performed wholly within that jurisdiction.

 

5.                                        Disputes .  The respective rights of the Assignor, on the one hand, and the Assignee, on the other, with respect to the Purchased Assets and the Assumed Liabilities assigned and assumed hereby shall be governed by the Agreement.  In the event of a conflict between this Assignment and the Agreement, the Agreement shall control.  All disputes between the Assignor and the Assignee arising out of the obligations of the parties under this Assignment or concerning the meaning or interpretation of any provisions contained herein shall be resolved in accordance with the Agreement.

 

6.                                        Counterparts .  This Assignment may be executed in one or more counterparts, each of which shall for all purposes be deemed to be an original and all of which shall constitute the same instrument.

 



 

IN WITNESS WHEREOF, the parties hereto have duly executed this Assignment as of the date first written above.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

 /s/ Joseph Kim

 

Name: Joseph Kim

 

Title: President & Chief Executive Officer

 

 

 

 

ADVISYS, INC.

 

 

 

 

 

 

 

By:

 /s/ Douglas R. Kern

 

Name: Douglas R. Kern

 

Title: President & Chief Executive Officer

 



 

EXHIBIT C

 

IP Assignment

 



 

EXHIBIT D

 

SUBSCRIPTION AGREEMENT

 

THIS SUBSCRIPTION AGREEMENT is made as of February 21, 2007, between VGX Pharmaceuticals, Inc. (the “Company”), a Delaware corporation, and ADViSYS, Inc., a Delaware corporation (the “Subscriber”).

 

WHEREAS, on the date hereof, the Company and the Subscriber entered into that certain Asset Purchase Agreement pursuant to which the Company agreed to purchase from the Subscriber, and the Subscriber agreed to sell to the Company the Purchased Assets, subject to the Asset Purchase Agreement; and

 

WHEREAS, in satisfaction of a portion of the purchase price for the Purchased Assets the Company will issue 924,219 shares of the Company’s Common Stock to the Subscriber;

 

WHEREAS, capitalized terms used but not otherwise defined herein shall have the meaning set forth in the Asset Purchase Agreement.

 

NOW, THEREFORE, in consideration of the foregoing, and of the mutual provisions and covenants contained herein, and for other good and valuable consideration, the receipt of which is hereby acknowledged, the Company and the Subscriber, intending to be legally bound, hereby agree as follows:

 

1.                                        Issuance of the Shares .  In partial consideration of the purchase of the Purchased Assets by the Company from the Subscriber, the Company agrees to issue to the Subscriber 924,219 shares of the Company’s Common Stock (the “Initial Shares”).  For purposes of this Agreement, the term “Shares” shall include the Initial Shares and any other shares of Common Stock or equity securities held by the Subscriber on or after the date hereof.

 

2.                                        Investment Representations .  The Subscriber hereby represents and warrants to the Company as follows:

 

(a)                                   The Subscriber is aware of the Company’s business affairs and financial condition and has had the opportunity to discuss the Company’s business, management and financial affairs with its management.  The Subscriber has substantial experience in evaluating and investing in private placement transactions of securities in companies similar to the Company so that it is capable of evaluating the merits and risks of its investment in the Company.  The Subscriber acknowledges that its investment in the Company is highly speculative and entails a substantial degree of risk.

 

(b)                                  The Subscriber is acquiring the Shares for investment for the Subscriber’s own account, not as a nominee or agent, and not with the view to, or for resale in connection with, any distribution thereof within the meaning of the Securities Act of 1933, as amended (the “Securities Act”), and the Subscriber has no present intention of selling, granting any participation in, or otherwise distributing the Shares.  The Subscriber does not presently have any contract, undertaking, agreement or arrangement with any person to sell, transfer or grant participation to such person or to any third person, with respect to any of the Shares.

 



 

(c)                                   The Subscriber understands that no public market now exists for any of the securities issued by the Company and that the Company has made no assurances that a public market will ever exist for the Company’s securities.  The Subscriber acknowledges that the Shares constitute “restricted securities” under the Securities Act and must be held indefinitely unless they are subsequently registered under the Securities Act or an exemption from such registration is available, and that the Company is under no obligation to register the Shares.

 

3.                                        Validity of Issuance .  The Initial Shares are validly issued, fully paid and nonassessable.

 

4.                                        Capitalization .  Exhibit A sets forth the authorized, issued and outstanding capital stock of the Company and a list of the holders of such capital stock as of the date of this Agreement.  Except as set forth on Exhibit A, the Company has not issued and is not obligated to issue any warrants, options or other rights to purchase or acquire any shares of its capital stock, or any securities convertible into such shares or any warrants, options or other rights to acquire any such convertible securities.

 

5.                                        Legends.   The certificate evidencing the Shares shall be endorsed with the following legend (in addition to any legend required under applicable securities laws or corporate laws or any other contract between the Subscriber and the Company):

 

THE SHARES EVIDENCED BY THIS CERTIFICATE HAVE BEEN ACQUIRED FOR INVESTMENT PURPOSES AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “ACT”), OR ANY STATE SECURITIES LAWS, AND MAY NOT BE PLEDGED, SOLD, OFFERED FOR SALE, TRANSFERRED OR OTHERWISE DISPOSED OF IN THE ABSENCE OF REGISTRATION UNDER OR EXEMPTION FROM SUCH ACT AND ALL APPLICABLE STATE SECURITIES LAWS.

 

THE SHARES REPRESENTED BY THIS CERTIFICATE ARE SUBJECT TO THE COMPANY’S RIGHTS OF FIRST REFUSAL AND A MARKET STAND-OFF RESTRICTION IN CONNECTION WITH ANY PUBLIC OFFERING BY THE COMPANY, WHICH ARE CONTAINED IN A STOCK SUBSCRIPTION AGREEMENT.  A COPY OF THE STOCK SUBSCRIPTION AGREEMENT IS ON FILE WITH THE SECRETARY OF THE COMPANY.

 

6.                                        Right of First Refusal .

 

(a)                                   The Subscriber shall give to the Company at least 60 days’ prior written notice of any proposed sale or other transfer by the Subscriber of any of the Shares.  Such notice shall describe the proposed sale or other transfer, the name and address of each party to the transaction and the price and other terms thereof.  Such notice shall constitute an offer from the Subscriber (the “Offer”) to sell the Shares to the Company at the same price and on the same other terms, which Offer by its terms shall remain open for a period of 30 days from the date of receipt of the Subscriber’s notice.

 

(b)                                  If the Company does not accept the Offer within such 30-day period, the Subscriber will have 60 days from the end of the 30-day period to complete the transaction with the persons specified in the Offer on terms and conditions that are no more favorable to such

 



 

persons or less favorable to the Subscriber than those set forth in the Offer.  If the transaction is not completed during such 60-day period, the procedures specified in this Agreement will thereafter apply to any proposed sale of such Shares.  As a condition to the transfer of any Shares other than to the Company in accordance with this Section 6, the Subscriber shall cause the transferee to execute and deliver to the Company an investment representation letter, which contains representations, warranties and agreements substantially identical to those set forth in this Section 6 and Sections 7 and 8  of this Agreement.

 

(c)                                   If all or a part of the consideration for the Shares under the Offer is not readily available to the Company (e.g., real estate or securities for which there is no established trading market) or otherwise cannot be precisely duplicated by the Company, a purchase by the Company will be made for a consideration and upon terms that constitute the reasonable economic equivalent of the price and terms of the Offer.  For these purposes, the promissory note of the Company will be considered the reasonable economic equivalent of the promissory note of the proposed transferee, notwithstanding any differences in financial condition.

 

(d)                                  The Company may assign its right to purchase Shares under this Section 6, in whole or in part, to any other person.

 

7.                                        Market Standoff Agreement .  In the event that the Company shall file a registration statement under the Securities Act (if at all) to register shares of its Common Stock or other securities, the undersigned agrees that the undersigned will not, to the extent requested by the Company and the underwriter of such securities, and during the period of duration specified by the Company and such underwriter following the effective date of each such registration statement, directly or indirectly sell, offer to sell, contract to sell (including, without limitation, any short sale), grant any option to purchase or otherwise transfer or dispose of (other than to donees who agree to be similarly bound) any securities of the Company held by the undersigned at any time during such period except Shares, if any, included in such registration (and the undersigned understands that there is no obligation on the part of the Company to register any securities of the Company held by the undersigned); provided, however, that: (a) all officers, directors and 1% or greater shareholders of the Company enter into similar agreements; and (b) such market stand-off time period may not exceed 180 days from the effective date of the registration statement.  Notwithstanding the foregoing, the obligations described in this Section 7 shall not apply to a registration relating solely to employee benefit plans on Form S-l or Form S-8 promulgated under the Securities Act or similar forms that may be promulgated in the future, or a registration relating solely to a Securities Exchange Commission Rule 145 transaction on Form S-4 or similar forms that may be promulgated in the future.  In order to enforce the foregoing covenant, the Company may impose stop transfer instructions with respect to the securities of the undersigned until the end of such market stand-off period.

 

8.                                        Drag-Along Rights .  In the event the Board of Directors of the Company approves a Sale Transaction (defined below), the Subscriber shall be obligated to, upon the request of the Board of Directors:  (a) sell, transfer and deliver, or cause to be sold, transferred and delivered, to the Company, his or her Shares on substantially the same terms applicable to the Sale Transaction (with appropriate adjustments to reflect the conversion of convertible securities, the redemption of redeemable securities and the exercise of exercisable securities as well as the relative preferences and priorities of preferred stock, if any); and (b) execute and

 



 

deliver such instruments of conveyance and transfer and take such other action as the Board of Directors may reasonably require in order to carry out the terms and provisions of this Section 8 (including, without limitation, voting the Subscriber’s Shares in favor of the Sale Transaction).  For purposes of this Section 8, “Sale Transaction” means (i) an acquisition of the Company by another entity by means of any transaction or series of related transactions (including, without limitation, any reorganization, merger, consolidation or sale of capital stock of the Company) that would result in the transfer of 50% or more of the outstanding voting power of the Company or in which the stockholders of the Company immediately prior to such transaction would own, as a result of such transaction, less than a majority of the voting securities, in the same relative proportions, of the successor or surviving entity immediately thereafter, or (ii) a sale of all or substantially all of the assets of the Company.

 

9.                                        Equitable Relief .  In the event of a breach by the Subscriber of any term of this Agreement, in addition to all of the other remedies that may be available under applicable law, the Company shall have the right to equitable relief, including, without limitation, the right to enforce specifically the terms of this Agreement by obtaining injunctive relief against any violation or non-performance hereof.

 

10.                                  General Provisions .

 

(a)                                   Any notice to be given under the terms of this Agreement to the Company shall be addressed to the Company in care of its Secretary, and any notice to be given to the Subscriber shall be addressed to the Subscriber at the address given beneath its signature hereto.  Either party may hereafter designate a different address for notices to be given to such party by a notice given pursuant to this Section 10(a).  Any notice shall have been deemed duly given when addressed as aforesaid and deposited (with postage prepaid) in the United States mail, sent by overnight courier (with charges prepaid), or sent by confirmed facsimile.

 

(b)                                  This Agreement shall be governed, construed and enforced in accordance with the internal laws of the State of Delaware.

 

(c)                                   Any provision of this Agreement may be amended and the observance thereof may be waived only by the prior written consent of the Company and the Subscriber.  No course of dealing between or among any persons having any interest in this Agreement shall be deemed effective to modify, amend or discharge any part of this Agreement or the Shares or any rights or obligations of any person under or by reason of this Agreement.

 

(d)                                  The Subscriber agrees upon request to execute any further documents or instruments necessary or desirable to carry out the purposes or intent of this Agreement.

 



 

IN WITNESS WHEREOF, the parties hereto have caused this Agreement to be duly executed as of the date first set forth above.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

/s/ Joseph Kim

 

Name:

Joseph Kim

 

Title:

President & Chief Executive Officer

 

 

 

 

ADVISYS, INC.

 

 

 

 

 

 

 

By:

/s/ Douglas R. Kern

 

Name:

Douglas R. Kern

 

Title:

President & Chief Executive Officer

 

 

 

 

Address and Facsimile Number of
Subscriber:

 

 

 

2700 Research Forest Drive, Suite 180

 

The Woodlands, TX 77381

 

Fax No.: 282-296-7333

 




EXHIBIT 10.33

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

Pf enex Expression Technology™

 

COMMERCIAL LICENSE AGREEMENT

 

This Agreement is effective as of the latest date of signing below and is by and between Dow Global Technologies Incorporated (“Dow”), a Delaware corporation having its principal offices at 2030 Dow Center, Midland, MI, 48674 USA and VGX Pharmaceuticals, Inc, a Delaware corporation (“VGX”) having a principal place of business at 450 Sentry Parkway, Blue Bell, PA 19422.

 

VGX further desires to secure a non-exclusive license to Dow’s Pf enex Expression Technology™ for the clinical and commercial production of Product.

 

Accordingly, in consideration of the premises and the mutual covenants of this Agreement, the parties hereto agree as follows:

 

Article 1                DEFINITIONS

 

1.01         Affiliates :  “Affiliates” shall mean any entity that, directly or indirectly through one or more intermediates, controls, is controlled by or is under common control with either VGX or Dow, where “controls”, “controlled by”, and “is under common control” means ownership, directly or indirectly, of fifty percent (50%) or more of the voting equity interest in the entity or the possession, direct or indirect, of the power to direct or cause the direction of the management and policies of that entity, whether through ownership or voting securities, by contract or otherwise.

 

1.02         Biological Material :  “Biological Material” shall mean Dow proprietary strains of transformed Pseudomonas fluorescens genetically engineered to express Product.  It includes Dow proprietary strains of Pseudomonas fluorescens , Dow proprietary plasmids and expression vectors for transforming Pseudomonas fluorescens , Dow proprietary nucleic acid and protein based probes relating to genetic transformation of Pseudomonas fluorescens , and Dow proprietary plasmids and expression vectors for transforming Pseudomonas fluorescens to express Product, and Dow proprietary nucleic acid and protein based probes relating to genetic transformation of Pseudomonas fluorescens that express Product.

 

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1.03         Calendar Year :  “Calendar Year” shall mean January 1 st  and ending December 31 st .

 

1.04         Calendar Quarter :  “Calendar Quarter” shall mean a three month period ending March 31, June 30, September 30 or December 31.

 

1.05         Commercially Reasonable Efforts :  “Commercially Reasonable Efforts” shall mean, with respect to the development, manufacture, or commercialization of a Product, that level of effort and resources customarily applied in the research-based biopharmaceutical industry to a product of similar commercial potential at a similar stage in its lifecycle, taking into consideration its safety and efficacy, cost to develop, the competitiveness of alternative products, its proprietary position, likelihood of regulatory approval, profitability and all other relevant factors.

 

1.06         Confidential Information :  “Confidential Information” shall mean any and all proprietary information including know-how, data, intellectual property, trade secrets, and other physical materials, and information (including without limitation, information related to technical, business, including customer names, information or addresses, and intellectual property matters), including information contained in Royalty Reports, Status Reports, Termination Royalty Report, Biological Material, Patent Rights, Know-How Technology, Product, information and know-how related to the Product owned or held by either party to this Agreement, now and in the future which is disclosed by either party to the other party in connection with this Agreement.  The Confidential Information shall include proprietary information disclosed in writing or other tangible form, including samples of materials.  If Confidential Information is disclosed orally, the Confidential Information shall be summarized in written form within thirty (30) days by the disclosing party and a copy provided to the recipient.

 

1.07         Contract Manufacturer :  “Contract Manufacturer” shall mean anyone under an agreement with VGX for the manufacture of Product.

 

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1.08         Effective Date :  “Effective Date” shall mean the last date of execution of this Agreement.

 

1.09         Field : “Field” shall mean production, clinical and commercial activities related to Product as it relates to human therapeutic use.

 

1.10         Foreign Regulatory Authority :  “Foreign Regulatory Authority” means any applicable regulatory agency, or other governmental entity or authority of any country or regulatory jurisdiction having responsibility in such country or regulatory jurisdiction for any regulatory approvals of any kind necessary for the development, pre-clinical and/or human clinical testing, manufacture, supply, marketing and/or sale of Product in such country or regulatory jurisdiction.  Such approvals include, but are not limited to, a new drug study or clinical license certificate under the Special Access Programme (SAP), the Medicines and Healthcare products Regulatory Agency, or the Federal Institute for Drugs and Medical Devices.

 

1.11         Improvements :  “Improvements” shall mean all discoveries and/or inventions (whether patented or not) made during the term of this Agreement by VGX which constitute (i) a modification of Biological Material; (ii) a modification of Know-How Technology; or (iii) which, if practiced, would infringe any of the claims of Patent Rights or which relate directly or indirectly to the Pf enex Expression Technology™.  Made as used herein means the discovery or invention was conceived or reduced to practice.   Improvements do not include any inventions or discoveries related to Product alone.

 

1.12         Improvement Report :  “Improvement Report” shall mean a written report that provides sufficient information so that Dow may practice such Improvement and if necessary such report shall also include the transfer of material necessary to practice Improvements.  Such report will be made January 31 st  of each year.

 

1.13         Know-How Technology :  “Know-How Technology” shall mean Dow’s technical

 

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information and materials, including without limitation, technology, data, bacterial strains, genetic constructs, computer software and algorithms for controlling fermentation vessels and related equipment, chemicals, inventions (patentable or otherwise), practices, methods, knowledge, know-how, skill, and experience related directly or indirectly to the Biological Material.

 

1.14         Licensed Territory :  “Licensed Territory” shall mean worldwide.

 

1.15         Net Sales :  “Net Sales” shall mean ******.

 

“Net sales” shall not include any consideration received with respect to a sale, use or other disposition of any Product as part of a clinical trial prior to the receipt of applicable Regulatory Approval for the Product.

 

Sales of a Product to an Affiliate or VGX Partner shall be excluded from Net Sales calculations, it being understood and agreed that sales of a Product by such Persons shall be included in Net Sales, as provided above.

 

******.

 

1.16         Parties :  “Parties” shall mean collectively Dow and VGX.

 

1.17         Party :  “Party” shall mean either Dow or VGX as the case may be.

 

1.18         Patent Rights :  “Patent Rights” shall mean Dow owned or controlled patent applications U.S. Application No. 10/590,095, 10/590,185, 10/994,138, 10/996,007, 11/400,840, 11/189,375 and U.S. Provisional Application titled “Codon Optimization Method” and any divisional, continuation, foreign equivalent, substitute, renewal, extension, reissue, reexamination, patents of addition, supplemental protection certificate, or application therefore or patent issuing therefrom.

 

1.19         Pf enex Expression Technology™ :  “ Pf enex Expression Technology™” shall mean Patent Rights and Know-How Technology related to or using directly or indirectly the Biological Material.

 

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1.20         Product :  “Product” shall mean the Vpr protein produced by the Production Strain as defined in the IND filing that shall be provided to DOW by VGX within ten (10) business days of the IND filing, expressed utilizing DOW’s proprietary Pf enex Expression Technology™, DOW Know-How Technology and/or the Production Strain. For the avoidance of doubt this Commercial License shall be for a single product. The amino acid sequence of the Product is defined in Appendix B of this Agreement.

 

1.21         Production Strain :  “Production Strain” shall mean a codon optimized Pseudomonas fluorescens strain that is derived from the Pf enex Expression Technology™ provided by Dow to VGX pursuant to this Agreement including VGX’s gene encoding for the Vpr protein and is the strain designated CS469-002 (cytoplasmic) created as part of the Services under the Letter Agreement between VGX and DOW with an effective date of February 9, 2006. Additionally, the five (5) other strains designated CS469-001, CS469-003, CS469-007, CS469-008, CS469-009 and developed under the services performed as part of the Letter Agreement between VGX and DOW (dated February 9, 2006) are also included under “Production Strain”.  The nucleotide sequences of each Production Strain are listed in Appendix C of this Agreement.

 

1.22         Royalty Report :  “Royalty Report” shall mean the written report due under this Agreement that report Royalties due under the Agreement.  The Royalty Report is due at the end of each Calendar Quarter.

 

1.23         Termination Royalty Report :  “Termination Royalty Report” shall mean the Royalty Report that is due after termination of this Agreement.

 

1.24         Third Party :  “Third Party” shall mean any person, organization, firm, corporation, partnership or entity other than Dow, VGX and their respective Affiliates.

 

1.25         VGX Partner :  “VGX Partner” shall mean anyone under an agreement with VGX relating to the development, marketing, promotion or distribution of Product.

 

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Article 2                                                LICENSE GRANT AND TRANSFER OF BIOLOGICAL MATERIAL

 

2.01         Grant to VGX :

 

(a)           Dow hereby grants to VGX and its Affiliates a non-exclusive, non-sublicensable, royalty-bearing license under the Patent Rights and Know-How Technology to use said Pf enex Expression Technology™ to make, have-made, use and sell Product for clinical and commercial use. In the exercise of its have-made rights under this section, VGX shall obtain Dow’s prior consent to VGX’s selection of a Contract Manufacturer, such consent not to be unreasonably withheld, delayed, or conditioned.  For the avoidance of doubt, it is understood that the purpose of requiring Dow’s consent is to provide reasonable assurance to Dow that the proposed Contract Manufacturer or VGX Partner is subject to enforceable agreements imposing the same confidentiality and limited use obligations with respect to Dow’s Confidential Information and the Pf enex Expression Technology™ as are undertaken by VGX under this Agreement, that the proposed Contract Manufacturer or VGX Partner is located in a country or countries subject to the rule of law and having functioning judicial systems for the enforcement, if necessary, of such obligations, and such parties agree in writing to be bound by terms and conditions at least as restrictive as those contained in this Agreement.  VGX, VGX Partner, and/or Contract Manufacturer shall not use any Biological Materials or Know-How Technology for research or production that is not specifically related to Product.   VGX shall not have any right to sublicense or transfer its rights under this Agreement.  Except for production of Product using the Pf enex Expression Technology™, VGX shall not use any Biological Materials or Know-How Technology for research or production.

 

(b)          Dow hereby grants to VGX and its Affiliates an exclusive, non-sublicensable, royalty-bearing license under the Patent Rights and Know-How Technology to the Pf enex Expression Technology™ to use the Production Strain to make and/or have made Product. In the exercise of its have-made rights under this section, VGX shall obtain Dow’s prior consent to VGX’s selection of a Contract Manufacturer, such consent not to be unreasonably withheld,

 

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delayed, or conditioned.

 

2.02         Notwithstanding the foregoing, VGX reserves the right to sublicense the Product to a Third Party.  Licensee shall assure the performance of the confidentiality and limited use obligations by its Contract Manufacturer or Licensee Partner and any such agreement shall include terms and conditions at least as restrictive as the terms and conditions in this Agreement.

 

2.03         Transfer of Biological Material and Technical Support :  Upon execution of this Agreement, Dow shall transfer Biological Material and the Know-How Technology package to VGX and the Know-How Technology package will be added as Appendix A.  Dow shall provide commercially reasonable technical assistance to VGX in the use of Biological Material and Know-How Technology at Dow’s prevailing hourly rate at the time technical assistance is provided.

 

2.04         Parties’ Roles :  VGX shall have complete control of purchasing and the detailed design, construction and operation (including maintenance) of the equipment necessary to produce Product using Pf enex Expression Technology TM .  Dow’s role is a technical advisor.  Among other things, this means that VGX is solely responsible for all of the following:  (i) safety, (ii) the selection, retention, supervision, performance, and payment of qualified engineer(s), constructor(s) and/or contractor(s), (iii) the detailed design, and the construction, operation and maintenance of the equipment necessary to produce Product using Pf enex Expression Technology TM  and all of its component parts, (iv) the inspection and the structural and mechanical conditions of any and all equipment and materials included in or added to the equipment necessary to produce Product using Pf enex Expression Technology TM , and (v) the training of the operating and maintenance personnel.

 

Article 3                                                MILESTONE AND MAINTENANCE PAYMENTS, ROYALTIES, AND ROYALTY REPORTS

 

3.01         Milestone & Maintenance  Payments:  As partial consideration for the

 

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granting of this license, VGX agrees to pay Dow:

 

(a)           the sum of ****** payable annually on each anniversary of the acceptance of an Investigational New Drug Application (IND) or the equivalent filing with a Foreign Regulatory Authority for the Product ******

 

(b)           the sum of ****** payable within thirty (30) days of submission for the Product of a Biologics License Application (BLA) or a New Drug Application (NDA) or the equivalent foreign regulatory authority anywhere in the world. ******;

 

(c)           the sum of ****** payable within thirty (30) days of receipt of marketing approval for the Product by the Food and Drug Administration or the equivalent foreign regulatory authority anywhere in the world.

 

For the avoidance of doubt these sums shall not be applied against any royalty payments due under Article IV hereof.

 

3.02         ******

 

3.03         Royalty and Royalty Reports :  Commencing in the calendar year in which the Product receives regulatory approval, VGX agrees to make written Royalty Reports to Dow quarterly, where Royalty Reports and Royalties are due quarterly, and VGX shall use commercially reasonable efforts to provide Royalty Reports within thirty (30) days of the end of each Calendar Quarter.  The Royalty Report must be submitted within sixty (60) days after the end of each Calendar Quarter.  Royalty Reports shall provide the total Net Sales of Product sold or value received during the preceding three (3) calendar months.  The first Royalty Report shall include all Net Sales of Product sold from the Effective Date of this Agreement to the date of said Royalty Report.  Such quarterly Royalty Reports shall provide the particulars of the sale of Product during such Calendar Quarter conducted by VGX during the preceding three (3) month period under this Agreement as are pertinent to a royalty accounting.  These shall include at least the following:

 

a.             total sale or transfer of Product and country of sale or transfer;

b.             deductions applicable, if any;

c.             total Royalties due on such sales or transfers; and

d.             payment of Royalty for the period of the Royalty Report based on Net Sales of Product.

 

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3.04         Royalty Report after Termination :  VGX shall provide a Termination Royalty Report to Dow within sixty (60) days after the date of any termination of this Agreement.  The Termination Royalty Report shall provide the total Product Net Sales up to such date of termination which were not previously reported to Dow.  Concurrently with the making of this Termination Royalty Report, VGX will pay to Dow all Royalties due.

 

3.05         Methods for Payment of Milestone Fees and Royalties:

 

(a)                       Each payment to Dow shall be made by wire transfer to the following destination:

 

Citibank NA, New York

ABA # 021000089

Account # 4074 – 8654

The Account of DGTI

Ref: royalty payment

 

(b)           Royalty reports shall be addressed to the following address:

 

DGTI

North American Financial and Statutory Accounting

2020 Dow Center

Midland, MI 48674

Attn: Treasury Accounting-MISC C.D.

 

or another location in the United States which Dow may subsequently designate from time to time by notice to VGX.

 

3.06         Late Payments :  If VGX fails to pay on the due date any amount which is payable under this Agreement, then, without prejudice to other sections of this Agreement, that amount shall bear interest compounded quarterly from the due date until payment is made in full, both before and after any judgment, at an annual rate of two (2) percentage points above the prime commercial lending rate quoted by Citibank, New York, NY on the day payment was due, until paid.

 

3.07         Status Reports :  Status reports shall be provided to Dow annually on January 31 st  

 

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of each Calendar Year. In each report VGX shall provide Licensor a clinical status report detailing the clinical status and projected commercialization date of each Product. VGX shall also provide the identity in each report of any research and development activities that employ the Patent Rights, Pf enex Expression Technology, Biological Material, or Know-How Technology.  These reports shall be sent to the address provided in Section 12.01, with a copy to the address provide in Section 3.05(b).

 

Article 4                                                RETENTION BY VGX AND ACCESS TO RECORDS

 

4.01         Records :  VGX shall keep records in accordance with customary accounting practices and in sufficient detail showing the amount of Products sold or otherwise transferred to Third Parties to permit the determination of royalties due to Dow.  VGX shall keep complete records relating to the activities and requirements under Article 3 such that records shall be in sufficient detail to enable the Royalties payable hereunder by VGX to be clearly and fully determined.  VGX further agrees to permit its books and records relating to the activities and requirements under Article 3, including without limitation such books and records relating to VGX Partner, to be examined no more than once in any two consecutive Calendar Quarters to verify the reports provided under this Agreement, such confidential examination to be made at Dow’s discretion by either: (i) an independent auditing firm appointed by and at the expense of Dow, which firm shall be reasonably acceptable to VGX, or (ii) Dow’s internal auditors.  Such records shall be kept and examination thereof shall be limited to a period of time no more than three (3) Calendar Years after the close of the fiscal year to which the records pertain.  In the event that VGX shall include a VGX Partner to the extent permitted hereunder, VGX shall (a) cause such VGX Partner to incorporate audit rights in favor of VGX substantially identical to the provisions of this Section 4.01, and (b) use commercially reasonable efforts to enforce such audit rights with respect to such VGX Partner.

 

4.02         Financial Information.  VGX shall provide to Dow annual audited financial statements, as may be prepared by or on behalf of VGX, within ninety (90) days after the close of each fiscal year during the Agreement Term, subject to assumption by Dow of customary and reasonable confidentiality obligations regarding such information.

 

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Article 5                                                CONFIDENTIALITY

 

5.01                        Confidential Information :  It is anticipated that it will be necessary, in connection with their obligations under this Agreement, for VGX and Dow to disclose to each other Confidential Information.

 

5.02                        Confidentiality and Limited Use :  With respect to all Confidential Information, both VGX and Dow agree as follows, it being understood that “recipient” indicates the Party receiving the confidential, proprietary information from the other “disclosing” Party. Confidential Information, Biological Material and Know-How Technology provided or disclosed to the recipient shall remain the property of the disclosing Party and shall be maintained in confidence by the recipient and shall not be provided or disclosed to Third Parties by the recipient and, further, shall not be used except for purposes contemplated in this Agreement.  Parties may disclose Confidential Information to officers, directors, employees, associates, agents, consultants, contractors, and Affiliates.  All confidentiality and limited use obligations with respect to the Confidential Information shall terminate fifteen (15) years after the termination date of this Agreement.

 

5.03                        Confidentiality Exceptions :  Notwithstanding any provision to the contrary, a Party may disclose Confidential Information of the other Party provided that the disclosing Party notifies the other Party and allows the other Party’s attorneys the chance to respond to the request to disclose Confidential Information directly with the court or government body, through the disclosing Party’s attorneys if necessary: (i) in connection with an order of a court or other government body or as otherwise required by or in compliance with law or regulations; provided that the disclosing Party provides the other Party with notice and cooperates with the other party in taking reasonable measures to obtain confidential treatment thereof; (ii) in confidence to recipient’s attorneys, accountants, banks and financial sources and its advisors, who are under an obligation of confidentiality; or (iii) in confidence, in connection with the sale of substantially all the business assets to which this Agreement relates, so long as, in the case of a disclosure under (ii) or (iii) hereof, the person or entity to which disclosure is made is bound to confidentiality on terms consistent with the terms set forth herein. The obligations of

 

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confidentiality and limited use shall not apply to any of the Confidential Information which:

 

(a)                               is publicly available by publication or other documented means or later becomes likewise publicly available through no act or fault of recipient; or

 

(b)                              is already known to recipient before receipt from the disclosing party, as demonstrated by recipient’s written records; or

 

(c)                               is made known to recipient by a Third Party who did not obtain it directly or indirectly from the disclosing party and who does not obligate recipient to hold it in confidence; or

 

(d)                              is independently developed by the recipient as evidenced by credible written research records of recipient’s employees or agents who did not have access to the disclosing party’s Confidential Information.

 

Specific information should not be deemed to be within any of these exclusions merely because it is embraced by more general information falling within these exclusions.

 

5.04                        Disclosures to Personnel :  Recipient agrees to advise those of its officers, directors, employees, associates, agents, consultants, contractors and Affiliates who become aware of the Confidential Information, of these confidentiality and limited use obligations and agrees, prior to any disclosure of Confidential Information to such individuals or entities, to make them bound by obligations of confidentiality and limited use no less onerous as those contained in this Agreement.  If VGX requests that Dow send information and/or materials to a third party contractor, VGX must make such request in writing to Dow and confirm that the third party contractor is bound by obligations of confidentiality and limited use no less onerous as those contained in this Agreement. If Dow requests that VGX send information and/or materials to a third party contractor, DOW must make such request in writing to VGX and confirm that the third party contractor is bound by obligations of confidentiality and limited use no less onerous

 

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as those contained in the agreement.

 

5.05                        Return of Confidential Information :  Upon termination of this Agreement, originals and copies of Confidential Information in written or other tangible form and all Biological Material shall be returned to the disclosing party by recipient or destroyed by recipient.  One copy of each document may be retained in the custody of the recipient’s legal counsel solely to provide a record of what disclosures were made.

 

5.06                        Confidential Status of Agreement :  Except insofar as required to be disclosed by law, rule, regulation, or order (including any of the rules and regulations of a relevant stock exchange or other governing body, specifically including the Securities & Exchange Commission (SEC)):  (a) this Agreement, the terms of this Agreement, and all financial records and reports kept and made in accordance with this Agreement, shall be deemed to be Confidential Information subject to the requirements of Sections 5.02, 5.03, and 5.04; and (b) neither Party shall (i) make public disclosures concerning this Agreement, its terms, or financial rights and obligations without obtaining the prior written consent of the other Party, which consent shall not be unreasonably withheld, conditioned, or delayed, (ii) respond to a request for information concerning this Agreement without informing the other Party before responding to such request, or (iii) publicly disclose financial terms, payments, records or reports kept or made hereunder unless under court order or under regulatory order, in each case after all appeals have been exhausted by the Parties.

 

5.07                        Remedies : Each Party acknowledges and agrees that due to the unique nature of the other Party’s Confidential Information, there may be no adequate remedy at law for any breach of its obligations hereunder, that any such breach may allow such Party or third parties to unfairly compete with such other Party resulting in irreparable harm to such other Party, except as otherwise noted in this Agreement.  Therefore, the breaching Party agrees to grant to the non-breaching Party, a world-wide, non-exclusive, sublicensable, irrevocable royalty-free license to make, use, or sell any patentable discovery resulting from breaching Party filing patent applications related to the unauthorized use of non-breaching Party’s Confidential Information.  Futhermore, upon

 

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any breach or any threat thereof, such other Party shall be entitled to seek appropriate equitable relief in addition to whatever remedies it might have at law.  Each Party will notify the other Party in writing immediately upon the occurrence of any such unauthorized release or other breach of which it is aware.

 

Article 6                                                DISCLAIMERS, INDEMNIFICATION, HOLD HARMLESS AND INSURANCE

 

6.01                        Representations and Warranties :  Dow has the right to license Patent Rights and Know-How Technology to the extent required for the grant of rights contained herein and has the power and authority to enter into this Agreement.

 

6.02                         No Other Warranties :

 

EXCEPT FOR THE EXPRESS WARRANTIES IN SECTION 6.01, DOW MAKES NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED, EITHER IN FACT OR BY OPERATION OF LAW, REGARDING:

 

PATENT RIGHTS, KNOW-HOW TECHNOLOGY, IMPROVEMENTS, PF ENEX EXPRESSION TECHNOLOGY™, PRODUCT AND BIOLOGICAL MATERIAL (INCLUDING, WITHOUT LIMITATION, THE VALIDITY OR SCOPE OF THE PATENT RIGHTS) OR INCLUDING, WITHOUT LIMITATION, PERFORMANCE, MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, OR THE NON-INFRINGEMENT OF ON THIRD PARTY PROPERTY RIGHTS.

 

6.03                        VGX Indemnification :  Except to the extent caused by the negligence or willful misconduct of Dow, VGX will defend and indemnify against, and hold Dow and its employees, directors, officers and agents harmless from, any loss, cost, liability or expense (including court costs and reasonable fees of attorneys and other professionals) incurred from any claim arising or alleged to arise out of the manufacture, use, distribution or sale of product by VGX; provided, however, that (i) VGX shall have sole control of such defense, (ii) Dow shall provide notice promptly to VGX of any actual or threatened claim of which Dow becomes aware, (iii) and VGX has no indemnification

 

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obligations or liability for any claim that is based solely upon the use by VGX of patent rights, biological material or Pf enex Expression Technology™.  In no event shall Dow be liable for any consequential, special, punitive, exemplary, indirect or incidental damages arising from this agreement or performance under this Agreement (including loss of anticipated profits, loss of use, or loss of product).  VGX will bear responsibility with regard to any matter arising out of or related to the VGX’s use of Dow’s Patent Rights, Know-How Technology, Improvements, Pf enex Expression Technology™, and Biological Material, except to the extent that such liability is due to negligence or willful misconduct of Dow. VGX has the duty to promptly notify Dow of any claim relating to Dow’s Patent Rights, Know-How Technology, Improvements, Pf enex Expression Technology™, and Biological Material or the Product.  Additionally, Dow has the right to assume and/or participate in the defense of any claim.

 

6.04                        Dow Indemnification :   Except to the extent caused by the negligence or willful misconduct of VGX, Dow will defend and indemnify against, and hold VGX, and its employees, officers, directors and agents harmless from any loss, cost, liability or expense *****.  Dow shall have sole control of such defense.  In no event shall VGX be liable for any consequential, special, punitive, exemplary, indirect or incidental damages arising from this agreement or performance under this Agreement (including loss of anticipated profits, loss of use, or loss of product).  This waiver applies regardless of whether or not the damages were foreseeable, and regardless of the theory or cause of action upon which the damages might be based.

 

6.05                        Limited Liability :  Neither party shall be liable to the other for any loss of profits, loss of business, interruption of business, indirect, special or consequential damages of any kind suffered by such other party for breach hereof, whether based on contract or tort claims or otherwise, even if such party has been advised of the possibility of such loss.

 

6.06                        VGX Insurance :  At all times while this Agreement is in effect, VGX will procure and maintain, at its own expense and for its own benefit, Comprehensive/Commercial General Liability Insurance, including coverage for Contractual Liability and Products Liability (including coverage for human clinical

 

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trials), having a bodily injury, death, and property damage combined single limit of at least ****** per occurrence.  Prior to commencement of any commercial product sales, VGX will procure and maintain, at its own expense and for its own benefit, Product Liability insurance having a bodily injury, death, and property damage combined single limit of at least ****** per occurrence.  The scope of the Product Liability coverage to be provided is to be similar to standard ISO forms (e.g. 1998 Commercial General Liability ISO form #CG 00 01 01 98 or CG 00 02 01 98). If the insurance to be provided is in a form similar to ISO policy form CG 00 02 01 98 (claims made form), then the policy shall contain an extended reporting period; of at least three (3) years; any Retroactive Date under said policy shall be no later than the Effective Date of this Agreement.

 

(a)  VGX will furnish Dow a certificate(s) from an insurance carrier or carriers (having a minimum AM Best rating of A-) showing all insurance set forth above.  The certificate(s) will include the following statement:  “The insurance certified hereunder is applicable to contracts between Dow Global Technologies Inc. and the Insured.  This insurance may be canceled or altered only after thirty (30) days written notice to Dow Global Technologies Inc.”  The insurance will be endorsed and the certificate(s) will confirm that the insurance (1) names Dow Global Technologies Inc. and its affiliates as additional insureds with respect to the liability of VGX arising from this Agreement; (2) provides that such insurance is primary and non-contributing to any liability insurance carried by Dow Global Technologies Inc.; and (3) provides that underwriters and insurance companies of VGX may not have any right of subrogation against Dow Global Technologies Inc. and its affiliates.  The insurance will contain no more than a typical industry deductible/SIR.

 

6.07                            Dow Insurance: At all times while this Agreement is in effect, Dow will maintain, at its own expense and for its own benefit, Comprehensive/Commercial General Liability (CGL) Insurance, including coverage for Contractual Liability, having a bodily injury, death, and property damage combined single limit of at least ****** per occurrence.  Upon request Dow will furnish VGX a certificate(s) from an insurance carrier or carriers (having a minimum AM Best rating of A-) showing all insurance set forth above.  The certificate(s) will include the

 

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following statement:  “The insurance certified hereunder is applicable to contracts between VGX Pharmaceuticals, Inc. and the Insured.  This insurance may be canceled or altered only after thirty (30) days written notice to VGX Pharmaceuticals, Inc.”  The insurance will be endorsed and the certificate(s) will confirm that (1) the insurance names VGX Pharmaceuticals, Inc and its Affiliates as additional insureds with respect to the liability of Dow arising from this Agreement; (2) provides that such insurance is primary and non-contributing to any liability insurance carried by VGX Pharmaceuticals, Inc.; and (3) provides that underwriters and insurance companies of Dow may not have any right of subrogation against VGX Pharmaceuticals, Inc. and its affiliates.  The insurance will contain no more than a typical industry deductible/SIR.

 

6.08                        Dow and VGX each agree to waive any right of recovery against the other and their respective Affiliates for any loss or damage of the type covered by the insurance to be procured and maintained under this Agreement regardless of whether or not such insurance is so maintained.

 

6.09                        Failure of any of the terms and conditions of the Insurance provision will be deemed a material breach of this Agreement.

 

Article 7                                                PATENTS, IMPROVEMENTS AND INFRINGEMENT OF DOW’S PATENT RIGHTS BY THIRD PARTIES

 

7.01 Grant-Back :

 

(a)  When an Improvement is made or discovered by VGX and/or its Affiliates, and such Improvement would not have arisen but for the presence of Pf enex Expression Technology TM , Biological Material, or Know-How Technology, and such Improvement relates to Pf enex Expression Technology TM , Biological Material, or Know-How Technology and do not include Product, VGX and its employees and/or its Affiliates hereby assign its entire right, title and interest in such Improvement to Dow and agree to cooperate with Dow in obtaining patent protection therefore at Dow’s cost, including, but not limited to the execution of any and all lawful papers in the U.S. and foreign patent offices.  Dow hereby grants VGX the ability to use such Improvement under the terms of

 

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this Agreement to the extent Dow has the right to convey the right to practice the Improvement to Licensee.

 

(b) Notwithstanding the foregoing, VGX shall not file any patent applications which disclose, describe or require the presence of Pf enex Expression Technology TM , Biological Material, or Know-How Technology absent consent from Dow.  For the avoidance of doubt, Dow agrees that it shall consent to disclosure in patent applications filed by VGX concerning VGX’s Product and the use of Dow’s Confidential Information as may be reasonably necessary to comply with the legal standards of disclosure and description.  Dow will have the right to review all sections and examples relating to Pf enex Expression Technology TM , Biological Material, or Know-How Technology thirty (30) days before the filing of such patent application.  If VGX files such an application outside the scope of 7.01(a), VGX and/or its Affiliates hereby grant Dow and its Affiliates irrevocable world-wide, exclusive, royalty-free licenses to such Improvement with the right to sublicense such rights to Third Parties, with the right to further sublicense.

 

7.02                        Patent Infringement :  Should VGX become aware of any infringement or alleged infringement of any Patent Rights, VGX shall promptly notify Dow in writing of the name and address of the alleged infringer and of the alleged acts of infringement, and provide any available evidence of the alleged acts of infringement.  Dow shall not be obligated to prosecute against any Third Party any suit for infringement of the aforesaid Patent Rights.  In the event that Dow decides to bring a patent infringement suit against the alleged Third Party infringer, VGX shall cooperate with Dow in the prosecution of any legal infringement action and agrees to provide Dow with pertinent data and evidence which may be helpful in the prosecution of such action of which it may have knowledge or which may be readily available to it.    Dow shall reimburse VGX for reasonable expenses incurred by VGX in assisting Dow in this matter.  Dow shall have the exclusive right (but not the obligation) to institute and conduct legal action against Third Party infringers of the Patent Rights, and to enter into such settlement agreements as may be deemed appropriate by Dow.  Dow shall receive the full benefits of any compensatory or punitive damages it obtains pursuant to bringing such suit.

 

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7.03                        Invalidity of Patent Rights :  If, at any time during this Agreement, Dow shall be unable to uphold the validity of any of the Patent Rights against any alleged infringer, VGX shall not have or assert any damage claim or a claim for refund or reimbursement against Dow.  In the event that Patent Rights are not upheld, royalties shall continue under this Agreement for VGX’s rights under Pf enex Expression Technology™.  However, in the event Patent Rights are not upheld and VGX is required to pay duplicate royalties to a Third Party, VGX shall pay Dow a reduced royalty rate of the royalty rate minus the duplicate royalty rate.  For the purpose of clarity any patent that has not been withdrawn, cancelled, abandoned, disclaimed, revoked or held unpatentable, invalid or unenforceable by a final decision of a court or other governmental agency of competent jurisdiction, which decision is unappealable or unappealed within the time allowed for appeal is considered to be valid and upheld.

 

7.04                        Challenges : VGX, VGX affiliates, VGX Partners, or sublicensees are not permitted directly or indirectly, to challenge the validity or enforceability of any of Patent Rights.  Such breach shall result in termination of this license.

 

Article 8                                                ASSIGNABILITY/SUCCESSION/CHANGE IN CONTROL

 

8.01                        VGX Assignability :  The rights acquired herein by VGX are not assignable or transferable in whole or part (by assignment, merger, succession, operation of law or otherwise) to any Third Party, without prior written permission from Dow, which Dow may withhold in its absolute discretion.  A change of control shall be considered for purposes of this paragraph a transfer of the Agreement.  A “change of control” means a change in the direct or indirect power to direct or cause the direction of the management and policies of VGX, whether through ownership or voting securities, by contract or otherwise, or the sale of fifty percent (50%) or more of the equity interest of VGX.  Any attempted assignment in violation of this provision shall be void.  In the event of a “change in control” of VGX, VGX shall promptly notify Dow of such change in control and Dow shall be permitted to terminate the Agreement subject to the provisions of Section 10.05.  Notwithstanding the foregoing, in the event that all of the equity and assets of VGX are acquired by a Third Party, Dow will provide its written permission for

 

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the Agreement to be transferred, provided such Third Party agrees in writing to be bound by the terms and conditions of this Agreement.

 

8.02                        Dow Assignability :   Dow shall have the right to assign this Agreement in connection with the reorganization, consolidation, spin-off, sale or transfer of assets related to that portion of its business pertaining to the subject matter of this Agreement, either alone or in conjunction with other Dow businesses.  In addition, Dow shall have the right to assign its respective rights or obligations and delegate its performance hereunder, in whole or in part, to any of its Affiliates.  In either event, the assignee shall agree in writing to be bound by all the terms of this Agreement.

 

Article 9                                                UNITED STATES GOVERNMENT EXPORT CONTROL REGULATIONS

 

9.01                        Export Control Regulations :  The Parties acknowledge that, in the course of performing under this Agreement, they may have access to certain information about the production and/or development of certain materials that are subject to export control regulations of the U.S. Department of Commerce and require a specific license from that agency before such technology can be transferred outside the United States or disclosed in the United States to nationals of other countries (unless such individuals have been granted U.S. citizenship, permanent residence, or legal status) (the “Controlled Technology”).  In addition to the obligations imposed by Article 5, each Party agrees not to release Controlled Technology that it may obtain from the other Party unless it is released to (i) a U.S. citizen, (ii) an individual who currently holds permanent resident or asylee status in the United States, or (iii) pursuant to a license granted by the U.S. Department of Commerce.

 

Article 10                                         TERM AND TERMINATION

 

10.01                  Term :  Unless previously terminated in accordance with the following provisions of this Article 10, this Agreement is effective as of the Effective Date of this Agreement and shall expire, on a country-by-country basis, (i) ten (10) years from the date of first sale of a Product, or (ii) expiration of the last to expire patent in the Patent Rights licensed hereunder, whichever is longer. Upon such expiration, all rights and licenses

 

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granted to VGX hereunder shall become irrevocable and fully paid-up.

 

10.02                    VGX’s Right to Terminate :  VGX shall have the right to terminate this Agreement one (1) Calendar Year after the Effective Date, provided VGX provides thirty (30) days written notice of such termination. Notwithstanding the previous sentence, in the event VGX withdraws its IND or no longer seeks regulatory approval for the Product, VGX shall have the right to terminate this agreement by providing thirty (30) days written notice of such termination.

 

10.03                    Dow’s Right to Terminate :  Dow shall have the right to terminate this Agreement by giving thirty (30) days written notice to VGX if substantial health and safety risks associated with the Pf enex Expression Technology™ used by VGX create a material risk to Dow (after taking into account VGX’s indemnification obligations, any insurance coverage provided by VGX or held by Dow, and defenses available to VGX (including without limitation product liability defenses and indemnification of government contractors) that cannot be mitigated short of termination.

 

10.04                    Termination of Agreement for Breach :

 

(a)                       Either Party may terminate this Agreement upon at least thirty (30) days written notice to the other Party should the other party commit a material breach of its obligations or be in default under any of the provisions of this Agreement if: (i) the Party in breach has failed to cure the breach or default within the same thirty (30) day notice period; (ii) if such breach or default cannot be cured within the thirty (30) day period, and the Party in breach has not taken reasonable steps to cure the breach or default.  If the breach or default can not be cured within the thirty (30) day period, the Party in breach shall notify the non-breaching Party of the steps taken toward curing such default or breach and the plans to totally cure such default or breach as soon as reasonably possible.  If the Party in breach fails to provide such notice, the non-breaching Party shall be free to terminate with immediate effect by notice to the Party in breach.

 

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(b)                      If VGX shall at any time default in the payment of any license fee, milestone fee or royalty or in the making of any report hereunder, or shall commit any material breach of any covenant herein contained, and shall fail to remedy any such default or breach within thirty (30) days after written notice thereof by DOW, then DOW may, at its option, terminate the license and all other rights herein granted, by giving notice to VGX in writing to such effect.

 

(c)                       Notwithstanding a Party’s right to terminate this Agreement as a result of a non-cured material breach by the other Party, the non-breaching Party shall not be prevented from seeking any other remedy which may be available to it in equity, including specific performance on the part of the party in breach.

 

(d)                      In the event that reasonable grounds for insecurity arise with respect to the performance of VGX’s obligations to timely pay any Royalty hereunder, Dow may in writing demand adequate assurance of due performance and, if VGX does not provide such adequate assurance in a manner reasonably satisfactory to Dow within thirty (30) days of such demand, Dow may, at it’s option, terminate this Agreement upon written notice to VGX.

 

10.05                    Insolvency :  Either Party may terminate this Agreement if, at any time:

 

(a)                       the other Party makes an assignment for the benefit of creditors or admits in writing its inability generally to pay or is generally not paying its debts as such debts become due;

 

(b)                      any decree or order for relief is entered against the other Party under any bankruptcy, reorganization, compromise, arrangement, insolvency, readjustment of debt, dissolution or liquidation or similar law;

 

(c)                       the other Party petitions or applies to any tribunal for, or consents to, the

 

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appointment of, or taking possession by, a trustee, receiver, custodian, liquidator or similar official, of such other Party or any substantial part of its assets, or commences a voluntary case under the bankruptcy law of any jurisdiction;

 

(d)                      any such petition or application is filed, or any such proceedings are commenced, against the other Party and such other Party by any act indicates its approval thereof, consent thereto or acquiescence therein, or an order, judgment or decree is entered appointing any such trustee, receiver, custodian, liquidator or similar official, or approving the petition in any such proceedings, and such order for relief, order, judgment or decree remains unstayed and in effect for more than sixty (60) days; or

 

(e)                       any order, judgment or decree is entered in any proceedings against the other Party decreeing the dissolution of such other Party and such order, judgment or decree remains unstayed and in effect for more than sixty (60) days.

 

10.06                    Effects of Termination/Survival :

 

(a)                       Expiration or termination of this Agreement shall not relieve the Parties of any obligation accruing prior to or upon such expiration or termination.  Accordingly, Dow rights under Article [7] shall survive expiration of termination of this Agreement for any reason.  Sections [3.04, Articles 5 and Article 6] shall survive expiration or termination of this Agreement and VGX shall not be relieved of any payment obligation that may have accrued prior to such expiration or termination.

 

(b)                      Upon an early termination of this Agreement due to a change of control of VGX, VGX shall, except in the case of a breach by VGX, insolvency by VGX as specified in this Article, be entitled to sell, for a period of twelve (12) months, remaining inventories of any Product(s) which are already in its possession.  Such sales shall be in accordance with this Agreement and

 

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the Parties shall continue to be obligated to make all applicable payments hereunder.

 

(c)                       After termination, except as provided in (b) above, any remaining Product and all Biological Material and Confidential Information relating, if any, shall be destroyed or shall be returned, respectively, and the destruction shall be certified to Dow by a representative of VGX.

 

10.07                    Termination for Violations :     Violation of the U.S. Export Control laws or regulations by VGX shall constitute grounds for Dow, in its sole discretion, to terminate this license agreement.  Failure to obtain any needed export control license may result in criminal liability under the United States law.

 

Article 11                                         ADVERTISING/PUBLICITY

 

11.01                    Neither the granting of the license herein granted by Dow nor the acceptance of the milestone payments or royalties hereunder by Dow shall constitute Dow’s approval of, or acquiescence in, advertising or other business practices of VGX, nor an approval of or acquiescence in any use of the corporate name of Dow, use of the name(s) of the inventors of the Patent Rights licensed, in connection with the manufacture, advertising, use or sale of Product, and Dow hereby expressly reserves all rights of actions with respect thereto.

 

11.02                    Dow and VGX hereby agree to issue a joint press release upon signing of this Agreement.  The wording of said press release shall be mutually agreed by both parties prior to issuance.

 

Article 12                                         NOTICES

 

12.01 Notices :  Any notice or other communication required or permitted to be given by either party under this Agreement shall be given in writing and shall be effective when delivered, if delivered by hand, reputable courier service or five days after mailing if mailed by registered or certified mail, postage prepaid and return receipt requested, addressed to each party at the following addresses or such other address as may be

 

24



 

designated by written notice by either Party:

For Dow Global Technologies Inc.:

Dowpharma – Business Leader

The Dow Chemical Company

5501 Oberlin Drive

San Diego, CA 92121

 

With a copy to:

The Dow Chemical Company

9330 Zionsville Road

Indianapolis, IN 46268

Attention: General Patent Counsel

 

For VGX:

 

VGX Pharmaceuticals, Inc.

450 Sentry Parkway

Blue Bell, PA 19422

Attention: J. Joseph Kim

 

Article 13                                         MISCELLANEOUS

 

13.01                    Severability :  If any clause, provision, or section of this Agreement attached hereto, shall, for any reason, be held illegal, invalid or unenforceable, the parties shall negotiate in good faith and in accordance with reasonable standards of fair dealing, a valid, legal, and enforceable substitute provision or provisions that most nearly reflect the original intent of the parties under this Agreement in a manner that is commensurate in magnitude and degree with the changes arising as a result of any such substitute provision or provisions.  All other provisions in this Agreement shall remain in full force and effect and shall be construed in order to carry out the original intent of the parties as nearly as possible (consistent with the necessary reallocation of benefits) and as if such invalid, illegal, or unenforceable provision had never been contained herein.

 

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13.02                    Merger of Understanding :  Except for the Confidentiality Agreement signed December 12, 2005 and the Services agreement signed on February 8, 2006 this Agreement constitutes the entire Agreement between the Parties regarding the subject matter hereof and all prior negotiations and understandings between the parties are deemed to be merged into this Agreement.

 

13.03                    Force Majeure :  Neither of the Parties shall be liable for any default or delay in performance of any obligation under this Agreement caused by any of the following: Act of God, war, terrorism, riot, fire, explosion, accident, flood, sabotage, compliance with governmental requests, laws, regulations, orders or actions, national defense requirements or any other event beyond the reasonable control of such Party; or labor trouble, strike, lockout or injunction (provided that neither of the Parties shall be required to settle a labor dispute against its own best judgment).   The party invoking the provisions of this Section shall give the other Party written notice and full particulars of such force majeure event.  Both Dow and VGX shall use reasonable business efforts to mitigate the effects of any force majeure on their respective part.

 

13.04                    Relationship of the Parties : The relationship of Dow and VGX is strictly one of independent contractors and the parties acknowledge that this Agreement does not create a joint venture, partnership, or the like, between them.  VGX and DOW shall always remain independent contractors in its performance of this Agreement.  Neither party to this Agreement shall have any authority to employ any person as an employee or agent for or on behalf of the other party to this Agreement for any purpose, and neither party to this Agreement, nor any person performing any duties or engaging in any work at the request of such party, shall be deemed to be an employee or agent of the other party to this Agreement.

 

13.05                    Choice of Law; Submission to Jurisdiction :  All questions with respect to the construction of this Agreement and the rights and liabilities of the Parties hereto shall be determined in accordance with the laws of the State of Delaware applicable to business arrangements entered into and performed entirely within the State of Delaware.  The

 

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Parties hereto irrevocably (a) submit to the exclusive personal jurisdiction of any state court or federal court in the State of Delaware in any suit, action or other legal proceeding relating to this Agreement; (b) agree that all claims in respect of any such suit, action or other legal proceeding may be heard and determined in, and enforced in and by, any such court; and (c) waive any objection that they may now or hereafter have to venue in any such court or that such court is an inconvenient forum.

 

13.06                    Provisions Contrary to Law :  In performing this Agreement, the Parties shall comply with all applicable laws and regulations.  Nothing in this Agreement shall be construed so as to require the violation of any law, and wherever there is any conflict between any provision of this Agreement and any law the law shall prevail, but in such event the affected provision of this Agreement shall be affected only to the extent necessary to bring it within the applicable law.

 

13.07                    Remedies :  Except as otherwise expressly stated in this Agreement, the rights and remedies of a party set forth herein with respect to failure of the other to comply with the terms of this Agreement (including, without limitation, rights of full termination of this Agreement) are not exclusive, the exercise thereof shall not constitute an election of remedies and the aggrieved party shall in all events be entitled to seek whatever additional remedies may be available in law or in equity.

 

13.08                    Fees :  Except as otherwise provided herein, each Party shall bear its own legal fees incurred in connection with the transactions contemplated hereby.

 

13.09                    Headings :  Headings herein are for convenience of reference only and shall in no way affect interpretation of this Agreement.

 

13.10                    Counterparts :  This Agreement may be executed in any number of counterparts with the same effect as if all parties had signed the same document. All such counterparts shall be deemed an original, shall be construed together and shall constitute one and the same instrument.

 

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13.11                    Appendices :  The appended Appendices and any modifications or amendments thereof form an integral part of this Agreement.

 

IN WITNESS WHEREOF, the Parties hereto have understood, agreed to and caused this Agreement to be executed in duplicate originals by their duly authorized representatives as of the date written beneath their respective signatures.

 

Dow Global Technologies Inc.

 

VGX Pharmaceuticals, Inc.

(Licensor)

 

(VGX)

 

 

 

 

 

By:

/s/ James M. Blatt

 

By:

/s/ J. Joseph Kim

 

 

 

 

 

Name:

James M. Blatt

 

Name:

J. Joseph Kim

 

 

 

 

 

Title:

President

 

Title:

President and C.E.O.

 

 

 

 

 

Date:

April 18, 2007

 

Date:

March 13, 2007

 

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EXHIBIT 10.34

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

EXCLUSIVE LICENSE AGREEMENT

BAYLOR COLLEGE OF MEDICINE

VGX PHARMACEUTICALS, INC.

 

RE: OTA 92-14, 98-24, 98-25, 98-36, 02-001, 02-028, 02-080, 03-025, 03-065, 07-019, and 07-055.

 

This Exclusive License Agreement (hereinafter called “Agreement”), to be effective as of the 9th day of May, 2007 (hereinafter called “Agreement Date”), is by and between Baylor College of Medicine (hereinafter called “BAYLOR”), a Texas nonprofit corporation having its principal place of business at One Baylor Plaza, Houston, Texas 77030, and VGX Pharmaceuticals, Inc., a corporation organized under the laws of Delaware and having a principal place of business at 455 Sentry Parkway, BlueBell, PA, 19422, and its Affiliates (hereinafter, collectively referred to as “VGX”).

 

WITNESSETH:

 

WHEREAS, BAYLOR is the owner of the Patent Rights as defined below; and

 

WHEREAS, BAYLOR is willing to grant a royalty bearing, worldwide, exclusive license to the Patent Rights to VGX on the terms set forth herein; and

 

WHEREAS, VGX desires to obtain said exclusive license under the Patent Rights.

 

NOW, THEREFORE, for and in consideration of the premises and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereto expressly agree as follows:

 

1.                                       DEFINITIONS AS USED HEREIN

 

1.1                                The term “Affiliates” shall mean any legal entity that is controlling, controlled by, or under common control with VGX or a corporation, partnership, joint venture or other entity of which the common stock or other equity ownership thereof is twenty five percent (25%) or more owned by VGX.

 

1.2                                The term “Field” shall mean any and all applications in humans.

 

1.3                                The term “Legal Costs” shall mean all legal fees and expenses, filing or maintenance fees, assessments and all other costs and expenses related to

 

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prosecuting, obtaining and maintaining patent protection on the Patent Rights in the United States and foreign countries.

 

1.4                                The term “Licensed Product(s)” shall mean any product, process or service that incorporates, utilizes or is made with the use of the Patent Rights.

 

1.5                                The term “Net Sales” shall mean the gross amount of monies or cash equivalent or other consideration which is billed, invoiced or received (whichever occurs first) for sales, leases or other modes of transfer of Licensed Products by VGX or sublicensees, less:

 

(i)

customary trade, quantity or cash discounts and rebates to the extent actually allowed and taken;

 

 

(ii)

amounts repaid or credited to customers by reason of rejections or returns;

 

 

(iii)

to the extent separately stated on purchase orders, invoices or other documents of sale, taxes and/or other governmental charges which are actually paid by or on behalf of VGX or sublicensees for the production, sale, transportation, delivery or use of a Licensed Product; and

 

 

(iv)

reasonable charges for delivery or transportation provided by third parties, if separately stated.

 

The term “Net Sales” in the case of non-cash sales, shall mean the fair market value of all equivalent or other consideration received by VGX or sublicensees for the sale, lease or transfer of Licensed Products.

 

1.7                                The term “Party” shall mean either VGX or BAYLOR, and “Parties” shall mean VGX and BAYLOR.

 

1.8                                The term “Patent Rights” shall mean the patents and/or patent applications identified in Appendix A.

 

1.9                                The term “Sublicensing Revenue” shall mean all (i) cash, (ii) sublicensing fees and (iii) all other payments and the cash equivalent thereof, which are paid to VGX by the sublicensees of the Patent rights hereunder, but excluding the following payments:

 

(a)

payments made in consideration for the issuance of equity or debt securities of VGX to the extent not exceeding the fair market value thereof;

 

 

(b)

that portion of payments for direct or fully burdened expenses (collectively not to exceed one hundred fifty percent (150%) of direct expenses) associated with research or development as calculated in accordance with GAAP, to the extent that such expenses are separately listed and part of the sublicense;

 

 

(c)

royalties on sales of Licensed Products by the sublicensee (payment for which has been otherwise provided in Paragraph 4.2 herein); and

 

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(d)

payments for supply of Licensed Products for use in clinical trials by or on behalf of, or for resale by, the sublicensee.

 

2.                                       GRANT OF LICENSE

 

2.1                                License Grant. Subject to the reservations of rights set forth in Paragraph 2.2, BAYLOR hereby grants to VGX an exclusive, worldwide, sublicensable license under the Patent Rights to make, have made, use, market, sell, offer to sell, lease and import Licensed Products in the Field.

 

2.2                                Restrictions on License. The grant in Section 2.1 shall be further subject to, restricted by and non-exclusive with respect to:

 

(i)                        t he making under or using of the Patent Rights by BAYLOR for non-commercial research, patient care, teaching and other educationally related purposes;

 

(ii)                     the making under or using of the Patent Rights by the developers for non-commercial research purposes at academic or research institutions;

 

(iii)                  any non-exclusive license of the Patent Rights that BAYLOR grants to other academic or research institutions for non-commercial research purposes;

 

(iv)                 the making under or using of the Patent Rights by academic and research institutions for non-commercial research purposes; and

 

(v)                    any non-exclusive license of the Patent Rights that BAYLOR is required by law or regulation to grant to the United States of America or to a foreign state pursuant to an existing or future treaty with the United States of America.

 

2.3                                Government Reservation.   Rights under this Agreement are subject to rights required to be granted to the Government of the United States of America pursuant to 35 USC Section 200-212, including a nonexclusive, nontransferable, irrevocable, paid-up license to practice or have practiced for or on behalf of the United States the subject inventions throughout the world.

 

3.                                       MARKETING EFFORTS

 

VGX shall use reasonable efforts, as defined herein, to effect assiduously the introduction of Licensed Products into the commercial market as soon as practicable.  VGX shall supply an annual progress report as per the terms of Paragraph 5.1.

 

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4.                                       PAYMENTS

 

4.1                                License Execution Fee. As partial consideration for the rights conveyed by BAYLOR under this Agreement, VGX shall pay BAYLOR a license fee of twenty five thousand dollars ($25,000) within ten (10) days of the Agreement Date.

 

4.2                                Royalty on Net Sales. In addition to the foregoing, VGX or its sublicensee shall pay BAYLOR a royalty of ****** of Net Sales.  Such royalties shall be payable as provided in Section 5.

 

4.3                                Annual Maintenance Fee. Beginning on the second (2 nd ) anniversary of the Agreement Date and up to the date upon which the first milestone payment becomes due, VGX shall pay an Annual Maintenance Fee of twenty five thousand dollars ($25,000), with the payment being due on the anniversary of the Agreement Date. This Annual Maintenance Fee shall be creditable against the milestone payment(s) stipulated in Paragraph 4.4, such that the Annual Maintenance Fee shall be creditable against a Milestone Payment paid to BAYLOR during the same calendar year. Only one (1) such Annual Maintenance Fee credit per calendar year can be assessed against a Milestone Payment.

 

4.4                                Milestone Payments. VGX shall also pay BAYLOR the following milestone payments set forth below:

 

(i) First Clinical Indication:

 

 

Initiation of a Phase I Clinical Trial:

 

Seventy five thousand dollars ($75,000)

Initiation of a Phase II Clinical Trial:

 

One hundred thousand dollars ($100,000)

Initiation of a Phase III Clinical Trial:

 

Two hundred fifty thousand dollars ($250,000)

First Commercial Sale of Licensed Product:

 

Five hundred thousand dollars ($500,000)

 

 

 

(ii) Second Clinical Indication:

 

 

Initiation of a Phase II Clinical Trial:

 

******

Initiation of a Phase III Clinical Trial:

 

******

First Commercial Sale of a Licensed Product:

 

******

 

 

 

(iii) Third Clinical Indication:

 

 

Initiation of a Phase II Clinical Trial:

 

******

Initiation of a Phase III Clinical Trial:

 

******

First Commercial Sale of Licensed Product:

 

******

 

VGX shall notify BAYLOR in writing within thirty (30) days upon the achievement of each milestone, such notice to be accompanied by payment of the appropriate milestone payment.  Milestones are to be paid regardless of whether VGX or VGX’s sublicensee attains such milestone.

 

4.5                                Sublicensing Revenue. In addition to the foregoing fees and royalties, VGX agrees to pay to BAYLOR the following percentage of all Sublicensing Revenue for any sublicense of the Patent Rights signed during the time intervals listed below:

 

4



 

(i)

From the Agreement Date to twelve (12) months after the Agreement Date:   ****** .

 

 

(ii)

From twelve (12) months and one day after the Agreement Date to twenty-four (24) months after the Agreement Date:   ****** .

 

 

(iii)

From twenty-four (24) months and one day after the Agreement Date to thirty-six (36) months after the Agreement Date:   ****** .

 

 

(iv)

From thirty-six (36) months and one day after the Agreement Date and thereafter:   ****** .

 

Monies paid to VGX to fund research and development or clinical studies, or paid in the form of loans to, or as an equity investment in, VGX, or royalties based upon Sales or Net Sales by the sublicensee (which are otherwise payable under Paragraph 4.2) are not subject to any payment to Baylor, except to the extent and only to the extent such monies are paid to VGX as a substitute, wholly or in part, for a royalty on Sales of Licensed Products or for license initiation, maintenance or other related fees and payments covered by this Agreement. Sublicensing Revenue that is a percentage of milestone payments received by VGX from a sublicensee shall be fully creditable against the milestone payments payable to BAYLOR by VGX under Paragraph 4.4 of this Agreement.

 

4.6                                Failure to Make Payment. Should VGX fail to make any payment whatsoever due and payable to BAYLOR hereunder, BAYLOR may, at its sole option, terminate this Agreement as provided in Section 10.

 

5.                                       REPORTING

 

5.1                                Annual Progress Report. No later than sixty (60) days after December 31 of each calendar year, VGX shall provide to BAYLOR a written annual progress report describing progress on research and development, regulatory approvals, manufacturing, sublicensing, marketing and sales during the most recent twelve (12) month period ending December 31 and plans for the forthcoming year as it relates to the technology covered by the Agreement.  If multiple technologies are covered by the Agreement, the progress report shall provide the information set forth above for each technology.  VGX shall also provide any reasonable additional data BAYLOR requires to evaluate VGX’s performance.

 

5.2                                Sale of Licensed Product. VGX shall report to BAYLOR the date of first sale of Licensed Products in each country within thirty (30) days of occurrence.

 

5.3                                Royalty Report Format. VGX shall submit to BAYLOR within thirty (30) days after March 31, June 30, September 30 and December 31, a royalty report setting forth for such calendar quarter at least the following information:

 

(i)                        the number of Licensed Products sold by VGX and sublicensees in each country;

 

(ii)                     total billings for such Licensed Products;

 

(iii)                  deductions applicable to determine the Net Sales thereof;

 

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(iv)                 the amount of Sublicensing Revenue received by VGX;

 

(v)                    the amount of royalty due thereon, or, if no royalties are due to BAYLOR for any reporting period, the statement that no royalties are due; and

 

(vi)                 the amount of other payments due BAYLOR, including but not limited to, milestone payments, minimum royalty payments and maintenance fee payments.

 

Such report shall be certified as correct by an officer of VGX and shall include a detailed listing of all deductions from royalties and other payments.  After termination or expiration of this Agreement, a final payment shall be made by VGX covering the whole or partial calendar quarter.  VGX shall pay to BAYLOR with each such royalty report the amount of royalties and other payments due with respect to such calendar quarter.  If multiple technologies are covered by the Agreement, VGX shall specify which Patent Rights are utilized for each Licensed Product included in the royalty report by citing the applicable BLG number listed on the front page of the Agreement.

 

5.4                                Payment Terms. All payments due hereunder shall be deemed received when funds are credited to BAYLOR’s bank account and shall be payable by check or wire transfer in United States dollars.  For sales of Licensed Products in currencies other than the United States, VGX shall use exchange rates published in The Wall Street Journal on the last business day of the calendar quarter that such payment is due.  No transfer, exchange, collection or other charges, including any wire transfer fees , shall be deducted from such payments.

 

5.5                                Late Payments. Late payments shall be subject to a charge of one and one-half percent (1.5%) per month, the interest being compounded annually, or two hundred fifty dollars ($250.00), whichever is greater.  VGX shall calculate the correct late payment charge, and shall add it to each such late payment.  Said late payment charge and the payment and acceptance thereof shall not negate or waive the right of BAYLOR to seek any other remedy, legal or equitable, to which it may be entitled because of the delinquency of any subsequent payment.

 

5.6                                Address for Payments. If payments are sent by check, they shall be sent to the address listed in Paragraph 15.1.  If payments are sent by wire transfer, they shall be sent using the wiring instructions sent by BAYLOR.

 

5.7                                Merger or Acquisition. In the event of acquisition, merger, change of corporate name, or change of make-up, organization, or identity, VGX shall notify BAYLOR in writing within thirty (30) days of such event.

 

5.8                                Small Entity Status. If VGX or sublicensee (or optionee) does not qualify as a “small entity” as provided by the United States Patent and Trademark Office, VGX must notify BAYLOR immediately.

 

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6.                                       RECORDS AND INSPECTION

 

VGX shall maintain or cause to be maintained a true and correct set of records pertaining to the Net Sales under this Agreement.  During the term of this Agreement and for a period of two (2) years thereafter, VGX agrees to permit an accountant selected and paid by BAYLOR and reasonably acceptable to VGX to have access during ordinary business hours to such records as are maintained by VGX as may be necessary, in the opinion of such accountant, to determine the correctness of any report and/or payment made under this Agreement.  In the event that the audit reveals an underpayment of royalty by more than five percent (5%) for the period being audited, the cost of the audit shall be paid by VGX.  If the underpayment is less than five percent (5%) but more than two percent (2%) for the period being audited, VGX and BAYLOR shall each pay fifty percent (50%) of the cost of the audit.  Such accountant shall maintain in confidence, and shall not disclose to BAYLOR, any information concerning VGX or its operations or properties other than information directly relating to the correctness of such reports and payments.

 

7.                                       SUBLICENSES

 

All sublicenses granted by VGX of the Patent Rights under this Agreement shall be subject to the terms of this Agreement.  VGX shall be responsible for its sublicensees and shall not grant any rights which are inconsistent with the rights granted to and obligations of VGX hereunder.  Any act or omission of a sublicensee which would be a breach of this Agreement if performed by VGX shall be deemed to be a breach by VGX of this Agreement.  Each sublicense agreement granted by VGX shall include an audit right by BAYLOR of the same scope as provided in Paragraph 6 hereof with respect to VGX.  No such sublicense agreement shall contain any provision which would cause it to extend beyond the term of this Agreement.  VGX shall give BAYLOR prompt notification of the identity and address of each sublicensee with whom it concludes a sublicense agreement and shall supply BAYLOR with a copy of each such sublicense agreement.

 

8.                                       PATENTS AND INFRINGEMENT

 

8.1                                Patent Prosecution Responsibility. For the term of this Agreement, VGX shall be primarily responsible for filing, prosecuting and maintaining all patent applications and patents included in the Patent Rights, and VGX agrees to pay all Legal Costs.

 

8.2                                Notification of Intent Not to Pursue. In the event that VGX decides not to pay for the costs associated with either: (i) the prosecution of the Patent Rights to issuance or (ii) maintenance of any United States or foreign issued patent on the Patent Rights, VGX shall timely notify BAYLOR in writing thereof with respect to the undesired patent. VGX’s right under this Agreement to practice the invention according to the claim scope of same undesired patent shall immediately terminate upon the giving of such notice.  If VGX fails to notify BAYLOR in sufficient time for BAYLOR to assume

 

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said costs prior to the abandonment or expiration of any Patent Rights, VGX shall be considered in default of this Agreement.

 

8.3                                Obligation to Inform. VGX agrees to keep BAYLOR fully informed, at VGX’s expense, of all prosecutions and other actions pursuant to this Section 8, by submitting to Baylor an annual summary of such prosecutions and other actions. In addition, VGX shall notify Baylor of a decision to abandon any Patent covered by the Agreement, in a timely manner so that Baylor is reasonably able to maintain the prosecution of said Patent.

 

8.4                                Obligation to Cooperate. BAYLOR agrees to reasonably cooperate with VGX to whatever extent is reasonably necessary to provide VGX the full benefit of the license granted to the Patent Rights under this Agreement.

 

8.5                                Infringement Procedures. During the term of this Agreement, each Party shall promptly inform the other of any suspected infringement of any claims in the Patent Rights or the misuse, misappropriation, theft or breach of confidence of other proprietary rights in the Patent Rights by a third party, and with respect to such activities as are suspected.  Any action or proceeding against such third party shall be instituted as following:

 

(i)  BAYLOR and VGX may agree to jointly institute an action for infringement, misuse, misappropriation, theft or breach of confidence of the proprietary rights against such third party.  Such joint action shall be brought in the names of both BAYLOR and VGX.  If BAYLOR or VGX decides to jointly prosecute an action or proceeding after it has been instituted by one Party, the action shall be continued in the name or names they both agree is expedient for efficient prosecution of such action.  VGX and BAYLOR shall agree to the manner in which they shall exercise control over any joint action or proceeding. However, should the parties disagree on a particular decision, BAYLOR may decide on such decision with input from VGX.  In such joint action or proceeding, the out-of-pocket costs shall be borne equally, and any recovery or settlement shall be shared equally.

 

(ii)  If VGX does not agree to participate in a joint action or proceeding then BAYLOR shall have the right, but not the obligation, to institute an action for infringement, misuse, misappropriation, theft or breach of confidence of the proprietary rights against such third party.  If BAYLOR elects to institute action, it does so at its own cost.  If BAYLOR fails to bring such an action or proceeding within a period of three (3) months after receiving notice or otherwise having knowledge of such infringement, then VGX shall have the right, but not the obligation, to prosecute the same at its own expense.  Should either BAYLOR or VGX commence action under the provisions of this Paragraph 8.5 and thereafter elect to abandon the same, it shall give timely notice to the other Party who may, if it so desires, continue prosecution of such action or proceeding.  All recoveries, whether by judgment, award, decree or settlement, from infringement or misuse of the Patent Rights shall be apportioned as follows: (a) the Party bringing the action or proceeding shall first recover an amount equal the costs and expenses incurred by such Party directly related to the prosecution of such action or proceeding,

 

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(b) the Party cooperating in such action or proceeding shall then recover costs and expenses incurred by such Party directly related to its cooperation in the prosecution of such action or proceeding and (c) the remainder shall be divided equally between VGX and BAYLOR.

 

8.6                                Consent to Settle. Neither BAYLOR nor VGX shall settle any action covered by Paragraph 8.5 without first obtaining the consent of the other Party, which consent will not be unreasonably withheld.

 

8.7                                Liability for Losses. BAYLOR shall not be liable for any losses incurred as the result of an action for infringement brought against VGX as the result of VGX’s exercise of any right granted under this Agreement.  The decision to defend or not defend shall be in VGX’s sole discretion.

 

9.                                       TERM AND EXPIRATION

 

Unless sooner terminated as otherwise provided in Section 10 herein below, the license to the Patent Rights granted to VGX shall expire on a per country basis, on the later of (i) the date of expiration of the last of the Patent Rights in the relevant country or (ii) in the event no patents included within the Patent Rights issue in a country, the first date following the tenth (10 th ) anniversary of the first commercial sale of Licensed Products by VGX in such country.  After such expiration, VGX shall have a perpetual, paid-in-full (i.e., royalty free) license in such country.

 

10.                                TERMINATION

 

10.1                         Termination by BAYLOR: Default: In the event of default or failure by VGX to perform any of the terms, covenants or provisions of this Agreement, VGX shall have thirty (30) days after the receipt of written notice of such default by BAYLOR to correct such default.  If such default is not corrected within the said thirty (30) day period, BAYLOR shall have the right, at its option, to cancel and terminate this Agreement.  The failure of BAYLOR to exercise such right of termination, for non-payment of royalties/ fees or otherwise, shall not be deemed to be a waiver of any right BAYLOR might have, nor shall such failure preclude BAYLOR from exercising or enforcing said right upon any subsequent failure by VGX.

 

10.2                         Termination by BAYLOR: Insolvency. BAYLOR shall have the right, at its option, to cancel and terminate this Agreement in the event that VGX shall (i) become involved in insolvency, dissolution, bankruptcy or receivership proceedings affecting the operation of its business or (ii) make an assignment of all or substantially all of its assets for the benefit of creditors, or in the event that (iii) a receiver or trustee is appointed for VGX and VGX shall, after the expiration of thirty (30) days following any of the events enumerated above, have been unable to secure a dismissal, stay or other suspension of such proceedings.

 

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10.3         Termination by VGX: VGX shall have the right in its sole discretion to terminate this Agreement upon sixty (60) days’ written notice to BAYLOR.

 

10.4         Effects of Termination. In the event of termination of this Agreement, all rights to the Patent Rights shall revert to BAYLOR.  At the date of any termination of this Agreement, VGX shall immediately cease using any of the Patent Rights; provided, however, that VGX may sell any Licensed Products actually in the possession of VGX on the date of termination, provided that VGX pays to BAYLOR royalties on all such sales in accordance with Paragraph 4.2 with respect thereto and otherwise complying with the terms of this Agreement.

 

10.5         Effect of Termination: Sublicenses. VGX shall provide, in all sublicenses granted by it under this Agreement, that VGX’s interest in such sublicenses shall, at BAYLOR’s option, terminate or be assigned to BAYLOR upon termination of this Agreement.

 

10.6         No Refund. In the event this Agreement is terminated pursuant to this Section 10, or expires as provided for in Section 9, BAYLOR is under no obligation to refund any payments made by VGX to BAYLOR prior to the effective date of such termination or expiration.

 

10.7         Survival of Termination. No termination of this Agreement shall constitute a termination or a waiver of any rights of either Party against the other Party accruing at or prior to the time of such termination.  The obligations of Sections 13, 15 and 16 shall survive termination of this Agreement.

 

11.          ASSIGNABILITY

 

Without the prior written approval of BAYLOR, which will not be unreasonably withheld, neither this Agreement nor the rights granted hereunder shall be transferred or assigned in whole or in part by VGX to any person or entity whether voluntarily or involuntarily, by operation of law or otherwise.  Notwithstanding the foregoing, VGX may assign this Agreement and its rights and obligations hereunder without BAYLOR’s consent, (i) in connection with the transfer or sale of all or substantially all of its assets or the business of VGX to which this Agreement relates or (ii) to any Affiliate; so long as VGX gives BAYLOR prompt notice of such action and the successor entity or Affiliate, as the case may be, acknowledges its consent and agreement to the terms of this Agreement in writing before such assignment; and so long as such action is not entered into solely to satisfy creditors of VGX.  This Agreement shall be binding upon and shall inure to the benefit of the respective successors, legal representatives and assignees of BAYLOR and VGX.

 

12.          GOVERNMENTAL COMPLIANCE

 

12.1        Compliance with Applicable Laws. VGX shall at all times during the term of this Agreement and for so long as it shall use the Patent Rights, or sell Licensed Products, comply and cause its sublicensees to comply with all laws that may control

 

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the import, export, manufacture, use, sale, marketing, distribution and other commercial exploitation of the Patent Rights, Licensed Products or any other activity undertaken pursuant to this Agreement.

 

12.2         Requirement for U.S. Manufacture. VGX agrees that, to the extent it is commercially practical, Licensed Products leased or sold in the United States shall be manufactured substantially in the United States.

 

12.3         Export Control Regulations.   The Patent Rights are subject to, and VGX agrees to comply in all respects with, U.S. law including but not limited to U.S. export controls under the Export Administration Regulations (15 C.F.R. Part 734 et seq.) and U.S. economic sanctions and embargoes codified in 31 C.F.R. Chapter V. VGX agrees that VGX bears sole responsibility for understanding and complying with current U.S. trade controls laws and regulations as applicable to its activities subject to this Agreement.  Without limitation on the general agreement to comply set forth in the first sentence of this Paragraph 12.3, VGX agrees not to sell any goods, services, or technologies subject to this Agreement, or to re-export the same: (1) to any destination prohibited by U.S. law, including any destination subject to U.S. economic embargo; (2) to any end-user prohibited by U.S. law, including any person or entity listed on the U.S. government’s Specially Designated Nationals list, Denied Parties List, Debarred Persons List, Unverified List, or Entities List.  Furthermore, VGX agrees that any transfer of Patent Rights from BAYLOR to VGX under this Agreement is subject to U.S. export license authorization as may be required under U.S. law.

 

13.          ARBITRATION

 

13.1        Amicable Resolution.   The Parties shall attempt to settle any controversy between them amicably.  To this end, a senior executive from each Party shall consult and negotiate to reach a solution.  The Parties agree that the period of amicable resolution shall toll any otherwise applicable statute of limitations.  However, nothing in this clause shall preclude any Party from commencing mediation if said negotiations do not result in a signed written settlement agreement within thirty (30) days after written notice that these amicable resolution negotiations have commenced.

 

13.2.       Mediation.   If a controversy arises out of or relates to this Agreement, or the breach thereof, and if the controversy cannot be settled through amicable resolution, the Parties agree to try in good faith to settle the controversy by mediation before resorting to final and binding arbitration.  The Party seeking mediation shall propose five mediators, each of whom shall be a lawyer licensed to practice by the state of Texas, having practiced actively in the field of commercial law for at least fifteen (15) years, to the other Party who shall select the mediator from the list. The Parties shall split the cost of the mediator equally.  The Parties agree that the period of mediation shall toll any otherwise applicable statute of limitations.  However, nothing in this clause shall preclude any Party from commencing arbitration if said negotiations do not result in a signed written settlement agreement within sixty (60) days after written notice that amicable resolution negotiations have commenced.

 

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13.3        Arbitration.   Any dispute, controversy, or claim arising out of or relating to this Agreement, or the breach, termination or invalidity thereof, including claims for tortious interference or other tortious or statutory claims arising before, during or after termination, providing only that such claim touches upon matters covered by this Agreement shall be finally settled by arbitration administered by the American Arbitration Association pursuant to the Commercial Arbitration Rules in force at the time of the commencement of the arbitration, except as modified by the specific provisions of this Agreement. It is the specific intent of the Parties that this arbitration provision is intended to be the broadest form allowed by law.

 

13.4        Parties to Arbitration.   This agreement to arbitrate is intended to be binding upon the signatories hereto, their principals, successors, assigns, subsidiaries and affiliates. This agreement to arbitrate is also intended to include any disputes, controversy or claims against any Party’s employees, agents, representatives, or outside legal counsel arising out of or relating to matters covered by this Agreement or any agreement in which this Agreement is incorporated.

 

13.5        Consolidation Permitted.   The Parties expressly agree that any court with jurisdiction may order the consolidation of any arbitrable controversy under this Agreement with any related arbitrable controversy not arising under this Agreement, as the court may deem necessary in the interests of justice or efficiency or on such other grounds as the court may deem appropriate.

 

13.6        Entry of Judgment.   The Parties agree that a final judgment on the arbitration award may be entered by any court having jurisdiction thereof.

 

13.7        Appointing Arbitrators.    The American Arbitration Association shall appoint the arbitrator(s) from its Large, Complex Claims Panel. If such appointment cannot be made from the Large, Complex Claims Panel, then from its Commercial Panel. The Parties hereby agree to and acquiesce in any appointment of an arbitrator or arbitrators that may be made by such appointing authority.

 

13.8        Qualifications of the Arbitrator(s).   The arbitrator(s) must be a lawyer, having practiced actively in the field of commercial law for at least fifteen (15) years.

 

13.9        Governing Substantive Law.    The arbitrator(s) shall determine the rights and obligations of the Parties according to the substantive laws of the State of Texas (excluding conflicts of law principles) as though acting as a court of the State of Texas.

 

13.10      Governing Arbitration Law.   The law applicable to the validity of the arbitration clause, the conduct of the arbitration, including any resort to a court for provisional remedies, the enforcement of any award and any other question of arbitration law or procedure shall be the Federal Arbitration Act.

 

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13.11      Governing Convention.   The Parties elect to have the New York Convention on the Recognition and Enforcement of Foreign Arbitral Awards of June 10, 1958 (instead of the Inter-American New York Convention on International Commercial Arbitration of August 15, 1990) govern any and all disputes that may be the subject of arbitration pursuant to this Agreement.

 

13.12      Preliminary Issues of Law.   The arbitrator(s) shall hear and determine any preliminary issue of law asserted by a Party to be dispositive of any claim, in whole or part, in the manner of a court hearing a motion to dismiss for failure to state a claim or for summary judgment, pursuant to such terms and procedures as the arbitrator(s) deems appropriate.

 

13.13      Confidentiality.   The Parties and the arbitrator(s) shall treat all aspects of the arbitration proceedings, including without limitation discovery, testimony and other evidence, briefs and the award, as strictly confidential.  Further, except as may be required by law, neither Party nor the arbitrator(s) may disclose the existence, content, or results of any arbitration hereunder without the prior written consent of both Parties.

 

13.14      Place of Arbitration.   The seat of arbitration shall be Houston, Texas, USA for actions or claims prosecuted by VGX, and the seat of arbitration shall be Philadelphia, Pennsylvania, USA, for actions or claims prosecuted by BAYLOR.

 

13.15      Language.   The arbitration shall be conducted in the English language. All submissions shall be made in English or with an English translation. Witnesses may provide testimony in a language other than English, provided that a simultaneous English translation is provided. Each Party shall bear its own translation costs.

 

13.16      Punitive Damages Prohibited.   The Parties hereby waive any claim to any damages in the nature of punitive, exemplary, or statutory damages in excess of compensatory damages, or any form of damages in excess of compensatory damages, and the arbitrator(s) is/are specially divested of any power to award any damages in the nature of punitive, exemplary, or statutory damages in excess of compensatory damages, or any form of damages in excess of compensatory damages.

 

13.17      Costs.   The Party prevailing on substantially all of its claims shall be entitled to recover its costs, including attorneys’ fees, for the arbitration proceedings, as well as for any ancillary proceeding, including a proceeding to compel or enjoin arbitration, to request interim measures or to confirm or set aside an award.

 

13.18      Survival.   The provisions of this Section 13 shall survive expiration or termination of this Agreement.

 

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14.          ADDRESSES

 

14.1        Addresses: Payments . All payments shall be made payable to “Baylor College of Medicine” and shall be sent to the address below, and shall reference the applicable BLG numbers listed on the front page of the Agreement.

 

BAYLOR Tax ID #: 74-1613878

Director, Baylor Licensing Group

Baylor College of Medicine

One Baylor Plaza, BCM210-600D

Houston, TX 77030

 

Telephone No.

713-798-6821

 

Facsimile No.

713-798-1252

 

E-Mail

blg@bcm.tmc.edu

 

14.2         For questions about payments, BAYLOR can contact VGX at the address below:

 

Title:

Chief Financial Officer

Name:

Gene Kim

Address:

450 Sentry Parkway

 

Blue Bell, PA 19422

 

Telephone No.

267-440-4205

 

Facsimile No.

267-440-4242

 

E-Mail.

gene@vgxp.com

 

14.3         Addresses: Notices. All notices, reports or other communication pursuant to this Agreement shall be sent to such Party via (i) United States Postal Service postage prepaid, (ii) overnight courier, or (iii) facsimile transmission, addressed to it at its address set forth below or as it shall designate by written notice given to the other Party.  Notice shall be sufficiently made, or given and received (a) on the date of mailing or (b) when a facsimile printer reflects transmission.

 

In the case of BAYLOR:

Patrick Turley

Associate General Counsel

Baylor College of Medicine

One Baylor Plaza, BCM210-600D

Houston, TX 77030

 

Telephone No.

713-798-6821

Facsimile No.

713-798-1252

E-Mail

blg@bcm.tmc.edu

 

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In the case of VGX:

J. Joseph Kim

President and CEO

450 Sentry Parkway

Blue Bell, PA 19422

 

Telephone No.

267-440-4201

Facsimile No.

267-440-4242

E-Mail

kim@vgxp.com

 

14.4          Baylor Reference Number. Each such report, notice or other communication shall include the applicable BLG numbers listed on the front page of the Agreement.

 

15.          INDEMNITY, INSURANCE & WARRANTIES

 

15.1        INDEMNITY.

 

(I)  EACH PARTY SHALL NOTIFY THE OTHER OF ANY CLAIM, LAWSUIT OR OTHER PROCEEDING RELATED TO THE PATENT RIGHTS.  VGX AGREES THAT IT WILL DEFEND, INDEMNIFY AND HOLD HARMLESS BAYLOR, ITS FACULTY MEMBERS, SCIENTISTS, RESEARCHERS, EMPLOYEES, STUDENTS, OFFICERS, TRUSTEES AND AGENTS AND EACH OF THEM (THE “INDEMNIFIED PARTIES”), FROM AND AGAINST ANY AND ALL CLAIMS, CAUSES OF ACTION, LAWSUITS OR OTHER PROCEEDINGS (THE “BAYLOR CLAIMS”) FILED OR OTHERWISE INSTITUTED AGAINST ANY OF THE INDEMNIFIED PARTIES RELATED DIRECTLY OR INDIRECTLY TO OR ARISING OUT OF THE DESIGN, PROCESS, MANUFACTURE OR USE BY ANY PERSON OR PARTY OF THE PATENT RIGHTS, LICENSED PRODUCTS OR ANY OTHER EMBODIMENT OF THE PATENT RIGHTS EVEN THOUGH SUCH BAYLOR CLAIMS AND THE COSTS (INCLUDING, BUT NOT LIMITED TO, THE PAYMENT OF ALL REASONABLE ATTORNEYS’ FEES AND COSTS OF LITIGATION OR OTHER DEFENSE) RELATED THERETO RESULT IN WHOLE OR IN PART FROM THE NEGLIGENCE OF ANY OF THE INDEMNIFIED PARTIES OR ARE BASED UPON DOCTRINES OF STRICT LIABILITY OR PRODUCT LIABILITY; PROVIDED, HOWEVER, THAT SUCH INDEMNITY SHALL NOT APPLY TO ANY BAYLOR CLAIMS ARISING FROM THE GROSS NEGLIGENCE OR INTENTIONAL MISCONDUCT OF ANY INDEMNIFIED PARTY.  VGX WILL ALSO ASSUME RESPONSIBILITY FOR ALL COSTS AND EXPENSES RELATED TO SUCH BAYLOR CLAIMS FOR WHICH IT IS OBLIGATED TO INDEMNIFY THE INDEMNIFIED PARTIES PURSUANT TO THIS PARAGRAPH 16.1, INCLUDING, BUT NOT LIMITED TO, THE PAYMENT OF ALL REASONABLE ATTORNEYS’ FEES AND COSTS OF LITIGATION OR OTHER DEFENSE.

 

(II)  VGX FURTHER AGREES NOT TO SETTLE ANY CLAIM AGAINST AN INDEMNIFIED PARTY WITHOUT THE INDEMNIFIED PARTY’S WRITTEN CONSENT WHICH CONSENT SHALL NOT BE UNREASONABLY WITHHELD.  VGX FURTHER AGREES TO KEEP THE INDEMNIFIED PARTIES FULLY APPRISED OF THE BAYLOR CLAIMS.

 

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15.2        Insurance.

 

(i)  VGX shall for so long as VGX manufactures, uses or sells any Licensed Product(s), maintain in full force and effect policies of (a) worker’s compensation insurance within statutory limits, (b) employers’ liability insurance with limits of not less than one million dollars ($1,000,000) per occurrence, (c) general liability insurance (with Broad Form General Liability endorsement) with limits of not less than one million dollars ($1,000,000) per occurrence with an annual aggregate of four million dollars ($4,000,000) and (d) product liability insurance in the event that VGX sells any Licensed Products, with limits of not less than two million dollars ($2,000,000) per occurrence with an annual aggregate of five million dollars ($5,000,000).

 

(ii)  Such coverage(s) shall be purchased from a carrier or carriers having an A. M. Best rating of at least A- (A minus) and shall name BAYLOR as an additional insured.  VGX shall provide to BAYLOR copies of certificates of insurance within thirty (30) days after execution of this Agreement.  Upon request by BAYLOR, VGX shall provide to BAYLOR copies of said policies of insurance.  It is the intention of the Parties hereto that VGX shall, throughout the term of this Agreement, continuously and without interruption, maintain in force the required insurance coverages set forth in this Paragraph 15.2.  Failure of VGX to comply with this requirement shall constitute a default of VGX allowing BAYLOR, at its option, to immediately terminate this Agreement.

 

(iii)  BAYLOR reserves the right to request additional policies of insurance where appropriate and reasonable in light of VGX’s business operations and availability of coverage.

 

15.3        DISCLAIMER OF WARRANTY.   BAYLOR REPRESENTS AND WARRANTS TO VGX THAT IT HAS THE FULL AUTHORITY TO EXECUTE AND DELIVER THIS LICENSE AGREEMENT; AND HAS RECEIVED NO MATERIAL CLAIM IN WRITING FROM ANY THIRD PARTY CONTESTING THE VALIDITY, ENFORCEABILITY, LICENSEABLITY, USE OR OWNERSHIP OF ANY SUCH BAYLOR PATENT RIGHTS. EXCEPT AS SET FORTH IN THE PREVIOUS SENTENCE, THE BAYLOR PATENT RIGHTS, LICENSED PRODUCTS AND ANY OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT ARE PROVIDED ON AN “AS IS” BASIS.  BAYLOR MAKES NO WARRANTIES OR REPRESENTATIONS, EXPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, WARRANTIES OF FITNESS OR MERCHANTABILITY, REGARDING OR WITH RESPECT TO THE PATENT RIGHTS OR LICENSED PRODUCTS AND BAYLOR MAKES NO WARRANTIES OR REPRESENTATIONS, EXPRESS OR IMPLIED, OF THE PATENTABILITY OF THE PATENT RIGHTS OR LICENSED PRODUCTS OR OF THE ENFORCEABILITY OF ANY PATENTS ISSUING THEREUPON, IF ANY, OR THAT THE PATENT RIGHTS OR LICENSED PRODUCTS ARE OR SHALL BE FREE FROM INFRINGEMENT OF ANY PATENT OR OTHER RIGHTS OF THIRD PARTIES.  NOTHING IN THIS AGREEMENT SHALL BE CONSTRUED AS CONFERRING BY IMPLICATION, ESTOPPEL OR OTHERWISE ANY LICENSE OR RIGHTS UNDER ANY PATENTS OF BAYLOR OTHER THAN THE PATENT RIGHTS; HOWEVER, BAYLOR AGREES IN GOOD FAITH TO NEGOTIATE WITH VGX A LICENSE UNDER ANY EXISTING

 

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PATENT RIGHTS OWNED BY BAYLOR THAT MAY PREVENT VGX FROM PRACTICING UNDER THE PATENT RIGHTS OF THIS AGREEMENT TO THE EXTENT THAT SAID PATENT RIGHTS ARE NOT OTHERWISE OBLIGATED TO OR CONTROLLED BY A THIRD PARTY.

 

16.           ADDITIONAL PROVISIONS

 

16.1        Use of BAYLOR Name .   VGX agrees that it shall not use in any way the name of “Baylor College of Medicine” or any logotypes or symbols associated with BAYLOR or the names of any of the scientists or other researchers at BAYLOR without the prior written consent of BAYLOR.

 

16.2        Confidentiality .   VGX agrees to maintain the Patent Rights in confidence, and to use the same only in accordance with this Agreement.  Such obligation of confidentiality shall not apply to information which VGX can demonstrate: (i) was at the time of disclosure in the public domain; (ii) has come into the public domain after disclosure through no fault of VGX; (iii) was known to VGX prior to disclosure thereof by BAYLOR; (iv) was lawfully disclosed to VGX by a third party which was not under an obligation of confidence to BAYLOR with respect thereto; (v) which VGX can reasonably demonstrate was independently developed by VGX without use of the Patent Rights; or (vi) which VGX shall be compelled to disclose by law or legal process.

 

16.3        BAYLOR’s Disclaimers .   Neither BAYLOR, nor any of its faculty members, scientists, researchers, employees, students, officers, trustees or agents assume any responsibility for the manufacture, product specifications, sale or use of the Patent Rights or Licensed Products which are manufactured by or sold by VGX.

 

16.4        Independent Contractors.   The Parties hereby acknowledge and agree that each is an independent contractor and that neither Party shall be considered to be the agent, representative, master or servant of the other Party for any purpose whatsoever, and that neither Party has any authority to enter into a contract, to assume any obligation or to give warranties or representations on behalf of the other Party.  Nothing in this relationship shall be construed to create a relationship of joint venture, partnership, fiduciary or other similar relationship between the Parties.

 

16.5        Non-Waiver .   The Parties covenant and agree that if a Party fails or neglects for any reason to take advantage of any of the terms provided for the termination of this Agreement or if a Party, having the right to declare this Agreement terminated, shall fail to do so, any such failure or neglect by such Party shall not be a waiver or be deemed or be construed to be a waiver of any separate cause for the termination of this Agreement subsequently arising, or as a waiver of any of the terms, covenants or conditions of this Agreement or of the performance thereof.  None of the terms, covenants and conditions of this Agreement may be waived by a Party except by other Party’s written consent.

 

16.6        Reformation.   The Parties hereby agree that neither Party intends to violate any public policy, statutory or common law, rule, regulation, treaty or decision of

 

17



 

any government agency or executive body thereof of any country or community or association of countries, and that if any word, sentence, paragraph or clause or combination thereof of this Agreement is found, by a court or executive body with judicial powers having jurisdiction over this Agreement or any of the Parties hereto, in a final, unappealable order to be in violation of any such provision in any country or community or association of countries, such words, sentences, paragraphs or clauses or combination shall be inoperative in such country or community or association of countries, and the remainder of this Agreement shall remain binding upon the Parties hereto.

 

16.7        Force Majeure.   No liability hereunder shall result to a Party by reason of delay in performance caused by force majeure, that is circumstances beyond the reasonable control of the Party, including, without limitation, acts of God, fire, flood, war, terrorism, civil unrest, labor unrest, or shortage of or inability to obtain material or equipment.

 

16.8        Entire Agreement.   The terms and conditions herein constitute the entire agreement between the Parties and shall supersede all previous agreements, either oral or written, between the Parties hereto with respect to the subject matter hereof.  No agreement of understanding bearing on this Agreement shall be binding upon either Party hereto unless it shall be in writing and signed by the duly authorized officer or representative of each of the Parties and shall expressly refer to this Agreement.

 

IN WITNESS WHEREOF, the Parties hereto have executed and delivered this Agreement in multiple originals by their duly authorized officers and representatives on the respective dates shown below, but effective as of the Agreement Date.

 

 

VGX

 

PHARMACEUTICALS, INC.

 

 

BAYLOR COLLEGE OF MEDICINE

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Name:

  /s/ J. Joseph Kim

 

 

Name:

  /s/ Cyndi M. Baily

 

J. Joseph Kim

 

 

 

Cyndi M. Baily

 

 

 

 

 

 

Title:

President and CEO

 

Title:

Senior Vice President &

 

 

 

 

 

 General Counsel

 

 

 

 

 

 

 

 

 

 

 

 

Date:

 5/9/07

 

 

Date:

 5/7/07

 

18




EXHIBIT 10.35

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

R&D COLLABORATION AND LICENSE AGREEMENT

 

 

BETWEEN

 

VGX PHARMACEUTICALS, INC.

 

(VGX)

 

 

AND

 

 

VGX INTERNATIONAL

 

(VI)

 



 

R&D COLLABORATION AND LICENSE AGREEMENT

 

This R&D Collaboration and License Agreement (“AGREEMENT”) is between VGX Pharmaceuticals, Inc. (“VGX”), a Delaware corporation, with offices located at 450 Sentry Parkway East, Blue Bell, Pennsylvania 19422, and VGX International Inc. (“VI”), a corporation having an address of Jung-Hun Building, #701, 944-1 Daechi 3-Dong, Gangnam-gu, Seoul, Korea.

 

A. Whereas VGX controls certain intellectual property related to VGX-100 (Recombinant Viral Protein R (rVpr)) (hereinafter referred to as “VGX-100”) a drug for treating all and any disease indications in humans and animals, including but not limited to those listed in Attachment I; and

 

B. Whereas VGX and VI desire to enter into an agreement for exclusive worldwide rights to conduct research, development activities, sale, licensing, and marketing of VGX-100 for Gastric Cancer for humans.

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties hereby agree as follows:

 

1.              DEFINITIONS

 

1.1    CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.2    CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.3    EFFECTIVE DATE means the date on which VI and VGX have both fully executed this AGREEMENT.

 

1.4    FAIR MARKET VALUE means the cash consideration which VGX or VI thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.5    NET SALES is defined as the gross amount of monies or cash equivalent or other consideration which is paid by unrelated third parties to VGX or VI for VGX-100 by sale or other mode of transfer, less all qualifying costs directly attributable to such sales, which are made, made for, used or sold by VI, its agents, employees and/or independent contractors.

 

NET SALES of a commercial product comprising one or more VGX R&D PRODUCTS and one or more other active ingredients (a “COMBINATION PRODUCT”) shall be calculated as set forth above, subject to the provisions of Section 3.1.3.

 

1



 

1.6    VGX R&D PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale for each indication and/or any agents and contractors(s) to unrelated third parties which (1) in the absence of this AGREEMENT would infringe at least one claim of VGX PATENT RIGHTS described in patents listed in Attachment I, or (2) use a process and/or machine covered by at least one claim of VGX PATENT RIGHTS described in patents listed in Attachment I or utilize VGX KNOW-HOW TECHNOLOGY.

 

1.7    SALE means any bona fide transaction for which consideration payment is received or expected for the sale, use, lease, transfer or other disposition of VGX R&D PRODUCT(S) to an unrelated third party.  A SALE of VGX R&D PRODUCT (S) shall be deemed completed at the time VGX or VI, their agents, or their contractors receive payment for such VGX R&D PRODUCT (S).

 

1.8    VGX KNOW-HOW TECHNOLOGY shall mean VGX’s technical information and materials, including without limitation, technology, preclinical or clinical data, bacterial strains, genetic constructs, chemicals, inventions (patentable or otherwise), practices, methods, knowledge, know-how, skill, and experience related directly or indirectly to VGX-100.

 

1.9    VGX PATENT RIGHTS means all of VGX’s interest in the rights represented by or issuing from (including all claims referenced within) those patent applications listed in ATTACHMENT I and all future interests in such rights anywhere in the world of the VGX-100 intellectual property.

 

2.              R&D COLLABORATION

 

Subject to the terms and conditions of this AGREEMENT, VGX and VI shall collaborate to research, develop and market VGX R&D PRODUCTS for GASTRIC CANCER. No other rights are granted by either party hereunder.  This agreement shall not impair VI’s freedom (without any restriction or any obligation to VGX) to research, develop, and market products for GASTRIC CANCER, except for the restrictions in this Agreement.

 

2.1    VGX shall provide VGX-100 (Recombinant Vpr Protein) necessary for the production or intended for production of VGX R&D PRODUCT(S) upon VI’s request. VI shall reimburse VGX for the costs of such VGX 100 at a price to be mutually agreed. VGX and VI shall share pre-clinical testing data, and clinical results for product development and clinical development.

 

3.              COST SHARING, FEES, AND ROYALTIES

 

3.1    Cost Sharing, Fees and Royalties.

 

3.1.1         VGX agrees to waive Upfront Fees.

 

3.1.2         Research and Development Costs.

 

2



 

3.1.2.1      VI and VGX agree to share the Research and Development costs on a mutually agreeable basis.

 

3.1.2.2      VI shall pay to VGX the following R&D milestone cost reimbursements to cover the costs of out-of-pocket, third-party expenses spent to conduct research and development of VGX-100 prior to the Effective Date.

 

Due Date

 

Payment

 

 

 

Upon completion of IND-enabling Toxicology Studies

 

******

 

 

 

Upon submission of an IND

 

******

 

3.1.3         In consideration of the exclusive worldwide rights granted to VI, VI shall pay to VGX, on a quarterly basis, a royalty of ****** of the NET SALES of each VGX R&D PRODUCT(S), which is sold by VI, its agent(s), and/or independent contractor(s) of VI for a period of ten (10) years from the date of the first SALE of VGX R&D PRODUCT(S) in any country covered by such patent issuance or until such time as the related patent protection on expires in such country, whichever is the later to occur.

 

3.1.4         In the event one or more VGX R&D PRODUCT(S) are sold in a COMBINATION PRODUCT, the amount of royalties and agents’ and/or contractors’ revenues paid to VGX pursuant to this Section 3.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the VGX R&D PRODUCT(S).

 

3.2    Diligence and Milestone Fees.

 

3.2.1         VI shall use commercially reasonable efforts to develop for SALE and to market VGX R&D PRODUCT(S) as drugs for treating GASTRIC CANCER indication.  VI agrees to pay VGX the following Milestone Payments.  The amount of the Milestone Payments (except for the one of Phase I clinical testing) shall be determined within 6 months prior to the scheduled initiation of a Phase II clinical trial for VGX-100.  The amount shall be determined based on the industry benchmark as described below, and  said payments are payable by VI to VGX within sixty (60) days after the achievement of the respective milestone event.  The data on industry benchmark on such license terms shall be based on the benchmark data gathered by firms such as Recombinant Capital (http://www.recap.com) or other similar data gathering or consulting firms.  If the parties cannot agree on the payment amount, the parties agree to hire two or more internationally reputable investment banks or accounting firms to determine said amount based on the firms’ own experience and expertise, or on the recommendation of an expert hired by them.

 

3



 

Due Date

 

Payment

 

 

 

Upon completion of Phase I safety and dose-escalation studies

 

To be determined (TBD) prior to the initiation of Phase I Studies

 

 

 

Upon completion of patient accrual for GASTRIC CANCER Phase II clinical trial for VGX-100

 

TBD

 

 

 

Upon completion of patient accrual for GASTRIC CANCER Phase III clinical trial for VGX-100

 

TBD

 

 

 

Upon NDA submission for VGX-100 for GASTRIC CANCER

 

TBD

 

 

 

Upon NDA approval for VGX-100 for GASTRIC CANCER

 

TBD

 

3.3    Currency, Payment Method.

 

All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to VGX under this AGREEMENT shall be made in United States dollars by check or wire-transfer.  If VI receives revenues from SALES of VGX R&D PRODUCTS in currency other than United States Dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

3.4 Option to Co-Development and Co-Marketing Rights.

 

3.4.1 Upon completion of Phase II for GASTRIC CANCER, VGX shall have an option to develop and market VGX-100 for GASTRIC CANCER in the United States and Europe.  Once the option is exercised, VGX shall assume all costs for development and filings in the U.S. and Europe for GASTRIC CANCER.  In return, VGX shall pay to VI, on a quarterly basis, a royalty of ****** of the NET SALES of each VGX R&D PRODUCT for GASTRIC CANCER only, which is sold by VGX, its agent(s), and/or independent contractor(s) of VGX in the U.S. and Europe,   VGX shall exercise the said option by providing a written notice to VI anytime during the effective term of this Agreement.

 

3.4.2  If VI, its agents, or contractors fails to lead VGX-100 to an initiation of Phase II Clinical trial for GASTRIC CANCER within 5 years from the effective date, VI shall return all rights specified in this Agreement back to VGX.

 

4



 

4.              CONFIDENTIALITY

 

4.1    CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and marked confidential or, if oral, should be reduced to writing within thirty (30) days of disclosure and marked confidential.

 

4.2    Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party during the term of this Agreement and for five (5) years after the date of termination of this Agreement.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this Agreement.  The foregoing obligation shall not apply to:

 

4.2.1         information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless  independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records; and

 

4.2.2         information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure; and

 

4.2.3         information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

4.2.4         information, which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

5



 

Note: Confidential information shall not be disclosed to third party and this rule shall apply to both VGX and VI. This is particularly true for process development data.

 

5.              TERM AND TERMINATION

 

5.1    This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the earlier of: (a) expiration of the last-to-expire patent or (b) twenty (20) years after the EFFECTIVE DATE.

 

5.2    VI may terminate this Agreement (a) upon thirty (30) days written notice to VGX, if the sale or other exploitation of the VGX R&D PRODUCT(s) becomes technologically or commercially unfeasible; or (b) upon sixty (60)-days written notice to VGX, and by doing all of the following:

 

5.2.1         ceasing to make, have made, use, import, sell and offer for sale all VGX R&D PRODUCTS; and

 

5.2.2         paying all monies owed to VGX up to the date of the termination excluding any future obligation under this AGREEMENT.

 

5.3    VGX may terminate this AGREEMENT, upon sixty (60)-days written notice to VI, if any of the following events of default (“Default”) occur:

 

5.3.1         VI is more than ninety (90) days late in paying to VGX royalties, expenses or any other monies due under this AGREEMENT and VI does not immediately pay VGX in full any amounts due upon demand; or

 

5.3.2         VI experiences a Trigger Event (defined below);

 

5.3.3         VI materially breaches this AGREEMENT and does not cure the material breach within ninety (90) days after the receipt of the written notice of such  breach.

 

5.4    “Trigger Event” means any of the following:

 

 If VI:

 

5.4.1.1      becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due; or

 

5.4.1.2      is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

6


 

5.4.1.3              makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

5.4.2         If proceedings under any International law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VI;

 

5.4.3         If any order for relief is entered relating to any of the proceedings described in Sections 5.4.2 ;

 

5.4.4         If VI shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

5.4.5         If VI shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 5.4.2, 5.4.3, 5.4.4.

 

5.4.6         I n the event of a “change in control” of VI, VI shall promptly notify VGX of such change in control and VGX shall be permitted to terminate this Agreement at VGX’s option.  A “change of control” means a change in the direct or indirect power to direct or cause the direction of the management and policies of VI, whether through ownership or voting securities, by contract or otherwise

 

5.5    The provisions of Sections 5.3 and 5.4 shall apply to a Default of, or a Trigger Event experienced by, any agents and/or contractors of VI ‘s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the agents and/or contractors(s) cause VI to fail to meet its diligence obligations under Section 3.2.

 

5.6    In the event of a termination under Section 5.1 or 5.3, all duties of VGX (other than under Sections 5.11) and all rights (but not duties) of VI (other than under Section 5.11) under this AGREEMENT immediately terminate without the necessity of any action being taken either by VI or by VGX, provided, however, that in no event shall the foregoing be construed to obligate VI to pay any amounts accruing under Sections 3.1  after the date of termination except under Section 5.10.  Upon and after any termination of this AGREEMENT, the rights covered by this agreement for VI and any agents and/or contractors thereof to manufacture, sale, marketing, importation and/or distribution of VGX R&DPRODUCT(s) shall terminate on the same date of the termination of the agreement, except otherwise specified in this agreement or agreed upon by both parties.

 

7



 

5.7    Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

5.8    Upon termination of this AGREEMENT under section 5.2 and 5.3, VI shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed VGX R&D PRODUCT(s) on hand, under the control of VI, its agents, or contractors thereof; and (b) such VGX R&D PRODUCT(s) as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be recorded in writing.  VI shall deliver copies of such written inventories, verified by an officer of VI, forthwith to VGX.  VGX shall have forty five (45) days after receipt of such verified inventories within which to challenge the physical inventory and request an audit thereof.

 

5.9    Upon termination of this agreement under section 5.1, VI shall pay all monies owed to VGX up to the date of the termination.

 

5.10 Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 5.3.1 or 5.3.2, VI shall have a period of six (6) months to sell off its inventory of VGX R&D PRODUCT(S) existing on the date of termination of this AGREEMENT and shall pay royalties to VGX with respect to such VGX R&D PRODUCT(S) within thirty (30) days following the expiration of such six-month period.

 

5.11 Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Articles 4, 5, 6, 7 and 8 shall survive such termination.

 

6.

REPRESENTATIONS AND WARRANTIES OF VGX AND VI; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

6.1    VGX represents and warrants to VI that VGX has the full authority to execute and deliver this AGREEMENT.

 

6.2    VI acknowledges that VGX holds world-wide exclusive rights, granted by PENN to VGX, to develop VGX-100 for the treatment of any indications.  VI agrees to assume all royalty obligations to PENN with regards to the GASTRIC CANCER indication as outlined in Section 3.1.3.

 

6.3    VGX and VI will work together to file and maintain the patents and/or patent applications listed in ATTACHMENT I before the deadline permitted by the relevant international and US patent laws.

 

8



 

6.4    From the Effective Date, VI agrees to pay a portion of the costs of maintaining and filing the patents and/or patent applications listed in ATTACHMENT I.  To fulfill this requirement, VI will directly pay IP maintenance payment of ****** to the Intellectual Property law firm (s) designated by VGX within thirty (30) days from the Effective Date and ****** annually thereafter.  A separate Client and Billing Agreement may be signed by VGX, VI, and the designated law firm(s) to facilitate these payments.

 

6.5    VGX shall defend and indemnify and hold VI (and its respective officers, directors and employees) harmless against any and all Losses, arising out of, relating to, based on, or caused by (A) the breach by VGX of any representation or warranty contained in this Agreement, (B) a claim that the formulation or manufacture of the VGX-100 by VGX for VI or other activities of VGX under this Agreement infringe on the patent or other intellectual property rights of a third party, (C) any governmental or regulatory action arising out of VGX, or (D) any negligence or intentional misconduct by VGX in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated in any substantial respect by the negligent acts of or failure to act by VI or its agents and/or  contractors.  VI will promptly notify VGX of any such Losses which come to VI’s attention, but failure to do so will not relieve VGX of its indemnification obligations under this Section 6.3 except to the extent any such delay results in a material prejudice to VGX.  Notwithstanding anything to the contrary in this Agreement, VGX shall not be liable for any Losses to the extent that the Losses suffered by VI (and its officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.6    VI shall defend and indemnify and hold VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) harmless against any Losses, arising out of, relating to, based on, or caused by (A) the breach by VI of any representation or warranty contained in this Agreement or (B) any negligence or intentional misconduct by VI in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated by the negligent acts of or failure to act by VGX, its agents and/or contractors.  VGX will promptly notify VI of any such Losses which come to VGX’s attention, but failure to do so will not relieve VI of its indemnification obligations under this Section 6.4 except to the extent any such delay results in a material prejudice to VI.  Notwithstanding anything to the contrary in this Agreement, VI shall not be liable for any Losses where the Losses suffered by VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.7    To best of VGX’s knowledge, there are no pending or threatened suits, claims, or actions of any type whatsoever against VGX with respect to the VGX-100.

 

9



 

6.8    All necessary corporate authorizations, consents and approvals which are necessary or required for VGX to enter into this Agreement have been duly obtained;

 

6.9    To the best of its knowledge, the entering into of this Agreement by VGX will not (i) violate any Applicable Law or(ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination, cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of VGX, under its organizational documents, as amended to date, or any material note, indenture, mortgage, lease, agreement, contract, purchase order or other instrument, document or agreement to which VGX is a party or by which it or any of its properties or assets is bound or affected.

 

7.              ADDITIONAL PROVISIONS

 

7.1    Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between VGX and VI, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

7.2    VI is not permitted to assign this AGREEMENT or any part of it to any person or entity, either directly or by operation of law, without the prior written consent of VGX in its sole discretion.

 

7.3    A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

7.4    Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by internationally recognized express couriers (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGX:

 

VGX Pharmaceutical, Inc.

450 Sentry Parkway East

Blue Bell, PA 19422

Attention: Senior Vice President

 

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If for VI:

 

VGX International

Jung-Hun Building, #701

944-1 Daechi 3-Dong

Gangnam-gu, Seoul, Korea

Attention: Vice President

 

Either party may change its official address upon written notice to the other party.

 

7.5    This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania in the United States of America, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the either federal or state courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.  The parties agree to accept original service of complaint via internationally recognized courier with receipt confirmation.  Also, the parties agree to waive the Hague Convention requirements relating to translation of certain documents to applicable foreign language which in this case is  Korean.

 

7.6    VI shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.

 

7.7    If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

7.8    This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

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[SIGNATURE PAGE FOLLOWS]

 

12



 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

VGX INTERNATIONAL, INC.

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

 

 

 

By:

      /s/ Jay Surh

 

By:

      /s/ Kevin W. Rassas

 

 

 

 

 

Name:

   Jay Surh

 

Name:

  Kevin W. Rassas

 

 

 

 

 

Title:

     Executive Director

 

Title:

   Senior Vice President

 

 

 

 

 

Date:

              6/19/2007

 

Date:

   6.27.07

 

13




EXHIBIT 10.36

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

NONEXCLUSIVE LICENSE

 

 

between

 

 

VGX PHARMACEUTICALS, INC.

 

(VGXP)

 

 

and

 

 

VGX ANIMAL HEALTH, INC.

 

(VGXAH)

 

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NONEXCLUSIVE LICENSE

 

This NONEXCLUSIVE LICENSE (“NONEXCLUSIVE LICENSE”), made on August 15, 2007 (“EFFECTIVE DATE”), is by and between VGX ANIMAL HEALTH, having a place of business at 2700 Research Forest Drive, The Woodlands, TX 77381 (“VGXAH”), and VGX Pharmaceuticals, Inc., having a place of business at 450 Sentry Parkway East, Blue Bell, PA 19422 (“VGXP”).

 

WHEREAS, VGXP owns and controls certain intellectual property related to electroporation devices and methods of using same to deliver biomolecules, including DNA plasmids (“DEVICE PATENT RIGHTS”) and materials and methods of plasmid manufacturing (“MFG PATENT RIGHTS”);

 

WHEREAS, VGXP owns and controls certain intellectual property related to biological products including Growth Hormone Releasing Hormone (GHRH) and VGXP has licensed intellectual property rights related to such products to VGXAH by way of an exclusive license agreement dated August 15, 2007 (“EXCLUSIVE PRODUCT LICENSE”);

 

WHEREAS, VGXAH desires access to the DEVICE PATENT RIGHTS and MFG PATENT RIGHTS in order to practice the rights provided by the EXCLUSIVE PRODUCT LICENSE, and VGXP desires to effectuate the license of DEVICE PATENT RIGHTS and MFG PATENT RIGHTS for such limited use to VGXAH;

 

NOW, THEREFORE, in consideration of the mutual promises and covenants contained herein and other good and valuable consideration, the sufficiency of which is hereby acknowledged, the parties agree as follows:

 

1.               DEFINITIONS

 

1.1 INTELLECTUAL PROPERTY is used herein to mean any and all legal right(s) that protect(s) any invention, improvement or discovery, whether or not patentable, and will include, but is not limited to, patent rights, patent applications, copyrights, trademarks, trade secrets, and know-how.

 

1.2 VGXAH INTELLECTUAL PROPERTY is used herein to mean and intellectual property that was conceived or reduced to practice by VGXAH solely that does not incorporate or extend from VGXP PATENT RIGHTS, DEVICE PATENT RIGHTS, and/or MFG PATENT RIGHTS.

 

1.3 VGXP LICENSED PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale by VGXAH and/or any sublicensee(s) of VGXAH to unrelated third parties which  in the absence of this AGREEMENT would infringe at least one claim of VGXP PATENT RIGHTS.

 

2



 

1.4  VGXP PATENT RIGHTS means all of VGXP’s interest in the rights represented by or issuing from (including all claims referenced within) those United States patents and patent applications listed in Attachment 1, including, in each case, any continuations, continuations-in-part, divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.5 SALE means any bona fide transaction for which consideration is received or expected for the sale, use, lease, transfer or other disposition of DEVICE FACILITATED PRODUCT(S) and/or PATENTED DEVICES to an unrelated third party.  A SALE shall be deemed completed at the time VGXAH invoices, ships or receives payment for the SALE, whichever occurs first.

 

1.6 NET SALES means the gross amount invoiced for SALES, less qualifying costs directly attributable to such SALES and actually identified on the invoice and borne by VGXAH.  Such qualifying costs shall be limited to the following:

 

1.6.1 Discounts and rebates, in amounts customary in the trade, for quantity purchases, prompt payments, for wholesalers and distributors;

 

1.6.2 Credits, allowances and/or refunds, not exceeding the original invoice amount, for rejections, claims and/or returns;

 

1.6.3  Prepaid outbound transportation expenses and transportation insurance premiums;

 

1.6.4 Sales and use taxes, tariffs, duties, surcharges and other fees imposed by a governmental agency; and

 

1.6.5  Retroactive price reductions actually applied in an invoice.

 

1.7 TERRITORY A shall mean the United States of America.  TERRITORY B shall mean any country that is a part of the European Union.  TERRITORY C shall mean any country that not the United States of America or a part of the European Union.

 

1.8  FIELD or FIELD OF USE is used interchangeably and means practice, including the making, using, selling, or offering to sell any product or services, in the field of animal health.  Such practice contemplates application of any product or services to an end user that is an animal that is non-human.  One example of such end use is the treatment of a farm animal with a DNA product for therapeutic purposes.

 

1.9  DEVICE PATENT RIGHTS means all of VGXP’s interest in the rights represented by United States Patent Number 7,245,963 and United States patent application Serial

 

3



 

Number 60/852,149, including, in each case, any continuations, continuations-in-part, divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.10  PATENTED DEVICES means any and all devices and use of same that is covered by the DEVICE PATENT RIGHTS, and in particular, the devices are those used for the electroporation of DNA to animals or cells of an animal that is not human.

 

1.11 DEVICE FACILITATED PRODUCT means any product that is delivered to an animal using the PATENTED DEVICES, and includes the animal that results from such use.

 

1.12 PRODUCT IMPROVEMENTS shall mean all inventions for which patent applications are or may be filed, whether ultimately patentable or not, that are conceived or first reduced to practice by VGXAH that incorporate or otherwise expand on inventions that are subject to DEVICE PATENT RIGHTS and that relate to the make, use, import, sale, or offer of sale of PATENTED DEVICES.

 

1.13 DEVICE IMPROVEMENTS is used herein to mean any and all inventions for which patent applications are or may be filed, whether ultimately patentable or not, that are conceived or first reduced to practice by VGXAH that incorporate or otherwise expand on inventions that are subject to the DEVICE PATENT RIGHTS.

 

1.14 MFG PATENT RIGHTS is used herein to mean all of VGXP’s interest in the rights represented by United States Patent Number 7,238,522, including, in each case, any continuations, continuations-in-part, divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.15 MFG PROCESSES is used herein to mean plasmid manufacturing methods and devices to accomplish the same as covered by MFG PATENT RIGHTS.

 

1.16 MFG IMPROVEMENTS is used herein to mean any and all inventions for which patent applications are or may be filed, whether ultimately patentable or not, that are conceived or first reduced to practice by VGXAH that incorporate or otherwise expand on inventions that are subject to the MFG PATENT RIGHTS.

 

1.17 AFFILIATE means any corporation, firm, limited liability company, partnership, or other entity that directly or indirectly controls, or is controlled by, or is under common control with a Party to this Agreement. For the purpose of this definition, control means ownership, directly or through one or more Affiliates, of fifty percent (50%) (or such lesser percentage which is the maximum allowed to be owned by a foreign entity in a

 

4



 

particular jurisdiction) or more of the shares of stock entitled to vote for the election of directors in the case of a corporation, or fifty percent (50%) (or such lesser percentage which is the maximum allowed to be owned by a foreign entity in a particular jurisdiction) or more of the equity interests in the case of any other type of legal entity, or status as a general partner in any partnership, or any other arrangement whereby a Party controls or has the right to control the board of directors or equivalent governing body of a corporation or other entity.

 

1.18 EXCLUDED PROCEEDS means all proceeds reasonably and fairly attributable to bona fide (i) debt financing; (ii) equity (and conditional equity, such as warrants, convertible debt and the like (iii) investments in VGXAH at fair market value; (iv) reimbursements of patent prosecution costs and patent maintenance expenses; (v) reimbursement for the cost of research and/or development services provided on the basis of full-time equivalent efforts of personnel not in excess of commercially reasonable full-time equivalent rates.

 

2.  LICENSE GRANT

 

2.1            VGXP grants to VGXAH for the agreed upon term, provided herein, a nonexclusive, world-wide right and license under the DEVICE PATENT RIGHTS to use the PATENTED DEVICES in the FIELD OF USE, including the right to sublicense to a third party (the “SUBLICENSEE”).

 

2.2           VGXP grants to VGXAH for the agreed upon term, provided herein, a nonexclusive, world-wide right and license under the MFG PATENT RIGHTS to use MFG PROCESSES in the FIELD OF USE, including the right to sublicense to SUBLICENSEE; however, such right to sublicense MFG PATENT RIGHTS will only extend to a SUBLICENSEE of DEVICE PATENT RIGHTS or to a SUBLICENSEE of VGXP LICENSED PRODUCT.

 

3.  TERM OF NONEXCLUSIVE LICENSE

 

3.1 Term.  This NONEXCLUSIVE LICENSE, unless sooner terminated as provided herein, shall terminate upon the later of:

 

(a) expiration or abandonment of the last patent that is a component of the DEVICE PATENT RIGHTS; or

 

(b) twenty-five (25) years after the EFFECTIVE DATE.

 

3.2 Termination.  The parties may terminate this Agreement under the following conditions:

 

5



 

3.2.1 VGXP, upon ten (10) days written notice to VGXAH, may terminate if VGXAH is more than sixty (60) days late in paying any amounts payable to VGXP or Ronald O. Bergan and Mary Alice Bergan (collectively, “BERGANS”) (see Section 4.1.5, below), provided herein, or if VGXAH, or SUBLICENSEE, breaches this NONEXCLUSIVE LICENSE and does not cure the breach within thirty (30) days after written notice of breach;

 

3.2.2 VGXAH, upon thirty (30) days written notice to VGXP, may terminate if the sale or other exploitation of the PATENTED DEVICES becomes technologically or commercially unfeasible; or

 

3.2.3 In the instant that the PRODUCT LICENSE AGREEMENT terminates, then parties agree that this NONEXCLUSIVE LICENSE shall hereby terminate concomitantly.

 

3.2.4  VGXP may terminate this AGREEMENT, upon ten (10) days written notice to VGXAH, if one of the following default events occur:

 

(a) If VGXAH becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

(b) If VGXAH is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment;

 

(c) If VGXAH makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

(d) If proceedings under any United States law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VGXAH;

 

(e) If any order for relief is entered relating to any of the proceedings described in subsections (a) through (d);

 

(f) If VGXAH shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

(g) If VGXAH shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in subsections (a) through (d).

 

6



 

3.2.5  Upon termination of this NONEXCLUSIVE LICENSE, VGXAH and SUBLICENSEE(S) shall refrain from further manufacture, sale, marketing, importation and/or distribution of PATENTED DEVICES and/or MFG PROCESSES.

 

3.2.6 Upon termination of this NONEXCLUSIVE LICENSE, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party, provided hereunder.

 

3.2.7 Upon termination of this NONEXCLUSIVE LICENSE, VGXAH shall inventory in writing as soon as commercially practicable and in any event no later than sixty (60) days after termination of: all devices and manufacturing protocols for purposes of MFG PROCESSES and all PATENTED DEVICES under the control of VGXAH or SUBLICENSEE(S); and all PATENTED DEVICES that are in the process of manufacture and component parts thereof, which inventories shall be reduced to writing.  VGXAH shall deliver copies of such written inventories, verified by an officer of VGXAH, forthwith to VGXP.  VGXP shall have forty five (45) days after receipt of such verified inventories within which to challenge the inventory and request an audit thereof.  Upon five (5) days written notice to VGXAH or SUBLICENSEE(S), VGXP and its agents shall be given access during normal business hours to the premises of respective company for the purpose of conducting an audit.  Upon the termination of this AGREEMENT, VGXAH shall at its own expense forthwith remove, efface or destroy all references to VGXP from all advertising or other materials used in the promotion of VGXAH’s, or SUBLICENSSE’s, business and VGXAH and SUBLICENSEE(S) shall not represent in any manner that it has rights in or to any one or more of the DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES.

 

4.  FEES AND ROYALTIES

 

4.1  License Initiation Fees and Royalties

 

In the event that VGXAH sublicenses DEVICE PATENT RIGHTS or a VGXP LICENSED PRODUCT to a SUBLICENSEE, the parties agree that VGXAH shall have the option to license MFG PATENT RIGHTS to same SUBLICENSEE, if desired by VGXAH.

 

4.1.1  As part of the consideration for the bundle of rights granted to VGXAH, VGXAH shall pay to VGXP, on a quarterly basis:  a) a royalty of ****** of the NET SALES of each DEVICE FACILITATED PRODUCT, including any PATENTED DEVICES, which is sold by VGXAH, including any sold by independent contractor(s) or agent(s) of VGXAH, and b) ****** of any royalties paid by any SUBLICENSEE of DEVICE PATENT RIGHTS to VGXAH.  In

 

7



 

determining the earned royalty payment, if any, such payment shall be made by VGXAH at the end of any CALENDAR QUARTER following the first SALE of a DEVICE FACILITATED PRODUCT or PATENTED DEVICE.  Such royalty payments shall terminate on a product-by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first SALE of such DEVICE FACILITATED PRODUCT or PATENTED DEVICE in such country, and (b) in any country in which patent rights exist for any DEVICE PATENT RIGHTS, the date of expiration of the last-to-expire patent in such country, within the definition of DEVICE PATENT RIGHTS, with an enforceable claim covering the PATENTED DEVICES.

 

4.1.2  In the event that a sold product is both a DEVICE FACILITATED PRODUCT and a VGXP LICENSED PRODUCT, royalty payment by VGXAH to VGXP shall include only one ****** royalty obligation for each sale event of such product.

 

4.1.3  Within thirty (30) days after the end of each of the periods specified below, VGXAH shall pay to VGXP the specified percentage of any sublicense initiation fee and any other non-royalty payment(s), net of all EXCLUDED PROCEEDS, including those resulting from co-marketing, strategic alliance, joint venture and other similar arrangement(s), actually received during such period by VGXAH from a SUBLICENSEE resulting from activities with PATENTED DEVICES.  Any non-cash consideration received by VGXAH from such sublicensee shall be valued at its FAIR MARKET VALUE as of the date of receipt by VGXAH.

 

Period

 

Percentage

 

 

 

EFFECTIVE DATE to 12 months after the EFFECTIVE DATE

 

******

 

 

 

12 months and one day after EFFECTIVE DATE to 24 months after the EFFECTIVE DATE

 

******

 

 

 

24 months and one day after EFFECTIVE DATE to 36 months after the EFFECTIVE DATE

 

******

 

4.1.4 In the event one or more DEVICE FACILITATED PRODUCTS and/or PATENTED DEVICES are sold in a COMBINATION PRODUCT, the amount of royalties paid to VGXP pursuant to this Section 4.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the DEVICE FACILITATED PRODUCTS and/or PATENTED DEVICES.

 

4.1.5  VGXAH acknowledges and agrees to assume from VGXP the payment obligation to BERGANS, which have been stipulated in the Asset Purchase

 

8



 

Agreement, section 2.1(a)(vii), made between VGXP and ADViSYS, dated February 21, 2007, such payments being related to the FIELD OF USE.

 

                4.2  Diligence and Milestone Fees

 

4.2.1  For the term of this agreement, VGXAH shall provide VGXP on each January 30 th , written progress reports, setting forth in such detail as VGXP may reasonably request, the progress of the development, evaluation, testing and commercialization of each DEVICE FACILITATED PRODUCT.  VGXAH shall also notify VGXP in writing within thirty (30) days of the first SALE of each DEVICE FACILITATED PRODUCT and/or PATENTED DEVICE.

 

4.2.2  Any of the events listed below that occur after the EFFECTIVE DATE shall require that the following milestone payments be paid by VGXAH to VGXP within sixty (60) days after the achievement of the respective milestone event. The aforementioned notwithstanding, VGXAH shall not be obligated to remit a milestone payment to VGXP until it has raised five million dollars ($ 5,000,000) in total capital. Any milestone payment obligation arising prior to raising five million dollars ($ 5,000,000) in total capital shall be accrued and become immediately payable upon reaching or surpassing this threshold. The milestone payments shall be made for each DEVICE FACILITATED PRODUCT that is not a VGXP LICENSED PRODUCT for each animal species.

 

9



 

Event

 

Amount

 

 

 

 

 

Filing of an INAD APPLICATION

 

$

250,000

 

 

 

 

 

Initiating of a Phase III or pivotal trial

 

$

500,000

 

 

 

 

 

Receipt of an NADA approval letter for the first DEVICE FACILITATED PRODUCT in TERRITORY A

 

$

1,000,000

 

 

 

 

 

Receipt of an NADA approval letter for the first DEVICE FACILITATED PRODUCT in TERRITORY B

 

$

1,000,000

 

 

 

 

 

Receipt of an NADA approval letter for the first DEVICE FACILITATED PRODUCT in TERRITORY C

 

$

1,000,000

 

 

4.3  Currency, Payment Method.

 

4.3.1  All dollar amounts referred to in this NONEXCLUSIVE LICENSE are United States dollars.  All payments to VGXP under this NONEXCLUSIVE LICENSE shall be made in United States dollars by check payable to “VGX Pharmaceuticals.”  If VGXAH receives revenues from SALES of DEVICE FACILITATED PRODUCTS or PATENTED DEVICES in currency other than United States dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

4.3.2  Amounts that are not paid when due shall accrue interest from the due date until paid, at a rate equal to one and one-half percent (1.5%) per month (or maximum allowed by law, if less).

 

5.  RECORDS AND REPORTS

 

5.1  VGXAH shall deliver to VGXP within forty-five (45) days after the end of each CALENDAR QUARTER following the first SALE of DEVICE FACILITATE PRODUCT(S) or PATENTED DEVICE, a written report, certified by the chief financial officer or treasurer of VGXAH (or an officer of VGXAH charged with the duties typically entrusted to the chief financial officer or treasurer of a Delaware corporation), setting forth the calculation of the royalties due to VGXP under Section 4.1 hereof for such CALENDAR QUARTER, including, without limitation:

 

10


 

5.1.1 Gross consideration for SALES of DEVICE FACILITATED PRODUCTS and/or PATENTED DEVICE(S), including all amounts invoiced, billed or received;

 

5.1.2 NET SALES of DEVICE FACILITATED PRODUCTS and/or PATENTED DEVICE(S) listed by country;

 

5.1.3  Royalties owed to VGXP, listed by category, including, without limitation, earned, and minimum royalty categories.

 

5.2  VGXAH shall pay the royalties due under Section 4.1 within forty-five (45) days following the last day of each CALENDAR QUARTER in which the royalties accrue.

 

5.3  VGXAH shall maintain complete and accurate books and records which enable the royalties payable under this NONEXCLUSIVE LICENSE to be verified.  The records for each CALENDAR QUARTER shall be maintained for three years after the submission of the report covering such period.  Upon reasonable prior notice to VGXAH, VGXAH shall provide VGXP (or an independent, certified public accounting firm selected by VGXP and reasonably acceptable to VGXAH) with access, during normal business hours, to all books and records relating to the SALES of DEVICE FACILITATED PRODUCTS and/or PATENTED DEVICE(S) by VGXAH to conduct a review or audit of those books and records solely for purposes of verifying royalties paid or due under this NONEXCLUSIVE LICENSE.  Access to VGXAH’s books and records for the applicable period(s) shall be available at least once each CALENDAR YEAR, during normal business hours, during the term of this NONEXCLUSIVE LICENSE and for three years after the expiration or termination of this NONEXCLUSIVE LICENSE.  If the audit is performed by an independent, certified public accounting firm selected by VGXP and reasonably acceptable to VGXAH and such auditor determines that VGXAH has underpaid royalties by five percent (5%) or more, then VGXAH shall pay the costs and expenses of VGXP and its accountants in connection with their review or audit, in addition to such underpayment.

 

5.4  VGXP is entitled to only one copy of any reports under this Section 4.5, and shall distribute such reports or audit results only to such persons as may reasonably require such reports or audit results in order for VGXP to fulfill its obligations, or enforce its rights, under this NONEXCLUSIVE LICENSE.

 

6.  INTELLECTUAL PROPERTY, PATENTS AND IMPROVEMENTS TO DEVICE PATENT RIGHTS

 

6.1  ASSIGNMENT.  When a DEVICE IMPROVEMENT and/or MFG IMPROVEMENT is made or discovered by VGXAH, VGXAH shall assign its entire right, title and interest in such DEVICE IMPROVEMENT and/or MFG IMPROVEMENT to VGXP.  Furthermore, VGXAH shall cooperate with VGXP in obtaining patent protection at VGXP’s cost, including, but not limited to the execution of any and all lawful papers in the U.S. and foreign patent offices. VGXP, in return for such cooperation, hereby grants VGXAH the ability to use such DEVICE IMPROVEMENT

 

11



 

and/or MFG IMPROVEMENT under the terms of this NONEXCLUSIVE LICENSE to the extent VGXP has the right to convey the right to practice the DEVICE IMPROVEMENT and/or MFG IMPROVEMENT to VGXAH.

 

6.2  PROHIBITION.  Notwithstanding the foregoing, VGXAH, AFFILIATE, and/or SUBLICENSEE shall not file any patent applications which disclose, describe or require the presence of inventions subject to the DEVICE PATENT RIGHTS or MFG PATENT RIGHTS absent written consent from VGXP.  VGXP will have the right to review all sections and examples relating to DEVICE PATENT RIGHTS and/or MFG PATENT RIGHTS forty five (45) days before the filing of such patent application.  If for any reason VGXAH files a patent application to a DEVICE IMPROVEMENT or MFG IMPROVEMENT, VGXAH shall immediately grant VGXP an irrevocable, fully paid-up, world-wide, exclusive, royalty-free license to such DEVICE IMPROVEMENT and MFG IMPROVEMENT with the right to sublicense such rights.

 

7.  LICENSE OPTION

 

7.1  VGXP SUPPORTED PATENTING  VGXAH hereby grants VGXP an exclusive option to acquire an exclusive or non-exclusive, worldwide, royalty-bearing license to any and all rights owned by VGXAH in the VGXAH INTELLECTUAL PROPERTY that results or is derived from VGXAH’s research and development related to the MFG PROCESSES or PATENTED DEVICES, exercisable at VGXP’s sole discretion.  Upon exercise of such option by VGXP, VGXAH and VGXP will negotiate in good faith the terms of such license agreement, reasonable per industry standards.  This exclusive option will terminate within twelve (12) months from the date of VGXP’s receipt of an enabling written disclosure from VGXAH of the VGXAH INTELLECTUAL PROPERTY (“Exclusive Period”).

 

If VGXP and VGXAH fail to execute a license agreement within the Exclusive Period, VGXAH shall be free to license the VGXAH INTELLECTUAL PROPERTY to any third parties for a period of one (1) year following the Exclusive Period, but not on more favorable terms than VGXAH offered to VGXP.

 

7.2  RESERVATION.  Any license granted to VGXP pursuant to this AGREEMENT shall be subject to VGXAH’s right to use VGXAH INTELLECTUAL PROPERTY for educational and internal research purposes, and if applicable, to the rights of the United States government reserved under Public Laws 96-517, 97-256 and 98-620, codified at 35 U.S.C. 200-212, and any regulations issued thereunder.

 

8.  INFRINGEMENT AND LITIGATION

 

8.1 VGXP and VGXAH are responsible for notifying each other promptly of any known or suspected infringement of DEVICE PATENT RIGHTS or MFG PATENT RIGHTS, which may come to their attention after the EFFECTIVE DATE.  VGXP and VGXAH shall consult one another in a timely manner concerning an appropriate response to the infringement.

 

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8.2 In any action to enforce any of the DEVICE PATENT RIGHTS or MFG PATENT RIGHTS, either party, at the request and reasonable expense of the other party, shall cooperate to the fullest extent reasonably possible.  This provision shall not be construed to require either party to undertake any activities, including legal discovery, at the request of any third party except as may be required by lawful process of a court of competent jurisdiction.

 

9.  CONFIDENTIAL INFORMATION, PUBLICATION, USE OF NAME

 

9.1  CONFIDENTIAL INFORMATION.            For purposes of this agreement, the term “Confidential Information” includes any confidential information of one of the parties hereto (the “Disclosing Party”) that is disclosed to the other party hereto (the “Receiving Party”).   “Confidential Information” includes but is not limited to the terms and conditions of this agreement, business and technical information and data, whether communicated in oral, written, graphic, physical or electronic form, as well as information or data generated or derived as a result of the discussions hereunder.

 

Any Confidential Information disclosed orally by the Disclosing Party must be set forth in writing and delivered to the Receiving Party, marked “confidential” or “trade secret”, within sixty (60) days after oral disclosure in order to be subject to the provisions of this agreement.

 

The term Confidential Information as used in this agreement shall not include any information:

 

a. which was in the public domain at the time of disclosure by the Disclosing Party to the Receiving Party;

 

b. which is published or otherwise comes into the public domain after its disclosure to the Receiving Party through no violation of this Agreement by the Receiving Party;

 

c. which is disclosed to the Receiving Party by a third party not under an obligation of confidence;

 

d. which is already known by the Receiving Party at the time of its disclosure to the Receiving Party by the Disclosing Party as evidenced by written documentation of the Receiving Party existing prior to such disclosure;

 

e. which is independently developed by the Receiving Party through persons who have not had, either directly or indirectly, access to or knowledge of the Confidential Information of the Disclosing Party, as evidenced by written documentation of the Receiving Party; or

 

f. which is required to be disclosed by any law or governmental regulation or produced under order of a court of competent jurisdiction; provided, however,

 

13



 

that the Receiving Party provide the Disclosing Party prompt written notice of such request or order and Disclosing Party is provided with an opportunity to attempt to limit such disclosure.

 

For seven (7) years from the date of disclosure of Confidential Information or the date of termination of this agreement, whichever is later, the parties agree to all the rights, promises and obligations provided in this agreement.  The Receiving Party agrees to treat as confidential all Confidential Information of the Disclosing Party made available to the Receiving Party.  The Receiving Party shall not disclose or use any Confidential Information for any reasons other than relevant to the Purpose, whether or not a written agreement results.

 

9.2            Prior to VGXAH making any oral or written disclosure relating to the DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES, VGXP shall be provided  a period of sixty (60) days to review proposed printed publication (including manuscripts and written abstracts) or oral presentation for improper disclosure of Confidential Information.  After review, if VGXP reasonably determines improper disclosure of CONFIDENTIAL INFORMATION of VGXP, VGXAH shall consider any amendments suggested by VGXP.

 

9.3            VGXAH agrees, upon written request of VGXP, to delay any publication or presentation contemplated under Section 9.2 for up to ninety (90) additional days in order to allow VGXP and VGXAH to protect intellectual property rights (or option rights under this agreement) of VGXP relating to the DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES, including, without limitation, allowing VGXP time to have patent applications filed or amended if VGXP reasonably determines that such filing and/or prosecution is necessary to protect any patentable DEVICE IMPROVEMENTS and/or MFG IMPROVEMENTS contained in such disclosure.

 

9.4            Any publication or disclosure of VGXAH INTELLECTUAL PROPERTY, or Results related thereto, that contains disclosure of DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES, or variants thereof, shall require VGXP’s  right of review as provided in Section 9.2, including the possible period of delay provided in Section 9.3.  Without prejudice to VGXP’s rights under Sections 9.2 and 9.3, VGXP shall use reasonable efforts to minimize delays.

 

9.5            VGXAH shall not use VGXP’s name, or the name of any director, officer or employee thereof, without VGXP’s prior written consent except that VGXAH may acknowledge VGXP’s contributions in scientific publications.  VGXP shall not use VGXAH’s name, or the name of any trustee, officer, faculty member, student or employee thereof, without VGXAH ‘s prior written consent.

 

10.  DISCLAIMER OF WARRANTIES

 

10.1          VGXP represents and warrants to VGXAH that to its KNOWLEDGE as of the date hereof:

 

14



 

 

10.1.1 VGXP has the full authority to execute and deliver this NONEXCLUSIVE LICENSE.

 

10.1.2 No material claim by any third party contesting the validity, enforceability, licensability, use or ownership of any of such DEVICE PATENT RIGHTS has been made, is currently outstanding or is threatened against VGXP.

 

10.1.3 No loss or expiration of any part of the DEVICE PATENT RIGHTS is currently pending.

 

10.2 EXCEPT AS SET FORTH IN SECTION 10.1, THE DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, AND MFG PROCESSES, AND ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT ARE PROVIDED ON AN “AS IS” BASIS AND VGXP MAKES NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED, WITH RESPECT THERETO.  BY WAY OF EXAMPLE, BUT NOT OF LIMITATION, VGXP MAKES NO REPRESENTATIONS OR WARRANTIES (i) OF COMMERCIAL UTILITY; (ii) OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE; OR (iii) THAT THE USE OF THE DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, OR MFG PROCESSES, OR ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADE SECRET OR TRADEMARK OR OTHER PROPRIETARY RIGHTS OF OTHERS.  VGXP SHALL NOT BE LIABLE TO VGXAH, VGXAH’S SUCCESSORS OR ASSIGNS OR ANY THIRD PARTY WITH RESPECT TO: ANY CLAIM ARISING FROM USE OF THE DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, OR MFG PROCESSES, OR ANY OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT OR FROM THE MANUFACTURE, USE OR SALE OF DEVICE FACILIATED PRODUCTS OR PATENTED DEVICES; OR ANY CLAIM FOR LOSS OF PROFITS, LOSS OR INTERRUPTION OF BUSINESS, OR FOR INDIRECT, SPECIAL OR CONSEQUENTIAL DAMAGES OF ANY KIND.

 

10.3  VGXAH shall defend, indemnify and hold harmless VGXP, its trustees, officers, agents and employees (individually, an “Indemnified Party”, and collectively, the “Indemnified Parties”), from and against any and all liability, loss, damage, action, claim or expense suffered or incurred by the Indemnified Parties (including attorney’s fees and expenses) (individually, a “Liability”, and collectively, the “Liabilities”) that results from or arises out of:  (a) the development, use, manufacture, promotion, sale or other disposition of any DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES by VGXAH, its vendors or other third parties; (b) any breach by VGXAH of this NONEXCLUSIVE LICENSE; and (c) the enforcement by an Indemnified Party of this Section.  Without limiting the foregoing, VGXAH shall defend, indemnify and hold harmless the Indemnified Parties from and against any Liabilities resulting from:

 

15



 

10.3.1  any product liability or other claim of any kind related to the use by a third party of a PATENTED DEVICE that was manufactured, sold or otherwise disposed by VGXAH or agents, other than such Liabilities arising from or related to the inaccuracy of any representation or warranty of VGXP in Section 10.1 of this NONEXCLUSIVE LICENSE; and

 

10.3.2  a claim by a third party that the DEVICE PATENT RIGHTS and/or MFG PATENT RIGHTS or the design, composition, manufacture, use, sale, or other disposition of any PATENTED DEVICES and/or MFG PROCESSES infringes or violates any patent, copyright, trademark or other intellectual property rights of such third party, except to the extent that any such claim may relate to the inaccuracy of any representation or warranty in Section 10.1; and

 

10.3.3 clinical trials or studies conducted by or on behalf of VGXAH and/or its agent relating to the PATENTED DEVICES, including, without limitation, any claim by or on behalf of a human subject of any such clinical trial or study.

 

10.4  VGXAH is not permitted to settle or compromise any claim or action giving rise to Liabilities in a manner that imposes any restrictions or obligations on VGXP or grants any rights to the DEVICE PATENT RIGHTS, MFG PATENT RIGHTS, PATENTED DEVICES, or MFG PROCESSES without VGXP’s prior written consent.  If VGXAH fails or declines to assume the defense of any such claim or action within thirty (30) days after notice thereof, VGXP may assume the defense of such claim or action for the account and at the risk of VGXAH, and any Liabilities related thereto shall be conclusively deemed a liability of VGXAH.  The indemnification rights of the parties or any other Indemnified Party contained herein are in addition to all other rights which the parties or such Indemnified Party may have at law or in equity or otherwise.

 

11.  ADDITIONAL PROVISIONS.

 

11.1  ASSIGNS AND SUCCESSORS.  This Agreement is personal to the parties and no rights hereunder may be assigned by VGXAH or VGXP, directly or by merger or other operation of law, without prior, express written consent of the other party.  Any prohibited assignment of this AGREEMENT or the rights hereunder shall be null and void.  No assignment shall relieve the assigning party of responsibility for the performance of any obligations that it has accrued prior to such assignment.

 

11.2  NO IMPLIED WAIVER.  A waiver by either party of a breach or violation of any provision of this AGREEMENT will not constitute or be construed as a waiver of any subsequent breach or violation of that provision or as a waiver of any breach or violation of any other provision of this AGREEMENT.

 

11.3  NO AGENCY.  Nothing herein shall be deemed to establish a relationship of principal and agent between VGXAH and VGXP, nor between or among any of their agents or employees, nor shall this AGREEMENT be construed as creating any form of legal association or arrangement which would impose liability upon one party for the act

 

16



 

or failure to act of the other party.  Nothing in this AGREEMENT, express or implied, is intended to confer on any person other than the parties hereto or their permitted assigns, any benefits, rights or remedies.

 

11.4  COMMUNICATIONS.  Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date dispatched if sent by public overnight courier (e.g., Federal Express) and addressed as follows:

 

If to VGXAH:

 

 

 

 

VGX Animal Health, INC.

 

2700 Research Forest Drive

 

Suite 180

 

The Woodlands, TX 77381

 

 

 

Attention:

Douglas R. Kern

 

 

Vice President Business Development

 

 

 

If to VGXP:

 

 

 

 

VGX Pharmaceuticals, Inc.

 

450 Sentry Parkway East

 

Blue Bell, PA 19422

 

 

 

Attention:

J.Joseph Kim

 

 

President and CEO

 

11.5  CHOICE OF LAW.  This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania, without giving effect to conflict of law provisions.  The parties hereby submit to the exclusive jurisdiction of and venue in any state or federal courts located within the Eastern District of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.

 

11.6  FORCE MAJEURE.  Neither party shall be liable for any failure to perform as required by this AGREEMENT to the extent such failure to perform is due to circumstances reasonably beyond such party’s control, including, without limitation, labor disturbances or labor disputes of any kind, accidents, failure of any governmental approval required for full performance, civil disorders or commotions, acts of aggression, acts of God, energy or other conservation measures imposed by law or regulation, explosions, failure of utilities, mechanical breakdowns, material shortages, disease, or other such occurrences.

 

11.7  LAWFUL CONDUCT.  The parties shall comply with all applicable laws, regulations and other legal requirements as it relates to the conduct of either party in the course of performance of this AGREEMENT.

 

17



 

11.8  AMENDMENTS.  No amendment, modification, waiver, termination or discharge of any provision of this AGREEMENT, nor consent to any departure by either party therefrom, will in any event be effective unless the same will be in writing, specifically identifying this Agreement and the provision intended to be amended, modified, waived, terminated or discharged and signed by the both parties, and each such amendment, modification, waiver, termination, or discharge will be effective only in the specific instance and for the specific purpose for which given. No provision of this Agreement will be varied, contradicted, or explained by any oral agreement, course of dealing or performance, or any other matter not set forth in an agreement in writing and signed by both parties.

 

11.9  ENTIRE AGREEMENT.  This AGREEMENT embodies the entire understanding between the parties relating to the subject matter hereof and supersedes all prior understandings and agreements, whether written or oral.  This AGREEMENT may not be varied except by a written document signed by duly-authorized representatives of each party. IN WITNESS WHEREOF, the duly-authorized representatives of the parties hereby execute this AGREEMENT as of the date first written above.

 

11.10 SURVIVAL.  Termination or expiration of this NONEXCLUSIVE LICENSE shall not affect the covenants, indemnities, obligations, rights, licenses, options, representations, and warranties of the parties as set forth in this NONEXCLUSIVE LICENSE or accrued prior to termination or expiration of this Agreement, unless expressly provided otherwise herein.

 

18



 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this NONEXCLUSIVE LICENSE to be executed by their duly-authorized representatives.

 

 

VGX ANIMAL HEALTH, INC.

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

By: Douglas R. Kern

 

By: J. Joseph Kim

 

 

 

Name:

/s/ Douglas R. Kern

 

Name:

/s/ J. Joseph Kim

 

 

 

Title: Vice President Business Development

 

Title: President and CEO

 

 

 

Date: September 1, 2007

 

Date: September 1, 2007

 

19




EXHIBIT 10.37

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

LICENSE AGREEMENT

 

 

BETWEEN

 

 

VGX ANIMAL HEALTH

 

(VGXAH)

 

 

AND

 

 

VGX PHARMACEUTICALS

 

(VGXP)

 



 

TABLE OF CONTENTS

 

 

 

 

Page

 

 

 

 

1.

DEFINITIONS

 

1

 

 

 

 

2.

LICENSE GRANT

 

4

 

 

 

 

3.

FEES AND ROYALTIES

 

4

 

 

 

 

4.

CONFIDENTIALITY

 

8

 

 

 

 

5.

TERM AND TERMINATION

 

9

 

 

 

 

6.

IMPROVEMENTS TO INVENTION

 

11

 

 

 

 

7.

PATENT MAINTENANCE and REIMBURSEMENT

 

12

 

 

 

 

8.

INFRINGEMENT AND LITIGATION

 

12

 

 

 

 

9.

REPRESENTATIONS AND WARRANTIES OF VGXP; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

13

 

 

 

 

10.

USE OF VGXP’S NAME

 

15

 

 

 

 

11.

ADDITIONAL PROVISIONS

 

15

 

1



 

LICENSE AGREEMENT

 

This License Agreement (“AGREEMENT”) is between VGX Animal Health Inc. (“VGXAH”), a Delaware corporation, with offices located at 2700 Research Forest Drive, The Woodlands, TX 77381, and VGX Pharmaceuticals, Inc., a Delaware corporation organized (“VGXP”), having a place of business at 450 Sentry Parkway, Blue Bell, PA 19422.

 

1.        DEFINITIONS

 

1.1    CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.2    CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.3    DEVELOPMENT PLAN means the plan, as it may be amended from time to time, for the development and/or marketing of the VGXP LICENSED PRODUCTS that demonstrates VGXAH’s commitment to bring the VGXP PATENT RIGHTS to practical application.  The initial DEVELOPMENT PLAN will be attached hereto, as Attachment 2, within 60 days of the EFFECTIVE DATE.

 

1.4    EFFECTIVE DATE means the date on which VGXAH and VGXP have both fully executed this AGREEMENT.

 

1.5    EXCLUDED PROCEEDS means all proceeds reasonably and fairly attributable to bona fide (i) debt financing; (ii) equity (and conditional equity, such as warrants, convertible debt and the like (iii) investments in VGXAH at fair market value; (iv) reimbursements of patent prosecution costs and patent maintenance expenses; (v) reimbursement for the cost of research and/or development services provided on the basis of full-time equivalent efforts of personnel not in excess of commercially reasonable full-time equivalent rates.

 

1.6    FAIR MARKET VALUE means the cash consideration which VGXAH or a sublicensee thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.7    INAD APPLICATION means an Investigational New Animal Drug Application filed with the United States Food & Drug Administration prior to administration of a pharmaceutical product to animals.

 

1.8    NADA means a New Animal Drug Application filed with the United States Food & Drug Administration or its foreign equivalents prior to sale of a pharmaceutical product to animal.

 

1



 

1.9 PATENT MAINTENANCE PAYMENT means an annual charge from VGXP to VGXAH to cover the estimated cost of maintaining the patents related to the field of animal health (“FIELD”) under the VGXP PATENT RIGHTS.

 

1.10 VGXP LICENSED PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale by VGXAH and/or any sublicensee(s) of VGXAH to unrelated third parties which fall under the scope of the VGXP PATENT RIGHTS.

 

1.11 VGXP PATENT RIGHTS means all of VGXP’s interest in the rights represented by or issuing from (including all claims referenced within) those United States patents and patent applications listed in Attachment 1, including, in each case, any continuations, continuations-in-part, divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.12 SALE means any bona fide transaction for which consideration is received or promised for the sale, use, lease, transfer or other disposition of VGXP LICENSED PRODUCT(S) to an unrelated third party.  A SALE of VGXP LICENSED PRODUCT(S) shall be deemed completed at the time VGXAH or its sublicensee invoices, ships or receives payment for such VGXP LICENSED PRODUCT(S), whichever occurs first.

 

1.13 NET SALES means the gross amount invoiced for SALES, less qualifying costs directly attributable to such SALES and actually identified on the invoice and borne by VGXAH or its sublicensee(s).  Such qualifying costs shall be limited to the following:

 

1.13.1 Discounts and rebates, in amounts customary in the trade, for quantity purchases, prompt payments, for wholesalers and distributors;

 

1.13.2 Credits, allowances and/or refunds, not exceeding the original invoice amount, for rejections, claims and/or returns;

 

1.13.3 Prepaid outbound transportation expenses and transportation insurance premiums;

 

1.13.4 Sales and use taxes, tariffs, duties, surcharges and other fees imposed by a governmental agency; and

 

1.13.5 Retroactive price reductions actually applied in an invoice.

 

NET SALES of a commercial product comprising one or more VGXP LICENSED PRODUCTS and one or more other active ingredients (a “COMBINATION PRODUCT”) shall be calculated as set forth above, subject to the provisions of Section 3.1.4.

 

2



 

1.14 TERRITORY A shall mean the United States of America.  TERRITORY B shall mean any country that is a part of the European Union.  TERRITORY C shall mean any country that is not the United States of America or a part of the European Union.

 

1.15 FIELD or FIELD OF USE is used interchangeably and means the practice, including the making, using, selling, or offering to sell any product or services, in the field of animal health.  Such practice contemplates application of any product or services to an end user that is an animal that is non-human.  One example of such end use is the treatment of a farm animal with a DNA product for therapeutic purposes.

 

1.16 DEVICE PATENT RIGHTS means all of VGXP’s interest in the rights represented by United States Patent Number 7,245,963 and United States patent application Serial Number 60/852,149, including, in each case, any continuations, continuations-in-part, divisions, provisionals, substitute applications, and any patent issuing therefrom, and any reissues, reexaminations, renewals and/or extensions (including any supplemental patent certificate) based thereon, and any confirmation patent or registration patent or patent of addition based on any such patent, and all foreign counterparts of any of the foregoing.

 

1.17 PATENTED DEVICES means any and all devices and use of same that is covered by the DEVICE PATENT RIGHTS, and in particular, the devices are those used for the electroporation of DNA to animals or cells of an animal.

 

1.18 DEVICE FACILITATED PRODUCT means any product that is delivered to an animal, or made for the purposes of delivering to an animal, using the PATENTED DEVICES.

 

1.19  PRODUCT IMPROVEMENTS shall mean all inventions for which patent applications are or may be filed, whether ultimately patentable or not, that are conceived or first reduced to practice by VGXAH and/or any sublicense(s) that incorporate or otherwise expand on inventions that are subject to VGXP PATENT RIGHTS and that relate to the make, use, import, sale, or offer of sale of VGXP LICENSED PRODUCT(S).

 

1.20.  AFFILIATE means any corporation, firm, limited liability company, partnership, or other entity that directly or indirectly controls, or is controlled by, or is under common control with a Party to this Agreement. For the purpose of this definition, control means ownership, directly or through one or more Affiliates, of fifty percent (50%) (or such lesser percentage which is the maximum allowed to be owned by a foreign entity in a particular jurisdiction) or more of the shares of stock entitled to vote for the election of directors in the case of a corporation, or fifty percent (50%) (or such lesser percentage which is the maximum allowed to be owned by a foreign entity in a particular jurisdiction) or more of the equity interests in the case of any other type of legal entity, or status as a general partner in any partnership, or any other arrangement whereby a Party controls or has the right to control the board of directors or equivalent governing body of a corporation or other entity.

 

3



 

2.              LICENSE GRANT

 

2.1 Subject to the terms and conditions of this AGREEMENT, VGXP grants to VGXAH for the term of this AGREEMENT an exclusive, world-wide right and license under the VGXP PATENT RIGHTS, with the right to grant sublicenses, to make, have made, use, import, sell and offer for sale VGXP LICENSED PRODUCT(S) in the FIELD OF USE.

 

2.2 VGXP agrees to provide VGXAH with limited rights under the DEVICE PATENT RIGHTS to the extent needed in order to enable the use of the VGXP LICENSED PRODUCT(S), and such agreement is provided in the NONEXCLUSIVE DEVICE AGREEMENT, executed by the parties on August 15, 2007, attached hereto as Attachment 3, and incorporated to this AGREEMENT in its entirety.

 

3.              FEES AND ROYALTIES

 

3.1    License Initiation Fee and Royalties

 

3.1.1         As part of the consideration for the bundle of rights granted to VGXAH hereunder, VGXAH shall pay to VGXP, on a quarterly basis: a) a royalty of ******  of the NET SALES of each VGXP LICENSED PRODUCT which is sold by VGXAH, including any sold by independent contractor(s) or agent(s) of VGXAH, and b) ****** of any royalties paid by a sublicensee(s) of VGXP PATENT RIGHTS to VGXAH.  In determining the earned royalty payment, if any, such payment shall be made by VGXAH at the end of any CALENDAR QUARTER following first SALE of a VGXP LICENSED PRODUCT.  Such royalty payments shall terminate on a product-by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first SALE of such VGXP LICENSED PRODUCT in such country, or (b) in any country in which patent rights exist for any VGXP LICENSED PRODUCT, the date of expiration of the last-to-expire patent in such country, within the definition of VGXP PATENT RIGHTS, with a valid claim covering the VGXP LICENSED PRODUCT.

 

3.1.2         In the event that a sold product is both a DEVICE FACILITATED PRODUCT and a VGXP LICENSED PRODUCT, royalty payment by VGXAH to VGXP shall include only one ****** royalty obligation for each sale event of such product.

 

3.1.3         Within thirty (30) days after the end of each of the periods specified below, VGXAH shall pay to VGXP the specified percentage of any sublicense initiation fee and any other non-royalty payment(s), net of all EXCLUDED PROCEEDS , including those resulting from co-marketing, strategic alliance, joint venture and other similar arrangement(s), actually received during such period by VGXAH from a sublicensee resulting from activities with VGXP LICENSED PRODUCT(S).  Any non-cash consideration received by VGXAH from such

 

4



 

sublicensee shall be valued at its FAIR MARKET VALUE as of the date of receipt by VGXAH.

 

Period

 

Percentage

 

 

 

 

 

EFFECTIVE DATE to 12 months after the EFFECTIVE DATE

 

******

 

 

 

 

 

12 months and one day after EFFECTIVE DATE to 24 months after the EFFECTIVE DATE

 

******

 

 

 

 

 

24 months and one day after EFFECTIVE DATE to 36 months after the EFFECTIVE DATE

 

******

 

 

3.1.4         In the event one or more VGXP LICENSED PRODUCTS are sold in a COMBINATION PRODUCT, the amount of royalties and sublicense revenues paid to VGXP pursuant to this Section 3.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the VGXP LICENSED PRODUCT(S).

 

3.1.5         VGXAH acknowledges and agrees to assume from VGXP all of the payment obligations from VGXP to Ronald O. Bergan and Mary Alice Bergan (collectively referred to as “BERGANS”), which have been stipulated in the Asset Purchase Agreement, section 2.1(a)(vii), made between VGXP and ADViSYS, dated February 21, 2007, such payments being related to the FIELD OF USE.

 

3.1.6         Upon the occurrence of the conditions in section 2.1(a)(iv) of the Asset Purchase Agreement, the parties agree to perform the following:

 

                (a) VGXP shall deliver ***** shares of VGXP stock to the BERGANS,

 

                (b) VGXAH shall deliver a number of shares of VGXAH stock that equals a fair market value of ****** at the time of VGXP’s delivery of the ****** shares of VGXP stock, and

 

                (c) Parties agree that the valuation of VGXAH stock shall be based on the per share price of the next round of financing, such round occurring within 6 months from date of VGXP delivering shares to BERGANS, provided that such round raised greater than ******.

 

5



 

3.2    Diligence and Milestone Fees

 

3.2.1         VGXAH shall use commercially-reasonable efforts to develop for SALE and to market VGXP LICENSED PRODUCTS in a manner consistent with the DEVELOPMENT PLAN.

 

3.2.2         For the term of the Agreement, VGXAH shall provide VGXP on each January 30 th , written progress reports, setting forth in such detail as VGXP may reasonably request, the progress of the development, evaluation, testing and commercialization of each VGXP LICENSED PRODUCT.  VGXAH shall also notify VGXP in writing within thirty (30) days of the first SALE of each VGXP LICENSED PRODUCT.

 

3.2.3         VGXAH shall provide VGXP with a written, current DEVELOPMENT PLAN once every twelve months, beginning upon attachment of the initial DEVELOPMENT PLAN, attached hereto as ATTACHMENT 2.

 

3.2.4         Any of the events listed below that occur after the EFFECTIVE DATE shall require that the following milestone payments be paid by VGXAH to VGXP within sixty (60) days after the achievement of the respective milestone event. The aforementioned notwithstanding, VGXAH shall not be obligated to remit a milestone payment to VGXP until it has raised five million dollars ($ 5,000,000) in total capital. Any milestone payment obligation arising prior to raising five million dollars ($ 5,000,000) in total capital shall be accrued and become immediately payable upon reaching or surpassing this threshold. The milestone payments shall be made for each VGXP LICENSED PRODUCT for each animal species.

 

Event

 

Amount

 

 

 

Filing of an INAD APPLICATION

 

$

250,000

 

 

 

Initiating of a Phase III or pivotal trial

 

$

500,000

 

 

 

Receipt of an NADA approval letter for the first VGXP LICENSED PRODUCT in TERRITORY A

 

$

1,000,000

 

 

 

Receipt of an NADA approval letter for the first VGXP LICENSED PRODUCT in TERRITORY B

 

$

1,000,000

 

 

 

Receipt of an NADA approval letter for the first VGXP LICENSED PRODUCT in TERRITORY C excluding Lifetide™ SW 5 in Australia

 

$

1,000,000

 

6



 

3.3    Reports and Records

 

3.3.1         VGXAH shall deliver to VGXP within forty-five (45) days after the end of each CALENDAR QUARTER following the first SALE of VGXP LICENSED PRODUCTS , a written report, certified by the chief financial officer or treasurer of VGXAH (or an officer of VGXAH charged with the duties typically entrusted to the chief financial officer or treasurer of a Delaware corporation), setting forth the calculation of the royalties due to VGXP under Section 3.1.1 and 3.1.2 herein for such CALENDAR QUARTER, including, without limitation:

 

3.3.1.1              Gross consideration for SALES of VGXP LICENSED PRODUCTS, including all amounts invoiced, billed or received;

 

3.3.1.2              NET SALES of VGXP LICENSED PRODUCTS listed by country;

 

3.3.1.3              Royalties owed to VGXP, listed by category, including, without limitation, earned, sublicensee-derived, and minimum royalty categories.

 

3.3.2         VGXAH shall pay the royalties due under Section 3.1.1 and 3.1.2 within forty-five (45) days following the last day of each CALENDAR QUARTER in which the royalties accrue.  With royalties, VGXAH shall send the report described in Section 3.3.

 

3.3.3         VGXAH shall maintain, and cause its sublicensees to maintain, complete and accurate books and records which enable the royalties payable under this AGREEMENT to be verified.  The records for each CALENDAR QUARTER shall be maintained for three years after the submission of the report covering such period.  Upon reasonable prior notice to VGXAH, VGXAH shall provide VGXP (or an independent, certified public accounting firm selected by VGXP and reasonably acceptable to VGXAH) with access, during normal business hours, to all books and records relating to the SALES of VGXP LICENSED PRODUCTS by VGXAH and its sublicensees to conduct a review or audit of those books and records solely for purposes of verifying royalties paid or due under this AGREEMENT.  Access to VGXAH’s and sublicensee’s books and records for the applicable period(s) shall be available at least once each CALENDAR YEAR, during normal business hours, during the term of this AGREEMENT and for three years after the expiration or termination of this AGREEMENT.  If the audit is performed by an independent, certified public accounting firm selected by VGXP and reasonably acceptable to VGXAH and such auditor determines that VGXAH has underpaid royalties by five percent (5%) or more, then VGXAH shall pay the costs and expenses of VGXP and its accountants in connection with their review or audit, in addition to such underpayment.

 

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3.3.4         VGXP is entitled to only one copy of any reports under this Section 3.3, and shall distribute such reports or audit results only to such persons as may reasonably require such reports or audit results in order for VGXP to fulfill its obligations, or enforce its rights, under this AGREEMENT.

 

3.4    Currency, Payment Method.

 

3.4.1         All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to VGXP under this AGREEMENT shall be made in United States dollars by check payable to “VGX Pharmaceuticals.”  If VGXAH receives revenues from SALES of VGXP LICENSED PRODUCTS in currency other than United States dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

3.4.2         Amounts that are not paid when due shall accrue interest from the due date until paid, at a rate equal to one and one-half percent (1.5%) per month (or maximum allowed by law, if less).

 

4.              CONFIDENTIALITY

 

4.1    CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and marked confidential or, if oral, should be reduced to writing within two weeks of disclosure and marked confidential.

 

4.2    Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party for the term of this Agreement and for five (5) years thereafter.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this AGREEMENT.  The foregoing obligation shall not apply to the below exceptions:

 

4.2.1         information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless received subject to non-disclosure and non-use obligations, or independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s

 

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CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records;

 

4.2.2         information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure;

 

4.2.3         information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

4.2.4         information which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

4.3 If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

4.4 VGXP shall not be obligated to maintain any CONFIDENTIAL INFORMATION of VGXAH except for the reports required in Section 3.3.  VGXP shall use reasonable efforts not to disclose those reports to any third party (subject to the exceptions of Section 4.2).  VGXP bears no institutional responsibility for maintaining the confidentiality of any other CONFIDENTIAL INFORMATION of VGXAH.

 

5.              TERM AND TERMINATION

 

5.1    This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the later of: (a) the expiration or abandonment of the last patent that is a component of the VGXP PATENT RIGHTS; or (b) twenty-five (25) years after the EFFECTIVE DATE.

 

5.2    VGXAH may terminate this Agreement upon: (a) thirty (30)-days written notice to VGXP, if the sale or other exploitation of the VGXP LICENSED PRODUCT(s) becomes technologically or commercially unfeasible, or (b) thirty (30)-days written notice to VGXP; and by completing all the following:

 

5.2.1         ceasing to make, have made, use, import, sell and offer for sale all VGXP LICENSED PRODUCTS;

 

5.2.2         terminating all sublicenses relating to VGXP LICENSED PRODUCTS, and causing all sublicensees to cease making, having made, using, importing, selling and offering for sale all VGXP LICENSED PRODUCTS; and

 

5.2.3         paying all monies owed to VGXP under this AGREEMENT.

 

9


 

5.3   VGXP may terminate this AGREEMENT, upon ten (10)-days written notice to VGXAH, if any of the following events of default (“Default”) occur:

 

5.3.1       VGXAH is more than sixty (60) days late in paying either VGXP or BERGANS (see Section 3.1.5, above) any royalties, expenses or any other monies due under this AGREEMENT and VGXAH does not immediately pay VGXP or BERGANS in full any amounts due upon demand; or

 

5.3.2       VGXAH experiences a Trigger Event (defined in Section 5.4, below);

 

5.3.3       VGXAH materially breaches this AGREEMENT and does not cure the material breach within thirty (30) days after written notice of such material breach.

 

5.4   “Trigger Event” means any of the following:

 

5.4.1        If VGXAH:

 

5.4.1.1     becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

5.4.1.2     is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

5.4.1.3     makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

5.4.2       If proceedings under any United States law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VGXAH;

 

5.4.3       If any order for relief is entered relating to any of the proceedings described in Section 5.4.;

 

5.4.4       If VGXAH shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

5.4.5       If VGXAH shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Section 5.4.

 

5.5   The provisions of Sections 5.3 and 5.4 shall apply to a Default of, or a Trigger Event experienced by, any sublicensee of VGXAH’s rights hereunder if and to the extent that

 

10



 

such Default of, or Trigger Event experienced by, the sublicensee causes VGXAH to fail to meet its diligence obligations under Section 3.2.

 

5.6   Upon and after any termination of this AGREEMENT, VGXAH and any sublicensee thereof shall refrain from further manufacture, sale, marketing, importation and/or distribution of VGXP LICENSED PRODUCT(s).

 

5.7   Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

5.8   Upon termination of this AGREEMENT, VGXAH shall inventory in writing as soon as commercially practicable and in any event no later than sixty (60) days after termination: (a) all completed VGXP LICENSED PRODUCT(s) on hand, under the control of VGXAH or sublicensee(s) thereof; and (b) all VGXP LICENSED PRODUCT(s) in the process of manufacture and component parts thereof.  VGXAH shall deliver copies of such written inventories, verified by an officer of VGXAH, forthwith to VGXP.  VGXP shall have forty five (45) days after receipt of such verified inventories within which to challenge the inventory and request an audit thereof.  Upon five (5)-days written notice to VGXAH, VGXP and its agents shall be given access during normal business hours to the premises of VGXAH, and/or sublicensees thereof for the purpose of conducting an audit.

 

5.9   Upon the termination of this AGREEMENT, VGXAH shall at its own expense forthwith remove, efface or destroy all references to VGXP from all advertising or other materials used in the promotion of VGXAH’s business or the business of any sublicensee of VGXAH and VGXAH and any sublicensee thereof shall not thereafter represent in any manner that it has rights in or to the VGXP PATENT RIGHTS or VGXP LICENSED PRODUCT(s).

 

5.10 Notwithstanding the foregoing, if this AGREEMENT terminates other than for reasons of default, Section 5.3, VGXAH shall have a period of six (6) months to sell off its inventory of VGXP LICENSED PRODUCT(s) existing on the date of termination of this AGREEMENT and shall pay royalties to VGXP with respect to such VGXP LICENSED PRODUCT(s) within thirty (30) days following the expiration of such six-month period.

 

5.11 Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.

 

6.             IMPROVEMENTS TO INVENTIONS COVERED BY VGXP PATENT RIGHTS

 

                When a PRODUCT IMPROVEMENT is conceived or reduced to practice by VGXAH and/or its sublicensee(s), and such PRODUCT IMPROVEMENT incorporates or otherwise expands on invention(s) that are covered by VGXP PATENT RIGHTS

 

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and/or relate to the make, use, import, sale, or offer of sale of VGXP LICENSED PRODUCT(S), VGXAH and/or its sublicense(s) hereby assign their entire right, title and interest in such PRODUCT IMPROVEMENT to VGXP.  Furthermore, VGXAH and/or sublicense(s) agree to cooperate with VGXP in obtaining patent protection to such PRODUCT IMPROVEMENT at VGXP’s cost, including but not limited to the execution of any and all lawful papers in the U.S. and foreign patent offices.  VGXP hereby grants VGXAH a license in the FIELD OF USE under any resulting patents related to same PRODUCT IMPROVEMENT under similar terms as that provided for VGXP PATENT RIGHTS under this AGREEMENT.

 

7.             PATENT MAINTENANCE AND REIMBURSEMENT

 

7.1   VGXP shall solely control, prosecute and maintain the VGXP PATENT RIGHTS during the term of this AGREEMENT.

 

7.2   VGXAH shall remit a PATENT MAINTENANCE PAYMENT to VGXP on each anniversary of this AGREEMENT. The initial PATENT MAINTENANCE PAYMENT shall be ****** and such amount shall be reviewed by the parties after the second anniversary of this AGREEMENT and from time to time. After each review the parties may in good faith adjust the PATENT MAINTENANCE PAYMENT upon mutual agreement in writing between VGXP and VGXAH.

 

8.             INFRINGEMENT AND LITIGATION

 

8.1   VGXP and VGXAH are responsible for notifying each other promptly of any known or suspected infringement of VGXP PATENT RIGHTS, which may come to their attention after the EFFECTIVE DATE.  VGXP and VGXAH shall consult one another in a timely manner concerning an appropriate response to the infringement.

 

8.2   VGXAH may prosecute such infringement at its own expense.  VGXAH shall not settle or compromise any such suit in a manner that imposes any obligations or restrictions on VGXP or grants any rights to the VGXP PATENT RIGHTS, without VGXP’s prior written permission.  Financial recoveries from any such litigation will first be applied to reimburse VGXAH for its litigation expenditures with additional recoveries being paid to VGXAH, subject to lost royalty due VGXP based on such infringement.

 

8.3   VGXAH’s rights under Section 8.2 are subject to the continuing right of VGXP to intervene at VGXP’s own expense and join VGXAH in any claim or suit for infringement of the VGXP PATENT RIGHTS.  Any consideration received by VGXP or VGXAH in settlement of any claim or suit shall be shared between VGXP and VGXAH in proportion with each party’s share of the litigation expenses reasonably incurred in such infringement action.

 

8.4   If VGXAH fails to prosecute any material infringement of VGXP PATENT RIGHTS, VGXP may prosecute such material infringement at its own expense.  In such event, financial recoveries will be entirely retained by VGXP.

 

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8.5   In any action to enforce any of the VGXP PATENT RIGHTS, either party, at the request and reasonable expense of the other party, shall cooperate to the fullest extent reasonably possible.  This provision shall not be construed to require either party to undertake any activities, including legal discovery, at the request of any third party except as may be required by lawful process of a court of competent jurisdiction.

 

9.

 

REPRESENTATIONS AND WARRANTIES OF VGXP; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

 

 

 

 

9.1    VGXP represents and warrants to VGXAH that to its KNOWLEDGE as of the date hereof:

 

9.1.1        VGXP has the full authority to execute and deliver this AGREEMENT.

 

9.1.2        No material claim by any third party contesting the validity, enforceability, licensability, use or ownership of any of such VGXP PATENT RIGHTS has been made, is currently outstanding or is threatened against VGXP.

 

9.1.3        No loss or expiration of any part of the VGXP PATENT RIGHTS is currently pending.

 

9.2   EXCEPT AS SET FORTH IN SECTION 9.1, THE VGXP PATENT RIGHTS,  VGXP LICENSED PRODUCTS AND ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT ARE PROVIDED ON AN “AS IS” BASIS AND VGXP MAKES NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED, WITH RESPECT THERETO.  BY WAY OF EXAMPLE, BUT NOT OF LIMITATION, VGXP MAKES NO REPRESENTATIONS OR WARRANTIES (i) OF COMMERCIAL UTILITY; (ii) OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE; OR (iii) THAT THE USE OF THE VGXP PATENT RIGHTS, VGXP LICENSED PRODUCTS OR ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADE SECRET OR TRADEMARK OR OTHER PROPRIETARY RIGHTS OF OTHERS.  VGXP SHALL NOT BE LIABLE TO VGXAH, VGXAH’S SUCCESSORS OR ASSIGNS OR ANY THIRD PARTY WITH RESPECT TO: ANY CLAIM ARISING FROM USE OF THE VGXP PATENT RIGHTS, VGXP LICENSED PRODUCTS AND ALL OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT OR FROM THE MANUFACTURE, USE OR SALE OF VGXP LICENSED PRODUCTS; OR ANY CLAIM FOR LOSS OF PROFITS, LOSS OR INTERRUPTION OF BUSINESS, OR FOR INDIRECT, SPECIAL OR CONSEQUENTIAL DAMAGES OF ANY KIND.

 

9.3   VGXAH shall defend, indemnify and hold harmless VGXP, its trustees, officers, agents and employees (individually, an “Indemnified Party”, and collectively, the “Indemnified Parties”), from and against any and all liability, loss, damage, action, claim or expense suffered or incurred by the Indemnified Parties (including attorney’s fees and expenses) (individually, a “Liability”, and collectively, the “Liabilities”) that results from or arises out of:  (a) the development, use, manufacture, promotion, sale or other disposition of any VGXP PATENT RIGHTS or VGXP LICENSED PRODUCTS by

 

13



 

VGXAH, its assignees, sublicensees, vendors or other third parties; (b) any breach by VGXAH of this AGREEMENT; and (c) the enforcement by an Indemnified Party of this Section.  Without limiting the foregoing, VGXAH shall defend, indemnify and hold harmless the Indemnified Parties from and against any Liabilities resulting from:

 

9.3.1     any product liability or other claim of any kind related to the use by a third party of a VGXP LICENSED PRODUCT that was manufactured, sold or otherwise disposed by VGXAH, its assignees, sublicensees, or agents, other than such Liabilities arising from or related to the inaccuracy of any representation or warranty of VGXP in Section 9.1 of this AGREEMENT; and

 

9.3.2     a claim by a third party that the VGXP PATENT RIGHTS or the design, composition, manufacture, use, sale, or other disposition of any VGXP LICENSED PRODUCT infringes or violates any patent, copyright, trademark or other intellectual property rights of such third party, except to the extent that any such claim may relate to the inaccuracy of any representation or warranty in Section 9.1; and

 

9.3.3     clinical trials or studies conducted by or on behalf of VGXAH and/or its sublicensees relating to the VGXP LICENSED PRODUCTS, including, without limitation, any claim by or on behalf of a human subject of any such clinical trial or study.

 

9.4   VGXAH is not permitted to settle or compromise any claim or action giving rise to Liabilities in a manner that imposes any restrictions or obligations on VGXP or grants any rights to the VGXP PATENT RIGHTS or VGXP LICENSED PRODUCTS without VGXP’s prior written consent.  If VGXAH fails or declines to assume the defense of any such claim or action within thirty (30) days after notice thereof, VGXP may assume the defense of such claim or action for the account and at the risk of VGXAH, and any Liabilities related thereto shall be conclusively deemed a liability of VGXAH.  The indemnification rights of the parties or any other Indemnified Party contained herein are in addition to all other rights which the parties or such Indemnified Party may have at law or in equity or otherwise.

 

9.5   Insurance

 

9.5.1     VGXAH shall procure and maintain a policy or policies of comprehensive general liability insurance, including broad form and contractual liability, in a minimum amount of $2,000,000 combined single limit per occurrence and in the aggregate, as respects personal injury, bodily injury and property damage arising out of VGXAH’s performance under this AGREEMENT.

 

9.5.2     VGXAH shall, upon commencement of clinical trials involving VGXP LICENSED PRODUCTS, procure and maintain a policy or policies of product liability insurance in a minimum amount of $3,000,000 combined single limit per occurrence and in the aggregate as respects bodily injury and property damage arising out of VGXAH’s performance of this AGREEMENT.

 

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9.5.3     The policy or policies of insurance described in this Section 8.5 shall be issued by a recognized insurance carrier with an A.M. Best rating of “A” or better and shall name VGXP as an additional insured with respect to VGXAH’s performance of this AGREEMENT.  VGXAH shall provide VGXP with certificates evidencing the insurance coverage required herein and all subsequent renewals thereof.  Such certificates shall provide that VGXAH’s insurance carrier(s) notify VGXP in writing at least 30 days prior to cancellation or material change in coverage.

 

9.6        VGXP may periodically review the adequacy of the minimum limits of liability insurance specified in Section 9.5 and VGXP reserves the right to require VGXAH to adjust the liability insurance coverages. The specified minimum insurance amounts do not constitute a limitation on VGXAH’s obligation to indemnify VGXP under this AGREEMENT.

 

10.           USE OF VGXP’S NAME

 

                VGXAH and its employees and agents shall not use, and VGXAH shall not permit its sublicensees to use, VGXP’s name or any adaptation thereof, or any VGXP seal, logotype, trademark, or service mark, or the name, mark, or logotype of any VGXP representative or organization in any way without the prior written consent of VGXP.

 

11.           ADDITIONAL PROVISIONS

 

11.1      Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between VGXP and VGXAH, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

11.2      VGXAH is not permitted to assign this AGREEMENT or any part of it to any person or entity other than an AFFILIATE of VGXAH, either directly or by operation of law, without the prior written consent of VGXP in its sole discretion.  Any prohibited assignment of this AGREEMENT or the rights hereunder shall be null and void.  No assignment relieves VGXAH of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

11.3      A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

11.4      Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by public courier (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

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If for VGXP:

VGX Pharmaceuticals

 

450 Sentry Parkway

 

Blue Bell, PA 19422

 

 

 

Attention: J. Joseph Kim

 

 

If for VGXAH:

VGX Animal Health

 

2700 Research Forest Drive

 

Suite 180

 

The Woodlands, TX 77381

 

 

 

Attention: Douglas R. Kern

 

Either party may change its official address upon written notice to the other party and allow for ten (10) business days for the change to be effective.

 

11.5      This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.

 

11.6      VGXP and VGXAH shall not discriminate against any employee or applicant for employment because of race, color, sex, sexual or affectional preference, age, religion, national or ethnic origin, handicap, or because he or she is a disabled veteran or a veteran of the Vietnam Era.

 

11.7      VGXAH shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.  The transfer of certain technical data and commodities may require a license from the cognizant agency of the United States Government and/or written assurances by VGXAH that VGXAH shall not export data or commodities to certain foreign countries without prior approval of such agency.  VGXP neither represents that a license is not required nor that, if required, it will issue.

 

11.8      If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such

 

16



 

provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

11.9      This AGREEMENT, including the attachments expressly referred to herein and attached, embody the entire agreement and understanding among the parties hereto and thereto and supersede all prior agreements and understandings relating to the subject matter.  This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

11.10    All agreements, covenants, indemnities, obligations, rights, licenses, options, representations, and warranties set forth in this Agreement or accrued prior to Termination or Expiration of this Agreement will survive the execution, delivery, Termination, or Expiration of this Agreement and remain in full effect, unless expressly provided otherwise herein.

 

[SIGNATURES BY PARTIES ON FOLLOWING PAGE]

 

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IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

VGX PHARMACEUTICALS, INC.

VGX ANIMAL HEALTH, INC.

 

 

 

 

 

 

By: J. Joseph Kim

 

By: Douglas R. Kern

 

 

 

Name:

/s/ J. Joseph Kim

 

Name:

 /s/ Douglas R. Kern

 

 

 

Title: President and CEO

 

Title: Vice President, Business Development

 

 

 

Date: September 1, 2007

 

Date: September 1, 2007

 

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EXHIBIT 10.38

 

ASSIGNMENT OF CONTINGENT PAYMENTS

 

This Agreement is made this 20 th  Day of October 2007 (“Effective Date”), by and between VGX Pharmaceuticals, Inc., a Delaware Corporation (hereinafter referred to as  “VGXP”), VGX Animal Health, Inc., a Delaware corporation  (hereinafter referred to as  “VGXAH”), and Ronald O. Bergan and Mary Alice Bergan(hereinafter collectively  referred to as “BERGANS”).

 

WHEREAS, under the Asset Purchase Agreement by and among VGX Pharmaceuticals, Inc., Advisys, Inc.,   and  BERGANS, dated February 21, 2007 (hereinafter referred to as the  “Purchase Agreement”),  VGXP promised to the BERGANS, among other things, certain contingent monetary payments under Article II paragraph 2.1 a(vii) in the Purchase Agreement. (hereinafter the above mentioned monetary obligations shall be referred to as “Bergan Payments”); and

 

WHEREAS, in addition to the licensing of some of VGXP’s technologies, VGXP desires to grant and VGXAH desires to assume the obligations for Bergan Payments; and

 

WHEREAS, the parties does not desire to disturb Bergan Payments and the right of BERGANS to Bergan Payments;

 

NOW, THEREFORE, in consideration of the mutual promises and conditions hereinafter set forth and intending to be legally bound, the parties hereto agree as follows:

 

1.              DEFINITIONS:

 

1.1. FIELD or FIELD OF USE is used interchangeably and means the practice, including the making, using, selling, or offering to sell any product or services, in the field of animal health.  Such practice contemplates application of any product or services to an end user that is an animal that is non-human.  One example of such end use is the treatment of a farm animal with a DNA product for therapeutic purposes.

 

1.2. GHRH means growth hormone releasing hormone.

 

1.3. “Bergan Payments” is used herein to mean the contingent payment obligations of VGXP as agreed to in the Purchase Agreement, Article II paragraph 2.1 a(vii), which relates to payments owed and payable to  BERGANS by VGX based on royalty and upfront and milestone payments made by a licensee of VGX that is a Nonrelated Party and VGX.

 

1.4 “Other Party” or “Nonrelated Party” is used herein interchangeably and means a third party that is not VGX, the BERGANS, or any entity that is wholly owned, majority controlled, or commonly controlled by VGX and/or the BERGANS.

 



 

2.              ASSUMPTION OF PAYMENT OBLIGATION.   VGXAH hereby assumes VGXP’s obligations for Bergan Payments that relate to the FIELD OF USE.   VGXAH assumes and agrees to perform and be bound by, all of the terms, covenants and conditions of the Bergan Payments, commencing as of the date of full execution of this Agreement, with the same force and effect as though VGXAH was originally obligated in the Purchase Agreement.

 

3.              BERGAN PAYMENTS

 

3.1    METHOD OF CALCULATING BERGAN PAYMENTS.  The terms agreed by VGXP and the BERGANS under the Purchase Agreement shall be applicable as though VGXAH is in the place of VGXP.

 

3.2.   Payment of Bergan Payments by VGXAH.  The Bergan Payments that relate to the FIELD OF USE shall be directly paid by VGXAH.

 

3.3.   VGXAH Default.  VGXP agrees to reassume the payment obligations assigned to VGXAH as a result of this Agreement should VGXAH be in default of Bergan Payments.

 

4.              Notices, payments, statements, reports and other communications under this Agreement shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by public courier (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGXP:

VGX Pharmaceuticals

 

 

 

450 Sentry Parkway

 

 

 

Blue Bell, PA 19422.

 

 

 

 

 

 

If for VGXAH:

VGX Animal Health

 

 

 

2700 Research Forest Drive,

 

 

 

The Woodlands, TX 77381

 

 

 

 

 

 

If for Ronald O. Bergen and Mary Alice Bergen:

 

 

 

 

 

 

 

3300 North 7 th  Avenue

 

 

 

Fargo, ND 58108

 

 

 

Any party may change its official address upon written notice to the other party.

 



 

5.              This Agreement shall be construed and governed in accordance with the laws of the Delaware, without giving effect to conflict of law provisions.  In the event that a party to this Agreement perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the courts located in Delaware with respect to any and all disputes concerning the subject of this Agreement.

 

[SIGNATURES ON FOLLOWING PAGE]

 

3



 

IN WITNESS WHEREOF, the parties have executed this AGREEMENT on the Effective Date.

 

 

VGX PHARMACEUTICALS, INC.

VGX ANIMAL HEALTH, INC.

 

 

 

 

By:

/s/ J. Joseph Kim

 

By:

/s/ Douglas R. Kern

 

 

Name:  J. Joseph Kim

 

Name: Douglas R. Kern

 

 

Title: President and CEO

Title: Vice President, Business Development

 

 

Date: October 20, 2007

Date: October 20, 2007

 

 

 

 

RONALD O. BERGAN

 

 

 

By:

/s/ Ronald O . Bergan

 

 

 

 

 

 

Date:

11-9-07

 

 

 

 

 

 

MARY ALICE BERGAN

 

 

 

 

 

By:

/s/ Mary Alice Bergan

 

 

 

 

 

 

Date:

11-9-07

 

 

 

4




EXHIBIT 10.39

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

R&D COLLABORATION AND LICENSE AGREEMENT

 

 

BETWEEN

 

VGX PHARMACEUTICALS, INC.

 

(VGX)

 

 

AND

 

 

VGX INTERNATIONAL

 

(VI)

 



 

R&D COLLABORATION AND LICENSE AGREEMENT

 

This R&D Collaboration and License Agreement (“AGREEMENT”) is between VGX Pharmaceuticals, Inc. (“VGX”), a Delaware corporation, with offices located at 450 Sentry Parkway East, Blue Bell, Pennsylvania 19422, and VGX International (“VI”), a corporation having an address of Jung-Hun Building, #701, 944-1 Daechi 3-Dong, Gangnam-gu, Seoul, Korea.

 

A. Whereas VGX controls certain intellectual property related to VGX-1027 (3-phenyl-4,5-dihydro-5-isoxazoleacetic acid) (hereinafter referred to as “VGX-1027”) a drug for treating all and any disease indications in humans and animals, including but not limited to those listed in Attachment I; and

 

B. Whereas VGX and VI desire to enter into an agreement for exclusive worldwide rights to conduct research, development activities, sales, licensing, and marketing of VGX-1027 for Type 1 Diabetes (hereinafter referred to as “T1D”).

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties hereby agree as follows:

 

1.              DEFINITIONS

 

1.1 CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.2 CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.3 EFFECTIVE DATE means the date on which VI and VGX have both fully executed this AGREEMENT.

 

1.4 FAIR MARKET VALUE means the cash consideration which VGX or VI thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.5 NET SALES is defined as the gross amount of monies or cash equivalent or other consideration which is paid by unrelated third parties to VGX or VI for VGX-1027 by sale or other mode of transfer, less all qualifying costs directly attributable to such sales, which are made, made for, used or sold by VI, its agents, employees and/or independent contractors .

 

NET SALES of a commercial product comprising one or more VGX R&D PRODUCTS and one or more other active ingredients (a “COMBINATION PRODUCT”) shall be calculated as set forth above, subject to the provisions of Section 3.1.3.

 

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1.6 VGX R&D PRODUCT(S) means product(s) which is/are made, made for, used by, imported by or for, sold by or offered for sale for each indication and/or any agents and contractors(s) to unrelated third parties which (1) in the absence of this AGREEMENT would infringe at least one claim of VGX PATENT RIGHTS described in patents listed in Attachment I, or (2) use a process and/or machine covered by at least one claim of VGX PATENT RIGHTS described in patents listed in Attachment I.

 

1.7 SALE means any bona fide transaction for which consideration payment is received or expected for the sale, use, lease, transfer or other disposition of VGX R&D PRODUCT(S) to an unrelated third party.  A SALE of VGX R&D PRODUCT (S) shall be deemed completed at the time VGX or VI, their agents, or their contractors receive payment for such VGX R&D PRODUCT (S).

 

1.8 VGX PATENT RIGHTS means all of VGX’s interest in the rights represented by or issuing from (including all claims referenced within) those patent applications listed in ATTACHMENT I and all future interests in such rights anywhere in the world of the VGX-1027 intellectual property.

 

2.              R&D COLLABORATION

 

Subject to the terms and conditions of this AGREEMENT, VGX and VI shall collaborate to research, develop and market VGX R&D PRODUCTS for T1D. No other rights are granted by either party hereunder.  This agreement shall not impair VI’s freedom (without any restriction or any obligation to VGX) to research, develop, and market products for T1D, except for the restrictions in this Agreement.

 

2.1            VGX shall provide VGX-1027 (3-phenyl-4,5-dihydro-5-isoxazoleacetic acid) necessary for the production or intended for production of VGX R&D PRODUCT(S) upon VI’s request. VI shall reimburse VGX for the costs of such VGX 1027 at a price to be mutually agreed. VGX and VI shall share pre-clinical testing data, and clinical results for product development and clinical development.

 

3.              COST SHARING, FEES, AND ROYALTIES

 

3.1  Cost Sharing, Fees and Royalties.

 

3.1.1         VGX agrees to waive upfront fees.

 

3.1.2         Research and Development Costs.   VI and VGX agree to share the Research and Development costs on a mutually agreeable basis.

 

3.1.3         In consideration of the exclusive worldwide rights granted to VI, VI shall pay to VGX, on a quarterly basis, a royalty of ****** of the NET SALES of each VGX R&D PRODUCT(S), which is sold by VI, its agent(s), and/or independent contractor(s) of VI for a period of ten (10) years from the date of the first SALE of VGX R&D PRODUCT(S) in any country covered by such patent issuance or until

 

2



 

such time as the related patent protection on expires in such country, whichever is the later to occur.

 

3.1.4         In further consideration of the exclusive worldwide rights granted to VI by Ganial Immunotherapeutics, Inc. (hereinafter referred to as “GIT”) through VGX, VI shall pay to GIT, on a quarterly basis, a royalty of ****** of the NET SALES of each VGX R&D PRODUCT(S), which is sold by VI and any agent(s) and/or independent contractor(s) of VI for a period of ten (10) years from the date of the first SALE of VGX R&D PRODUCT(S) in any country covered by such patent issuance or until such time as the related patent protection  expires in such country, whichever is the later to occur.

 

3.1.5         In the event one or more VGX R&D PRODUCT(S) are sold in a COMBINATION PRODUCT, the amount of royalties and agents’ and/or contractors’ revenues paid to VGX pursuant to this Section 3.1 shall be based on the portion of the FAIR MARKET VALUE of such combination of products reasonably attributable to the VGX R&D PRODUCT(S).

 

3.2  Diligence and Milestone Fees.

 

3.2.1         VI shall use commercially reasonable efforts to develop for SALE and to market VGX R&D PRODUCT(S) as drugs for treating T1D indication.  VI and VGX agree to the following R&D milestones.  The amount of the Milestone payments shall be determined within 6 months prior to the scheduled initiation of a Phase II clinical trial for VGX 1027.  The amount shall be determined based on the industry benchmark as described below, and  said payments are payable by VI to VGX within sixty (60) days after the achievement of the respective milestone event.  The data on industry benchmark on such license terms shall be based on the benchmark data gathered by firms such as Recombinant Capital (http://www.recap.com) or other similar data gathering or consulting firms.  If the parties cannot agree on the payment amount, the parties agree to hire two or more internationally reputable investment banks or accounting firms to determine  said amount based on the firms’ own experience and expertise, or on the recommendation of an expert hired by them.

 

Due Date

 

Payment

Upon completion of Phase I safety and dose-escalation studies

 

TBD

Upon completion of patient accrual for T1D Phase II clinical trial for VGX-1027

 

 TBD

Upon completion of patient

 

TBD

 

3



 

accrual for T1D Phase III clinical trial for VGX-1027

 

 

Upon NDA submission for VGX-1027 for T1D

 

TBD

Upon NDA approval for VGX-1027 for T1D

 

TBD

 

3.3  Currency, Payment Method.

 

All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to VGX under this AGREEMENT shall be made in United States dollars by check or wire-transfer.  If VI receives revenues from SALES of VGX R&D PRODUCTS in currency other than United States Dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

3.4  Option to Co-Development and Co-Marketing Rights.

 

3.4.1 Upon successful completion of Phase II  for T1D, VGX shall have an option to develop and market VGX-1027 for T1D in the United States.  Once the option is exercised, VGX shall assume all costs for development and filings in the U.S. for T1D.  In return, VGX shall pay to VI, on a quarterly basis, a royalty of ****** of the NET SALES of each VGX R&D PRODUCT for T1D only, which is sold by VGX, its agent(s), and/or independent contractor(s) of VGX in the U.S.  VGX shall exercise the said option by providing a written notice to VI anytime during the effective term of this Agreement.

 

3.4.2  If VI, its agents, or contractors fails to lead VGX-1027 to an initiation of Phase II Clinical trial for T1D within 5 years from the effective date, VI shall return all rights specified in this Agreement back to VGX.

 

4.              CONFIDENTIALITY

 

4.1 CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and

 

4



 

marked confidential or, if oral, should be reduced to writing within thirty (30) days of disclosure and marked confidential.

 

4.2 Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party during the term of this Agreement and for five (5) years after the date of termination of this Agreement.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this Agreement.  The foregoing obligation shall not apply to:

 

4.2.1         information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless  independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records; and

 

4.2.2         information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure; and

 

4.2.3         information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

4.2.4         information, which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

Note: Confidential information shall not be disclosed to third party and this rule shall apply to both VGX and VI. This is particularly true for process development data.

 

5.              TERM AND TERMINATION

 

5.1 This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the earlier of: (a) expiration of the last-to-expire patent or (b) twenty (20) years after the EFFECTIVE DATE.

 

5



 

5.2 VI may terminate this Agreement (a) upon thirty (30) days written notice to VGX, if the sale or other exploitation of the VGX R&D PRODUCT(s) becomes technologically or commercially unfeasible; or (b) upon sixty (60)-days written notice to VGX, and by doing all of the following:

 

5.2.1         ceasing to make, have made, use, import, sell and offer for sale all VGX R&D PRODUCTS; and

 

5.2.2         paying all monies owed to VGX up to the date of the termination excluding any future obligation under this AGREEMENT.

 

5.3 VGX may terminate this AGREEMENT, upon sixty (60)-days written notice to VI, if any of the following events of default (“Default”) occur:

 

5.3.1         VI is more than ninety (90) days late in paying to VGX royalties, expenses or any other monies due under this AGREEMENT and VI does not immediately pay VGX in full any amounts due upon demand; or

 

5.3.2         VI experiences a Trigger Event (defined below);

 

5.3.3         VI materially breaches this AGREEMENT and does not cure the material breach within ninety (90) days after the receipt of the written notice of such  breach.

 

5.4 “Trigger Event” means any of the following:

 

If VI:

 

5.4.1.1     becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due; or

 

5.4.1.2     is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

5.4.1.3     makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

6


 

5.4.2     If proceedings under any International law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VI;

 

5.4.3     If any order for relief is entered relating to any of the proceedings described in Sections 5.4.2 ;

 

5.4.4     If VI shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

5.4.5     If VI shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 5.4.2, 5.4.3, 5.4.4.

 

5.4.6     I n the event of a “change in control” of VI, VI shall promptly notify VGX of such change in control and VGX shall be permitted to terminate this Agreement at VGX’s option.  A “change of control” means a change in the direct or indirect power to direct or cause the direction of the management and policies of VI, whether through ownership or voting securities, by contract or otherwise

 

5.5 The provisions of Sections 5.3 and 5.4 shall apply to a Default of, or a Trigger Event experienced by, any agents and/or contractors of VI ’s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the agents and/or contractors(s) cause VI to fail to meet its diligence obligations under Section 3.2.

 

5.6 In the event of a termination under Section 5.1 or 5.3, all duties of VGX (other than under Sections 5.11) and all rights (but not duties) of VI (other than under Section 5.11) under this AGREEMENT immediately terminate without the necessity of any action being taken either by VI or by VGX, provided, however, that in no event shall the foregoing be construed to obligate VI to pay any amounts accruing under Sections 3.1  after the date of termination except under Section 5.10.  Upon and after any termination of this AGREEMENT, the rights covered by this agreement for VI and any agents and/or contractors thereof to manufacture, sale, marketing, importation and/or distribution of VGX R&DPRODUCT(s) shall terminate on the same date of the termination of the agreement, except otherwise specified in this agreement or agreed upon by both parties.

 

5.7 Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

5.8 Upon termination of this AGREEMENT under section 5.2 and 5.3, VI shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed VGX R&D PRODUCT(s) on hand, under the control of VI, its agents, or contractors thereof; and (b) such VGX R&D PRODUCT(s) as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be recorded in writing.  VI shall deliver copies of such written inventories, verified by an officer of VI,

 

7



 

forthwith to VGX.  VGX shall have forty five (45) days after receipt of such verified inventories within which to challenge the physical inventory and request an audit thereof.

 

5.9 Upon termination of this agreement under section 5.1, VI shall pay all monies owed to VGX up to the date of the termination.

 

5.10 Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 5.3.1 or 5.3.2, VI shall have a period of six (6) months to sell off its inventory of VGX R&D PRODUCT(S) existing on the date of termination of this AGREEMENT and shall pay royalties to VGX with respect to such VGX R&D PRODUCT(S) within thirty (30) days following the expiration of such six-month period.

 

5.11 Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Articles 4, 5, 6, 7 and 8 shall survive such termination.

 

6.                                        REPRESENTATIONS AND WARRANTIES OF VGX AND VI; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

6.1    VGX represents and warrants to VI that:

 

6.1.1         VGX has the full authority to execute and deliver this AGREEMENT.

 

6.1.2         No material claim by any third party contesting the validity, enforceability, collaborations, use or ownership of any of such VGX PATENT RIGHTS has been made, is currently outstanding or is threatened against VGX.

 

6.2 VI acknowledges that VGX holds world-wide exclusive rights, granted by GIT to VGX, to develop VGX-1027 for the treatment of any human and animal indications.  VI agrees to assume all royalty obligations to GIT with regards to the T1D indication as outlined in Section 3.1.3.

 

6.3 VGX and VI will work together to file the patents and/or patent applications listed in ATTACHMENT I before the deadline permitted by the relevant international and US patent laws.

 

6.4 VGX shall defend and indemnify and hold VI (and its respective officers, directors and employees) harmless against any and all Losses, arising out of, relating to, based on, or caused by (A) the breach by VGX of any representation or warranty contained in this Agreement, (B) a claim that the formulation or manufacture of the VGX-1027 by VGX for VI or other activities of VGX under this Agreement infringe on the patent or other intellectual property rights of a third party, (C) any governmental or regulatory action arising out of VGX, or (D) any negligence or intentional misconduct by VGX in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated in any substantial respect by the

 

8



 

negligent acts of or failure to act by VI or its agents and/or contractors.  VI will promptly notify VGX of any such Losses which come to VI’s attention, but failure to do so will not relieve VGX of its indemnification obligations under this Section 6.3 except to the extent any such delay results in a material prejudice to VGX.  Notwithstanding anything to the contrary in this Agreement, VGX shall not be liable for any Losses to the extent that the Losses suffered by VI (and its officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.5 VI shall defend and indemnify and hold VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) harmless against any Losses, arising out of, relating to, based on, or caused by (A) the breach by VI of any representation or warranty contained in this Agreement or (B) any negligence or intentional misconduct by VI in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated by the negligent acts of or failure to act by VGX, its agents and/or contractors.  VGX will promptly notify VI of any such Losses which come to VGX’s attention, but failure to do so will not relieve VI of its indemnification obligations under this Section 6.4 except to the extent any such delay results in a material prejudice to VI.  Notwithstanding anything to the contrary in this Agreement, VI shall not be liable for any Losses where the Losses suffered by VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

6.6 To best of VGX’s knowledge, there are no pending or threatened suits, claims, or actions of any type whatsoever against VGX with respect to the VGX-1027.

 

6.7 All necessary corporate authorizations, consents and approvals which are necessary or required for VGX to enter into this Agreement have been duly obtained;

 

6.8 To the best of its knowledge, the entering into of this Agreement by VGX will not (i) violate any Applicable Law or(ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination, cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of VGX, under its organizational documents, as amended to date, or any material note, indenture, mortgage, le ase, agreement, contract, purchase order or other instrument, document or agreement to which VGX is a party or by which it or any of its properties or assets is bound or affected.

 

7.              ADDITIONAL PROVISIONS

 

7.1 Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between VGX and VI, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be

 

9



 

construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

7.2 INTENTIONALLY LEFT BLANK

 

7.3 VI is not permitted to assign this AGREEMENT or any part of it to any person or entity, either directly or by operation of law, without the prior written consent of VGX in its sole discretion.  However, VI has the rights to contract out the manufacturing of the products covered in this agreement and rights to establish collaboration, development, and marketing partnership with a third party. In case any products covered in this agreement is sold by a marketing partnership, VI shall have the responsibility to pay royalty that is calculated on the bases of the combined net sales of VI and its marketing partners. No assignment relieves VI of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

7.4 A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

7.5 Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by internationally recognized express couriers (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGX:

 

VGX Pharmaceutical, Inc.

450 Sentry Parkway East

Blue Bell, PA 19422

Attention: Chief Executive Officer

 

 

If for VI:

 

VGX International

Jung-Hun Building, #701

944-1 Daechi 3-Dong

Gangnam-gu, Seoul, Korea

Attention: Vice President

 

Either party may change its official address upon written notice to the other party.

 

7.6 This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania in the United States of America, without giving

 

10



 

effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the either federal or state courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.  The parties agree to accept original service of complaint via internationally recognized courier with receipt confirmation.  Also, the parties agree to waive the Hague Convention requirements relating to translation of certain documents to applicable foreign language which in this case is Korean.

 

7.7 VI shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.

 

7.8 If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

7.9 This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

[SIGNATURE PAGE FOLLOWS]

 

11



 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

VGX INTERNATIONAL, INC.

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

By:

 

/s/ Harry Chung

 

By:

 

/s/ Kevin W. Rassas

 

Name:

Harry Chung

 

Name:

Kevin W. Rassas

 

Title:

 

Vice President

 

Title:

 

Senior Vice President

 

Date:

 

 

Date:

 

 

12



 

ATTACHMENT I

 

List of the PCT Patents filed and filings planned:

 

Patent Application Title:

 

13



 

FIRST AMENDMENT TO THE R&D COLLABORATION AND LICENSE AGREEMENT BETWEEN VGX PHARMACEUTICALS, INC. AND VGX INTERNATIONAL DATED DECEMBER, 18, 2006

 

This is the First Amendment (“Amendment”) to the R&D Collaboration and License Agreement Between VGX Pharmaceuticals, Inc. (“VGX”)  and VGX International (“VGXI”) dated as of 29th day of October, 2007 (the “Effective Date”), amending the R&D Collaboration and License Agreement (“Agreement”)  dated December 18, 2006 between VGX and VGXI.  All undefined terms contained herein shall have the meaning set forth in the Agreement.

 

WHEREAS, both parties wishes to amend the Agreement as follows:

 

NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

 

1.                                        Research and Development costs to be borne by VGXI include all costs incurred and charged by third-party organizations or persons providing services to properly initiate and complete Phase I clinical trials for VGX-1027.  These development costs include preclinical toxicity tests, completion of lab work, payments for non-VGX personnel at clinical study sites working on the trial, and creation of case report forms, IND preparation and filing and support costs, API and placebo manufacturing costs, fill/finish/encapsulation/packing/labeling and shipment costs, statistical analysis and data management, and pharmacokinetic analysis of drug levels.  In return, VGX will be responsible for all direct internal costs (including salaries. supplies, and overhead costs) of program managers, R&D scientists, clinical scientists and other support staff involved in the overseeing and management of product and clinical development processes for VGX-1027.

 

VGX International

VGX Pharmaceuticals

Jung-Hun Bldg, #701

450 Sentry Parkway

944-1 Daechi 3-Dong

Blue Bell, PA 19422

Gangnam-Gu, Seoul, Korea

Telephone: 267-440-4201

 

 

 

 

/s/ Bryan Byong Jin Kim

 

/s/ Gene J. Kim

Bryan Byong Jin Kim, DMD

Gene J. Kim

Vice President

Chief Financial Officer

 

 

 

 

Date:

10/29/07

 

Date:

10/31/07

 



 

SECOND AMENDMENT TO THE R&D COLLABORATION AND LICENSE AGREEMENT BETWEEN VGX PHARMACEUTICALS, INC. AND VGX INTERNATIONAL DATED DECEMBER, 18, 2006

 

This is the Second Amendment (“Amendment”) to the R&D Collaboration and License Agreement Between VGX Pharmaceuticals, Inc. (“VGX”)  and VGX International (“VGXI”) dated as of 4th day of August, 2008 (the “Effective Date”), amending the R&D Collaboration and License Agreement dated December 18, 2006 between VGX and VGXI and the First Amendment to the R&D Collaboration and License Agreement Between VGX Pharmaceuticals, Inc. (“VGX”) and VGX International (“VGXI”) dated October 31, 2007. (Both the license agreement and the First Amendment shall be collectively referred to as “the Agreement”) All undefined terms contained herein shall have the meaning set forth in the Agreement.

 

WHEREAS, both parties wishes to amend the Agreement as follows:

 

NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

 

1.                                        The parties are amending certain terms in the Agreement.  Specifically, the parties are amending the terms of payment relating to the 3 rd  party costs associated with the VGX-1027 MAD study, which is expected to begin in 3 rd  quarter of 2008. (hereinafter referred to as “the 3 rd  party costs”)  The total estimated 3 rd  party cost is currently expected to be approximately 1.2 million USD.  The study is critical to successfully completing the Phase I trial of VGX-1027.  By way of this Amendment, VGX agrees to pay for the 3 rd  party costs with the understanding that such costs shall be reimbursed by VGXI at the conculusion of the MAD study.  Therefore, VGXI agrees to reimburse VGX for all 3 rd  party costs of the MAD study paid by VGX within 60 days of the conclusion of the study. All other terms in the Agreement shall remain the same.

 

VGX International

VGX Pharmaceuticals

Jung-Hun Bldg, #701

450 Sentry Parkway

944-1 Daechi 3-Dong

Blue Bell, PA 19422

Gangnam-Gu, Seoul, Korea

Telephone: 267-440-4201

 

 

 

 

/s/ Bryan Byong Jin Kim

 

/s/ Gene J. Kim

Bryan Byong Jin Kim, DMD

Gene J. Kim

Vice President

Chief Financial Officer

 

 

 

 

Date:

08/04/08

 

Date:

08/04/08

 




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EXHIBIT 10.40

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated November 1, 2007, is made by and between VGX Pharmaceuticals, Inc, a Delaware corporation (the " Company "), and with its principal offices at 450 Sentry Parkway E., Blue Bell, PA, 19422 and Dr. Niranjan Sardesai ("Executive"), whose address is 102 Savory Lane, North Wales, PA 19454.

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Mr. Sardesai as Senior Vice President, Research & Development and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on November 1, 2007 (the " Commencement Date ") and continue for a period of three (3) years from the Commencement Date; provided , however , that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Mr. Sardesai throughout the Term with such responsibilities, duties and authority as are assigned to him by the Board of Directors (the "Board") of the Company, Chief Executive Officer or its designee. Mr. Sardesai shall report to the Chief Executive Officer.

        b.     Executive shall faithfully devote his full business/working time, attention and energy to the business and affairs of the Company and the performance of his duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of Executive's Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $140,000 per annum (the " Base Salary "), which shall be paid to Executive by the Company or any of its affiliates on a monthly basis.

        b.     Increases in the Base Salary shall be reviewed annually by the Board during the Term and any such increases, if any, will be at the Board's or its designee's sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.

4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at twenty percent (20%) or more of the Base Salary. The amount shall be determined by the Board, in its



sole and absolute discretion, which shall be binding and final, and shall be paid in a one-time lump sum payment (less payroll taxes). To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated.

5.     Benefits; Stock Options and Warrant.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

        a.     The Executive, Mr. Sardesai, will be granted options to purchase Seventy Five (75,000) shares of Common Stock of the Company at a strike price of $5.00 per share pursuant to an Option Grant Agreement in substantially the form attached hereto as Exhibit A . These options are subject to the rules and regulations of the 2001 Equity Incentive Plan. In addition, all shares of the Company's stock will be subject to those restrictions contained in the anticipated future Company's Stockholder's Agreement.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or his personal representative terminate Executive's employment on account of his death or total disability. In the case of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if he shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of his death or such Total Disability, such termination shall be effective immediately upon

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notice, in which case Executive or his representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board and/or Chief Executive Officer; provided , however , that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days written notice (" Termination

3



Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of his termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate his employment for good reason (" Termination For Good Reason ") upon 30 days written notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean voluntary termination by Executive of his employment with the Company based on one of the following events:

        e.     Voluntary Termination.     Executive may otherwise terminate his employment without Good Reason upon 30 days written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of his Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

        f.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

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8.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

9.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

10.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

11.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:

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        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

12.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

13.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

14.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

15.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

16.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

17.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

18.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

19.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

20.     Termination of Other Agreements.     

        The execution of this Agreement by Viral Genomix and the Executive terminates and voids for all purposes any other Agreements, if any, between the parties.

[SIGNATURE PAGE FOLLOWS]

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         IN WITNESS WHEREOF , the parties hereto have executed this Employment Agreement as of the date first written above.

    VGX PHARMACEUTICALS, INC.

 

 

By:

 

/s/ J. Joseph Kim

    Name:   Dr. J. Joseph Kim, Ph.D.
    Title:   President & CEO

 

 

EXECUTIVE:

 

 

/s/ Niranjan Sardesai

DR. NIRANJAN SARDESAI

7


FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
NOVEMBER 17, 2007

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and Niranjan Sardesai ("Executive") dated as of 20th day of August, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated November 17, 2007 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Dr. Niranjan Sardesai
102 Savory Lane
North Wales, PA, 19454
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Niranjan Sardesai

Niranjan Sardesai
Sr. Vice President
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

August 20, 2008


 

Date:

 

August 20, 2008

SECOND AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
NOVEMBER 17, 2007

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and Niranjan Sardesai ("Executive") dated as of            day of October 1, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated November 17, 2007 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Dr. Niranjan Sardesai
102 Savory Lane
North Wales, PA, 19454
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Niranjan Sardesai

Niranjan Sardesai
Sr. Vice President
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

October 1, 2008


 

Date:

 

October 1, 2008



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EXHIBIT 10.41

 

LEASE AGREEMENT

 

VENTURE TECHNOLOGY CENTER XI BUILDING

2700 RESEARCH FOREST DRIVE, SUITE 180

THE WOODLANDS, MONTGOMERY COUNTY, TEXAS

 

THIS LEASE AGREEMENT (“Lease”), effective August 20 , 2001, is between WOODLANDS VTO 2000 LAND, L.P” a Texas limited partnership (“Lessor”), and APPLIED VETERINARY SYSTEMS, INC., a Delaware corporation (“Lessee”).

 

1.  Premises . Upon the terms and conditions hereinafter set forth, Lessor does hereby lease, demise and let to Lessee and Lessee does hereby lease, and take from Lessor, approximately 13,185 net rentable square feet of floor space (“Premises”), subject to Section 48, together with all appurtenances thereto, in a building known and referred to as Venture Technology Center XI Building (“Building”), located at 2700 Research Forest Drive, The Woodlands, Montgomery County, Texas. The Building is located on that certain 8.016 acre tract of land, located in the John Taylor Survey, A-547 in Montgomery County, Texas, more particularly described in Exhibit “A” (“Land”). The Premises is shown on the floor plan attached hereto as Exhibit “A-I”. The address of the Premises is 2700 Research Forest Drive, Suite 180, The Woodlands, Texas 77380. Lessor reserves the right to change the name of the Building whenever it desires without any liability or consent of Lessee.

 

2. Loading Dock and Parking . In addition to the Premises, Lessee and its invitees are hereby granted the exclusive right to use the loading dock to be affixed to the Premises pursuant to the Tenant Improvement Letter attached hereto as Exhibit “B”. Lessee shall also have forty (40) parking permits, each for the non-exclusive use by a single automobile in the parking areas provided by Lessor on the Land. Lessor shall keep in good condition throughout the Term described below the parking areas for and vehicular access ways to the Premises. The use of such parking and access areas shall at all times be subject to such reasonable rules and regulations as Lessor may promulgate.

 

3. Term . The term of this Lease (“Term”) shall commence on October 1, 2001 (“Commencement Date”) and shall expire on the last day of the seventy-third (73 rd) full calendar month following the Commencement Date, subject to earlier termination as hereinafter provided. Lessor shall tender possession of the Premises to Lessee upon execution of this Lease by Lessor. Within 15 days following Lessee’s receipt from Lessor of a memorandum of this Lease specifying the Commencement Date and date of expiration of the Term, Lessee agrees to execute the memorandum.

 

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4. Use . Lessee shall use the entire Premises solely for pharmaceutical manufacturing, standard research laboratory and for office and for no other use.

 

5. Acceptance of the Premises . Lessee agrees to accept the Premises “as-is”, “where-is”, “with all faults”. However, all improvements, if any, shall be constructed in the Premises, and the cost thereof paid, in accordance with Exhibit B . Except as expressly provided in this Lease or such Exhibit B , Lessor has not undertaken to perform any alteration or improvement to the Premises. By taking possession of the Premises, Lessee shall be deemed to have accepted the Premises, and to have acknowledged that Lessor’s obligations under Exhibit B have been fully performed. Lessee hereby waives (i) any claims due to defects in the Premises and/or the Building except (A) minor finish adjustments in work performed by Lessor (“Punchlist Items”) specified in reasonable detail by Lessee contemporaneously with taking possession, and (B) latent defects in Lessor’s Work as described under Exhibit B , if any, of which Lessee notifies Lessor within 180 days after taking possession; and (ii) all express and implied warranties of suitability, habitability and fitness for any particular purpose. Lessee waives the right to terminate this Lease due to the condition of the Premises or the Building; Punchlist Items; or Lessor’s failure to perform its construction obligations under this Lease.

 

6. Security Deposit . Lessee contemporaneously with the execution of this Lease has deposited with Lessor the sum of $46,147.50 receipt of which is hereby acknowledged by Lessor, said security deposit being given to secure the faithful performance by Lessee of all of the terms, covenants and conditions of this Lease to be kept and performed by Lessee. If Lesseeshall fail to pay the rent herein reserved promptly when due or if Lessee violates any of the other terms, covenants or conditions of this Lease, said security deposit may, at the option of Lessor, be applied to any rent due and unpaid or to any damages suffered by Lessor as a result of Lessee’s default. Nothing contained in this Section shall in any way diminish or be construed as waiving any of Lessor’s other remedies as provided elsewhere in this Lease or at law or in equity. Should the entire security deposit or any portion thereof be applied by Lessor for the payment of sums due and payable to Lessor hereunder, Lessee shall, on the written demand of Lessor, remit to Lessor a sufficient amount in cash to restore said security deposit to its original amount. Should Lessee comply with all of the terms, covenants and conditions of this Lease and promptly pay all of the rental herein provided for as it falls due, (including any Additional Rent due at the end of the Fiscal Year, which term is defined in Section 8 below, during which the Term expires or terminates), and all other sums payable by Lessee to Lessor hereunder, said security deposit or remaining balance thereof shall be returned in full to Lessee. Lessor shall have the right to commingle the security deposit with other funds of Lessor, and any interest earned shall be the property of Lessor. Lessor may deliver the security deposit to any purchaser of Lessor’s interest in the Premises, and thereupon be discharged from further liability with respect to such deposit.

 

7. Base Rent . The Base Rent, which Lessee hereby agrees to pay to Lessor monthly, in advance, at Lessor’s address stated above, shall be the sum per month set forth below, due and payable on the first day of each calendar month during the Term hereof, without offset or deduction, with a pro rata portion being due and payable in advance for any partial month occurring at the beginning of the Term.

 

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Month

 

Base Rent Amount

 

1

 

$5,000.00

 

2-25

 

$12.00/PSF/yr.

 

26-49

 

$13.00/PSF/yr.

 

50-73

 

$14.00/PSF/yr.

 

 

8.  Additional Rent . Lessor agrees to pay all Operating Expenses (as defined in Section 10 below) (which includes the Management Fee described in Section 10) up to a maximum amount of $3.00 per year for each square foot of rentable floor area in the Building (“Operating Cost Allowance”). In the event the Operating Expenses shall, in any Fiscal Year exceed the product of the Operating Cost Allowance times the rentable square feet of the Building (prorated for any partial Fiscal Year at the beginning or end of the Term), Lessee agrees to pay to Lessor, as Additional Rent, Lessee’s pro rata share of any such excess (“Excess Operating Expenses”). The term “Fiscal Year”, as used herein, shall mean Lessor’s fiscal year for accounting purposes which currently is the 12-month period beginning January I and ending December 31. Lessor shall have the right to change the Fiscal Year, from time to time, and, in such event, Lessor shall notify Lessee in writing of such change. Lessee’s pro rata share shall be determined by multiplying the Excess Operating Expenses by a fraction, the numerator of which shall be the number of net rentable square feet in the Premises, and the denominator of which shall be 95% of the net rentable square footage in the Building, which may change from time to time utilizing BOMA (Building Owners and Managers Association) standards. Within 90 days following the completion of each Fiscal Year, Lessor will provide to Lessee a statement showing in reasonable detail the Operating Expenses for the preceding Fiscal Year, the Additional Rent due with regard to Lessee’s share of the Excess Operating Expenses, and Lessor’s reasonable estimate of Excess Operating Expenses for the then current Fiscal Year. Lessee shall, on or before 30 days following receipt of said statement, pay to Lessor the amount of Additional Rent due as provided herein, less the amount of Additional Rent paid in advance (if any) during the preceding Fiscal Year. Any overpayment will be credited by Lessor to Lessee’s pro rata share of the estimated Excess Operating Expenses for the then current Fiscal Year. Lessee agrees to pay Additional Rent each month thereafter, in addition to Base Rent, in an amount necessary to amortize the estimated Excess Operating Expenses for the then current Fiscal Year (or the pro rata portion thereof, if applicable) over a period equal to the lesser of (i) the number of months remaining in the Term or (ii) the number of months remaining in the current Fiscal Year. Notwithstanding that the Term has expired or been terminated, Lessee shall remain liable for and agrees to pay to Lessor within 30 days following receipt of an invoice therefore, its pro rata portion of Excess Operating Expenses for the Fiscal Year (or portion thereof) during which the Term expired or was terminated.

 

Lessee shall have the right, at its expense and at a reasonable time, but, in any event within twelve (12) months following the end of any Fiscal Year, to audit Lessor’s books relevant to the Additional Rent due under this Section provided that (i) the audit shall be prepared by a

 

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certified public accounting firm of recognized regional standing or by Lessee=s in-house audit staff; (ii) such firm or audit staff is not compensated on a contingency fee@ basis; (iii) such audit is pursued to its conclusion within thirty (30) days following the date of its commencement and is conducted at the location where Lessor maintains its books and records and shall not unreasonably interfere with the conduct of Lessor=s business; and (iv) the audit report shall be simultaneously delivered to Lessor at no charge. In the event that Lessor=s statement of Operating Expenses exceeds Lessee=s actual pro rata share of Excess Operating Expenses for  any Fiscal Year by more than five percent (5%), Lessor agrees to reimburse Lessee Lessee=s reasonable and actual cost of such audit, not to exceed $1,500.

 

9. Payment of Rentals . Lessee covenants to promptly pay all rentals when due and payable. A late charge of 10% per cent shall be added to any payment of Base Rent or Additional Rent which is more than 10 days past due in order to compensate Lessor for the extra administrative expenses incurred. If Lessor shall pay any monies or incur any expenses in correction of violations of the covenants herein set forth, the amounts so paid or incurred shall, on notice to Lessee, be considered additional rent payable by Lessee with the first installment of Base Rent thereafter to become due and payable, and may be collected or enforced as by law provided in respect of rentals.

 

10. Operating Expenses . The term “Operating Expenses” means all of Lessor’s costs, expenses and disbursements (but not acquisition of capital investment items, except as hereinafter expressly provided or specific costs billed to specific lessees) to operate and maintain the Land, the Building, and all improvements on the Land from time to time, including, but not limited to, Lessor’s costs of providing utilities, including, but not limited to lighting; porter services and supplies; refuse removal (if Lessor elects to furnish this service); landscaping, including irrigation; and general maintenance and repairs, including, but not limited to, repairs to roof surface and preventive maintenance, parking area restriping, exterior painting and other activities. Operating Expenses shall also include a reasonable amortization charge on account of any capital expenditure incurred to effect a reduction of Operating Expenses and a reasonable charge for amortization of all capital items Lessor installs (a) to reduce Operating Expenses, or (b) to promote safety, or (c) which Lessor is required to install on or for the benefit of the Building by any governmental law, code or regulation passed or enacted on or after the Commencement Date, or (d) which is a replacement (as opposed to additions or new improvements) of items located in the common areas adjacent to the Building, the parking area and other facilities used in connection with the Building, or involving the exterior of the Building, including, but not limited to, the roof and structural elements. Additionally, Operating Expenses shall include all ad valorem taxes or assessments, and annual assessments of The Woodlands Community Association, Inc. and The Woodlands Commercial Owners Association, whichever is applicable, which accrue against the Building or the Land during the Term, together with all insurance premiums and deductibles which Lessor is required to pay or deems necessary to pay with respect to the Building or the Land, including, but not limited to, casualty insurance and liability insurance, and a management fee (“Management Fee”) of 5% of the gross rental for the Building. Lessor agrees that those items listed on Exhibit  “E” attached hereto shall not be included within the definition of “Operating Expenses.” Notwithstanding anything contained

 

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herein to the contrary, it is agreed that in the event not more than 95% of the rentable area in the Building is occupied during any Fiscal Year or in the event not more than 95% of the rentable area in the Building is provided with building standard services during any Fiscal Year, an adjustment shall be made in computing the Operating Expenses for such year so that those Operating Expenses which vary with occupancy of the Building shall be computed for such year as though the Building had been 95% occupied during such year and as though 95% of the Building had been provided with building standard services during such year. Lessor agrees that it shall not be permitted to recover more than 100% of Operating Expenses for any Fiscal Year.

 

Notwithstanding anything contained herein to the contrary, if at the end of the Fiscal Year, the Land, with the Building thereon, has not yet been placed on the tax rolls, the Fiscal Year ad valorem taxes and assessment shall be adapted and increased as if it had been.

 

11. Utilities . Lessor shall make available to the Building electricity, water and sewer Facilities. Lessee agrees to assume all costs and expenses for water and sewer, except as herein provided, electricity, and telephone, including any license or deposit required to establish or maintain such services, and the costs of installation, hook-up and metering. Lessor agrees to pay all costs and expenses for water and sewer service. The cost of these services shall be included with Operating Expenses as defined in Section 10 hereof. Lessor, however, reserves the right to submeter, at Lessee’s cost and expense, Lessee’s water and sewer usage, charging Lessee at cost plus 15% overhead. Lessee shall promptly pay for all utility services furnished to the Premises during the term of this Lease. Failure by Lessor to any extent to furnish these defined services or any cessation thereof shall not constitute a breach of this Lease, render Lessor liable in any respect for damages to either person or property, nor be construed as an eviction of Lessee, nor work an abatement of rent, nor relieve Lessee from fulfillment of any covenant or agreement herein, Lessee hereby waiving all claims against Lessor arising from service interruptions. In the event of any such interruption other than a service interruption for scheduled maintenance, tests and inspections, however, Lessor shall use reasonable diligence during normal business hours to restore such service in any circumstance in which such restoration is within the reasonable control of Lessor.

 

In the event that there is any interruption of utility services to the Premises that (a) is within Lessor=s actual control, and (b) Lessee is unable to operate (and Lessee does not actually operate) its business at the Premises, and such interruption continues for a period of ten (10) consecutive days, then Base Rent shall abate commencing on the eleventh (11th) consecutive day of such interruption until such time as such utility services are resumed.

 

12. Peaceful Enjoyment . Lessee shall and may peacefully have, hold and enjoy the Premises for the Term, subject to the terms and conditions of this Lease, provided that Lessee pays the rentals and other sums herein recited and performs all of its covenants and agreements herein contained. It is understood and agreed that this covenant and any and all other covenants of Lessor contained in this Lease shall be binding upon Lessor and its successors and assigns, but only with respect to breaches occurring during its and their respective ownership of Lessor’s interest hereunder.

 

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13. Alterations, Additions and Improvements . Lessee shall not make or allow to be made any alterations or physical additions in or to the Premises without first obtaining the written consent of Lessor, which consent shall not be unreasonably withheld, delayed or conditioned; provided, however, that Lessee acknowledges and agrees that it shall not be unreasonable for Lessor to withhold its approval to any alterations or physical additions which are structural in nature or which could affect adversely the mechanical, plumbing or electrical systems for the Building. Lessor shall not be liable as a result of any such consent for completeness, design sufficiency, or compliance with any law, ordinance, order, rule, or regulation and Lessee shall indemnify, defend and hold Lessor harmless from all claims, demands, damages, causes of action or litigation, arising out of or resulting from such alterations.

 

Any and all alterations, additions or improvements, other than that portion of the initial Tenant improvements which are to be provided by Lessor pursuant to the terms of Exhibit “B” hereto, shall be made at Lessee’s sole expense in a good and workmanlike manner, in compliance with all applicable laws, ordinances and regulations, with a contractor approved by Lessor, which approval shall not be unreasonably withheld, conditioned or delayed. At Lessor’s option, all such alterations, additions or improvements upon the earlier to occur of (i) the termination date of the Lease or (ii) Lessor’s termination of Lessee’s right of possession of the Premises pursuant to Section 29 of the Lease, shall become the property of Lessor and shall be surrendered to Lessor upon the termination of this Lease by lapse of time or otherwise; provided, however this clause shall not apply to removable equipment or furniture owned by Lessee and which can be removed without damage to the Building or the Premises, provided there is no default by Lessee in any of the terms and conditions of the Lease. Notwithstanding anything foregoing to the contrary, upon the earlier to occur of (i) the termination date of this Lease, or (ii) Lessor’s termination of Lessee’s possession of the Premises pursuant to Section 29 hereof, Lessor may require Lessee to remove the “Identified Alterations” or any part thereof, and restore the same to the customary condition of so-called “second generation space” and to restore any portion of the Building shell affected by such removal to its condition prior to installation of said Identified Alterations, reasonable wear and tear excepted. The rights conferred to Lessor hereunder shall be in addition to (and not in conflict with) any other rights conferred on Lessor by this Lease, in equity or at law. At such time as Lessor approves the plans for the Tenant Improvements (as provided for in Exhibit “B”), Lessor shall identify which alterations, additions or improvements to the Premises, including without limitation, any cabling or other computer, satellite or telecommunications equipment or hardware, either located in the Premises or elsewhere within the Building or the Land, which Lessor may require be removed at expiration or earlier termination of this Lease (the “Identified Alterations”); provided, however, Lessor shall have the right until the date of expiration or earlier termination, by written notice to Lessee, to select which of the Identified Alterations shall be removed and which shall not be removed.

 

14. Exterior Repairs . Lessor will keep the exterior of the Building, including any doors, windows, or glass, in repair, provided Lessee shall give Lessor written notice of the necessity for such repairs, and provided that the damage thereto shall not have been caused by the negligence of Lessee, its agents, employees, licensees or invitees, in which event Lessee shall be responsible therefor for the cost. Lessor shall be under no liability for repair, maintenance, alteration or any

 

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other action with reference to any plumbing, electrical or other mechanical installation within or serving the Premises or any part thereof, except for the service lines leading to the Premises, provided that the damage thereto shall not have been caused by the negligence of Lessee, its agents, employees, licensees or invitees, in which event Lessee shall be responsible therefor for the cost.

 

15. Operation by Lessee . Lessee agrees to (a) keep the inside of all glass in the doors and windows of the Premises clean; (b) keep all interior surfaces of the Premises clean; (c) replace promptly, at its expense, any cracked or broken window glass inside the Premises with glass of like kind and quality; (d) maintain the Premises in a clean, orderly and sanitary condition and free of insects, rodents, vermin and other pests; (e) keep any garbage, trash, rubbish or refuse in rat-proof containers within the interior of the Premises until removed from the area; (f) have such garbage, trash, rubbish and refuse removed at its expense on a regular basis from location points and at such times as designated by Lessor, if said service is not provided by Lessor; (g) keep all mechanical apparatus free of vibration, noise or pollution which may be transmitted beyond the Premises; (h) comply with all laws, ordinances, rules and regulations of the Fire Underwriters Rating Bureau now or hereafter in affect; (i) shall not commit or allow any waste or damage to be committed to the Premises, any portion of the Building or the Land; and (j) conduct its business in all respects in a dignified manner in accordance with high standards of business operation.

 

In addition, Lessee shall not (a) place or maintain any merchandise or other articles in any vestibule or entry of the Premises, on the footwalks adjacent thereto or elsewhere on the exterior of the Premises or Building without the written consent of Lessor; (b) permit undue accumulation of garbage, trash, rubbish or other refuse within or without the Premises; (c) cause or permit objectionable odors to emanate or be dispelled from the Premises; (d) cause or permit the parking of vehicles so as to interfere with the use of any driveway, walk, parking area, dock or other common facility in the area; (e) occupy, use or permit the use or occupancy of any portion of the Premises for any business or purpose which is immoral, disreputable or in violation of any legal direction of any public officer; or (f)  occupy, use or permit the use or occupancy of any portion of the Premises for any business or purpose which, in the opinion of Lessor, reasonably formed, constitutes a public or private nuisance or unduly disturbs the business of other tenants in the Building.

 

Lessor shall have the right, upon written notice to Lessee, to provide for rubbish and refuse removal services as required of Lessee above, and if such cost is not otherwise included in Operating Expenses, Lessee agrees to reimburse Lessor for the cost incurred in providing such service within 30 days after receipt of a statement setting forth the cost of such service. Lessee agrees to discharge all waste materials from the Premises in compliance with the rules and regulations as set forth in The Woodlands Metro Center Municipal Utility District Policy Manual - Industrial Waste Discharges - Permits and Charges - No. R&S-50, issued July 12, 1979, with an effective date of July 12, 1979, as it may be amended from time to time. Lessee shall haul away for disposal at its own expense, any waste material not meeting the standards for discharge set forth in the above-referenced manual.

 

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Lessee shall comply, at Lessee’s cost and expense, with all private restrictions encumbering the Land and all present and future laws, ordinances, orders, rules, regulations and requirements of all federal, state, and municipal governments, including all municipal and road utility districts and municipal utility districts, and all departments, commissions, boards and officers thereof, and any other body exercising similar functions, which now or hereafter may be applicable to the Premises, the improvements in the Premises, or to the use or manner of use of the Premises or the improvements, including but not limited to, all environmental laws and the Americans With Disabilities Act. In the event of a violation of any environmental law by Lessee and cleanup of contamination is required, in addition to all other remedies of Lessor under this Lease or at law or in equity, Lessee shall conduct a cleanup so that there is a total and complete removal of all contaminates from the Premises. Lessee agrees that no such cleanup shall be subject to a risk reduction Standard 2 or 3 or Remedy Standard B, and no deed recordation notice shall be recorded against the Premises.

 

Lessee also agrees to comply with the Rules and Regulations of the Building, a copy of which is attached as Exhibit “C” . Lessor may amend said Rules and Regulations, from time to time, if reasonably necessary for the safety, care, or cleanliness of the Building, provided that no amendment shall alter any covenant or provision contained in this Lease. Lessee agrees to comply with any amendment which is made to said rules and Regulations in compliance with the terms of this subsection.

 

Lessee shall promptly pay directly to the taxing authority all sales and/or ad valorem taxes now or hereafter levied on Lessee’s personal property and leasehold improvements. Lessee waives all rights under applicable law to protest appraised values or receive notice of reappraisal regarding the Land and Building (including Lessor’s personalty), irrespective of whether Lessor contests same. To the extent such waiver is prohibited, Lessee appoints Lessor as Lessee’s attorney-in-fact, coupled with an interest, to appear and take all actions which Lessee would otherwise be entitled to take under applicable law.

 

16. Interior Repairs and Maintenance . Lessee will, at Lessee’s cost and expense, keep the interior of the Premises, together with all electrical, plumbing and other mechanical installations therein, all heating and air conditioning equipment, and all interior windows or doors serving the Premises, in good order and repair, and will make all replacements thereto as its expense. Lessee will surrender the Premises at the expiration or earlier termination of this Lease, in as good condition as when received, excepting depreciation caused by ordinary wear and tear. Lessee will not overload the electrical wiring serving the Premises or within the Premises, and will install at its expense, but only after obtaining Lessor’s written approval, which approval shall not be unreasonably withheld, delayed or conditioned, any additional electrical service which may be required in connection with Lessee’s use or occupancy. Notwithstanding anything herein to the contrary, Lessor, and not Lessee, shall be liable for any and all interior repairs which may result from any structural failure of the Building, unless caused by Lessee, its agents, employees or invitees. Lessee will repair promptly, at its expense, any damage to the Premises caused by bringing into the Premises any property for Lessee’s use, or by the installation or removal of such

 

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property, regardless of fault or by whom such damage was caused, unless caused by the gross negligence or willful misconduct of the Lessor or Lessor Parties (hereinafter defined). Upon execution of this Lease, Lessee, at its own cost and expense, shall enter into a regularly scheduled preventative maintenance/service contract with Lessor, or a maintenance contractor approved by Lessor, which approval shall not be unreasonably withheld, conditioned or delayed, for servicing all hot water, heating, and air-conditioning systems and equipment within the Premises. If Lessee fails to make such repairs and/or to perform the maintenance and repairs to the Premises which are Lessee’s obligation under this Lease, Lessor may make same, and Lessee agrees to pay, as additional rent, the cost thereof, plus 15% overhead, to Lessor promptly upon Lessor’s demand therefor.

 

17. Roof and Walls . Lessor or its designee shall have the exclusive right (a) to use all or any part of the roof of the Building for any purpose including to erect additional stories or other structures over all or any part of the Premises, and to erect in connection with the construction thereof temporary scaffolds and other aids to construction on the exterior of the Premises, provided that access to the Premises shall not be denied; and (b) upon reasonable prior written notice to Lessee, to install, maintain, use, repair and replace within the Premises, pipes, ducts, conduits, wires and all other mechanical equipment serving other parts of the Building, the same to be in locations within the Premises as will not materially interfere with Lessee’s use thereof. Lessee shall have no right to penetrate or erect improvements on the roof without the prior written consent of Lessor, such approval not to be unreasonably withheld, conditioned or delayed. Lessee shall be liable in damages to Lessor for any breach of this provision, including damages for loss of any and all warranties.

 

18. Signs and Advertising . Lessee will not place or suffer to be placed or maintained on or displaced to the exterior of the Premises, any sign, advertising matter or other thing of any kind, and will not place or maintain any decoration, lettering or advertising matter on the glass of any window or door of the Premises without first obtaining the written approval of Lessor and anybody having a right to approve signs pursuant to any restrictive covenants agreements. Lessee will maintain any approved sign, decoration, lettering, advertising matter or other thing in good condition and repair at all times, in compliance with all laws and private covenants affecting the Landlord or the Building.

 

So long as the square footage occupied by Lessee in the Building under this Lease is such that Lessee is one of the four (4) largest tenants in the Building (i.e., no more than three (3) other tenants in the Building occupy more square footage than Lessee), then Lessee shall have the right to locate a sign advertising Lessee upon both of the Building’s monument structures. If Lessee should become the fifth (5 th ) largest tenant in the Building, then Lessor shall have the right to require that Lessee’s sign panel on the Building’s monument structures be removed. Lessor shall maintain such panels on the monument structures for so long as Lessee is not in default under the terms of this Lease. The cost of installation, the cost of the sign itself, and any costs incurred by Lessor in repairing such sign shall be at the sole cost and expense of Lessee, and Lessee shall indemnify and hold Lessor harmless with respect to any claim, charge, expense, or liability for same. The placement of any such sign upon the monument structures and the design and criteria

 

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thereof shall be governed by such rules, regulations and requirements as Lessor may, from time to time, promulgate. Upon default hereunder, expiration, or earlier termination of this Lease, any sign advertising Lessee upon the monument structures shall be removed by Lessee at its sole cost and expense within thirty (30) days after the occurrence of such default, expiration, or termination. If Lessee fails to perform any of its obligations under this paragraph, Lessor shall be entitled to perform Lessee=s obligations on Lessee=s behalf and for Lessee=s account, in which event Lessee shall, within thirty (30) days following receipt of Lessor=s invoice accompanied by supporting evidence of such expenditures incurred by Lessor, reimburse Lessor for all reasonable costs and expense incurred in connection with performing such obligations. If Lessee fails to timely reimburse Lessor, Lessor shall have the right to file suit against Lessee in a court of competent jurisdiction and recover from Lessee amounts due Lessor, together with interest thereon from the due date until paid at the lesser of (a) the highest non-usurious rate of interest allowed by applicable law, or (b) eighteen percent (18%) per annum.

 

19. Entry by Lessor . Lessee shall permit Lessor or Lessor’s agents, representatives, or employees to enter upon the Premises at reasonable times, and upon having given Lessee reasonable advance notice, (a) to inspect the Premises, to determine whether Lessee is in compliance with the terms of this Lease; (b) to show the Premises to prospective purchasers, lessees, mortgagees, beneficiaries under trust deeds, or insurers (but as to prospective lessees only during the last 7 months of the Term), and (c) to make repairs, improvements, additions and alterations thereto, as Lessor is permitted to make according to the terms of the Lease. Any inspections of the Premises pursuant to this subsection shall be at Lessor’s cost and expense; provided, however, in the event it is determined by Lessor that an environmental study should be conducted on the Premises and said environmental study determines that Lessee has not complied with all then existing environmental laws, Lessee shall reimburse Lessor for the cost of the study within 15 days after receipt of an invoice setting forth the cost, and Lessee shall promptly take all action necessary, at Lessee’s sole expense, to remedy any noncompliance by Lessee discovered by such study in accordance with Section 15 above.

 

20. Liens . In the event that any mechanic’s, materialman’s, or other lien shall at any time be filed against the Premises, the Building or the Land purporting to be for work, labor, services or materials performed for or furnished to Lessee or anyone holding the Premises through or under Lessee, or arising out of any alleged act or omission of Lessee, Lessee shall forthwith cause the same to be properly bonded or released. If Lessee shall fail to cause such lien to be bonded or released within 15 days after being notified of the filing thereof, then, in addition to any other right or remedy of Lessor, Lessor may, but shall not be obligated to, discharge the same by posting a bond or paying the amount claimed to be due, and the amount so paid by Lessor, and all costs and expenses incurred by Lessor in procuring the discharge of such lien, including reasonable attorney’s fees, shall be due and payable by Lessee to Lessor as additional rent on the first day of the next succeeding month. Lessor shall not be liable for any labor or materials furnished to Lessee upon credit, and no mechanics’, materialman’s or other liens for any such labor or materials shall attach to or affect the estate or interest of Lessor in and to the Land or Building.

 

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21. Subordination . Lessee agrees that this Lease is and shall be subordinate to any mortgage or deed of trust which may now or hereafter encumber the Building or the Land, and to all renewals, modifications, consolidations, replacements and extensions thereof. In confirmation of such subordination, Lessee shall at Lessor’s request execute promptly any appropriate certificate or instrument that Lessor may reasonably request. In the event of the enforcement by the trustee or the beneficiary under a mortgage or deed of trust of the remedies provided for by law or by such mortgage or deed of trust, Lessee will, upon request of any person or party succeeding to the interest of Lessor as a result of such enforcement, attorn to and automatically become the lessee of such successor in interest without change in the terms or other provisions of this Lease; provided, however, that such successor in interest shall not be bound by (i) any payment of Base Rent or Additional Rent for more than one month in advance except prepayments in the nature of security for the performance by Lessee of its obligations under this Lease; (ii) any amendment or modifications under this Lease made without the written consent of such trustee, beneficiary, or successor in interest; (iii) any default by the prior owner or Landlord in the observance or performance of any of its covenants or obligations hereunder, or (iv) any right of offset which Lessee may have had against the prior owner or Landlord. Upon request by any successor in interest, Lessee shall execute and deliver an instrument or instruments confirming the attornment herein provided for. Lessee further agrees that in the event Lessee is notified of the existence of any mortgage or deed of trust and of the address of the holder of any such instrument, Lessee agrees that it will give the holder thereof notice of any claimed default under this Lease, and will exercise no remedies which it may have on account thereof until forty-five (45) days have elapsed after the receipt of such notice by the holder of such instrument without cure thereof.

 

Lessee has requested that Lessor provide a non-disturbance agreement from Lessor’s current mortgagee. Lessor agrees to use Lessor’s best reasonable efforts to provide such an agreement in form and substance acceptable to such mortgagee as soon as reasonably possible following Lessor’s execution of this Lease.

 

Within 15 days after Lessor’s request, Lessee agrees to execute an estoppel certificate or other agreement certifying to Lessor and/or any mortgagee of the Building or any successor thereto or designee thereof, such facts and agreeing to such reasonable notice provisions as such mortgagee may request in connection with Lessor’s financing. If Lessee fails or refuses to give a certificate hereunder within the time period herein specified, then the information contained in such certificate as submitted by Lessor shall be deemed correct for all purposes, and all notice provisions and other matters in the certificate shall be deemed agreed to, but Lessor shall have the right to treat such failure or refusal as a default by Lessee.

 

This Lease and all rights of Lessee hereunder are further subject and subordinate to the extent that the same relate to the Premises to all ground or underlying leases covering the Land/or any part thereof which may now or hereinafter affect the Land or the Building, and any renewals or modifications thereof.

 

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22. Condemnation . If the whole or any part of the Premises shall be taken under the power of eminent domain, this Lease shall terminate as to the part so taken on the date Lessee is required to yield possession thereof to the condemning authority. Lessor shall, with reasonable diligence, make such repairs and alterations as may be necessary in order to restore the part not taken to a useful condition, and the Base Rent shall be reduced proportionately to the portion of the Premises so taken. If the amount of the Premises so taken substantially impairs the usefulness of the Premises for the purposes set forth in Section 4, either party may terminate this Lease within 30 days after Lessee is dispossessed, effective as of the date when Lessee is required to yield possession. All compensation awarded for any taking shall belong to and be the property of Lessor, except that Lessee shall have the right to assert a claim for any personalty of Lessee that is taken and for Lessee’s moving costs.

 

23. Fire and Casualty . In the event of a fire or other casualty in the Premises, Lessee shall immediately give notice thereof to Lessor. If the Premises, shall be destroyed by fire or other casualty so as to render the Premises untenantable, the rental herein shall be reduced proportionally to the portion of the Premises rendered untenantable until such time as the Premises are made tenantable by Lessor. If from such cause the same shall be so damaged that Lessor shall decide not to rebuild, or if Lessor’s lender or mortgagee does not make adequate insurance proceeds available to make such repairs, then all rent and other sums owed hereunder up to the time of such destruction or casualty shall be paid by Lessee, and thenceforth this Lease shall cease and come to an end. If Lessor elects to rebuild the Premises, then Lessor shall have a period of 180 days in which to substantially complete such rebuilding. If Lessor is unable to substantially complete such rebuilding within such 180-day period, then Lessee shall have the right, exercisable until such time as Lessor has actually substantially completed such rebuilding (but not thereafter), to terminate this Lease by written notice to Lessor.

 

24. Casualty Insurance . Lessor shall, at all times during the Term, maintain a policy or policies of insurance with the premiums thereon fully paid in advance, issued by and binding upon some solvent insurance company, licensed to do business in the State of Texas, insuring Lessor’s interest in the Building against loss or damage by fire and other hazards with coverages and in amounts as customarily carried by owners of similar buildings in the Montgomery County, Texas area, as determined by Lessor, with payments for losses thereunder payable solely to Lessor or its designee.

 

25. Liability and Personal Property Insurance . Lessee shall maintain, at its expense, at all times during the Term, a policy or policies of commercial general liability insurance, an all-risk policy insuring against loss or damage by fire or other hazards for the full replacement value of Lessee’s personal property, trade fixtures, equipment, inventory, and any alterations or improvements Lessee constructs on the Premises (with extended coverage limits), and builder’s risk coverage in such amounts as are reasonably required by Lessor in the event Lessee performs any alterations or improvements to the Premises, with the premiums thereon fully paid in advance, each issued by (i) an insurance company or companies rated “A-” or higher under the most current edition of A.M. Best’s Key Rating Guide, (ii) a Lloyds of London underwriter, or (iii) an insurance company agreed to by Lessor. All insurers must be licensed to do business in

 

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the State of Texas. The insurance shall afford protection of not less than $1,000,000 combined single limit bodily injury and property damage per occurrence. The policy or policies shall name Lessor as an additional insured. As to any injury or damage occurring in or on the Premises, Lessee’s insurance shall be primary. Lessee’s policy shall contain an agreement by the insurer that such policy, or policies may not be canceled or materially modified without 30 days’ prior notice to Lessor. Lessee shall provide Lessor a copy of the required policy or policies, or a certificate evidencing the required coverage, before beginning any work in the Premises or taking occupancy of same. Additionally, Lessee shall provide Lessor evidence of the renewal of each policy at least 30 days before the expiration of the policy.

 

26. Release of Claims: Waiver of Subrogation . Anything in this Lease to the contrary notwithstanding, Lessor and Lessee each waive any and all right of recovery, claim, action or cause of action against the other and its partners (if any), and the agents, officers, and employees of the other party or its partners, for any loss or damage:

 

(i)                                     to the Premises, the Building, or any improvements thereto, or any personal property of such party therein, by reason of fire, the elements or any other cause which could have been insured against under a Texas standard special form extended coverage insurance policy, or

(ii)                                  arising out of any business interruption, including but not limited to loss of profits, by reason of fire, the elements or any other cause,

 

regardless of cause or origin, including the sole or concurrent negligence of the other party or its  partners, or the agents, officers, or employees of the other party or its partners. Lessor and Lessee covenant that its insurance policies shall provide that the insurer shall not hold any right of subrogation against the other party for losses which must be insured against by the terms of this Lease. This Section shall survive the termination of this Lease.

 

27. Release and Indemnification by Lessee . Subject to the terms of Section 26, above, notwithstanding that joint or concurrent liability may be imposed upon Lessor by law, Lessee shall indemnify and hold harmless (and at Lessor’s option, defend) Lessor, and Lessor’s property managers, lenders, employees, agents, contractors and invitees, and any affiliates or subsidiaries thereto (individually, “Lessor Party”, collectively, “Lessor Parties”) at Lessee’s sole cost and expense, against any loss, cost, damage or expense (including attorneys’ fees and court costs) relating to or as a result of (a) any default or failure to comply with the terms hereof (whether in connection with termination hereof or otherwise) by Lessee, its agents, contractors, employees and invitees (individually, “Lessee Party”, collectively, “Lessee Parties”); (b) any act, omission or negligence of Lessee or any Lessee Parties; and (c) all claims for damages to persons or property by reason of the use or occupancy of the Premises not caused by the gross negligence or willful misconduct of Lessor or the Lessor Parties. Notwithstanding any other provision hereof, the preceding indemnity shall survive the termination, cancellation or expiration of this Lease. Moreover, Lessor shall not be liable, and Lessee covenants not to bring any action against Lessor, for any damage or injury to the Premises, Lessee’s furniture, personal property, trade fixtures,

 

13



 

inventory or equipment, Lessee, or any Lessee Parties, arising from any use or condition of the Premises, Building, or Land, the act or neglect of co-tenants or of any other person, or malfunction of any equipment or apparatus serving the Premises, Building, or Land. Any and all claims against Lessor for any damage or injury referred to in this paragraph are hereby waived and released by Lessee.

 

28. Holding Over . In the event of holding over by Lessee after the expiration or termination of the Term and without the written consent of Lessor, there shall be no renewal of this Lease by operation of law, but at Lessor’s sole option, Lessee shall be a tenant at sufferance and shall pay monthly rent during the holdover period equal to double the amount of all Base Rent and Additional Rent payable during the last month of the Term. Further, Lessee shall indemnify Lessor against all claims for damages by any other lessee to whom Lessor may have leased all or any part of the Premises. Lessee shall vacate and deliver the Premises to Lessor upon Lessee’s receipt of notice from Lessor to vacate. No holding over by Lessee with or without the consent and acquiescence of Lessor or the acceptance of rent shall operate to extend, reinstate or continue the Term of this Lease.

 

29. Default by Lessee . If (a) Lessee fails to timely pay any sum to be paid by Lessee under this Lease and such failure continues for a period of 10 days following the date on which written notice thereof is given (or deemed given) by Lessor; provided, however, that Lessor shall be required to give only two (2) such notices in any 12-month period, per calendar year, and upon the third such failure in any l2-month period, per calendar year, Lessor shall have the right to avail itself of any or all remedies afforded to Lessor hereunder without any further notice to Lessee; (b) Lessee fails to perform any of its other duties or obligations under this Lease and such default continues for 20 days after Lessor delivers written notice to Lessee or deposits written notice in the U. S. Mail addressed to Lessee’s address above; provided, however, that if such failure is one which is not reasonably susceptible of being cured within a 20-day period, then Lessor shall not be deemed to be in default hereunder so long as Lessee commences its cure of such failure within such 20-day period and diligently and continuously prosecutes the cure thereof to completion within ninety (90) days after delivery or deposit of Lessor’s written notice of such failure; (c) any of the following actions occur and Lessee fails to contest same using Lessee’s best reasonable efforts and cause same to be removed, dismissed, or vacated within 30 days from the date of entry or filing: (i) Lessee’s interest under this Lease is levied on under execution or other legal process, or (ii) any petition is filed by or against Lessee to declare Lessee a bankrupt or to delay, reduce or modify Lessee’s debts or obligations, or (iii) any petition under the Bankruptcy Code is filed or other action taken to reorganize or modify Lessee’s capital structure, or (iv) Lessee is declared insolvent according to law, or (v) any general assignment of Lessee’s property is made for the benefit of creditors, or (vi) a receiver or trustee is appointed for Lessee or its property; (d) Lessee vacates or abandons the Premises and ceases payment of rent; (e) if Lessee is a corporation, Lessee ceases to exist as a corporation in good standing in the State of Texas; or (f) if Lessee is a partnership or other entity, Lessee is dissolved or otherwise liquidated, then Lessor may treat the occurrence of anyone or more of the foregoing events as a breach of this Lease. Upon the occurrence of any of the foregoing events, at Lessor’s option, Lessor shall have anyone or more of the following described remedies, in addition to all other rights and remedies provided at law or in equity:

 

14



 

A.            Lessor may continue this Lease in full force and effect, and this Lease shall continue in full force and effect as long as Lessor does not terminate this Lease, and Lessor shall have the right to collect Rent, Additional Rent and other charges when due.

 

B.            Lessor may terminate this Lease and forthwith repossess the Premises and recover damages in a sum of money equal to the total of (i) the cost of recovering the Premises, including the cost of the removal and storage of any of Lessee’s possessions left within the Premises, (ii) the unpaid Base Rent and Additional Rent earned at the time of termination, plus interest thereon at the lesser of 18% or the then maximum interest rate permitted to be charged by applicable law (“Interest”) from the due date until paid, (iii) the balance of the Base Rent and Additional Rent for the remainder of the Term, discounted to its present value at the rate of 6% per annum, less the fair market rental value (allowing a reasonable period for reletting) of the Premises for said period (provided said sum shall not be less than zero), and (iv) any other sum of money and/or damages owed by Lessee to Lessor.

 

C.            Without terminating this Lease, Lessor may terminate Lessee’s right of possession and repossess the Premises by forcible detainer suit or otherwise, without demand or notice of any kind to Lessee, and without terminating this Lease, without acceptance of surrender of the Premises, and without becoming liable for damages, or guilty of trespass. If Lessor pursues this remedy and if and to the extent required by law, Lessor shall use reasonable efforts to relet the Premises for Lessee’s account, for such rent and upon such terms and conditions as Lessor deems satisfactory. Lessor shall be deemed to have used “reasonable efforts” to relet the Premises if Lessor offers the Premises “for lease” and entertains in good faith, bona fide offers to lease submitted to Lessor. In no event shall Lessor be obligated to lease the Premises in priority of other space in the Building or adjacent buildings owned by Lessor or any affiliate thereof. If Lessor so relets, Lessor is authorized to decorate or to make any repairs, changes, alterations or modifications in or to the Premises as it deems necessary to prepare the Premises to relet at Lessee’s expense. If Lessor fails to relet the Premises, then Lessee shall pay to Lessor as damages a sum equal to the amount of the Base Rent and Additional Rent provided for in this Lease for such period or periods. If Lessor relets the Premises and fails to realize a sufficient sum from such reletting to pay all Base Rent and Additional Rent due and payable hereunder after deducting (a) the due and unpaid Base Rent and Additional Rent, (b) the accrued Interest thereon, (c) the cost of recovering possession, (d) the costs and expenses of all decorations, repairs, changes, alteration and modifications, (e) the expense of such reletting and the collection of the rent accruing therefrom, (f) the cost of any brokerage fees or commissions payable by Lessor in connection with such reletting or attempted related; (g) the cost of removing and storing the furniture, trade fixtures, equipment, inventory and/or personal property of Lessee or any other occupant’s property left on the Premises, Parking, or Land after reentry, (h) any other costs incurred by Lessor in such reletting; and (i) any other sum or money or damages owed by Lessee to Lessor at law, in equity, or hereunder, then Lessee shall pay to Lessor any such deficiency upon demand from time to time, Lessor shall in no event be obligated to pay any excess proceeds from such reletting to Lessee after deduction of the foregoing from such proceeds. Lessor may file one or more suits to recover any sums falling due under this Section 

 

15



 

from time to time. Any reletting shall not be an election by Lessor to terminate this Lease or acceptance of surrender of the Premises unless Lessor gives a written notice of such intention to Lessee. Notwithstanding any such reletting without termination, Lessor may at any time thereafter elect to terminate this Lease for such previous default.

 

D.            Lessor may change the locks on the Premises and not return the new key to the Lessee unless the Lessee cures the default(s). The Lessor will not have to give the Lessee a new key unless the Lessee cures the default(s); the new key will be provided only during Lessor’s regular business hours.

 

E.             Lessor may enter upon the Premises and do whatever Lessee is obligated to do under the terms of this Lease; and Lessee agrees to reimburse Lessor on demand for any expenses which Lessor may incur in effecting compliance with Lessee’s obligations under this Lease plus fifteen percent (15%) of such cost to cover overhead, plus Interest, and Lessee further agrees that Lessor shall not be liable for any damages resulting to Lessee from such action, except for Lessor’s gross negligence or willful misconduct. No action taken by Lessor under this section shall relieve Lessee from any of its obligations under this Lease or from any consequences or liabilities arising from the failure to perform such obligations.

 

F.             Any furniture, trade fixtures, equipment, inventory or other personal property of Lessee which remains on the Premises following (i) the termination date of this Lease, or (ii) Lessor’s termination of Lessee’s possession of the Premises pursuant to this Section 29, shall conclusively be deemed abandoned, and without notice to Lessee, Lessor may dispose of the same in any manner deemed suitable by Lessor, sell such property and retain the proceeds therefor, or store such property at Lessee’s expense.

 

G.            Lessor shall have the right to exercise any and all other remedies available to Lessor in this Lease, at law or in equity.

 

30. Waiver . Failure of Lessor to declare any default immediately upon occurrence thereof, or delay in taking any action in connection therewith, shall not waive such default, but Lessor shall have the right to declare any such default at any time and take such action as might be lawful or authorized hereunder, either in law or at equity.

 

31. Intentionally Omitted Prior to Execution .

 

32. Assignment by Lessor . Lessor shall have the right to sell, transfer or assign, in whole or in part, all of its rights and obligations hereunder and in the Building and the Land. In such event and upon the assumption by such transferee of Lessor’s obligations hereunder, no further liability or obligation shall thereafter accrue against Lessor hereunder.

 

33. Assignment by Lessee . Lessee shall not, without Lessor’s prior written consent in each instance, convey, assign Dr encumber this Lease or any interest herein, directly or

 

16



 

indirectly, voluntarily or by operation of law, including the merger or conversion of Lessee with Dr into another entity, or sublet all or any portion of the Premises, or permit the use Dr occupancy of any part of the Premises by anyone other than Lessee (collectively, “Transfer”). Except as otherwise hereinafter set forth, if Lessee is other than an individual, any change in “control” of Lessee shall constitute a Transfer, and the surviving party in control shall be the Transferee. “Control” means the direct or indirect power to direct or cause direction of the management and policies of an entity, whether through ownership of voting securities, by contract or otherwise. Conversely, Lessee shall not sublease space from, or assume the lease obligations of, another lessee in the Project without Lessor’s prior written consent. Following any Transfer, Lessee (and any guarantors) shall remain fully liable under this Lease, as then or thereafter amended with or without notice to or consent of Lessee (or any guarantors), and Lessor may proceed directly under this Lease against Lessee (or any guarantor) without first proceeding against any other party. Lessee shall give Lessor written notice of any proposed Transfer at least 30 days prior to the anticipated effective date of the proposed Transfer, which notice shall include a complete detailed written description of the Transfer; the name, address, business and intended use of the Transferee; a current audited financial statement for the Transferee certified by a recognized accounting firm; a copy of the proposed Transfer document; appropriate evidence of the existence, good standing and signature authority of the Transferee in the state that the Land is located in; and such other pertinent information as Lessor reasonably requests, together with Lessor’s then-quoted Transfer processing fee as stipulated under the last paragraph of this section. If the proposed Transferee is subject to any new requirements under applicable law (including the Americans with Disabilities Act of 1990), (i) Lessee shall be liable for any costs or expenses to comply with such requirements, and (ii) to the extent such requirements require alterations, Lessee shall deliver for Lessor’s approval plans and specifications complying with such additional requirements and acceptable security assuring timely, lien-free completion of construction. If the aggregate consideration, including Base Rent, paid to Lessee for a Transfer exceeds that payable by Lessee under this Lease (prorated according to the Transferred interest), then Lessee shall, within 15 days after receipt, pay 50% of such excess to Lessor.

 

Within 30 days after receipt of all required Transfer information, Lessor shall give Lessee written notice of its election (i) to consent to the Transfer; or (ii) to terminate this Lease as of the effective date of the Transfer as to the space covered by such Transfer for the remainder of the Term, in which event Lessee shall be relieved of its obligations accruing after the termination date with respect to the terminated interest (provided, however, that Lessee shall have the right, for a period of 5 days following the giving by Lessor of its decision to terminate this Lease, to rescind its request for consent to a Transfer); or (iii) not to consent to the Transfer, in which event this Lease shall continue in full force and effect. If Lessor fails to timely make such election, Lessor shall be deemed to have elected option (iii) above. Any Transfer occurring without Lessor’s consent shall be void and shall constitute a Default hereunder. In any event, all renewal and expansion options and other preferential rights under this Lease are personal to the original Lessee under this Lease and shall not be exercisable by any Transferee. Neither Lessor’s acceptance of any name for listing on the Building directory or other signage, nor Lessor’s acceptance of rent from any Transferee, shall be deemed, or substitute for, Lessor’s consent to a

 

17



 

Transfer. Lessor agrees not to unreasonably withhold, delay or condition its consent to any assignment of this Lease or sublease of the entirety of the Premises; provided that the proposed Transferee is (A) creditworthy, (B) has a good reputation in the business community, (C)  will use the Premises for only the use permitted in Section 4 of this Lease, and (D) is not then an occupant of the Building or person or entity with whom Lessor is then negotiating to lease space in the Building and for which Lessor has reasonably comparable space available in the Building to accommodate such proposed Transferee’s space needs, Additionally, notwithstanding anything to the contrary or apparent contrary set forth in this Lease, a transfer of “control” of Lessee. occurring as a result of a merger of Lessee into another entity shall not constitute a Transfer requiring Lessor’s consent so long as, within a period of thirty (30) days following such merger, Lessee (or the surviving entity) provides Lessor with written notice of such merger accompanied by a copy of the merger documents filed with the Secretary of State of the State of Delaware.

 

Notwithstanding anything contained herein to the contrary, Lessor shall not be obligated to entertain or consider any request by Lessee to consent to any proposed assignment of this Lease or sublease of all or any part of the Premises unless each request by Lessee is accompanied by a nonrefundable fee payable to Lessor in the amount of $500.00 to cover Lessor’s administrative, legal, and other costs and expenses incurred in processing each of Lessee’s requests. Neither Lessee’s payment nor Lessor’s acceptance of the foregoing fee shall be construed to impose any obligation whatsoever upon Lessor to consent to Lessee’s request.

 

34. Transfer of Control. Subject to the exception set forth in Section 33, if Lessee is a corporation, and if at any time during the term of this Lease, corporate shares of Lessee shall be transferred by sale, assignment, bequest, inheritance, operation of law or other disposition so as to result in a change in the present control of said corporation by the person or persons now owning a majority of said corporate shares, Lessee shall be in default of this Lease and Lessor may exercise its rights in respect of default hereunder.

 

35. Notices . Any notice required or permitted to be given pursuant to the terms of this Lease shall be sent by certified or registered U.S. mail return receipt requested, hand delivery or nationally recognized overnight courier, if to Lessor, at 2201 Timberloch Place, The Woodlands, Texas 77380, Attn: Property Management, with a copy to Crescent Real Estate Equities Limited Partnership, 777 Main Street, Suite 2100, Fort Worth, Texas 76102, Attn: Legal Department, and if to Lessee, at 2700 Research Forest Dr., Suite 180, The Woodlands, TX 77381, Attn: Douglas R. Kern. The place to which such notices shall be sent may be changed by either party giving notice of such change to the other party in the manner hereinabove provided, and such address changes shall be effective within five (5) days of receipt of such notice. A notice shall be deemed given and received (i) if by certified or registered mail, on the 3rd business day following deposit in the U. S. Mail; (ii) if by hand delivery, upon tender of delivery; and (iii) if by overnight courier, the first (lst) business day following deposit.

 

36. Severability . If any of the provisions of this Lease shall contravene or be invalid under the laws of the particular state, county, or jurisdiction where applied, such contravention or invalidity shall not invalidate the Lease or any other portions thereof and the remainder of this

 

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Lease or the application thereof to other persons or circumstances shall not be affected thereby.

 

37. Corporate Authority . If Lessee signs as a corporation, or other entity each of the persons executing this Lease on behalf of Lessee represents and warrants that Lessee is a duly organized and existing corporation, partnership, limited liability company or other entity, that Lessee has and is qualified to do business in Texas, that the corporation or other entity has full right and authority to enter into this Lease, and that all persons signing on behalf of the corporation or other entity were authorized to do so by appropriate corporate or entity actions.

 

38. Title . This Lease is subject to all matters of record in the Real Property Records of Montgomery County, Texas. By execution of this Lease, Lessee consents to all plats and replats of the Land, if any, in compliance with all applicable laws.

 

39. Not an Offer . The submission of this Lease to Lessee shall not be construed as an offer, nor shall Lessee have any rights with respect thereto unless Lessor executes a copy of this Lease and delivers the same to Lessee.

 

40. Exhibits, Riders and Addenda . This Lease also includes and incorporates herein for all purposes all attached Exhibits, Riders, and Addenda, if any.

 

41. Joint and Several Tenancy . If more than one person executes this Lease as Lessee, their obligations hereunder are joint and several, and any act or notice of or to, or refund to, or the signature of, anyone or more of them, in relation to the renewal or termination of this Lease, or under or with respect to any of the terms hereof shall be fully binding on each and all of the persons executing this Lease as a Lessee.

 

42. Binding Effect . This Lease shall be binding upon and inure to the benefit of the heirs, successors or assigns of Lessor and Lessee, subject to the limitation on subleasing and assignment herein contained.

 

43. Entire Agreement . This Lease shall constitute the sole and only agreement of Lessor and Lessee with regard to the Lease of the Premises, and shall supercede any prior or contemporaneous oral or written agreements. This Lease may not be altered, changed or amended, except by an instrument in writing, signed by both parties hereto.

 

44. Pronouns. Pronouns which refer to either Lessor or Lessee shall be construed to mean the appropriate number and gender intended.

 

45. Force Majeure . If either party shall be delayed or prevented from the performance of any act required hereunder by reason of acts of God, strikes, lockouts, labor troubles, inability to procure materials, restrictive governmental laws or regulations or other cause without fault and beyond the control of the party obligated (Lessee’s financial inability, such as inability to obtain financing or lack of capital, excepted), performance of such act shall be excused for the period of the delay, and the period for the performance of any such act shall

 

19



 

be extended by a period equal to the period of such delay; provided, however, nothing in this Section shall excuse Lessee from the prompt payment of any rental or other charge required of Lessee hereunder, except as may be expressly provided elsewhere in this Lease.

 

46. Lessor’s Liability . Any judgment recovered by any Lessee Party against any Lessor Party shall be satisfied solely out of proceeds received at a judicial sale upon execution and levy made against Lessor’s right, title and interest in the Building. Lessee waives (i) all right to levy against the Building or Land or any other properly of Lessor or any Lessor Party for any deficiency or claim against Lessor or any Lessor Party or to otherwise claim against Lessor or any Lessor Party for consequential, special or punitive damages allegedly suffered by any Lessee Party, including without limitation, lost profits and business interruption.

 

47. General . Time is of the essence of this Lease. All rights and remedies of Lessor and Lessee under this Lease shall be cumulative and none shall exclude any other rights or remedies allowed by law. This Lease shall be declared to be a Texas lease, and all of the terms hereof shall be construed according to the Jaws of the State of Texas. Said Lease shall be performable only in Montgomery County, Texas, and venue for any action hereunder shall lie exclusively in Montgomery County, Texas or in the Southern District of Texas, Houston Division, as appropriate.

 

48. Brokers . Lessor and Lessee warrant and represent to the other that it has not dealt with any real estate broker and/or salesman in connection with the negotiation or execution of this Lease and no such broker or salesman has been involved in connection with this Lease, and each party agrees to defend, indemnify and hold harmless the other party from and against any and all costs, expenses, attorneys’ fees or liability for any compensation, commission and charges claimed by any real estate broker and/or salesman due to acts of such party or such party’s representatives.

 

49. Relocation . Lessor shall have the right to require Lessee, upon 90 days notice, to relocate the Premises to any other premises of equal or greater size with improvements to be equal or greater than those prior to the relocation within the Building or to other buildings in the Project (“Relocated Premises”) on a date of relocation (the “Relocation Date”) specified therein. In such event, all reasonable expenses of moving Lessee and decorating the Relocated Premises with substantially the same leasehold improvements shall be at the expense of Lessor, including the physical move, telephone installation and stationery costs. Lessor shall have the option to tender the Relocated Premises to Lessee on any date within a 30 day period prior to or after the Relocation Date, in which event the Relocation Date shall become the date of tender of possession of the Relocated Premises. From the Relocation Date through the expiration date of the Lease, the aggregate Base Rent for the Relocated Premises shall be the same as for the original Premises. Lessee’s failure to comply with these provisions shall constitute a Default hereunder.

 

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50. Guaranty . Contemporaneously with the execution of this Lease, Douglas R. Kern (“Guarantor”), a principal of Lessee, is delivering to Lessor a guarantee all of the covenants, duties, and obligations of Lessee that accrue under this Lease pursuant to a Guaranty in the form attached hereto as Exhibit “D”.

 

IN TESTIMONY WHEREOF, the parties hereto have executed this Lease in multiple counterparts, each of which shall constitute an original but collectively shall constitute only one document, such execution to be effective on the date first above written.

 

 

LESSOR:

 

WOODLANDS VTO 2000 LAND, L.P.,

 

a Texas limited partnership

 

By: WOODLANDS VTO 2000 LAND G.P., L.L.C.,

 

 

its General Partner

 

 

 

 

 

 

 

 

By:

/s/ Michael Richmond

 

 

Name: Michael Richmond

 

 

Title:   President and CEO

 

 

 

 

 

LESSEE:

 

APPLIED VETERINARY SYSTEMS, INC., a Delaware

 

Corporation

 

 

 

 

 

 

By:

/s/ Douglas R. Kern

 

 

Name: Douglas R. Kern

 

 

Title:   President/CEO

 

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EXHIBIT “A”

The Land

 

22



 

EXHIBIT “B”

 

Tenant Improvement Letter

 

ESFORMS\GTenant Improvement Add\3·20-01

(Lessee does work)

 

1.                                        Construction of Leasehold Improvements . Lessor shall provide, at Lessor’s expense and utilizing the services of Fretz Construction, tenant improvements consisting of 2 single-wide glass entry doors, 2 single-wide glass entry doors, side by side causing a double door entrywayand 1 loading dock. Lessee shall construct all other leasehold improvements required by Lessee for the Premises (“Tenant Improvements”).

 

2.                                        Construction Costs . Lessee shall be responsible for all costs associated with the construction of the Tenant Improvements. Lessee shall pay to Lessor the sum of $ 0, said amount to be Lessor’s administrative fee for construction management, including, but not limited to, review of the plans, drawings, and specifications for the Tenant Improvements, including the mechanical systems, and periodic inspections of the construction.

 

3.                                        Approval of Plans . All plans, drawings, and specifications for the Tenant Improvements (“Plans”) must be submitted, prior to commencement of construction of the Tenant Improvements, to Lessor for its prior. written approval, which approval shall not be unreasonably withheld. The Plans must be prepared by an architect licensed to practice in the State of Texas and Lessee’s architect must represent and warrant that the designs for the Premises embodied in the Plans submitted to Lessor on behalf of Lessee shall comply with all applicable building and life safety laws, rules, regulations and codes including, but not limited to, the Texas Elimination of Architectural Barriers Act, and all City of Houston building codes as adopted and modified by the Committee described in numbered paragraph 13 below. The Plans also must be provided as electronic files in .dwg, .dxf, or other Autodesk AutoCAD compatible format. Lessor shall not be liable for damages resulting from its approval or disapproval of the Plans or any action taken by Lessee. If Lessor fails to respond to Lessee’s request for approval within five (5) business days following Lessee’s submittal of all plans, drawings, specifications and other information requested by Lessor and Tenant is unable to complete the Tenant Improvements by October 1, 2001, and such failure constitutes the sole reason for such inability, then Tenant shall be entitled to an abatement of one (1) day of Base Rent for each day of such delay.

 

4.                                        Contractor . Lessee’s choice for the contractor to perform the construction of the Tenant Improvements shall be subject to Lessor’s prior, written approval, which approval shall be given at Lessor’s sole discretion. Upon its execution, Lessee shall provide to Lessor a copy of the contract for construction with the approved contractor. Lessor shall have no liability for review or failure to review such Contract. By its execution of this Lease, Lessor approves the selection by Lessee of Fretz Construction as its contractor.

 

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5.                                        Lessor’s Liability . Lessee acknowledges that Lessor is not an architect or engineer. Accordingly, Lessor does not guaranty or warrant that the approved Plans will comply with all applicable laws, be free from errors or omissions, or result in construction of a safe place of habitation. nor that the Tenant Improvements will be free from defects or unsafe conditions and Lessor will have no liability therefor.

 

6. Electrical Service . The Lessee shall put electrical service in its own name before construction can commence. Requests for service should be made to Entergy. 1/800/840-4478.  If any charges are incurred by Lessor for electricity to the Premises after the commencement of construction. these charges will be reimbursed by Lessee.

 

7. Insurance . Prior to the commencement of construction of the Tenant Improvements. Lessee shall cause the contractor to provide to Lessor a certificate of insurance evidencing that the contractor has obtained the following insurance:

 

(a)                                   Workers Compensation Insurance in accordance with the laws of the State of Texas and Employers Liability Insurance with minimum limits of not less than the following:

 

 

Each Accident

 

$

1,000,000

 

 

 

 

 

 

Disease Policy Limit

 

$

1,000,000

 

 

 

 

 

 

Disease Each Employee

 

$

250,000

 

 

 

 

 

 

(b)                                  Comprehensive General Liability

 

Combined single limit bodily injury and property damage

 

 

- each occurrence

 

$

1,000,000

 

 

 

 

 

 

- aggregate

 

$

1,000,000

 

 

 

 

 

 

Such insurance shall include the following:

 

(i) Premises - Operations

 

(ii) Contractor’s Protective Liability, covering all work sublet.

 

(iii) Completed Operations and Products Liability coverage, which shall be maintained for a minimum period of three years after final payment and Contractor shall continue to provide evidence of such coverage to Owner on an annual basis during such period.

 

(iv) Broad Form Property Damage

 

(v) Property Damage Liability Insurance which shall include coverage for Collapse and Underground.

 

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(vi) Contractual Liability (Hold Harmless Coverage)

 

(vii) Personal Injury (with Employment Exclusion deleted. if applicable)

 

- aggregate

 

$

1,000,000

 

 

(c)                                   Comprehensive Automobile Liability Insurance, with limits of liability of not less than the following:

 

Combined single limit bodily injury and property damage

 

- each occurrence

 

$

1,000,000

 

 

Such coverage shall include owned, hired, and non-owned vehicles.

 

(d)                                  Umbrella Liability Insurance in an amount of not less than $2,000,000 providing limits of liability in excess of limits provided in (a), (b), and (c) above.

 

(e)                                   Builder’s Risk insurance for the complete replacement value of the Tenant Improvements.

 

All insurance policies arranged by the contractor shall contain a clause waiving any right of subrogation against Lessor. All insurance policies, except the policy listed in 7(a) above, shall name Lessor as an additional insured.

 

8.                                        Completion of Construction . Lessee shall cause the contractor to diligently pursue, until completion, the construction of the Tenant Improvements in accordance with the plans, drawings, and specifications approved by Lessor. Prior to the Commencement Date, Lessee shall provide to Lessor the following items:

 

(1)                                   an affidavit that payroll, bills for materials and equipment, and other indebtedness connected with the construction of the Tenant Improvements have been paid or otherwise satisfied;

 

(2)                                   properly executed releases and affidavits of payment establishing payment of the Lessee’s and the contractor’s obligations related to the construction of the Tenant Improvements; and

 

(3)                                   a complete list of all materialman, suppliers, and subcontractors supplying materials or work costing in excess of $5,000, including addresses, telephone numbers, and names of individuals to contact who are familiar with the portion of the construction of the Tenant Improvements accomplished by such entity.

 

(4)                                   if applicable, proof of approval from the Texas Department of Licensing and Regulation of the plans and specifications for the Tenant Improvements.

 

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9.                                        Performance Standards . Lessee shall require that the contractor perform all labor in a workmanlike manner, in strict compliance with the Lease, including this Tenant Improvement Addendum, all applicable Federal, state, local, and agency laws, ordinances, and regulations, and according to the standard industry practice.

 

10.                                  Trash . Lessee shall require that the contractor shall clean the job site and haul away all accumulated trash and debris on a daily basis. The contractor shall supply its own trash receptacles and Lessor’s facilities shall not be for this purpose.

 

11.                                  Warranties . Lessee shall cause contractor to warrant to Lessor that materials and equipment furnished for construction of the Tenant Improvements will be of good quality and new unless otherwise required or permitted by the Lessee, that the Tenant Improvements will be free from defects not inherent in the quality required or permitted, and that the Tenant Improvements will conform with the requirements of the plans, drawings, and specifications approved by Lessor.

 

12.                                  INDEMNIFICATION . LESSEE HEREBY AGREES TO INDEMNIFY AND HOLD LESSOR HARMLESS FROM AND AGAINST AND TO REIMBURSE LESSOR WITH RESPECT TO ANY AND ALL CLAIMS, DEMANDS, CAUSES OF ACTION, LOSS, DAMAGE, LIABILITIES, COSTS, AND EXPENSES (INCLUDING ATTORNEY’S FEES AND COURT COSTS) OF ANY AND EVERY KIND OR CHARACTER, INCLUDING, WITHOUT LIMITATION, INJURY TO OR DEATH OF ANY PERSON, OR FOR DAMAGE TO ANY PROPERTY, KNOWN OR UNKNOWN, FIXED OR CONTINGENT, ASSERTED AGAINST OR INCURRED BY LESSOR AT ANY TIME AND FROM TIME TO TIME BY REASON OF OR ARISING OUT OF THE CONSTRUCTION OF THE TENANT IMPROVEMENTS BY LESSEE, LESSEE’S CONTRACTOR AND LESSEE’S SUBCONTRACTORS OR FROM LESSOR’S FAILURE TO COMPLY WITH THE TERMS OF THIS TENANT IMPROVEMENT ADDENDUM.

 

Additionally, Lessee shall discharge at once or bond or otherwise secure against all liens and attachments which are filed in connection with the construction of the Tenant Improvements by the contractor or any materialman, supplier, or subcontractor, and shall indemnify, protect, defend, and hold Lessor harmless from and against all claims, demands, causes of action, loss, damage, liability, costs, and expenses (including attorneys fees and court costs) relating to such liens and attachments.

 

13.                  The Woodlands Covenants and Standards . Lessee shall cause all construction to be in accordance with The Woodlands Covenants and the Commercial/Industrial Development Standards (“Standards”) adopted by the Committee under authority granted by The Woodlands Covenants, and any other applicable standards. The Woodlands Covenants shall mean and refer to:

 

· the Covenants, Restrictions, Easements, Charges and Liens of The Woodlands, which are

 

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imposed upon the Land and recorded in the Real Property Records of Montgomery County, Texas and which are substantially similar in form and substance as those recorded under:

 

·                                           County Clerk File No. 9210558 of the Real Property Records of Montgomery County, Texas (WCA)

 

·                                           County Clerk’s File No. 9348561 of the Real Property Records of Montgomery County, Texas (TWA)

 

the Declaration of Covenants and Restrictions of The Woodlands Commercial Owners Association which are imposed upon the Land and recorded in the Real Property Records of Montgomery County, Texas, and are substantially similar in for and substance as those recorded under County Clerk’s File No. 9357930.

 

“Committee” as used herein shall mean and refer to the committee organized pursuant to The Woodlands Covenants for the purpose of establishing rules, regulations, policies and procedures governing the improvement of property in The Woodlands.

 

Approval of plans by the Committee shall not entitle Lessee to rely thereon with respect to conformity with laws, regulations, codes, or ordinances, or with respect to the physical condition of The Property. Lessee hereby waives any claims, demands, or causes of action growing out of any plan approvals by the Committee.

 

14.                                  Approval of Improvements to the Premises . Lessee understands that when it performs any construction, renovation, modification, or alteration on the Premises which is expected to cost $50,000.00 or more, Lessee must (i) submit its plans and specifications to the Texas Department of Licensing and Regulation for its review and approval before commencing such work, (ii) provide evidence to Lessor of such submission to and approval by this department, and (iii) indemnify, defend, and hold Lessor harmless against any liability, claim, loss, damage or penalty (including court costs and reasonable attorneys fees and court costs) resulting from Lessee’s failure to comply with the Texas Elimination of Architectural Barriers Act, as amended from time to time, or its associated rules and regulations.

 

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EXHIBIT C

 

TO LEASE AGREEMENT

 

RULES AND REGULATIONS

 

PASSAGE WAY OBSTRUCTION

 

The sidewalks, entries, passages, courts, corridors and stairways shall not be obstructed by any Lessee, its employees or agents, or used by them for purposes other than for ingress and egress to and from their respective Premises.

 

SIGNAGE

 

No sign, advertisement, display, notice or other lettering shall be exhibited, inscribed, painted or affixed on any part of the outside of the Premises or inside, if visible from the outside, of the Building of which they form a part without the prior written approval of Lessor. All signs and notices of Lessee, so approved by Lessor, shall be maintained by Lessee in good and attractive condition at Lessee’s expense and risk. Lessor shall have the right to remove all signs erected in violation of this rule without notice to Lessee, at the expense of Lessee. Signage must comply with sign standards of The Woodlands Development Standards Committee, The Woodlands Development Review Committee or The Woodlands Community Standards Committee, whichever is applicable.

 

NOISE AND DISTURBANCE

 

No loud speakers, television sets, phonographs, radios, security systems, or other devices shall be used in a manner so as to be heard or seen outside of the Premises without the prior written consent of Lessor.

 

Lessee shall not make or permit any noise or odor which Lessor deems objectionable or unpleasant to emanate from the Premises.

 

ANTENNAE AND AERIALS

 

No aerial or antenna, including, but not limited to, a satellite dish, shall be erected on the roof or exterior walls of the Premises or Building in which the Premises is a part, without, in each instance, the prior written consent of Lessor. Any aerial or antenna so installed without such written consent shall be subject to removal by Lessor without notice at any time.

 

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USE OF PREMISES

 

No portion of the Premises shall be used for a purpose other than as permitted under the terms of this Lease. No portion of the Premises shall be used for living, sleeping, residential or lodging purposes.

 

FIRE PROTECTION

 

Lessee shall not do or permit anything to be done in the Premises, or in the common areas of the Building, or bring or keep anything therein, which will in any way increase the rate of, or make inoperative, fire insurance on the Building or property kept therein, or any other insurance policy carried by Lessor on the Building, or obstruct or interfere with the rights of other Lessees, or in any way injure or annoy them, or conflict with the laws relating to fire, or with any regulations of the fire department, or with any insurance policy upon the Building or any part thereof, or conflict with any of the rules or ordinances of any county, state or federal authority. Should Lessee utilize flammable or combustible liquids, all such flammables and combustibles will be stored and maintained in OSHA approved cabinets.

 

PARKING

 

Lessee and Lessee’s employees shall park their cars only in those portions of the parking area designated for that purpose by Lessor.

 

All vehicles will be parked within striped lanes. Parking across the stripes or in unmarked areas, blocking of walkways, loading area, entrances or driveways will not be permitted. Should such a situation exist, Lessor, at its option, shall have the right to tow such vehicle away at the owner’s expense.

 

MAINTENANCE OF PREMISES

 

Lessee shall keep the Premises at a temperature sufficiently high to prevent freezing of water in pipes and fixtures.

 

No awning or other projections shall be attached to the outside walls of the Premises or the Building of which they form a part without, in each instance, the prior written consent of Lessor.

 

DELIVERIES AND MOVES

 

All loading and unloading of goods shall be done only at such times, in the areas and through the entrances designated for such purpose by Lessor.

 

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TRASH REMOVAL

 

All garbage, refuse and waste (“Waste Material”) shall be kept in the kind of container specified by Lessor, and shall be placed outside of the Premises, prepared for collection in the manner and at the times and places specified by Lessor. In no event shall Lessee dispose of Waste Material in public areas of the Building. If Lessor shall provide or designate a service for picking up Waste Material, Lessee shall use the same at Lessee’s cost, provided such cost shall be competitive to any similar service available to Lessee. Waste Material includes only solid waste generated by Lessee and specifically excludes, and Lessee agrees not to deposit in the place for collection, any radioactive, volatile, corrosive, highly flammable, explosive, infectious, biohazardous, toxic or hazardous material as defined by applicable federal, state, or local laws or regulations.

 

PEST CONTROL

 

Lessee shall use at Lessee’s cost such pest extermination contractors as Lessor may direct and at such intervals as Lessor may require, provided the cost thereof is competitive to any similar service available to Lessee.

 

ELECTRICAL AND TELEPHONE SERVICE

 

If Lessee desires telegraphic, telephonic or other electric connections, Lessor or its agents will direct the electricians as to where and how the wires may be introduced, and without such direction no boring or cutting for wires will be permitted. Access to any mechanical, electrical or telephone rooms must be approved by Lessor.

 

EXCESS TRASH DISPOSAL

 

In the event Lessee must dispose of crates, boxes, etc., which will not fit into a standard exterior trash container, it will be the responsibility of Lessee to dispose of same. In no event will Lessee set such items in the common areas of the Building. Lessor may provide a common trash receptacle for Lessee’s use.

 

WATER USAGE

 

The water closets and other water fixtures shall not be used for any purpose other than those for which they were intended, and any damage resulting to them from misuse, or the defacing or injury of any part of the Building shall be borne by the person who shall occasion it. No person shall waste water by interfering with the faucets or otherwise.

 

ALTERATIONS AND CONTRACTOR APPROVAL

 

All contractors and/or technicians performing any alterations for Lessee within the Premises must be referred to Lessor for approval and shall, prior to commencement, execute proper lien waivers.

 

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NOTICE TO RENT SIGNS

 

Lessor may place on the windows or doors of the Premises, or upon the bulletin board, a notice “To Rent” for one month prior to the expiration of the Term of the Lease.

 

LOCKS AND KEYS

 

Lessor agrees to furnish Lessee two keys for the doors entering the Building, Lessee’s suite and each entry door therein. Any additional keys will be furnished at a charge by Lessor equal to its cost plus 15% overhead. No additional locks shall be placed upon any doors without the written consent of Lessor, nor shall any duplicate keys be made. All necessary keys shall be furnished by Lessor, and the same shall be surrendered upon the termination of this lease, and Lessee shall then give to Lessor or its agents explanation of the combination of all locks upon the doors of vaults.

 

UPKEEP OF PREMISES

 

All glass. locks and trimmings in or about the doors and windows. and all electric globes and shades belonging to the Building shall be kept whole, and whenever broken by the Lessee or its agents or invitees. shall be immediately replaced or repaired and put in order by Lessee under the direction and to the satisfaction of Lessor and on vacating Premises shall be left whole and in good repair.

 

SKYLIGHTS AND WINDOWS

 

No floors, skylights or windows that reflect or admit light into the corridors or passage-ways, or to any other place in the Building. shall be covered or obstructed by any Lessee. If Lessee desires blinds or window coverings, they must be of such shade, color, material and make as shall be prescribed by Lessor (and any awning proposed may be prohibited by Lessor).

 

ADDITIONAL RULES AND REGULATIONS

 

Lessor reserves the right to make such other and further reasonable rules and regulations as in its judgment may from time to time be necessary for the safety care and cleanliness of the Building and its occupants and for the preservation of good order therein.

 

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GUARANTY OF LEASE

 

THIS GUARANTY is given by DOUGLAS R. KERN (“Guarantor”), whose address is 64 Autumn Crescent, The Woodlands, TX  77381 , in favor of WOODLANDS VTO 2000 LAND, L.P., a Texas limited partnership, with offices at 2201 Timberloch Place, The Woodlands, Texas (“Lessor”) as of this 20 th  day of August , 2001.

 

APPLIED VETERINARY SYSTEMS, INC., a Delaware corporation (“Lessee”) wishes to enter into a lease (“Lease”) with Lessor for 13,185 rentable square feet of floor space in a building known as Venture Technology Center XI located at 2700 Research Forest Blvd., Suite 180, The Woodlands, Texas; and

 

WHEREAS, Lessor has refused to enter into said Lease unless the obligations of Lessee under said Lease are guaranteed in the manner hereinafter set forth;

 

NOW, THEREFORE, in consideration of Lessor entering into the Lease, dated this date and being executed simultaneously herewith, the Guarantor hereby agrees as follows:

 

1.                                        Guarantor unconditionally guarantees to Lessor and its successors and assigns the full and punctual performance and observance by Lessee of all of the terms, covenants and conditions to be kept, performed or observed by Lessee pursuant to the Lease. If at any time Lessee shall default in the performance or observance of any of the terms, covenants or conditions in the Lease and such default shall continue beyond any applicable grace or cure period provided for therein, Guarantor will promptly and fully keep, perform and observe the same in the place and stead of Lessee. Guarantor shall pay, reimburse and indemnify Lessor for all damages, costs, expenses, losses and other liabilities arising or resulting from Lessee’s failure to perform or satisfy the required terms. Guarantor does not waive notice of any breach or default by Lessee; however, Guarantor agrees that any notice given to Lessee c/o Guarantor at the address for notice set forth in the Lease also constitutes notice to Guarantor of any such breach or default. Guarantor assumes all responsibility for being and keeping itself informed of Lessee’s financial condition and assets and all other circumstances bearing upon the risk of nonperformance by Lessee under the Lease.

 

2.                                        Any act of the Lessor, or the successors or assigns of Lessor, consisting of a waiver of any of the terms or conditions of the Lease, or the giving of any consent to any matter or thing relating to the Lease, or the granting to Lessee of any indulgences or extensions of time of payment of any amount due from Lessee or the time of performance of any obligation of Lessee may be done without notice to, or assent from, the Guarantor and without releasing the obligations of the Guarantor.

 

3.                                        The obligations of the Guarantor hereunder shall not be released by Lessor’s receipt, application or release of the security deposit or any other collateral given for the

 

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performance and observance of covenants and conditions in the Lease contained on Lessee’s part to be performed or observed; nor by any modification of any of the terms or conditions of the Lease, but in case of any such modification the liability of the Guarantor, shall be deemed modified In accordance with the terms of any such modification of the Lease.

 

4.                                        The liability of Guarantor hereunder shall in no way be affected by a) the release or discharge of Lessee in any receivership, bankruptcy or other similar proceeding, b) the impairment, limitation or modification of the liability of Lessee or the estate of Lessee in bankruptcy, or of any remedy for the enforcement of Lessee’s liability under the Lease resulting from the operation of any present or future provision of the National Bankruptcy Act, c) the rejection or disaffirmance of the Lease in any such proceeding, d) the assignment or transfer of the Lease by Lessee, or e) any disability or other defense of Lessee, f) the release or termination from any cause whatsoever of the liability of Lessee pursuant to the Lease.

 

5.                                        Until all the covenants and conditions in the Lease on the Lessee’s part to be performed and observed are fully performed and observed, the Guarantor: (a) shall have no right of subrogation against the Lessee by reason of any payments or acts of performance by the Guarantor, in compliance with the obligations of the Guarantor hereunder; (b) waives any right to enforce any remedy which the Guarantor now or hereafter shall have against the Lessee by reason of anyone or more payment or acts of performance in compliance with the obligations of the Guarantor hereunder; and (c) subordinates any liability or indebtedness of the Lessee now or hereafter held by the Guarantor to the obligations of the Lessee to the Lessor under the Lease.

 

6.                                        This guaranty extends to any successor, assignee or Lessee of Lessee, to any extensions or renewals of the Lease, and any term established by reason of the holdover of Lessee or any assignee of Lessee.

 

7.                                        This guaranty is binding upon Guarantor. its legal representatives and assigns and is binding upon and shall inure to the benefit of Lessor, its successors and assigns. No assignment or delegation by Guarantor shall release Guarantor of its obligations under this guaranty. The term “Lessee” used in this guaranty includes also the first and any successive assignee or Lessee of Lessee.

 

8.                                        This instrument may not be changed, modified, discharged or terminated orally or in any manner other than by an agreement in writing signed by the Guarantor and the Lessor.

 

9.                                        This guaranty and the rights and obligations of the Lessee and of the Guarantor shall be governed and construed in accordance with the laws of the State of Texas, and it is further agreed that this contract is performable in Montgomery County, Texas, and the Guarantor waives the right to be sued elsewhere.

 

Guarantor has signed this guaranty on the date stated above.

 

 

 

/s/ DOUGLAS R. KERN

 

DOUGLAS R. KERN

 

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EXHIBIT “E”

 

EXCLUSIONS FROM OPERATING EXPENSES

 

Notwithstanding anything in the Lease to the contrary, Lessor and Lessee agree that the following items shall be excluded from Operating Expenses:

 

1.      Capital expenditures in accordance with generally accepted accounting principles except that Operating Expenses shall include the costs (amortized over such period as Landlord shall determine, together with interest thereon at the Prime Rate adjusted daily on the unamortized balance thereof) of any capital improvement:

 

a.              which acts in any manner to reduce Operating Expenses;

 

b.              which is required under any governmental law, code or regulation passed or enacted on or after the effective date of this Lease;

 

c.              which is a replacement (as opposed to additions or new improvements) of items located in the common areas adjacent to the Building, the parking area and other facilities used in connection with the Building, or involving the exterior of the Building, including, but not limited to the roof and structural elements.

 

Prime Rate, as used herein, shall mean the varying per annum rate of interest which shall from day to day be equal to the per annum rate of interest then most recently established and announced by Chase Bank of Texas, N.A. as its prime lending rate of interest, with each such change in such per annum rate of interest to become effective on the effective date of each such change.

 

2.              Costs of correcting defects in the Building, the common areas adjacent thereto and the parking area and other facilities used in connection therewith, or the equipment used therein and the replacement of defective equipment to the extent such costs are covered by warranties of manufacturers, suppliers, or contractors, or are otherwise borne by parties other than Lessor, except that conditions resulting from ordinary wear and tear will not be deemed defects for the purpose of this category.

 

3.              Costs of bringing the Building, the common areas adjacent thereto and the parking area and other facilities used in connection therewith into compliance with building codes, laws, rules, regulations, ordinances, or any other governmental rules or requirements,

 

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including, without limitation, the Americans With Disabilities Act of 1990, which compliance was required prior to the effective date of this Lease.

 

4.              Costs of repairs or other work occasioned by fire, windstorm, or other casualty of an insurable nature, whether or not Lessor carries such insurance, and costs reimbursable to Lessor by governmental authorities in eminent domain or condemnation proceedings, except that the amount of any insurance deductible up to the amount of $25,000.00 shall be included in Operating Expenses.

 

5.              Any expenses or costs that, under generally accepted accounting principles attributable to losses due to uncollected rent or fees or reserves for bad debts.

 

6.              Any expenses that are or should be separately metered or billed directly to or separately paidby another lessee or other third party.

 

7.              Costs of preparation of space, including buildout, renovating, or otherwise improving, changing, decorating, or redecorating space, for new lessees, prospective lessees, or other occupants in the Building, or vacant space in the Building except for routine, periodic repair, and replacement not considered to be capital items under generally accepted accounting principles.

 

8.              Costs incurred in removing the property or improvements of former lessees or other occupants of the Building.

 

9.              Architectural fees, leasing commissions, attorneys’ fees, costs and disbursements, and ther expenses incurred in connection with negotiations or disputes with lessees, prospective lessees, or other occupants of the Building and any such expenses incurred in connection with this Lease.

 

10.            Specific costs incurred for third parties (including other lessees), including without limitation, above Building standard electrical and/or janitorial services, and other services above Building standard.

 

11.            All utility costs for which Lessee directly contracts with local utility companies.

 

12.            Costs incurred due to acts of Lessor, any other lessee, or other occupant of the Building causing an increase in the rate of insurance on the Building or its contents.

 

13.            Costs, fines, interest penalties, attorneys’ fees, and costs of litigation incurred due to late payment of taxes (except for penalties associated with Lessor’s good faith contest of real estate taxes), utility bills, ground rentals, or mortgage debt, and other such costs incurred by Lessor’s failure to make such payments when due.

 

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14.            Penalties, fines, and other costs incurred due to violations or alleged violations by Lessor, any other lessee, or any third party of any laws, rules, regulations, codes, or ordinances. It is understood and agreed that Operating Expenses shall include costs to comply with laws, rules, regulations passed or enacted by the governmental authority on or after the effective date of this Lease.

 

15.            Costs incurred due to violations or alleged violations by Lessor, any other lessee, or other occupant of the Building of the terms and conditions of any lease or other rental arrangement covering space in the Building.

 

16.            Wages, salaries, and other compensation of any kind or nature paid to any executive employees above the grade of director of property management (manager) and any related overhead, administrative and general office expense other than the management fee specifically provided for in the Lease.

 

17.            Costs incurred in the operation of any concession serving the Building, including, without limitation, parking facilities.

 

18.            Compensation paid to clerks, attendants, and other persons in any concessions operated   by Lessor.

 

19.            Ground rentals, payment of principal and interest on debt (and other debt costs), amortization payments on any mortgage or mortgages executed by Lessor covering the    Building or the Land (or any portion thereof) (except to the extent that any of the foregoing may include payments or prepayments of insurance premiums or taxes that would be included in Operating Expenses if paid directly by Lessor), rental concessions, and negative cash flow guarantees.

 

20.            Costs incurred in connection with the sale, refinancing, mortgaging, or selling, or change    of ownership of the Building or the Land, including, without limitation, brokerage commissions, attorneys’ and accountants’ fees, loan brokerage fees, closing costs, interest charges and property transfer taxes.

 

21.            State, local, federal, personal and corporate income taxes measured by the income of Lessor from all sources or from sources other than rent alone; estate and inheritance taxes; franchise, succession and transfer taxes.

 

22.            All costs incurred by Lessor in connection with any dispute relating to the Lessor’s title to or ownership of the Building or the Land.

 

23.            Advertising and promotional expenditures.

 

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24.            Costs and expenses in excess of $10,000.00 in the aggregate for owning, leasing, and maintaining sculpture, painting, and other works of art installed in and/or on the Building or the Land.

 

25.            Contributions to charitable organizations.

 

26.            Expenses and costs relating in any way whatsoever to the identification, testing,   monitoring and control, encapsulation, removal, replacement, repair, or abatement of any hazardous materials within the Building of the Land (a) which material was classified as Ahazardous@ prior to the effective date of this Lease and (b) was required to be removed, replaced, repaired or abated prior to the effective date of this Lease.

 

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FIRST AMENDMENT TO LEASE AGREEMENT

 

This FIRST AMENDMENT TO LEASE AGREEMENT (this “ First Amendment ”) is executed to be effective as of the 12th day of November , 2007 (the “ First Amendment Effective Date ”), by and between all those entities set forth on Exhibit “A” attached hereto and hereby incorporated herein for all purposes, each a Delaware limited liability company, as lessor (collectively, “ Lessor ”), successor from the original lessor, Woodlands VTO 2000 Land, L.P., a Texas limited partnership (“ Original Lessor ”), by an assignment or series of successive assignments, and, VGX PHARMACEUTICALS, INC. a Delaware corporation, as lessee (“ Lessee ”), successor from the original lessee, Applied Veterinary Systems, Inc., a Delaware corporation (“ Original Lessee ”), by an assignment or series of successive assignments.

 

W I T N E S S E T H :

 

WHEREAS , Original Lessor and Original Lessee executed that certain Lease Agreement dated as of August 20, 2001 (as amended, the “ Lease ”), pursuant to which Original Lessor leased to Original Lessee that approximately 13,185 net rentable square feet of floor space in a building known and referred to as Venture Technology Center XI Building, located at 2700 Research Forest Drive, The Woodlands, Montgomery County, Texas (as more particularly described in the Lease, the “ Premises ”), the term of which Lease commenced on October 1, 2001;

 

WHEREAS , Lessor succeeded to the interests of Original Lessor under the Lease by virtue of transfer (or a series of transfers) of the Premises ending with Lessor and an assignment (or series of assignments) of the lessor’s interest in the Lease ending with Lessor;

 

WHEREAS , Lessee succeeded to the interests of Original Lessee under the Lease by virtue of transfer (or a series of transfers) of the Premises ending with Lessee and an assignment (or series of assignments) of the lessee’s interest in the Lease ending with Lessee;

 

WHEREAS , Lessor and Lessee desire to amend the Lease to:  (i) extend the term of the Lease; (ii) provide for Lessee’s construction of certain “Modifications” (as herein defined) to the improvements located on the land; (iii) amend the rent due under the Lease; and (iv) make certain other modifications to the Lease as stated herein;

 

NOW, THEREFORE , for and in consideration of the sum of TEN DOLLARS ($10.00), the mutual covenants and agreements set forth herein, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, Lessor and Lessee hereby agree as follows:

 

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1 .              Defined Terms .  Reference is hereby made to the Lease.  Each capitalized term used herein and not otherwise defined herein shall have the meaning ascribed to it in the Lease.  The provisions in this First Amendment shall control over any conflicting provisions in the Lease.

 

2.              Extension of Term .  The term of the Lease is extended to a date that is ten (10) years from November 1, 2007 (the “ Extension Commencement Date ”) (even though a portion thereof overlaps the existing term, this 10-year period is herein called the “ Extended Term ”).

 

3.              Use .  Commencing on the First Amendment Effective Date, Section 4 of the Lease shall be and hereby is amended, superseded and replaced, to read in its entirety as follows:

 

“4.            Use .         Lessee shall use the entire Premises solely for pharmaceutical manufacturing, standard research laboratory, general office and for such other purposes as are incidental or related thereto.  Lessee may maintain (for use by Lessee and its employees and incidental use by their invitees and visitors) in the Premises employee lunch rooms, employee coffee bars, research library, kitchens for the foregoing, printing and copying facilities, storage, telecommunications and data rooms, and any other facility or equipment utilized in the normal conduct of Lessee’s business and not inconsistent with the primary use of the Premises as a business office.”

 

4.              Adjustments to Base Rent .  Until the Extension Commencement Date, Lessee will continue to pay Base Rent (per Section 7 of the Lease) in the amount of $15,382.50 per month.  Notwithstanding anything in the Lease to the contrary, the Lease is hereby amended to provide that the Base Rent amount due from Lessee to Lessor during the remainder of the initial Term of the Lease following the Extension Commencement Date and during the Extended Term shall be as follows:

 

(a)            First twelve (12) months of the Extended Term:  $ 20,326.88 per month; and

 

(b)            Next twelve (12) months of the Extended Term (i.e., months 13-24 of the Extended Term):  $ 20,601.56 per month; and

 

(c)            Next twelve (12) months of the Extended Term (i.e., months 25-36 of the Extended Term):  $ 20,876.25 per month; and

 

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(d)            Next twelve (12) months of the Extended Term (i.e., months 37-48 of the Extended Term):  $ 21,150.94 per month; and

 

(e)            Next twelve (12) months of the Extended Term (i.e., months 49-60 of the Extended Term):  $ 21,425.63 per month; and

 

(f)             Next twelve (12) months of the Extended Term (i.e., months 61-72 of the Extended Term):  $ 21,700.31 per month; and

 

(g)            Next twelve (12) months of the Extended Term (i.e., months 73-84 of the Extended Term):  $ 21,975.00 per month; and

 

(h)            Next twelve (12) months of the Extended Term (i.e., months 85-96 of the Extended Term):  $ 22,249.69 per month; and

 

(i)             Next twelve (12) months of the Extended Term (i.e., months 97-108 of the Extended Term):  $ 22,524.38 per month; and

 

(j)             Last twelve (12) months of the Extended Term (i.e., months 109-120 of the Extended Term):  $ 22,799.06 per month.

 

5.              Adjustments to Operating Cost Allowance .  Commencing on the Extension Commencement Date, the first sentence of Section 8 of the Lease shall be and hereby is amended, superseded and replaced, to read in its entirety as follows:

 

“Lessor agrees to pay all Operating Expenses (as defined in Section 10 below) ( which includes the Management Fee described in Section 10 ) up to a maximum amount of the greater of actual Operating Expenses for the 2007 Fiscal Year grossed up to reflect a 95% occupancy level, or $5.93 per year for each square foot of rentable area in the Building (“Renewal Operating Cost Allowance”).”

 

Lessor and Lessee further agree that, in order to implement the foregoing amendment to the Operating Cost Allowance during the 2007 Fiscal Year, the Operating Cost Allowance for the 2007 Fiscal

 

40



 

Year shall be an amount equal to a blended rate of $3.00 per year for each square foot of rentable area in the Building for the first ten (10) months of the 2007 Fiscal Year and the Renewal Operating Cost Allowance for the last two (2) months of the 2007 Fiscal Year.

 

6.              Approved Alterations; Lessor’s Allowance .  The Lease is hereby amended to provide the following:

 

(a)            Lessee is hereby granted consent and approval from Lessor, as long as the work contemplated in this section is completed within two (2) years from the Extension Commencement Date, to make alterations or improvements to the Premises as described on Exhibit “B” attached hereto and incorporated herein by this reference (the “ Approved Alterations ”).  Construction of the Approved Alterations shall be performed in accordance with the terms, provisions and conditions of Exhibit “B-1” attached hereto.

 

(b)            Upon completion of all of the Approved Alterations by Lessee, Lessee shall give written notice thereof to Lessor accompanied by documentation establishing the amount expended for the Approved Alterations (“ Verified Expenditures ”), requesting payment by Lessor of the Verified Expenditures, which shall not to exceed ONE HUNDRED THIRTY-ONE THOUSAND, EIGHT HUNDRED FIFTY AND NO/100 DOLLARS ($131,850.00) in the aggregate (the “ Allowance ”).  Lessor and Lessee acknowledge and agree that the Verified Expenditures may include costs related to architectural and engineering fees related to the Approved Alterations and costs related to moving operations and personnel to the Premises.  Lessee shall submit a single draw request for all completed work on an AIA request for payment appropriately signed, accompanied by lien waivers for all completed work.  Lessee may not draw from the Allowance more than once.  Lessor may audit Lessee’s books, records and receipts should it desire to do so, at any time upon reasonable notice to Lessee, to further verify and confirm the Verified Expenditures made the subject of the draw.  Within twenty (20) days from the date of the request, as long as Lessee is not in material default of the Lease, Lessor will pay Lessee a cash sum equal to the lesser of the Verified Expenditures made the subject of the draw or the Allowance (the “ Required Payment ”).

 

(c)            Notwithstanding anything in the Lease to the contrary, Lessor shall in no way be responsible for (i) correction or repair of any defect in construction or design of the Approved Alterations (the same to be Lessee’s affirmative responsibility as an additional repair obligation of Lessee under the Lease), or (ii) any consequence to Lessee as a result of any defective design or construction of the Approved Alterations, including damage to Lessee property, loss of use of the Premises or interruption or loss of business activity of Lessee, and Lessee hereby releases Lessor from, and agrees to indemnify Lessor against, any claims, actions, losses, suits, costs and expenses arising out of any defective design or

 

41



 

construction of the Additional Alterations made by Lessee or Lessee’s contractors, subcontractors, employees or agents.

 

7.              Lessor’s Limited HVAC Warranty .  Lessor agrees to make, at its expense, any necessary repair to or replacement of the current roof-top HVAC units serving the Premises for a period of one year after the First Amendment Effective Date.  Lessee agrees to give Lessor written notice of need for repairs to the roof-top HVAC units during the one-year repair warranty period.  Lessor shall not be in default of the Lease or otherwise liable in any way to Lessee or any third party by reason of the foregoing roof-top HVAC units being or becoming out of repair until Lessor has been notified in writing by Lessee of the necessity of repair by Lessee and has had reasonable opportunity to repair the same.  Notwithstanding the above, Lessor agrees to make any necessary repairs or replacements as soon as commercially reasonable.  After the expiration of the one (1) year warranty period, Lessee will be responsible for any and all maintenance costs and repair costs related to the HVAC system.

 

8.              Subordination .  Commencing on the First Amendment Effective Date, the second paragraph of Section 21 of the Lease shall be and hereby is amended, superseded and replaced, to read in its entirety as follows:

 

“Lessor agrees to use reasonable efforts to secure and deliver to Lessee a commercially reasonable non-disturbance agreement from and executed by Lessor’s mortgagee (“ Mortgagee ”), for the benefit of Lessee whereby, as a condition to any attornment or subordination by Lessee to Lessor’s mortgagee, Lessee shall not be disturbed in its possession of the Premises or its rights under the Lease so long as Lessee is not in default under the Lease.  Lessee acknowledges and agrees that a form of non-disturbance agreement (an “ SNDA Agreement ”), acceptable to Lessee is attached hereto as Attachment I ; provided, however, that Lessee acknowledges and agrees that any future SNDA Agreement may contain, among other terms and conditions (a) any provision (or the substantial equivalent thereof) contained in any previous SNDA Agreement executed by Lessee (or any predecessor lessee hereunder), (b) a provision requiring that notices of Lessor default be given to the Mortgagee and the Mortgagee allowed a reasonable time in addition to Lessor’s cure period hereunder to cure such default before Lessee shall be entitled to take its remedies hereunder or by law, (c) a provision stating that the terms of the Mortgagee’s mortgage govern over any conflicting provision of this Lease pertaining to the Mortgagee’s obligation to make insurance or condemnation proceeds available for reconstruction of any part of the Premises, (d) provisions by which such Mortgagee or successor-in-interest upon foreclosure is agreed not to be bound by (excepting those provisions of a continual nature with respect to the maintenance or repairs of the Property and Premises to the extent first arising after the date such Mortgagee or successor-in-interest obtains title to the Premises) (i) any payment of rent or additional rent for more than one (1) month in advance, including prepayment in the nature of

 

42



 

security for the performance by Lessee of its obligations under this Lease (unless actually received by such successor in interest), (ii) any amendment or modification of this Lease (or implied waiver of Lessee’s obligations) made without the written consent of such trustee or such beneficiary or such successor in interest, (iii) any representations or defaults by any prior Lessor, and (iv) any other commercially reasonable matters that such Mortgagee is not directly responsible for causing, as such Mortgagee may specify, and/or (e) such other provisions and protections as such Mortgagee may request that are reasonably customary in the commercial mortgage lending community at the time.”

 

9.              Assignment by Lessee Commencing on the First Amendment Effective Date, Section 33 of the Lease shall be and hereby is amended, superseded and replaced, to read in its entirety as follows:

 

“33.          Assignment by Lessee .  Lessee shall not, without Lessor’s prior written consent in each instance, such consent shall not unreasonably withheld, conditioned or delayed, convey, assign or encumber this Lease or any interest herein, directly or indirectly, voluntarily or by operation of law, including the merger or conversion of Lessee with or into another entity, or sublet all or any portion of the Premises, or permit the use or occupancy of any part of the Premises by anyone other than Lessee (collectively, “Transfer”).  Except as otherwise hereinafter set forth, if Lessee is other than an individual, any change in “control” of Lessee shall constitute a Transfer, and the surviving party in control shall be the Transferee.  “Control” means the direct or indirect power to direct or cause direction of the management and policies of an entity, whether through ownership of voting securities, by contract or otherwise.  Conversely, Lessee shall not sublease space from, or assume the lease obligations of, another lessee in the Project without Lessor’s prior written consent, such consent shall not be unreasonably withheld, conditioned or delayed.  Following any Transfer, Lessee (and any guarantors) shall remain fully liable under this Lease, as then or thereafter amended with or without notice to or consent of Lessee (or any guarantors), and Lessor may proceed directly under this Lease against Lessee (or any guarantor) without first proceeding against any other party.  Lessee shall give Lessor written notice of any proposed Transfer at least 15 days prior to the anticipated effective date of the proposed Transfer, which notice shall include a complete detailed written description of the Transfer, the name, address, business and intended use of the Transferee; a current audited financial statement for the Transferee certified by a recognized accounting firm; a copy of the proposed Transfer document; appropriate evidence of the existence, good standing and signature authority of the Transferee in the state that the Land is located in; and such other pertinent information as Lessor reasonably requests, together with Lessor’s then-quoted Transfer processing fee as stipulated under the last paragraph of this section.  If the proposed Transferee is subject to any new requirements under applicable law (including the Americans with Disabilities Act of 1990) affecting the Premises, (i) Lessee shall be liable for any costs or expenses to comply with such requirements, and (ii) to the

 

43



 

extent such requirements require alterations, Lessee shall deliver for Lessor’s approval plans and specifications complying with such additional requirements and acceptable security assuring timely, lien-free completion of construction.  If the aggregate consideration, including Base Rent, after deductions are made for concessions, tenant improvement costs and lease commissions incurred as a result of procuring such Transfer, paid to Lessee for a Transfer exceeds that payable by Lessee under this Lease (prorated according to the Transferred interest), then Lessee shall, within 15 days after receipt, pay 50% of such excess to Lessor.

 

“Within 15 days after receipt of all required Transfer information, Lessor shall give Lessee written notice of its election (i) to consent to the Transfer; or (ii) to terminate this Lease as of the effective date of the Transfer as to the space covered by such Transfer for the remainder of the Term, in which event Lessee shall be relieved of its obligations accruing after the termination date with respect to the terminated interest (provided, however, that Lessee shall have the right, for a period of 5 days following the giving by Lessor of its decision to terminate this Lease to rescind its request for consent to a Transfer); or (iii) not to consent to the Transfer, in which event this Lease shall continue in full force and effect.  If Lessor fails to timely make such election, Lessor shall be deemed to have elected option (iii) above.  Any Transfer occurring without Lessor’s consent, which shall not be unreasonably withheld, conditioned or delayed, shall be void and shall constitute a Default hereunder.  In any event, all renewal and expansion options and other preferential rights under this Lease are personal to the original Lessee under this Lease and shall not be exercisable by any Transferee unless such conveyance is approved and consented to by Lessor in its sole and absolute discretion.  Neither Lessor’s acceptance of any name for listing on the Building directory or other signage, nor Lessor’s acceptance of rent from any Transferee, shall be deemed, or substituted for, Lessor’s consent to a Transfer.

 

“Lessor agrees not to unreasonably withhold, delay or condition its consent to any assignment of this Lease or sublease of the entirety of the Premises, provided that the proposed Transferee is (A) creditworthy defined as having a comparable net worth to that of Lessee as of the Extension Commencement Date, (B) an entity of good standing in its particular state of incorporation, (C) will use the Premises for only the use permitted in Section 4 of this Lease, and (D) not then an occupant of the Building or a person or entity with whom Lessor is then negotiating to lease space in the Building for which Lessor has reasonably comparable space available in the Building to accommodate such proposed Transferee’s space needs.  Additionally, notwithstanding anything to the contrary or apparent set forth in this Lease, (Y) a transfer of “control” of Lessee occurring as a result of a merger of Lessee into another entity shall not constitute a Transfer requiring Lessor’s consent so long as, within a period of thirty (30) days following such merger, Lessee (or the surviving entity) provides Lessor with written notice of such merger accompanied by a copy of the merger documents filed with the Secretary of State of the State of Delaware if applicable, and (Z) any Transfer to any entity which controls, is

 

44



 

controlled by, or is under common control with, Lessee shall not constitute a Transfer requiring Lessor’s consent so long as, within a period of thirty (30) days following such Transfer, Lessee (or the Transferee) provides Lessor with written notice of such Transfer accompanied by a copy of all documents effecting such Transfer.

 

“Notwithstanding anything contained herein to the contrary, Lessor shall not be obligated to entertain or consider any request of Lessee to consent to any proposed assignment of this Lease or sublease of all or any part of the Premises unless each request by Lessee is accompanied by a nonrefundable fee payable to Lessor in the amount of $500.00 to cover Lessor’s administrative, legal, and other costs and expenses incurred in processing each of Lessee’s requests.  Neither Lessee’s payment nor Lessor’s acceptance of the foregoing fee shall be construed to impose any obligation whatsoever upon Lessor to consent to Lessee’s request.”

 

10.            Notices .  Commencing on the First Amendment Effective Date, Section 35 of the Lease shall be and hereby is amended, superseded and replaced, to read in its entirety as follows:

 

“35.          Notices .  Any notice required or permitted to be given pursuant to the terms of this Lease shall be sent by certified or registered U.S. mail return receipt requested, hand delivery or nationally recognized overnight courier, if to Lessor, at 4545 Post Oak Place, Suite 200, Houston, Texas 77027, Attn:  Property Management, with a copy to Boyar & Miller, 4265 San Felipe, Suite 1200, Houston, Texas 77027, Attn:  Timothy J. Heinrich, and if to Lessee, at 2700 Research Forest Dr., Suite 180, The Woodlands, Texas 77381, Attn: Gene Kim, with a copy to PalermoBarr, Commercial Real Estate Advisors, 10200 Grogan’s Mill Road, Suite 550, The Woodlands, Texas  77380, Attn: Damon Palermo.  The place to which such notices shall be sent may be changed by either party giving notice of such change to the other party in the manner hereinabove provided, and such address changes shall be effective within five (5) days of receipt of such notice.  A notice shall be deemed given and received (i) if by certified or registered mail, on the 3rd business day following deposit in the U.S. Mail; (ii) if by hand delivery, upon tender of delivery; and (iii) if by overnight courier, the first (1st) business day following deposit.”

 

11.            Relocation .  Commencing on the First Amendment Effective Date, Section 49 of the Lease shall be and hereby is omitted and deleted in its entirety.

 

45


 

12.                                  Renewal Option .  Lessee shall have an option to renew the term of the Lease in accordance with the terms and conditions set forth in Exhibit “C” attached hereto and made a part hereof for all purposes.

 

13.                                  Preferential Lease Right . Lessee shall have the preferential right to lease certain space in the Building in accordance with the terms and conditions set forth in Exhibit “D” attached hereto and made a part hereof for all purposes.

 

14.                                  Early Termination Right .  Lessee shall have the option to terminate the Lease, but only in strict accordance with the terms and conditions set forth in Exhibit “E” attached hereto and made a part hereof for all purposes.

 

15.                                  Estoppel Certifications .  Lessee hereby acknowledges and certifies to Lessor that:  (a) as of the First Amendment Effective Date, Lessor is not in default under the Lease and Lessor has fully performed all of its obligations and responsibilities under the Lease, and Lessor is not in default of the Lease; (b) there is no existing sublease of the Premises or any part thereof and Lessee has not assigned the Lease or any right or interest therein, either directly or indirectly; (c) Lessee has received no notice and has no knowledge of any violation of any law, ordinance or regulation pertaining to the Premises; (d) Lessee has paid in full for any labor and materials provided to improve, alter, repair or modify the Premises, and no right of lien has been claimed or asserted against Lessee or the Premises in regard to any such work authorized by Lessee; (e) the Lease is not amended, either orally or in writing or by course of conduct or otherwise; (f) Lessee has expended no monies for which it claims any right of offset or abatement under the Lease; and (g) Lessee’s current sole address for notice and/or billing under the Lease is:  2700 Research Forest Dr., Suite 180, The Woodlands, Texas 77381, Attn: Gene Kim, with a copy notice to Palermo Barr, Commercial Real Estate Advisors, 10200 Grogan’s Mill Road, Suite 550, The Woodlands, Texas  77380, Attn: Damon Palermo.  But for these acknowledgements and certifications of Lessee, Lessor would not enter into this First Amendment.

 

16.                                  Amendments .  This First Amendment sets forth the entire understanding of Lessor and Lessee in connection with amending the Lease.  Except as otherwise expressly amended herein, the Lease remains in full force and effect in accordance with its terms.

 

17.                                  Binding Agreement .  This First Amendment shall be binding upon, and shall inure to the benefit of, the parties hereto and their respective legal representatives, successors and permitted assigns.  This First Amendment is not binding until executed and delivered by Lessor and Lessee.

 

46



 

18.                                  Severability .  If any provision of this First Amendment, or the application thereof to any person or circumstance, shall, for any reason and to any extent, be invalid or unenforceable, the remainder of this First Amendment and the application of such provision to other persons or circumstances shall not be affected thereby but rather shall be enforced to the greatest extent permitted by applicable law.

 

19.                                  Counterparts .  This First Amendment may be executed in multiple counterparts, each of which shall constitute an original, but all of which shall constitute one and the same agreement.  Execution and delivery of this First Amendment by facsimile transmission is binding the same as if original signed copies had been exchanged by the parties hereto.

 

20.                                  Brokers .  Lessee and Lessor each hereby represents to the other that it has not been represented by, has not engaged, and has not involved in this transaction any broker, agent or other commissionable party in connection with or relating to the transaction described in this First Amendment, except Palermo REI, LP d/b/a PalermoBarr, Commercial Real Estate Advisors (“ Lessee’s Broker ”), and except involvement of Lessor’s broker, for which Lessor is solely responsible.   Within ten (10) days after the Extension Commencement Date and provided that Lessee is not then in default under the Lease, but only if such conditions are satisfied, Lessor agrees to pay Lessee’s Broker an amount equal to four percent (4%) of the aggregate Base Rent to be paid by Lessee to Lessor during the Extension Term.  Lessee and Lessor each agrees to indemnify, defend and hold harmless the other party from and against any and all claims, suits, actions, proceedings, judgments, liabilities, losses, expenses and costs, including without limitation, costs of court, litigation expense, and reasonable attorney’s fees, resulting from or arising out of any breach of its foregoing representation, or by any claim by any broker asserting a claim contrary to its above representation (or, in the case of the indemnity by Lessor, any claims by the broker it has engaged, if any, and any claim by Lessee’s Broker for the commission Lessor has agrees to pay as set forth above when the same is in fact due and payable).

 

21.                                  Amendment Not Binding on Lessor UNLESS Executed and Delivered by Lessor .  Nothing in this First Amendment constitutes an offer or agreement of Lessor unless and until Lessor has executed this First Amendment and returned one (1) fully executed original to Lessee after it has been signed and delivered by Lessee.  Lessee shall not rely on the drafting of this First Amendment by Lessor (or Lessor’s request for Lessee to execute and submit the same to Lessor) as constituting an agreement to allow modification of the Lease, and until the execution and return of this First Amendment by Lessor to Lessee, Lessee shall be responsible and liable for performance of the Lease without regard to the proposed terms of this First Amendment.  Lessee acknowledges that Lessor has not made any verbal agreements with or given any verbal assurance to Lessee, of any nature or kind, with regard to Lessor’s willingness to enter into this First Amendment, and it has not relied on any such anticipated signature of Lessor hereon.

 

47



 

22.                                  Guaranty .  Lessor and Lessee hereby acknowledge and agree that the Guaranty of Lease, dated August 20, 2001, between CREEKSTONE WOODLANDS, LLC , a Texas limited liability company, as Lessor, successor from the original lessor, Woodlands VTO 2000 Land, L.P., a Texas limited partnership, by an assignment or series of successive assignments, and DOUGLAS R. KERN , an individual, no longer applies and is hereby deleted in its entirety.

 

[SIGNATURES BEGIN ON FOLLOWING PAGE]

 

48



 

IN WITNESS WHEREOF , the parties hereto have duly executed this First Amendment on the date across from their respective signatures, below, to be effective as of the First Amendment Effective Date.

 

 

 

 

 

LESSOR:

 

 

 

 

 

 

 

 

Date:

11/12, 2007

 

/s/ Michael F. Preston

 

 

 

MICHAEL F. PRESTON , President of

 

 

 

Creekstone Management GP, L.L.C., a

 

 

 

Delaware limited liability company, general

 

 

 

partner of Creekstone Management, L.P.,

 

 

 

a Texas limited partnership,

 

 

 

acting solely in its capacity as

 

 

 

attorney-in-fact of Lessor

 

 

 

 

 

 

 

 

Acknowledged and agreed:

 

 

 

 

 

 

 

 

CREEKSTONE WOODLANDS, LLC , a
Delaware limited liability company

 

 

 

 

 

 

 

 

 

 

 

 

 

By:

Creekstone Woodlands Holdings, LLC,

 

 

 

 

a Delaware limited liability company,

 

 

 

 

its managing member

 

 

 

 

 

 

 

 

 

 

 

Date:

11/12, 2007

 

 

By:

/s/ Michael F. Preston

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Name:

MICHAEL F. PRESTON

 

 

 

 

Title:

President

 

49



 

 

 

 

LESSEE :

 

 

 

 

 

 

 

 

 

 

 

VGX PHARMACEUTICALS, INC. , a Delaware
corporation

 

 

 

 

 

 

 

 

 

 

Date:

10/26, 2007

 

By:

/s/ J. J. Kim

 

 

 

 

 

 

 

 

 

 

 

 

 

Name:

J. J. Kim

 

 

 

 

 

 

 

 

 

 

 

 

 

Title:

President& CEO

 

50



 

EXHIBIT “A”

 

TENANTS-IN-COMMON

 

Creekstone Woodlands, LLC

 

Creekstone Woodlands 1, LLC

 

Creekstone Woodlands 2, LLC

 

Creekstone Woodlands 5, LLC

 

Creekstone Woodlands 6, LLC

 

A-1



 

EXHIBIT “B”

 

APPROVED ALTERATIONS

 

B-1



 

EXHIBIT “B-1”

 

CONSTRUCTION OF APPROVED ALTERATIONS

 

1.                                        [Intentionally Deleted.]

 

2.                                        [Intentionally Deleted.]

 

3.                                        Approval of Plans .  All plans, drawings, and specifications for the Approved Alterations (“Plans”) must be submitted, prior to commencement of construction of the Approved Alterations, to Lessor for its prior, written approval, which approval shall not be unreasonably withheld, conditioned or delayed.  The Plans must be prepared by an architect licensed to practice in the State of Texas and selected by Lessee, subject to Lessor’s reasonable approval.  Lessee’s architect must represent and warrant that the designs for the Approved Alterations embodied in the Plans submitted to Lessor on behalf of Lessee shall comply with all applicable building and life safety laws, rules, regulations and codes including, but not limited to, the Americans with Disabilities Act, the Texas Elimination of Architectural Barriers Act, and all City of Houston building codes as adopted and modified by the Committee described in numbered paragraph 13 below.  The Plans also must be provided as electronic files in .dwg, .dxf or other Autodesk Auto CAD compatible format.  Lessor shall not be liable for damages resulting from its approval or disapproval of the Plans or any action taken by Lessee.  If Lessor fails to respond to Lessee’s request for approval within five (5) business days following Lessee’s submittal of all plans, drawings, specifications and other information requested to Lessor, then such request for approval shall be deemed approved.

 

Due to the age of construction of the existing improvements, no current asbestos survey is required.  However, Lessor shall supply Lessee summary pages from the third party Phase I report Lessor received during Lessor’s due diligence prior to the Extension Commencement Date.

 

4                                           Contractor .  Lessee shall bid the Lessor-approved construction documents to not less than three (3) general contractors mutually acceptable to Lessor and Lessee.  Lessee shall choose the general contractor, with Lessor’s consent, which consent shall not be unreasonably withheld, delayed or

 

1



 

conditioned, to construct the Approved Alterations and Lessee shall promptly enter into a construction agreement with the chosen general contractor.  Upon its execution, Lessee shall provide to Lessor a copy of the contract for construction with the approved contractor.  Lessor shall have no liability for review or failure to review such contract.

 

5.                                        Lessor’s Liability .  Lessee acknowledges that Lessor is not an architect or engineer.  Accordingly, Lessor does not guaranty or warrant that the approved Plans will comply with all applicable laws, be free from errors or omissions, or result in construction of a safe place of habitation, nor that the Approved Alterations will be free from defects or unsafe conditions and Lessor will have no liability therefor.

 

6.                                        Electrical Service .  [Intentionally Deleted.]

 

7.                                        Insurance .  Prior to the commencement of construction of the Approved Alterations, Lessee shall cause the contractor to provide to Lessor a certificate of insurance evidencing that the contractor has obtained the following insurance:

 

(a)                                   Workers Compensation Insurance in accordance with the laws of the State of Texas and Employers Liability Insurance with minimum limits of not less than the following:

 

Each Accident

 

$

1,000,000

 

 

 

Disease Policy Limit

 

$

1,000,000

 

 

 

Disease Each Employee

 

$

250,000

 

(b)                                  Comprehensive General Liability

 

Combined single limit bodily injury and property damage

 

- each occurrence

 

$

1,000,000

 

 

 

 

-aggregate

 

$

1,000,000

 

2



 

Such insurance shall include the following:

 

(i)                                      Premises – Operations

 

(ii)                                   Contractor’s Protective Liability, covering all work sublet.

 

(iii)                                Completed Operations and Products Liability coverage, which shall be maintained for a minimum period of three years after final payment and Contractor shall continue to provide evidence of such coverage to Owner on an annual basis during such period.

 

(iv)                               Broad Form Property Damage

 

(v)                                  Property Damage Liability Insurance, which shall include coverage for Collapse and Underground.

 

(vi)                               Contractual Liability (Hold Harmless Coverage)

 

(vii)                            Personal Injury (with Employment Exclusion deleted, if applicable)

 

-aggregate

 

$

1,000,000

 

(c)                                   Comprehensive Automobile Liability Insurance, with limits of liability of not less than the following:

 

Combined single limit bodily injury and property damage

 

-each occurrence

 

$

1,000,000

 

Such coverage shall include owned, hired and non-owned vehicles.

 

(d)                                  Umbrella Liability Insurance in an amount of not less than $2,000,000 providing limits of liability in excess of limits provided in (a), (b) and (c) above.

 

3


 

(e)            Builder’s Risk insurance for the complete replacement of the Approved Alterations.

 

All insurance policies arranged by the contractor shall contain a clause waiving any right of subrogation against Lessor.  All insurance policies, except the policy listed in 7(a) above, shall name Lessor as an additional insured.

 

8.              Completion of Construction .  Lessee shall cause the contractor to diligently pursue, until completion, the construction of the Approved Alterations in accordance with the plans, drawings, and specifications approved by Lessor.  Within seventy-five (75) days following substantial completion of the Approved Alterations, Lessee shall provide to Lessor the following items:

 

(1)            a complete architectural and engineered set of documents describing the scope of work;

 

(2)            an affidavit that payroll, bills for materials and equipment, and other indebtedness connected with the construction of the Approved Alterations have been paid or otherwise satisfied;

 

(3)            properly executed releases and affidavits of payment establishing payment of the Lessee’s contractor’s obligations related to the construction of the Approved Alterations;

 

(4)            a complete list of all materialmen, suppliers, and subcontractors supplying materials or work costing in excess of $5,000, including addresses, telephone numbers, and names of individuals to contact who are familiar with the portion of the construction of the Approved Alterations accomplished by such entity;

 

(5)            if applicable, proof of approval from the Texas Department of Licensing and Regulation of the plans and specifications for the Approved Alterations; and

 

B-4



 

(6)            a warranty book and any other customary and reasonable information that is requested by the Lessor.

 

9.              Performance Standards .  Lessee shall require that the contractor perform all labor in a workmanlike manner, in strict compliance with the Lease, including this Exhibit “B-1” , all applicable Federal, state, local and agency laws, ordinances, and regulations, and according to the standard industry practice.  Lessor shall have the right to supervise all “base building” and other construction related activities affecting the plumbing and structural systems of the building.  Due to the laboratory nature of the Approved Alterations, Lessee shall have the right to “self-perform” any design and renovation construction work once the plans for such work are approved by Lessor (such approval shall not be unreasonably withheld, delayed or denied).  Lessee shall not use any materials containing asbestos or hazardous substances unless these substances are incorporated within construction materials approved for such use by the Environmental Protection Agency.

 

10.            Trash .  Lessee shall require that the contractor clean the job site and deposit all accumulated trash and debris on a daily basis in the designated construction dumpster(s).  The contractor shall supply its own trash receptacles and Lessor’s facilities shall not be for this purpose.

 

11.            Warranties .  Lessee shall cause contractor to warrant to Lessor that materials and equipment furnished for construction of the Approved Alterations will be of good quality and new unless otherwise required or permitted by the Lessor, that the Approved Alterations will be free from defects not inherent in the quality required or permitted, and that the Approved Alterations will conform with the requirements of the plans, drawings, and specifications approved by Lessor.

 

12.            INDEMNIFICATION .  LESSEE HEREBY AGREES TO INDEMNIFY AND HOLD LESSOR HARMLESS FROM AND AGAINST AND TO REIMBURSE LESSOR WITH RESPECT TO ANY AND ALL CLAIMS, DEMANDS, CAUSES OF ACTION, LOSS, DAMAGE, LIABILITIES, COSTS, AND EXPENSES (INCLUDING ATTORNEY’S FEES AND COURT COSTS) OF ANY AND EVERY KIND OR CHARACTER, INCLUDING, WITHOUT LIMITATION, INJURY TO OR DEATH OF ANY PERSON, OR FOR DAMAGE TO ANY PROPERTY, KNOWN OR UNKNOWN, FIXED OR CONTINGENT, ASSERTED AGAINST OR INCURRED BY LESSOR AT ANY TIME AND FROM TIME TO TIME BY REASON OF OR ARISING OUT OF THE CONSTRUCTION OF THE APPROVED ALTERATIONS BY LESSEE, LESSEE’S CONTRACTOR AND LESSEE’S SUBCONTRACTORS OR FROM LESSOR’S FAILURE TO COMPLY WITH THE TERMS OF THIS EXHIBIT “B-1” .

 

B-5



 

Additionally, Lessee shall discharge as soon as commercially reasonable (but in no event later than any date specified in any mortgage indebtedness secured by the Premises), or bond or otherwise secure against all liens and attachments which are filed in connection with the construction of the Approved Alterations by the contractor or any materialman, supplier, or subcontractor, and shall indemnify, protect, defend and hold Lessor harmless from and against all claims, demands, causes of action, loss, damage, liability, costs and expenses (including attorneys fees and court costs) relating to such liens and attachments.

 

13.            The Woodlands Covenants and Standards .  Lessee shall cause all construction to be in accordance with The Woodlands Covenants and the Commercial/Industrial Development Standards (“Standards”) adopted by the Committee under authority granted by The Woodlands Covenants, and any other applicable standards.  The Woodlands Covenants shall mean and refer to:

 

·       the Covenants, Restrictions, Easements, Charges and Liens of The Woodlands, which are imposed upon the Land and recorded in the Real Property Records of Montgomery County, Texas, and which are substantially similar in form and substance as those recorded under (i) County Clerk File No. 9210558 of the Real Property Records of Montgomery County, Texas (WCA); and (ii) County Clerk’s File No. 9348561 of the Real Property Records of Montgomery County, Texas (TWA).

 

·       the Declaration of Covenants and Restrictions of The Woodlands Commercial Owners Association which are imposed upon the Land and recorded in the Real Property Records of Montgomery County, Texas, and are substantially similar in form and substance as those recorded under County Clerk’s File No. 9357930 of the Real Property Records of Montgomery County, Texas.

 

“Committee” as used herein shall mean and refer to the committee organized pursuant to The Woodlands Covenants for the purpose of establishing rules, regulations, policies and procedures governing the improvement of property in The Woodlands.

 

Approval of plans by the Committee shall not entitle Lessee to rely thereon with respect to conformity with laws, regulations, codes or ordinances, or with respect to the physical condition of the Property.  Lessee hereby waives any claims, demands, or causes of action growing out of any plan approvals by the Committee.

 

B-6



 

14.            Approval of Improvements to the Premises .  Lessee understands that when it performs any construction, renovation, modification or alteration on the Premises which is expected to cost $50,000.00 or more, Lessee must (i) submit its plans and specifications to the Texas Department of Licensing and Regulation for its review and approval before commencing such work, (ii) provide evidence to Lessor of such submission to and approval by this department, and (iii) indemnify, defend and hold Lessor harmless against any liability, claim, loss, damage or penalty (including court costs and reasonable attorneys fees and court costs) resulting from Lessee’s failure to comply with the Texas Elimination of Architectural Barriers, as amended from time to time, or its associated rules and regulations.

 

B-7



 

EXHIBIT “C”

 

RENEWAL OPTIONS

 

(a)            Provided that (i) the Lease is in full force and effect as of the date of the applicable Renewal Notice (as such term is hereinafter defined), and (ii) Lessee shall not be in default beyond any applicable notice and cure period under the Lease, Lessee shall have the option to extend the Term of the Lease for two (2) additional terms of five (5) years each (each, a “ Renewal Term ”), commencing on the day after the expiration of the initial term of this Lease or the day after the expiration of the first Renewal Term, as applicable (each, an “ Expiration Date ”).  Lessee’s option with respect to a Renewal Term shall be exercisable by written notice (the “ Renewal Notice ”), to Lessor given not more than eight (8) months nor less than four (4) months prior to the applicable Expiration Date.  Each Renewal Term shall constitute an extension of the Term of the Lease and shall be upon all of the same terms and conditions as the initial Term, except that (i) there shall be no further option to renew the Term of the Lease after the expiration of the second Renewal Term, (ii) Lessor shall not be required to furnish any materials or perform any work to prepare the Premises for Lessee’s occupancy and Lessor shall not be required to make any Allowance or reimburse Lessee for any improvements made or to be made by Lessee, or grant Lessee any rent concession, and (iii) the Base Rent for each Renewal Term shall be as determined pursuant to the provisions of (b), (c) and (d) , below, and shall commence on the first day of the applicable Renewal Term.

 

(b)            The annual Base Rent for the Premises for each Renewal Term shall be an amount equal to ninety-five percent (95%) of the Market Rental Rate.  “ Market Rental Rate ” means the effective rental rate (as of the first day of the applicable Renewal Term) for comparable space in Class “A”, single story flex buildings in the Research Forest area of The Woodlands, Texas that a willing lessee would pay and a willing lessor would accept for the Premises during the applicable Renewal Term, in arms length, bona fide negotiations, for a new lease of the Premises, based upon other lease transactions made in the Building and other comparable office buildings in The Woodlands submarket, taking into consideration all relevant terms and conditions of any comparable leasing transactions, including, without limitation:  (i) location, quality and age of the building; (ii) use and size of the space in question; (iii) location and/or floor level within the building; (iv) extent of leasehold improvement allowances; (v) the amount of any abatement of rental or other charges; parking charges or inclusion of same in rental; (vi) lease takeovers/assumptions; (vii) club memberships; (viii) relocation allowances; (ix) refurbishment and repainting allowances; (x) any and all other concessions or inducements; (xi) extent of services provided or to be provided; (xii) distinction between “gross” and “net” lease; (xiii) base year or dollar amount for escalation purposes (both operating costs and ad valorem/real estate taxes); (xiv) any other adjustments (including by way of indexes) to base rental; (xv) credit standing and financial stature of the tenant; and (xvi) length of term.  As used herein, “effective rental rate” means the stated net base rental rate (i.e., the base rental exclusive of any “expense stop” or “base year” operating expense amount).

 

C-1



 

(c)            If Lessee timely exercises the renewal option pursuant to this Exhibit “C” , Lessor shall notify Lessee (the “ Rent Notice ”), not later than 30 days after receipt of the Renewal Notice, of Lessor’s determination of the Market Rental Rate (“ Lessor’s Determination ”).  Lessee shall notify Lessor (“ Lessee’s Notice ”), within 30 days after Lessee’s receipt of the Rent Notice, whether Lessee accepts or disputes Lessor’s Determination, and if Lessee disputes Lessor’s Determination, Lessee’s Notice shall set forth Lessee’s determination (“ Lessee’s Determination ”) of the Market Rental Rate.  If Lessee fails to give Lessee’s Notice within such 30 day period, Lessee shall be deemed to have accepted Lessor’s Determination.

 

(d)            If Lessee timely disputes Lessor’s Determination, and Lessor and Lessee fail to agree as to the Market Rental Rate within 30 days after the giving of Lessee’s Notice, then the Market Rental Rate shall be determined as follows:  An MAI member of the Houston chapter of the Appraisal Institute (the “ Baseball Arbitrator ”), shall be selected and paid for jointly by Lessor and Lessee.  If Lessor and Lessee are unable to agree upon the Baseball Arbitrator, then the same shall be designated by the American Arbitration Association (the “ AAA ”).  The Baseball Arbitrator selected by the parties or designated by the AAA shall have at least five years experience in (i) the leasing of first class office space in The Woodlands, Texas, or (ii) the appraisal of Class “A” office buildings in The Woodlands, Texas.  Lessor and Lessee shall each submit to the Baseball Arbitrator, and to the other, Lessor’s Determination and Lessee’s Determination of the Market Rental Rate of the Premises.  The Baseball Arbitrator shall determine which of the two rent determinations more closely represents the Market Rental Rate of the Premises.  The Baseball Arbitrator may not select any other rental value for the Premises other than one submitted by Lessor or Lessee.  The determination of the party so selected or designated shall be binding upon Lessor and Lessee and shall serve as the basis for the determination of the Base Rent payable for the Renewal Term, subject to further adjustment as provided in the Lease.  After a determination has been made of the Market Rental Rate, the parties shall execute and deliver an instrument setting forth the Market Rental Rate, but the failure to so execute and deliver any such instrument shall not affect the determination of Market Rental Rate.

 

(e)            If Lessee disputes Lessor’s Determination and if the final determination of Market Rental Rate shall not be made on or before the first day of the applicable Renewal Term then, Lessee shall have the option to:  (i) withdraw the Renewal Notice prior to the first day of such Renewal Term and not be obligated to pay any Base Rent applicable to the Premises due under such Renewal Term (and the Lease shall expire as of the end of the Extension Term or, if previously exercised in accordance with the terms hereof, the first Renewal Term), or (ii) pending such final determination, pay as Base Rent for the Renewal Term, an amount equal to the Lessor’s Determination, and if based upon the final determination of the Market Rental Rate, the Base Rent payments made by Lessee for such portion of the Renewal Term were (i) less than the Market Rental Rate payable for the Renewal Term, Lessee shall pay to Lessor the amount of such deficiency within 10 days after demand therefor, or (ii) greater than the Market Rental Rate payable for the Renewal Term, Lessor shall credit the amount of such excess against installments of Base Rent and/or Additional Rent payable by Lessee next coming due.

 

It is an express condition of the option granted to Lessee pursuant to the terms of this Exhibit “C” that time is of the essence with respect to Lessee’s exercise of such option by the date specified in this Exhibit “C” .

 

C-2



 

EXHIBIT “D”

 

PREFERENTIAL LEASE RIGHT

 

(a)            As used herein:

 

Available ” means, as to any space, that (i) the existing tenant’s lease expires within the next twelve (12) months and is not subject to any extension option that may validly be exercised by the tenant, (ii) Lessor has the right to cancel an existing lease or “recapture” any space due to a tenant’s request for Lessor’s consent to a proposed assignment or subletting, and such cancellation occurs prior to or simultaneous with the Offer Notice as herein after defined, (iii) Lessor terminates an existing lease by mutual agreement with the tenant or by exercise of its remedies following a default thereunder by the tenant, or (iv) the space is unleased.  Anything to the contrary contained herein notwithstanding, Lessee’s right of first offer pursuant to this Exhibit “D” is subordinate to (i) any right of offer, right of first refusal, preferential lease right, expansion option, renewal right or similar right or option in favor of any other tenant existing as of the First Amendment Effective Date, (ii) Lessor’s right to extend the term of lease of existing occupants on a floor located within the Offer Space (as defined below), whether or not such occupant occupies such space as of the date hereof or pursuant to an agreement entered into after the date hereof for Offer Space that Lessee failed to exercise its right to lease, and whether or not pursuant to an option to renew, and (iii) any right of offer, right of first refusal, preferential lease right, expansion option, renewal right or similar right or option in favor of any other tenant who has a right to occupy all or a portion of the Offer Space.  Items (i) – (iii) collectively are referred to as “Senior Rights” .

 

Offer Space ” means the space in the Building that is not leased to Lessee as of the date of this First Amendment.  As hereinafter used in this Exhibit “D” , the terms “such Offer Space” and “applicable Offer Space” and “Offer Space”, where the context so requires, shall refer to the particular portion of the entire Offer Space that is set forth in the applicable Offer Notice from time to time.  If the Offer Space is the subject of lease negotiations which include other portions of the Building, the Offer Space Option, as hereinafter defined, shall, at Lessor’s option, apply to the entire space which is subject to such negotiations, and, at Lessor’s option, Lessee shall be obligated to either accept or refuse the opportunity to lease such entire space on the terms provided in the Offer Notice.

 

(b)            Provided (i) the Lease shall not have been terminated, (ii) Lessee shall not be in default beyond any applicable notice and grace period provided under the Lease, (iii) as of the Anticipated Inclusion Date, there shall be at least two (2) years remaining in the Term or any Renewal Term if Lessee shall have exercised any Renewal Option, and (iv) Lessee shall physically occupy the entire rentable area of the Premises, if at any time during the Term, either the Offer Space becomes, or Lessor reasonably anticipates that the Offer Space will become, Available, Lessor shall give to Lessee notice (an “ Offer Notice ”) thereof, specifying (A) the location and rentable square footage of such Offer Space, (B) Lessor’s determination of the Fair

 

D-1



 

Offer Rental for such Offer Space, which shall constitute the maximum thereof Lessor can claim as the Fair Offer Rental for such space in any arbitration thereof (“ Lessor’s Maximum Offer Determination ”), and (C) the date or estimated date that such offer space has or shall become Available (the “ Anticipated Inclusion Date ”).  “ Fair Offer Rental ” means the fixed annual rent that a willing lessee would pay and a willing lessor would accept for the applicable Offer Space, taking into account all relevant factors, including, but not limited to:  (i) location, quality and age of the building; (ii) use and size of the space in question; (iii) location and/or floor level within the building; (iv) extent of leasehold improvement allowances; (v) the amount of any abatement of rental or other charges; parking charges or inclusion of same in rental; (vi) lease takeovers/assumptions; (vii) club memberships; (viii) relocation allowances; (ix) refurbishment and repainting allowances; (x) any and all other concessions or inducements; (xi) extent of services provided or to be provided; (xii) distinction between “gross” and “net” lease; (xiii) base year or dollar amount for escalation purposes (both operating costs and ad valorem/real estate taxes); (xiv) any other adjustments (including by way of indexes) to base rental; (xv) credit standing and financial stature of the tenant; and (xvi) length of term.

 

(c)            Provided that on the date that Lessee exercises the Offer Space Option and on the Offer Space Inclusion Date (as hereinafter defined) (i) the Lease, as amended, shall not have been terminated, (ii) Lessee shall not be in default beyond any applicable notice and grace period provided under the Lease, as amended, (iii) at the time that Lessee exercises the Offer Space Option and on the Anticipated Inclusion Date, there shall be at least two (2) years remaining in the Term or the Renewal Term if Lessee shall have exercised its Renewal Option, and (iv) Lessee shall physically occupy the entire rentable area of the Premises, Lessee shall have the option (the “ Offer Space Option ”), exercisable by notice (an “ Acceptance Notice ”) given to Lessor on or before the date that is ten (10) business days after the giving of the Offer Notice (time being of the essence) to include the Offer Space in the Premises.  Lessee shall not have the option to include in the Premises less than the entire Offer Space described in the Offer Notice.  Lessee shall notify Lessor in the Acceptance Notice whether Lessee accepts or disputes Lessor’s Maximum Offer Determination, and if Lessee disputes Lessor’s Maximum Offer Determination, the Acceptance Notice shall set forth Lessee’s good faith determination of the Fair Offer Rental for such Offer Space, which shall constitute the minimum that Lessee can claim as the Fair Offer Rental for such space in any arbitration thereof (“ Lessee’s Minimum Offer Determination ”).  If Lessee fails to object to Lessor’s Maximum Offer Determination in the Acceptance Notice and to set forth therein Lessee’s Minimum Offer Determination, then Lessee shall be deemed to have accepted Lessor’s Maximum Offer Determination as the Fair Offer Rental for such Offer Space.

 

(d)            If Lessee timely delivers the Acceptance Notice, then, on the date on which Lessor delivers vacant possession of the Offer Space to Lessee (the “ Offer Space Inclusion Date ”), the Offer Space shall become part of the Premises, upon all of the terms and conditions set forth in the Lease, except (i) Base Rent for the Offer Space shall be equal to the Fair Offer Rental, (ii) Lessee’s pro-rata share, proportionate share or words of like import with respect to such Offer Space shall be a fraction, expressed as a percentage, the numerator of which is the number of rentable square feet in the Offer Space and the denominator of which is the number of rentable square feet in the Building, measured according to the same methodology Lessor used to measure the size of the Offer Space, (iii) Lessor shall not be required to, but may in Lessor’s sole discretion, perform any Lessor’s work or any other work, pay a Lessor’s contribution or an Allowance or any other amount, or render any services to make the Building or the Offer Space

 

D-2



 

ready for Lessee’s use or occupancy, and Lessee shall accept the Offer Space in its “AS IS” condition and “WITH ALL FAULTS” on the Offer Space Inclusion Date latent defects excepted, and (iv) the term of the lease of the Offer Space shall be co-terminous with the Term of the Lease.

 

(e)            If, in the Acceptance Notice, Lessee disputes Lessor’s determination of Fair Offer Rental, and Lessor and Lessee fail to agree as to the amount thereof within 20 business days after the giving of the Acceptance Notice, then the dispute shall be resolved consistent to the methodology employed in the determination of the Market Rental Rate as outlined in Section (d) of Exhibit “C”.  If the dispute shall not have been resolved on or before the Offer Space Inclusion Date, then pending such resolution, Lessee shall have the option to:  (i) withdraw its Acceptance Notice and not be responsible for any Base Rent applicable to the Offer Space, or (ii) pay, as Base Rent for the applicable Offer Space, an amount equal to Lessor’s Maximum Offer Determination on a month-to-month basis until such time that a resolution is reached or Lessee withdraws its Acceptance Notice.  If such resolution shall be in favor of Lessee, then within 20 days after the final determination of Fair Offer Rental, Lessor shall refund to Lessee any overpayment or credit Lessee against Rent next coming due, at Lessor’s option.

 

(f)             If Lessor is unable to deliver possession of the Offer Space to Lessee for any reason on or before the date on which Lessor anticipates that the Offer Space shall be Available as set forth in the Offer Notice, the Offer Space Inclusion Date shall be the date on which Lessor is able to so deliver possession and Lessor shall have no liability to Lessee therefor and the Lease, as amended, shall not in any way be impaired.  Notwithstanding anything contained in this subsection (f) to the contrary, if Lessor is delayed in the delivery of the Offer Space due to a prior tenant’s holdover (the “Holdover Tenant”), and such holdover exceeds 90 days, then Lessee may have the option to:  (i) cancel such Offer Space Option by delivering to Lessor written notification of such termination and not be responsible for any Base Rent applicable to the Offering Space, or (ii) participate in fifty percent (50%) of the holdover proceeds payable by the Holdover Tenant.  Lessor shall use commercially reasonable efforts to pursue its rights under said Lease to evict, in addition to its other remedies, the Holdover Tenant occupying the Offer Space.

 

(g)            If Lessee fails timely to give an Acceptance Notice, then (i) Lessor may enter into one or more leases of the particular Offer Space with respect to which Lessee did not give an Acceptance Notice with third parties on such terms and conditions as Lessor shall determine, the Offer Space Option with respect only to the particular space that was the subject of the Offer Notice shall no longer be deemed Available.

 

(h)            Promptly after the occurrence of the Offer Space Inclusion Date, Lessor and Lessee shall confirm the occurrence thereof and the inclusion of the Offer Space in the Premises by executing an instrument reasonably satisfactory to Lessor and Lessee; provided , that failure by Lessor or Lessee to execute such instrument shall not affect the inclusion of the Offer Space in the Premises in accordance with this Exhibit.

 

D-3



 

EXHIBIT “E”

 

EARLY TERMINATION RIGHT

 

(a)            Subject to and upon the terms, provisions and conditions set forth in this Exhibit “E” , Lessee, but not any assignee or subtenant thereof, shall have the one time right (the “ Termination Right ”), to terminate the Lease as to the entire Premises, effective on the last day of any full calendar month following the Extension Commencement Date that is prior to the end of the seventy-second (72 nd ) full calendar month after the Extension Commencement Date (the “ Termination Date ”).  In order to exercise the Termination Right, Lessee must give Lessor written notice of Lessee’s exercise of the Termination Right at least six (6) months prior to the Termination Date, and pay the Termination Fee, as hereinafter defined, prior to the Termination Date.  If Lessee fails to give notice of exercise of the Termination Right on or prior to the required notice date, the Termination Right shall be deemed waived and of no further force and effect.  If Lessee gives timely notice of exercise of the Termination Right but fails to timely pay the Termination Fee to Lessor when due, Lessor may at its option either (i) deem the Termination Right waived and of no further force and effect, or (ii) enforce the termination of this Lease, effective as of the Termination Date, and Lessee’s obligation to pay the Termination Fee.  The provisions of this paragraph shall survive the expiration or termination of this Lease.

 

(b)            Notwithstanding the foregoing, Lessor shall have the option to revoke and nullify any purported exercise of the Termination Right by Lessee if at the time of exercise or thereafter Lessee is in default under the Lease.

 

(c)            The “ Termination Fee ” shall be an amount equal to the unamortized portion of the Lease Costs (as hereinafter defined) as of the Termination Date.  For purposes hereof, “ Lease Costs ” shall mean all unamortized actual (i) lease commissions paid to Lessee’s Broker, and (ii) construction costs, architectural and engineering fees, cabling design and installation costs, and other costs, if any, incurred by Lessor in connection with Lessee’s lease of the Premises, specifically including, but not limited to, the Allowance granted to Lessee.  For purposes of calculating Lease Costs, each component or item of Lease Costs will be deemed to be amortized in equal monthly installments over the remaining Lease term(s) applicable to the space(s) in question at the rate of eight percent (8%) per annum beginning on the date that such component or item of Lease Costs was actually paid by Lessor.

 

D-4




EXHIBIT 10.42

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

SALES AND MARKETING AGREEMENT

 

BETWEEN

 

VGX PHARMACEUTICALS, INC.

 

(VGX)

 

AND

 

VGX INTERNATIONAL

 

(VI)

 



 

SALES AND MARKETING AGREEMENT

 

This Sales and Marketing Agreement (“AGREEMENT”) is between VGX Pharmaceuticals, Inc. (“VGX”), a Delaware corporation, with offices located at 450 Sentry Parkway, Blue Bell, Pennsylvania 19422, and VGX International (“VI”), a corporation having an address of Jung-Hun Building, #701, 944-1 Daechi 3-Dong, Gangnam-gu, Seoul, Korea.

 

A. Whereas VGX controls certain intellectual property related to VGX-1027 (3-phenyl-4,5-dihydro-5-isoxazoleacetic acid) a drug for treating a variety of diseases including Rheumatoid Arthritis (hereinafter referred to as “VGX-1027 for RA”) currently in Phase I clinical trials in the US;

 

B. Whereas VGX and VI desire to enter into an agreement for exclusive rights to sell and market VGX-1027 for RA in Asia (excluding Japan), and Africa and the Middle East.

 

C. Whereas VGX provides VI with the right to first negotiate an exclusive marketing and sales agreement in Japan.

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties hereby agree as follows:

 

1.                                        DEFINITIONS

 

1.1          CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.2          CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.3          EFFECTIVE DATE means the date on which VI and VGX have both fully executed this AGREEMENT.

 

1.4          FAIR MARKET VALUE means the cash consideration which VGX or VI thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.5          NET SALES is defined as the gross amount of monies or cash equivalent or other consideration which is paid by unrelated third parties to VI for VGX-1027 for RA by sale or other mode of transfer, less all qualifying costs directly attributable to such sales, which are made, made for, used or sold by VI, its agents, employees and/or independent contractors.

 

1.6          SALE means any bona fide transaction for which consideration payment is received or expected for the sale, use, or other disposition of VGX-1027 for RA to an unrelated

 

1



 

third party.  A SALE of VGX-1027 for RA shall be deemed completed at the time VI, its agents, or its contractors receive payment for such VGX-1027 for RA.

 

1.7          TERRITORY means countries in Asia (excluding Japan), and Africa and the Middle East.

 

2.                                        FEES AND ROYALTIES

 

2.1          Fees and Royalties.

 

2.1.1                 VGX agrees to waive upfront fees.

 

2.1.2                 As a partial consideration of the exclusive rights granted to VI, VI shall pay for developmental costs incurred and charged by third-party organizations or persons providing services to properly initiate and complete Phase I clinical trials for VGX-1027. These development costs include preclinical toxicity tests, completion of lab work, payments for non-VGX personnel at clinical study sites working on the trial, and creation of case report forms, IND preparation and filing and support costs, API and placebo manufacturing costs, fill/finish/encapsulation/packaging/labeling and shipment costs, statistical analysis and data management, and pharmacokinetic analysis of drug levels.  In return, VGX will be responsible for all direct internal costs (including salaries. supplies, and overhead costs) of program managers, R&D scientists, clinical scientists and other support staff involved in the overseeing and management of product and Phase I clinical development processes for VGX-1027. VI shall have rights to access and to reference data from Phase I clinical studies.

 

2.1.3                 In further consideration of the exclusive rights granted to VI, VI shall pay to VGX, on a quarterly basis, a royalty of ****** of the NET SALES, which is sold by VI, its agent(s), and/or independent contractor(s) of VI for a period of ten (10) years from the date of the first SALE of  VGX-1027 for RA in any country covered in the TERRITORY or until such time as the related patent protection expires in such country, whichever is the later to occur.

 

2.1.4                 In further consideration of the exclusive rights granted to VI, VI shall pay to Ganial Immunotherapeutics, Inc. (hereinafter referred to as “GIT”), on a quarterly basis, a royalty of ****** of the NET SALES of each VGX-1027 for RA, which is sold by VI and any agent(s) and/or independent contractor(s) of VI for a period of ten (10) years from the date of the first SALE of VGX-1027 for RA, in any country covered by such patent issuance or until such time as the related patent protection  expires in such country, whichever is the later to occur.

 

2



 

2.2          Diligence and Milestone Fees.

 

2.2.1                 As a partial consideration of the exclusive rights granted to VI, VI agrees to pay the following milestones.

 

Due Date

 

Payment

 

Upon initiation of Phase II clinical trial s for VGX-1027 for RA

 

$

1,500,000

 

 

 

 

 

Upon initiation of Phase III clinical trial s for VGX-1027 for RA

 

$

3,000,000

 

 

 

 

 

Upon NDA submission for VGX-1027 for RA in the US or any country in the TERRITORRY

 

$

3,000,000

 

 

 

 

 

Upon NDA approval for VGX-1027 for RA in the US or any country in the TERRITORRY

 

$

5,000,000

 

 

2.3                    Currency, Payment Method: All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to VGX under this AGREEMENT shall be made in United States dollars by check or wire-transfer.  If VI receives revenues from SALES of VGX-1027 for RA in currency other than United States Dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

2.4                    Late Payments: If VI fails to pay on the due date any amount which is payable under this Agreement, then, without prejudice to other sections of this Agreement, that amount shall bear interest compounded quarterly from the due date until payment is made in full, both before and after any judgment, at an annual rate of four (4) percentage points above the prime commercial lending rate quoted by Citibank, New York, NY on the day payment was due, until paid.

 

2.5                    Right to First Negotiate in Japan:  During the time period from the Effective Date and the completion of final Phase II clinical studies, VI shall have the right to first negotiate an exclusive sale and marketing agreement to sell VGX-1027 for RA in Japan.

 

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3.                                        CONFIDENTIALITY

 

3.1          CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers). CONFIDENTIAL INFORMATION should be in writing and marked confidential or, if oral, should be reduced to writing within thirty (30) days of disclosure and marked confidential.

 

3.2          Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party during the term of this AGREEMENT and for five (5) years after the date of termination of this AGREEMENT.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this AGREEMENT.  The foregoing obligation shall not apply to:

 

3.2.1                 information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless  independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records; and

 

3.2.2                 information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure; and

 

3.2.3                 information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

3.2.4                 information, which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

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Note: Confidential information shall not be disclosed to third party and this rule shall apply to both VGX and VI. This is particularly true for process development data.

 

4.                                        TERM AND TERMINATION

 

4.1          This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the earlier of: (a) expiration of the last-to-expire patent or (b) twenty (20) years after the EFFECTIVE DATE.

 

4.2          VI may terminate this AGREEMENT (a) upon sixty (60) days written notice to VGX, if the sale or other exploitation of the VGX-1027 for RA becomes technologically or commercially unfeasible; or (b) upon sixty (60)-days written notice to VGX, and by doing all of the following:

 

4.2.1                 ceasing to make, have made, use, import, sell and offer for sale VGX-1027 for RA; and

 

4.2.2                 paying all monies owed to VGX up to the date of the termination excluding any future obligation under this AGREEMENT.

 

4.3          VGX may terminate this AGREEMENT, upon sixty (60)-days written notice to VI, if any of the following events of default (“Default”) occur:

 

4.3.1                 VI is more than ninety (90) days late in paying to VGX royalties, expenses or any other monies due under this AGREEMENT and VI does not immediately pay VGX in full any amounts due upon demand; or

 

4.3.2                 VI experiences a Trigger Event (defined below);

 

4.3.3                 VI materially breaches this AGREEMENT and does not cure the material breach within sixty (60) days after the receipt of the written notice of such breach;

 

4.3.4                 VI fails, within a reasonable period of time, to make a good faith effort to establish the necessary marketing and sales organization to achieve commercially reasonable sales of VGX-1027 for RA in the TERRITORY.

 

4.3.5                 VI fails, within two years from regulatory approval of VGX-1027 for RA in a country in the TERRITORY, to have established, or to be substantially in the process of having established, the necessary marketing and sales organization in said country.

 

4.4          “Trigger Event” means any of the following if VI:

 

4.4.1.1                becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

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4.4.1.2                is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment; or

 

4.4.1.3                makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

4.4.2                 If proceedings under any International law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VI;

 

4.4.3                 If any order for relief is entered relating to any of the proceedings described in Sections 4.4.2 ;

 

4.4.4                 If VI shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts; or

 

4.4.5                 If VI shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 4.4.2, 4.4.3, 4.4.4.

 

4.4.6                 In the event of a “change in control” of VI, VI shall promptly notify VGX of such change in control and VGX shall be permitte d to terminate this Agreement at VGX’s option.  A “change of control” means a change in the direct or indirect power to direct or cause the direction of the management and policies of VI, whether through ownership or voting securities, by contract, or otherwise

 

4.5          The provisions of Sections 4.3 and 4.4 shall apply to a Default of, or a Trigger Event experienced by, any agents and/or contractors of VI ‘s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the agents and/or contractors(s) cause VI to fail to meet its diligence obligations under Section 2.2.

 

4.6          In the event of a termination under Section 4.1 or 4.3, all duties of VGX (other than under Sections 4.11) and all rights (but not duties) of VI (other than under Section 4.11) under this AGREEMENT immediately terminate without the necessity of any action being taken either by VI or by VGX, provided, however, that in no event shall the foregoing be construed to obligate VI to pay any amounts accruing under Sections 2.1  after the date of termination except under Section 4.10.  Upon and after any termination of this AGREEMENT, the rights covered by this AGREEMENT for VI and any agents

 

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and/or contractors thereof to manufacture, sale, marketing, importation and/or distribution of VGX R&DPRODUCT(s) shall terminate on the same date of the termination of the AGREEMENT, except otherwise specified in this AGREEMENT or agreed upon by both parties.

 

4.7          Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

4.8          Upon termination of this AGREEMENT under section 4.2 and 4.3, VI shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed VGX-1027 FOR RA on hand, under the control of VI, its agents, or contractors thereof; and (b) such VGX-1027 FOR RA as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be recorded in writing.  VI shall deliver copies of such written inventories, verified by an officer of VI, forthwith to VGX.  VGX shall have forty five (45) days after receipt of such verified inventories within which to challenge the physical inventory and request an audit thereof.

 

4.9          Upon termination of this AGREEMENT under section 4.1, VI shall pay all monies owed to VGX up to the date of the termination.

 

4.10              Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 4.3.1 or 4.3.2, VI shall have a period of six (6) months to sell off its inventory of VGX-1027 for RA existing on the date of termination of this AGREEMENT and shall pay royalties to VGX with respect to such VGX-1027 for RA within thirty (30) days following the expiration of such six-month period.

 

4.11              Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Articles 2, 3, 4, 5, 6, 7, and 8 shall survive such termination.

 

5.                                        REPRESENTATIONS AND WARRANTIES OF VGX AND VI; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

5.1          VGX represents and warrants to VI that:

 

5.1.1                 VGX has the full authority to execute and deliver this AGREEMENT.

 

5.1.2                 To best of VGX’s knowledge, there are no pending or threatened suits, claims, or actions of any type whatsoever against VGX with respect to the VGX-1027 for RA.

 

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5.1.3        All necessary corporate authorizations, consents and approvals which are necessary or required for VGX to enter into this AGREEMENT have been duly obtained.

 

5.1.4        To the best of its knowledge, the entering into of this AGREEMENT by VGX will not (i) violate any Applicable Law or (ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination, cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of VGX, under its organizational documents.

 

5.2           VI represents and warrants to VGX that:

 

5.2.1  all necessary corporate and other authorizations, consents, and approvals which are necessary or required for VI to enter into this AGREEMENT have been duly obtained.

 

5.2.2  to the best of its knowledge the entering into of this AGREEMENT by VI will not (i) violate any Applicable Law or any applicable ruling, writ, injunction, order, judgment or decree of any court, administrative agency or other governmental body or (ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination, cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of VGX under its organizational documents.

 

5.2.3  VI shall not, during the course of any manufacturing, marketing, using or selling by it of VGX-1027 FOR RA, engage in any act which results in VGX-1027 for RA being adulterated or misbranded within the meaning of Applicable Law.

 

5.2.4  VI shall comply with all Applicable Law related to their importation, manufacture, use or sale of VGX-1027 for RA in the TERRITORY.

 

5.2.5  to the best of its knowledge, VGX-1027 for RA, and its manufacture, use or sale by VI and/or its Affiliates, will not violate any patents, patent rights, copyrights, confidential information or trade secrets of any other person.

 

5.2.6  VI shall, and shall obligate its Affiliates, subcontractors, joint venture partners, and any other person or entity performing services under this AGREEMENT to substantially comply with all of the terms in this AGREEMENT, including confidentiality provisions, and comply all their operations relating to VGX-1027 for RA with all Applicable Laws in the TERRITORY.

 

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5.2.7  VI shall use its best efforts to prevent sales of VGX-1027 for RA outside of the listed VI TERRITORY above.  Breach of this clause shall be considered a material breach of this AGREEMENT.

 

THE WARRANTIES CONTAINED IN THIS SECTION 5.1 and 5.2 ARE THE EXCLUSIVE WARRANTIES MADE BY THE PARTIES IN RESPECT TO VGX-1027 FOR RA, AND ALL OTHER WARRANTIES RELATING THERETO, EXPRESSED, STATUTORY OR IMPLIED, INCLUDING BUT NOT LIMITED TO WARRANTIES OF FITNESS FOR A PARTICULAR PURPOSE, AND MERCHANTABILITY ARE HEREBY WAIVED AND EXCLUDED.

 

5.3  VGX shall defend and indemnify and hold VI (and its respective officers, directors and employees) harmless against any and all Losses, arising out of, relating to, based on, or caused by (A) the breach by VGX of any representation or warranty contained in this AGREEMENT, (B) a claim that the formulation or manufacture of the VGX-1027 for RA by VGX for VI or other activities of VGX under this AGREEMENT infringe on the patent or other intellectual property rights of a third party, (C) any governmental or regulatory action arising out of VGX, or (D) any negligence or intentional misconduct by VGX in connection with performing its obligations under this AGREEMENT, in each case except to the extent that such Losses arise from or are aggravated in any substantial respect by the negligent acts of or failure to act by VI or its agents and/or contractors.  VI will promptly notify VGX of any such Losses which come to VI’s attention, but failure to do so will not relieve VGX of its indemnification obligations under this Section 5.3 except to the extent any such delay results in a material prejudice to VGX.  Notwithstanding anything to the contrary in this AGREEMENT, VGX shall not be liable for any Losses to the extent that the Losses suffered by VI (and its officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

5.4  VI shall defend and indemnify and hold VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) harmless against any Losses, arising out of, relating to, based on, or caused by (A) the breach by VI of any representation or warranty contained in this AGREEMENT or (B) any negligence or intentional misconduct by VI in connection with performing its obligations under this AGREEMENT, in each case except to the extent that such Losses arise from or are aggravated by the negligent acts of or failure to act by VGX, its agents and/or contractors.  VGX will promptly notify VI of any such Losses which come to VGX’s attention, but failure to do so will not relieve VI of its indemnification obligations under this Section.

 

6              RETENTION BY VI AND ACCESS TO RECORDS

 

6.1           Records:             VI shall keep records in accordance with customary accounting practices and in sufficient detail showing the amount of VGX-1027 for RA sold or otherwise transferred to third parties to permit the determination of royalties due to VGX.  VI shall keep complete records related to activities such that records shall be in sufficient

 

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detail to enable the Royalties payable hereunder by VI to be clearly and fully determined.  VI further agrees to permit its books and records, including without limitation such books and records relating to VI’s parties, agents, etc, to be examined no more than once in any two consecutive Calendar Quarters to verify the reports provided under this Agreement, such confidential examination to be made at VGX’s discretion by either: (i) an independent auditing firm appointed by and at the expense of VGX, which firm shall be reasonably acceptable to VI, or (ii) VGX’s internal auditors.  Such records shall be kept and examination thereof shall be limited to a period of time no more than three (3) Calendar Years after the close of the fiscal year to which the records pertain.  In the event that VI shall include a VI’s partner to the extent permitted hereunder, VI shall (a) cause such VI partner to incorporate audit rights in favor of VGX substantially identical to the provisions of this Section 6.1 , and (b) use commercially reasonable efforts to enforce such audit rights with respect to such VI’s partner.

 

6.2  Financial Information.  VI shall provide to VGX (a) annual audited financial statements and (b) such other quarterly financial statements as may be prepared by or on behalf of VI, within ninety (90) days, subject to assumption by VGX of customary and reasonable confidentiality obligations regarding such information.

 

7              Insurance:  Prior to commencement of any commercial product sales, VI will procure and maintain, at its own expense and for its own benefit, Product Liability insurance having a bodily injury, death, and property damage combined single limit of at least U.S. $5,000,000 per occurrence.  If the above-mentioned policy or the limit is not available in any of the countries in the listed TERRITORY, VI agrees to use its best efforts to procure the best policy and limit available in such countries.

 

7.1  VI will furnish VGX a certificate(s) from an insurance carrier or showing all insurance set forth above.  The certificate(s) will include the following statement:  “The insurance certified hereunder is applicable to contracts between VGX. and the Insured.  This insurance may be canceled or altered only after thirty (30) days written notice to VGX.”  The insurance will be endorsed and the certificate(s) will confirm that the insurance (1) names VGX. and its affiliates as additional insureds with respect to matters arising from this Agreement; (2) provides that such insurance is primary and non-contributing to any liability insurance carried by VGX; and (3) provides that underwriters and insurance companies of VI may not have any right of subrogation against VGX and its affiliates.  The insurance will contain no more than a typical industry deductible.

 

7.2  VI agrees to waive any right of recovery against VGX, and its affiliates for any loss or damage of the type covered by the insurance to be procured and maintained under this Agreement regardless of whether or not such insurance is so maintained.  Failure of any of the terms and conditions of the Insurance provision will be deemed a material breach of this Agreement.

 

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8              ADDITIONAL PROVISIONS

 

8.1  Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between VGX and VI, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

8.2  VI is not permitted to assign this AGREEMENT or any part of it to any person or entity, either directly or by operation of law, without the prior written consent of VGX in its sole discretion.  However, VI has the rights to contract out the manufacturing of the VGX-1027 FOR RA covered in this AGREEMENT and rights to establish sales and marketing partnership with a third party.  In case any product covered in this AGREEMENT is sold by a marketing partnership, VI shall have the responsibility to pay royalty that is calculated on the bases of the combined net sales of VI and its marketing partners. No assignment relieves VI of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

8.3  A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

8.4  Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by internationally recognized express couriers (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGX:

 

VGX Pharmaceutical, Inc.

450 Sentry Parkway East

Blue Bell, PA 19422

Attention: Chief Executive Officer

 

If for VI:

 

VGX International

Jung-Hun Building, #701

944-1 Daechi 3-Dong

Gangnam-gu, Seoul, Korea

Attention: Vice President

 

Either party may change its official address upon written notice to the other party.

 

8.5  This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania in the United States of America, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve

 

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the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the either federal or state courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.  The parties agree to accept original service of complaint via internationally recognized courier with receipt confirmation.  Also, the parties agree to waive the Hague Convention requirements relating to translation of certain documents to applicable foreign language which in this case is Korean.

 

8.6  VI shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.

 

8.7  If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

8.8   Fees :  Except as otherwise provided herein, each Party shall bear its own legal fees incurred in connection with the transactions contemplated hereby.

 

8.9  This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

[SIGNATURE PAGE FOLLOWS]

 

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IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

VGX INTERNATIONAL, INC.

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

 

 

 

By:

/s/ Bryan Kim

 

By:

/s/ Kevin W. Rassas

 

 

 

 

 

Name:

Bryan Kim

 

Name:

  Kevin W. Rassas

 

 

 

 

 

Title:

   Vice President

 

Title:

    Senior Vice President

 

 

 

 

 

Date:

2/28/08

 

Date:

    2/28/08

 

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EXHIBIT 10.43

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated March 31, 2008, is made by and between VGX Pharmaceuticals, Inc., a Delaware corporation (the " Company "), and Dr. J. Joseph Kim (" Executive ").

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         WHEREAS , Executive and the Company previously entered into a Non-Disclosure, Assignment of Inventions, Non-Solicitation and Non-Compete Agreement (the " Non-Compete Agreement "), which continues in full force and effect.

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Executive as Chief Executive Officer and President and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on the date hereof (the " Commencement Date ") and continue for a period of three years from the Commencement Date; provided, however, that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Executive throughout the Term as Chief Executive Officer and President of the Company with such responsibilities, duties and authority as are assigned to him by the Board of Directors (the " Board ") of the Company or its designee.

        b.     Executive shall faithfully devote his full business/working time, attention and energy to the business and affairs of the Company and the performance of his duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of the Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $240,000 per annum (the " Base Salary "), which shall be paid to Executive by the Company or any of its affiliates on a monthly basis.

        b.     Increases in the Base Salary shall be reviewed annually by the Board during the Term and any such increases, if any, will be at the Board's or its designee's sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.


4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at thirty percent (30%) or more of the Base Salary. The amount shall be determined by the Board, in its sole and absolute discretion, which shall be binding and final, and shall be paid in a one-time lump sum payment (less payroll taxes). To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated. Notwithstanding the foregoing, all bonuses shall be paid within two and one-half months after the close of each year.

5.     Benefits; Stock Options.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or his personal representative terminate Executive's employment on account of his death or total disability. In the case of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if he shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of his death or such Total Disability, such termination shall be effective immediately upon



notice, in which case Executive or his representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board; provided, however, that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days' written notice (" Termination Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:


        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of his termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate his employment for good reason (" Termination For Good Reason ") by providing 30 days' written notice of a breach constituting Good Reason, which notice shall be provided within 90 days after the initial existence of the breach, provided, that such breach is not cured in all material respects to the reasonable satisfaction of Executive within 30 days after such notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean voluntary termination by Executive of his employment with the Company based on one of the following events:

provided, however, that, with respect to subsections (i) and (ii) above, in the event that Executive terminates his employment within six months prior to a Change in Control (as such term is defined below) or within 12 months after a Change in Control, " Good Reason " shall be defined to be (y) the material diminution in Executive's position, title, responsibilities or authority from those in effect, or (z) a relocation of Executive's principal executive offices more than fifty miles from its location existing at, six months prior to a Change in Control.

        e.     Voluntary Termination.     Executive may otherwise terminate his employment without Good Reason upon 30 days' written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of his Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

        f.     Section 409A.     The Base Salary continuation set forth in Sections 7 (a), (c) and (d) hereof shall be intended to satisfy either (i) the safe harbor set forth in the regulations issued under Section 409A (as defined below) of the Internal Revenue Code of 1986, as amended (the "Code") (Treas. Regs. 1.409A-1(n)(2)(ii)), or (ii) be treated as a Short-term Deferral as that term is defined



under Section 409A (Treas. Regs. 1.409A-1(b)(4)). To the extent that such continuation payments exceed the applicable safe harbor amount or do not constitute a Short-term Deferral, the excess amount shall be treated as deferred compensation under Section 409A and as such shall be payable pursuant to the following schedule: such excess amount shall be paid via standard payroll in periodic installments in accordance with the Company's usual practice for its senior executives.

        Notwithstanding any provision in this Agreement to the contrary, in the event that Executive is a "specified employee" as defined in Section 409A, any continuation payment, continuation benefits or other amounts payable under this Agreement that would be subject to the special rule regarding payments to "specified employees" under Section 409A(a)(2)(B) of the Code shall not be paid before the expiration of a period of six months following the date of Executive's termination of employment or before the date of Executive's death, if earlier.

        g.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

        h.     Release.     Executive shall not be entitled to any compensation under this Section 7 unless Executive executes and delivers to the Company within 10 days after termination, a Separation of Employment Agreement and General Release (the " Release ") in the form attached hereto as Exhibit A by which Executive releases the Company from any obligations and liabilities of any type whatsoever, except for the Company's obligation to provide the compensation and benefits specified in this Section 7 and those Release Exclusions (as such term is defined in the Release) set forth in the Release. The parties hereto acknowledge that the payments to be provided under this Section 7 are to be provided in consideration for the Release.

8.     Change in Control Provisions.     

        a.     Effect of Termination Following Change in Control.     In the event of a Change in Control (as such term is defined below) during the Term, and a termination of Executive's employment, either as a Termination Without Cause or Termination For Good Reason, occurring either within six months prior to or within 12 months following such Change in Control, whether or not such termination is during the Term, Executive shall be entitled to receive (i) the payments and other rights provided in Section 7(c) hereof and (ii) a lump sum cash severance payment, paid within 15 days of the date of termination, equal to the sum of Executive's monthly base salary (as in effect immediately prior to such termination) and the Pro-Rata Bonus Amount (as determined under Section 7(c)(iv) above) multiplied by 24, but discounted to present value from the dates such payments would be made if paid on a monthly basis for such 24-month period, based on the 100% short-term Applicable Federal Rate (compounded annually) under Section 1274(d) of the Internal Revenue Code of 1986, as amended (the " Code "), as in effect at the time of payment.

        b.     Definition of Change in Control.     For purposes of this Agreement, a " Change in Control " shall be deemed to have occurred upon:


9.     Parachute Tax Indemnity.     

        a.     If it shall be determined that any amount paid, distributed or treated as paid or distributed by the Company to or for Executive's benefit (whether paid or payable or distributed or distributable pursuant to the terms of this Agreement or otherwise, but determined without regard to any additional payments required under this Section 9) (a " Payment ") would be subject to the excise tax imposed by Section 4999 of the Code, or any interest or penalties are incurred by Executive with respect to such excise tax (such excise tax, together with any such interest and penalties, being hereinafter collectively referred to as the " Excise Tax "), then Executive shall be entitled to receive an additional payment (a " Gross-Up Payment ") in an amount such that after payment by Executive of all federal, state and local taxes (including any interest or penalties imposed with respect to such taxes), including, without limitation, any income taxes (and any interest and penalties imposed with respect thereto) and Excise Tax imposed upon the Gross-Up Payment, Executive retains an amount of the Gross-Up Payment equal to the Excise Tax imposed upon all the Payments.

        b.     All determinations required to be made under this Section 9, including whether and when a Gross-Up Payment is required and the amount of such Gross-Up Payment and the assumptions to be utilized in arriving at such determination, shall be made by a nationally recognized accounting firm as may be designated by Executive (the " Accounting Firm ") which shall provide detailed supporting calculations both to the Company and Executive within 15 business days of the receipt of notice from Executive that there has been a Payment, or such earlier time as is requested by the Company. In the event that the Accounting Firm is serving as accountant or auditor for the individual, entity or group effecting the Change in Control, Executive shall appoint another nationally recognized accounting firm to make the determinations required hereunder (which accounting firm shall then be referred to as the Accounting Firm hereunder). All fees and expenses of the Accounting Firm shall be borne by the Company. Any Gross-Up Payment, as determined pursuant to this Section 9, shall be paid by the Company to Executive within five days of the receipt of the Accounting Firm's determination. Any determination by the Accounting Firm shall be binding upon the Company and Executive. As a result of the uncertainty in the application of Section 4999 of the Code at the time of the initial determination by the Accounting Firm hereunder, it is possible that Gross-Up Payments which will not



have been made by the Company should have been made (" Underpayment "), consistent with the calculations required to be made hereunder. In the event that the Company exhausts its remedies pursuant to this Section 9 and Executive thereafter is required to make a payment of any Excise Tax, the Accounting Firm shall determine the amount of the Underpayment that has occurred and any such Underpayment shall be promptly paid by the Company to or for Executive's benefit.

        c.     Executive shall notify the Company in writing of any claim by the Internal Revenue Service that, if successful, would require the payment by the Company of the Gross-Up Payment. Such notification shall be given as soon as practicable but no later then 10 business days after Executive is informed in writing of such claim and shall apprise the Company of the nature of such claim and the date on which such claim is requested to be paid. Executive shall not pay such claim prior to the expiration of the 30-day period following the date on which he gives such notice to the Company (or such shorter period ending on the date that any payment of taxes with respect to such claim is due). If the Company notifies Executive in writing prior to the expiration of such period that the Company desires to contest such claim, Executive shall:

        d.     If, after Executive's receipt of an amount advanced by the Company pursuant to this Section 9, Executive becomes entitled to receive any refund with respect to such claim, Executive shall (subject to the Company's complying with the requirements of this Section 9) promptly pay to the Company the amount of such refund (together with any interest paid or credited thereon after taxes applicable thereto). If, after Executive's receipt of an amount advanced by the Company pursuant to this Section 9, a determination is made that Executive shall not be entitled to any refund with respect to such claim and the Company does not notify Executive in writing of its intent to contest such denial of refund prior to the expiration of 30 days after such determination, then such advance shall be


forgiven and shall not be required to be repaid and the amount of such advance shall offset, to the extent thereof, the amount of Gross-Up Payment required to be paid.

10.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

11.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

12.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

13.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:


        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

14.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

15.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

16.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

17.     Section 409A.     

        It is intended that this Agreement be drafted and administered in compliance with section 409A of the Code, including, but not limited to, any future amendments to Code section 409A, and any other Internal Revenue Service or other governmental rulings or interpretations (collectively, " Section 409A ") issued pursuant to Section 409A so as not to subject Executive to payment of interest or any additional tax under Section 409A. The parties intend for any payments under this Agreement to either satisfy the requirements of Section 409A or to be exempt from the application of Section 409A, and this Agreement shall be construed and interpreted accordingly. In furtherance thereof, if payment or provision of any amount or benefit hereunder that is subject to Section 409A at the time specified herein would subject such amount or benefit to any additional tax under Section 409A, the payment or provision of such amount or benefit shall be postponed to the earliest commencement date on which the payment or provision of such amount or benefit could be made without incurring such additional tax. In addition, to the extent that any Internal Revenue Service guidance issued under Section 409A would result in Executive being subject to the payment of interest or any additional tax under Section 409A, the parties agree, to the extent reasonably possible, to amend this Agreement in order to avoid the imposition of any such interest or additional tax under Section 409A, which amendment shall have the minimum economic effect necessary and be reasonably determined in good faith by the Company and Executive.


18.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

19.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

20.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

21.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

22.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

[SIGNATURE PAGE FOLLOWS]


        IN WITNESS WHEREOF, the parties hereto have executed this Employment Agreement as of the date first written above.

    VGX PHARMACEUTICALS, INC.

 

 

By:

 



        Name:    
        Title:    

 

 

EXECUTIVE

 

 

/s/ J. Joseph Kim

Dr. J. Joseph Kim, Ph.D.

EXHIBIT A

SEPARATION OF EMPLOYMENT AGREEMENT AND GENERAL RELEASE

        WHEREAS Dr. J. Joseph Kim, Ph.D. ("Executive") has been employed by VGX Pharmaceuticals, Inc. (the "Company"), and because Executive's employment with the Company will terminate effective                        , Executive and the Company agree as follows:

        1.     In consideration of the promises of the Company set forth in Paragraph 3 below, Executive, and his heirs, executors and administrators, intending to be legally bound, hereby permanently and irrevocably agrees to the termination of Executive's employment with the Company effective on                        (or such earlier date as may be communicated in writing by                         ) (the "Termination Date") and hereby REMISE, RELEASE and FOREVER DISCHARGE the Company and any individual or organization related to the Company and against whom or which Executive could assert a claim, including                        (hereinafter, together with the Company, referred to collectively as "Releasees"), of and from any and all causes of action, suits, debts, claims and demands whatsoever, which he had, has or may have against Releasees up until the date of his execution of this Separation of Employment Agreement and General Release (this "Release Agreement"), other than the Release Exclusions (as such term is defined below). Particularly, but without limitation, Executive so releases and waives all claims relating in any way to his employment or the termination of his employment relationship with the Company, including without limitation claims under Title VII of the Civil Rights Act of 1964, as amended , §§ 42 U.S.C. 2000e et seq . ("Title VII"), the Americans with Disabilities Act, 42 U.S.C. §§ 12101 et seq . (the "ADA"), the Employee Retirement Income Security Act 29 U.S.C. §§ 1001 et seq . ("ERISA"), the Age Discrimination in Employment Act, as amended 29 U.S.C. §§ 621 et seq . (the "ADEA"), any and all other federal and/or state statutes, including without limitation the Pennsylvania Human Relations Act ("PHRA"), and all federal, state or common law claims, including all tort and contract claims of whatever nature or form, and all claims for counsel fees and costs. Executive agrees that Executive will not file any civil complaint or lawsuit against the Company or any of Releasees under Title VII, ERISA, the ADA, the ADEA, the PHRA or any other federal, state or local law. Executive further agrees and covenants that should any person, organization or other entity file, charge, claim, sue, or cause or permit to be filed any civil action, suit or legal proceeding involving any matter occurring at any time in the past, Executive will not seek or accept any personal relief in such civil action, suit or legal proceeding. This release does not relinquish Executive's rights, if any, to the following specific claims that Executive has or may have (the "Release Exclusions"): (i) to seek indemnification pursuant to applicable state law and the Company's By-laws; (ii) to seek coverage under directors' and officers' liability insurance policies maintained by the Company; (iii) to enforce the Company's obligations under this Agreement or (iv) to seek relief for any claims that Executive has arising from his interest in the Company as a stockholder, including those claims that arise from any stockholder agreement to which Executive is or was a party.

        2.     Executive shall promptly take all steps necessary to dismiss with prejudice any and all pending complaints, lawsuits and/or grievances against the Releasees, regardless of whether they are or have been filed internally or externally. Executive waives his right to institute or have pursued on his behalf any complaints, lawsuits, or grievances whatsoever against the Releasees for any matter occurring up to the present, regardless of the forum, other than the Release Exclusions. Executive also agrees that the payment in Paragraph 3 is in full satisfaction of any liability or obligation to Executive under the Employment Agreement, dated as of March     , 2008, between the Company and Executive.

        3.     In full consideration of Executive's execution of this Release Agreement, and his agreement to be legally bound by its terms, the Company will provide Executive with the following consideration, to which Executive acknowledges he would not otherwise be entitled:

A-1


        Executive understands and expressly agrees that each benefit enhancement and payment under paragraphs (a) and (b) above is expressly contingent on Executive's continued employment through                        , or such earlier date as may be communicated in writing by the Company.

        Executive acknowledges that, other than the payments described in this Paragraph 3, he has received payment in full of all of the compensation, wages, benefits and/or payments of any kind otherwise due to him from the Company. Except as set forth in this Release Agreement, it is expressly agreed and understood that Releasees do not have, and will not have, any obligation to provide Executive at any time in the future with any payments, benefits or considerations other than those recited in this Paragraph, required by law or as may be claimed as a right under the Release Exclusions.

        4.     If Executive brings a legal action for claims against any of the Releasees in contravention of any part of this Release Agreement, including Paragraph 1 of this Release Agreement, and other than the Release Exclusions, Executive agrees and acknowledges that he will reimburse such Releasees for their reasonable attorneys' fees and costs in defending any such action, provided, however, that this reimbursement requirement shall be inapplicable in any matter regarding the ADEA.

        5.     The parties acknowledge that the performance of the promises of each are expressly contingent upon the fulfillment and satisfaction of the obligations of the other party as set forth in this Release Agreement.

        6.     Executive hereby agrees and recognizes that, as of his Termination Date, Executive's employment relationship with the Company or Releasees will be permanently and irrevocably severed, Executive promises never to seek employment with the Company or Releasees in the future, and that Executive waives his right to be hired or rehired in the future by the Company and any of its affiliates. It is further agreed and understood that Executive will continue to be available and cooperate in a reasonable manner in providing assistance to the Company in concluding any matters which are reasonably related to the duties and responsibilities that Executive had while employed by the Company, provided that such cooperation and assistance does not interfere with any subsequent employment obtained by Executive.

        7.     Executive agrees and acknowledges that this Release Agreement is not and shall not be construed to be an admission of any violation of any federal, state or local statute or regulation, or of any duty owed by Releasees.

        8.     Executive agrees, covenants and promises that Executive will not communicate or disclose the terms of this Release Agreement to any persons with the exception of members of Executive's immediate family and Executive's attorney and financial advisor. Executive further agrees to refrain from using or disclosing for the benefit of any person, business or entity other than the Company, any confidential information relating to the Company's business, which includes but is not limited to information relating to the Company's employees, suppliers, customers, services, plans, research, marketing studies or analyses, and financial or business affairs. Executive represents that any and all documents containing such confidential information will be returned to the Company by the Termination Date and that, in addition, he will otherwise retain no equipment or property of the Company, including any documents and files, whether electronically stored or maintained in hard copy.

        9.     This Release Agreement, and the provisions of the Employment Agreement and the Non-Disclosure, Assignment of Inventions, Non-Solicitation and Non-Compete Agreement (attached as Exhibit A to the Employment Agreement) that survive Executive's termination of employment, constitute the complete and entire understanding between the parties, and supersede any and all prior agreements and understandings between the parties to the extent they are inconsistent with this Release Agreement.

A-2


        10.   Executive hereby certifies that Executive has read the terms of this Release Agreement, that Executive has been advised by the Company, and is again hereby advised, to consult with an attorney of his own choice prior to executing this Release Agreement, that Executive has had an opportunity to do so, and that Executive understands this Release Agreement's terms and effects. Executive further certifies that neither Releasees nor any representative of Releasees have made any representations to Executive concerning this Release Agreement other than those contained herein.

        11.   Executive acknowledges that Executive has been informed that this Release Agreement includes a waiver of claims under the ADEA, and that Executive has the right to consider this Release Agreement for a period of 21 days. Executive also understands that he has the right to revoke this Release Agreement for a period of seven days following his execution of this Release Agreement by giving written notice to the Company in care of                        . Executive also understands and agrees that this Release Agreement will not be binding or enforceable until after the seven day revocation period has expired.

        12.   If any provision of this Release Agreement is deemed invalid, the remaining provisions shall not be affected.

        13.   The provisions of this Release Agreement shall be governed by the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

        14.   Executive certifies and acknowledges that: (a) he has carefully read this Release Agreement; (b) it is written in a manner understandable to him and he fully understood it; (c) he is entering into it knowingly and voluntarily; and (d) he intends to be legally bound by the promises contained in this Release Agreement for the aforesaid consideration.

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        IN WITNESS WHEREOF, and intending to be legally bound hereby, the parties have executed the foregoing Separation of Employment Agreement and General Release on the dates indicated below.

WITNESS:  

   
Dr. J. Joseph Kim, Ph.D.

 

 

 

 

DATE:

 




WITNESS:

 




 

VGX PHARMACEUTICALS, INC.

 

 

 

 

BY:

 



        NAME:  

        TITLE:  

        DATE:  

A-4




QuickLinks


EXHIBIT 10.44

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

CELLECTRA™ DEVICE

 

 

LICENSE AGREEMENT

 

 

BETWEEN

 

VGX PHARMACEUTICALS, INC.

 

AND

 

 

VGX INTERNATIONAL, INC.

 



 

CELLECTRA™ DEVICE LICENSE AGREEMENT

 

This License Agreement (“AGREEMENT”) is between VGX Pharmaceuticals, Inc.  (“VGX”), a Delaware corporation, with offices located at 450 Sentry Parkway East, Blue Bell, Pennsylvania 19422, and VGX International, Inc.  (“VI”), a corporation having an address of Jung-Hun Building, #701, 944-1 Daechi 3-Dong, Gangnam-gu, Seoul, Korea.

 

A.  Whereas VGX controls certain intellectual property related to a CELLECTRA™ Device (hereinafter referred to as “CELLECTRA™ DEVICE”) a medical device that utilizes electroporation technology for delivery of plasmids into skeletal muscle cells and skin of humans.

 

B.  Whereas VGX and VI desire to enter an agreement for exclusive rights to the development, sales, licensing, and marketing of the CELLECTRA™ DEVICE in humans in the Republic of Korea.

 

NOW, THEREFORE, in consideration of the promises and covenants contained in this AGREEMENT and intending to be legally bound, the parties hereby agree as follows:

 

1.                                        DEFINITIONS

 

1.1            APPROVED PRODUCT means a drug and/or vaccine product approved for delivery in humans using a CELLECTRA™ DEVICE.

 

1.2           CALENDAR QUARTER means each three-month period, or any portion thereof, beginning on January 1, April 1, July 1 and October 1.

 

1.3            CALENDAR YEAR means each 12-month period beginning on January 1.

 

1.4            CELLECTRA™ DEVICE means VGX’s electroporation device, including applicators and needle arrays, for delivery of plasmids into skeletal muscle cells and skin in humans which is/are made, made for, used by, imported by or for, sold by or offered for sale for each indication and/or any agents and contractors(s) to unrelated third parties which (1) in the absence of this AGREEMENT would infringe on any claim of VGX PATENT RIGHTS described in patents listed in Attachment I, or (2) use a process and/or machine covered by any claim of VGX PATENT RIGHTS described in patents listed in Attachment I.

 

1.5           EFFECTIVE DATE means the date on which VGX and VI have both fully executed this AGREEMENT.

 

1.6           FAIR MARKET VALUE means the cash consideration which VGX or VI thereof would realize from an unaffiliated, unrelated buyer in an arm’s length sale of an identical item sold in the same quantity and at the same time and place of the transaction.

 

1.7           IMPROVEMENT means all discoveries and/or inventions (whether patented or not) made during the term of this Agreement by VI which constitute (i) a modification of

 

1



 

CELLECTRA™ DEVICE (ii) a modification of KNOW-HOW TECHNOLOGY; or (iii) which, if practiced, would infringe any claims of PATENT RIGHTS or which relate directly or indirectly to the CELLECTRA™ DEVICE.  Made as used herein means the discovery or invention was conceived or reduced to practice.  Improvements do not include any inventions or discoveries related to LICENSED PRODUCTS alone.

 

1.8            KNOW-HOW TECHNOLOGY means VGX’s technical information and materials, including without limitation, technology, data, computer software and algorithms for controlling the CELLECTRA™ DEVICE and related equipment, inventions (patentable or otherwise), practices, methods, knowledge, know-how, skill and experience related directly or indirectly to the CELLECTRA™ DEVICE.

 

1.9            LICENSED PRODUCT means any product where therapeutic genetic constructs are used together with the CELLECTRA™ DEVICE in administering treatments to humans.

 

1.10          NET SALES is defined as the gross amount of monies or cash equivalent or other consideration which is paid by unrelated third parties to VI for a CELLECTRA™ DEVICE and/or LICENSED PRODUCT by sale or other mode of transfer, less all qualifying costs directly attributable to such sales, which are made, made for, used or sold by VI, its agents, employees and/or independent contractors .

 

1.11          PATENT RIGHTS mean those patents listed in ATTACHMENT I.

 

1.12          SALE means any bona fide transaction for which consideration payment is received or expected for the sale, use, lease, transfer or other disposition of a CELLECTRA™ DEVICE and/or LICENSED PRODUCT to an unrelated third party.  A SALE of CELLECTRA™ DEVICE and/or LICENSED PRODUCT shall be deemed completed at the time VGX or VI, their agents, or their contractors receive payment for such CELLECTRA™ DEVICE and/or LICENSED PRODUCT.

 

1.13          SUBLICENSE means when used as a verb to, directly or indirectly, sublicense, or grant any other right with respect to, or agree not to assert, any intellectual property right granted to a Party under this Agreement.  When used as a noun, “Sublicense” shall mean any agreement to Sublicense.

 

1.14          TERRITORY means the Republic of Korea.

 

1.15          VGX PATENT RIGHTS means all of VGX’s interest in the rights represented by or issuing from (including all claims referenced within) those patent applications listed in Attachment I and all future interests in such rights anywhere in the world of the CELLECTRA™ DEVICE intellectual property.

 

2.              LICENSE

 

Subject to the terms and conditions of this AGREEMENT, VGX shall grant VI an exclusive license to research, develop and market the CELLECTRA™ DEVICE for human use in the TERRITORY.  No other rights are granted by either party hereunder. 

 

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This agreement shall not impair VI’s freedom (without any restriction or any obligation to VGX) to research, develop, and market products for the CELLECTRA™ DEVICE, except for the restrictions in this Agreement.

 

2.1            VGX shall provide the CELLECTRA™ DEVICE including applicators and arrays, upon VI’s request.  VI shall reimburse VGX for the costs of such CELLECTRA™ DEVICE, applicators and needle arrays at the prices set forth in Attachment II such prices may be adjusted form time to time upon mutual agreement.  VI will pay VGX for all shipping, insurance, handling and other costs related to delivery of the CELLECTRA™ DEVICE, applicators and needle arrays to VI.

 

2.2            VGX and VI shall share pre-clinical testing data, and clinical results related to the product development and clinical development of the CELLECTRA™ DEVICE.

 

3.              COST SHARING, FEES, AND ROYALTIES

 

3.1            Cost Sharing, Fees and Royalties.

 

3.1.1         VI shall pay a cost sharing fee of $100,000 to reimburse VGX for the costs in part of patents, agency fees, attorneys fees, and preclinical development of CELLECTRA™ DEVICE upon execution of this agreement.

 

3.1.2         In consideration of the exclusive rights to CELLECTRA™ DEVICE in the TERRITORY VI shall pay to VGX, on a quarterly basis, a royalty of ****** the NET SALES of LICENSED PRODUCT in the TERRRITORY, which is sold by VI, its agent(s), and/or sub-licensees of VI for a period of ten (10) years from the date of the first SALE of CELLECTRA™ DEVICE in the TERRITORY or until such time as the related patent protection expires in such TERRITORY, whichever is the later to occur.  Said payments are due within ten (10) days after each CALENDAR QUARTER.

 

3.1.3         VI shall pay VGX an annual maintenance fee of $25,000 to cover, among other things, product enhancements, a portion of the on-going patent costs, agency fees, attorneys fees for patents listed in Attachment I.  Said payments are due within ten (10) days after each anniversary of the EFFECTIVE DATE.

 

3.1.4

 

3.2            Diligence and Milestone Fees.

 

3.2.1         VI shall use commercially reasonable efforts to develop for SALE and to market CELLECTRA™ DEVICE in the TERRITORY.  VI and VGX agree to the following R&D milestones payments related to the use of CELLECTRA™ DEVICE to develop LICENSED PRODUCT in the TERRITORY.  Said payments are due within sixty (60) days after the achievement of the respective milestone event:

 

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Milestone

 

Payment

 

Upon Filing of each IND

 

$

100,000

 

Upon initiation of each Phase II

 

$

150,000

 

Upon initiation of each Phase III clinical trial

 

$

250,000

 

Upon each BLA approval

 

$

500,000

 

Upon first commercial sale CELLECTRA™ DEVICE for each BLA

 

$

750,000

 

 

3.3            Currency, Payment Method.

 

All dollar amounts referred to in this AGREEMENT are United States dollars.  All payments to VGX under this AGREEMENT shall be made in United States dollars by check or wire-transfer.  If VI receives revenues from SALES of CELLECTRA™ DEVICE and/or LICENSED PRODUCT in currency other than United States Dollars, revenues shall be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of The Wall Street Journal as of the last business day of the applicable CALENDAR QUARTER.

 

4.              SUB-LICENSES

 

4.1            VI shall have the right to sub-license the rights to CELLECTRA™ DEVICE in the TERRITORY such sub-licenses may not be granted without the prior written approval of VGX, such approval not to be unreasonably withheld.

 

4.1.1         VI shall pay to VGX ****** of any and all Sub-license Fees that VI receives.  Sub-license Fees shall include the net proceeds of cash payments or non-cash compensation provided by Sub-licensees to VI, including equity or rights to purchase equities.

 

5.              PATENTS

 

5.1            Grant-Back.  When an IMPROVMENT is made or discovered by VI and/or its Affiliates, and such Improvement would not have arisen but for the presence of CELLECTRA™ DEVICE , or KNOW-HOW TECHNOLOGY, and such IMPROVEMENT relates to CELLECTRA™ DEVICE , or KNOW-HOW TECHNOLOGY and does not include LICENSED PRODUCT, VI and its employees and/or its Affiliates hereby assign its entire right, title and interest in such IMPROVEMENT to VGX and agree to cooperate with VGX in obtaining patent protection therefore at VGX’s cost, including, but not limited to the execution of any and all lawful papers in the U.S.  and foreign patent offices.  VGX hereby grants VI the ability to use such IMPROVEMENT under the terms of this Agreement to the extent VGX has the right to convey the right to practice the Improvement to Licensee.

 

5.2            Patent Applications.  Notwithstanding the foregoing, VI shall not file any patent applications which disclose, describe or require the presence of CELLECTRA™

 

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DEVICE , or KNOW-HOW TECHNOLOGY absent consent from VGX.  For the avoidance of doubt, VGX agrees that it shall consent to disclosure in patent applications filed by VI concerning VI’s Product and the use of VGX’s Confidential Information as may be reasonably necessary to comply with the legal standards of disclosure and description.  VGX will have the right to review all sections and examples relating to CELLECTRA™ DEVICE , or KNOW-HOW TECHNOLOGY thirty (30) days before the filing of such patent application.  If VI files such an application outside the scope of 5.1, VI and/or its Affiliates hereby grant VGX and its Affiliates irrevocable world-wide, exclusive, royalty-free licenses to such IMPROVMENT with the right to sublicense such rights to Third Parties, with the right to further sublicense.

 

5.3            Patent Infringement.  Should VI become aware of any infringement or alleged infringement of any PATENT RIGHTS, VI shall promptly notify VGX in writing of the name and address of the alleged infringer and of the alleged acts of infringement, and provide any available evidence of the alleged acts of infringement.  VGX shall not be obligated to prosecute against any Third Party any suit for infringement of the aforesaid Patent Rights.  In the event that VGX decides to bring a patent infringement suit against the alleged Third Party infringer, VI shall cooperate with VGX in the prosecution of any legal infringement action and agrees to provide VGX with pertinent data and evidence which may be helpful in the prosecution of such action of which it may have knowledge or which may be readily available to it.  VGX shall reimburse VI for reasonable expenses incurred by VI in assisting VGX in this matter.  VGX shall have the exclusive right (but not the obligation) to institute and conduct legal action against Third Party infringers of the PATENT RIGHTS, and to enter into such settlement agreements as may be deemed appropriate by VGX.  VGX shall receive the full benefits of any compensatory or punitive damages it obtains pursuant to bringing such suit.

 

5.4            Invalidity of PATENT RIGHTS If, at any time during this Agreement, VGX shall be unable to uphold the validity of any of the PATENT RIGHTS against any alleged infringer, VI shall not have or assert any damage claim or a claim for refund or reimbursement against VGX.  In the event that PATENT RIGHTS are not upheld, royalties shall continue under this Agreement for VI’s rights under CELLECTRA™ DEVICE.  However, in the event PATENT RIGHTS are not upheld and VI is required to pay duplicate royalties to a Third Party, VI shall pay VGX a reduced royalty rate of the royalty rate minus the duplicate royalty rate.  For the avoidance of doubt any patent that has not been withdrawn, cancelled, abandoned, disclaimed, revoked or held unpatentable, invalid or unenforceable by a final decision of a court or other governmental agency of competent jurisdiction, which decision is unappealable or unappealed within the time allowed for appeal is considered to be valid and upheld.

 

5.5            Challenges.  VI, VI affiliates, VI Partners, or sublicensees are not permitted directly or indirectly, to challenge the validity or enforceability of any of Patent Rights.  Such breach shall result in termination of this license.

 

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6.              CONFIDENTIALITY

 

6.1            CONFIDENTIAL INFORMATION means and includes all technical and business information, plans, inventions, developments, discoveries, improvements, software, know-how, procedures, methods, techniques, formulae, data, processes, studies, and other proprietary ideas, whether or not patentable or copyrightable, that a party hereto identifies as confidential or proprietary at the time it is delivered or communicated to the other party hereto, or any other information that should reasonably be recognizable by its nature to be confidential or trade secret information of a party (including, without limitation, information respecting such party’s business plans, sales and sales methods, customers and prospective customers).  CONFIDENTIAL INFORMATION should be in writing and marked confidential or, if oral, should be reduced to writing within thirty (30) days of disclosure and marked confidential.

 

6.2            Each party shall maintain in confidence and not disclose to any third party any CONFIDENTIAL INFORMATION of the other party during the term of this Agreement and for five (5) years after the date of termination of this Agreement.  Each party shall ensure that its employees have access to CONFIDENTIAL INFORMATION of the other party only on a need-to-know basis, and are obligated to abide by such party’s obligations under this Agreement.  The foregoing obligation shall not apply to:

 

6.2.1         Information that is known to the receiving party prior to the time of disclosure, and was not received directly or indirectly from the disclosing party hereunder in violation of a confidentiality obligation, unless independently developed by or for the receiving party, without exposure to or benefit of the disclosing party’s CONFIDENTIAL INFORMATION, in each case, to the extent evidenced by written records; and

 

6.2.2         Information disclosed to the receiving party, without restriction, by a third party that has a right to make such disclosure; and

 

6.2.3         Information that was or becomes patented, published or otherwise part of the public domain as a result of acts by the disclosing party or a third person developing or obtaining such information as a matter of right; and

 

6.2.4         Information, which the disclosing party permits, in writing, the receiving party to publicly disclose.

 

If a receiving party is required to disclose any of the disclosing party’s CONFIDENTIAL INFORMATION by order of a governmental authority or a court of competent jurisdiction; the receiving party shall timely inform its disclosing party, reasonably cooperate at the disclosing parties expense with any reasonable action the disclosing party takes to attempt to obtain confidential treatment of such information by the authority or court, and limit its disclosure of such information to the extent practical.

 

7.              TERM AND TERMINATION

 

7.1            This AGREEMENT, unless sooner terminated as provided in this AGREEMENT, shall terminate upon the earlier of: (a) expiration of the last-to-expire patent or (b) twenty (20) years after the EFFECTIVE DATE.

 

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7.2            VI may terminate this Agreement (a) upon thirty (30) days written notice to VGX, if the sale or other exploitation of the CELLECTRA™ DEVICE becomes technologically or commercially unfeasible; or (b) upon sixty (60)-days written notice to VGX, and by doing all of the following:

 

7.2.1         Ceasing to make, have made, use, import, sell and offer for sale CELLECTRA™ DEVICE ; and

 

7.2.2         Paying all monies owed to VGX up to the date of the termination excluding any future obligation under this AGREEMENT.

 

7.3            VGX may terminate this AGREEMENT, upon sixty (60)-days written notice to VI, if any of the following events of default (“Default”) occur:

 

7.3.1         VI is more than ninety (90) days late in paying to VGX royalties, expenses or any other monies due under this AGREEMENT and VI does not immediately pay VGX in full any amounts due upon demand; or

 

7.3.2         VI experiences a Trigger Event (defined in Section 7.4 below);

 

7.3.3         VI materially breaches this AGREEMENT and does not cure the material breach within ninety (90) days after the receipt of the written notice of such breach.

 

7.3.4         Is materially behind the Development Plan timeline set forth in Attachment II and is unlikely or unable to cure such delinquency in a reasonable period of time.

 

7.4            “Trigger Event” means any of the following:

 

If VI:

 

7.4.1         Becomes insolvent, bankrupt or generally fails to pay its material debts as such debts become due;

 

7.4.2         Is adjudicated insolvent or bankrupt; admits in writing its inability to pay its debts; or shall suffer a custodian, receiver or trustee for it or substantially all of its property to be appointed and, if appointed without its consent, is not discharged within thirty (30) days of such appointment;

 

7.4.3         Makes an assignment for the benefit of creditors; or suffers proceedings under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or the release of debtors to be instituted against it and, if contested by it, not dismissed or stayed within thirty (30) days;

 

7.4.4         If proceedings under any International law related to bankruptcy, insolvency, liquidation, or the reorganization, readjustment or the release of debtors are instituted or commenced by VI;

 

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7.4.5         If any order for relief is entered relating to any of the proceedings described in Sections 7.4.4;

 

7.4.6         If VI shall call a meeting of its creditors with a view to arranging a composition or adjustment of its debts;

 

7.4.7         If VI shall, by any act or failure to act, indicate its consent to, approval of or acquiescence in any of the proceedings described in Sections 7.4.4, 7.4.5 or 7.4.6;

 

7.4.8         If VI has a “change of control”.  A “change of control” means a change in the direct or indirect power to direct or cause the direction of the management and policies of VI, whether through ownership or voting securities, by contract or otherwise.  In the event of a “change in control” of VI, VI shall promptly notify VGX of such change in control and VGX shall be permitted to terminate this Agreement at VGX’s option.

 

7.5            The provisions of Sections 7.3 and 7.4 shall apply to a Default of, or a Trigger Event experienced by, any agents and/or contractors of VI ‘s rights hereunder if and to the extent that such Default of, or Trigger Event experienced by, the agents and/or contractors(s) cause VI to fail to meet its diligence obligations under Section 3.2.

 

7.6            In the event of a termination under Section 7.1 or 7.3, all duties of VGX (other than under Sections 7.11) and all rights (but not duties) of VI (other than under Section 7.11) under this AGREEMENT immediately terminate without the necessity of any action being taken either by VI or by VGX, provided, however, that in no event shall the foregoing be construed to obligate VI to pay any amounts accruing under Sections 3.1 and 3.2 after the date of termination except under Section 7.10.  Upon and after any termination of this AGREEMENT, the rights covered by this agreement for VI and any agents and/or contractors thereof to manufacture, sale, marketing, importation and/or distribution of CELLECTRA™ DEVICE shall terminate on the same date of the termination of the agreement, except otherwise specified in this agreement or agreed upon by both parties.

 

7.7            Upon termination of this AGREEMENT, each (receiving) party shall, at the other (disclosing) party’s request, return to the other party all CONFIDENTIAL INFORMATION (except for one copy for archival purposes) of the other party provided hereunder.

 

7.8            Upon termination of this AGREEMENT under section 7.2 and 7.3, VI shall cause physical inventories to be taken as soon as commercially practicable and in any event no later than sixty (60) days after termination of: (a) all completed CELLECTRA™ DEVICE on hand, under the control of VI, its agents, or contractors thereof; and (b) such CELLECTRA™ DEVICE as are in the process of manufacture and component parts thereof as of the date of termination of this AGREEMENT, which inventories shall be recorded in writing.  VI shall deliver copies of such written inventories, verified by an officer of VI, forthwith to VGX.  VGX shall have forty five (45) days after receipt of

 

8



 

such verified inventories within which to challenge the physical inventory and request an audit thereof.

 

7.9            Upon termination of this agreement under section 7.1, VI shall pay all monies owed to VGX up to the date of the termination.

 

7.10          Notwithstanding the foregoing, if this AGREEMENT terminates other than pursuant to Section 7.3.1 or 7.3.2 or 7.3.3, VI shall have a period of six (6) months to sell off its inventory of CELLECTRA™ DEVICE existing on the date of termination of this AGREEMENT and shall pay royalties to VGX with respect to such CELLECTRA™ DEVICE within thirty (30) days following the expiration of such six-month period.

 

7.11          Each party’s obligation to pay all monies owed and accruing as of the date of termination under this AGREEMENT shall survive termination of this AGREEMENT.  In addition, the provisions of Sections 4, 5, 6, 7 and 8 shall survive such termination.

 

8.              REPRESENTATIONS AND WARRANTIES OF VGX AND VI; DISCLAIMER OF ADDITIONAL WARRANTIES; INDEMNIFICATION

 

8.1            VGX represents and warrants to VI that:

 

8.1.1         VGX has the full authority to execute and deliver this AGREEMENT.

 

8.1.2         No material claim by any third party contesting the validity, enforceability, collaborations, use or ownership of any of such VGX PATENT RIGHTS has been made, is currently outstanding or is threatened against VGX.

 

8.2            VGX and VI will work together to file the patents and/or patent applications listed in ATTACHMENT I before the deadline permitted by the relevant international and US patent laws.

 

8.3            VGX shall defend and indemnify and hold VI (and its respective officers, directors and employees) harmless against any and all Losses, arising out of, relating to, based on, or caused by (A) the breach by VGX of any representation or warranty contained in this Agreement, (B) a claim that the manufacture of the CELLECTRA™ DEVICE by VGX for VI or other activities of VGX under this Agreement infringe on the patent or other intellectual property rights of a third party, (C) any governmental or regulatory action arising out of VGX, or (D) any negligence or intentional misconduct by VGX in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated in any substantial respect by the negligent acts of or failure to act by VI or its agents and/or contractors.  VI will promptly notify VGX of any such Losses which come to VI’s attention, but failure to do so will not relieve VGX of its indemnification obligations under this Section 8.3 except to the extent any such delay results in a material prejudice to VGX.  Notwithstanding anything to the contrary in this Agreement, VGX shall not be liable for any Losses to the extent that the Losses suffered by VI (and its officers, directors and employees) are the result of or in

 

9



 

consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

8.4            VI shall defend and indemnify and hold VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) harmless against any Losses, arising out of, relating to, based on, or caused by (A) the breach by VI of any representation or warranty contained in this Agreement or (B) any negligence or intentional misconduct by VI in connection with performing its obligations under this Agreement, in each case except to the extent that such Losses arise from or are aggravated by the negligent acts of or failure to act by VGX, its agents and/or contractors.  VGX will promptly notify VI of any such Losses which come to VGX’s attention, but failure to do so will not relieve VI of its indemnification obligations under this Section 6.4 except to the extent any such delay results in a material prejudice to VI.  Notwithstanding anything to the contrary in this Agreement, VI shall not be liable for any Losses where the Losses suffered by VGX (and its affiliates, including its agents and/or contractors, and their respective officers, directors and employees) are the result of or in consequence of any failure by the indemnified party to take reasonable and prudent action to mitigate any Losses.

 

8.5            To best of VGX’s knowledge, there are no pending or threatened suits, claims, or actions of any type whatsoever against VGX with respect to the CELLECTRA™ DEVICE.

 

8.6            All necessary corporate authorizations, consents and approvals which are necessary or required for VGX to enter into this Agreement have been duly obtained;

 

8.7            To the best of its knowledge, the entering into of this Agreement by VGX will not (i) violate any Applicable Law or (ii) conflict with or result in any breach of any of the terms, conditions or provisions of, or constitute a default (or give rise to any right of termination, cancellation or acceleration) under, or result in the creation of any lien, security interest, charge or encumbrance upon any of the properties or assets of VGX, under its organizational documents, as amended to date, or any material note, indenture, mortgage, le a se, agreement, contract, purchase order or other instrument, document or agreement to which VGX is a party or by which it or any of its properties or assets is bound or affected.

 

9.              ADDITIONAL PROVISIONS

 

9.1            Nothing in this AGREEMENT shall be deemed to establish a relationship of principal and agent between VGX and VI, or between or among any of either party’s agents or employees for any purpose whatsoever, nor shall this AGREEMENT be construed as creating any other form of legal association or arrangement which would impose liability upon one party for the act or failure to act of the other party.

 

9.2            VI is not permitted to assign this AGREEMENT or any part of it to any person or entity, either directly or by operation of law, without the prior written consent of VGX in

 

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its sole discretion.  However, VI has the rights to contract out the manufacturing of the products covered in this agreement and rights to establish collaboration, development, and marketing partnership with a third party.  In case any product covered in this agreement is sold by a marketing partnership, VI shall have the responsibility to pay royalty that is calculated on the bases of the combined net sales of VI and its marketing partners.  No assignment relieves VI of responsibility for the performance of any accrued obligations, which it has prior to such assignment.

 

9.3            A waiver by either party of a breach of any provision of this AGREEMENT will not constitute a waiver of any subsequent breach of that provision or a waiver of any breach of any other provision of this AGREEMENT.

 

9.4            Notices, payments, statements, reports and other communications under this AGREEMENT shall be in writing and shall be deemed to have been received as of the day after the date sent if sent by internationally recognized express couriers (e.g., Federal Express) or by Express Mail, receipt requested, and addressed as follows:

 

If for VGX:

 

VGX Pharmaceutical, Inc.

450 Sentry Parkway East

Blue Bell, PA 19422

Attention: Chief Executive Officer

 

If for VI:

 

VGX International

Jung-Hun Building, #701

944-1 Daechi 3-Dong

Gangnam-gu, Seoul, Korea

Attention: Vice President

 

Either party may change its official address upon written notice to the other party.

 

9.5            This AGREEMENT shall be construed and governed in accordance with the laws of the Commonwealth of Pennsylvania in the United States of America, without giving effect to conflict of law provisions.  In the event that a party to this AGREEMENT perceives the existence of a dispute with the other party concerning any right or duty provided for herein, the parties will, as soon as practicable, confer in an attempt to resolve the dispute.  If the parties are unable to resolve such dispute amicably, then the parties hereby submit to the exclusive jurisdiction of and venue in the either federal or state courts located in the Eastern District of the Commonwealth of Pennsylvania with respect to any and all disputes concerning the subject of this AGREEMENT.  The parties agree to accept original service of complaint via internationally recognized courier with receipt confirmation.  Also, the parties agree to waive the Hague Convention

 

11



 

requirements relating to translation of certain documents to applicable foreign language which in this case is Korean.

 

9.6            VI shall comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this AGREEMENT.  Without limiting the foregoing, it is understood that this AGREEMENT may be subject to United States laws and regulations controlling the export of technical data, computer software, laboratory prototypes and other commodities, articles and information, including the Arms Export Control Act as amended in the Export Administration Act of 1979, and that the parties’ obligations are contingent upon compliance with applicable United States export laws and regulations.

 

9.7            If any provision of this AGREEMENT shall be held to be illegal, invalid or unenforceable, then such illegality, invalidity or unenforceability shall attach only to such provision, and shall not in any manner affect or render illegal, invalid or unenforceable any other provision of this AGREEMENT, and this AGREEMENT shall be carried out as if any such illegal, invalid or unenforceable provision were not contained herein.

 

9.8            This AGREEMENT may not be changed, modified, extended or terminated except by written amendment executed by an authorized representative of each party.

 

[SIGNATURE PAGE FOLLOWS]

 

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IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this AGREEMENT to be executed by their duly-authorized representatives.

 

 

VGX INTERNATIONAL, INC.

  VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

 

By:

  /s/ Bryan Kim

 

 

  By:

/s/ Kevin W.  Rassas

 

 

 

 

Name:

Bryan Kim

 

Name:

  Kevin W.  Rassas

 

 

 

 

Title:

Vice President

 

Title:

  Senior Vice President

 

 

 

 

Date:

4/16/08

 

Date:

  4.16.08

 

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EXHIBIT 10.45

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated December 17, 2005, is made by and between Viral Genomix, Inc. (VGX Pharmaceuticals), a Delaware corporation (the " Company "), and with its principal offices at 450 Sentry Parkway E., Blue Bell, PA, 19422 and MR. KEVIN W. RASSAS ("Executive"), whose address is 717 Larchwood Lane, Villanova, PA 19085.

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Mr. Rassas as Vice President of Business Development and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on December 17, 2005 (the " Commencement Date ") and continue for a period of three (3) years from the Commencement Date; provided , however , that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Mr. Rassas throughout the Term as Vice President of Business Development of the Company with such responsibilities, duties and authority as are assigned to him by the Board of Directors (the "Board") of the Company, Chief Executive Officer or its designee. The Vice President of Business Development shall report to the Chief Executive Officer and/or the Board of Directors.

        b.     Executive shall faithfully devote his full business/working time, attention and energy to the business and affairs of the Company and the performance of his duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of Executive's Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $60,000 per annum (the " Base Salary ") which shall be paid to Executive by the Company or any of its affiliates on a monthly basis until April 30 th , 2006. The annual salary rate will increase to $120,000 per annum starting May 1 st  of 2006.

        b.     Increases in the Base Salary shall be reviewed annually by the Board during the Term and any such increases, if any, will be at the Board's or its designee's sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.


4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at thirty percent (30%) or more of the Base Salary. The amount shall be determined by the Board, in its sole and absolute discretion, which shall be binding and final, and shall be paid in a one-time lump sum payment (less payroll taxes). To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated.

5.     Benefits; Stock Options and Warrant.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

        a.     On or about December 17, 2005, the Board Resolution granted Mr. Rassas options to purchase One Hundred Thousand (120,000) shares of Common Stock of the Company at a strike price of $0.30 per share pursuant to an Option Grant Agreement in substantially the form attached hereto as Exhibit A . These options are subject to the rules and regulations of the 2001 Equity Incentive Plan. In addition, all shares of the Company's stock will be subject to those restrictions contained in the anticipated future Company's Stockholder's Agreement.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or his personal representative terminate Executive's employment on account of his death or total disability. In the case of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if he shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a

2



licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of his death or such Total Disability, such termination shall be effective immediately upon notice, in which case Executive or his representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board and/or Chief Executive Officer; provided , however , that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less

3


than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days written notice (" Termination Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of his termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate his employment for good reason (" Termination For Good Reason ") upon 30 days written notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean voluntary termination by Executive of his employment with the Company based on one of the following events:

        e.     Voluntary Termination.     Executive may otherwise terminate his employment without Good Reason upon 30 days written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of his Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

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        f.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

8.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

9.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

10.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

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11.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:

        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

12.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

13.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

14.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

15.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

16.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

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17.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

18.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

19.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

20.     Termination of Other Agreements.     

        The execution of this Agreement by Viral Genomix and the Executive terminates and voids for all purposes any other Agreements, if any, between the parties.

[SIGNATURE PAGE FOLLOWS]

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         IN WITNESS WHEREOF , the parties hereto have executed this Employment Agreement as of the date first written above.

    VIRAL GENOMIX, INC.

 

 

By:

 

/s/ J. Joseph Kim

    Name:   Dr. J. Joseph Kim, Ph.D.
    Title:   President & CEO

 

 

EXECUTIVE:

 

 

/s/ Kevin W. Rassas

Mr. KEVIN W. RASSAS

8


FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
DECEMBER 17, 2005

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and Kevin Rassas ("Executive") dated as of 20th day of August, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated December 17, 2005 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Mr. Kevin Rassas
717 Larchwood Lane
Villanova, PA, 19085
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Kevin Rassas

Kevin Rassas
Sr. VP of Business Development
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

August 20, 2008


 

Date:

 

August 20, 2008

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EXHIBIT 10.46

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated August 1, 2005, is made by and between Viral Genomix, Inc. (VGX Pharmaceuticals), a Delaware corporation (the " Company "), and with its principal offices at 450 Sentry Parkway, Blue Bell, PA 19422, and Dr. C. Jo White ("Executive"), whose address is 1007 Stonebridge Road, Lower Gwynedd, PA 19002.

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         WHEREAS , Executive agrees to execute and shall be bound by the terms and conditions of the Non-Disclosure, Assignment of Inventions, Non-Solicitation and Non-Compete Agreement (the " Non-Compete Agreement "), attached hereto as Exhibit A .

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Dr. White as Chief Medical Officer (CMO) and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on August 1, 2005 (the " Commencement Date ") and continue for a period of three (3) years from the Commencement Date; provided , however , that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Dr. White throughout the Term as CMO of the Company with such responsibilities, duties and authority as are assigned to him by the Board of Directors (the "Board") of the Company, Chief Executive Officer or its designee. The CMO shall report to the Chief Executive Officer and/or the Board of Directors.

        b.     Executive shall faithfully devote his business/working time, attention and energy to the business and affairs of the Company and the performance of her duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of Executive's Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $200,000 per annum (the " Base Salary ") which shall be paid to Executive by the Company or any of its affiliates on a monthly basis.

        b.     Increases in the Base Salary shall be reviewed annually by the Board during the Term and any such increases, if any, will be at the Board's or its designee's sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.


4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at twenty percent (20%) or more of the Base Salary. The amount shall be determined by the Board, in its sole and absolute discretion, which shall be binding and final, and shall be paid in a lump sum payment (less payroll taxes). Upon execution of this Agreement, ten percent (10%) of Base Salary bonus will be paid immediately. To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated.

5.     Benefits; Stock Options and Vacation.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

        a.     On or about August 1, 2005, by Sole Director's Written Consent of Viral Genomix, Inc., the Executive was elected as CMO. The Board Resolution granted Dr. White options to purchase Three Hundred Thousand (300,000) shares of Common Stock of the Company. Upon execution of this Agreement by the Executive and the Company, the Executive will be awarded Three Hundred Thousand (300,000) Incentive Stock Options (ISO) to purchase Common Shares of the Company's Stock at a strike price of $0.25 per share pursuant to an Option Grant Agreement in substantially the form attached hereto as Exhibit B over three years. These options are subject to the rules and regulations of the 2001 Equity Incentive Plan. In addition, all shares of the Company's stock will be subject to those restrictions contained in the anticipated future Company's Stockholder's Agreement.

        b.     In addition, the Executive is entitled 25 business days (5 weeks) as a Company paid vacation days annually. The Executive will have an office and a dedicated laptop to improve Executive ability to concentrate at work, and increase her productivity.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or her personal representative terminate Executive's employment on account of her death or total disability. In the case

2



of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if she shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of her death or such Total Disability, such termination shall be effective immediately upon notice, in which case Executive or her representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and

3


determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board and/or Chief Executive Officer; provided , however , that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days written notice (" Termination Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of her termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate her employment for good reason (" Termination For Good Reason ") upon 30 days written notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean voluntary termination by Executive of her employment with the Company based on one of the following events:

4


        e.     Voluntary Termination.     Executive may otherwise terminate her employment without Good Reason upon 30 days written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of her Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

        f.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

8.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

9.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

10.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

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11.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:

        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

12.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

13.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

14.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

15.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

16.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

6


17.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

18.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

19.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

20.     Termination of Other Agreements.     

        The execution of this Agreement by Viral Genomix and the Executive terminates and voids for all purposes any other Agreements, if any, between the parties.

[SIGNATURE PAGE FOLLOWS]

7


         IN WITNESS WHEREOF , the parties hereto have executed this Employment Agreement as of the date first written above.

    VIRAL GENOMIX, INC.

 

 

By:

 

/s/ J. Joseph Kim

    Name:   J. Joseph Kim, Ph.D.
    Title:   President & CEO

 

 

EXECUTIVE:

 

 

/s/ C. Jo White

Dr. C. Jo White

8


FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
AUGUST 1, 2005

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and C. Jo. White ("Executive") dated as of 20 th  day of August, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated August 1, 2005 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Dr. C. Jo. White
1007 Stonebridge Road
Lower Gwynedd, PA, 19002
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ C. Jo. White

C. Jo. White
Chief Medical Officer
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

August 20, 2008

 

Date:

 

August 20, 2008

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EXHIBIT 10.47

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated May 1, 2005, is made by and between Viral Genomix, Inc. (VGX Pharmaceuticals), a Delaware corporation (the " Company "), and with its principal offices at 450 Sentry Parkway East, Blue Bell, PA 19422, and DR. BRYAN BYONGJIN KIM ("Executive"), whose address is 3 Forrest Ct., Mt. Laurel, New Jersey, 08054.

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         WHEREAS , Executive agrees to execute and shall be bound by the terms and conditions of the Non-Disclosure, Assignment of Inventions, Non-Solicitation and Non-Compete Agreement (the " Non-Compete Agreement "), attached hereto as Exhibit A .

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Dr. Kim as Director, Corporate Development and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on May 1, 2005 (the " Commencement Date ") and continue for a period of three (3) years from the Commencement Date; provided , however , that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Dr. Kim throughout the Term as Director, Corporate Development of the Company with such responsibilities, duties and authority as are assigned to him by the Chief Executive Officer and/or Chief Operating Officer or its designee. The Director, Corporate Development shall report to the Chief Executive Officer and/or Chief Operating Officer.

        b.     Executive shall faithfully devote his business/working time, attention and energy to the business and affairs of the Company and the performance of his duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of Executive's Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $100,000 per annum (the " Base Salary ") which shall be paid to Executive by the Company or any of its affiliates on a monthly basis.

        b.     Increases in the Base Salary shall be reviewed annually by the Chief Executive Officer and/or Chief Operating Officer during the Term and any such increases, if any, will be at the Chief Executive



Officer and/or Chief Operating Officer sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.

4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at twenty percent (20%) or more of the Base Salary. The amount shall be determined by the Board, in its sole and absolute discretion, which shall be binding and final, and shall be paid in a one-time lump sum payment (less payroll taxes). To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated.

5.     Benefits; Stock Options and Vacation.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

        a.     On or about May 1, 2005, the Board Resolution granted Dr. Kim options to purchase One Hundred Fifty Thousand (150,000) shares of Common Stock of the Company. Upon execution of this Agreement by the Executive and the Company, the Executive will be awarded One Hundred Fifty Thousand (150,000) Incentive Stock Options (ISO) to purchase Common Shares of the Company's Stock at a strike price of $0.25 per share pursuant to an Option Grant Agreement in substantially the form attached hereto as Exhibit B over three years. These options are subject to the rules and regulations of the 2001 Equity Incentive Plan. In addition, all shares of the Company's stock will be subject to those restrictions contained in the anticipated future Company's Stockholder's Agreement.

        b.     The Company offers the medical benefits to Executive and his family.

        c.     In addition, the Executive is entitled 15 business days (3 weeks) as a Company paid vacation days annually. The Executive will have an office and a dedicated laptop to improve Executive ability to concentrate at work, and increase his productivity.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

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7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or his personal representative terminate Executive's employment on account of his death or total disability. In the case of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if he shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of his death or such Total Disability, such termination shall be effective immediately upon notice, in which case Executive or his representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

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        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board and/or Chief Executive Officer; provided , however , that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days written notice (" Termination Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of his termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate his employment for good reason (" Termination For Good Reason ") upon 30 days written notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean

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voluntary termination by Executive of his employment with the Company based on one of the following events:

        e.     Voluntary Termination.     Executive may otherwise terminate his employment without Good Reason upon 30 days written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of his Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

        f.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

8.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

9.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

10.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may

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immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

11.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:

        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

12.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

13.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

14.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

15.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

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16.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

17.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

18.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

19.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

20.     Termination of Other Agreements.     

        The execution of this Agreement by Viral Genomix and the Executive terminates and voids for all purposes any other Agreements, if any, between the parties.

[SIGNATURE PAGE FOLLOWS]

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         IN WITNESS WHEREOF , the parties hereto have executed this Employment Agreement as of the date first written above.

    VIRAL GENOMIX, INC.

 

 

By:

 

/s/ J. Joseph Kim

    Name:   J. Joseph Kim, Ph.D.
    Title:   President & CEO

 

 

EXECUTIVE:

 

 

/s/ Bryan ByonJin Kim

DR. BRYAN BYONGJIN KIM

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FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
MAY 1, 2005

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and Bryan ByongJin Kim ("Executive") dated as of            day of August, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated May 1, 2005 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Mr. Bryan ByongJin Kim
3 Forrest Ct.
Mt. Laurel, NJ, 08054
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Bryan ByonJin Kim

Bryan ByongJin Kim
Vice President
  /s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer

Date:

 

August 20, 2008

 

Date:

 

August 20, 2008

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EXHIBIT 10.48

 

ASSET PURCHASE AGREEMENT

 

THIS ASSET PURCHASE AGREEMENT (this “ Agreement ”) is made and entered into as of June 10, 2008, between VGXI, Inc. (the “ Purchaser ”), a Delaware corporation, and VGX Pharmaceuticals, Inc. (the “ Company ”), a Delaware corporation.

 

BACKGROUND:

 

The Purchaser wishes to purchase from the Company, and the Company wishes to sell to the Purchaser, the Purchased Assets, subject to the Assumed Liabilities (as both terms are defined below), upon the terms and subject to the conditions set forth herein.  Certain capitalized terms used but not defined herein shall have the respective meanings given to them in Article XIII hereof.

 

NOW , THEREFORE, for good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, and intending to be legally bound hereby, the parties hereto hereby agree as follows:

 

ARTICLE I
PURCHASE AND SALE

 

1.1            Purchased Assets .  At the Closing, the Company shall sell, transfer, convey and deliver to the Purchaser, free and clear of all Encumbrances other than the Permitted Encumbrances, all of the Company’s right, title and interest in and to all of the following assets and properties (the “ Purchased Assets ”):

 

(a)            All equipment, machinery, furniture, fixtures, inventory and other tangible assets of the Company listed on Schedule 1.1(a)  hereto (for the purpose of evaluating the value of the Purchased Assets listed on Schedule 1.1(a) , it is noted that the value of the inventory for purposes of determining the Purchase Price was calculated by the parties in the factory cost basis);

 

(b)            The Contracts set forth on Schedule 1.1(b)  hereto (the “ Assigned Contracts ”); and

 

(c)            All of the Company’s patents and patent applications set forth on Schedule 1.1(c)  hereto, and all goodwill associated therewith (the “ Transferred Intellectual Property ”).

 

Schedule 1.1(a) Schedule 1.1(b)  and Schedule 1.1(c)  shall contain an accurate and complete description of any and all the Purchased Assets.

 

1.2            Assumption of Liabilities .  At the Closing, the Company shall assign to the Purchaser, and the Purchaser shall assume and agree to pay, perform and discharge, from and after the Closing, the following liabilities of the Company (the “ Assumed Liabilities ”).

 

(a)            Any and all Liabilities arising out of or relating to the DNA plasmid products of the Company (the “Products”), whether or not manufactured or sold on, prior to or after the

 



 

Closing Date, including, without limitation, claims under warranties and other product liability matters with respect thereto;

 

(b)            Any and all Liabilities to fill orders for Products that remain open as of the Closing Date;

 

(c)            Any and all Liabilities under the Assigned Contracts and the Assigned Intellectual Property, whether or not arising on, prior to or after the Closing Date; and

 

(d)            Any and all other Liabilities arising out of or relating to the Purchased Assets.

 

Except as specifically disclosed in this Section 1.2, the Purchaser may not assume and agree to pay, perform and discharge any liabilities of the Company.

 

ARTICLE II
PURCHASE PRICE

 

2.1            Purchase Price .

 

(a)            The consideration payable to the Company for the purchase of the Purchased Assets (the “ Purchase Price ”) shall be:

 

(i)             Cash in an amount equal to $9,110,000 according to the following schedule:

 

Closing Date

$1,750,000 (the “Closing Payment”)

 

 

June 30, 2008

$1,360,000

 

 

December 15, 2008

$4,000,000

 

 

March 31, 2009

$2,000,000

 

(ii)            The assumption by the Purchaser of the Assumed Liabilities at the Closing as set forth in Schedule 2.1(a)(ii).

 

2.2            Allocation of the Purchase Price .  At least 30 days before the required due date of Form 8594 under Section 1060 of the Code (or any successor form or successor provision of any future Tax law) (“ Form 8594 ”), the Purchaser and the Company shall agree upon an allocation of the Purchase Price, which shall be allocated among the Purchased Assets in accordance with the requirements of such Section 1060, using the unconsolidated assets of the Company.  The Purchaser and the Company shall each report the federal, state and local income and other Tax consequences of the transactions contemplated by this Agreement in a manner consistent with such allocation, including the preparation and filing of Form 8594 with their respective federal income Tax returns for the taxable year that includes the Closing Date, and neither the Purchaser

 

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nor the Company shall take any position or other action inconsistent with such allocation unless otherwise required by applicable Legal Requirements.  In the event that the agreed upon allocation is disputed by any Governmental Authority, the party receiving notice of such dispute shall promptly notify and consult with the other parties hereto concerning resolution of such dispute, and shall keep such other parties apprised of the status of such dispute and the resolution thereof.

 

ARTICLE III
CLOSING; DELIVERIES

 

3.1            Closing .  The consummation of the purchase and sale of the Purchased Assets and the assignment and assumption of the Assumed Liabilities (the “ Closing ”) shall take place at 10:00 a.m. (Philadelphia time) on the second Business Day after the satisfaction or waiver of the conditions (excluding conditions that, by their terms, cannot be satisfied until the Closing Date) set forth in Articles VIII and IX hereof (the “ Closing Date ”), unless another time or date is agreed to by the parties hereto.  The Closing shall be held at the offices of Duane Morris LLP, 30 South 17th Street, Philadelphia, PA 19103, unless another place is agreed to by the parties hereto.

 

3.2            Deliveries by the Purchaser .  At the Closing, the Purchaser shall deliver or cause to be delivered the following to the Company:

 

(a)            The Closing Payment, by wire transfer of immediately available funds to an account designated by the Company at each installment time as stated in Section 2.1 (a)(i);

 

(b)            The Purchaser Closing Certificate (as defined in Section 9.3 hereof) and the Ancillary Agreements required to be executed by the Purchaser pursuant to Article IX hereof, executed by the Purchaser; and

 

(c)            Such other Contracts, certificates and documents as shall be contemplated hereby or as shall be reasonably requested by the Company.

 

3.3            Deliveries by the Company .  At the Closing, the Company shall deliver or cause to be delivered the following to the Purchaser:

 

(a)            The Company Closing Certificate (as defined in Section 8.3 hereof) and the Ancillary Agreements required to be executed by the Company pursuant to Article VIII hereof, executed by the Company; and

 

(b)            Such other Contracts, consents, certificates and documents as shall be contemplated hereby or as shall be reasonably requested by the Purchaser.

 

ARTICLE IV
REPRESENTATIONS AND WARRANTIES OF THE COMPANY AND THE STOCKHOLDERS

 

The Company and the Stockholders hereby jointly and severally represent and warrant to the Purchaser as follows:

 

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4.1            Authority; Enforceability .  The execution, delivery and performance by the Company of this Agreement and each Ancillary Agreement to which it is a party, and the consummation of the transactions contemplated hereby and thereby, have been duly authorized by all necessary action on the part of the Company (including Board of Directors and stockholder approval).  This Agreement has been, and each Ancillary Agreement to which the Company is a party will be, duly and validly executed and delivered by the Company and constitutes, and will constitute, the valid and binding obligation of the Company, enforceable against it in accordance with its respective terms, except (a) as limited by Legal Requirements of general application relating to bankruptcy, insolvency and relief of debtors or (b) as limited by Legal Requirements governing specific performance, injunctive relief or other equitable remedies and by general principles of equity.  The Company has the requisite power and authority to execute and deliver this Agreement and each Ancillary Agreement to which it is a party and to consummate the transactions contemplated hereby and thereby.

 

4.2            Consents; Non-Contravention .

 

(a)            Except as set forth on Schedule 4.2 , no consent, approval, authorization, exemption or waiver of, or notice or filing with, any Person is required to be obtained, given or made, as applicable, by the Company in connection with the execution, delivery and performance by the Company of this Agreement or any Ancillary Agreement to which it is a party, or to consummate the transactions contemplated hereby and thereby.

 

(b)            Except as set forth on Schedule 4.2 , the execution, delivery and performance by the Company of this Agreement and each Ancillary Agreement to which it is a party or by which it is bound and the consummation by the Company of the transactions contemplated hereby and thereby does not and will not, with or without the giving of notice or the lapse of time or both, (i) contravene, conflict with or violate any Legal Requirement to which the Company is subject; (ii) contravene, conflict with or violate any Order applicable to the Company; (iii) contravene, conflict with or violate any provision of the Governing Documents of the Company; (iv) contravene, conflict with, violate, result in a breach of, constitute a default under, result in or permit the termination or amendment of any provision of, or result in or permit the acceleration of the maturity or cancellation of performance of any obligation under, any Contract to which the Company is a party or (v) result in the creation or imposition of any Encumbrance (except the Permitted Encumbrances) upon any of the Purchased Assets or give to any other Person any interests or rights therein, other than any of the foregoing events that would not reasonably be expected to adversely affect (A) the validity or enforceability of this Agreement or any Ancillary Agreement or (B) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements.

 

4.3            Organization .  The Company is a corporation duly organized, validly existing and in good standing under the laws of the State of Delaware, and has all requisite power and authority to carry on its business and to own, lease and/or use its assets and properties.

 

4.4            Title to Assets . The Company has good and valid title to all of the Purchased Assets and, in the case of leased Purchased Assets, to its leasehold interests, free and clear of all Encumbrances, except for the Permitted Encumbrances.

 

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4.5            Litigation .  There is no outstanding Order or Proceeding pending or, to the Knowledge of the Company, threatened, against or affecting the Company except for any such matter that would not reasonably be expected to adversely affect (i) the validity or enforceability of this Agreement or any Ancillary Agreement; or (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements.

 

4.6            Brokers .  The Company has not retained any broker, finder or investment banking firm or any other Person to act on its behalf in connection with the transactions contemplated by this Agreement and, to the Company’s knowledge, no other Person is entitled to receive any brokerage commission, finder’s fee or other similar compensation in connection with the transactions contemplated by this Agreement and the Ancillary Agreements.

 

ARTICLE V
REPRESENTATIONS AND WARRANTIES OF THE PURCHASER

 

The Purchaser hereby represents and warrants to the Company as follows:

 

5.1            Authority; Enforceability .  The execution, delivery and performance by the Purchaser of this Agreement and each Ancillary Agreement to which it is a party, and the consummation by the Purchaser of the transactions contemplated hereby and thereby, have been duly authorized by all necessary action on the part of the Purchaser.  This Agreement has been, and each Ancillary Agreement to which the Purchaser is a party will be, duly and validly executed and delivered by the Purchaser and constitutes, and will constitute, the valid and binding obligation of the Purchaser, enforceable against it in accordance with its respective terms, except (a) as limited by Legal Requirements of general application relating to bankruptcy, insolvency and relief of debtors or (b) as limited by Legal Requirements governing specific performance, injunctive relief or other equitable remedies and by general principles of equity.  The Purchaser has the requisite power and authority to execute and deliver this Agreement and each Ancillary Agreement to which it is a party and to consummate the transactions contemplated hereby and thereby.

 

5.2            Organization .  The Purchaser is a corporation duly organized, validly existing and in good standing under the laws of the State of Delaware, and has all requisite power and authority to carry on its business and to own, lease and/or use its assets and properties.

 

5.3            Consents; Non-Contravention .

 

(a)            Except as set forth on Schedule 5.3 , no consent, approval, authorization, exemption or waiver of, or notice or filing with, any Person is required to be obtained, given or made, as applicable, by the Purchaser in connection with the execution, delivery and performance by the Purchaser of this Agreement or any Ancillary Agreement to which it is a party, or to consummate the transactions contemplated hereby and thereby.

 

(b)            Except as set forth on Schedule 5.3 , the execution, delivery and performance by the Purchaser of this Agreement and each Ancillary Agreement to which it is a party or by which it is bound and the consummation of the transactions contemplated hereby and thereby does not

 

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and will not, with or without the giving of notice or the lapse of time or both, (i) contravene, conflict with or violate any Legal Requirement to which the Purchaser is subject; (ii) contravene, conflict with or violate any Order applicable to the Purchaser; (iii) contravene, conflict with or violate any provision of the Governing Documents of the Purchaser or (iv) contravene, conflict with, violate, result in a breach of, constitute a default under, result in or permit the termination or amendment of any provision of, or result in or permit the acceleration of the maturity or cancellation of performance of any obligation under, any Contract to which the Purchaser is a party, other than any of the foregoing events that would not reasonably be expected to adversely affect (A) the validity or enforceability of this Agreement or any Ancillary Agreement or (B) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements.

 

5.4            Brokers .  The Purchaser has not retained any broker, finder or investment banking firm to act on its behalf in connection with the transactions contemplated by this Agreement and, to the Purchaser’s knowledge, no other Person is entitled to receive any brokerage commission, finder’s fee or other similar compensation in connection with the transactions contemplated by this Agreement.

 

5.5            Litigation .  There is no outstanding Order or Proceeding pending or, to the knowledge of the Purchaser, threatened, against or affecting the Purchaser except for any such matter that would not reasonably be expected to adversely affect (i) the validity or enforceability of this Agreement or any Ancillary Agreement; or (ii) the consummation of the transactions contemplated by this Agreement and the Ancillary Agreements.

 

5.6            Disclaimer of Warranties .  The Purchaser acknowledges that, except as expressly set forth in Article IV of this Agreement, the Company has not made any representations or warranties, express or implied, regarding the Company, the Purchased Assets or the Assumed Liabilities.  The Purchaser further acknowledges that all warranties with regard to merchantability, fitness for a particular purpose, condition or design or arising by statute or otherwise in law are expressly excluded and that, except as otherwise set forth in Article IV hereof, the Purchaser is accepting the Purchased Assets and the Assumed Liabilities on an “as-is where-is, with all faults” basis.

 

ARTICLE VI
COVENANTS OF THE COMPANY

 

6.1            Further Assurances .  At any time or from time to time after the Closing, the Company shall, at the sole cost and expense of the Purchaser, execute and deliver any further instruments or documents and take all such further action as the Purchaser shall reasonably request to evidence the consummation of the transactions contemplated hereby.

 

6.2            Confidentiality .  Unless otherwise consented to by the Purchaser, the Company shall keep strictly confidential, and shall not disclose to any Person, the terms or existence of this Agreement, the Ancillary Agreements or the transactions contemplated hereby or thereby; provided, however, that the Company may disclose such information to the extent required by any Legal Requirement, in which event the Company shall provide the Purchaser with prompt written notice of such requirement, so that the Purchaser may seek an appropriate protective

 

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order or other remedy (as to which the Company shall provide reasonable cooperation) and may disclose such information to the extent required by the third party with whom the Company is engaged in discussions regarding a possible strategic transaction.

 

6.3            Books and Records .  From the Closing Date until the fifth anniversary thereof, the Company shall provide the Purchaser with access to the business records, contracts and other information the Company existing at the Closing Date and relating to the Purchased Assets and the Assumed Liabilities as is reasonably necessary for (a) the preparation for or the prosecution or defense of any Proceeding or investigation; (b) the preparation and filing of any tax return or election relating the Purchased Assets or the Assumed Liabilities and any audit by any taxing authority of any returns of the Purchaser relating thereto and (c) the preparation and filing of any other documents required by any Governmental Authority to be prepared and filed by or on behalf of the Purchaser.  The Purchaser shall reimburse the Company for all reasonable out-of-pocket costs and expenses incurred by the Company in providing such information and in rendering such assistance.  The access to files, books and records contemplated by this Section 6.3 shall be during normal business hours and upon reasonable notice and shall be subject to such reasonable limitations as the party having custody or control thereof may impose to preserve the confidentiality of information contained therein.

 

6.4            Access .  Prior to the Closing, the Company shall provide the Purchaser and advisors and other representatives reasonable access during regular business hours and upon reasonable notice to the Company’s properties, books and records and shall provide to the Purchaser such financial and operating data and other information concerning the Purchased Assets and Assumed Liabilities as the Purchaser shall from time to time reasonably request.

 

6.5            Purchase of Plasmid .  Within 30 Days after the Closing, the Company shall enter into a Supply Agreement on commercially reasonable terms with respect to the supply of Products by the Purchaser to the Company for its internal use (the “Supply Agreement”) with the Purchaser.

 

6.6            Assignments of Assumed Contracts .  The Company shall provide such reasonable assistance as the Purchaser shall request (which in no event shall include performance by the Company of any obligations under such Assumed Contracts) in providing for a smooth transition of the Assigned Contracts that are supply contracts to the Purchaser.

 

ARTICLE VII
COVENANTS OF THE PURCHASER

 

7.1            Further Assurances .  At any time or from time to time after the Closing, the Purchaser shall, at the sole cost and expense of the Company, execute and deliver any further instruments or documents and take all such further action as the Company shall reasonably request to evidence the consummation of the transactions contemplated hereby.

 

7.2            Confidentiality .  Unless otherwise consented to by the Company, the Purchaser shall keep strictly confidential, and shall not disclose to any Person, the terms or existence of this Agreement, the Ancillary Agreements or the transactions contemplated hereby or thereby; provided, however, that the Purchaser may disclose such information to the extent required by

 

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any Legal Requirement, in which event the Purchaser shall provide the Company with prompt written notice of such requirement, so that the Company may seek an appropriate protective order or other remedy (as to which the Purchaser shall provide reasonable cooperation).

 

7.3            Books and Records .  From the Closing Date until the fifth anniversary thereof, the Purchaser shall provide the Company with access to the business records, contracts and other information of the Purchaser existing at the Closing Date and relating to the Purchased Assets and the Assumed Liabilities as is reasonably necessary for (a) the preparation for or the prosecution or defense of any Proceeding or investigation; (b) the preparation and filing of any tax return or election relating the Purchased Assets or the Assumed Liabilities and any audit by any taxing authority of any returns of the Company relating thereto and (c) the preparation and filing of any other documents required by any Governmental Authority to be prepared and filed by or on behalf of the Company.  The Company shall reimburse the Purchaser for all reasonable out-of-pocket costs and expenses incurred by the Purchaser in providing such information and in rendering such assistance.  The access to files, books and records contemplated by this Section 7.3 shall be during normal business hours and upon reasonable notice and shall be subject to such reasonable limitations as the Purchaser may impose to preserve the confidentiality of information contained therein.

 

7.4            Arrangement with Administaff and Other Employee Matters .  The Purchaser shall offer full-time employment to all employees of the Company who are listed on Schedule 7.4 hereto other than those who as of immediately prior to the Closing are no longer employed by the Company (such employees who are offered employment, the “ Employees ”) upon terms (including with respect to compensation, benefits, vacation and recognition of service time and seniority) substantially similar to (or, at the option of the Purchaser, more favorable to) the Employees as those on which the Employees were employed by the Company as of the date hereof.  Employment of the Employees by the Purchaser will be in accordance with the Purchaser’s employment practices and policies and without a commitment to any particular term.  For purposes of this Section 7.4 , “Employees” shall include those individuals performing services for the Company who are co-employed by the Company and Administaff under the Administaff Agreement and for purposes of satisfying its obligations hereunder, the Purchaser may employ such employees in conjunction with Administaff.  For avoidance of doubt, any and all the salaries accrued but not fully paid to the Employees as of the Closing Date shall not be included as the Assumed Liabilities and the Company itself shall have the sole responsibility thereto.

 

7.5            Purchase of Plasmid.  Within 30 Days after the Closing , the Purchaser shall enter into the Supply Agreement with the Company.

 

7.6           Purchase Price.  Except with respect to the Closing Payment (the payment of which is addressed in Section 3.2(a)) , the Purchaser shall make all payments of the Purchase Price, by wire transfer of immediately available funds to an account designated by the company from time to time, as and when the same shall become due, as specified in Section 2.2(a)(i)  hereof.

 

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ARTICLE VIII
CONDITIONS TO THE PURCHASER’S OBLIGATIONS

 

The obligations of the Purchaser to consummate the transactions contemplated hereby at the Closing shall be subject to the satisfaction on or prior to the Closing Date of each of the following conditions:

 

8.1            Representations and Warranties True and Correct .  All of the representations and warranties of the Company contained in this Agreement shall be true and correct in all material respects (i) on and as of the date of this Agreement and (ii) on and as of the Closing Date, as if made on and as of the Closing Date, except in both cases for representations and warranties that contain material adverse effect or other materiality qualifications, which shall be true and correct in all respects.

 

8.2            Covenants and Agreements Performed .  The Company shall have performed or complied with, in all material respects, all covenants and obligations required by this Agreement to be performed or complied with by it prior to or on the Closing Date.

 

8.3            Company Closing Certificate .  The Purchaser shall have been furnished with a certificate executed by the Company (the “ Company Closing Certificate ”), dated the Closing Date, certifying that the conditions set forth in Sections 8.1 and 8.2 with respect to the Company have been fulfilled at or prior to the Closing Date.

 

8.4            No Prohibition .  No Legal Requirement or Order shall be in effect, or Proceeding pending or threatened, that restrains or prevents, or would restrain or prevent, the Purchaser from consummating the transactions contemplated hereby or would adversely affect the conduct of the Business substantially in the manner that the Business was being conducted immediately prior to the Closing.

 

8.5            Consents .  The Company shall have obtained the consents set forth on Schedule 4.2(1) all in forms reasonably acceptable to the Purchaser.

 

8.6            Assignment .  The Company shall have executed an Assignment and Assumption Agreement substantially in the form of Exhibit A hereto (the “ Assignment ”).

 

8.7            Intellectual Property Assignments .  The Company shall have executed the Intellectual Property Assignment substantially in the form of Exhibit B hereto (the “ IP Assignment ”).

 

8.8            Sublease .  The Company shall have executed the Sublease with respect to the Purchaser’s facility at 2700 Research Forest Boulevard, Suite 180a, The Woodlands, Texas 77381 in form and substance satisfactory to the Company and the Purchaser (the “ Sublease ”) within 15 days of signing of this Agreement

 

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ARTICLE IX
CONDITIONS TO THE COMPANY’S OBLIGATIONS

 

The obligations of the Company to consummate the transactions contemplated hereby at the Closing shall be subject to the satisfaction on or prior to the Closing Date of each of the following conditions:

 

9.1            Representations and Warranties True and Correct .  All of the representations and warranties of the Purchaser contained in this Agreement shall be true and correct in all material respects (i) on and as of the date of this Agreement and (ii) on and as of the Closing Date, as if made on and as of the Closing Date, except in both cases for representations and warranties that contain material adverse effect or other materiality qualifications, which shall be true and correct in all respects.

 

9.2            Covenants and Agreements Performed .  The Purchaser shall have performed or complied with, in all material respects, all covenants and agreements required by this Agreement to be performed or complied with by the Purchaser prior to or on the Closing Date.

 

9.3            Purchaser Closing Certificate .  The Company shall have been furnished with a certificate executed by an officer of the Purchaser (the “ Purchaser Closing Certificate ”), dated the Closing Date, certifying that the conditions set forth in Sections 9.1 and 9.2 have been fulfilled at or prior to the Closing Date.

 

9.4            No Prohibition .  No Legal Requirement or Order shall be in effect that restrains or prevents, or would restrain or prevent, the Stockholders or the Company from consummating the transactions contemplated hereby.

 

9.5            Consents .  The Purchaser shall have obtained the consents set forth on Schedule 5.2 in forms reasonably acceptable to the Stockholders and the Company.

 

9.6            Payment of Closing Payment .  The Purchaser shall have delivered the Closing Payment to the Company in the manner set forth in Section 3.2(a) .

 

9.7            Assignment .  The Purchaser shall have executed the Assignment.

 

9.8            Sublease.  The Purchaser shall have executed the Sublease within 15 days of signing of this Asset Purchase Agreeement

 

ARTICLE X
TERMINATION PRIOR TO CLOSING; REORGANIZATION

 

10.1          Termination .  This Agreement may be terminated at any time prior to the Closing:

 

(a)            By the written consent of the Purchaser and the Company;

 

(b)            By either the Purchaser, on the one hand, or the Company and the Stockholders, on the other hand, by written notice given to the other, if the Closing shall not occur on or before [July 31, 2008] (other than through the failure of the party seeking to terminate this Agreement to comply fully with such party’s covenants or obligations under this Agreement); or

 

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(c)                                  By either the Purchaser, on the one hand, or the Company and the Stockholders, on the other hand, by written notice given to the other, if there has been a material breach of any provision of this Agreement by (i) the Company, in the case of notice from the Purchaser or (ii) the Purchaser, in the case of notice from the Company, provided, however, that the Person receiving such notice shall have the opportunity to cure any such breach for seven Business Days after the date the notice is provided before any such termination shall be effective.

 

10.2                           Effect on Obligations .  Termination of this Agreement pursuant to Section 10.1 hereof shall terminate all obligations of the parties hereunder, except for their obligations under Article XI and Article XII hereof and Sections 6.2 and 7.2 hereof.

 

ARTICLE XI

SURVIVAL; INDEMNIFICATION AND OFFSET

 

11.1                           Survival .  The covenants, agreements, representations and warranties contained herein shall survive the Closing until the expiration of the statute of limitations applicable thereto.

 

11.2                           Indemnification .

 

(a)                                  The Company shall indemnify and defend the Purchaser and each of its directors, officers, employees, agents and other Affiliates and their respective successors and assigns (together, the “ Purchaser Indemnitees ”), and shall hold each of them harmless from and against, all Losses that are incurred or suffered by any of them in connection with, arising out of or resulting from:

 

(i)                                      Any misrepresentation or breach of any warranty made by the Company in this Agreement or any Ancillary Agreement; and

 

(ii)                                   Any breach of any covenant or obligation of any of the Company in this Agreement or any Ancillary Agreement to which such Person is a party.

 

(b)                                 The Purchaser shall indemnify the Company and each of its directors, officers, employees, agents and other Affiliates, as applicable (together, the “ Company Indemnitees ”), and shall hold each of them harmless from and against, all Losses that are incurred or suffered by any of them in connection with, arising out of or resulting from:

 

(i)                                      Any misrepresentation or breach of any warranty made by the Purchaser in this Agreement or any Ancillary Agreement;

 

(ii)                                   Any breach of any covenant or obligation of the Purchaser in this Agreement or any Ancillary Agreement; and

 

(iii)                                The Purchased Assets and the Assumed Liabilities.

 

11.3                           Notice of Indemnity Claims .  If any Purchaser Indemnitee or Company Indemnitee entitled to or seeking indemnification hereunder (an “ Indemnified Party ”) (i) determines that any event, occurrence, fact, condition or Claim gives rise, or could reasonably be

 

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expected to give rise to, Losses for which such Indemnified Party is or may be entitled to, or may seek, indemnification under this Agreement; (ii) otherwise identifies an event, occurrence, fact, condition or Claim giving rise, or that could reasonably be expected to give rise, to a right of indemnification hereunder in favor of such Indemnified Party or (iii) with respect to any Third Party Claim, becomes aware of the assertion of any Claim or of the commencement of any Proceeding at law or in equity (any of the foregoing, an “ Indemnity Claim ”), such Indemnified Party shall promptly notify the party obligated to provide indemnification or from whom indemnification is being or will be sought (the “ Indemnifying Party ”) in writing of such Indemnity Claim (a “ Claim Notice ”), describing in reasonable detail the facts giving rise to the claim for indemnification under this Agreement and shall include in such Claim Notice the amount or the method of computation of the amount of such Indemnity Claim (if then known) and a reference to the provision of this Agreement upon which such Indemnity Claim is based; provided, however, that the failure of any Indemnified Party to give timely notice thereof shall not affect any of the Indemnified Party’s rights to indemnification hereunder nor relieve the Indemnifying Party from any of the Indemnified Party’s indemnification obligations hereunder, except to the extent the Indemnifying Party is actually prejudiced by such failure in the Indemnified Party’s defense of the Indemnity Claim.  Any Claim Notice not relating to a Third Party Claim shall specify the nature of the Losses and the estimated amount thereof.

 

11.4                            Third-Party Claims .  Any obligation to provide indemnification hereunder with respect to any Proceeding by or against any Person other than any party hereto, including any Governmental Authority (a “ Third Party Claim ”), shall be subject to the following terms and conditions:

 

(a)                                   Upon receipt of a Claim Notice in respect of any Third Party Claim, the Indemnifying Party shall be entitled, at its option and its sole cost and expense and upon written notice (the “ Defense Notice ”) to the Indemnified Party within 30 days of its receipt of such Claim Notice, to assume and control the defense, compromise, settlement and investigation of such Third Party Claim, and to employ and engage counsel reasonably acceptable to the Indemnified Party; provided, however, that the Indemnified Party may, at its option, participate in such defense, compromise, settlement and investigation at its sole cost and expense; provided, further, however, that if there exists a material conflict of interest between the Indemnified Party, on the one hand, and the Indemnifying Party, on the other hand, or if the Indemnified Party has been advised by counsel that there may be one or more defenses available to it that are different from or additional to those available to the Indemnifying Party, then the Indemnified Party shall be entitled to retain its own counsel at the cost and expense of the Indemnifying Party.

 

(b)                                  If the Indemnifying Party fails to undertake the defense and investigation of any such Third Party Claim as provided in Section 12.5(a) , the Indemnified Party against which such Indemnity Claim has been asserted shall have the right to undertake the defense, compromise, settlement and investigation of such Indemnity Claim on behalf of, and at the reasonable cost and expense of and for the account and risk of, the Indemnifying Party.

 

11.5                            Settlement of Indemnity Claims .  The Indemnifying Party shall not, without the prior written consent of the Indemnified Party settle or compromise any Indemnity Claim or consent to the entry of any final Judgment that does not include as an unconditional term thereof the delivery by the claimant or plaintiff of a written release or releases from all Liability in

 

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respect of such Indemnity Claim of all Indemnified Parties affected by such Indemnity Claim and the sole relief for which are monetary damages that are paid in full by the Indemnifying Party.

 

11.6                            Exclusive Remedy . The indemnification provisions of this Article XI shall be the sole and exclusive remedy of each party hereto for any breach of any representation, warranty or pre-closing covenant and each party hereby waives its right to seek any other remedy therefor.

 

ARTICLE XII

MISCELLANEOUS

 

12.1                            Entire Agreement .  This Agreement together with the Ancillary Agreements and the certificates delivered hereunder constitutes the sole understanding of the parties with respect to the subject matter hereof.

 

12.2                            Successors and Assigns .  The terms and conditions of this Agreement shall inure to the benefit of and be binding upon the respective successors and assigns of the parties hereto; provided however, that this Agreement may not be assigned (either by operation of law or otherwise) (a) by the Company without the prior written consent of the Purchaser or (b) by the Purchaser without the prior written consent of the Company; provided, however, that the Company may assign this Agreement to a successor in connection with a sale of its business.

 

12.3                            Headings .  The headings of the Articles, Sections, and paragraphs of this Agreement are inserted for convenience only and shall not be deemed to constitute part of this Agreement or to affect the construction hereof.

 

12.4                            Amendment; Modification and Waiver .  No amendment, modification, or waiver of the terms of this Agreement shall be binding unless the same shall be in writing and duly executed by all of the parties hereto, except that any terms of this Agreement may be waived in writing at any time by the party that is entitled to the benefits of such waived term.  No single waiver of any term of this Agreement shall be deemed to or shall constitute, absent an express statement otherwise, a continuous waiver of such term or a waiver of any other term hereof.  No delay on the part of any party in exercising any right, power, or privilege hereunder shall operate as a waiver thereof.

 

12.5                            Expenses .  Except as otherwise expressly provided herein, each of the parties hereto shall bear the expenses incurred by that party incident to this Agreement and the transactions contemplated hereby, including all fees and disbursements of counsel and accountants retained by such party, whether or not the transactions contemplated hereby shall be consummated.

 

12.6                            Notices .  Any notice, request, instruction, or other document to be given hereunder by any party hereto to any other party shall be in writing and shall be given by delivery in person, by electronic facsimile transmission, by a nationally recognized overnight courier or by registered or certified mail, postage prepaid (and shall be deemed given when delivered if delivered by hand, when transmission confirmation is received if sent by facsimile, three days after mailing if mailed, one Business Day after deposited for domestic delivery with a nationally recognized overnight courier service if delivered by overnight courier, and three

 

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Business Days after deposited for international delivery with an internationally recognized overnight courier service), as follows:

 

if to the Company, to:

 

VGX Pharmaceuticals, Inc.
450 Sentry Parkway
Blue Bell, PA  19422
Attention:  Joseph Kim
Fax No.:  267-440-4242

 

with a copy to:

 

Duane Morris LLP
30 South 17th Street
Philadelphia, PA  19103
Attention:  Kathleen M. Shay
Fax No.:  215-979-1020

 

if to the Purchaser to:

 

VGXI, Inc.
2700 Research Forest Drive,

The Woodlands, Texas 7738

(Fax): 281.296.7333

 

or at such other address for a party as shall be specified by like notice.

 

12.7                            Governing Law; Consent to Jurisdiction .  This Agreement shall be construed in accordance with and governed by the laws of the Commonwealth of Pennsylvania applicable to agreements made and to be performed wholly within that jurisdiction and without regard to the principles of conflicts of law.  Each party hereto, for itself and its successors and assigns, irrevocably agrees that any Proceeding arising out of or relating to this Agreement shall be instituted in the United States District Court for the Eastern District of Pennsylvania or in the absence of jurisdiction, the state courts of Philadelphia County, Pennsylvania, and generally and unconditionally accepts and irrevocably submits to the exclusive jurisdiction of the aforesaid courts and irrevocably agrees to be bound by any final judgment rendered thereby from which no appeal has been taken or is available in connection with this Agreement.  Each party, for such party and such party’s successors and assigns, irrevocably waives any objection such party may have now or hereafter to the laying of the venue of any such Proceeding, including any objection based on the grounds of forum non conveniens, in the aforesaid courts.  Each of the parties, for such party and such party’s successors and assigns, irrevocably agrees that all process in any such Proceedings in any such court may be effected by mailing a copy thereof by registered or certified mail (or any substantially similar form of mail), postage prepaid, to it at its address set forth in Section 12.6 of this Agreement or at such other address of which the other parties shall have been notified in accordance with the provisions of Section 12.6 of this Agreement such service being hereby acknowledged by the parties to be effective and binding service in every

 

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respect.  Nothing herein shall affect the right to serve process in any other manner permitted by law.

 

12.8                            No Third Party Beneficiaries .  This Agreement is intended and agreed to be solely for the benefit of the parties hereto and their permitted successors and assigns, and no other Person, including any employee of the Company shall be entitled to rely on this Agreement or accrue any Claim pursuant to, under, by, or through this Agreement.

 

12.9                            Counterparts .  This Agreement may be executed in one or more counterparts, each of which shall for all purposes be deemed to be an original and all of which shall constitute the same instrument.

 

12.10                      Drafting of Agreement .  Each party acknowledges that such party has had the opportunity to participate in the drafting of this Agreement and to review this Agreement with legal counsel of its choice, and there shall be no presumption that ambiguities shall be construed or interpreted against the drafter, and no presumptions made or inferences drawn because of the inclusion of a term not contained in a prior draft or the deletion of a term contained in a prior draft.

 

12.11                      Savings Clause .  If any one or more of the terms hereof shall be adjudged, adjudicated, declared or deemed by a Governmental Authority to be invalid, illegal or void or unenforceable in any particular respect, this Agreement shall be construed as if the invalid, illegal, void or unenforceable term or part thereof had never been contained herein, and the remaining portions of this Agreement shall nonetheless continue in full force and effect.  If one or more of the terms, or part thereof, of this Agreement shall, for any reason, be adjudged, adjudicated, declared or deemed by any Governmental Authority to be excessive, then such terms shall be deemed reformed to the maximum limitations permitted by applicable law, and this Agreement shall be construed, by limiting and reducing its terms, so as to be enforceable to the extent compatible with the applicable law.

 

ARTICLE XIII

CERTAIN DEFINITIONS

 

13.1                            Administaff ” means Administaff Companies II, L.P.

 

13.2                            Administaff Agreement ” means that certain Client Services Agreement entered into between Administaff and the Company on March 17, 2003.

 

13.3                            Affiliate ” means, with respect to any Person, any Person directly or indirectly controlling, controlled by or under common control with, such Person.  For the purposes of this definition, “control” (including, with correlative meaning, the terms “controlling,” “controlled by” and “under common control with”) shall mean the possession, directly or indirectly, of the power to direct or cause the direction of management and policies of such Person, whether through the ownership of voting securities, by contract or otherwise.

 

13.4                            Ancillary Agreements ” means (a) the Assignment; (b) the IP Assignment; and (c) any other document specifically identified therein as an Ancillary Agreement.

 

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13.5                            Business Day ” means any day other than a day on which banks in Philadelphia, Pennsylvania are required or authorized to be closed.

 

13.6                            Claim ” means any claim, suit, demand, cause of action, chose in action, right of recovery or right of set-off of whatever kind or description asserted by the claimant against any Person.

 

13.7                            Code ” means the Internal Revenue Code of 1986, as amended.

 

13.8                            Contract ” means any agreement, purchase order, sales order, contract or similar instrument, arrangement or commitment.

 

13.9                            Encumbrances ” means liens, security interests, pledges, equities, proxies, claims, charges, adverse claims, mortgages, rights of first refusal, preemptive rights, restrictions, encumbrances, easements, covenants, licenses, options or title defects of any kind whatsoever.

 

13.10                      Governing Documents ” means, with respect to the Company or the Purchaser, the articles or certificate of incorporation and the bylaws of the applicable corporation; (b) all Security holders’ Contracts, voting Contracts, voting trust Contracts, joint venture Contracts, registration rights Contracts or other Contracts or documents relating to the organization, management or operation of such corporation or relating to the rights, duties and obligations of the Security holders of any such corporation and (c) any amendment or supplement to any of the foregoing.

 

13.11                      Governmental Authority ” means any government, court, department, authority, commission, board, bureau, agency or official or other regulatory, administrative authority, whether (in each case) federal, foreign, state or local.

 

13.12                      Governmental Authorization ” means any permit, license or other authorization given or otherwise made available by or under the authority of any Governmental Authority or pursuant to any Legal Requirement and required to:  (a) conduct the Business as currently conducted or (b) occupy, maintain, operate or use the Company’s assets or properties as currently maintained, operated or used.

 

13.13                      IRS ” means the Internal Revenue Service.

 

13.14                      Legal Requirement ” means any federal, state, local, municipal, foreign, international, multinational or other constitution, law, ordinance, principle of common law, code, regulation, statute or treaty.

 

13.15                      Losses ” means any and all losses, Liabilities, damages (including incidental and consequential damages), penalties, obligations, awards, fines, deficiencies, interest, Claims, diminution in value, costs and expenses whatsoever (excluding attorneys’, consultants’ and other professional fees and disbursements) resulting from, arising out of or incident to any matter for which indemnification is provided under this Agreement.

 

13.16                      Liabilities ” means with respect to any Person, means any liability or obligation of such Person of any kind, character or description, whether known or unknown, absolute or

 

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contingent, accrued or unaccrued, disputed or undisputed, liquidated or unliquidated, secured or unsecured, joint or several, due or to become due, vested or unvested, executory, determined, determinable or otherwise, and whether or not the same is required to be accrued on the financial statements of such Person.

 

13.17                      Order ” means any award, decision, injunction, judgment, order, ruling, subpoena or verdict entered, issued, made or rendered by any Governmental Authority or any arbitrator.

 

13.18                      Permitted Encumbrances ” means minor imperfections of title, none of which, individually or in the aggregate, detract from the value of the affected assets or properties, or impairs the use of the affected assets or properties or Liens for taxes that are not yet due or payable , .

 

13.19                      Person ” means an individual, corporation, partnership, association, limited liability company, trust, unincorporated organization, Governmental Authority, other entity or group.  For purposes of this definition, “group” means when two or more persons act as a partnership, limited partnership, syndicate, or other group for the purpose of acquiring, holding, or disposing of securities of an issuer.

 

13.20                      Proceeding ” means any action, arbitration, audit, hearing, investigation, litigation or suit commenced, brought, conducted or heard by or before, or otherwise involving, any Governmental Authority or arbitrator.

 

[SIGNATURE PAGE FOLLOWS]

 

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IN WITNESS WHEREOF , each of the parties hereto has caused this Agreement to be executed on its behalf as of the date first above written.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

By:

/s/

Niranjan Y. Sardesai

 

 

 

Niranjan Y. Sardesai

 

Title:

Senior VP, Research & Development

 

 

 

 

 

 

 

VGXI, INC.

 

 

 

By:

/s/

Byong Jin Kim

 

 

 

Byong Jin Kim

 

Title:

CEO

 



 

EXHIBIT A

 

ASSIGNMENT AND ASSUMPTION AGREEMENT

 

THIS ASSIGNMENT AND ASSUMPTION AGREEMENT (this “Assignment”), dated as of June 10, 2008 , between VGXI, Inc., a Delaware corporation (the “Assignee”), and VGX Pharmaceuticals, Inc., a Delaware corporation (the “Assignor”).

 

Background :

 

WHEREAS , the Assignor and the Assignee, have entered into an Asset Purchase Agreement dated as of June 10, 2008 (the “Agreement”);

 

WHEREAS , pursuant to the Agreement, the Assignor has agreed to sell, assign, convey, transfer and deliver the Purchased Assets to the Assignee;

 

WHEREAS , pursuant to the Agreement, the Assignee has agreed to assume the Assumed Liabilities; and

 

WHEREAS , capitalized terms used but not otherwise defined herein shall have the meanings ascribed to them in the Agreement.

 

NOW, THEREFORE , in consideration of the foregoing and the respective representations, warranties, covenants and agreements set forth herein, and intending to be legally bound hereby, the parties hereto agree as follows:

 

1.                                        Assignment of Purchased Assets .  The Assignor, for good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, and intending to be legally bound, hereby sells, transfers, conveys and delivers to the Assignee, and the Assignee does hereby accept from the Assignor, all of the right, title and interest of the Assignor in and to all of the Purchased Assets free and clear of all Encumbrances, other than the Permitted Encumbrances.

 

2.                                        Assumption of Liabilities .  The Assignee hereby assumes and agrees to pay, perform and discharge the Assumed Liabilities.

 

3.                                        Modification and Waiver .  No amendment, modification, or alteration of the terms or provisions of this Assignment shall be binding unless the same shall be in writing and duly executed by the parties hereto, except that any of the terms or provisions of this Assignment may be waived in writing at any time by the party that is entitled to the benefits of such waived terms or provisions.  No single waiver of any of the provisions of this Assignment shall be deemed to or shall constitute, absent an express statement otherwise, a continuous waiver of such provision or a waiver of any other provision hereof (whether or not similar).  No delay on the part of any party in exercising any right, power, or privilege hereunder shall operate as a waiver thereof.

 

4.                                        Governing Law .  This Agreement shall be construed in accordance with and governed by the laws of the Commonwealth of Pennsylvania applicable to agreements made and to be performed wholly within that jurisdiction.

 



 

5.                                        Disputes .  The respective rights of the Assignor, on the one hand, and the Assignee, on the other, with respect to the Purchased Assets and the Assumed Liabilities assigned and assumed hereby shall be governed by the Agreement.  In the event of a conflict between this Assignment and the Agreement, the Agreement shall control.  All disputes between the Assignor and the Assignee arising out of the obligations of the parties under this Assignment or concerning the meaning or interpretation of any provisions contained herein shall be resolved in accordance with the Agreement.

 

6.                                        Counterparts .  This Assignment may be executed in one or more counterparts, each of which shall for all purposes be deemed to be an original and all of which shall constitute the same instrument.

 



 

IN WITNESS WHEREOF , the parties hereto have duly executed this Assignment as of the date first written above.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

/s/

Niranjan Y. Sardesai

 

 

 

Niranjan Y. Sardesai

 

Title:

Senior VP, Research & Development

 

 

 

 

 

 

 

VGXI, INC.

 

 

 

By:

/s/

Byong Jin Kim

 

 

 

Byong Jin Kim

 

Title:

CEO

 




EXHIBIT 10.49

 

SUBLEASE

 

THIS SUBLEASE , dated June 10, 2008, with an effective date of June 1, 2008 (the “Effective Date”) is by and between VGX PHARMACEUTICALS, INC. , a Delaware corporation “Sublandlord”, and VGXI, INC., a Delaware corporation, hereinafter referred to as “Subtenant”.

 

W I T N E SS E T H:

 

WHEREAS, Sublandlord is a tenant of, and leases from Creekstone Woodlands, LLC; Creekstone Woodlands 1, LLC; Creekstone Woodlands 2, LLC; Creekstone Woodlands 5, LLC; and Creekstone Woodlands 6, LLC (collectively “Prime Landlord”), the following described premises: (the “Premises”) approximately 13,185 net rentable square feet of floor space in a building known and referred to as Venture Technology Center XI Building, located at 2700 Research Forest Drive, Suite 180, The Woodlands, Texas 77380 as further described in the attached Exhibit “A” (the “Prime Lease”);

 

WHEREAS, Subtenant desires to sublease from Sublandlord and Sublandlord desires to sublease to Subtenant approximately 11,537 net rentable square feet of the Premises as more specifically set forth on Exhibit “B” attached hereto and made a part hereof (the “Sublease Premises”);

 

WHEREAS, capitalized terms not otherwise defined herein shall have the meaning ascribed to them in the Prime Lease;

 

NOW, THEREFORE, for good and valuable consideration, the Sublandlord and Subtenant hereby covenant and agree with each other as follows:

 

1. - INCORPORATION OF WHEREAS CLAUSES:  The “Whereas” clauses set forth above are hereby incorporated into and made part of this Sublease.

 

2. - INCORPORATION OF PRIME LEASE:   Except as modified by this Sublease, the Prime Lease is incorporated herein by reference and this Sublease is expressly made subject to all the terms and conditions of the Prime Lease.  Any conflict between this Sublease and the Prime Lease shall be governed by this Sublease.  Except as otherwise provided herein, Subtenant expressly assumes all obligations under the Prime Lease arising from and after the Sublease Commencement Date and the Subtenant agrees to use the Sublease Premises in

 

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accordance with the terms of the Prime Lease and not do or omit to do anything which will breach any of the terms thereof.  Except as specifically provided herein, nothing in this Sublease shall be construed to create a privity of estate or contract between Subtenant and the Prime Landlord. This Sublease shall be expressly subject and subordinate to all of the terms, covenants and conditions contained in the Prime Lease, except: (a) any and all referenced to and any obligation on the part of Prime Landlord and/or Sublandlord to perform tenant work, construction and/or improvements in respect of the Sublease Premises, except that this Sublease shall be expressly subject to Paragraph 6 of the First Amendment to Lease Agreement and the Exhibits referenced therein, regarding the Approved Alterations, as that term is defined in the First Amendment to Lease Agreement, and the cost of the Approved Alterations and the benefits of the Allowance and Required Payment, as those terms are defined in the First Amendment to Lease Agreement, shall be shared equally by Sublandlord and Subtenant; and (b) all references to any right(s) to surrender any portion of the Sublease Premises.  If Prime Landlord under the Prime Lease fails to perform its obligations, Subtenant shall notify Sublandlord in writing.  In such event Sublandlord shall use commercially reasonable efforts to cause said Prime Landlord to perform its obligations, but Sublandlord shall not be obligated to incur any cost (unless Subtenant agrees to reimburse Sublandlord for such cost) or liability therefore, nor shall Sublandlord be responsible or liable for any such failure of the Prime Landlord. Except as otherwise provided in this Sublease, Subtenant expressly assumes the Sublandlord’s obligations arising under the Prime Lease from and after the Sublease Commencement Date.  In the event of a conflicting termination date in this Sublease, the termination date in the Prime Lease shall govern.

 

3. - TERM AND SCHEDULE OF BASE RENT:  Sublandlord hereby subleases to the Subtenant the Sublease Premises for a term commencing on the Effective Date (the “Sublease Commencement Date”), and expiring on the date the Prime Lease expires or is terminated pursuant to the terms of the Prime Lease (the “Sublease Term”), at the monthly rent (“Base Rent”) pursuant to the following schedule:

 

(a)                                    June 1, 2008 through October 31, 2008:  $17,786.02 per month; and

 

(b)                                  November 1, 2008 through October 31, 2009:  $18,026.37 per month; and

 

(c)                                   November 1, 2009 through October 31, 2010:  $18,266.72 per month; and

 

(d)                                  November 1, 2010 through October 31, 2011:  $18,507.07 per month; and

 

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(e)                                   November 1, 2011 through October 31, 2012:  $18,747.43 per month; and

 

(f)                                     November 1, 2012 through October 31, 2013:  $18,987.77 per month; and

 

(g)                                  November 1, 2013 through October 31, 2014:  $19,288.13 per month; and

 

(h)                                  November 1, 2014 through October 31, 2015:  $19,468.48 per month; and

 

(i)                                      November 1, 2015 through October 31, 2016:  $19,708.83 per month; and

 

(j)                                      November 1, 2016 through October 31, 2017:  $19 , 949.18 per month.

 

4. - PAYMENT OF BASE RENT: The Base Rent is payable in advance without any offsets, or deductions, on the first business day of each and every month during the Sublease Term. Notwithstanding the foregoing, Subtenant shall pay to Sublandlord Base Rent for the first full month of the Sublease Term in the amount of Seventeen Thousand Seven Hundred Eighty Six and 02/100 dollars ($17,786.02) upon Subtenant’s execution of this Sublease.  Subtenant shall pay the Base Rent to Sublandlord at VGX Pharmaceuticals, 450 Sentry Parkway, Blue Bell, PA 19422 Attention: Gene Kim .  If the Subtenant fails to pay the Base Rent within 5 business days after it is due, the Subtenant shall also pay a late charge equal to 5% of the unpaid Base Rent, plus interest at 2% per month or the maximum allowable by law, whichever is less, on the remaining unpaid balance, retroactive to the date originally due until paid.  These charges are not penalties but are designed to reasonably compensate Sublandlord for its administrative, processing and accounting costs.

 

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5. - ADDITIONAL RENT:  Subtenant shall be responsible for and pay to Sublandlord, payable in advance without any offsets, or deductions, on the first business day of each and every month during the Sublease Term, its pro rata share of the Additional Rent, including, without limitation, Operating Expenses and Utilities, as set forth under the Prime Lease.  Subtenant’s pro rata share of Additional Rent is 87.5% of the Additional Rent owed under the Prime Lease.  If Sublandlord shall make any expenditure for which Subtenant is responsible, or if Subtenant shall fail to make any payment which Subtenant is obliged to make hereunder, then the amount thereof may, at Sublandlord’s option, be added to any installment of Base Rent then due or thereafter becoming due as Additional Rent, and such amounts shall be subject to the appropriate charges as set forth in this Sublease.

 

6. - USE OF SUBLEASE PREMISES:   Subtenant shall use the Sublease Premises solely for the intended use as per Section 3 of the First Amendment to Lease.

 

7. - COMPLIANCE WITH LAWS, ORDINANCES, AND ENVIRONMENTAL: Subtenant shall fully comply with all laws, ordinances, requirements, and regulations of the federal, state, county, municipal, and other authorities, regulations, codes (including all building codes, zoning codes, fire, health, air quality, police or sanitary codes) and any other government requirement, including ADA and OSHA requirements, environmental requirements and underwriter requirements, as well as any private restrictions or covenants recorded against the property, which directly or indirectly impose a duty upon Sublandlord with respect to the use, occupancy, alteration or condition of the Sublease Premises.  In the event of a violation of any environmental law by Subtenant, Subtenant represents, covenants and warrants that it will indemnify and hold Sublandlord harmless from any claim under the Prime Lease, at law or in equity to which Sublandlord may be subjected.

 

8. - VIEWING SUBLEASE PREMISES:   Subtenant shall use the Sublease Premises exclusively for the purpose set forth herein. However, in the event Subtenant does not execute a direct lease with Landlord prior to or during the last three (3) months of this Sublease, or any extension thereof, Subtenant shall permit the Landlord to display the usual “To Let” signs and to show the Sublease Premises to prospective tenants.  Subtenant further agrees that at a reasonable time after reasonable notice to Subtenant during the Sublease Term Sublandlord, Prime Landlord, or their agents, may enter the Sublease Premises for the purpose of examining the condition thereof, or to make repairs in any part of the Building, but in making such reservation, Sublandlord does not assume any liability for the care or supervision of the Sublease Premises or appurtenances.

 

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9. - ALTERATIONS AND ASSIGNMENT:   Subtenant will not make or permit to be made any alterations or additions to said Sublease Premises, nor assign, mortgage, or pledge this Sublease, nor sublet the whole or any part of the Sublease Premises without Sublandlord’s written consent, subject to any limitations contained in the Prime Lease, and such consent shall not be unreasonably withheld, conditioned, or delayed.  Any consent by Sublandlord shall apply solely to the particular transaction consented to and shall not constitute a waiver by Sublandlord of any other provision of this Sublease.

 

10. - INSURANCE:   Subtenant will not by any act of commission or omission cause an increase in the rate of insurance or the cancellation of any insurance policy.  In the event of any increase in the rate of insurance caused by Subtenant’s occupancy, Subtenant agrees to pay on demand the amount of any such increase, and in default of such payment, such amount may be added to the next installment of Base Rent as Additional Rent. Subtenant shall, at its sole cost and expense, obtain and maintain during the Sublease Term, Commercial General Liability Insurance, including Contractual Liability coverage, with limits of not less than One Million Dollars ($1,000,000).  All insurers must be licensed to do business in Texas and must by rated “A-” or higher under the most current edition of A.M. Best’s Key Rating Guide, a Lloyds of London underwriter, or an insurance company  agreed to by the Prime Landlord. Subtenant shall deliver to Sublandlord prior to taking possession a certificate evidencing such coverage.  Such insurance policies shall provide for no cancellation or material alteration without thirty (30) days prior written notice to Sublandlord. Sublandlord and Subtenant shall cause each insurance policy carried by it and insuring the Sublease Premises and its fixtures and contents against loss by fire and causes covered by standard extended coverage to be written in a manner so as to provide that the insurance company waives all right of recovery by way of subrogation against the other in connection with any loss or damage covered by any such policies.  Neither party shall be liable to the other for, and each party hereby waives and releases the other party from any claims and liability for, any loss or damage caused by fire or any of the risks enumerated in standard extended coverage insurance, provided such insurance was obtainable at the time of such loss or damage, regardless of whether such insurance was actually maintained by either party, AND EVEN IF THE LOSS OR DAMAGE WAS CAUSED BY THE NEGLIGENCE OF THE OTHER PARTY . Each party shall provide a certificate evidencing such coverage, upon request, and provide for no cancellation or material alteration without 30 days written notice to the insured and additional insured(s).

 

11. - SIGNS: Subtenant shall not install any awnings, advertisements, or signs on any part of the Sublease Premises without Sublandlord’s written consent, subject to any limitations contained in the Prime Lease.

 

12. - INDEMNIFICATION:   Sublandlord shall not be responsible for any defect or change of condition in said Sublease Premises, nor for any damage thereto, nor to any person, nor to

 

5



 

goods or things contained therein due to any cause whatsoever except for the negligence or willful misconduct of the Sublandlord, and subject to the waiver of claims and liability set forth in Section 10 above, Subtenant will indemnify Sublandlord from and against any claims, demands, and actions arising in connection with Subtenant’s use of the Sublease Premises, or the use by any person occupying said Sublease Premises during the Sublease Term, or by reason of any breach or non-performance of any covenant herein by Subtenant, or the violation of any law or regulation by Subtenant.  Subtenant’s obligation to indemnify Sublandlord shall apply to actions and claims for damages or liability only to the extent that such actions or claims arise out of the use and occupancy of the Sublease Premises by Subtenant.

 

Sublandlord shall defend, indemnify and hold Subtenant harmless from and against any and all claims and/or demands for liability, losses, damages and/or costs and expenses, including, without limitation, penalties, fines and reasonable attorneys’ fees and costs (“Claims”) to the extent that such Claims result from or arise out of (a) Sublandlord’s negligence or failure to perform any of its obligations under this Sublease or the Prime Lease; (b) breach or default in the performance of any obligation to be performed by Sublandlord under the terms of this Sublease or the Prime Lease; or (c) any act or omission of Sublandlord or of its agents or employees; provided that the provisions of this paragraph shall not apply to any Claims to the extent arising from or in connection with any negligent or intentional conduct of the Subtenant or of any of its related parties or agents.

 

13. - FIRE AND CASUALTY:   If the Sublease Premises shall be so damaged by fire, other casualty, or act of the public enemy so as to be substantially destroyed, then this Sublease shall terminate and any unearned Base Rent or Additional Rent paid in advance by Subtenant shall be apportioned and refunded to it, but in case the Sublease Premises are not substantially destroyed, Sublandlord will endeavor to have the Prime Landlord restore the Sublease Premises and a just proportion of the Base Rent and Additional Rent shall abate according to the extent to which Sublease Premises have been rendered untenantable until the Sublease Premises have been restored.  The Subtenant agrees to give the Sublandlord immediate notice of any damage to the Sublease Premises.

 

14. - DEFAULT:   In the event Subtenant fails to perform or observe any of the covenants contained herein on its part to be observed and performed for ten (10) days after written notice by Sublandlord to Subtenant (provided, however, if such failure cannot reasonably be cured within ten (10) days, then such failure shall not be a default provided that Subtenant commences to cure the failure within said ten (10) day period and thereafter diligently and in good faith continues to cure the failure), (a) Sublandlord may forthwith terminate or cancel this Sublease by notifying Subtenant as hereinafter provided, and upon such

 

6



 

termination or cancellation, Subtenant shall be liable to Sublandlord for the actual damages Sublandlord sustains by reason of Subtenant’s breach of covenant and of such termination or cancellation, but in no event shall actual damages exceed the net present value of the difference between the Base Rent provided for herein and the fair market sublease rental value of the Sublease Premises for the remainder of the Sublease Term; or (b) Sublandlord may forthwith re-enter the Sublease Premises without notice and upon re-entry may let the Sublease Premises or any part thereof as agent for Subtenant and receive the rent therefor, applying the same first to the payment of such expense as Sublandlord may be out of pocket by way of entering and letting the Sublease Premises and then to the payment of the Base Rent and the fulfillment of Subtenant’s covenants hereunder; and Subtenant agrees to pay and shall be liable for amounts equal to the several installments of rent as they would, under the terms of this Sublease, become due if no default had occurred, whether the Sublease Premises be re-let or remain vacant in whole or in part for a period less than the remainder of the Sublease Term, or for the whole thereof, but Subtenant shall be entitled to be credited at the end of each month with any net amounts actually received by Sublandlord during such months for the use or occupancy of the Sublease Premises or any part thereof; provided, however, that all sums paid and liabilities incurred by Sublandlord for any of the purposes aforesaid (which Subtenant also agrees to pay and shall be liable for) shall have been first paid in full to Sublandlord, either directly by Subtenant or out of moneys actually received for renting said Sublease Premises after Sublandlord shall have received undisputed possession thereof, and the maintenance of any action or proceeding to recover possession of the Sublease Premises or any installment or installments of Base Rent, Additional Rent or any other moneys that may be due or become due from Subtenant to Sublandlord shall not preclude Sublandlord from thereafter instituting and maintaining subsequent actions or proceedings for the recovery of possession of the Sublease Premises or of any subsequent payment or payments of Base Rent, Additional Rent or any other moneys that may be due or become due from Subtenant to Sublandlord. A waiver by Sublandlord of any breach or breaches by Subtenant of any one or more of the covenants or conditions hereof shall not bar forfeiture or waive any other rights or remedies of Sublandlord for any subsequent breach of any such or other covenants and conditions. All notices to quit or vacate being hereby expressly waived, any law, usage or custom to the contrary notwithstanding.

 

15. - CONDEMNATION: In the event the Sublease Premises or any part thereof are taken or condemned for a temporary or permanent public or quasi-public use, Sublandlord may, at its option, terminate this Sublease and in such event any unearned Base Rent or Additional Rent paid in advance shall be returned to Subtenant.

 

16. - NOTICES:   All notices to be given hereunder by either party shall be in writing and shall be sent by registered mail addressed to the party intended to be notified at the address

 

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set forth herein or as may be from time to time designated in writing to the other party and giving such notice shall be a sufficient service thereof. Any such notice shall be sent to the Sublandlord addressed as VGX Pharmaceuticals Inc., 2700 Research Forest Dr., Suite 180, The Woodlands, Texas 77381, Attn: Gene Kim; and to the Subtenant addressed as VGXI, Inc., 2700 Research Forest Dr., Suite 180, The Woodlands, Texas 77381, Attn: Henry Hebel .  Sublandlord and Subtenant each reserve the right to designate additional persons to whom required copies of notices shall be sent.

 

17. - TERMINATION:   If at any time proceedings in bankruptcy, or pursuant to any other act for the relief of debtors, shall be instituted by or against Subtenant, or if Subtenant shall assign over Subtenant’s estate or effects for payment thereof, or if any execution shall issue against Subtenant or any of Subtenant’s effects whatsoever, or if a receiver or trustee shall be appointed of Subtenant’s property, or if this Sublease shall by operation of law, devolve upon or pass to any person or persons other than Subtenant, then and in each of said cases, Sublandlord may terminate this Sublease forthwith by notifying Subtenant as herein provided.  Upon such termination all sums due and payable or to become due and payable by Subtenant shall at once become due and payable.

 

18. - QUIET POSSESSION:   Sublandlord hereby covenants that Subtenant, upon paying the Base Rent and Additional Rent and performing all the covenants and agreements agreed to herein, may quietly enjoy the Sublease Premises, except as herein otherwise provided, subject, however, to the terms of the Sublease, and to the terms of any mortgages which may now or hereafter affect the Sublease Premises.

 

19. - WAIVER OF SUBROGATION:   Sublandlord and Subtenant waive all rights, each against the other, for damages caused by fire or other perils where such damages are sustained in connection with the occupancy of the Sublease Premises.

 

20. - HOLDOVER:   Should Subtenant continue to hold the Sublease Premises after the Sublease term expires, Subtenant shall be responsible for any damages suffered by Sublandlord under the Prime Lease and any and all actual damages incurred by Sublandlord.  This provision shall not be construed, however, as permission by Sublandlord for Subtenant to holdover.

 

21 - SUBLEASE CONDITIONED ON CONSENT:   This Sublease is subject to, and conditioned upon, Sublandlord’s obtaining the written consent of the Prime Landlord under the Prime Lease if such consent is required by the Prime Lease.  In the event that such consent is not obtained within fifteen (15) days after the date of this Sublease, Subtenant shall have the right to terminate this Sublease by giving written notice thereof to Sublandlord.  If Prime Landlord’s consent to this Sublease is not required under the terms of

 

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the Prime Lease, then the Parties agree to provide Prime Landlord with written notice, in accordance with the notice provisions of the Prime Lease , within a period of thirty (30) days following the date of execution of this Sublease accompanied by a copy of this Sublease and any other documents necessary to complete this Sublease.

 

22. – OTHER:   This Sublease is subject to the following provisions:

 

(A)                             Subtenant shall not be obligated to perform any obligations of Sublandlord under the Prime Lease that pertain to areas of the Building or the Premises other than the Sublease Premises.  Subtenant is not to be obligated to make any improvements or alterations to the Sublease Premises or the Building systems located therein in order to comply with applicable laws or otherwise.

 

(B)                               Subtenant shall have no obligation to cure a default under the Prime Lease caused by the acts or omissions of Sublandlord, its agents, contractors, employees or invitees.

 

(C)                               Subtenant shall not be required to pay any Base Rent, Additional Rent or other rent owed by Sublandlord under the Prime Lease to Prime Landlord.  Sublandlord shall pay all such Base Rent, Additional Rent and other rent as and when the same are due and payable under the Prime Lease.

 

(D)                              Subtenant shall not be responsible for the acts and omissions of Sublandlord, its agents, employees, contractors or invitees nor required to perform Sublandlord’s obligations under the Prime Lease as a result of such acts or omissions.  Sublandlord shall indemnify and hold Subtenant harmless from any claims, liabilities, obligations, losses, costs, or expenses arising out of, the acts or omissions of Sublandlord, its agent, employees, contractors, licensees or invitees.

 

(E)                                Subtenant shall not be required to maintain Sublandlord’s insurance under the Lease (which Sublandlord shall continue to maintain as required thereunder) but shall maintain the types and amounts of insurance in its name as required of Sublandlord under the Lease naming Landlord and Sublandlord as additional insureds.

 

(F)                                Subtenant shall not be responsible for any representations made by Sublandlord, its agents or employees under the Prime Lease.

 

(G)                               Subtenant shall not be required to remove any alterations, additions or improvements existing in the Sublease Premises as of the Sublease Commencement Date that Sublandlord is required to remove under the Prime Lease, including, without limitation, the Approved Alterations.

 

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(H)                                Any occupancy of the Sublease Premises by Subtenant prior to the Sublease Commencement Date shall be subject to all terms and conditions of this Sublease; however, no Base Rent or Additional Rent shall be payable with respect to such early occupancy.

 

(I)                                     Sublandlord shall use reasonable efforts to obtain an agreement from Landlord that the waiver and release of claims set forth in Section 26 of the Prime Lease shall inure to the benefit of Subtenant, its officer, employees and agents.

 

(J)                                    Sublandlord represents and warrants that (1) the copy of the Prime Lease and any amendments thereto attached hereto as Exhibit “A” is a true and complete copy of the Prime Lease and such amendments and the Prime Lease have not been amended, modified or supplemented except as reflected on Exhibit “A”, and (2) neither Prime Landlord nor Sublandlord is in default under the Prime Lease, and no condition or circumstance exists which, with notice or the passage of time, would be a default by either Prime Landlord or Sublandlord under the Prime Lease.

 

(K)                                Sublandlord shall not modify or amend the Prime Lease in any manner that would (1) adversely affect Subtenant’s rights under this Sublease in any way other than a de minimis manner or (2) increase Subtenant’s obligations under this Sublease.  Sublandlord shall not terminate the Prime Lease unless Sublandlord provides Subtenant with an executed non-disturbance and recognition agreement from Landlord that permits Subtenant to continue in occupancy of the Sublease Premises on the terms and conditions of this Sublease for the remainder of the Sublease Term following any such termination (assuming the Sublease had not terminated).  If for any reason the term of the Prime Lease shall terminate prior to October 31, 2017 as a result of the voluntary termination thereof by Sublandlord or any default by Sublandlord under the Prime Lease, then Sublandlord shall be liable to Subtenant for, and Sublandlord shall indemnify Subtenant from and against, all damages resulting therefrom, provided that such termination was not a result of a default under the Prime Lease caused by a default by Subtenant hereunder.

 

(L)                                  Notwithstanding anything to the contrary contained in this Sublease, in no event shall Sublandlord or Subtenant be liable for any claim for special, indirect, consequential, exemplary, punitive or incidental damages, including without limitation, any claims for loss of profits and/or loss of business opportunity, each party to this Sublease knowingly and voluntarily waiving and releasing any such claims other than for actual damages.

 

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(M)                             If, as a result of this Sublease, Subtenant or the Sublease Property is subject to any new requirements under applicable law (including the Americans with Disabilities Act of 1990), then Sublandlord and Subtenant shall share equally the costs or expenses to comply with such requirements.  Similarly, Sublandlord and Subtenant shall share equally in the maintenance costs and repair costs related to the HVAC system for the Sublease Premises after the Prime Landlord’s one-year warranty expires on October 31, 2008 in accordance with Paragraph 7 of the First Amendment to Lease Agreement.

 

(N)                                Subject to the approval and consent of the Prime Landlord, the following provisions of the First Amendment to Lease Agreement are expressly made part of this Sublease and shall inure to the benefit of Sublandlord and Subtenant: (1) The Renewal Option contained in Paragraph 12 and Exhibit “C”; (2) the Preferential Lease Right contained in Paragraph 13 and Exhibit “D”; and (3) the Early Termination Right contained in Paragraph 14 and Exhibit “E.”

 

21. - BROKERS: Subtenant and Sublandlord each hereby represents to the other that it has not been represented by, has not engaged, and has not involved in this transaction any broker, agent or other commissionable party in connection with or relating to the transaction described in this Sublease, except Palermo REI, LP d/b/a PalermoBarr Commercial Real Estate Advisors (“Sublandlord’s Broker”), for which Subtenant is solely responsible.  Subtenant and Sublandlord each agree to indemnify, defend and hold harmless the other party from and against any and all claims, suits, actions, proceedings, judgments, liabilities, losses, expenses and costs, including without limitation, costs of court, litigation expense, and reasonable attorney’s fees, resulting from or arising out of any breach of its foregoing representation, or by any claim by any broker asserting a claim contrary to its above representation (or, in the case of the indemnity by Subtenant, any claims by the broker it has engaged, if any), and any claim by Sublandlord’s Broker for any commission.

 

Remainder of page left intentionally blank.

 

11



 

The covenants and agreements contained in the foregoing Sublease are binding upon the parties hereto and their respective executors, administrators, successors, legal representatives and assigns.

 

IN WITNESS WHEREOF, the parties have executed this Sublease as of the date first written above.

 

 

 

SUBLANDLORD:

 

 

 

VGX PHARMACEUTICALS, INC., a Delaware
corporation

 

 

 

 

 

By:

 

/s/Gene Kim

 

 

 

Name:

 

Gene Kim

 

 

 

Title:

 

CFO

 

 

 

 

 

SUBTENANT:

 

 

 

VGXI, Inc., a Delaware corporation

 

 

 

By:

 

/s/Henry Hebel

 

 

 

Name:

 

Henry Hebel

 

 

 

Title:

 

V.P. Operations

 

12



 

Exhibit “A”

 

(the “Prime Lease”)

 

Lease dated August 20, 2001 by and between Woodlands VTO 2000 Land, L.P., predecessor in interest to Prime Landlord, and Applied Veterinary Systems, Inc., predecessor in interest to Sublandlord and modified by First Amendment to Lease Agreement, dated November 12, 2007 by and between the Prime Landlord and Sublandlord.  Copies of the Prime Lease, as amended by the First Amendment to Lease Agreement are attached hereto.

 

13



 

Exhibit “B”

 

(the “Sublease Premises”)

 

14




EXHIBIT 10.50

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

UNIVERSITY of PENNSYLVANIA

 

Patent License Agreement

 

This Patent License Agreement (this “ Agreement ”) is between The Trustees of the University of Pennsylvania, a Pennsylvania nonprofit corporation (“ Penn ”), and VGX Pharmaceuticals, Inc (“VGX”) , a corporation organized and existing under the laws of the State of Delaware.  This Agreement will become effective on the date on which Penn and VGX have fully executed the Agreement, (the “ Effective Date” ).

 

BACKGROUND

 

Penn owns certain intellectual property developed by Dr. David B. Weiner (“Dr. Weiner”) of Penn’s School of Medicine relating to therapeutic and prophylactic applications of viral constructs.  Penn also owns certain letters patent and/or applications for letters patent relating to the intellectual property.  VGX desires to obtain an exclusive license under the patent rights to exploit the intellectual property.  VGX also desires to fund further research by Dr. Weiner under a separate agreement.  Penn has determined that the exploitation of the intellectual property by VGX is in the best interest of Penn and is consistent with its educational and research missions and goals.

 

In consideration of the mutual obligations contained in this Agreement, and intending to be legally bound, the parties agree as follows:

 

1                                          LICENSE

 

1.1                                  License Grant .  Penn grants to VGX an exclusive, world-wide license (the “ License ”) to make, have made, use, import, offer for sale and sell Licensed Products in the Field of Use during the Term (as such terms may be defined in Sections 1.2 and 6.1).  The License includes the right to sublicense as permitted by this Agreement.  No other rights or licenses are granted by Penn. Any intellectual property created or conceived during the performance of the Sponsored Research Agreement between Penn and VGX being entered into simultaneously with this Agreement (the “ Sponsored Research Agreement ”) will be governed by the terms of the Sponsored Research Agreement.

 

1.2                                  Related Definitions . The term “ Licensed Products ” means products that are made, made for, used, imported, offered for sale or sold by VGX or its Affiliates or sublicensees and that either (i) in the absence of this Agreement, would infringe at least one claim of the Patent Rights or (ii) use a process or machine covered by a claim of Patent Rights, in either case whether or not the claim is issued or pending.  The term “ Patent Rights ” means all of Penn’s patent rights represented by or issuing from: (a) the United States patents and patent applications listed in Exhibit A; (b) any continuation, divisional and re-issue applications of (a); and (c) any foreign counterparts and extensions of (a) or (b).  The term “ Affiliate ” means a legal entity that is controlling, controlled by, or under common control with VGX and that has executed either this Agreement or a written Joinder Agreement agreeing to be bound by all of the terms and

 



 

conditions of this Agreement.  For purposes of this Section 1.2, the word “ control ” means (x) the direct or indirect ownership of more than fifty percent (50%) of the outstanding voting securities of a legal entity, (y) the right to receive fifty percent (50%) or more of the profits or earnings of a legal entity, or (z) the right to determine the policy decisions of a legal entity.  The term “ Field of Use ” means therapeutic and prophylactic use in all applications.

 

1.3                                  Reservation of Rights by Penn .  Penn reserves the right to use, and to permit other non-commercial entities to use, the Patent Rights for educational and research purposes.

 

1.4                                  U.S. Government Rights .  The parties acknowledge that the United States government retains rights in intellectual property funded under any grant or similar contract with a Federal agency.  The License is expressly subject to all applicable United States government rights, including, but not limited to, any applicable requirement that products, which result from such intellectual property and are sold in the United States, must be substantially manufactured in the United States.

 

1.5                                  Sublicense Conditions .  The VGX’s right to sublicense granted by Penn under the License is subject to each of the following conditions:

 

(a)           In each sublicense agreement, VGX will prohibit the sublicensee from further sublicensing to more than one additional sublicense in any jurisdiction and require the sublicensee to comply with the terms and conditions of this Agreement.

 

(b)                                  Within thirty (30) days after VGX enters into a sublicense agreement, VGX will deliver to Penn a complete and accurate copy of the entire sublicense agreement written in the English language.  Penn’s receipt of the sublicense agreement, however, will constitute neither an approval of the sublicense nor a waiver of any right of Penn or obligation of VGX under this Agreement.

 

(c)                                   In the event that VGX causes or experiences a Trigger Event (as defined in Section 7.4), all payments due to VGX from its Affiliates or sublicensees under the sublicense agreement will, upon notice from Penn to such Affiliate or sublicensee, become payable directly to Penn for the account of VGX.  Upon receipt of any such funds, Penn will remit to VGX the amount by which such payments exceed the amounts owed by VGX to Penn.

 

(d)                                  VGX’s execution of a sublicense agreement will not relieve VGX of any of its obligations under this Agreement.  VGX is primarily liable to Penn for any act or omission of an Affiliate or sublicensee of VGX that would be a breach of this Agreement if performed or omitted by VGX, and VGX will be deemed to be in breach of this Agreement as a result of such act or omission.

 

2



 

2                                          DILIGENCE

 

2.1                                  Development Plan .  Attached as Exhibit B is an outline of a Development plan. VGX will deliver to Penn, within ninety (90) days after the Effective Date, a copy of a detailed development plan for the Patent Rights (the “ Development Plan ”).  The purpose of the Development Plan is (a) to demonstrate VGX’s capability to bring the Patent Rights to commercialization, (b) to project the timeline for completing the necessary tasks, and (c) to measure VGX’s progress against the projections. Thereafter, VGX will deliver to Penn an annual updated Development Plan no later than December 1 of each year during the Term.  The Development Plan will include, at a minimum, the information listed in Exhibit B.

 

2.2                                  VGX’s Efforts .  VGX will use commercially reasonable efforts to develop, commercialize, market and sell Licensed Products in a manner consistent with the Development Plan.

 

2.3                                  Diligence Efforts.   Until the first commercial sale of the first Licensed Product, VGX will commit financial resources to the development and commercialization of Licensed Products in amounts not less that specified below (“ Development Expenditures ”) in each 12 month period following the Effective Date.  Development Expenditures shall include all monies spent directly for development of Licensed Product by VGX, its subsidiaries, sub-licensees, business partners and independent contractors in any given year and shall be applied as a credit against due diligence fees due at the end of the year.  In the event that VGX’s total Development Expenditures for Licensed Products in any such 12 month period do not meet or exceed the required minimum, then VGX will pay to Penn the amount of the shortfall.

 

Year 1

 

$

200,000

 

Year 2

 

$

250,000

 

Year 3

 

$

300,000

 

All years thereafter

 

$

400,000

 

 

3                                          FEES AND ROYALTIES

 

3.1                                  License Initiation Fee .  In lieu of Initiation and License Maintenance fees, VGX will pay to Penn $100,000 upon execution of this Agreement.

 

3.2                                  Milestone Payments .  In partial consideration of the License, VGX will pay to Penn the applicable milestone payment listed in the table below after achievement of each milestone event for the first Licensed Product.  VGX will provide Penn with written notice within thirty (30) days after achieving each milestone.

 

MILESTONE

 

PAYMENT

 

Filing of an IND Application

 

$

125,000

 

Enrollment of First Subject in Phase II Clinical Trial

 

$

250,000

 

Enrollment of First Subject in Phase III Clinical Trial

 

$

375,000

 

Filing of NDA

 

$

250,000

 

Receipt of Approval in US, EU or Japan (whichever is first to occur)

 

$

1,500,000

 

 

3



 

3.3                                  Earned Royalties .  In partial consideration of the License, within 45 days after the end of each calendar quarter, VGX will pay to Penn a royalty of ****** of worldwide Net Sales during the quarter and deliver to Penn a report detailing net sales for the quarter. Such royalty payments shall terminate on a product –by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first Sale of such Licensed Product in such country, or (b) in any country in which patent rights exist for any Licensed Product, the date of expiration of the last-to-expire patent in such country, within the definition of Patent Rights, with a valid claim covering the Licensed Product.

 

3.4                                  Related Definitions .  The term “ Sale ” means any bona fide transaction for which consideration is received or expected by VGX or its Affiliate or sublicensee for the sale, use, lease, transfer or other disposition of a Licensed Product to a third party.  A Sale is deemed completed at the time that VGX or its Affiliate or sublicensee invoices, ships or receives payment for a Licensed Product, whichever occurs first.  The term “ Quarter ” means each three-month period beginning on January 1, April 1, July 1 and October 1.  The term “ Net Sales ” means the consideration received or expected from, or the fair market value attributable to, each Sale, less Qualifying Costs that are directly attributable to a Sale, specifically identified on an invoice or other documentation and actually borne by VGX or its Affiliates or sublicensees.  For purposes of determining Net Sales, the words “ fair market value ” mean the cash consideration that VGX or its Affiliates or sublicensees would realize from an unrelated buyer in an arms length sale of an identical item sold in the same quantity and at the time and place of the transaction.  The term “Q ualifying Costs ” means:  (a) customary discounts in the trade for quantity purchased, for prompt payment or for wholesalers and distributors; (b) credits or refunds for claims or returns that do not exceed the original invoice amount; (c) prepaid outbound transportation expenses and transportation insurance premiums; and (d) sales and use taxes and other fees imposed by a governmental agency.

 

3.5                                  Minimum Royalties .  In partial consideration of the License, VGX will pay to Penn the amount, if any, that the applicable minimum royalty listed in the table below, exceeds VGX’s actual earned royalties under Section 3.3 for each Quarter after the first Sale of a Licensed Product.

 


QUARTER:

 

First 8
Quarters

 

Next 8
Quarters

 

Next 8
Quarters

 

All Quarters
thereafter

 

MINIMUM:

 

******

 

******

 

******

 

******

 

 

3.6                                  Sublicense Fees .  In partial consideration of the License, VGX will pay to Penn a sublicense fee of ****** plus the fair market value of all other consideration of any kind, received by VGX from sublicensees during the Quarter. Monies paid to VGX that are specifically targeted to fund research and development or clinical studies, or paid in the form of loans to, or as an equity investment in, VGX, or royalties based upon Sales or Net Sales by the sublicensee are not subject to any payment to Penn, except to the extent and only to the extent such monies are paid to VGX as a substitute, wholly or in part, for a royalty on Sales of Licensed Products or for license initiation, maintenance or other related fees and payments covered by this Agreement.

 

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4                                          TRANSACTION FEE

 

4.1        VGX shall pay all reasonable documented out-of-pocket expenses of Penn incurred in connection with the negotiation of this Agreement, including legal fees and expenses provided however, that the total amount of such out-of-pocket expenses shall not exceed $5,000. VGX shall pay such expenses directly, within thirty (30) days of presentment of invoices by Penn

 

5                                          REPORTS AND PAYMENTS

 

5.1                                  Royalty Reports .  Within forty-five (45) days after the end of each Quarter following the first Sale, VGX will deliver to Penn a report, certified by the chief financial officer of VGX, detailing the calculation of all royalties, fees and other payments due to Penn for such Quarter.  The report will include, at a minimum, the following information for the Quarter, each listed by product, by country:  (a) the number of units of Licensed Products constituting Sales; (b) the gross consideration invoiced, billed or received for Sales; (c) Qualifying Costs, listed by category of cost; (d) Net Sales; (e) the gross amount of any payments and other consideration received by VGX from sublicensees and the amounts of any deductions permitted by Section 3.6; (f) the royalties, fees and other payments owed to Penn, listed by category; and (g) the computations for any applicable currency conversions.  Each royalty report will be substantially in the form of the sample report attached as Exhibit C.

 

5.2                                  Payments .  VGX will pay all royalties, fees and other payments due to Penn under Sections 2.3, 3.2, 3.3, 3.5, and 3.6 within forty-five (45) days after the end of the Quarter in which the royalties, fees or other payments accrued.

 

5.3                                  Records .  VGX will maintain, and will cause its Affiliates and sublicensees to maintain, complete and accurate books, records and related background information to verify Sales, Net Sales, and all of the royalties, fees, and other payments due or paid under this Agreement, as well as the various computations reported under Section 5.1.  The records for each Quarter will be maintained for at least five (5) years after submission of the applicable report required under Section 5.1.

 

5.4                                  Audit Rights .  Upon reasonable prior written notice to VGX, VGX and its Affiliates and sublicensees will provide Penn and its accountants, which accounts are reasonably acceptable to VGX, with access to all of the books, records and related background information required by Section 5.3 to conduct a review or audit of Sales, Net Sales, and all of the royalties, fees, and other payments payable under this Agreement.  Access will be made available: (a) during normal business hours; (b) in a manner reasonably designed to facilitate Penn’s review or audit without unreasonable disruption to VGX’s business; and (c) no more than once each calendar year during the Term (as defined below) and for a period of five (5) years thereafter.  VGX will promptly pay to Penn the amount of any underpayment determined by the review or audit, performed by accountants reasonably acceptable to, plus accrued interest.  If the review or audit determines that VGX has underpaid any payment by five percent (5%) or more, then VGX will also promptly pay the costs and expenses of Penn and its accountants in connection with the review or audit.  In addition, once annual Sales of Licensed Products exceed ****** VGX will conduct, at least once every two (2) years at its own expense, an independent audit of Sales, Net Sales, and all of the royalties, fees, and other payments due or paid under this Agreement.  Promptly after completion of the audit, VGX will provide to Penn a copy of the report of the independent auditors.

 

5



 

5.5                                  Information Rights .  Until the closing of the VGX’s initial public offering, VGX will provide to Penn, at least as frequently as the following reports are distributed to the Board of Directors or management of VGX, copies of:  (a) all Board and managerial reports that relate to the Patent Rights or the Licensed Products. After the closing of the VGX’s initial public offering, VGX will provide to Penn, promptly after filing, a copy of each annual report, proxy statement, 10-K, 10-Q and other material report filed with the U.S. Securities and Exchange Commission.

 

5.6                                  Currency .  All dollar amounts referred to in this Agreement are expressed in United States dollars.  All payments will be made in United States dollars.  If VGX receives payment from a third party in a currency other than United States dollars for which a royalty or fee is owed under this Agreement, then (a) the payment will be converted into United States dollars at the conversion rate for the foreign currency as published in the eastern edition of the Wall Street Journal as of the last business day of the Quarter in which the payment was received by VGX, and (b) the conversion computation will be documented by VGX in the applicable report delivered to Penn under Section 5.1.

 

5.7                                  Place of Payment .  All payments by VGX are payable to “The Trustees of the University of Pennsylvania” and will be made to the following addresses:

 

By Electronic Transfer :

 

By Check :

 

 

 

Wachovia Bank, N.A.

 

The Trustees of the University of Pennsylvania

ABA #031-201-467

 

c/o Center for Technology Transfer

Account No.: 2000030009804

 

P.O. Box 785546

c/o: CTT/T. Dunn

 

Philadelphia, PA 19178-5546

 

5.8                                  Interest .  All amounts that are not paid by VGX when due will accrue interest from the date due until paid at a rate equal to one and one-half percent (1.5%) per month (or the maximum allowed by law, if less).

 

6                                          CONFIDENTIALITY AND USE OF PENN’S NAME

 

6.1                                  Confidentiality Agreement .  If VGX and Penn entered into one or more Confidential Disclosure Agreements prior to the Effective Date, then such agreements will continue to govern the protection of confidential information under this Agreement, and each Affiliate and sublicensee of VGX will be bound to VGX’s obligations under such agreements.  If, however, no Confidential Disclosure Agreement has been entered into between VGX and Penn prior to the Effective Date, then in connection with the execution of this Agreement, the parties will enter into a Confidential Disclosure Agreement substantially similar to Penn’s standard form.  The term “ Confidentiality Agreement ” means all Confidential Disclosure Agreements between the parties that remain in effect after the Effective Date.

 

6.2                                  Other Confidential Matters .  Penn is not obligated to accept any confidential information from VGX, except for the reports required by Sections 2.1, 5.1, 5.4, and 7.6.  Penn, acting through its Center for Technology Transfer and finance offices, will use reasonable efforts not to disclose to any third party outside of Penn any confidential information of VGX contained in those reports, for so long as such information remains confidential.  Penn bears no institutional responsibility for maintaining the confidentiality of any other information of VGX.  VGX may

 

6



 

elect to enter into confidentiality agreements with individual investigators at Penn that comply with Penn’s internal policies.

 

6.3                                  Use of Penn’s Name .  VGX and its Affiliates, sublicensees, employees, and agents may not use the name, logo, seal, trademark, or service mark (including any adaptation of them) of Penn or any Penn school, organization, employee, student or representative, without the prior written consent of Penn.

 

7                                          TERM AND TERMINATION

 

7.1                                  Term .  This Agreement will commence on Effective Date and terminate upon the later of:  (a) the expiration or abandonment of the last patent to expire or become abandoned of the Patent Rights; or (b) ten (10) years after the first Sale of the first Licensed Product if no patent has issued from the Patent Rights (as the case may be, the “ Term ”).

 

7.2                                  Early Termination by VGX .  VGX may terminate this Agreement at any time effective upon completion of each of the following conditions:  (a) providing at least sixty (60) days prior written notice to Penn of such intention to terminate; (b) ceasing to make, have made, use, import, offer for sale and sell all Licensed Products; (c) terminating all sublicenses and causing all Affiliates and sublicensees to cease making, having made, using, importing, offering for sale and selling all Licensed Products; and (d) paying all amounts owed to Penn under this Agreement and any Sponsored Research Agreement between Penn and VGX related to the Patent Rights, through the effective date of termination.

 

7.3                                  Early Termination by Penn .  Penn may terminate this Agreement if:  (a) VGX is more than sixty (60) days late in paying to Penn any amounts owed under this Agreement and does not immediately pay Penn in full, including accrued interest, upon demand (a “Payment Default”); (b) other than a Payment Default, VGX or its Affiliate or sublicensee breaches this Agreement and does not cure the breach within sixty (60) days after written notice of the breach; or (c) VGX or its Affiliate or sublicensee experiences a Trigger Event.

 

7.4                                  Trigger Event .  The term “ Trigger Event ” means any of the following:    (a) a material default by VGX under any Sponsored Research Agreement between VGX and Penn related to the Patent Rights (whether entered prior to, contemporaneous with, or subsequent to the Effective Date) that is not cured during any specified cure periods; (b) if VGX or its Affiliate or sublicensee (i) becomes insolvent, bankrupt or generally fails to pay its debts as such debts become due, (ii) is adjudicated insolvent or bankrupt, (iii) admits in writing its inability to pay its debts, (iv) suffers the appointment of a custodian, receiver or trustee for it or its property and, if appointed without its consent, not discharged within thirty (30) days, (v) makes an assignment for the benefit of creditors, or (vi) suffers proceedings being instituted against it under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or release of debtors and, if contested by it, not dismissed or stayed within thirty (30) days; (c) the institution or commencement by VGX or its Affiliate or sublicensee of any proceeding under any law related to bankruptcy, insolvency, liquidation or the reorganization, readjustment or release of debtors; (d) the entering of any order for relief relating to any of the proceedings described in Section 7.4(b) or (c) above; (e) the calling by VGX or its Affiliate or sublicensee of a meeting of its creditors with a view to arranging a composition or adjustment of its debts; (f) the act or failure to act by VGX or its Affiliate or sublicensee indicating its consent to, approval of or acquiescence in any of the proceedings described in Section7.4 (b)– (e) above; (g) failure by

 

7



 

VGX to pay patent counsel pursuant to the terms of a Client and Billing Agreement, if any; or (h) the commencement by VGX of any action against Penn, including an action for declaratory judgment, to declare or render invalid or unenforceable the Patent Rights, or any claim thereof.

 

7.5                                  Effect of Termination .  Upon the termination of this Agreement for any reason:  (a) the License terminates; (b) VGX and all its Affiliates and sublicensees will cease all making, having made, using, importing, offering for sale and selling all Licensed Products, except to extent permitted by Section 7.6; (c) VGX will pay to Penn all amounts, including accrued interest, owed to Penn under this Agreement and any Sponsored Research Agreement related to the Patent Rights, through the date of termination, including royalties on Licensed Products invoiced or shipped through the date of termination and any sell off period permitted by Section 7.6, whether or not payment is received prior to termination: or expiration of the sell off period permitted by Section 7.6; (d) VGX will, at Penn’s request, return to Penn all confidential information of Penn and provide to Penn one complete copy of all data with respect to Licensed Products generated by VGX during the Term that will facilitate the further development of the technology licensed under this Agreement; and (e) in the case of termination under Section 7.3, all duties of Penn and all rights (but not duties) of VGX under this Agreement immediately terminate without further action required by either Penn or VGX.

 

7.6                                  Inventory & Sell Off .  Upon the termination of this Agreement for any reason, VGX will cause physical inventories to be taken immediately of:  (a) all completed Licensed Products on hand under the control of VGX or its Affiliates or sublicensees; and (b) such Licensed Products as are in the process of manufacture and any component parts on the date of termination of this Agreement.  VGX will deliver promptly to Penn a copy of the written inventory, certified by an officer of the VGX.  Upon termination of this Agreement for any reason, VGX will promptly remove, efface or destroy all references to Penn from any advertising, labels, web sites or other materials used in the promotion of the business of VGX or its Affiliates or sublicensees, and VGX and its Affiliates and sublicensees will not represent in any manner that it has rights in or to the Patent Rights or the Licensed Products.  Upon the termination of this Agreement for any reason other than pursuant to Section 7.3 (a) or (c), VGX may sell off its inventory of Licensed Products existing on the date of termination for a period of six (6) months and pay Penn royalties on Sales of such inventory within thirty (30) days following the expiration of such six (6) month period.

 

7.7                                  Survival .  VGX’s obligation to pay all amounts, including accrued interest, owed to Penn under this Agreement will survive the termination of this Agreement for any reason.  Sections 14.10 and 14.11  and Articles 5, 6, 7, 10, 11,and 12 will survive the termination of this Agreement for any reason in accordance with their respective terms.

 

8                                          PATENT PROSECUTION AND MAINTENANCE

 

8.1                                  Patent Control .  Penn controls the preparation, prosecution and maintenance of the Patent Rights and the selection of patent counsel, with input from VGX.  If, however, VGX desires a greater degree of control over the Patent Rights, then VGX and Penn will use good faith efforts to enter into a Client and Billing Agreement with patent counsel in substantially in the form attached as Exhibit D.  During the term of the Client and Billing Agreement, VGX will manage the preparation, prosecution and maintenance of the Patent Rights, with input from Penn. In the absence of or upon termination of a Client and Billing Agreement for any reason, control reverts to Penn under the first sentence of this Section 8.1.  For purposes of this Article 8, the

 

8



 

word “ maintenance ” includes any interference negotiations, claims, or proceedings, in any forum, brought by Penn, VGX, a third party, or the United States Patent and Trademark Office, and any requests by Penn or VGX that the United States Patent and Trademark Office reexamine or reissue any patent in the Patent Rights.

 

8.2                                  Payment and Reimbursement .  Within thirty (30) days after the Effective Date, VGX will reimburse Penn for all historically accrued attorneys fees, expenses, official fees and all other charges accumulated prior to the Effective Date incident to the preparation, filing, prosecution and maintenance of the Patent Rights.  Thereafter, VGX will either pay directly under a Client and Billing Agreement or reimburse Penn for all documented attorneys fees, expenses, official fees and all other charges accumulated on or after the Effective Date incident to the preparation, filing, prosecution, and maintenance of the Patent Rights, within thirty (30) days after VGX’s receipt of invoices for such fees, expenses and charges.  Penn reserves the right to require the VGX to provide a deposit in advance of incurring out of pocket patent expenses estimated by counsel to exceed $2,500.  If VGX fails to reimburse patent expenses under Paragraph 8.2, or provide a requested deposit with respect to a Patent Right, then Penn will be free at its discretion and expense to either abandon such applications or patents related to such Patent Right or to continue such preparation, prosecution and/or maintenance activities, and any patent rights associated with such patent action will be automatically excluded from the term “Patent Rights” hereunder, on a patent by patent or country by country basis, as applicable.

 

9                                          INFRINGEMENT

 

9.1                                  Notice .  VGX and Penn will notify each other promptly of any infringement of the Patent Rights that may come to their attention.  VGX and Penn will consult each other in a timely manner concerning any appropriate response to the infringement.

 

9.2                                  Prosecution of Infringement .  VGX may prosecute any infringement of the Patent Rights at VGX’s expense, including defending against any counterclaims or cross claims brought by any party against VGX or Penn regarding the Patent Rights and defending against any claim that the Patent or Patent Rights are invalid in the course of any infringement action or in a declaratory judgment action.  Penn reserves the right to intervene voluntarily and join VGX in any such infringement litigation.  If Penn chooses not to intervene voluntarily, but Penn is a necessary party to the action brought by VGX, then VGX may join Penn in the infringement litigation.  If VGX decides not to prosecute any infringement of the Patent Rights, then Penn may elect to prosecute such infringement independently of VGX in Penn’s sole discretion.

 

9.3                                  Cooperation .  In any litigation under this Article 9, either party, at the request and sole expense of the other party, will cooperate to the fullest extent reasonably possible.  This Section 9.3 will not be construed to require either party to undertake any activities, including legal discovery, at the request of any third party, except as may be required by lawful process of a court of competent jurisdiction.  If, however, either party is required to undertake any activity, including legal discovery, as a right of lawful process of a court of competent jurisdiction, then VGX will pay all expenses incurred by VGX and by Penn.

 

9.4                                  Control of Litigation .  VGX controls any litigation or potential litigation involving the prosecution of infringement claims regarding the Patent Rights in which Penn is not a party, including the selection of counsel, all with input from Penn.  VGX must not settle or compromise any such litigation in a manner that imposes any obligations or restrictions on Penn

 

9



 

or grants any rights to the Patent Rights, other than any permitted sublicenses, without Penn’s prior written permission.  Penn controls any litigation or potential litigation involving the prosecution of infringement claims regarding the Patent Rights in which Penn has elected to prosecute the infringement independently of VGX or has voluntarily or involuntarily joined VGX in the infringement litigation, including the selection of counsel, all with input from VGX.  In all instances in which Penn is a party, Penn reserves the right to select its own counsel.  If Penn is involuntarily joined as a party, Penn retains the right to select its own counsel, but VGX will be responsible for all litigation expenditures as set forth in Section 9.5.

 

9.5                                  Recoveries from Litigation .  If VGX prosecutes any infringement claims either without Penn as a party or with Penn involuntarily joined as a party, then VGX will reimburse Penn for Penn’s litigation expenditures, including any attorneys’ fees, expenses, official fees and other charges incurred by Penn, even if there are no financial recoveries from the infringement action.  VGX will reimburse Penn within thirty (30) days after receiving each invoice from Penn.  After reimbursing Penn for its expenditures, VGX will use the financial recoveries from such claims, if any, (a) first, to reimburse VGX for its litigation expenditures; and (b) second, to retain any remainder but to treat the remainder as either (i) Net Sales for the purpose of determining the royalties due to Penn under Section 3.6 or (ii) sublicense consideration for the purpose of determining the sublicense fees due to Penn under Section 3.10, whichever would result in a larger payment to Penn.  If VGX prosecutes any infringement claims with Penn joined as a voluntary party, then any financial recoveries from such claims will be (x) first, shared between VGX and Penn in proportion with their respective shares of the aggregate litigation expenditures by VGX and Penn; and (y) second, shared equally by VGX and Penn as to any remainder after VGX and Penn have fully recovered their aggregate litigation expenditures.  If Penn prosecutes any infringement claims independent of VGX, then Penn will prosecute such infringement at Penn’s expense and will retain any financial recoveries in their entirety.

 

10                                   DISCLAIMER OF WARRANTIES

 

10.1                            Disclaimer .  PENN REPRESENTS AND WARRANTS TO VGX THAT IT HAS THE FULL AUTHORITY TO EXECUTE AND DELIVER THIS LICENSE AGREEMENT; THAT TO THE KNOWLEDGE OF THE CURRENT STAFF OF THE UNIVERSITY OF PENNSYLVANIA CENTER FOR TECHNOLOGY TRANSFER (CTT) AND OFFICE OF THE GENERAL COUNSEL (COLLECTIVELY “CTT/GC”), CTT/GC HAVE RECEIVED NO MATERIAL CLAIM IN WRITING FROM ANY THIRD PARTY CONTESTING THE VALIDITY, ENFORCEABILITY, LICENSABILITY, USE OR OWNERHIP OF ANY SUCH PENN PATENT RIGHTS AND CTT/GC HAVE RECEIVED NO NOTICE IN WRITING OF ANY LOSS OR EXPIRATION OF ANY PART OF PENN PATENT RIGHTS. EXCEPT AS SET FORTH IN THE PREVIOUS SENTENCE, THE PENN PATENT RIGHTS, LICENSED PRODUCTS AND ANY OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT ARE PROVIDED ON AN “AS IS” BASIS.  PENN MAKES NO REPRESENTATIONS OR WARRANTIES, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO ANY WARRANTY OF ACCURACY, COMPLETENESS, PERFORMANCE, MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, COMMERCIAL UTILITY, NON-INFRINGEMENT OR TITLE.

 

10



 

11.                                LIMITATION OF LIABILITY

 

11.1                            Limitation of Liability .  PENN WILL NOT BE LIABLE TO VGX, ITS AFFILIATES, SUBLICENSEES, SUCCESSORS OR ASSIGNS, OR ANY THIRD PARTY WITH RESPECT TO ANY CLAIM:  ARISING FROM VGX’S USE OF THE PENN PATENT RIGHTS, LICENSED PRODUCTS OR ANY OTHER TECHNOLOGY LICENSED UNDER THIS AGREEMENT; OR ARISING FROM THE DEVELOPMENT, TESTING, MANUFACTURE, USE OR SALE OF LICENSED PRODUCTS.  PENN WILL NOT BE LIABLE TO VGX, ITS AFFILIATES, SUBLICENSEES, SUCCESSORS OR ASSIGNS, OR ANY THIRD PARTY FOR LOST PROFITS, BUSINESS INTERRUPTION, OR INDIRECT, SPECIAL OR CONSEQUENTIAL DAMAGES OF ANY KIND.

 

12.                                INDEMNIFICATION

 

12.1                            Indemnfication .  VGX will defend, indemnify, and hold harmless each Indemnified Party from and against any and all Liabilities with respect to an Indemnification Event.  The term “ Indemnified Party ” means each of Penn and its trustees, officers, faculty, students, employees, contractors, and agents.  The term “ Liabilities ” means all damages, awards, deficiencies, settlement amounts, defaults, assessments, fines, dues, penalties, costs, fees, liabilities, obligations, taxes, liens, losses, lost profits and expenses (including, but not limited to, court costs, interest and reasonable fees of attorneys, accountants and other experts) that are incurred by an Indemnified Party or awarded or otherwise required to be paid to third parties by an Indemnified Party.  The term “ Indemnification Event ” means any Claim against one or more Indemnified Parties arising out of or resulting from: (a) the development, testing, use, manufacture, promotion, sale or other disposition of any Penn Patent Rights or Licensed Products by VGX, its Affiliates, sublicensees, assignees or vendors or third parties, including, but not limited to, (x) any product liability or other Claim of any kind related to use by a third party of a Licensed Product, (y) any Claim by a third party that the practice of any of the Patent Rights or the design, composition, manufacture, use, sale or other disposition of any Licensed Product infringes or violates any patent, copyright, trade secret, trademark or other intellectual property right of such third party, and (z) any Claim by a third party relating to clinical trials or studies for Licensed Products; (b) any material breach of this Agreement by VGX or its Affiliates or sublicensees; and (c) the enforcement of this Article 12 by any Indemnified Party.  The term “Claim” means any charges, complaints, actions, suits, proceedings, hearings, investigations, claims or demands.

 

12.2                            Reimbursement of Costs .  VGX will pay directly all Liabilities incurred for defense or negotiation of any Claim or will reimburse Penn for all documented Liabilities incident to the defense or negotiation of any Claim within thirty (30) days after VGX’s receipt of invoices for such fees, expenses and charges.

 

12.3                            Control of Litigation .  VGX controls any litigation or potential litigation involving the defense of any Claim, including the selection of counsel, with input from Penn.  Penn reserves the right to protect its interest in defending against any Claim by selecting its own counsel, with any attorneys’ fees and litigation expenses paid for by VGX, pursuant to Sections 12.1 and 12.2.

 

12.4                            Other Provisions .  VGX will not settle or compromise any Claim giving rise to Liabilities in any manner that imposes any restrictions or obligations on Penn or grants any rights to the Penn Patent Rights or the Licensed Products without Penn’s prior written consent.  If VGX fails or declines to assume the defense of any Claim within thirty (30) days after notice of the

 

11



 

Claim, or fails to reimburse an Indemnified Party for any Liabilities pursuant to Sections 12.1 and 12.2 within the thirty (30) day time period set forth in Section 12.2, then Penn may assume the defense of such Claim for the account and at the risk of VGX, and any Liabilities related to such Claim will be conclusively deemed a liability of VGX.  The indemnification rights of the Indemnified Parties under this Article 12 are in addition to all other rights that an Indemnified Party may have at law, in equity or otherwise.

 

13.                                INSURANCE

 

13.1                            Coverages .  VGX will procure and maintain insurance policies for the following coverages with respect to personal injury, bodily injury and property damage arising out of VGX’s performance under this Agreement:  (a) during the Term, comprehensive general liability, including broad form and contractual liability, in a minimum amount of $2,000,000 combined single limit per occurrence and in the aggregate; (b) prior to the commencement of clinical trials involving Licensed Products, clinical trials coverage in a minimum amount of $3,000,000 combined single limit per occurrence and in the aggregate; and (c) prior to the Sale of the first Licensed Product, product liability coverage, in a minimum amount of $2,000,000 combined single limit per occurrence and in the aggregate.  Penn may review periodically the adequacy of the minimum amounts of insurance for each coverage required by this Section 13.1, and Penn reserves the right to require VGX to adjust the limits accordingly.  The required minimum amounts of insurance do not constitute a limitation on VGX’s liability or indemnification obligations to Penn under this Agreement.

 

13.2                            Other Requirements .  The policies of insurance required by Section 13.1 will be issued by an insurance carrier with an A.M. Best rating of “A” or better and will name Penn as an additional insured with respect to VGX’s performance under this Agreement.  VGX will provide Penn with insurance certificates evidencing the required coverage within thirty (30) days after the Effective Date and the commencement of each policy period and any renewal periods.  Each certificate will provide that the insurance carrier will notify Penn in writing at least thirty (30) days prior to the cancellation or material change in coverage.

 

14.                                ADDITIONAL PROVISIONS

 

14.1                            Independent Contractors .  The parties are independent contractors. Nothing contained in this Agreement is intended to create an agency, partnership or joint venture between the parties.  At no time will either party make commitments or incur any charges or expenses for or on behalf of the other party.

 

14.2                            No Discrimination .  Neither Penn nor VGX will discriminate against any employee or applicant for employment because of race, color, sex, sexual or affectional preference, age, religion, national or ethnic origin, handicap, or veteran status.

 

14.3                            Compliance with Laws .  VGX must comply with all prevailing laws, rules and regulations that apply to its activities or obligations under this Agreement.  For example, VGX will comply with applicable United States export laws and regulations.  The transfer of certain technical data and commodities may require a license from the applicable agency of the United States government and/or written assurances by VGX that VGX will not export data or commodities to certain foreign countries without prior approval of the agency.  Penn does not represent that no license is required, or that, if required, the license will issue.

 

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14.4                            Modification, Waiver & Remedies .  This Agreement may only be modified by a written amendment that is executed by an authorized representative of each party.  Any waiver must be express and in writing.  No waiver by either party of a breach by the other party will constitute a waiver of any different or succeeding breach.  Unless otherwise specified, all remedies are cumulative.

 

14.5                            Assignment & Hypothecation .  VGX may not assign this Agreement or any part of it, either directly or by merger or operation of law, without the prior written consent of Penn.  Penn will not unreasonably withhold or delay its consent, provided that: (a) at least thirty (30) days before the proposed transaction, VGX gives Penn written notice and such background information as may be reasonably necessary to enable Penn to give an informed consent; (b) the assignee agrees in writing to be legally bound by this Agreement and to deliver to Penn an updated Development Plan within forty-five (45) days after the closing of the proposed transaction; and (c) VGX provides Penn with a copy of assignee’s undertaking.  Any permitted assignment will not relieve VGX of responsibility for performance of any obligation of VGX that has accrued at the time of the assignment.  VGX will not grant a security interest in the License or this Agreement during the Term.  Any prohibited assignment or security interest will be null and void.

 

14.6                            Notices .  Any notice or other required communication (each, a “ Notice ”) must be in writing, addressed to the party’s respective Notice Address listed on the signature page, and delivered: (a) personally; (b) by certified mail, postage prepaid, return receipt requested; (c) by recognized overnight courier service, charges prepaid; or (d) by facsimile.  A Notice will be deemed received:  if delivered personally, on the date of delivery; if mailed, five (5) days after deposit in the United States mail; if sent via courier, one (1) business day after deposit with the courier service; or if sent via facsimile, upon receipt of confirmation of transmission provided that a confirming copy of such Notice is sent by certified mail, postage prepaid, return receipt requested.

 

14.7                            Severability & Reformation .  If any provision of this Agreement is held to be invalid or unenforceable by a court of competent jurisdiction, then the remaining provisions of this Agreement will remain in full force and effect. Such invalid or unenforceable provision will be automatically revised to be a valid or enforceable provision that comes as close as permitted by law to the parties’ original intent.

 

14.8                            Headings & Counterparts .  The headings of the articles and sections included in this Agreement are inserted for convenience only and are not intended to affect the meaning or interpretation of this Agreement.  This Agreement may be executed in several counterparts, all of which taken together will constitute the same instrument.

 

14.9                            Governing Law .  This Agreement will be governed in accordance with the laws of the Commonwealth of Pennsylvania, without giving effect to the conflict of law provisions of any jurisdiction.

 

14.10                      Dispute Resolution .  If a dispute arises between the parties concerning any right or duty under this Agreement, then the parties will confer, as soon as practicable, in an attempt to resolve the dispute.  If the parties are unable to resolve the dispute amicably, then the parties will

 

13



 

submit to the exclusive jurisdiction of, and venue in, the state and Federal courts located in the Eastern District of Pennsylvania with respect to all disputes arising under this Agreement.

 

14.11                      Integration .  This Agreement with its Exhibits and the Sponsored Research Agreement, , contain the entire agreement between the parties with respect to the Patent Rights and the License and supersede all other oral or written representations, statements, or agreements with respect to such subject matter, including but not limited to the Term Sheet.

 

Each party has caused this Agreement to be executed by its duly authorized representative.

 

THE TRUSTEES OF THE

 

VGX PHARMACEUTICALS, INC.

UNIVERSITY OF PENNSYLVANIA

 

 

 

 

 

 

 

 

By:

/s/ Michael E. Breton

 

By:

/s/ J. Joseph Kim

Name:

Michael E. Breton

 

Name:

J. Joseph Kim

Title:

Assoc Vice Provost

 

Title:

President/CEO

 

Address:

 

Center for Technology Transfer

 

Address:  450 Sentry Parkway

 

 

University of Pennsylvania

 

 

Blue Bell, PA 19422

 

 

3160 Chestnut Street, Suite 200

 

 

 

 

Philadelphia, PA 19104-6283

 

 

 

 

Attention: Managing Director

 

 

 

Required copy to:

 

University of Pennsylvania

 

 

 

 

Office of General Counsel

 

 

 

 

133 South 36 th  Street, Suite 300

 

 

 

 

Philadelphia, PA 19104-3246

 

 

 

 

Attention: General Counsel

 

 

 

14



 

EXHIBIT INDEX

 

Exhibit A

 

Patents and Patent Applications in Patent Rights

 

 

 

Exhibit B

 

Development Plan Outline

 

 

 

Exhibit C

 

Format of Royalty Report

 

 

 

Exhibit D

 

Form of Patent Management Agreement

 

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Exhibit A

Patents and Patent Applications in Patent Rights

 

S4229 – “Improved HIV Vaccines and Methods for Using the Same” was invented by Drs. David Weiner and Jian Yan. It relates to improved HIV vaccines, improved methods for inducing immune responses and for prophylactically and/or therapeutically immunizing individuals against HIV. A US Provisional Patent Application Serial No. 60/833,856 was filed on July 28, 2006

 

S4253 – HPV and HCV Vaccines and Methods of Using the Same” was invented by Drs. David Weiner and Jian Yan. The invention provides expression optimized sequences for HPV and HCV antigens which are useful in expression constructs such as vaccines, particularly but not limited to DNA vaccines. A US Provisional Patent Application Serial No: 60/833,861 was filed on July 28, 2006.

 

T4383 – “Consensus Sequences for Influenza Constructs” was invented by Drs. David Weiner and Jian Yan. A US Provisional Patent Application was filed (Serial Number not yet assigned).

 

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Exhibit B

Development Plan Outline

 

VGX Pharmaceuticals DNA Vaccines Development Plan Outline

 

Target Activity

 

Estimated Time

Conduct R&D Studies in Preclinical Animal Models

 

2Q 2007 – 2Q 2008

Select Lead DNA Vaccine Clinical Candidate

 

3/4Q 2007

Conduct IND-enabling Animal Toxicity Testing on Lead Candidate

 

4Q 2007 – 1/2Q 2008

Perform GMP manufacturing of Lead Candidate

 

4Q 2007 – 1/2Q 2008

File IND on Lead Candidate

 

2/3Q 2008

Conduct Phase I Clinical Trial for Lead Candidate

 

4Q 2008 – 3Q 2009

Conduct Phase II Clinical Trial for Lead Candidate

 

2010-2011 (TBD)

Conduct Phase III Clinical Trial for Lead Candidate

 

2012-2014 (TBD)

Select Additional or Follow-on Clinical Candidates

 

2008 –2009

 

17



 

Exhibit C

Royalty Report

 

INSERT Excel File “10.2 Penn Patent License-Exhibit C Royalty Report 04-16-07”

 

18



 

Exhibit D

Client and Billing Agreement

 

The Trustees of the University of Pennsylvania (“Penn”), a Pennsylvania non-profit corporation doing business at 3160 Chestnut Street, Suite 200, Philadelphia, PA 19104-6283; and VGX Pharmaceuticals, Inc. (“VGX”), a corporation doing business at 450 Sentry Parkway, Blue Bell, PA 19422, have entered into a License Agreement with respect to certain inventions which are the subject of the patent applications and patents listed in Appendix A hereto, including any continuations, divisions, extensions thereof, and any foreign counterpart patents, applications, or registrations (“Patent Rights”);

 

Penn has retained the services of Pepper Hamilton LLP (“Law Firm”), with offices at Berwyn, PA 19312-1183, to prepare, file and prosecute the pending patent applications constituting the Patent Rights and to maintain the patents that issue thereon;

 

Penn, Company and Law Firm, intending to formalize their business relationships, agree as follows:

 

1.                                        Penn is the owner of the Patent Rights.

 

2.                                        Company is the licensee of Penn’s interest in the Patent Rights.

 

3.                                        Penn shall maintain an attorney-client relationship with Law Firm in furtherance of efforts to secure and maintain the Patent Rights.

 

4.                                        Law Firm will interact directly with Company on all patent prosecution and patent maintenance matters related to the Patent Rights and will copy Penn on all correspondence related thereto.  Company and Law Firm agree to use all reasonable efforts to notify Penn in writing at least thirty (30) days prior to the due date or deadline for any action which could adversely affect the pending status of any patent application within the Patent Rights, the maintenance of any granted patent within the Patent Rights, Penn’s right to file any continuing application or foreign counterpart application based on the Patent Rights, or the breadth of any claim within the Patent Rights.  In any case, Company shall give Penn written notice of any final decision regarding the action to be taken or not to be taken on such matters prior to instructing Law Firm to implement the decision.  Penn reserves the right to countermand any instruction given by Company to Law Firm.

 

5.                                        Law Firm’s legal services relating to the Patent Rights will be performed on behalf of Penn.  Law Firm shall invoice Company directly for all work relating to the filing, prosecution and maintenance of the Patent Rights and shall provide copies of all invoices to Penn.  Company is responsible for the payment of all charges and fees so invoiced by Law Firm.  Company will pay invoices directly to Law Firm and copy Penn on each payment.

 

6.                                        To clarify each party’s position with regard to prosecution and maintenance of the Patent Rights, either Penn or Company will notify Law Firm in writing of all decisions to authorize the performance of any desired service(s), which shall be subject to Penn’s right to countermand, as provided in paragraph 4, above.  In the event Penn countermands any decision or instruction of Company, such countermand shall be promptly communicated in writing to Law Firm.

 

7.                                        This agreement represents the complete understanding of each of the undersigned parties as to the client and billing arrangements defined herein.  Additions or deletions of dockets identified in Appendix A will become effective only by written addendum to Appendix A.  All such additions

 

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or deletions of individual patents or applications filed in the US, or as foreign counterparts thereof are considered to be within the terms of this client and billing agreement.

 

8.                                        Notices and copies of all correspondence relating to the Patent Rights should be sent to the following:

 

To PENN:

 

To COMPANY:

 

 

 

Center for Technology Transfer

 

VGX Pharmaceuticals Inc

University of Pennsylvania

 

450 Sentry Parkway

3160 Chestnut Street, Suite 200

 

Blue Bell, PA 19422

Philadelphia, PA 19104-6283

 

Attn: Chief Executive Officer

Attn:  Director, Intellectual Property

 

 

 

 

 

To Law Firm:

 

 

 

 

 

Pepper Hamilton LLP

 

 

Berwyn, PA 19312-1183

 

 

 

ACCEPTED AND AGREED TO:

 

 

 

 

 

THE TRUSTEES OF THE

 

VGX PHARMACEUTICALS INC.

UNIVERSITY OF PENNSYLVANIA

 

 

 

 

 

 

 

 

By:

/s/ Michael E. Breton

 

By:

/s/ J. Joseph Kim

 

 

 

 

 

Name:

Michael E. Breton

 

Name:

J. Joseph Kim

 

 

 

 

 

Title:

Assoc Vice Provost

 

Title:

President/CEO

 

 

 

 

 

Date:

4-12-07

 

Date:

4-16-07

 

 

 

 

 

 

 

 

 

LAW FIRM

 

 

 

 

 

 

 

 

 

 

 

 

By:

/s/ Marc DeLuca

 

 

 

 

 

 

 

 

Name:

Marc DeLuca

 

 

 

 

 

 

 

 

Title:

Partner

 

 

 

 

 

 

 

 

Date:

4/27/07

 

 

 

 

20



 

UNIVERSITY of PENNSYLVANIA

 

First Amendment to Patent License Agreement

 

This First Amendment to Patent License Agreement dated June 12, 2008 (this “ First Amendment ”), is made by and between The Trustees of the University of Pennsylvania (“ Penn ”) and VGX Pharmaceuticals, Inc. (“ Compan y”) and amends the Patent License Agreement between the parties, effective as of April 16, 2007 (the “ License Agreement ”).

 

BACKGROUND

 

The License Agreement relates to certain intellectual property developed by Dr. David B. Weiner of Penn’s School of Medicine which intellectual property is the subject of patents or patent applications (the “ Penn Dockets ”). Company desires to add new dockets to the Penn Dockets, to establish license terms for the new dockets and to add terms related to certain combination products.  The parties wish to amend the License Agreement to reflect these changes.

 

Now, therefore, the parties hereby agree as follows:

 

1)                Exhibit A to the License Agreement is hereby amended and restated in its entirety, and is replaced by Exhibit A to this Amendment.

 

2)                Section 3.3 of the License Agreement shall be replaced with the following language:

 

3.3                     Earned Royalties. In partial consideration of the License, within 45 days after the end of each Quarter, VGX will pay to Penn a royalty of ******of worldwide Net Sales during the quarter; except that VGX will pay to Penn a royalty of ****** worldwide Net Sales of Combination Products.  For the sake of clarity, the royalty on a Combination Product is based on the total Net Sales for such Combination Product, regardless of the number of components or their relative value.  Such royalty payments shall terminate on a product-by-product and country-by-country basis upon the later of (a) the date which is ten (10) years after the date of the first Sale of such Licensed Product or Combination Product in such country, or (b) in any country in which patent rights exist for any Licensed Product, the date of expiration of the last-to-expire patent in such country, within the definition of Patent Rights, with a valid claim covering the Licensed Product.

 

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3)                Section 3.4 of the License Agreement shall be replaced with the following language:

 

3.4                     Related Definitions. The term “Sale” means any bona fide transaction for which consideration is received or expected by VGX or its Affiliate or sublicensee for the sale, use, lease, transfer or other disposition of a Licensed Product or Combination Product to a third party.  A Sale is deemed completed at the time that VGX or its Affiliate or sublicensee invoices, ships or receives payment for a Licensed Product or Combination Product, whichever occurs first. The term “Quarter” means each three month period beginning on January 1, April 1, July 1 and October 1. The term “Net Sales” means the consideration received or expected from, or the fair market value attributable to, each Sale, less Qualifying Costs that are directly attributable to a Sale, specifically identified on an invoice or other documentation and actually borne by VGX or its Affiliates or sublicensees.  For purposes of determining Net Sales, the words “fair market value” mean the cash consideration that VGX or its Affiliates or sublicensees would realize from an unrelated buyer in an arms-length sale of an identical item sold in the same quantity and at the time and place of the transaction.  The term “Qualifying Costs” means: (a) customary discounts in the trade for quantity purchased or for wholesalers and distributors; (b) credits or refunds for claims or returns that do not exceed the original invoice amount; (c) prepaid outbound transportation expenses and transportation insurance premiums; and (d) sales and use taxes and other fees imposed by a governmental agency.  The term “Combination Products” means products that are made, made for, used, imported, offered for sale or sold by VGX or its Affiliates or sublicensees that contain (a) one or more Licensed Product and (b) one or more active ingredients that are not Licensed Products.

 

4)                Section 5.1 of the License Agreement shall be replaced with the following language:

 

5.1                     Royalty Reports. Within forty-five (45) days after the end of each Quarter following the first Sale, VGX will deliver to Penn a report, certified by the chief financial officer of VGX, detailing the calculation of all royalties, fees and other payments due to Penn for such Quarter. The report will include, at a minimum, the following information for the Quarter, each listed by product, by country: (a) the number of units of Licensed Products  constituting Sales; (b) the number of units of Combination Products constituting Sales (c) the gross consideration invoiced, billed or received for Sales; (d) Qualifying Costs, listed by category of cost; (e) Net Sales; (f) the gross amount of any payments and other consideration received by VGX from sublicensees and the amounts of any deductions permitted by Section 3.6; (g) the royalties, fees and other payments owed to Penn, listed by category; and (h) the computations for any applicable currency conversions. Each royalty report will be substantially in the form of the sample report attached as Exhibit C.

 

5)                A new section 8.3 shall be added after section 8.2 as follows.

 

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8.3                     Within thirty (30) days of the execution date of this First Amendment, VGX will reimburse Penn for all historically accrued attorney fees, expenses, official fees and all other charges accumulated since the first filing of the patent application under dockets S4231, R3791, O2725, L2092 and L2056 incident to the preparation, filing, prosecution and maintenance of the Patent Rights.

 

6)                In partial consideration of the amendments included in this First Amendment, VGX will pay Penn ****** upon execution hereof.

 

7)    This First Amendment, together with the License Agreement, constitutes the entire agreement between the parties.  All other terms and provisions of the License Agreement, except as expressly amended by this First Amendment, remain in full force and effect.

 

IN WITNESS WHEREOF, the parties, intending to be legally bound, have caused this First Amendment to be executed by their duly authorized representatives.

 

 

THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

By:

   /s/ Michael J. Cleare

 

By:

   /s/ J. Joseph Kim

 

 

 

Name: Michael J. Cleare, Ph.D.

 

Name: J. Joseph Kim, Ph.D.

 

 

 

Title: Associate Vice Provost for Research and
Executive Director, Center for Technology
Transfer

 

Title: President and Chief Executive Officer

 

 

 

Date:

   6/12/08

 

Date:

   6/16/08

 

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EXHIBIT 10.51

EMPLOYMENT AGREEMENT

        This Employment Agreement (the " Agreement "), dated October 1, 2005, is made by and between Viral Genomix, Inc. (VGX Pharmaceuticals), a Delaware corporation (the " Company "), and with its principal offices at 450 Sentry Parkway East, Blue Bell, PA 19422, and MR. GENE J. KIM ("Executive").

R E C I T A L S

         WHEREAS , the Company desires to employ Executive and to have the benefit of his skills and services, and Executive desires to accept employment with the Company, on the terms and conditions set forth herein; and

         WHEREAS , Executive agrees to execute and shall be bound by the terms and conditions of the Non-Disclosure, Assignment of Inventions, Non-Solicitation and Non-Compete Agreement (the " Non-Compete Agreement "), attached hereto as Exhibit A .

         NOW, THEREFORE , in consideration of the mutual promises, terms, covenants and conditions set forth herein and in the Non-Compete Agreement, and the performance of each, the parties hereto, intending legally to be bound, hereby agree as follows:

1.     Employment; Term.     

        a.     The Company hereby agrees to employ Mr. Kim as Director of Finance and Executive hereby agrees to accept such employment with the Company in accordance with the terms and conditions of this Agreement.

        b.     The " Term " of this Agreement shall commence on October 1, 2005 (the " Commencement Date ") and continue for a period of three (3) years from the Commencement Date; provided , however , that the Term of this Agreement may be terminated earlier at any time as provided in Section 7 below.

2.     Position and Duties.     

        a.     The Company agrees to employ Mr. Kim throughout the Term as Director of Finance of the Company with such responsibilities, duties and authority as are assigned to him by the Chief Executive Officer and/or Chief Operating Officer or its designee. The Director of Finance shall report to the Chief Executive Officer and/or Chief Operating Officer.

        b.     Executive shall faithfully devote his business/working time, attention and energy to the business and affairs of the Company and the performance of his duties hereunder and to use reasonable efforts to perform such responsibilities faithfully and efficiently.

        c.     Without limiting the generality of the foregoing paragraph, during the Term, upon prior written consent of the Board or its designee, Executive shall be permitted to serve on other Boards of Directors, professional associations and otherwise be involved with any family business or trust to the extent that, in the reasonable judgment of the Board or its designee, such other business pursuits and activity do not materially (i) interfere with Executive's ability to discharge Executive's duties and responsibilities to the Company, whether or not such activity is pursued for gain, profit or other pecuniary advantage, or (ii) violate the Conflicts provision of Executive's Non-Compete Agreement.

3.     Compensation.     

        a.     Executive shall be entitled to receive as compensation for his employment a base annual salary at a rate of $100,000 per annum (the " Base Salary ") which shall be paid to Executive by the Company or any of its affiliates on a monthly basis.

        b.     Increases in the Base Salary shall be reviewed annually by the Chief Executive Officer and/or Chief Operating Officer during the Term and any such increases, if any, will be at the Chief Executive



Officer and/or Chief Operating Officer sole discretion and will otherwise be consistent with the Company's annual policies and budget for payroll increases.

4.     Bonus.     

        During the Term, Executive shall be eligible to receive an incentive cash bonus up to the amount, based upon the criteria, and payable at such times, as may be determined by the Board and targeted at twenty percent (20%) or more of the Base Salary. The amount shall be determined by the Board, in its sole and absolute discretion, which shall be binding and final, and shall be paid in a one-time lump sum payment (less payroll taxes). To the extent that such cash bonus is to be determined in light of financial performance during a specified fiscal period and the Agreement commences on a date after the start of such fiscal period, any cash bonus payable in respect of such fiscal period's results may be prorated. In addition, if the period of Executive's employment hereunder expires before the end of a fiscal period, and if Executive is eligible to receive a cash bonus at such time (such eligibility being subject to the restrictions set forth in Section 7 below), any cash bonus payable in respect of such fiscal period's results may be prorated.

5.     Benefits; Stock Options and Vacation.     

        In addition to the salary and cash bonus referred to above, Executive shall be entitled during the Term to participate in such employee benefits plans or programs of the Company, and shall be entitled to such other fringe benefits, as are from time to time adopted by the Board and made available by the Company generally to employees of Executive's position, tenure, salary, age, health and other qualifications. Without limiting the generality of the foregoing, Executive shall be eligible for such awards, if any, under the Company's employee benefits plans or programs as shall be granted to Executive in the sole discretion of the Board or its designee. Executive acknowledges and agrees that the Company does not guarantee the adoption or continuance of any particular employee benefits plan or program or other fringe benefits during the Term, and participation by Executive in any such plan or program shall be subject to the rules and regulations applicable thereto.

        a.     On or about October 1, 2005, the Board Resolution granted Mr. Kim options to purchase One Hundred Fifty Thousand (150,000) shares of Common Stock of the Company. Upon execution of this Agreement by the Executive and the Company, the Executive will be awarded One Hundred Fifty Thousand (150,000) Incentive Stock Options (ISO) to purchase Common Shares of the Company's Stock at a strike price of $0.30 per share pursuant to an Option Grant Agreement in substantially the form attached hereto as Exhibit B over three years. These options are subject to the rules and regulations of the 2001 Equity Incentive Plan. In addition, all shares of the Company's stock will be subject to those restrictions contained in the anticipated future Company's Stockholder's Agreement.

        b.     The Company offers the medical benefits to Executive and his family.

        c.     In addition, the Executive is entitled 15 business days (3 weeks) as a Company paid vacation days annually. The Executive will have an office and a dedicated laptop to improve Executive ability to concentrate at work, and increase his productivity.

6.     Expenses.     

        The Company will reimburse Executive, in accordance with the practices in effect from time to time for other officers or staff personnel of the Company, for all reasonable and necessary business and traveling expenses and other disbursements incurred by Executive for or on behalf of the Company in the performance of Executive's duties hereunder, upon presentation by Executive to the Company of appropriate vouchers and supporting documentation.

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7.     Termination.     

        Executive's employment by the Company pursuant hereto is subject to termination as follows:

        a.     Death or Disability.     The Company may by written notice to Executive or his personal representative terminate Executive's employment on account of his death or total disability. In the case of Executive's death, Executive's employment shall be deemed to terminate on the date of Executive's death. For purposes hereof, Executive shall be deemed to experience a " Total Disability " if Executive is considered totally disabled under any group disability plan maintained by the Company and in effect at that time, or in the absence of any such plan, Executive shall be deemed to experience a Total Disability if he shall have been unable to perform his duties hereunder on a full-time basis for 90 consecutive days or longer, or for shorter periods aggregating 120 days in any 360-day period. In the event of any dispute under this Section 7(a), Executive shall submit to a physical examination by a licensed physician mutually satisfactory to the Company and Executive, the cost of such examination to be paid by the Company, and the determination of such physician shall be determinative. In the case of a Total Disability, until the Company shall have terminated Executive's employment hereunder in accordance with the foregoing, Executive shall be entitled to receive compensation provided for herein notwithstanding any such Total Disability. In the event of the termination of Executive's employment on account of his death or such Total Disability, such termination shall be effective immediately upon notice, in which case Executive or his representative will have no rights or claims against the Company under this Agreement except as follows:

        b.     Involuntary Termination for Cause.     In the event the Company terminates Executive's employment for Cause (as such term is defined below), such termination (" Termination For Cause ") shall be effective immediately upon notice thereof, in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

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        " Cause " shall mean: (1) conviction of Executive of any felony; (2) participation by Executive in any fraud or act of dishonesty against the Company; (3) material violation by Executive of (i) any contract between the Company and Executive, or (ii) any statutory duty of Executive to the Company; (4) conduct of Executive that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Executive's gross unfitness to serve; or (5) the continued, willful refusal or failure by Executive to perform any material duties reasonably requested by the Board and/or Chief Executive Officer; provided , however , that in the case of conduct described in clauses (3), (4) and (5) hereof, such conduct shall not constitute "Cause" unless (a) the Board shall have given Executive written notice setting forth with specificity (i) the conduct deemed to constitute "Cause," (ii) reasonable action that would remedy the objectionable conduct and (iii) a reasonable time (not less than 10 days) within which Executive may take such remedial action, and (b) Executive shall not have taken such specified remedial action within such specified reasonable time.

        c.     Involuntary Termination Without Cause.     The Company may terminate Executive's employment, other than on account of death, Total Disability or for Cause, on 30 days written notice (" Termination Without Cause "), in which case Executive will have no rights or claims against the Company under this Agreement except as follows:

        For the purposes of this Agreement, " Pro Rata Bonus Amount " shall mean one-twelfth ( 1 / 12 th) of the greater of (A) the most recent annual cash bonus paid to Executive prior to the date of his termination, or (B) the average of the three most recent annual cash bonuses paid to Executive prior to the date of his termination. The rights of Executive and the obligations of the Company under this Section 7(c) shall remain in full force and effect notwithstanding the expiration of the Term, whether by failure of the Board to extend such Term or otherwise, and the failure of the Board to extend such Term shall be deemed a Termination Without Cause under this Section 7(c).

        d.     Voluntary Termination For Good Reason.     Executive may terminate his employment for good reason (" Termination For Good Reason ") upon 30 days written notice. In the event of Termination for Good Reason, Executive shall be entitled to receive the payments and other rights provided in Section 7(c) hereof. For purposes of this Agreement, termination for " Good Reason " shall mean

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voluntary termination by Executive of his employment with the Company based on one of the following events:

        e.     Voluntary Termination.     Executive may otherwise terminate his employment without Good Reason upon 30 days written notice, in which case Executive (or his estate or representative, as applicable) shall be paid (A) any unpaid portion of his Base Salary on a pro rata basis through the date of the termination, and (B) any unreimbursed expenses.

        f.     Forfeiture of Rights.     In the event that, subsequent to termination of Executive's employment hereunder, Executive breaches any of the provisions of the Non-Compete Agreement in any material respect, all payments and benefits to which Executive may otherwise have been entitled to pursuant to this Section 7 hereof shall immediately terminate and be forfeited.

8.     Remedies.     

        In addition to other remedies provided by law or equity, upon a breach by Executive of any of the covenants contained herein or in the Non-Compete Agreement, the Company shall be entitled to have a court of competent jurisdiction enter an injunction against Executive enjoining Executive and prohibiting any further breach of the covenants contained herein. Executive acknowledges that a breach or threatened breach by Executive of the provisions of this Agreement will cause irreparable damage to the Company because Executive's services to be performed hereunder are of a unique, special and extraordinary character. Thus, the Company shall be entitled to injunctive relief without the necessity of proving actual damages and the Company shall not be required to post a bond or other security in support of such injunctive relief.

9.     Arbitration.     

        Any claim, dispute or controversy arising out of or in connection with this Agreement, or any breach thereof, shall be arbitrated by the parties before a sole arbitrator (who shall have substantial experience in the pharmaceutical and life sciences industry) conducted in accordance with the National Rules for the Resolution of Employment Disputes of the American Arbitration Association then in effect. The arbitrator shall have the authority to order discovery but shall not have the authority to add to, detract from or modify any provision hereof nor to award punitive damages to any injured party. A decision by the sole arbitrator shall be final and binding. Judgment may be entered on the arbitrator's award in any court having jurisdiction. The direct expense of any arbitration proceeding shall be borne by the Company. Each party shall bear its own counsel fees. Such arbitration shall take place in Philadelphia, Pennsylvania. The parties hereto consent to the jurisdiction of the state and federal courts located in the Commonwealth of Pennsylvania with respect to any action arising under this Agreement. Notwithstanding the foregoing, the Company shall be entitled to seek injunctive or other equitable relief, as contemplated by Section 10 hereof, from any court of competent jurisdiction, without the need to resort to arbitration.

10.     Assignment; Binding Nature.     

        This Agreement shall be binding upon and inure to the benefit of the parties and their respective successors, heirs (in the case of Executive) and permitted assigns. No rights or obligations of the Company under this Agreement may be assigned or transferred by the Company except that such rights or obligations may be assigned or transferred to the successor of the Company or its business if the assignee or transferee assumes all of the liabilities, obligations and duties of the Company, as contained in this Agreement, either contractually or as a matter of law. If any such successor of the Company or its business does not agree to so assume such liabilities, obligations and duties, Executive may

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immediately resign, which shall be deemed a Termination For Good Reason under the provisions of this Agreement. No rights or obligations of Executive under this Agreement may be assigned or transferred by Executive other than Executive's rights to compensation and benefits, which may be transferred only by will or operation of law, except as otherwise specifically provided or permitted hereunder.

11.     Notice.     

        Any notice (including notice of a change of address) permitted or required to be given pursuant to the provisions of this Agreement shall be in writing and sent by certified mail, postage pre-paid, return receipt requested, or by hand delivery to the parties at the following addresses:

        Notice properly given by mail shall be deemed effective three business days after mailing, and if hand-delivered, upon receipt.

12.     Entire Agreement.     

        This Agreement and the Non-Compete Agreement constitute the complete agreements and understandings between the Company and Executive concerning Executive's employment by the Company, and supersede any and all previous agreements or understandings concerning such employment, whether written or oral, between Executive and the Company.

13.     Modification.     

        This Agreement may not be waived, amended or modified without the express written consent of the party against whom enforcement of such Agreement is sought.

14.     Waiver.     

        Except as set forth herein, no delay or omission to exercise any right, power or remedy accruing to any party shall impair any such right, power or remedy or shall be construed to be a waiver of or an acquiescence to any breach hereof. No waiver by either party of any breach by the other party of any condition or provision contained in this Agreement to be performed by such other party shall be deemed a waiver of a similar or dissimilar condition or provision at the same or any prior or subsequent time. Any waiver must be in writing and signed by Executive and the Chairman of the Board.

15.     Invalidity of Any Provision.     

        If any portion of this Agreement is held invalid or inoperative, the other portions of this Agreement shall be deemed valid and operative and, so far as is reasonable and permitted by the law, effect shall be given to the intent manifested by the portion held invalid or inoperative.

16.     Applicable Law.     

        This Agreement shall be governed by and construed in accordance with the laws of the Commonwealth of Pennsylvania, without regard to the principles of conflict of laws thereof.

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17.     Counterparts.     

        This Agreement may be executed simultaneously in any number of counterparts, each of which shall be deemed an original but all of which together shall constitute one and the same agreement.

18.     Headings.     

        The Section headings contained in this Agreement are for reference purposes only and will not affect in any way the meaning or interpretation of this Agreement.

19.     Binding Effect.     

        The provisions of this Agreement will be binding upon, and will inure to the benefit of, the respective heirs, legal representatives and successors of the parties thereto.

20.     Termination of Other Agreements.     

        The execution of this Agreement by Viral Genomix and the Executive terminates and voids for all purposes any other Agreements, if any, between the parties.

[SIGNATURE PAGE FOLLOWS]

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         IN WITNESS WHEREOF , the parties hereto have executed this Employment Agreement as of the date first written above.

    VIRAL GENOMIX, INC.

 

 

By:

 

/s/ J. Joseph Kim

    Name:   J. Joseph Kim, Ph.D.
    Title:   President & CEO

 

 

EXECUTIVE:

 

 

/s/ Gene J. Kim

MR. GENE J. KIM

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FIRST AMENDMENT TO THE EMPLOYMENT AGREEMENT DATED
OCTOBER 1, 2005

        This is the First Amendment ("Amendment") to the Employment Agreement between VGX Pharmaceuticals, Inc. ("VGX") and Gene J Kim ("Executive") dated as of 20th day of August, 2008 (the "Effective Date"), amending the Employment Agreement ("Agreement") dated December 17, 2005 between VGX and Executive. All undefined terms contained herein shall have the meaning set forth in the Agreement.

        WHEREAS, both parties wishes to amend the Agreement as follows:

        NOW, THEREFORE, for good and valuable consideration and intending to be legally bound, the parties hereby agree as follows:

Mr. Gene J Kim
220 Huntsman Ln
Blue Bell, PA, 19422
  VGX Pharmaceuticals
450 Sentry Parkway
Blue Bell, PA 19422
Telephone: 267-440-4205
             
/s/ Gene J. Kim

Gene J. Kim
Chief Financial Officer
  /s/ J. Joseph Kim

Dr. J. Joseph Kim
Chief Executive Officer

Date:

 

August 20, 2008


 

Date:

 

August 20, 2008

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QuickLinks


EXHIBIT 10.52

 

FORM OF VGX PHARMACEUTICALS

 

NOTE PURCHASE AGREEMENT

 

THIS NOTE PURCHASE AGREEMENT (the “Purchase Agreement”), dated this          day of               ,           , is by and between [NAME OF HOLDER]., an individual (the “Buyer”), and VGX PHARMACEUTICALS, INC., a Delaware corporation (the “Company”).

 

WHEREAS, the Buyer wishes to purchase from the Company and the Company wishes to sell to the Buyer, upon the terms and subject to the conditions of this Purchase Agreement, a convertible promissory note of the Company, in the principal amount of $ ###,### .

 

NOW THEREFORE, in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties agree as follows:

 

1.                                        Sale and Issuance of Note.   Upon the terms and subject to the conditions of this Purchase Agreement, the Buyer agrees to purchase from the Company, and the Company agrees to sell and issue to the Buyer, a convertible promissory note, in the form attached hereto as Exhibit A which is made a part of this Purchase Agreement (the “Note”), in the principal amount of $###,### (the “Principal Sum”), subject to the terms and conditions contained herein and in the Note.

 

2.                                        Representations and Warranties of the Company .  By executing this Purchase Agreement, the Company makes the following representations and, warranties to the Buyer, with the intent and understanding that the Buyer will rely thereon:

 

2.1                                  Organization of the Company; Authorization; Good Standing .  The Company is a corporation duly organized, validly existing and in good standing under the laws of the State of Delaware and has all requisite corporate power and authority to own and lease its property, to carry on its business as presently conducted and as proposed to be conducted (as previously disclosed to the Buyer) and to execute and deliver, and to perform all of its obligations under, this Purchase Agreement and the Note (collectively, the “Company Documents”).

 

2.2                                  Enforceability .  The creation and issue of the Note and the execution and delivery by the Company of the Company Documents and the consummation of the transactions contemplated thereby have been duly authorized by all requisite corporate action on the part of the Company, and the Company Documents have been duly executed and delivered by the Company and constitute the legal, valid and binding obligation of the Company, enforceable in accordance with its terms.

 



 

2.3                                  Complete and Accurate Information . All information provided by the Company in whatever form in connection with the transactions contemplated by the Company Documents are complete and accurate and provide a true and fair view of the financial position of the Company.

 

3.                                        Representations and Warranties of the Buyer .  By executing this Purchase Agreement, the Buyer makes the following representations and warranties to the Company, with the intent and understanding that the Company will rely thereon:

 

3.1                                  Investment Representations .  The Buyer has knowledge and experience in financial and business matters sufficient to enable him to evaluate the merits and risks of an investment in the Note, the shares of the Company’s Common stock issuable upon conversion of the Note (the “Shares”) and the Company.  The Buyer has assets sufficient to enable him to bear the economic risk of the Buyer’s investment in the Note.  The Buyer is acquiring the Note for investment purposes only, for his, her or its own account, and not with a present view to, or for sale in connection with, any distribution thereof.  The Buyer understands that the Note and the Shares have not been registered under the Securities Act by reason of their issuance in a transaction exempt from the registration requirements of the Securities Act pursuant to the exemption provided in Section 4 thereof, that the Note and the Shares have not been registered under applicable state securities laws by reason of their issuance in a transaction exempt from such registration requirements, and that the Note and the Shares may not be sold or otherwise disposed of unless registered under the Securities Act and applicable state securities laws (the Company being under no obligation to register such Note or the Shares) or exempted from registration.  The Buyer further acknowledges that the Note and the Shares are subject to the restrictions on transfers set forth in the Company Documents, and that each transferee of the Note or the Shares as a condition to such transfer may be required to agree in writing to be bound by such restrictions.

 

3.2                                  Buyer’s Acknowledgment as to Information .  The Buyer or representatives of the Buyer have received from the Company such information (including exhibits to this Purchase Agreement and of such documents referred to herein and therein as he or they have requested) with respect to the Company as the Buyer has deemed necessary and relevant in connection with the transactions contemplated by the Company Documents, and the Buyer has had the opportunity, directly or through such representatives, to ask questions of and receive answers from persons acting on behalf of the Company necessary to verify the information so obtained.

 

4.                                        Legend .  Each certificate evidencing the Note and the Company’s securities issuable upon conversion of the Note and Warrant, and each certificate evidencing the Note and the Company’s securities issuable upon conversion of the Note held by subsequent transferees of any such certificate, shall be stamped or otherwise imprinted with a legend in substantially the following form:

 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE NOTE PURCHASE AGREEMENT DATED AS OF           ,        BETWEEN VGX PHARMACEUTICALS, INC.

 

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(THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF SUCH SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

5.                                        Miscellaneous.

 

5.1                                  Legal Fees and Expenses .  Each party hereto agrees to pay its own legal fees and expenses incurred in connection with the transactions contemplated hereunder.

 

5.2                                  No Waiver .  The failure of a party to insist upon strict adherence to any term of this Purchase Agreement on any occasion shall not be considered a waiver or deprive that party of the right thereafter to insist upon strict adherence to that term or any other term of this Purchase Agreement.  Any waiver of any term of this Purchase Agreement must be in writing.

 

5.3                                  Entire Agreement; Amendment .  This Purchase Agreement and all Exhibits hereto, set forth the entire agreement of the parties with respect to the subject matter hereof and supersede all prior agreements relating thereto, written or oral.  This Purchase Agreement may be amended or modified only by a written instrument executed by the Company and the Buyer.

 

5.4                                  Parties in Interest; Limitation on Assignment .  This Purchase Agreement shall inure to the benefit of and be binding upon the parties and their respective permitted successors and assigns; provided , however , that this Purchase Agreement shall not be assigned or assignable by either party without the prior written consent of the other party.

 

5.5                                  Counterparts .  This Purchase Agreement may be executed in any number of counterparts, each of which shall be considered an original, but all of which together shall constitute one and the same instrument.

 

5.6                                  Governing Law .  This Purchase Agreement shall be governed by, construed, interpreted and enforced in accordance with the laws of the Commonwealth of Pennsylvania as applied to contracts entered into and performed entirely within the Commonwealth of Pennsylvania among Pennsylvania residents without regard to conflicts of laws principles.

 

5.7                                  Notices .  All notices, consents and other communications under this Purchase Agreement shall be in writing and shall be deemed to have been duly given when (a) delivered by hand, (b) sent by telex or telecopier (with receipt confirmed), provided that a copy is mailed by registered mail, return receipt requested, or (c) when received by the addressee, if sent by

 

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Express Mail, Federal Express or other express delivery service (receipt requested), in each case to the appropriate addresses, telex numbers and telecopier numbers set forth below (or to such other addresses, telex numbers and telecopier numbers as a party may designate as to itself by notice to the other party ):

 

5.7.1                         If to the Company:

 

 VGX Pharmaceuticals

 450 Sentry Parkway

 Blue Bell, PA 19422

 FAX:  267-440-4242

 Attention:  Corporate Secretary

 

5.7.2                         If to the Buyer:

 

5.8                                  Severability .  In the event that any court having jurisdiction shall determine that any provision contained in this Purchase Agreement shall be unreasonable or unenforceable in any respect, then such covenant or other provision shall be deemed limited to the extent that such court deems it reasonable and enforceable, and as so limited shall remain in full force and effect.  In the event that such court shall deem any such covenant or other provision wholly unenforceable, the remaining covenants and other provisions of this Purchase Agreement shall nevertheless remain in full force and effect.

 

5.9                                  Headings and Captions .  The headings and captions used herein to identify sections and subsections are for convenience only and shall not be used for interpretation of any provisions herein.

 

5.10                            Indemnity .  The representations, warranties and agreements made by the Company and the Buyer herein shall survive the execution of this Purchase Agreement.  The Company and the Buyer hereby agree to indemnify and hold harmless the other party from and against any and all loss, liability, claim, damage and expense (including, without limitation, attorneys’ fees and disbursements) suffered or incurred as a result of a misrepresentation or breach of any warranty or agreement made by the defaulting party in this Purchase Agreement.

 

[Signature Page Follows]

 

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IN WITNESS WHEREOF , each of the parties has caused this Purchase Agreement to be executed on its behalf with the intent to be legally bound as of the day and year first above written.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

BUYER:

 

 

 

 

 

 

 

By:

 

 

Name:  [HOLDER]

 



 

EXHIBIT A

 

FORM OF CONVERTIBLE PROMISSORY NOTE

 

( see attached)

 




EXHIBIT 10.53

 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE NOTE PURCHASE AGREEMENT DATED AS OF                             BETWEEN VGX PHARMACEUTICALS, INC.  (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF THESE SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THESE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

CONVERTIBLE SUBORDINATED PROMISSORY NOTE

 

US $ ###,###

Blue Bell, Pennsylvania

 

[ENTER DATE]

 

FOR VALUE RECEIVED, the undersigned, VGX PHARMACEUTICALS, INC., a DELAWARE corporation (the “Borrower”), hereby promises to pay to the order of [HOLDER], an individual (hereinafter, with any subsequent holder, the “Holder”), the principal sum of                                      Dollars ($ ###,### ) (the “Principal Sum”), together with interest on the balance of the Principal Sum outstanding at a per annum rate of five percent (5%), upon the terms set forth below.  Interest shall be calculated on the basis of the actual number of days elapsed over a 360-day year and shall commence to accrue on the date hereof.

 

1.                                        Note Purchase Agreement .  This convertible subordinated promissory note (the “Note”) is being issued pursuant to the terms and conditions of the Note Purchase Agreement (the “Purchase Agreement”) dated as of the date hereof to which the Borrower and the Holder are parties.  All notices with respect to this Note shall be made in accordance with Section 5.7 of the Purchase Agreement

 

2.                                        Maturity .  Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section 7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable       months from the date hereof (the “Maturity Date”).  No payments of principal or interest are required hereunder until the Maturity Date.  The Maturity Date shall be automatically

 

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extended to another 12 months at an option of the Holder.  If the Holder desires to extend the Maturity Date, the Maturity Date will be automatically renewed for another 12 months after the first       months on terms and conditions to be informed by the Holder and the Holder does not need to provide any advance notices.  However, if the Holder elects not to extend the Maturity Date, the Holder will provide a termination notice in writing sixty (60) days prior to the Maturity Date to the Borrower.  Upon payment in full of the Principal Sum and interest payable hereunder, or upon conversion of this Note in accordance with Section 3 hereof, the Holder shall surrender this Note to the Borrower for cancellation.

 

3.                                        Conversion .  If, prior to the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, the Borrower shall issue shares of Common Stock to one or more investors, the Note shall be convertible, at the option of the Holder, by written notice to the Borrower, in whole but not in part, into that number of fully paid, validly issued and non-assessable shares of Common Stock equal to the $       price per share, as adjusted for any stock splits, reverse stock splits or stock dividends occurring after the date hereof.  Notwithstanding the above, provided the value of the Borrower’s Common Stock is equal or greater than $3.00 per share at the time of conversion, the value of this Note shall automatically convert to Common Stock of the Borrower upon occurrence of the following:  If, prior to the Maturity Date, the Borrower enters into and performs its obligations under an underwriting agreement, in usual and customary form, with the managing underwriter of such offering, or enters into an agreement of purchase and sale with a public company; the Note shall be automatically converted, in whole but not in part, into that number of fully paid, validly issued and non-assessable shares of Common Stock equal to the $3.00 price per share, as adjusted for any stock splits, reverse stock splits or stock dividends occurring after the date hereof.  Upon such conversion of this Note, the value of the Note to be converted shall include all accrued and outstanding interest, and all other fees, costs and charges, if any, due or payable under this Note on the date of conversion, and all rights of the Holder of this Note, except the right to receive such shares of Common Stock in accordance with this Section 3, shall cease and this Note shall no longer be deemed to be outstanding.  In addition, no fractional shares of Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

4.                                        Payment .  Any payment of principal, interest and all other fees, costs and charges, if any, shall be in lawful money of the United States of America by wire transfer of same day funds to the account of the Holder at such banking institution as the Holder designates or, if requested by the Holder, by certified or bank cashier’s check payable to the Holder mailed to the Holder at the address of the Holder as set forth on the records of the Borrower or such other address as shall be designated in writing by the Holder to the Borrower.

 

5.                                        Credits .  The Borrower’s payments will be credited first to any interest then due, and the remainder to the Principal Sum.  Interest will cease to accrue on any amount credited to the Principal Sum as of the date any such amount is paid.

 

6.                                        Financial Reports .      The Borrower shall furnish Holder the following financial statements prepared in accordance with generally accepted accounting principles consistently applied: (i) within thirty (30) days after the end of each calendar quarter, the Company’s

 

2



 

unaudited or if available, audited balance sheet and statements of income and cash flows for the quarter just ended; and (ii) as soon as possible after the end of each fiscal year of the Company, a balance sheet as of the end of its fiscal year and the related statements of income and cash flows for the fiscal year then ended, unaudited or if available, audited by an independent certified public accounting firm that is acceptable to the Holder in its reasonable judgment.

 

7.                                        Event of Default .  Repayment of all principal and interest under this Note will be accelerated and shall be immediately due in full in the event of any of the following:

 

(a)                                   default shall be made in the payment of the Principal Sum of this Note or any part thereof when and as the same shall become due and payable, either on the Maturity Date or at a date fixed by the parties in writing for prepayment or by acceleration or otherwise and such default continues for a period of 10 days;

 

(b)                                  default shall be made in the payment of interest on this Note when and as the same shall become due and payable and such default continues for a period of 10 days;

 

(c)                                   the Borrower shall (i) apply for or consent to the appointment of a receiver, trustee or liquidator of the Borrower or any of its property, (ii) make a general assignment for the benefit of creditors, (iii) commence a voluntary case under the federal bankruptcy laws or file a petition or answer seeking reorganization or an arrangement with creditors to take advantage of any other bankruptcy, reorganization, insolvency, readjustment of debt, dissolution or liquidation law or statute, or file an answer admitting the material allegations of a petition filed against it in any proceeding under any such law, or (iv) take corporate action for the purpose of effecting any of the foregoing; or an order, judgment or decree shall be entered, without the application, approval or consent of the Borrower, by any court of competent jurisdiction, approving a petition seeking reorganization of the Borrower, or of all or a substantial part of the assets of the Borrower and such order, judgment or decree shall continue unstayed and in effect for a period of 60 days;

 

(d)                                  The Borrower’s failure to observe and perform any of the material terms, covenants, conditions or agreements required to be observed and performed by the Borrower under this Note or the Purchase Agreement, and such failure shall remain unremedied for 30 days after written notice shall have been provided to the Borrower by the Holder of such default; or

 

(e)                                   Any representation or warranty made by the Borrower under this Note or Purchase Agreement or in any other loan document relating to this transaction, or in any certificate or writing delivered pursuant to any loan document relating to this transaction, shall be incorrect in any material respect.

 

Nothing in this Section 7 shall, in any manner, be construed to prohibit or otherwise affect the rights of the Holder to enforce payment of this Note in accordance with its terms.

 

8.                                        Subordination .  All principal and accrued interest on this Note shall be subordinate in right and time of payment to the payment in full of all Senior Indebtedness.  Notwithstanding

 

3



 

anything to the contrary set forth in this Note, unless and until the Senior Indebtedness shall have been indefeasibly satisfied and paid in full in cash and all lending commitments thereunder have terminated: (a) the Holder may not demand payment of any of the Principal Sum; (b) no accrued interest on this Note shall be payable to the Holder; provided, however, that interest on this Note shall accrue in accordance with the terms of this Note; (c) the indebtedness evidenced by this Note shall be unsecured, and (d) the holder of this Note shall not, without the written consent of the holders of the Senior Indebtedness, take any action with respect to collection or enforcement or other like action hereunder or exercise any remedies the Holder may have at law or equity in respect of any amounts owing under this Note, regardless of whether an Event of Default exists pursuant to Section 7 hereof and regardless of any remedies provision contained in this Note.  The provisions of this Section 8 shall continue in effect until all amounts under the Senior Indebtedness are indefeasibly satisfied and paid in full in cash and all lending commitments of the holders thereof under such Senior Indebtedness shall have terminated, notwithstanding any delay or failure of such holder in the exercise of any right or remedy with respect to the Senior Indebtedness.  For purposes hereof, “Senior Indebtedness” shall mean all present and future obligations due from the Borrower, its successors and assignees, arising in respect of borrowed money, or from any bank or other financial institution, which obligations are secured by any assets of the Borrower, including without limitation, any principal and all interest thereon and all related fees and expenses.

 

9.                                        Co-Sale Rights .  Upon the conversion of the Note entered in connection herewith, the Company hereby covenants and agrees as follows:

 

(a)  If at any time, Dr. J. Joseph Kim (the “Founding Stockholder”) desires to sell all or any of the capital stock beneficially owned by each of them respectively (the “Take-Along Shares”) to any unrelated person or entity or any affiliate of such unrelated person or entity (a “Proposed Transferee”) as part of a bona fide written offer (a “Bona Fide Offer”), the Founding Stockholders shall make effective arrangement on the terms of the Bona Fide Offer (which shall be a condition to any sale by either of the Founding Stockholders) so that the Purchaser shall have the right to sell to the Proposed Transferee, at the same price per share and other terms and conditions as involved in such sale by such selling Founding Stockholder, such number of shares of capital stock equal to the Take-Along Shares multiplied by a fraction, (i) the numerator of which is the number of shares of capital stock owned by the Purchaser, and (ii) the denominator of which is the sum of all shares of capital stock owned by the selling Founding Stockholder(s) and the Purchaser.

 

(b)  Notice of Intent to Participate .  If the Purchaser wishes to participate in any sale under this Section 9, the Purchaser shall notify in writing the selling Founding Stockholder of such intention as soon as practicable after the Purchaser’s receipt of the Notice, and in any event within 15 days after the date the Notice was given.

 

(c)    Sale to Proposed Transferee .  The selling Founding Stockholder and the Purchaser, if participating, shall sell to the Proposed Transferee all, or at the option of the Proposed Transferee, any part of the shares proposed to be sold by them at not less than the price and upon other terms and conditions, if any, not more favorable to the Proposed Transferee than those in the Bona Fide Offer; provided, however, that any purchase of less than all of such shares by the Proposed Transferee shall be made from the selling Founding Stockholder and the

 

4



 

Purchaser pro rata based upon the relative amount of the shares that each of them would otherwise be entitled to sell pursuant to Section 9(a).

 

(d)   Effect of Failure to Provide Timely Notice .  The failure of the Purchaser to provide notice within the specified period under this Section 9 shall be deemed a rejection of the respective right or option given to that Purchaser, provided, however, that such failure shall be without prejudice to such Purchaser’s rights with respect to any future sales of shares pursuant to a Bone Fide Offer.

 

10.                                  Transfer of Securities .

 

(a)                                  Prior to any sale, assignment, transfer, pledge, hypothecation or other disposition of these Securities or of any legal or beneficial interest herein (a “Transfer”), the Holder shall give written notice to the Borrower of the Holder’s intention to effect such Transfer and to comply in all other respects with the provisions of this Section 10.  Each such notice shall contain (a) a statement setting forth the intention of the Holder’s prospective transferee with respect to its retention or disposition of the Securities, and (b) unless waived by the Borrower, an opinion of counsel for the Holder, which opinion shall be reasonably acceptable to the Borrower, addressed to the Borrower as to the necessity or non-necessity for registration under the Securities Act of 1933, as amended (the “Securities Act”), and applicable state securities laws in connection with such Transfer and stating the factual and statutory bases relied upon by counsel.  The following provisions shall then apply:

 

(1)                                   If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may be effected without registration or qualification under the Securities Act and any applicable state securities laws, then the registered holder of the Securities shall be entitled to Transfer [all or any portion thereof in accordance with the intended method of disposition specified in the statement delivered by such holder to the Borrower;

 

(2)                                   If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may not be effected without registration under the Securities Act or registration or qualification under any applicable state securities laws, the registered holder of the Securities shall not be entitled to Transfer all or any portion thereof until the requisite registration or qualification is effective; and

 

(3)                                   No Transfers shall be permitted hereunder unless the transferee agrees in writing to be bound by the provisions of this Note.

 

(b)                                 Each instrument issued upon a Transfer of this Note [(and each instrument evidencing any balance of such Securities not transferred)] shall bear the legend set forth in the Purchase Agreement unless (1) in the opinion of counsel for the Holder, addressed to the Borrower, the registration of future Transfers is not required by the applicable provisions of the Securities Act and applicable state securities laws, (2) the Borrower shall have waived the requirement of such legend or (3) in the reasonable opinion of counsel to the Borrower, such

 

5



 

Transfer shall have been made in connection with an effective registration statement filed pursuant to the Securities Act or in compliance with the requirements of Rule 144 or Rule 144A (or any similar or successor rule) promulgated under the Securities Act, and in compliance with applicable state securities laws.

 

11.                                  Collection .  Should the indebtedness evidenced by this Note, or any part hereof, be collected at law or in equity or in bankruptcy, receivership or other court proceedings, or this Note placed in the hands of attorneys for collection, the Borrower agrees to pay, in addition to the balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, due and payable hereon, all costs of collection, including reasonable attorneys’ fees, incurred by the Holder in collecting or enforcing this Note.

 

12.                                  Demand .  The Borrower hereby waives demand, presentment, notice, notice of demand, notice for payment, protest and notice of dishonor.

 

13.                                  Waiver .  Holder will not be deemed to waive any of his rights under this Note unless his waiver is in writing.  No delay or omission by the Holder in exercising any of his rights will operate as a waiver of his rights.  A waiver in writing on one occasion will not be construed as a consent to or a waiver of any of the Holder’s right or remedy on any future occasion.

 

14.                                  Governing Law .  This Note shall be governed by and construed and enforced in accordance with the laws of the Commonwealth of Pennsylvania and will take effect as an instrument under seal.  Whenever possible, each provision of this Note will be interpreted in such manner as to be effective and valid under applicable law, but if any provision of this Note will be prohibited by or invalid under applicable law, such provision will be ineffective only to the extent of such prohibition or invalidity, without invalidating the remainder of such provision or the remaining provisions of this Note.

 

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IN WITNESS WHEREOF, the Company has caused this Note to be issued this        day of              .

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

1



 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE NOTE PURCHASE AGREEMENT DATED AS OF                             BETWEEN VIRAL GENOMIX, INC.  (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF THESE SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THESE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

CONVERTIBLE SUBORDINATED PROMISSORY NOTE

 

US $ ###,###

Philadelphia, Pennsylvania

 

[ENTER DATE]

 

FOR VALUE RECEIVED, the undersigned, VIRAL GENOMIX, INC., a DELAWARE corporation (the “Borrower”), hereby promises to pay to the order of [HOLDER] , an individual  (hereinafter, with any subsequent holder, the “Holder”), the principal sum of                                                    DOLLARS ($ ###,### ) (the “Principal Sum”), together with interest on the balance of the Principal Sum outstanding at a per annum rate of five percent (5%), upon the terms set forth below.  Interest shall be calculated on the basis of the actual number of days elapsed over a 360-day year and shall commence to accrue on the date hereof.

 

15.                                  Note Purchase Agreement .  This convertible subordinated promissory note (the “Note”) is being issued pursuant to the terms and conditions of the Note Purchase Agreement (the “Purchase Agreement”) dated as of the date hereof to which the Borrower and the Holder are parties.  All notices with respect to this Note shall be made in accordance with Section 5.7 of the Purchase Agreement

 

16.                                  Maturity .  Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section 7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable       months from the date hereof (the “Maturity Date”).  No payments of principal or interest are required hereunder until the Maturity Date.  The Maturity Date shall be automatically extended to another 12 months at an option of the Holder.  If the Holder desires to extend the

 

2



 

Maturity Date, the Maturity Date will be automatically renewed for another 12 months after the first       months on terms and conditions to be informed by the Holder and the Holder does not need to provide any advance notices.  However, if the Holder elects not to extend the Maturity Date, the Holder will provide a termination notice sixty (60) days prior to the Maturity Date to the Borrower.  Upon payment in full of the Principal Sum and interest payable hereunder, or upon conversion of this Note in accordance with Section 3 hereof, the Holder shall surrender this Note to the Borrower for cancellation.

 

17.                                  Conversion .  If, prior to the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, the Borrower shall issue shares of Common Stock to one or more investors, the Note shall be convertible, at the option of the Holder, by written notice to the Borrower, in whole but not in part, into that number of fully paid, validly issued and non-assessable shares of Common Stock equal to the $          price per share, as adjusted for any stock splits, reverse stock splits or stock dividends occurring after the date hereof.  Upon such conversion of this Note, the value of the Note to be converted shall include all accrued and outstanding interest, and all other fees, costs and charges, if any, due or payable under this Note on the date of conversion, and all rights of the Holder of this Note, except the right to receive such shares of Common Stock in accordance with this Section 3, shall cease and this Note shall no longer be deemed to be outstanding.  In addition, no fractional shares of Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

18.                                  Payment .  Any payment of principal, interest and all other fees, costs and charges, if any, shall be in lawful money of the United States of America by wire transfer of same day funds to the account of the Holder at such banking institution as the Holder designates or, if requested by the Holder, by certified or bank cashier’s check payable to the Holder mailed to the Holder at the address of the Holder as set forth on the records of the Borrower or such other address as shall be designated in writing by the Holder to the Borrower.

 

19.                                  Credits .  The Borrower’s payments will be credited first to any interest then due, and the remainder to the Principal Sum.  Interest will cease to accrue on any amount credited to the Principal Sum as of the date any such amount is paid.

 

20.                                  Intentionally Omitted

 

21.                                  Event of Default .  Repayment of all principal and interest under this Note will be accelerated and shall be immediately due in full in the event of any of the following:

 

(a)                                   default shall be made in the payment of the Principal Sum of this Note or any part thereof when and as the same shall become due and payable, either on the Maturity Date or at a date fixed by the parties in writing for prepayment or by acceleration or otherwise and such default continues for a period of 10 days;

 

(b)                                  default shall be made in the payment of interest on this Note when and as the same shall become due and payable and such default continues for a period of 10 days;

 

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(c)                                   the Borrower shall (i) apply for or consent to the appointment of a receiver, trustee or liquidator of the Borrower or any of its property, (ii) make a general assignment for the benefit of creditors, (iii) commence a voluntary case under the federal bankruptcy laws or file a petition or answer seeking reorganization or an arrangement with creditors to take advantage of any other bankruptcy, reorganization, insolvency, readjustment of debt, dissolution or liquidation law or statute, or file an answer admitting the material allegations of a petition filed against it in any proceeding under any such law, or (iv) take corporate action for the purpose of effecting any of the foregoing; or an order, judgment or decree shall be entered, without the application, approval or consent of the Borrower, by any court of competent jurisdiction, approving a petition seeking reorganization of the Borrower, or of all or a substantial part of the assets of the Borrower and such order, judgment or decree shall continue unstayed and in effect for a period of 60 days;

 

(d)                                  The Borrower’s failure to observe and perform any of the material terms, covenants, conditions or agreements required to be observed and performed by the Borrower under this Note or the Purchase Agreement, and such failure shall remain unremedied for 30 days after written notice shall have been provided to the Borrower by the Holder of such default; or

 

(e)                                   any representation or warranty made by the Borrower under this Note or Purchase Agreement or in any other loan document relating to this transaction, or in any certificate or writing delivered pursuant to any loan document relating to this transaction, shall be incorrect in any material respect.

 

Nothing in this Section 7 shall, in any manner, be construed to prohibit or otherwise affect the rights of the Holder to enforce payment of this Note in accordance with its terms.

 

 

22.                                  Subordination .  All principal and accrued interest on this Note shall be subordinate in right and time of payment to the payment in full of all Senior Indebtedness.  Notwithstanding anything to the contrary set forth in this Note, unless and until the Senior Indebtedness shall have been indefeasibly satisfied and paid in full in cash and all lending commitments thereunder have terminated: (a) the Holder may not demand payment of any of the Principal Sum; (b) no accrued interest on this Note shall be payable to the Holder; provided, however, that interest on this Note shall accrue in accordance with the terms of this Note; (c) the indebtedness evidenced by this Note shall be unsecured, and (d) the holder of this Note shall not, without the written consent of the holders of the Senior Indebtedness, take any action with respect to collection or enforcement or other like action hereunder or exercise any remedies the Holder may have at law or equity in respect of any amounts owing under this Note, regardless of whether an Event of Default exists pursuant to Section 7 hereof and regardless of any remedies provision contained in this Note.  The provisions of this Section 8 shall continue in effect until all amounts under the Senior Indebtedness are indefeasibly satisfied and paid in full in cash and all lending commitments of the holders thereof under such Senior Indebtedness shall have terminated, notwithstanding any delay or failure of such holder in the exercise of any right or remedy with respect to the Senior Indebtedness.  For purposes hereof, “Senior Indebtedness” shall mean all present and future obligations due from the Borrower, its successors and assignees, arising in respect of borrowed

 

4



 

money, or from any bank or other financial institution, which obligations are secured by any assets of the Borrower, including without limitation, any principal and all interest thereon and all related fees and expenses.

 

 

23.                                  Transfer of Securities .

 

(a)                                  Prior to any sale, assignment, transfer, pledge, hypothecation or other disposition of these Securities or of any legal or beneficial interest herein (a “Transfer”), the Holder shall give written notice to the Borrower of the Holder’s intention to effect such Transfer and to comply in all other respects with the provisions of this Section 10.  Each such notice shall contain (a) a statement setting forth the intention of the Holder’s prospective transferee with respect to its retention or disposition of the Securities, and (b) unless waived by the Borrower, an opinion of counsel for the Holder, which opinion shall be reasonably acceptable to the Borrower, addressed to the Borrower as to the necessity or non-necessity for registration under the Securities Act of 1933, as amended (the “Securities Act”), and applicable state securities laws in connection with such Transfer and stating the factual and statutory bases relied upon by counsel.  The following provisions shall then apply:

 

(1)                                   If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may be effected without registration or qualification under the Securities Act and any applicable state securities laws, then the registered holder of the Securities shall be entitled to Transfer [all or any portion thereof in accordance with the intended method of disposition specified in the statement delivered by such holder to the Borrower;

 

(2)                                   If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may not be effected without registration under the Securities Act or registration or qualification under any applicable state securities laws, the registered holder of the Securities shall not be entitled to Transfer all or any portion thereof until the requisite registration or qualification is effective; and

 

(3)                                   No Transfers shall be permitted hereunder unless the transferee agrees in writing to be bound by the provisions of this Note.

 

(b)                                 Each instrument issued upon a Transfer of this Note [(and each instrument evidencing any balance of such Securities not transferred)] shall bear the legend set forth in the Purchase Agreement unless (1) in the opinion of counsel for the Holder, addressed to the Borrower, the registration of future Transfers is not required by the applicable provisions of the Securities Act and applicable state securities laws, (2) the Borrower shall have waived the requirement of such legend or (3) in the reasonable opinion of counsel to the Borrower, such Transfer shall have been made in connection with an effective registration statement filed pursuant to the Securities Act or in compliance with the requirements of Rule 144 or Rule 144A (or any similar or successor rule) promulgated under the Securities Act, and in compliance with applicable state securities laws.

 

5


 

24.           Collection .  Should the indebtedness evidenced by this Note, or any part hereof, be collected at law or in equity or in bankruptcy, receivership or other court proceedings, or this Note placed in the hands of attorneys for collection, the Borrower agrees to pay, in addition to the balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, due and payable hereon, all costs of collection, including reasonable attorneys’ fees, incurred by the Holder in collecting or enforcing this Note.

 

25.           Demand .  The Borrower hereby waives demand, presentment, notice, notice of demand, notice for payment, protest and notice of dishonor.

 

26.           Waiver .  Holder will not be deemed to waive any of his rights under this Note unless his waiver is in writing.  No delay or omission by the Holder in exercising any of his rights will operate as a waiver of his rights.  A waiver in writing on one occasion will not be construed as a consent to or a waiver of any of the Holder’s right or remedy on any future occasion.

 

27.           Governing Law .  This Note shall be governed by and construed and enforced in accordance with the laws of the Commonwealth of Pennsylvania and will take effect as an instrument under seal.  Whenever possible, each provision of this Note will be interpreted in such manner as to be effective and valid under applicable law, but if any provision of this Note will be prohibited by or invalid under applicable law, such provision will be ineffective only to the extent of such prohibition or invalidity, without invalidating the remainder of such provision or the remaining provisions of this Note.

 

6



 

IN WITNESS WHEREOF, the Company has caused this Note to be issued this      day of                  .

 

 

VIRAL GENOMIX, INC.

 

(VGX PHARMACE U TICALS)

 

 

 

 

 

By:

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

1



 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE NOTE PURCHASE AGREEMENT DATED AS OF                    BETWEEN VIRAL GENOMIX, INC.  (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF THESE SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THESE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

CONVERTIBLE SUBORDINATED PROMISSORY NOTE

 

US $ ###,###

 

Blue Bell, Pennsylvania

 

 

[ENTER DATE]

 

FOR VALUE RECEIVED, the undersigned, VIRAL GENOMIX, INC., a DELAWARE corporation (the “Borrower”), hereby promises to pay to the order of [HOLDER]  (hereinafter, with any subsequent holder, the “Holder”), the principal sum of                 Dollar ($ ###,### ) (the “Principal Sum”), together with interest on the balance of the Principal Sum outstanding at a per annum rate of five percent (5%), upon the terms set forth below.  Interest shall be calculated on the basis of the actual number of days elapsed over a 360-day year and shall commence to accrue on the date hereof.

 

28.           Note Purchase Agreement .  This convertible subordinated promissory note (the “Note”) is being issued pursuant to the terms and conditions of the Note Purchase Agreement (the “Purchase Agreement”) dated as of the date hereof to which the Borrower and the Holder are parties.  All notices with respect to this Note shall be made in accordance with Section 5.7 of the Purchase Agreement

 

29.           Maturity .  Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section 7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable       months from the date hereof (the “Maturity Date”).  No payments of principal or interest are required hereunder until the Maturity Date.  The Maturity Date shall be automatically extended to another 12 months at an option of the Holder.  If the Holder desires to extend the

 

2



 

Maturity Date, the Maturity Date will be automatically renewed for another 12 months after the first       months on terms and conditions to be informed by the Holder and the Holder does not need to provide any advance notices.  However, if the Holder elects not to extend the Maturity Date, the Holder will provide a termination notice sixty (60) days prior to the Maturity Date to the Borrower.  Upon payment in full of the Principal Sum and interest payable hereunder, or upon conversion of this Note in accordance with Section 3 hereof, the Holder shall surrender this Note to the Borrower for cancellation.

 

30.           Conversion .  If, prior to the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, the Borrower shall issue shares of Common Stock to one or more investors, the Note shall be convertible, at the option of the Holder, by written notice to the Borrower, in whole but not in part, into that number of fully paid, validly issued and non-assessable shares of Common Stock equal to the $      price per share, as adjusted for any stock splits, reverse stock splits or stock dividends occurring after the date hereof.  Upon such conversion of this Note, the value of the Note to be converted shall include all accrued and outstanding interest, and all other fees, costs and charges, if any, due or payable under this Note on the date of conversion, and all rights of the Holder of this Note, except the right to receive such shares of Common Stock in accordance with this Section 3, shall cease and this Note shall no longer be deemed to be outstanding.  In addition, no fractional shares of Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

31.           Payment .  Any payment of principal, interest and all other fees, costs and charges, if any, shall be in lawful money of the United States of America by wire transfer of same day funds to the account of the Holder at such banking institution as the Holder designates or, if requested by the Holder, by certified or bank cashier’s check payable to the Holder mailed to the Holder at the address of the Holder as set forth on the records of the Borrower or such other address as shall be designated in writing by the Holder to the Borrower.

 

32.           Credits .  The Borrower’s payments will be credited first to any interest then due, and the remainder to the Principal Sum.  Interest will cease to accrue on any amount credited to the Principal Sum as of the date any such amount is paid.

 

33.           Financial Reports .  The Borrower shall furnish Holder the following financial statements prepared in accordance with generally accepted accounting principles consistently applied: (i) within thirty (30) days after the end of each calendar quarter, the Company’s unaudited or if available, audited balance sheet and statements of income and cash flows for the quarter just ended; and (ii) as soon as possible after the end of each fiscal year of the Company, a balance sheet as of the end of its fiscal year and the related statements of income and cash flows for the fiscal year then ended, unaudited or if available, audited by an independent certified public accounting firm that is acceptable to the Holder in its reasonable judgment.

 

34.           Event of Default .  Repayment of all principal and interest under this Note will be accelerated and shall be immediately due in full in the event of any of the following:

 

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(a)           default shall be made in the payment of the Principal Sum of this Note or any part thereof when and as the same shall become due and payable, either on the Maturity Date or at a date fixed by the parties in writing for prepayment or by acceleration or otherwise and such default continues for a period of 10 days;

 

(b)           default shall be made in the payment of interest on this Note when and as the same shall become due and payable and such default continues for a period of 10 days;

 

(c)           the Borrower shall (i) apply for or consent to the appointment of a receiver, trustee or liquidator of the Borrower or any of its property, (ii) make a general assignment for the benefit of creditors, (iii) commence a voluntary case under the federal bankruptcy laws or file a petition or answer seeking reorganization or an arrangement with creditors to take advantage of any other bankruptcy, reorganization, insolvency, readjustment of debt, dissolution or liquidation law or statute, or file an answer admitting the material allegations of a petition filed against it in any proceeding under any such law, or (iv) take corporate action for the purpose of effecting any of the foregoing; or an order, judgment or decree shall be entered, without the application, approval or consent of the Borrower, by any court of competent jurisdiction, approving a petition seeking reorganization of the Borrower, or of all or a substantial part of the assets of the Borrower and such order, judgment or decree shall continue unstayed and in effect for a period of 60 days;

 

(d)           The Borrower’s failure to observe and perform any of the material terms, covenants, conditions or agreements required to be observed and performed by the Borrower under this Note or the Purchase Agreement, and such failure shall remain unremedied for 30 days after written notice shall have been provided to the Borrower by the Holder of such default; or

 

(e)           any representation or warranty made by the Borrower under this Note or Purchase Agreement or in any other loan document relating to this transaction, or in any certificate or writing delivered pursuant to any loan document relating to this transaction, shall be incorrect in any material respect.

 

Nothing in this Section 7 shall, in any manner, be construed to prohibit or otherwise affect the rights of the Holder to enforce payment of this Note in accordance with its terms.

 

35.           Subordination .  All principal and accrued interest on this Note shall be subordinate in right and time of payment to the payment in full of all Senior Indebtedness.  Notwithstanding anything to the contrary set forth in this Note, unless and until the Senior Indebtedness shall have been indefeasibly satisfied and paid in full in cash and all lending commitments thereunder have terminated: (a) the Holder may not demand payment of any of the Principal Sum; (b) no accrued interest on this Note shall be payable to the Holder; provided, however, that interest on this Note shall accrue in accordance with the terms of this Note; (c) the indebtedness evidenced by this Note shall be unsecured, and (d) the holder of this Note shall not, without the written consent of the holders of the Senior Indebtedness, take any action with respect to collection or enforcement or other like action hereunder or exercise any remedies the Holder may have at law or equity in respect of any amounts owing under this Note, regardless of whether an Event of Default exists

 

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pursuant to Section 7 hereof and regardless of any remedies provision contained in this Note.  The provisions of this Section 8 shall continue in effect until all amounts under the Senior Indebtedness are indefeasibly satisfied and paid in full in cash and all lending commitments of the holders thereof under such Senior Indebtedness shall have terminated, notwithstanding any delay or failure of such holder in the exercise of any right or remedy with respect to the Senior Indebtedness.  For purposes hereof, “Senior Indebtedness” shall mean all present and future obligations due from the Borrower, its successors and assignees, arising in respect of borrowed money, or from any bank or other financial institution, which obligations are secured by any assets of the Borrower, including without limitation, any principal and all interest thereon and all related fees and expenses.

 

36.           Collateral.   The Borrower shall provide the Holder as collateral with       shares of Common Stock of VGX International, Inc. (formerly Dong-Il Fabrics Co., Ltd.) that the Borrower owns at the Closing.

 

37.           C o-Sale Rights .  Upon the conversion of the Note entered in connection herewith, the Company hereby covenants and agrees as follows:

 

(a)  If at any time, Dr. J. Joseph Kim (the “Founding Stockholder”) desires to sell all or any of the capital stock beneficially owned by each of them respectively (the “Take-Along Shares”) to any unrelated person or entity or any affiliate of such unrelated person or entity (a “Proposed Transferee”) as part of a bona fide written offer (a “Bona Fide Offer”), the Founding Stockholders shall make effective arrangement on the terms of the Bona Fide Offer (which shall be a condition to any sale by either of the Founding Stockholders) so that the Purchaser shall have the right to sell to the Proposed Transferee, at the same price per share and other terms and conditions as involved in such sale by such selling Founding Stockholder, such number of shares of capital stock equal to the Take-Along Shares multiplied by a fraction, (i) the numerator of which is the number of shares of capital stock owned by the Purchaser, and (ii) the denominator of which is the sum of all shares of capital stock owned by the selling Founding Stockholder(s) and the Purchaser.

 

(b)  Notice of Intent to Participate .  If the Purchaser wishes to participate in any sale under this Section  10, the Purchaser shall notify the selling Founding Stockholder of such intention as soon as practicable after the Purchaser’s receipt of the Notice, and in any event within 15 days after the date the Notice was given.

 

(c)  Sale to Proposed Transferee .  The selling Founding Stockholder and the Purchaser, if participating, shall sell to the Proposed Transferee all, or at the option of the Proposed Transferee, any part of the shares proposed to be sold by them at not less than the price and upon other terms and conditions, if any, not more favorable to the Proposed Transferee than those in the Bona Fide Offer; provided, however, that any purchase of less than all of such shares by the Proposed Transferee shall be made from the selling Founding Stockholder and the Purchaser pro rata based upon the relative amount of the shares that each of them would otherwise be entitled to sell pursuant to Section  10(a).

 

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(d)  Effect of Failure to Provide Timely Notice .  The failure of the Purchaser to provide notice within the specified period under this Section  10 shall be deemed a rejection of the respective right or option given to that Purchaser, provided, however, that such failure shall be without prejudice to such Purchaser’s rights with respect to any future sales of shares pursuant to a Bone Fide Offer.

 

38.           Transfer of Securities .

 

(a)          Prior to any sale, assignment, transfer, pledge, hypothecation or other disposition of these Securities or of any legal or beneficial interest herein (a “Transfer”), the Holder shall give written notice to the Borrower of the Holder’s intention to effect such Transfer and to comply in all other respects with the provisions of this Section 11.  Each such notice shall contain (a) a statement setting forth the intention of the Holder’s prospective transferee with respect to its retention or disposition of the Securities, and (b) unless waived by the Borrower, an opinion of counsel for the Holder, which opinion shall be reasonably acceptable to the Borrower, addressed to the Borrower as to the necessity or non-necessity for registration under the Securities Act of 1933, as amended (the “Securities Act”), and applicable state securities laws in connection with such Transfer and stating the factual and statutory bases relied upon by counsel.  The following provisions shall then apply:

 

(1)           If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may be effected without registration or qualification under the Securities Act and any applicable state securities laws, then the registered holder of the Securities shall be entitled to Transfer [all or any portion thereof in accordance with the intended method of disposition specified in the statement delivered by such holder to the Borrower;

 

(2)           If in the opinion of counsel for the Borrower the proposed Transfer of the Securities may not be effected without registration under the Securities Act or registration or qualification under any applicable state securities laws, the registered holder of the Securities shall not be entitled to Transfer all or any portion thereof until the requisite registration or qualification is effective; and

 

(3)           No Transfers shall be permitted hereunder unless the transferee agrees in writing to be bound by the provisions of this Note.

 

(b)          Each instrument issued upon a Transfer of this Note [(and each instrument evidencing any balance of such Securities not transferred)] shall bear the legend set forth in the Purchase Agreement unless (1) in the opinion of counsel for the Holder, addressed to the Borrower, the registration of future Transfers is not required by the applicable provisions of the Securities Act and applicable state securities laws, (2) the Borrower shall have waived the requirement of such legend or (3) in the reasonable opinion of counsel to the Borrower, such Transfer shall have been made in connection with an effective registration statement filed pursuant to the Securities Act or in compliance with the requirements of Rule 144 or Rule 144A (or any similar or successor rule) promulgated under the Securities Act, and in compliance with applicable state securities laws.

 

6



 

39.           Collection .  Should the indebtedness evidenced by this Note, or any part hereof, be collected at law or in equity or in bankruptcy, receivership or other court proceedings, or this Note placed in the hands of attorneys for collection, the Borrower agrees to pay, in addition to the balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, due and payable hereon, all costs of collection, including reasonable attorneys’ fees, incurred by the Holder in collecting or enforcing this Note.

 

40.           Demand .  The Borrower hereby waives demand, presentment, notice, notice of demand, notice for payment, protest and notice of dishonor.

 

41.           Waiver .  Holder will not be deemed to waive any of his rights under this Note unless his waiver is in writing.  No delay or omission by the Holder in exercising any of his rights will operate as a waiver of his rights.  A waiver in writing on one occasion will not be construed as a consent to or a waiver of any of the Holder’s right or remedy on any future occasion.

 

42.           Governing Law .  This Note shall be governed by and construed and enforced in accordance with the laws of the Commonwealth of Pennsylvania and will take effect as an instrument under seal.  Whenever possible, each provision of this Note will be interpreted in such manner as to be effective and valid under applicable law, but if any provision of this Note will be prohibited by or invalid under applicable law, such provision will be ineffective only to the extent of such prohibition or invalidity, without invalidating the remainder of such provision or the remaining provisions of this Note.

 

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IN WITNESS WHEREOF, the Company has caused this Note to be issued this        day of                .

 

 

VIRAL GENOMIX, INC.

 

(VGX PHARMACETUICALS)

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 




EXHIBIT 10.54

 

AMENDMENT TO THE CONVERTIBLE SUBORDINATED PROMISSORY NOTE

 

THIS AMENDMENT is made 19 th  day of January 2008 by and between VGX Pharmaceuticals , Inc. (previously D.B.A. Viral Genomix, Inc.) , a Delaware Corporation, (hereinafter called “ Borrower ”) and  DONG KOOK PHARM, CO. LTD.,  a Korea Corporation, (hereinafter called “ Holder ”).

 

WHEREAS, the Borrower executed and issued to the Holder the Convertible Subordinated Promissory Note in the amount of US $1,000,000.00 and dated December 30, 2005 (hereinafter called “ Note ” and attached hereto as “Exhibit A”); and

 

WHEREAS, the Note is made in favor of the Holder and has the Original Maturity Date of December 30, 2007; and

 

WHEREAS , the Parties desire to modify certain terms on the Note.

 

NOW, THEREFORE , for and in consideration of the mutual promises, terms and conditions set forth herein and intending to be legally bound hereby, the Parties agree as follows:

 

1.                                        The Original Maturity Date of the Note is hereby extended for 6 months for the first $500,000 and the New Maturity Date for the first $500,000 shall be June 30, 2008 . Provided, the Parties agree that the Borrower shall immediately repay the  principal of the first $500,000 to the Holder on the New Maturity Date.

 

2.                                        The Original Maturity Date of the Note is hereby extended for 12 months for the remaining $500,000 and the New Maturity Date for the remaining $500,000 shall be December 30, 2008. Provided, t he Parties agree that the Borrower shall immediately repay the principal of the remaining $500,000 to the Holder on the New Maturity Date.

 



 

3.                                        Upon execution of this Amendment, the Borrower shall pay Holder $97,392, which represents accrued interest on the Principal from the Borrowing Date to the Original Maturity Date of December 30, 2007.

 

4 .                                        At the time of paying each principal amount, the Borrower agrees to pay the interest of 5% per annum in addition to each principal amount.

 

5 .                                        The Borrower represents and warrants that the name of the Borrower has been changed from Viral Genomix, Inc. to VGX Pharmaceuticals, Inc.

 

6.                                        All other terms in the Note shall remain the same.

 

IN WITNESS THEREOF, the Parties hereto, intending to be legally bound hereby, have caused this Amendment to the Convertible Subordinated Promissory Note to be duly executed on the above date.

 

 

BORROWER:

HOLDER:

 

 

 

VGX Pharmaceuticals, Inc.

DONG KOOK PHARM, CO. LTD.

 

 

 

 

 

 

BY:

/s/ J. Joseph Kim

 

By:

/s/ Gi Beom Kwon

 

J. Joseph Kim, CEO

 

 

Gi Beom Kwon, President and CEO

 




EXHIBIT 10.55

 

AMENDMENT TO THE CONVERTIBLE SUBORDINATED PROMISSORY NOTE

 

THIS AMENDMENT is made this 11th day of  June 2008 by and between   VGX Pharmaceuticals, a Delaware Corporation , (hereinafter called “ Borrower ”) and   Huvitz Co., Ltd. ,  (hereinafter called “ Holder ”).

 

WHEREAS, the Borrower executed the Convertible Subordinated Promissory Note in the amount of $1,500,000.00 and  dated October 24, 2005 (hereinafter called “ Note ); and

 

WHEREAS, the Note is made in favor of the Holder and has the Maturity Date of October 24, 2008; and

 

WHEREAS , the parties desire to modify certain terms in the Note.

 

NOW, THEREFORE , for and in consideration of the mutual promises, terms and conditions set forth herein and intending to be legally bound hereby, the parties hereto agree as follows:

 

1.                                        The Maturity Date of the Note is extended for 6 months and shall be April 24, 2009.

 

2 .                                        The Parties acknowledge that the name of the Borrower has been changed from Viral Genomix, Inc. to VGX Pharmaceuticals.

 

3 .                                        All other terms in the Note shall remain the same.

 



 

IN WITNESS THEREOF, the parties hereto, intending to be legally bound hereby, have caused this Amendment to the Convertible Subordinated Promissory Note to be duly executed on the above date.

 

 

BORROWER:

 

HOLDER:

 

 

 

VGX Pharmaceuticals, Inc.

 

Huvitz Co., Ltd.

 

 

 

 

 

 

BY:

/s/ J. Joseph Kim

 

By:

/s/ Hyun Soo Kim

 

J. Joseph Kim, CEO

 

 

Hyun Soo Kim, Ph.D.
President and CEO

 




EXHIBIT 10.57

 

CONSENT TO ASSIGNMENT

 

WHEREAS , on [               ] , VGX Pharmaceuticals, Inc. issued a Promissory Note (the “Note”) in the principal amount of $ [               ] in favor of [               ] (the “Holder”); and

 

WHEREAS , the Holder has informed the Company that he wishes to transfer the Note to [                   ] (the “Transferee”).

 

NOW, THEREFORE , the undersigned, intending to be legally bound, hereby consents to and approves the assignment of the Note by the Holder to the Transferee.

 

IN WITNESS WHEREOF , the undersigned has executed this Consent as of December      , 2006.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

Title:

 

 




EXHIBIT 10.58

 

ALLONGE

 

Note:                      Convertible Subordinated Promissory Note dated [ ORIGINAL DATE OF NOTE] (the “Note”)

 

Borrower:               VGX Pharmaceuticals, Inc. (the “Borrower”)

 

Holder:                   [NAME OF HOLDER] (the “Holder”)

 

Principal

Sum:                       $ [PRINCIPAL]

 

THIS ALLONGE TO CONVERTIBLE SUBORDINATED PROMISSORY NOTE (this “Allonge”) is made as of June        , 2008, between the Borrower and the Holder.  Capitalized terms used but not defined herein shall have the meanings ascribed to them in the Note.

 

WHEREAS, on [ORIGINAL DATE OF NOTE] , the Borrower issued the Note to the Holder in an aggregate principal amount of $[###,###] , all which remains outstanding as of the date hereof; and

 

WHEREAS, the Borrower and the Holder now wish to amend certain provisions of the Note, as set forth herein.

 

NOW THEREFORE, in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties, intending to be legally bound, hereby agree to the following amendments to the Note:

 

1.             Section 3 of the Note titled “Conversion” shall be amended by adding a new subsection at the end of such section as follows:

 

“Notwithstanding any provision to the contrary contained herein, prior to the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued but unpaid, interest and all other fees, costs and charges, if any, at the effective time of the Merger (as defined below), 100% of the Principal Sum of $ 2,000,000 outstanding immediately prior to such effective time shall automatically be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock (as defined below) at a conversion price per share equal average of the closing sales prices for one share of Acquiror Common Stock as reported on the exchange for the ten consecutive Trading Days ending on (and including) the Trading Day prior to public announcement of the execution of the Definitive Merger Agreement (rounded up to the nearest whole cent). For clarity, if announcement of the execution of the Definitive Merger Agreement is made after the close of trading on the Exchange, the calculation of the Execution Share Value shall include the closing sales price for one

 



 

share of Acquiror Common Stock as reported on the day of announcement.   For purposes of this Note, the “Merger” shall mean the merger transaction involving the Borrower and a third party public company (“Acquiror”) pursuant to an agreement and plan of merger that is currently in the process of being negotiated by the Borrower and Acquiror, as a result of which the Borrower will [ become a wholly owned subsidiary of ] Acquiror and the holders of securities of the Borrower will receive shares of Acquiror Common Stock.  For purposes of this Note, “Acquiror Common Stock” shall mean the common stock of the Acquiror.  For purposes of this Note, “Trading Day” shall mean a day on which trades occur on the exchange on which Acquiror Common Stock is traded and for which a last sale price is reported for Acquiror Common Stock.  Upon such conversion of the Principal Sum outstanding immediately prior to the effective time of the Merger pursuant to this subsection, all rights of the Holder of this Note, except the right to receive such shares of Acquiror Common Stock as provided in and in accordance with this subsection, shall cease and this Note shall no longer be deemed to be outstanding.  In addition, no fractional shares of Acquiror Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Acquiror Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

Holder hereby agrees that such Holder shall not sell or otherwise transfer or dispose Securities of the Company held by such Holder for a period not to exceed ninety (90) days following the effective date of the Close of the Merger for the first 50% of shares acquired through conversion. Holder shall not sell or otherwise transfer or dispose Securities of the Company held by such Holder for a period not to exceed one hundred eighty (180) days following the effective date of the Close of the Merger for the remaining 50% of shares acquired through conversion.

 

This Allonge is intended to be and shall remain attached to, and shall constitute an integral part of, the Note from and after the date hereof.  Except as modified hereby, all of the terms and provisions of the Note are hereby ratified and confirmed and, as amended by this Allonge, shall continue in full force and effect.

 

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Intending to be legally bound hereby, each of the undersigned have duly executed this Allonge as of the        day of                           , 2008.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 J. Joseph Kim, Ph.D.

 

 President and Chief Executive Officer

 

 

 

 

 

HOLDER

 

 

 

 

 

By:

 

 

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EXHIBIT 10.59

 

THIS NOTE HAS BEEN ACQUIRED FOR INVESTMENT AND HAS NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THIS NOTE IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE NOTE PURCHASE AGREEMENT DATED AS OF               BETWEEN VGX PHARMACEUTICALS, INC.  (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF THIS NOTE SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS NOTE TO THE SECRETARY OF THE COMPANY.  NEITHER THIS NOTE NOR ANY INTEREST HEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

AMENDED AND RESTATED SUBORDINATED PROMISSORY NOTE

 

US $ [PRINCIPAL]

 

Blue Bell, Pennsylvania

 

 

Original Issuance Date:            

 

 

Date of Amendment and Restatement: November      , 2008

 

FOR VALUE RECEIVED, the undersigned, VGX PHARMACEUTICALS, INC., a Delaware corporation (the “Borrower”), hereby promises to pay to the order of               , (hereinafter, with any subsequent holder, the “Holder”), the principal sum of                      ($ ###,### ) (the “Principal Sum”), together with interest on the balance of the Principal Sum outstanding at a per annum rate of five percent (5%), upon the terms set forth below.  Interest shall be calculated on the basis of the actual number of days elapsed over a 360-day year and shall commence to accrue on the date hereof.

 

1.              Note Purchase Agreement .  This amended and restated subordinated promissory note (this “Note”) amends and restates, and supersedes in its entirety, that certain convertible subordinated promissory note that was issued by the Borrower to the Holder on                (the “Original Note”) pursuant to the terms and conditions of the Note Purchase Agreement (the “Purchase Agreement”) dated as of                 to which the Borrower and the Holder are parties.  All notices with respect to this Note shall be made in accordance with Section 5.7 of the Purchase Agreement

 

2.              Maturity .  Unless this Note has been repaid pursuant to Section 6 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable on the earliest to occur of :

 



 

(i)  [Maturity Date] or (ii) the date of the closing of the transactions contemplated by that certain Agreement and Plan of Merger dated as of July 7, 2008 among the Company, Inovio Biomedical Corporation and Inovio Acquisition Corporation, as the same may be amended and/or restated from time to time (the “Maturity Date”).  No payments of principal or interest are required hereunder until the Maturity Date.  Upon payment in full of the Principal Sum and interest payable hereunder, the Holder shall surrender this Note to the Borrower for cancellation.

 

3.              Payment .  Any payment of principal, interest and all other fees, costs and charges, if any, shall be in lawful money of the United States of America by wire transfer of same day funds to the account of the Holder at such banking institution as the Holder designates or, if requested by the Holder, by certified or bank cashier’s check payable to the Holder mailed to the Holder at the address of the Holder as set forth on the records of the Borrower or such other address as shall be designated in writing by the Holder to the Borrower.

 

4.              Credits .  The Borrower’s payments will be credited first to any interest then due, and the remainder to the Principal Sum.  Interest will cease to accrue on any amount credited to the Principal Sum as of the date any such amount is paid.

 

5.              Financial Reports .  The Borrower shall furnish Holder the following financial statements prepared in accordance with generally accepted accounting principles consistently applied: (i) within thirty (30) days after the end of each calendar quarter, the Company’s unaudited or if available, audited balance sheet and statements of income and cash flows for the quarter just ended; and (ii) as soon as possible after the end of each fiscal year of the Company, a balance sheet as of the end of its fiscal year and the related statements of income and cash flows for the fiscal year then ended, unaudited or if available, audited by an independent certified public accounting firm; provided, however, that, in the event that the Borrower or any of its successors or parent entities becomes subject to the financial statement delivery requirements of the Securities and Exchange Commission, all such financial statements shall be deliverable by the Borrower promptly after they are required to be filed with the Securities and Exchange Commission (and not before such date), notwithstanding anything to the contrary contained in this Section 5.

 

6.              Event of Default .  Repayment of all principal and interest under this Note will be accelerated and shall be immediately due in full in the event of any of the following:

 

(a)            default shall be made in the payment of the Principal Sum of this Note or any part thereof when and as the same shall become due and payable, either on the Maturity Date or at a date fixed by the parties in writing for prepayment or by acceleration or otherwise and such default continues for a period of 10 days;

 

(b)            default shall be made in the payment of interest on this Note when and as the same shall become due and payable and such default continues for a period of 10 days;

 

(c)            the Borrower shall (i) apply for or consent to the appointment of a receiver, trustee or liquidator of the Borrower or any of its property, (ii) make a general assignment for the benefit of creditors, (iii) commence a voluntary case under the federal bankruptcy laws or file a petition or answer seeking reorganization or an arrangement with

 

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creditors to take advantage of any other bankruptcy, reorganization, insolvency, readjustment of debt, dissolution or liquidation law or statute, or file an answer admitting the material allegations of a petition filed against it in any proceeding under any such law, or (iv) take corporate action for the purpose of effecting any of the foregoing; or an order, judgment or decree shall be entered, without the application, approval or consent of the Borrower, by any court of competent jurisdiction, approving a petition seeking reorganization of the Borrower, or of all or a substantial part of the assets of the Borrower and such order, judgment or decree shall continue unstayed and in effect for a period of 60 days;

 

(d)            The Borrower’s failure to observe and perform any of the material terms, covenants, conditions or agreements required to be observed and performed by the Borrower under this Note or the Purchase Agreement, and such failure shall remain unremedied for 30 days after written notice shall have been provided to the Borrower by the Holder of such default; or

 

(e)            Any representation or warranty made by the Borrower under this Note or Purchase Agreement or in any other loan document relating to this transaction, or in any certificate or writing delivered pursuant to any loan document relating to this transaction, shall be incorrect in any material respect.

 

Nothing in this Section 7 shall, in any manner, be construed to prohibit or otherwise affect the rights of the Holder to enforce payment of this Note in accordance with its terms.

 

7.              Subordination .  All principal and accrued interest on this Note shall be subordinate in right and time of payment to the payment in full of all Senior Indebtedness.  Notwithstanding anything to the contrary set forth in this Note, unless and until the Senior Indebtedness shall have been indefeasibly satisfied and paid in full in cash and all lending commitments thereunder have terminated: (a) the Holder may not demand payment of any of the Principal Sum; (b) no accrued interest on this Note shall be payable to the Holder; provided, however, that interest on this Note shall accrue in accordance with the terms of this Note; (c) the indebtedness evidenced by this Note shall be unsecured; and (d) the holder of this Note shall not, without the written consent of the holders of the Senior Indebtedness, take any action with respect to collection or enforcement or other like action hereunder or exercise any remedies the Holder may have at law or equity in respect of any amounts owing under this Note, regardless of whether an Event of Default exists pursuant to Section 7 hereof and regardless of any remedies provision contained in this Note.  The provisions of this Section 8 shall continue in effect until all amounts under the Senior Indebtedness are indefeasibly satisfied and paid in full in cash and all lending commitments of the holders thereof under such Senior Indebtedness shall have terminated, notwithstanding any delay or failure of such holder in the exercise of any right or remedy with respect to the Senior Indebtedness.  For purposes hereof, “Senior Indebtedness” shall mean all present and future obligations due from the Borrower, its successors and assignees, arising in respect of borrowed money, or from any bank or other financial institution, which obligations are secured by any assets of the Borrower, including without limitation, any principal and all interest thereon and all related fees and expenses.

 

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8.              Transfer of Note .

 

(a)            Prior to any sale, assignment, transfer, pledge, hypothecation or other disposition of this Note or of any legal or beneficial interest herein (a “Transfer”), the Holder shall give written notice to the Borrower of the Holder’s intention to effect such Transfer and to comply in all other respects with the provisions of this Section 8.  Each such notice shall contain (a) a statement setting forth the intention of the Holder’s prospective transferee with respect to its retention or disposition of this Note, and (b) unless waived by the Borrower, an opinion of counsel for the Holder, which opinion shall be reasonably acceptable to the Borrower, addressed to the Borrower as to the necessity or non-necessity for registration under the Securities Act of 1933, as amended (the “Securities Act”), and applicable state securities laws in connection with such Transfer and stating the factual and statutory bases relied upon by counsel.  The following provisions shall then apply:

 

(1)            If in the opinion of counsel for the Borrower the proposed Transfer of this Note may be effected without registration or qualification under the Securities Act and any applicable state securities laws, then the registered holder of this Note in accordance with the intended method of disposition specified in the statement delivered by such holder to the Borrower;

 

(2)            If in the opinion of counsel for the Borrower the proposed Transfer of this Note may not be effected without registration under the Securities Act or registration or qualification under any applicable state securities laws, the registered holder of this Note shall not be entitled to Transfer all or any portion thereof until the requisite registration or qualification is effective; and

 

(3)            No Transfers shall be permitted hereunder unless the transferee agrees in writing to be bound by the provisions of this Note.

 

(b)            Each instrument issued upon a Transfer of this Note shall bear the legend set forth in the Purchase Agreement unless (1) in the opinion of counsel for the Holder, addressed to the Borrower, the registration of future Transfers is not required by the applicable provisions of the Securities Act and applicable state securities laws, (2) the Borrower shall have waived the requirement of such legend or (3) in the reasonable opinion of counsel to the Borrower, such Transfer shall have been made in connection with an effective registration statement filed pursuant to the Securities Act or in compliance with the requirements of Rule 144 or Rule 144A (or any similar or successor rule) promulgated under the Securities Act, and in compliance with applicable state securities laws.

 

9.              Collection .  Should the indebtedness evidenced by this Note, or any part hereof, be collected at law or in equity or in bankruptcy, receivership or other court proceedings, or this Note placed in the hands of attorneys for collection, the Borrower agrees to pay, in addition to the balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, due and payable hereon, all costs of collection, including reasonable attorneys’ fees, incurred by the Holder in collecting or enforcing this Note.

 

10.            Demand .  The Borrower hereby waives demand, presentment, notice, notice of demand, notice for payment, protest and notice of dishonor.

 

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11.            Waiver .  Holder will not be deemed to waive any of his rights under this Note unless his waiver is in writing.  No delay or omission by the Holder in exercising any of his rights will operate as a waiver of his rights.  A waiver in writing on one occasion will not be construed as a consent to or a waiver of any of the Holder’s right or remedy on any future occasion.

 

12.            Governing Law .  This Note shall be governed by and construed and enforced in accordance with the laws of the Commonwealth of Pennsylvania and will take effect as an instrument under seal.  Whenever possible, each provision of this Note will be interpreted in such manner as to be effective and valid under applicable law, but if any provision of this Note will be prohibited by or invalid under applicable law, such provision will be ineffective only to the extent of such prohibition or invalidity, without invalidating the remainder of such provision or the remaining provisions of this Note.

 

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IN WITNESS WHEREOF, the Company has caused this Note to be issued this      day of November, 2008.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

The Holder consents to the amendment and restatement of the Original Note effected by this Note.

 

 

 

 

 

 

 

 

Name of Holder (please print)

 

 

 

 

 

 

 

 

Signature of Holder

 

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EXHIBIT 10.62

 

VIRAL GENOMIX, INC.

 

EQUITY COMPENSATION PLAN

 

The purpose of the Viral Genomix, Inc. Equity Compensation Plan (the “Plan”) is to provide (i) designated employees of Viral Genomix, Inc. (the “Company”) and its subsidiaries, (ii) certain consultants and advisors who perform services for the Company or its subsidiaries and (iii) non-employee members of the Board of Directors of the Company (the “Board”) with the opportunity to receive grants of incentive stock options, nonqualified stock options, and stock awards.  The Company believes that the Plan will encourage the participants to contribute materially to the growth of the Company, thereby benefiting the Company’s stockholders, and will align the economic interests of the participants with those of the stockholders.

 

1.                                        Administration

 

(a)                                   Committee .  The Plan shall be administered and interpreted by the Board or by a committee or individual appointed by the Board (the “Committee”).  After an initial public offering of the Company’s stock as described in Section 18(b) (a “Public Offering”), the Plan shall be administered by a Committee, which may consist of two or more persons who are “outside directors” as defined under section 162(m) of the Internal Revenue Code of 1986, as amended (the “Code”), and related Treasury regulations and “non-employee directors” as defined under Rule 16b-3 under the Securities Exchange Act of 1934, as amended (the “Exchange Act”).  However, the Board may ratify or approve any grants as it deems appropriate.  If the Board or an individual administers the Plan, references in the Plan to the “Committee” shall be deemed to refer to the Board or individual.

 

(b)                                  Committee Authority .  The Committee shall have the sole authority to (i) determine the individuals to whom grants shall be made under the Plan, (ii) determine the type, size and terms of the grants to be made to each such individual, (iii) determine the time when the grants will be made and the duration of any applicable exercise or restriction period, including the criteria for exercisability and the acceleration of exercisability, (iv) amend the terms of any previously issued grant, and (v) deal with any other matters arising under the Plan.

 

(c)                                   Committee Determinations .  The Committee shall have full power and authority to administer and interpret the Plan, to make factual determinations and to adopt or amend such rules, regulations, agreements and instruments for implementing the Plan and for the conduct of its business as it deems necessary or advisable, in its sole discretion.  The Committee’s interpretations of the Plan and all determinations made by the Committee pursuant to the powers vested in it hereunder shall be conclusive and binding on all persons having any interest in the Plan or in any awards granted hereunder.  All powers of the Committee shall be executed in its sole discretion, in the best interest of the Company, not as a fiduciary, and in keeping with the objectives of the Plan and need not be uniform as to similarly situated individuals.

 



 

2.                                        Grants

 

Awards under the Plan may consist of grants of incentive stock options as described in Section 5 (“Incentive Stock Options”), nonqualified stock options as described in Section 5 (“Nonqualified Stock Options”) (Incentive Stock Options and Nonqualified Stock Options are collectively referred to as “Options”), and stock awards as described in Section 6 (“Stock Awards”) (hereinafter collectively referred to as “Grants”).  All Grants shall be subject to the terms and conditions set forth herein and to such other terms and conditions consistent with this Plan as the Committee deems appropriate and as are specified in writing by the Committee to the individual in a grant instrument or an amendment to the grant instrument (the “Grant Instrument”).  The Committee shall approve the form and provisions of each Grant Instrument.  Grants under a particular Section of the Plan need not be uniform as among the grantees.

 

3.                                        Shares Subject to the Plan

 

(a)                                   Shares Authorized .  Subject to adjustment as described below, the aggregate number of shares of common stock of the Company (“Company Stock”) that may be issued or transferred under the Plan is 11,060,000 shares.  After a Public Offering, the maximum aggregate number of shares of Company Stock that shall be subject to Grants made under the Plan to any individual during any calendar year shall be 500,000 shares, subject to adjustment as described below.  The shares may be authorized but unissued shares of Company Stock or reacquired shares of Company Stock, including shares purchased by the Company on the open market for purposes of the Plan.  If and to the extent Options granted under the Plan terminate, expire, or are canceled, forfeited, exchanged or surrendered without having been exercised or if any Stock Awards are forfeited, the shares subject to such Grants shall again be available for purposes of the Plan.

 

(b)                                  Adjustments .  If there is any change in the number or kind of shares of Company Stock outstanding (i) by reason of a stock dividend, spin-off, recapitalization, stock split, or combination or exchange of shares, (ii) by reason of a merger, reorganization or consolidation, (iii) by reason of a reclassification or change in par value, or (iv) by reason of any other extraordinary or unusual event affecting the outstanding Company Stock as a class without the Company’s receipt of consideration, or if the value of outstanding shares of Company Stock is substantially reduced as a result of a spin-off or the Company’s payment of an extraordinary dividend or distribution, the maximum number of shares of Company Stock available for Grants, the maximum number of shares of Company Stock that any individual participating in the Plan may be granted in any year, the number of shares covered by outstanding Grants, the kind of shares issued under the Plan, and the price per share or the applicable market value of such Grants may be appropriately adjusted by the Committee to reflect any increase or decrease in the number of, or change in the kind or value of, issued shares of Company Stock to preclude, to the extent practicable, the enlargement or dilution of rights and benefits under such Grants; provided, however, that any fractional shares resulting from such adjustment shall be eliminated.  Any adjustments determined by the Committee shall be final, binding and conclusive.

 

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4.                                        Eligibility for Participation

 

(a)                                   Eligible Persons .  All employees of the Company and its subsidiaries (“Employees”), including Employees who are officers or members of the Board, and members of the Board who are not Employees (“Non-Employee Directors”) shall be eligible to participate in the Plan.  Consultants and advisors who perform services for the Company or any of its subsidiaries (“Key Advisors”) shall be eligible to participate in the Plan if the Key Advisors render bona fide services to the Company or its subsidiaries, the services are not in connection with the offer and sale of securities in a capital-raising transaction and the Key Advisors do not directly or indirectly promote or maintain a market for the Company’s securities.

 

(b)                                  Selection of Grantees .  The Committee shall select the Employees, Non-Employee Directors and Key Advisors to receive Grants and shall determine the number of shares of Company Stock subject to a particular Grant in such manner as the Committee determines.  Employees, Key Advisors and Non-Employee Directors who receive Grants under this Plan shall hereinafter be referred to as “Grantees.”

 

5.                                        Granting of Options

 

(a)                                   Number of Shares .  The Committee shall determine the number of shares of Company Stock that will be subject to each Grant of Options to Employees, Non-Employee Directors and Key Advisors.

 

(b)                                  Type of Option and Price .

 

(i)                                      The Committee may grant Incentive Stock Options that are intended to qualify as “incentive stock options” within the meaning of section 422 of the Code or Nonqualified Stock Options that are not intended to qualify or any combination of Incentive Stock Options and Nonqualified Stock Options, all in accordance with the terms and conditions set forth herein.  Incentive Stock Options may be granted only to Employees.  Nonqualified Stock Options may be granted to Employees, Non-Employee Directors and Key Advisors.

 

(ii)                                   The purchase price (the “Exercise Price”) of Company Stock subject to an Option shall be determined by the Committee and may be equal to, greater than, or less than the Fair Market Value (as defined below) of a share of Company Stock on the date the Option is granted; provided, however, that (x) the Exercise Price of an Incentive Stock Option shall be equal to, or greater than, the Fair Market Value of a share of Company Stock on the date the Incentive Stock Option is granted and (y) an Incentive Stock Option may not be granted to an Employee who, at the time of grant, owns stock possessing more than 10% of the total combined voting power of all classes of stock of the Company or any parent or subsidiary of the Company, unless the Exercise Price per share is not less than 110% of the Fair Market Value of Company Stock on the date of grant.

 

(iii)                                If the Company Stock is publicly traded, then the Fair Market Value per share shall be determined as follows: (x) if the principal trading market for the Company Stock is a national securities exchange or the Nasdaq National Market, the last reported sale price thereof on the relevant date or (if there were no trades on that date) the latest preceding date upon which a sale was reported, or (y) if the Company Stock is not principally traded on such exchange or

 

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market, the mean between the last reported “bid” and “asked” prices of Company Stock on the relevant date, as reported on Nasdaq or, if not so reported, as reported by the National Daily Quotation Bureau, Inc. or as reported in a customary financial reporting service, as applicable and as the Committee determines.  If the Company Stock is not publicly traded or, if publicly traded, is not subject to reported transactions or “bid” or “asked” quotations as set forth above, the Fair Market Value per share shall be as determined by the Committee.

 

(c)                                   Option Term .  The Committee shall determine the term of each Option.  The term of any Option shall not exceed 10 years from the date of grant.  However, an Incentive Stock Option that is granted to an Employee who, at the time of grant, owns stock possessing more than 10% of the total combined voting power of all classes of stock of the Company, or any parent or subsidiary of the Company, may not have a term that exceeds five years from the date of grant.

 

(d)                                  Exercisability of Options .

 

(i)                                      Options shall become exercisable in accordance with such terms and conditions, consistent with the Plan, as may be determined by the Committee and specified in the Grant Instrument.  The Committee may accelerate the exercisability of any or all outstanding Options at any time for any reason.

 

(ii)                                   The Committee may provide in a Grant Instrument that the Grantee may elect to exercise part or all of an Option before it otherwise has become exercisable.  Any shares so purchased shall be restricted shares and shall be subject to a repurchase right in favor of the Company during a specified restriction period, with the repurchase price equal to the Exercise Price, or such other restrictions as the Committee deems appropriate.

 

(e)                                   Grants to Non-Exempt Employees .  Notwithstanding the foregoing, Options granted to persons who are non-exempt employees under the Fair Labor Standards Act of 1938, as amended, shall have an Exercise Price not less than 85% of the Fair Market Value of the Company Stock on the date of grant, and may not be exercisable for at least six months after the date of grant (except that such Options may become exercisable, as determined by the Committee, upon the Grantee’s death, Disability or retirement, or upon a Change in Control or other circumstances permitted by applicable regulations).

 

(f)                                     Termination of Employment, Disability or Death .

 

(i)                                      Except as provided below, an Option may only be exercised while the Grantee is employed by, or providing service to, the Company as an Employee, Key Advisor or member of the Board.  In the event that a Grantee ceases to be employed by, or provide service to, the Company for any reason other than Disability, death, or termination for Cause (as defined below), any Option which is otherwise exercisable by the Grantee shall terminate unless exercised within 90 days after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options that are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

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(ii)                                   In the event the Grantee ceases to be employed by, or provide service to, the Company on account of a termination for Cause by the Company (as defined below), any Option held by the Grantee shall terminate as of the date the Grantee ceases to be employed by, or provide service to, the Company.  In addition, notwithstanding any other provisions of this Section 5, if the Committee determines that the Grantee has engaged in conduct that constitutes Cause at any time while the Grantee is employed by, or providing service to, the Company or after the Grantee’s termination of employment or service, any Option held by the Grantee shall immediately terminate and the Grantee shall automatically forfeit all shares underlying any exercised portion of an Option for which the Company has not yet delivered the share certificates, upon refund by the Company of the Exercise Price paid by the Grantee for such shares.  Upon any exercise of an Option, the Company may withhold delivery of share certificates pending resolution of an inquiry that could lead to a finding resulting in a forfeiture.

 

(iii)                                In the event the Grantee ceases to be employed by, or provide service to, the Company because the Grantee is Disabled, any Option which is otherwise exercisable by the Grantee shall terminate unless exercised within one year after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options which are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

(iv)                               If the Grantee dies while employed by, or providing service to, the Company or within 90 days after the date on which the Grantee ceases to be employed or provide service on account of a termination specified in Section 5(f)(i) above (or within such other period of time as may be specified by the Committee), any Option that is otherwise exercisable by the Grantee shall terminate unless exercised within one year after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options that are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

(v)                                  For purposes of this Section 5(f) and Section 6:

 

(1)                                   “Company” shall mean the Company and its parent and subsidiary corporations or other entities, as determined by the Committee.

 

(2)                                   “Employed by, or provide service to, the Company” shall mean employment or service as an Employee, Key Advisor or member of the Board (so that, for purposes of exercising Options and satisfying conditions with respect to Stock Awards, a Grantee shall not be considered to have terminated employment or service until the Grantee ceases to be an Employee, Key Advisor and member of the Board), unless the Committee determines otherwise.

 

(3)                                   “Disability” shall mean a Grantee’s becoming disabled within the meaning of section 22(e)(3) of the Code.

 

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(4)                                   “Cause” shall mean, except to the extent specified otherwise by the Committee, a finding by the Committee of the following:  (i) conviction of Grantee of any felony; (ii) participation by Grantee in any fraud or act of dishonesty against the Company; (iii) material violation by Grantee of (a) any contract between the Company and Grantee or (b) any statutory duty of Grantee to the Company; (iv) conduct of Grantee that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Grantee’s gross unfitness to serve in the capacity as an employee, director or consultant; or (v) the continued, willful refusal or failure by Grantee to perform any material duties reasonably requested by the Board; provided, however, that in the case of conduct described in clauses (iii), (iv) and (v) hereof, such conduct shall not constitute “Cause” unless:  (a) the Board shall have given Grantee written notice setting forth with specificity (1) the conduct deemed to constitute “Cause,” (2) reasonable action that would remedy the objectionable conduct and (3) a reasonable time (not less than 10 days) within which Grantee may take such remedial action; and (b) Grantee shall not have taken such specified remedial action within such specified reasonable time.

 

(g)                                  Exercise of Options .  A Grantee may exercise an Option that has become exercisable, in whole or in part, by delivering a notice of exercise to the Company with payment of the Exercise Price.  The Grantee shall pay the Exercise Price for an Option as specified by the Committee (i) in cash, (ii) with the approval of the Committee, by delivering shares of Company Stock owned by the Grantee (including Company Stock acquired in connection with the exercise of an Option, subject to such restrictions as the Committee deems appropriate) and having a Fair Market Value on the date of exercise equal to the Exercise Price or by attestation (on a form prescribed by the Committee) to ownership of shares of Company Stock having a Fair Market Value on the date of exercise equal to the Exercise Price, (iii) after a Public Offering, payment through a broker in accordance with procedures permitted by Regulation T of the Federal Reserve Board, or (iv) by such other method as the Committee may approve.  The Committee may authorize loans by the Company to Grantees in connection with the exercise of an Option, upon such terms and conditions as the Committee, in its sole discretion, deems appropriate.  Shares of Company Stock used to exercise an Option shall have been held by the Grantee for the requisite period of time to avoid adverse accounting consequences to the Company with respect to the Option.  The Grantee shall pay the Exercise Price and the amount of any withholding tax due (pursuant to Section 7) at the time of exercise.

 

(h)                                  Limits on Incentive Stock Options .  Each Incentive Stock Option shall provide that, if the aggregate Fair Market Value of the stock on the date of the grant with respect to which Incentive Stock Options are exercisable for the first time by a Grantee during any calendar year, under the Plan or any other stock option plan of the Company or a parent or subsidiary, exceeds $100,000, then the Option, as to the excess, shall be treated as a Nonqualified Stock Option.  An Incentive Stock Option shall not be granted to any person who is not an Employee of the Company or a parent or subsidiary (within the meaning of section 424(f) of the Code).

 

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6.                                        Stock Awards

 

The Committee may issue or transfer shares of Company Stock to an Employee, Non-Employee Director or Key Advisor under a Stock Award, upon such terms as the Committee deems appropriate.  The following provisions are applicable to Stock Awards:

 

(a)                                   General Requirements .  Shares of Company Stock issued or transferred pursuant to Stock Awards may be issued or transferred for consideration or for no consideration, and subject to restrictions or no restrictions, as determined by the Committee.  The Committee may establish conditions under which restrictions on Stock Awards shall lapse over a period of time or according to such other criteria as the Committee deems appropriate.  The period of time during which the Stock Awards will remain subject to restrictions will be designated in the Grant Instrument as the “Restriction Period.”

 

(b)                                  Number of Shares .  The Committee shall determine the number of shares of Company Stock to be issued or transferred pursuant to a Stock Award and the restrictions applicable to such shares.

 

(c)                                   Requirement of Employment or Service .  If the Grantee ceases to be employed by, or provide service to, the Company (as defined in Section 5(f)) during a period designated in the Grant Instrument as the Restriction Period, or if other specified conditions are not met, the Stock Award shall terminate as to all shares covered by the Grant as to which the restrictions have not lapsed, and those shares of Company Stock must be immediately returned to the Company.  The Committee may, however, provide for complete or partial exceptions to this requirement as it deems appropriate.

 

(d)                                  Restrictions on Transfer and Legend on Stock Certificate .  During the Restriction Period, a Grantee may not sell, assign, transfer, pledge or otherwise dispose of the shares of a Stock Award except to a Successor Grantee under Section 8(a).  Each certificate for a share of a Stock Award shall contain a legend giving appropriate notice of the restrictions in the Grant.  The Grantee shall be entitled to have the legend removed from the stock certificate covering the shares subject to restrictions when all restrictions on such shares have lapsed.  The Committee may determine that the Company will not issue certificates for Stock Awards until all restrictions on such shares have lapsed, or that the Company will retain possession of certificates for shares of Stock Awards until all restrictions on such shares have lapsed.

 

(e)                                   Right to Vote and to Receive Dividends .  Unless the Committee determines otherwise, during the Restriction Period, the Grantee shall have the right to vote shares of Stock Awards and to receive any dividends or other distributions paid on such shares, subject to any restrictions deemed appropriate by the Committee.

 

(f)                                     Lapse of Restrictions .  All restrictions imposed on Stock Awards shall lapse upon the expiration of the applicable Restriction Period and the satisfaction of all conditions imposed by the Committee.  The Committee may determine, as to any or all Stock Awards, that the restrictions shall lapse without regard to any Restriction Period.

 

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7.                                        Withholding of Taxes

 

(a)                                   Required Withholding .  All Grants under the Plan shall be subject to applicable federal (including FICA), state and local tax withholding requirements.  The Company may require that the Grantee or other person receiving or exercising Grants pay to the Company the amount of any federal, state or local taxes that the Company is required to withhold with respect to such Grants, or the Company may deduct from other wages paid by the Company the amount of any withholding taxes due with respect to such Grants.

 

(b)                                  Election to Withhold Shares .  If the Committee so permits, a Grantee may elect to satisfy the Company’s income tax withholding obligation with respect to Options or Stock Awards paid in Company Stock by having shares withheld up to an amount that does not exceed the Grantee’s minimum applicable withholding tax rate for federal (including FICA), state and local tax liabilities.  The election must be in a form and manner prescribed by the Committee and may be subject to the prior approval of the Committee.

 

8.                                        Transferability of Grants

 

(a)                                   Nontransferability of Grants .  Except as provided below, only the Grantee may exercise rights under a Grant during the Grantee’s lifetime.  A Grantee may not transfer those rights except (i) by will or by the laws of descent and distribution or (ii) with respect to Grants other than Incentive Stock Options, if permitted in any specific case by the Committee, pursuant to a domestic relations order or otherwise as permitted by the Committee.  When a Grantee dies, the personal representative or other person entitled to succeed to the rights of the Grantee (“Successor Grantee”) may exercise such rights.  A Successor Grantee must furnish proof satisfactory to the Company of his or her right to receive the Grant under the Grantee’s will or under the applicable laws of descent and distribution.

 

(b)                                  Transfer of Nonqualified Stock Options .  Notwithstanding the foregoing, the Committee may provide, in a Grant Instrument, that a Grantee may transfer Nonqualified Stock Options to family members, or one or more trusts or other entities for the benefit of or owned by family members, consistent with the applicable securities laws, according to such terms as the Committee may determine; provided that the Grantee receives no consideration for the transfer of an Option and the transferred Option shall continue to be subject to the same terms and conditions as were applicable to the Option immediately before the transfer.

 

9.                                        Right of First Refusal; Repurchase Right

 

(a)                                   Offer .  Prior to a Public Offering, if at any time an individual desires to sell, encumber, or otherwise dispose of shares of Company Stock that were issued or distributed to him or her under this Plan and that are transferable, the individual may do so only pursuant to a bona fide written offer, and the individual shall first offer the shares to the Company by giving the Company written notice disclosing: (i) the name of the proposed transferee of the Company Stock; (ii) the certificate number and number of shares of Company Stock proposed to be transferred or encumbered; (iii) the proposed price; (iv) all other terms of the proposed transfer; and (v) a written copy of the proposed offer.  Within 60 days after receipt of such notice, the Company shall have the option to purchase all or part of such Company Stock at the then current Fair Market Value (as defined in Section 5(b)) and may pay such price in installments over a period not to exceed four years, at the discretion of the Committee.

 

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(b)                                  Sale .  In the event the Company (or a stockholder, as described below) does not exercise the option to purchase Company Stock, as provided above, the individual shall have the right to sell, encumber, or otherwise dispose of the shares of Company Stock described in Subsection (a) on the terms of the transfer set forth in the written notice to the Company, provided such transfer is effected within 15 days after the expiration of the option period.  If the transfer is not effected within such period, the Company must again be given an option to purchase, as provided above.

 

(c)                                   Assignment of Rights .  The Board, in its sole discretion, may waive the Company’s right of first refusal and repurchase right under this Section 9.  If the Company’s right of first refusal or repurchase right is so waived, the Board may, in its sole discretion, assign such right to the remaining stockholders of the Company in the same proportion that each stockholder’s stock ownership bears to the stock ownership of all the stockholders of the Company, as determined by the Board.  To the extent that a stockholder has been given such right and does not purchase his or her allotment, the other stockholders shall have the right to purchase such allotment on the same basis.

 

(d)                                  Purchase by the Company .  Prior to a Public Offering, if a Grantee ceases to be employed by, or provide service to, the Company, the Company shall have the right to purchase all or part of any Company Stock issued or distributed to him or her under this Plan at its then current Fair Market Value (as defined in Section 5(b)) (or at such other price as may be established in the Grant Instrument); provided, however, that such repurchase shall be made in accordance with applicable accounting rules to avoid adverse accounting treatment.

 

(e)                                   Public Offering .  On and after a Public Offering, the Company shall have no further right to purchase shares of Company Stock under this Section 9.

 

(f)                                     Stockholders’ Agreement .  Notwithstanding the provisions of this Section 9, if the Board requires that a Grantee execute a stockholders’ agreement with respect to any Company Stock issued or distributed pursuant to this Plan, which contains a right of first refusal or repurchase right, the provisions of this Section 9 shall not apply to such Company Stock, unless the Board determines otherwise.

 

10.                                  Change in Control of the Company

 

For purposes of this Agreement, a “Change in Control” shall be deemed to have occurred upon:

 

(a)                                   an acquisition subsequent to the date hereof by any person, entity or group (within the meaning of Section 13(d)(3) or 14(d)(2) of the Exchange Act) (a “Person”), of beneficial ownership (within the meaning of Rule 13d-3 promulgated under the Exchange Act) of 30% or more of either (i) the then outstanding shares of Company Stock or (ii) the combined voting power of the then outstanding voting securities of the Company entitled to vote generally in the election of directors; excluding, however, the following:  (1)  any acquisition directly from the Company, other than an acquisition by virtue of the exercise of a conversion privilege unless the security being so converted was itself acquired directly from the Company; (2) any acquisition by the Company; and (3) any acquisition by an employee benefit plan (or related trust) sponsored or maintained by the Company;

 

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(b)                                  a change in the composition of the Board such that during any period of two consecutive years, individuals who at the beginning of such period constitute the Board, and any new director (other than a director designated by a person who has entered into an agreement with the Company to effect a transaction described in Subsections 10(a), 10(c) or 10(d)) whose election by the Board or nomination for election by the Company’s stockholders was approved by a vote of at least two-thirds of the directors then still in office who either were directors at the beginning of the period or whose election or nomination for election was previously so approved, cease for any reason to constitute at least a majority of the members thereof;

 

(c)                                   the approval by the stockholders of the Company of a merger, consolidation, reorganization or similar corporate transaction, whether or not the Company is the surviving corporation in such transaction, in which outstanding shares of Company Stock are converted into (i) shares of stock of another company, other than a conversion into shares of voting common stock of the successor corporation (or a holding company thereof) representing 51% or more of the voting power of all capital stock thereof outstanding immediately after the merger or consolidation or (ii) other securities (of either the Company or another company) or cash or other property;

 

(d)                                  the approval by stockholders of the Company of the issuance of shares of Company Stock in connection with a merger, consolidation, reorganization or similar corporate transaction in an amount in excess of 49% of the number of shares of Company Stock outstanding immediately prior to the consummation of such transaction; or the approval by the stockholders of the Company of (i) the sale or other disposition of all or substantially all of the assets of the Company or (ii) a complete liquidation or dissolution of the Company.

 

11.                                  Consequences of a Change in Control

 

(a)                                   Assumption of Grants .  Upon a Change in Control where the Company is not the surviving corporation (or survives only as a subsidiary of another corporation), unless the Committee determines otherwise, all outstanding Options that are not exercised shall be assumed by, or replaced with comparable options by the surviving corporation (or a parent or subsidiary of the surviving corporation), and other outstanding Grants shall be converted to similar grants of the surviving corporation (or a parent or subsidiary of the surviving corporation).

 

(b)                                  Other Alternatives .  Notwithstanding the foregoing, subject to Subsection 11(c) below, in the event of a Change in Control, the Committee may take any of the following actions with respect to any or all outstanding Grants: the Committee may (i) determine that outstanding Options shall automatically accelerate and become fully exercisable and that the restrictions and conditions on outstanding Stock Awards shall immediately lapse, (ii) require that Grantees surrender their outstanding Options in exchange for a payment by the Company, in cash or Company Stock as determined by the Committee, in an amount equal to the amount by which the then Fair Market Value of the shares of Company Stock subject to the Grantee’s unexercised Options exceeds the Exercise Price of the Options, as applicable or (iii) after giving Grantees an opportunity to exercise their outstanding Options, terminate any or all unexercised Options at such time as the Committee deems appropriate.  Such surrender, termination or settlement shall take place as of the date of the Change in Control or such other date as the Committee may specify.  The Committee shall have no obligation to take any of the foregoing actions, and, in the

 

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absence of any such actions, outstanding Grants shall continue in effect according to their terms (subject to any assumption pursuant to Subsection 11(a)).

 

(c)                                   Limitations .  Notwithstanding anything in the Plan to the contrary, in the event of a Change in Control, the Committee shall not have the right to take any actions described in the Plan (including without limitation actions described in Subsection 11(b), above, that would make the Change in Control ineligible for pooling of interests accounting treatment or that would make the Change in Control ineligible for desired tax treatment if, in the absence of such right, the Change in Control would qualify for such treatment and the Company intends to use such treatment with respect to the Change in Control.

 

12.                                  Requirements for Issuance or Transfer of Shares

 

(a)                                   Stockholders’ Agreement .  The Committee may require that a Grantee execute a stockholders’ agreement, with such terms as the Committee deems appropriate, with respect to any Company Stock issued or distributed pursuant to this Plan.

 

(b)                                  Limitations on Issuance or Transfer of Shares .  No Company Stock shall be issued or transferred in connection with any Grant hereunder unless and until all legal requirements applicable to the issuance or transfer of such Company Stock have been complied with to the satisfaction of the Committee.  The Committee shall have the right to condition any Grant made to any Grantee hereunder on such Grantee’s undertaking in writing to comply with such restrictions on his or her subsequent disposition of such shares of Company Stock as the Committee shall deem necessary or advisable, and certificates representing such shares may be legended to reflect any such restrictions.  Certificates representing shares of Company Stock issued or transferred under the Plan will be subject to such stop-transfer orders and other restrictions as may be required by applicable laws, regulations and interpretations, including any requirement that a legend be placed thereon.

 

(c)                                   Lock-Up Period .  If so requested by the Company or any representative of the underwriters (the “Managing Underwriter”) in connection with any underwritten offering of securities of the Company under the Securities Act of 1933, as amended (the “Securities Act”), a Grantee (including any successors or assigns) shall not sell or otherwise transfer any shares or other securities of the Company during the 30-day period preceding and the 180-day period following the effective date of a registration statement of the Company filed under the Securities Act for such underwriting (or such shorter period as may be requested by the Managing Underwriter and agreed to by the Company) (the “Market Standoff Period”).  The Company may impose stop-transfer instructions with respect to securities subject to the foregoing restrictions until the end of such Market Standoff Period.

 

13.                                  Amendment and Termination of the Plan

 

(a)                                   Amendment .  The Board may amend or terminate the Plan at any time; provided, however, that the Board shall not amend the Plan without stockholder approval if such approval

 

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is required in order to comply with the Code or other applicable laws, or to comply with applicable stock exchange requirements.

 

(b)                                  Termination of Plan .  The Plan shall terminate on the day immediately preceding the tenth anniversary of its effective date, unless the Plan is terminated earlier by the Board or is extended by the Board with the approval of the stockholders.

 

(c)                                   Termination and Amendment of Outstanding Grants .  A termination or amendment of the Plan that occurs after a Grant is made shall not materially impair the rights of a Grantee unless the Grantee consents or unless the Committee acts under Section 19(b).  The termination of the Plan shall not impair the power and authority of the Committee with respect to an outstanding Grant.  Whether or not the Plan has terminated, an outstanding Grant may be terminated or amended under Section 19(b) or may be amended by agreement of the Company and the Grantee consistent with the Plan.

 

(d)                                  Governing Document .  The Plan shall be the controlling document.  No other statements, representations, explanatory materials or examples, oral or written, may amend the Plan in any manner.  The Plan shall be binding upon and enforceable against the Company and its successors and assigns.

 

14.                                  Funding of the Plan

 

This Plan shall be unfunded.  The Company shall not be required to establish any special or separate fund or to make any other segregation of assets to assure the payment of any Grants under this Plan.  In no event shall interest be paid or accrued on any Grant, including unpaid installments of Grants.

 

15.                                  Rights of Participants

 

Nothing in this Plan shall entitle any Employee, Key Advisor, Non-Employee Director or other person to any claim or right to be granted a Grant under this Plan.  Neither this Plan nor any action taken hereunder shall be construed as giving any individual any rights to be retained by or in the employ of the Company or any other employment rights.

 

16.                                  No Fractional Shares

 

No fractional shares of Company Stock shall be issued or delivered pursuant to the Plan or any Grant.  The Committee shall determine whether cash, other awards or other property shall be issued or paid in lieu of such fractional shares or whether such fractional shares or any rights thereto shall be forfeited or otherwise eliminated.

 

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17.                                  Headings

 

Section headings are for reference only.  In the event of a conflict between a title and the content of a Section, the content of the Section shall control.

 

18.                                  Effective Date of the Plan

 

(a)                                   Effective Date .  Subject to approval by the Company’s stockholders, the Plan shall be effective on May 15, 2001.

 

(b)                                  Public Offering .  The provisions of the Plan that refer to a Public Offering, or that refer to, or are applicable to persons subject to, section 16 of the Exchange Act or section 162(m) of the Code, shall be effective, if at all, upon the initial registration of the Company Stock under section 12(g) of the Exchange Act, and shall remain effective thereafter for so long as such stock is so registered.

 

19.                                  Miscellaneous

 

(a)                                   Grants in Connection with Corporate Transactions and Otherwise .  Nothing contained in this Plan shall be construed to (i) limit the right of the Committee to make Grants under this Plan in connection with the acquisition, by purchase, lease, merger, consolidation or otherwise, of the business or assets of any corporation, firm or association, including Grants to employees thereof who become Employees of the Company, or for other proper corporate purposes, or (ii) limit the right of the Company to grant stock options or make other awards outside of this Plan.  Without limiting the foregoing, the Committee may make a Grant to an employee of another corporation who becomes an Employee by reason of a corporate merger, consolidation, acquisition of stock or property, reorganization or liquidation involving the Company or any of its subsidiaries in substitution for a stock option or stock awards grant made by such corporation.  The terms and conditions of the substitute grants may vary from the terms and conditions required by the Plan and from those of the substituted stock incentives.  The Committee shall prescribe the provisions of the substitute grants.

 

(b)                                  Compliance with Law .  The Plan, the exercise of Options and the obligations of the Company to issue or transfer shares of Company Stock under Grants shall be subject to all applicable laws and to approvals by any governmental or regulatory agency as may be required.  With respect to persons subject to section 16 of the Exchange Act, after a Public Offering it is the intent of the Company that the Plan and all transactions under the Plan comply with all applicable provisions of Rule 16b-3 or its successors under the Exchange Act.  In addition, it is the intent of the Company that the Plan and applicable Grants under the Plan comply with the applicable provisions of section 162(m) of the Code, after a Public Offering, and section 422 of the Code.  To the extent that any legal requirement of section 16 of the Exchange Act or section 162(m) or 422 of the Code as set forth in the Plan ceases to be required under section 16 of the Exchange Act or section 162(m) or 422 of the Code, that Plan provision shall cease to apply.  The Committee may revoke any Grant if it is contrary to law or modify a Grant to bring it into compliance with any valid and mandatory government regulation.  The Committee may also

 

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adopt rules regarding the withholding of taxes on payments to Grantees.  The Committee may, in its sole discretion, agree to limit its authority under this Section.

 

(c)                                   Employees Subject to Taxation Outside the United States .  With respect to Grantees who are subject to taxation in countries other than the United States, the Committee may make Grants on such terms and conditions as the Committee deems appropriate to comply with the laws of the applicable countries, and the Committee may create such procedures, addenda and subplans and make such modifications as may be necessary or advisable to comply with such laws.

 

(d)                                  Governing Law .  The validity, construction, interpretation and effect of the Plan and Grant Instruments issued under the Plan shall be governed and construed by and determined in accordance with the laws of Delaware, without giving effect to the conflict of laws provisions thereof.

 

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EXHIBIT 10.63

 

VGX ANIMAL HEALTH, INC.

 

EQUITY COMPENSATION PLAN

 

The purpose of the VGX Animal Health, Inc. Equity Compensation Plan (the “Plan”) is to provide (i) designated employees of VGX Animal Health, Inc. (the “Company”) and its subsidiaries, (ii) certain consultants and advisors who perform services for the Company or its subsidiaries and (iii) non-employee members of the Board of Directors of the Company (the “Board”) with the opportunity to receive grants of incentive stock options, nonqualified stock options, and stock awards.  The Company believes that the Plan will encourage the participants to contribute materially to the growth of the Company, thereby benefiting the Company’s stockholders, and will align the economic interests of the participants with those of the stockholders.

 

1.                                       Administration

 

(a)                                   Committee .  The Plan shall be administered and interpreted by the Board or by a committee or individual appointed by the Board (the “Committee”).  After an initial public offering of the Company’s stock as described in Section 18(b) (a “Public Offering”), the Plan shall be administered by a Committee, which may consist of two or more persons who are “outside directors” as defined under section 162(m) of the Internal Revenue Code of 1986, as amended (the “Code”), and related Treasury regulations and “non-employee directors” as defined under Rule 16b-3 under the Securities Exchange Act of 1934, as amended (the “Exchange Act”).  However, the Board may ratify or approve any grants as it deems appropriate.  If the Board or an individual administers the Plan, references in the Plan to the “Committee” shall be deemed to refer to the Board or individual.

 

(b)                                  Committee Authority .  The Committee shall have the sole authority to (i) determine the individuals to whom grants shall be made under the Plan, (ii) determine the type, size and terms of the grants to be made to each such individual, (iii) determine the time when the grants will be made and the duration of any applicable exercise or restriction period, including the criteria for exercisability and the acceleration of exercisability, (iv) amend the terms of any previously issued grant, and (v) deal with any other matters arising under the Plan.

 

(c)                                   Committee Determinations .  The Committee shall have full power and authority to administer and interpret the Plan, to make factual determinations and to adopt or amend such rules, regulations, agreements and instruments for implementing the Plan and for the conduct of its business as it deems necessary or advisable, in its sole discretion.  The Committee’s interpretations of the Plan and all determinations made by the Committee pursuant to the powers vested in it hereunder shall be conclusive and binding on all persons having any interest in the Plan or in any awards granted hereunder.  All powers of the Committee shall be executed in its sole discretion, in the best interest of the Company, not as a fiduciary, and in keeping with the objectives of the Plan and need not be uniform as to similarly situated individuals.

 



 

2.                                       Grants

 

Awards under the Plan may consist of grants of incentive stock options as described in Section 5 (“Incentive Stock Options”), nonqualified stock options as described in Section 5 (“Nonqualified Stock Options”) (Incentive Stock Options and Nonqualified Stock Options are collectively referred to as “Options”), and stock awards as described in Section 6 (“Stock Awards”) (hereinafter collectively referred to as “Grants”).  All Grants shall be subject to the terms and conditions set forth herein and to such other terms and conditions consistent with this Plan as the Committee deems appropriate and as are specified in writing by the Committee to the individual in a grant instrument or an amendment to the grant instrument (the “Grant Instrument”).  The Committee shall approve the form and provisions of each Grant Instrument.  Grants under a particular Section of the Plan need not be uniform as among the grantees.

 

3.                                       Shares Subject to the Plan

 

(a)                                   Shares Authorized .  Subject to adjustment as described below, the aggregate number of shares of common stock of the Company (“Company Stock”) that may be issued or transferred under the Plan is 1,500,000 shares.  After a Public Offering, the maximum aggregate number of shares of Company Stock that shall be subject to Grants made under the Plan to any individual during any calendar year shall be 500,000 shares, subject to adjustment as described below.  The shares may be authorized but unissued shares of Company Stock or reacquired shares of Company Stock, including shares purchased by the Company on the open market for purposes of the Plan.  If and to the extent Options granted under the Plan terminate, expire, or are canceled, forfeited, exchanged or surrendered without having been exercised or if any Stock Awards are forfeited, the shares subject to such Grants shall again be available for purposes of the Plan.

 

(b)                                  Adjustments .  If there is any change in the number or kind of shares of Company Stock outstanding (i) by reason of a stock dividend, spin-off, recapitalization, stock split, or combination or exchange of shares, (ii) by reason of a merger, reorganization or consolidation, (iii) by reason of a reclassification or change in par value, or (iv) by reason of any other extraordinary or unusual event affecting the outstanding Company Stock as a class without the Company’s receipt of consideration, or if the value of outstanding shares of Company Stock is substantially reduced as a result of a spin-off or the Company’s payment of an extraordinary dividend or distribution, the maximum number of shares of Company Stock available for Grants, the maximum number of shares of Company Stock that any individual participating in the Plan may be granted in any year, the number of shares covered by outstanding Grants, the kind of shares issued under the Plan, and the price per share or the applicable market value of such Grants may be appropriately adjusted by the Committee to reflect any increase or decrease in the number of, or change in the kind or value of, issued shares of Company Stock to preclude, to the extent practicable, the enlargement or dilution of rights and benefits under such Grants; provided, however, that any fractional shares resulting from such adjustment shall be eliminated.  Any adjustments determined by the Committee shall be final, binding and conclusive.

 

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4.                                       Eligibility for Participation

 

(a)                                  Eligible Persons .  All employees of the Company and its subsidiaries (“Employees”), including Employees who are officers or members of the Board, and members of the Board who are not Employees (“Non-Employee Directors”) shall be eligible to participate in the Plan.  Consultants and advisors who perform services for the Company or any of its subsidiaries (“Key Advisors”) shall be eligible to participate in the Plan if the Key Advisors render bona fide services to the Company or its subsidiaries, the services are not in connection with the offer and sale of securities in a capital-raising transaction and the Key Advisors do not directly or indirectly promote or maintain a market for the Company’s securities.

 

(b)                                 Selection of Grantees .  The Committee shall select the Employees, Non-Employee Directors and Key Advisors to receive Grants and shall determine the number of shares of Company Stock subject to a particular Grant in such manner as the Committee determines.  Employees, Key Advisors and Non-Employee Directors who receive Grants under this Plan shall hereinafter be referred to as “Grantees.”

 

5.                                       Granting of Options

 

(a)                                  Number of Shares .  The Committee shall determine the number of shares of Company Stock that will be subject to each Grant of Options to Employees, Non-Employee Directors and Key Advisors.

 

(b)                                 Type of Option and Price .

 

(i)                                      The Committee may grant Incentive Stock Options that are intended to qualify as “incentive stock options” within the meaning of section 422 of the Code or Nonqualified Stock Options that are not intended to qualify or any combination of Incentive Stock Options and Nonqualified Stock Options, all in accordance with the terms and conditions set forth herein.  Incentive Stock Options may be granted only to Employees.  Nonqualified Stock Options may be granted to Employees, Non-Employee Directors and Key Advisors.

 

(ii)                                   The purchase price (the “Exercise Price”) of Company Stock subject to an Option shall be determined by the Committee and may be equal to, greater than, or less than the Fair Market Value (as defined below) of a share of Company Stock on the date the Option is granted; provided, however, that (x) the Exercise Price of an Incentive Stock Option shall be equal to, or greater than, the Fair Market Value of a share of Company Stock on the date the Incentive Stock Option is granted and (y) an Incentive Stock Option may not be granted to an Employee who, at the time of grant, owns stock possessing more than 10% of the total combined voting power of all classes of stock of the Company or any parent or subsidiary of the Company, unless the Exercise Price per share is not less than 110% of the Fair Market Value of Company Stock on the date of grant.

 

(iii)                                If the Company Stock is publicly traded, then the Fair Market Value per share shall be determined as follows: (x) if the principal trading market for the Company Stock is a national securities exchange or the Nasdaq National Market, the last reported sale price thereof on the relevant date or (if there were no trades on that date) the latest preceding date upon which a sale was reported, or (y) if the Company Stock is not principally traded on such exchange or

 

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market, the mean between the last reported “bid” and “asked” prices of Company Stock on the relevant date, as reported on Nasdaq or, if not so reported, as reported by the National Daily Quotation Bureau, Inc. or as reported in a customary financial reporting service, as applicable and as the Committee determines.  If the Company Stock is not publicly traded or, if publicly traded, is not subject to reported transactions or “bid” or “asked” quotations as set forth above, the Fair Market Value per share shall be as determined by the Committee.

 

(c)                                  Option Term .  The Committee shall determine the term of each Option.  The term of any Option shall not exceed 10 years from the date of grant.  However, an Incentive Stock Option that is granted to an Employee who, at the time of grant, owns stock possessing more than 10% of the total combined voting power of all classes of stock of the Company, or any parent or subsidiary of the Company, may not have a term that exceeds five years from the date of grant.

 

(d)                                 Exercisability of Options .

 

(i)                                      Options shall become exercisable in accordance with such terms and conditions, consistent with the Plan, as may be determined by the Committee and specified in the Grant Instrument.  The Committee may accelerate the exercisability of any or all outstanding Options at any time for any reason.

 

(ii)                                   The Committee may provide in a Grant Instrument that the Grantee may elect to exercise part or all of an Option before it otherwise has become exercisable.  Any shares so purchased shall be restricted shares and shall be subject to a repurchase right in favor of the Company during a specified restriction period, with the repurchase price equal to the Exercise Price, or such other restrictions as the Committee deems appropriate.

 

(e)                                  Grants to Non-Exempt Employees .  Notwithstanding the foregoing, Options granted to persons who are non-exempt employees under the Fair Labor Standards Act of 1938, as amended, shall have an Exercise Price not less than 100% of the Fair Market Value of the Company Stock on the date of grant, and may not be exercisable for at least six months after the date of grant (except that such Options may become exercisable, as determined by the Committee, upon the Grantee’s death, Disability or retirement, or upon a Change in Control or other circumstances permitted by applicable regulations).

 

(f)                                    Termination of Employment, Disability or Death .

 

(i)                                      Except as provided below, an Option may only be exercised while the Grantee is employed by, or providing service to, the Company as an Employee, Key Advisor or member of the Board.  In the event that a Grantee ceases to be employed by, or provide service to, the Company for any reason other than Disability, death, or termination for Cause (as defined below), any Option which is otherwise exercisable by the Grantee shall terminate unless exercised within 90 days after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options that are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

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(ii)                                 In the event the Grantee ceases to be employed by, or provide service to, the Company on account of a termination for Cause by the Company (as defined below), any Option held by the Grantee shall terminate as of the date the Grantee ceases to be employed by, or provide service to, the Company.  In addition, notwithstanding any other provisions of this Section 5, if the Committee determines that the Grantee has engaged in conduct that constitutes Cause at any time while the Grantee is employed by, or providing service to, the Company or after the Grantee’s termination of employment or service, any Option held by the Grantee shall immediately terminate and the Grantee shall automatically forfeit all shares underlying any exercised portion of an Option for which the Company has not yet delivered the share certificates, upon refund by the Company of the Exercise Price paid by the Grantee for such shares.  Upon any exercise of an Option, the Company may withhold delivery of share certificates pending resolution of an inquiry that could lead to a finding resulting in a forfeiture.

 

(iii)                              In the event the Grantee ceases to be employed by, or provide service to, the Company because the Grantee is Disabled, any Option which is otherwise exercisable by the Grantee shall terminate unless exercised within one year after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options which are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

(iv)                             If the Grantee dies while employed by, or providing service to, the Company or within 90 days after the date on which the Grantee ceases to be employed or provide service on account of a termination specified in Section 5(f)(i) above (or within such other period of time as may be specified by the Committee), any Option that is otherwise exercisable by the Grantee shall terminate unless exercised within one year after the date on which the Grantee ceases to be employed by, or provide service to, the Company (or within such other period of time as may be specified by the Committee), but in any event no later than the date of expiration of the Option term.  Except as otherwise provided by the Committee, any of the Grantee’s Options that are not otherwise exercisable as of the date on which the Grantee ceases to be employed by, or provide service to, the Company shall terminate as of such date.

 

(v)                                For purposes of this Section 5(f) and Section 6:

 

(1)                                   “Company” shall mean the Company and its parent and subsidiary corporations or other entities, as determined by the Committee.

 

(2)                                   “Employed by, or provide service to, the Company” shall mean employment or service as an Employee, Key Advisor or member of the Board (so that, for purposes of exercising Options and satisfying conditions with respect to Stock Awards, a Grantee shall not be considered to have terminated employment or service until the Grantee ceases to be an Employee, Key Advisor and member of the Board), unless the Committee determines otherwise.

 

(3)                                   “Disability” shall mean a Grantee’s becoming disabled within the meaning of section 22(e)(3) of the Code.

 

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(4)                                   “Cause” shall mean, except to the extent specified otherwise by the Committee, a finding by the Committee of the following:  (i) conviction of Grantee of any felony; (ii) participation by Grantee in any fraud or act of dishonesty against the Company; (iii) material violation by Grantee of (a) any contract between the Company and Grantee or (b) any statutory duty of Grantee to the Company; (iv) conduct of Grantee that, based upon a good faith and reasonable factual investigation and determination by the Board, demonstrates Grantee’s gross unfitness to serve in the capacity as an employee, director or consultant; or (v) the continued, willful refusal or failure by Grantee to perform any material duties reasonably requested by the Board; provided, however, that in the case of conduct described in clauses (iii), (iv) and (v) hereof, such conduct shall not constitute “Cause” unless:  (a) the Board shall have given Grantee written notice setting forth with specificity (1) the conduct deemed to constitute “Cause,” (2) reasonable action that would remedy the objectionable conduct and (3) a reasonable time (not less than 10 days) within which Grantee may take such remedial action; and (b) Grantee shall not have taken such specified remedial action within such specified reasonable time.

 

(g)                                  Exercise of Options .  A Grantee may exercise an Option that has become exercisable, in whole or in part, by delivering a notice of exercise to the Company with payment of the Exercise Price.  The Grantee shall pay the Exercise Price for an Option as specified by the Committee (i) in cash, (ii) with the approval of the Committee, by delivering shares of Company Stock owned by the Grantee (including Company Stock acquired in connection with the exercise of an Option, subject to such restrictions as the Committee deems appropriate) and having a Fair Market Value on the date of exercise equal to the Exercise Price or by attestation (on a form prescribed by the Committee) to ownership of shares of Company Stock having a Fair Market Value on the date of exercise equal to the Exercise Price, (iii) after a Public Offering, payment through a broker in accordance with procedures permitted by Regulation T of the Federal Reserve Board, or (iv) by such other method as the Committee may approve.  The Committee may authorize loans by the Company to Grantees in connection with the exercise of an Option, upon such terms and conditions as the Committee, in its sole discretion, deems appropriate.  Shares of Company Stock used to exercise an Option shall have been held by the Grantee for the requisite period of time to avoid adverse accounting consequences to the Company with respect to the Option.  The Grantee shall pay the Exercise Price and the amount of any withholding tax due (pursuant to Section 7) at the time of exercise.

 

(h)                                  Limits on Incentive Stock Options .  Each Incentive Stock Option shall provide that, if the aggregate Fair Market Value of the stock on the date of the grant with respect to which Incentive Stock Options are exercisable for the first time by a Grantee during any calendar year, under the Plan or any other stock option plan of the Company or a parent or subsidiary, exceeds $100,000, then the Option, as to the excess, shall be treated as a Nonqualified Stock Option.  An Incentive Stock Option shall not be granted to any person who is not an Employee of the Company or a parent or subsidiary (within the meaning of section 424(f) of the Code).

 

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6.                                       Stock Awards

 

The Committee may issue or transfer shares of Company Stock to an Employee, Non-Employee Director or Key Advisor under a Stock Award, upon such terms as the Committee deems appropriate.  The following provisions are applicable to Stock Awards:

 

(a)                                   General Requirements .  Shares of Company Stock issued or transferred pursuant to Stock Awards may be issued or transferred for consideration or for no consideration, and subject to restrictions or no restrictions, as determined by the Committee.  The Committee may establish conditions under which restrictions on Stock Awards shall lapse over a period of time or according to such other criteria as the Committee deems appropriate.  The period of time during which the Stock Awards will remain subject to restrictions will be designated in the Grant Instrument as the “Restriction Period.”

 

(b)                                  Number of Shares .  The Committee shall determine the number of shares of Company Stock to be issued or transferred pursuant to a Stock Award and the restrictions applicable to such shares.

 

(c)                                   Requirement of Employment or Service .  If the Grantee ceases to be employed by, or provide service to, the Company (as defined in Section 5(f)) during a period designated in the Grant Instrument as the Restriction Period, or if other specified conditions are not met, the Stock Award shall terminate as to all shares covered by the Grant as to which the restrictions have not lapsed, and those shares of Company Stock must be immediately returned to the Company.  The Committee may, however, provide for complete or partial exceptions to this requirement as it deems appropriate.

 

(d)                                  Restrictions on Transfer and Legend on Stock Certificate .  During the Restriction Period, a Grantee may not sell, assign, transfer, pledge or otherwise dispose of the shares of a Stock Award except to a Successor Grantee under Section 8(a).  Each certificate for a share of a Stock Award shall contain a legend giving appropriate notice of the restrictions in the Grant.  The Grantee shall be entitled to have the legend removed from the stock certificate covering the shares subject to restrictions when all restrictions on such shares have lapsed.  The Committee may determine that the Company will not issue certificates for Stock Awards until all restrictions on such shares have lapsed, or that the Company will retain possession of certificates for shares of Stock Awards until all restrictions on such shares have lapsed.

 

(e)                                   Right to Vote and to Receive Dividends .  Unless the Committee determines otherwise, during the Restriction Period, the Grantee shall have the right to vote shares of Stock Awards and to receive any dividends or other distributions paid on such shares, subject to any restrictions deemed appropriate by the Committee.

 

(f)                                     Lapse of Restrictions .  All restrictions imposed on Stock Awards shall lapse upon the expiration of the applicable Restriction Period and the satisfaction of all conditions imposed by the Committee.  The Committee may determine, as to any or all Stock Awards, that the restrictions shall lapse without regard to any Restriction Period.

 

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7.                                       Withholding of Taxes

 

(a)                                   Required Withholding .  All Grants under the Plan shall be subject to applicable federal (including FICA), state and local tax withholding requirements.  The Company may require that the Grantee or other person receiving or exercising Grants pay to the Company the amount of any federal, state or local taxes that the Company is required to withhold with respect to such Grants, or the Company may deduct from other wages paid by the Company the amount of any withholding taxes due with respect to such Grants.

 

(b)                                  Election to Withhold Shares .  If the Committee so permits, a Grantee may elect to satisfy the Company’s income tax withholding obligation with respect to Options or Stock Awards paid in Company Stock by having shares withheld up to an amount that does not exceed the Grantee’s minimum applicable withholding tax rate for federal (including FICA), state and local tax liabilities.  The election must be in a form and manner prescribed by the Committee and may be subject to the prior approval of the Committee.

 

8.                                       Transferability of Grants

 

(a)                                   Nontransferability of Grants .  Except as provided below, only the Grantee may exercise rights under a Grant during the Grantee’s lifetime.  A Grantee may not transfer those rights except (i) by will or by the laws of descent and distribution or (ii) with respect to Grants other than Incentive Stock Options, if permitted in any specific case by the Committee, pursuant to a domestic relations order or otherwise as permitted by the Committee.  When a Grantee dies, the personal representative or other person entitled to succeed to the rights of the Grantee (“Successor Grantee”) may exercise such rights.  A Successor Grantee must furnish proof satisfactory to the Company of his or her right to receive the Grant under the Grantee’s will or under the applicable laws of descent and distribution.

 

(b)                                  Transfer of Nonqualified Stock Options .  Notwithstanding the foregoing, the Committee may provide, in a Grant Instrument, that a Grantee may transfer Nonqualified Stock Options to family members, or one or more trusts or other entities for the benefit of or owned by family members, consistent with the applicable securities laws, according to such terms as the Committee may determine; provided that the Grantee receives no consideration for the transfer of an Option and the transferred Option shall continue to be subject to the same terms and conditions as were applicable to the Option immediately before the transfer.

 

9.                                       Right of First Refusal; Repurchase Right

 

(a)                                   Offer .  Prior to a Public Offering, if at any time an individual desires to sell, encumber, or otherwise dispose of shares of Company Stock that were issued or distributed to him or her under this Plan and that are transferable, the individual may do so only pursuant to a bona fide written offer, and the individual shall first offer the shares to the Company by giving the Company written notice disclosing: (i) the name of the proposed transferee of the Company Stock; (ii) the certificate number and number of shares of Company Stock proposed to be transferred or encumbered; (iii) the proposed price; (iv) all other terms of the proposed transfer; and (v) a written copy of the proposed offer.  Within 60 days after receipt of such notice, the Company shall have the option to purchase all or part of such Company Stock at the then current Fair Market Value (as defined in Section 5(b)) and may pay such price in installments over a period not to exceed four years, at the discretion of the Committee.

 

8



 

(b)                                  Sale .  In the event the Company (or a stockholder, as described below) does not exercise the option to purchase Company Stock, as provided above, the individual shall have the right to sell, encumber, or otherwise dispose of the shares of Company Stock described in Subsection (a) on the terms of the transfer set forth in the written notice to the Company, provided such transfer is effected within 15 days after the expiration of the option period.  If the transfer is not effected within such period, the Company must again be given an option to purchase, as provided above.

 

(c)                                   Assignment of Rights .  The Board, in its sole discretion, may waive the Company’s right of first refusal and repurchase right under this Section 9.  If the Company’s right of first refusal or repurchase right is so waived, the Board may, in its sole discretion, assign such right to the remaining stockholders of the Company in the same proportion that each stockholder’s stock ownership bears to the stock ownership of all the stockholders of the Company, as determined by the Board.  To the extent that a stockholder has been given such right and does not purchase his or her allotment, the other stockholders shall have the right to purchase such allotment on the same basis.

 

(d)                                  Purchase by the Company .  Prior to a Public Offering, if a Grantee ceases to be employed by, or provide service to, the Company, the Company shall have the right to purchase all or part of any Company Stock issued or distributed to him or her under this Plan at its then current Fair Market Value (as defined in Section 5(b)) (or at such other price as may be established in the Grant Instrument); provided, however, that such repurchase shall be made in accordance with applicable accounting rules to avoid adverse accounting treatment.

 

(e)                                   Public Offering .  On and after a Public Offering, the Company shall have no further right to purchase shares of Company Stock under this Section 9.

 

(f)                                     Stockholders’ Agreement .  Notwithstanding the provisions of this Section 9, if the Board requires that a Grantee execute a stockholders’ agreement with respect to any Company Stock issued or distributed pursuant to this Plan, which contains a right of first refusal or repurchase right, the provisions of this Section 9 shall not apply to such Company Stock, unless the Board determines otherwise.

 

10.                                 Change in Control of the Company

 

For purposes of this Agreement, a “Change in Control” shall be deemed to have occurred upon:

 

(a)                                   an acquisition subsequent to the date hereof by any person, entity or group (within the meaning of Section 13(d)(3) or 14(d)(2) of the Exchange Act) (a “Person”), of beneficial ownership (within the meaning of Rule 13d-3 promulgated under the Exchange Act) of 30% or more of either (i) the then outstanding shares of Company Stock or (ii) the combined voting power of the then outstanding voting securities of the Company entitled to vote generally in the election of directors; excluding, however, the following:  (1)  any acquisition directly from the Company, other than an acquisition by virtue of the exercise of a conversion privilege unless the security being so converted was itself acquired directly from the Company; (2) any acquisition by the Company; and (3) any acquisition by an employee benefit plan (or related trust) sponsored or maintained by the Company;

 

9



 

(b)                                  a change in the composition of the Board such that during any period of two consecutive years, individuals who at the beginning of such period constitute the Board, and any new director (other than a director designated by a person who has entered into an agreement with the Company to effect a transaction described in Subsections 10(a), 10(c) or 10(d)) whose election by the Board or nomination for election by the Company’s stockholders was approved by a vote of at least two-thirds of the directors then still in office who either were directors at the beginning of the period or whose election or nomination for election was previously so approved, cease for any reason to constitute at least a majority of the members thereof;

 

(c)                                   the approval by the stockholders of the Company of a merger, consolidation, reorganization or similar corporate transaction, whether or not the Company is the surviving corporation in such transaction, in which outstanding shares of Company Stock are converted into (i) shares of stock of another company, other than a conversion into shares of voting common stock of the successor corporation (or a holding company thereof) representing 51% or more of the voting power of all capital stock thereof outstanding immediately after the merger or consolidation or (ii) other securities (of either the Company or another company) or cash or other property;

 

(d)                                  the approval by stockholders of the Company of the issuance of shares of Company Stock in connection with a merger, consolidation, reorganization or similar corporate transaction in an amount in excess of 49% of the number of shares of Company Stock outstanding immediately prior to the consummation of such transaction; or the approval by the stockholders of the Company of (i) the sale or other disposition of all or substantially all of the assets of the Company or (ii) a complete liquidation or dissolution of the Company.

 

11.                                 Consequences of a Change in Control

 

(a)                                   Assumption of Grants .  Upon a Change in Control where the Company is not the surviving corporation (or survives only as a subsidiary of another corporation), unless the Committee determines otherwise, all outstanding Options that are not exercised shall be assumed by, or replaced with comparable options by the surviving corporation (or a parent or subsidiary of the surviving corporation), and other outstanding Grants shall be converted to similar grants of the surviving corporation (or a parent or subsidiary of the surviving corporation).

 

(b)                                  Other Alternatives .  Notwithstanding the foregoing, subject to Subsection 11(c) below, in the event of a Change in Control, the Committee may take any of the following actions with respect to any or all outstanding Grants: the Committee may (i) determine that outstanding Options shall automatically accelerate and become fully exercisable and that the restrictions and conditions on outstanding Stock Awards shall immediately lapse, (ii) require that Grantees surrender their outstanding Options in exchange for a payment by the Company, in cash or Company Stock as determined by the Committee, in an amount equal to the amount by which the then Fair Market Value of the shares of Company Stock subject to the Grantee’s unexercised Options exceeds the Exercise Price of the Options, as applicable or (iii) after giving Grantees an opportunity to exercise their outstanding Options, terminate any or all unexercised Options at such time as the Committee deems appropriate.  Such surrender, termination or settlement shall take place as of the date of the Change in Control or such other date as the Committee may specify.  The Committee shall have no obligation to take any of the foregoing actions, and, in the

 

10



 

absence of any such actions, outstanding Grants shall continue in effect according to their terms (subject to any assumption pursuant to Subsection 11(a)).

 

(c)                                   Limitations .  Notwithstanding anything in the Plan to the contrary, in the event of a Change in Control, the Committee shall not have the right to take any actions described in the Plan (including without limitation actions described in Subsection 11(b), above, that would make the Change in Control ineligible for pooling of interests accounting treatment or that would make the Change in Control ineligible for desired tax treatment if, in the absence of such right, the Change in Control would qualify for such treatment and the Company intends to use such treatment with respect to the Change in Control.

 

12.                                 Requirements for Issuance or Transfer of Shares

 

(a)                                   Stockholders’ Agreement .  The Committee may require that a Grantee execute a stockholders’ agreement, with such terms as the Committee deems appropriate, with respect to any Company Stock issued or distributed pursuant to this Plan.

 

(b)                                  Limitations on Issuance or Transfer of Shares .  No Company Stock shall be issued or transferred in connection with any Grant hereunder unless and until all legal requirements applicable to the issuance or transfer of such Company Stock have been complied with to the satisfaction of the Committee.  The Committee shall have the right to condition any Grant made to any Grantee hereunder on such Grantee’s undertaking in writing to comply with such restrictions on his or her subsequent disposition of such shares of Company Stock as the Committee shall deem necessary or advisable, and certificates representing such shares may be legended to reflect any such restrictions.  Certificates representing shares of Company Stock issued or transferred under the Plan will be subject to such stop-transfer orders and other restrictions as may be required by applicable laws, regulations and interpretations, including any requirement that a legend be placed thereon.

 

(c)                                   Lock-Up Period .  If so requested by the Company or any representative of the underwriters (the “Managing Underwriter”) in connection with any underwritten offering of securities of the Company under the Securities Act of 1933, as amended (the “Securities Act”), a Grantee (including any successors or assigns) shall not sell or otherwise transfer any shares or other securities of the Company during the 30-day period preceding and the 180-day period following the effective date of a registration statement of the Company filed under the Securities Act for such underwriting (or such shorter period as may be requested by the Managing Underwriter and agreed to by the Company) (the “Market Standoff Period”).  The Company may impose stop-transfer instructions with respect to securities subject to the foregoing restrictions until the end of such Market Standoff Period.

 

13.                                 Amendment and Termination of the Plan

 

(a)                                   Amendment .  The Board may amend or terminate the Plan at any time; provided, however, that the Board shall not amend the Plan without stockholder approval if such approval

 

11



 

is required in order to comply with the Code or other applicable laws, or to comply with applicable stock exchange requirements.

 

(b)                                  Termination of Plan .  The Plan shall terminate on the day immediately preceding the tenth anniversary of its effective date, unless the Plan is terminated earlier by the Board or is extended by the Board with the approval of the stockholders.

 

(c)                                   Termination and Amendment of Outstanding Grants .  A termination or amendment of the Plan that occurs after a Grant is made shall not materially impair the rights of a Grantee unless the Grantee consents or unless the Committee acts under Section 19(b).  The termination of the Plan shall not impair the power and authority of the Committee with respect to an outstanding Grant.  Whether or not the Plan has terminated, an outstanding Grant may be terminated or amended under Section 19(b) or may be amended by agreement of the Company and the Grantee consistent with the Plan.

 

(d)                                  Governing Document .  The Plan shall be the controlling document.  No other statements, representations, explanatory materials or examples, oral or written, may amend the Plan in any manner.  The Plan shall be binding upon and enforceable against the Company and its successors and assigns.

 

14.                                 Funding of the Plan

 

This Plan shall be unfunded.  The Company shall not be required to establish any special or separate fund or to make any other segregation of assets to assure the payment of any Grants under this Plan.  In no event shall interest be paid or accrued on any Grant, including unpaid installments of Grants.

 

15.                                 Rights of Participants

 

Nothing in this Plan shall entitle any Employee, Key Advisor, Non-Employee Director or other person to any claim or right to be granted a Grant under this Plan.  Neither this Plan nor any action taken hereunder shall be construed as giving any individual any rights to be retained by or in the employ of the Company or any other employment rights.

 

16.                                 No Fractional Shares

 

No fractional shares of Company Stock shall be issued or delivered pursuant to the Plan or any Grant.  The Committee shall determine whether cash, other awards or other property shall be issued or paid in lieu of such fractional shares or whether such fractional shares or any rights thereto shall be forfeited or otherwise eliminated.

 

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17.                                 Headings

 

Section headings are for reference only.  In the event of a conflict between a title and the content of a Section, the content of the Section shall control.

 

18.                                 Effective Date of the Plan

 

(a)                                   Effective Date .  Subject to approval by the Company’s stockholders, the Plan shall be effective on June 1, 2007.

 

(b)                                  Public Offering .  The provisions of the Plan that refer to a Public Offering, or that refer to, or are applicable to persons subject to, section 16 of the Exchange Act or section 162(m) of the Code, shall be effective, if at all, upon the initial registration of the Company Stock under section 12(g) of the Exchange Act, and shall remain effective thereafter for so long as such stock is so registered.

 

19.                                 Miscellaneous

 

(a)                                   Grants in Connection with Corporate Transactions and Otherwise .  Nothing contained in this Plan shall be construed to (i) limit the right of the Committee to make Grants under this Plan in connection with the acquisition, by purchase, lease, merger, consolidation or otherwise, of the business or assets of any corporation, firm or association, including Grants to employees thereof who become Employees of the Company, or for other proper corporate purposes, or (ii) limit the right of the Company to grant stock options or make other awards outside of this Plan.  Without limiting the foregoing, the Committee may make a Grant to an employee of another corporation who becomes an Employee by reason of a corporate merger, consolidation, acquisition of stock or property, reorganization or liquidation involving the Company or any of its subsidiaries in substitution for a stock option or stock awards grant made by such corporation.  The terms and conditions of the substitute grants may vary from the terms and conditions required by the Plan and from those of the substituted stock incentives.  The Committee shall prescribe the provisions of the substitute grants.

 

(b)                                  Compliance with Law .  The Plan, the exercise of Options and the obligations of the Company to issue or transfer shares of Company Stock under Grants shall be subject to all applicable laws and to approvals by any governmental or regulatory agency as may be required.  With respect to persons subject to section 16 of the Exchange Act, after a Public Offering it is the intent of the Company that the Plan and all transactions under the Plan comply with all applicable provisions of Rule 16b-3 or its successors under the Exchange Act.  In addition, it is the intent of the Company that the Plan and applicable Grants under the Plan comply with the applicable provisions of section 162(m) of the Code, after a Public Offering, and section 422 of the Code.  To the extent that any legal requirement of section 16 of the Exchange Act or section 162(m) or 422 of the Code as set forth in the Plan ceases to be required under section 16 of the Exchange Act or section 162(m) or 422 of the Code, that Plan provision shall cease to apply.  The Committee may revoke any Grant if it is contrary to law or modify a Grant to bring it into compliance with any valid and mandatory government regulation.  The Committee may also

 

13



 

adopt rules regarding the withholding of taxes on payments to Grantees.  The Committee may, in its sole discretion, agree to limit its authority under this Section.

 

(c)                                   Employees Subject to Taxation Outside the United States .  With respect to Grantees who are subject to taxation in countries other than the United States, the Committee may make Grants on such terms and conditions as the Committee deems appropriate to comply with the laws of the applicable countries, and the Committee may create such procedures, addenda and subplans and make such modifications as may be necessary or advisable to comply with such laws.

 

(d)                                  Governing Law .  The validity, construction, interpretation and effect of the Plan and Grant Instruments issued under the Plan shall be governed and construed by and determined in accordance with the laws of Delaware, without giving effect to the conflict of laws provisions thereof.

 

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EXHIBIT 10.64

 

ALLONGE

 

Note:

 

Convertible Subordinated Promissory Note dated [ORIGINAL DATE OF NOTE] (the “Note”)

 

 

 

Borrower:

 

VGX Pharmaceuticals, Inc. (the “Borrower”)

 

 

 

Holder:

 

[NAME OF HOLDER] (the “Holder”)

 

 

 

Principal Sum:

 

$ [PRINCIPAL]

 

THIS ALLONGE TO CONVERTIBLE SUBORDINATED PROMISSORY NOTE (this “Allonge”) is made as of November        , 2008, between the Borrower and the Holder.  Capitalized terms used but not defined herein shall have the meanings ascribed to them in the Note.

 

WHEREAS , on [ ORIGINAL DATE OF NOTE] , the Borrower issued the Note to the Holder in an aggregate principal amount equal to the Principal Sum (as defined in the Note), all which remains outstanding as of the date hereof;

 

WHEREAS , on [AMENDMENT DATE] , the Borrower and the Holder entered into an amendment pursuant to which certain provisions of the Note were amended;

 

WHEREAS , on [FIRST ALLONGE DATE] , the Borrower and the Holder entered into an Allonge WHEREAS, the Borrower and the Holder now wish to amend further certain provisions of the Note, as set forth herein.

 

NOW THEREFORE , in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties, intending to be legally bound, hereby agree as follows:

 

1.             The first sentence of Section 2 of the Note (titled “Maturity”) is hereby amended and restated in its entirety to read as follows:  “Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section 7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable on December 30, 2009; provided, however, that such date shall be extended one additional year, upon written notice of extension given either by the Borrower to the Holder or by the Holder to the Borrower at any time prior to December 31, 2009 (such maturity date is hereafter referred to as the “Maturity Date”).

 

2.             Section 3 of the Note (titled “Conversion”) is hereby amended by deleting the additional paragraphs thereto that were added pursuant to Section 1 of Allonge No. 1 and by adding the following additional paragraphs to such Section 3:

 



 

“Notwithstanding any provision to the contrary contained herein, if the Merger (as defined below) is consummated, at any time from and after such consummation until the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued but unpaid interest thereon and all other fees, costs and charges, if any (such period of time, the “Conversion Period”), this Note shall be converted into shares of Acquiror Common Stock as follows:

 

(i)            At the option of the Holder, one-half (1/2) of the Principal Sum outstanding hereunder, together with all accrued but unpaid interest on such portion of the Principal Sum, and one-half (1/2) of all other fees, costs and charges, if any, shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock (as defined below) as determined by the application of a conversion price equal to $1.05 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares) (the “Conversion Price”).   Such option shall be exercisable by the Holder by providing written notice of conversion to the Company at any time prior to the expiration of the Conversion Period.

 

(ii)           In the event that, at any time during the Conversion Period, the average of the closing sales prices for one share of Acquiror Common Stock as reported on the exchange on which Acquiror Common Stock is traded for the five consecutive Trading Days (as defined below) at a price per share equal to or greater than $2.10 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares), one-half (1/2) of the Principal Sum outstanding hereunder, together with all accrued but unpaid interest on such portion of the Principal Sum and one-half (1/2) of all other fees, costs and charges, if any, under this Note shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock as determined by the application of a conversion price per share equal to the Conversion Price.

 

No fractional shares of Acquiror Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Acquiror Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

With respect to any shares of Acquiror Common Stock issued in a conversion pursuant to clauses (i) or (ii) above at any time from the date of the occurrence of the Merger through the date that is 180 days after the such date, the Holder shall not (A) sell, assign, exchange, transfer, pledge, hypothecate, distribute or otherwise dispose of (other than by operation of law where the transferee remains subject to and bound by the provisions of this paragraph) any such shares of Acquiror Common Stock or any interest (including, without limitation, an option to buy or sell) in any such shares, in whole or in part, and no such attempted transfer shall be treated as effective for any purpose, or (B) engage in any transaction with respect to such shares or any interest therein, the intent or effect of which is the effective economic disposition of such shares (including, but not limited to, engaging in put, call, short-sale, straddle or similar market transactions), for a

 

2



 

period of time commencing on the date of conversion through the date that is 180 days after the occurrence of the Merger, provided, however, that such restrictions in the foregoing clauses (A) and (B) shall lapse as to 50% of such shares 90 days after the date of the occurrence of the Merger.  The Holder agrees, promptly after the Company’s or the Acquiror’s request, to enter into a written agreement to memorialize in further detail the restrictions contained in this paragraph.

 

For purposes of this Note, the “Merger” shall mean the merger transaction involving the Borrower and Inovio Biomedical Corporation (the “Acquiror”), pursuant to an Agreement and Plan of Merger dated as of July 7, 2008 by and among the Borrower, the Acquiror and the other parties listed therein, as the same may be amended and/or restated from time to time; “Acquiror Common Stock” shall mean the common stock of the Acquiror; and “Trading Day” shall mean a day on which trades occur on the exchange on which Acquiror Common Stock is traded and for which a last sale price is reported for Acquiror Common Stock.”

 

3 .             Effective as of the time of the Merger, the conversion provisions set forth in Section 3 of the Note shall be deleted in their entirety.  For the avoidance of doubt, the conversion provisions added to such Section 3 pursuant to this Allonge shall remain in full force and effect in the event of such deletion.

 

4.             Effective at the time of the Merger, the delivery dates for the financial statements contained in Section 6 of the Note (titled “Financial Reports”) are hereby modified so as to provide that such financial statements shall be deliverable by the Company promptly after they are required to be filed with the Securities and Exchange Commission (and not before such date), notwithstanding anything to the contrary contained in such Section 6.

 

5.             Effective as of the effective time of the Merger, Section 9 of the Note (“Co-Sale Rights”) shall be deleted in its entirety.

 

This Allonge is intended to be and shall remain attached to, and shall constitute an integral part of, the Note from and after the date hereof.  Except as modified hereby, all of the terms and provisions of the Note are hereby ratified and confirmed and, as amended by this Allonge, shall continue in full force and effect.

 

3



 

Intending to be legally bound hereby, each of the undersigned have duly executed this Allonge as of the     day of             , 2008.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

 

 

 

 

HOLDER

 

 

 

 

 

 

 

 

 

4



 

ADDENDUM TO ALLONGE TO NOTE

 

Note:

 

Convertible Subordinated Promissory Note dated [ORIGINAL DATE OF NOTE] (the “Note”)

 

 

 

Borrower:

 

VGX Pharmaceuticals, Inc. (the “Borrower”)

 

 

 

Holder:

 

[NAME OF HOLDER] (the “Holder”)

 

 

 

Principal Sum:

 

$ [PRINCIPAL]

 

The Borrower and the Holder previously executed an Allonge dated November             , 2008 relating to the Note.  Capitalized terms used but not defined herein shall have the meanings ascribed to them in the Note.

 

The Borrower and the Holder agree, for good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, to supplement the Allonge as follows:

 

1.             In the event that the Holder elects to convert one-half (1/2) of the entire Principal Sum, together with all accrued but unpaid interest on such portion of the Principal Sum and one-half (1/2) of all other fees, costs and charges, if any, relating to the Note, as provided in paragraph (i) of Section 3 of the Note (titled “Conversion”), as amended by Section 2 of the Allonge, at the Holder’s option, all remaining amounts of the Principal Sum, interest and other fees, costs and charges, if any, relating to the Note shall, simultaneously with such optional conversion, be converted into a number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock determined by application of a conversion price per share equal to the Conversion Price.  Such option shall be exercisable by the Holder by providing written notice of conversion to the Company of such conversion elected pursuant to this paragraph 1 at the same time that the notice of optional conversion required by the Note is provided by the Holder to the Borrower.

 

2.             In the event that, at any time during the Conversion Period, the average of the closing sales prices for one share of Acquiror Common Stock as reported on the exchange on which Acquiror Common Stock is traded for the five consecutive Trading Days (as defined below) at a price per share equal to or greater than $2.10 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares), all remaining amounts of the Principal Sum, interest and other fees, costs and charges, if any, relating to the Note shall, simultaneously with the automatic conversion provided in paragraph (ii) of Section 3 of the Note (titled “Conversion”), as amended by Section 2 of the Allonge, be automatically converted into a number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock determined by application of a conversion price per share equal to the Conversion Price.

 

5



 

The provisions in the Allonge regarding limitations on transfer of shares of Acquiror Common Stock acquired upon conversion of the Note shall likewise apply to all shares of Acquiror Common Stock acquired upon any conversion pursuant to this Addendum.

 

This Addendum is intended to be and shall remain attached to, and shall constitute an integral part of, the Allonge and the Note from and after the date hereof.  Except as modified hereby, all of the terms and provisions of the Note and the Allonge are hereby ratified and confirmed and, as supplemented by this Addendum, shall continue in full force and effect.

 

6



 

Intending to be legally bound hereby, each of the undersigned have duly executed this Addendum to Allonge as of the      day of                   , 2008.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

 

 

 

 

HOLDER

 

 

 

 

 

 

 

 

ALLONGE

 

Note:

 

Convertible Subordinated Promissory Note dated [ORIGINAL DATE OF NOTE] (the “Note”)

 

 

 

Borrower:

 

VGX Pharmaceuticals, Inc. (the “Borrower”)

 

 

 

Holder:

 

[NAME OF HOLDER] (the “Holder”)

 

 

 

Principal Sum:

 

$ [PRINCIPAL]

 

 

 

Coupon Rate:

 

5%

 

THIS ALLONGE TO CONVERTIBLE SUBORDINATED PROMISSORY NOTE (this “Allonge”) is made as of November       , 2008, between the Borrower and the Holder.  Capitalized terms used but not defined herein shall have the meanings ascribed to them in the Note.

 

WHEREAS , [ ORIGINAL DATE OF NOTE] , the Borrower issued the Note to the Holder in an aggregate principal amount equal to the Principal Sum (as defined in the Note), all which remains outstanding as of the date hereof;

 

WHEREAS , on [FIRST ALLONGE DATE] , the Borrower and the Holder entered into an Allonge (“Allonge No. 1”), pursuant to which certain provisions of the Note were amended; and

 

7



 

WHEREAS , the Borrower and the Holder now wish to amend further certain provisions of the Note, as set forth herein.

 

NOW THEREFORE , in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties, intending to be legally bound, hereby agree as follows:

 

1.             The first sentence of Section 2 of the Note (titled “Maturity”) is hereby amended and restated in its entirety to read as follows:  “Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section  7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable on July 10, 2010 (the “Maturity Date”).

 

2.             Section 3 of the Note (titled “Conversion”) is hereby amended by deleting the additional paragraphs thereto that were added pursuant to Section 1 of Allonge No. 1 and by adding the following additional paragraphs to such Section 3:

 

“Notwithstanding any provision to the contrary contained herein, if the Merger (as defined below) is consummated, at any time from and after such consummation until the Maturity Date or the repayment by the Borrower of the Principal Sum (such period of time, the “Conversion Period”), the entire Principal Sum , shall be converted into shares of Acquiror Common Stock as follows:

 

(i)            At the option of the Holder, all of the Principal Sum outstanding hereunder shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock (as defined below) as determined by the application of a conversion price equal to $1.05 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares) (the “Conversion Price”).   Such option shall be exercisable by the Holder by providing written notice of conversion to the Company at any time prior to the expiration of the Conversion Period.

 

(ii)           In the event that, at any time during the Conversion Period, the average of the closing sales prices for one share of Acquiror Common Stock as reported on the exchange on which Acquiror Common Stock is traded for the five consecutive Trading Days (as defined below) at a price per share equal to or greater than $2.10 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares), this Note shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock at a conversion price per share equal to the Conversion Price.

 

No fractional shares of Acquiror Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Acquiror Common

 

8



 

Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

With respect to any shares of Acquiror Common Stock issued in a conversion pursuant to clauses (i) or (ii) above at any time from the date of the occurrence of the Merger through the date that is 180 days after the such date, the Holder shall not (A) sell, assign, exchange, transfer, pledge, hypothecate, distribute or otherwise dispose of (other than by operation of law where the transferee remains subject to and bound by the provisions of this paragraph) any such shares of Acquiror Common Stock or any interest (including, without limitation, an option to buy or sell) in any such shares, in whole or in part, and no such attempted transfer shall be treated as effective for any purpose, or (B) engage in any transaction with respect to such shares or any interest therein, the intent or effect of which is the effective economic disposition of such shares (including, but not limited to, engaging in put, call, short-sale, straddle or similar market transactions), for a period of time commencing on the date of conversion through the date that is 180 days after the occurrence of the Merger, provided, however, that such restrictions in the foregoing clauses (A) and (B) shall lapse as to 50% of such shares 90 days after the date of the occurrence of the Merger.  The Holder agrees, promptly after the Company’s or the Acquiror’s request, to enter into a written agreement to memorialize in further detail the restrictions contained in this paragraph.

 

For purposes of this Note, the “Merger” shall mean the merger transaction involving the Borrower and Inovio Biomedical Corporation (the “Acquiror”), pursuant to an Agreement and Plan of Merger dated as of July 7, 2008 by and among the Borrower, the Acquiror and the other parties listed therein, as the same may be amended and/or restated from time to time; “Acquiror Common Stock” shall mean the common stock of the Acquiror; and “Trading Day” shall mean a day on which trades occur on the exchange on which Acquiror Common Stock is traded and for which a last sale price is reported for Acquiror Common Stock.”

 

3 .             Effective as of the time of the Merger, the conversion provisions set forth in Section 3 of the Note shall be deleted in their entirety.  For the avoidance of doubt, the conversion provisions added to such Section 3 pursuant to this Allonge shall remain in full force and effect in the event of such deletion.

 

4.             Effective at the time of the Merger, the delivery dates for the financial statements contained in Section 6 of the Note (titled “Financial Reports”) are hereby modified so as to provide that such financial statements shall be deliverable by the Company promptly after they are required to be filed with the Securities and Exchange Commission (and not before such date), notwithstanding anything to the contrary contained in such Section 6.

 

5.             Effective as of the effective time of the Merger, Section 9 of the Note (“Co-Sale Rights”) shall be deleted in its entirety.

 

9



 

This Allonge is intended to be and shall remain attached to, and shall constitute an integral part of, the Note from and after the date hereof.  Except as modified hereby, all of the terms and provisions of the Note are hereby ratified and confirmed and, as amended by this Allonge, shall continue in full force and effect.

 

10


 

Intending to be legally bound hereby, each of the undersigned have duly executed this Allonge as of the          day of                               , 2008.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

 

 

HOLDER

 

 

 

 

 

11



 

ALLONGE

 

Note:

 

Convertible Subordinated Promissory Note dated [ORIGINAL DATE OF NOTE] (the “Note”)

 

 

 

Borrower:

 

VGX Pharmaceuticals, Inc. (the “Borrower”)

 

 

 

Holder:

 

[NAME OF HOLDER] (the “Holder”)

 

 

 

Principal

 

 

Sum:

 

$ [PRINCIPAL]

 

THIS ALLONGE TO CONVERTIBLE SUBORDINATED PROMISSORY NOTE (this “Allonge”) is made as of October        , 2008, between the Borrower and the Holder.  Capitalized terms used but not defined herein shall have the meanings ascribed to them in the Note.

 

WHEREAS , on [ORIGINAL DATE OF NOTE] the Borrower issued the Note to the Holder in an aggregate principal amount equal to the Principal Sum (as defined in the Note), all which remains outstanding as of the date hereof;

 

WHEREAS , on [FIRST ALLONGE DATE] , the Borrower and the Holder entered into an Allonge (“Allonge No. 1”), pursuant to which certain provisions of the Note were amended; and

 

WHEREAS , the Borrower and the Holder now wish to amend further certain provisions of the Note, as set forth herein.

 

NOW THEREFORE , in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties, intending to be legally bound, hereby agree as follows:

 

1.             The first sentence of Section 2 of the Note (titled “Maturity”) is hereby amended and restated in its entirety to read as follows:  “Unless this Note has been converted pursuant to Section 3 or repaid pursuant to Section 7 below, the entire unpaid balance of the Principal Sum outstanding, together with all accrued, but unpaid, interest and all other fees, costs and charges, if any, shall be due and payable on October 24, 2010 (the “Maturity Date”).

 

2.             Section 3 of the Note (titled “Conversion”) is hereby amended by deleting the additional paragraphs thereto that were added pursuant to Section 1 of Allonge No. 1 and by adding the following additional paragraphs to such Section 3:

 

“Notwithstanding any provision to the contrary contained herein, if the Merger (as defined below) is consummated, at any time from and after such consummation until the Maturity Date or the repayment by the Borrower of the Principal Sum, together with all accrued but unpaid interest thereon and all other fees, costs and charges, if any (such

 

12



 

period of time, the “Conversion Period”), the entire Principal Sum, together with all accrued but unpaid interest thereon and all other fees, costs and charges, if any, shall be converted into shares of Acquiror Common Stock as follows:

 

(i)            At the option of the Holder, all of the Principal Sum outstanding hereunder, together with all accrued but unpaid interest thereon and all other fees, costs and charges, if any, shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock (as defined below) as determined by the application of a conversion price equal to $1.05 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares) (the “Conversion Price”).   Such option shall be exercisable by the Holder by providing written notice of conversion to the Company at any time prior to the expiration of the Conversion Period.

 

(ii)           In the event that, at any time during the Conversion Period, the average of the closing sales prices for one share of Acquiror Common Stock as reported on the exchange on which Acquiror Common Stock is traded for the five consecutive Trading Days (as defined below) at a price per share equal to or greater than $2.10 per share (as adjusted for any stock splits, stock dividends, recapitalizations or the like with respect to such shares), this Note shall be converted into that number of fully paid, validly issued and non-assessable shares of Acquiror Common Stock at a conversion price per share equal to the Conversion Price.

 

No fractional shares of Acquiror Common Stock shall be issued upon the conversion of this Note.  With respect to any fraction of a share of Acquiror Common Stock called for upon the conversion of this Note, a cash amount equal to such fraction shall be paid to the Holder.

 

With respect to any shares of Acquiror Common Stock issued in a conversion pursuant to clauses (i) or (ii) above at any time from the date of the occurrence of the Merger through the date that is 180 days after the such date, the Holder shall not (A) sell, assign, exchange, transfer, pledge, hypothecate, distribute or otherwise dispose of (other than by operation of law where the transferee remains subject to and bound by the provisions of this paragraph) any such shares of Acquiror Common Stock or any interest (including, without limitation, an option to buy or sell) in any such shares, in whole or in part, and no such attempted transfer shall be treated as effective for any purpose, or (B) engage in any transaction with respect to such shares or any interest therein, the intent or effect of which is the effective economic disposition of such shares (including, but not limited to, engaging in put, call, short-sale, straddle or similar market transactions), for a period of time commencing on the date of conversion through the date that is 180 days after the occurrence of the Merger, provided, however, that such restrictions in the foregoing clauses (A) and (B) shall lapse as to 50% of such shares 90 days after the date of the occurrence of the Merger.  The Holder agrees, promptly after the Company’s or the Acquiror’s request, to enter into a written agreement to memorialize in further detail the restrictions contained in this paragraph.

 

13



 

For purposes of this Note, the “Merger” shall mean the merger transaction involving the Borrower and Inovio Biomedical Corporation (the “Acquiror”), pursuant to an Agreement and Plan of Merger dated as of July 7, 2008 by and among the Borrower, the Acquiror and the other parties listed therein, as the same may be amended and/or restated from time to time; “Acquiror Common Stock” shall mean the common stock of the Acquiror; and “Trading Day” shall mean a day on which trades occur on the exchange on which Acquiror Common Stock is traded and for which a last sale price is reported for Acquiror Common Stock.”

 

3 .             Effective as of the time of the Merger, the conversion provisions set forth in Section 3 of the Note shall be deleted in their entirety.  For the avoidance of doubt, the conversion provisions added to such Section 3 pursuant to this Allonge shall remain in full force and effect in the event of such deletion.

 

4.             Effective at the time of the Merger, the delivery dates for the financial statements contained in Section 6 of the Note (titled “Financial Reports”) are hereby modified so as to provide that such financial statements shall be deliverable by the Company promptly after they are required to be filed with the Securities and Exchange Commission (and not before such date), notwithstanding anything to the contrary contained in such Section 6.

 

This Allonge is intended to be and shall remain attached to, and shall constitute an integral part of, the Note from and after the date hereof.  Except as modified hereby, all of the terms and provisions of the Note are hereby ratified and confirmed and, as amended by this Allonge, shall continue in full force and effect.

 

14



 

Intending to be legally bound hereby, each of the undersigned have duly executed this Allonge as of the          day of                               , 2008.

 

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

 

 

HOLDER

 

 

 

 

 

15




EXHIBIT 10.65

 

Portions Subject to Confidential Treatment Request Under Rule 406

 

 

LICENSE AGREEMENT

 

 

by and between

 

VGX PHARMACEUTICALS, INC.,

 

 

and

 

GENETRONICS, INC.

 

 

November 9, 2006

 



 

TABLE OF CONTENTS

 

 

 

Page(s)

 

 

 

1.

DEFINITIONS

1

 

 

 

1.1.

Additional Third Party License

1

 

 

 

1.2.

Affiliate(s)

1

 

 

 

1.3.

Applicator

2

 

 

 

1.4.

Calendar Quarter

2

 

 

 

1.5.

Calendar Year

2

 

 

 

1.6.

Change of Control

2

 

 

 

1.7.

Clinical Trial

2

 

 

 

1.8.

Commercialize

2

 

 

 

1.9.

Confidential Information

2

 

 

 

1.10.

Control or Controlled

3

 

 

 

1.11.

Develop

3

 

 

 

1.12.

Development Term

3

 

 

 

1.13.

Device

3

 

 

 

1.14.

EP

4

 

 

 

1.15.

Existing EP Intellectual Property

4

 

 

 

1.16.

Existing Genetronics Know-How

4

 

 

 

1.17.

Existing Genetronics Patent Rights

4

 

 

 

1.18.

Existing Genetronics Patents

4

 

 

 

1.19.

FDA

4

 

 

 

1.20.

FD&C Act

4

 

 

 

1.21.

First Commercial Sale

4

 

 

 

1.22.

FTE

4

 



 

1.23.

GAAP

4

 

 

 

1.24.

Genetic Construct

4

 

 

 

1.25.

Generator

4

 

 

 

1.26.

Genetronics Competitor

5

 

 

 

1.27.

Genetronics Costs

5

 

 

 

1.28.

Genetronics Product Enhancements

5

 

 

 

1.29.

Genetronics EP Technology

5

 

 

 

1.30.

Genetronics Know-How

5

 

 

 

1.31.

Genetronics Licensed Technology

5

 

 

 

1.32.

Genetronics Patent Rights

5

 

 

 

1.33.

Genetronics Third Party Agreement

5

 

 

 

1.34.

IND

5

 

 

 

1.35.

Indication

6

 

 

 

1.36.

Joint IP

6

 

 

 

1.37.

Joint Know-How

6

 

 

 

1.38.

Joint Patent Right

6

 

 

 

1.39.

Joint Collaboration Technology

6

 

 

 

1.40.

Know-How

6

 

 

 

1.41.

Licensed Fields

6

 

 

 

1.42.

Licensed Product

6

 

 

 

1.43.

Major Market Country

6

 

 

 

1.44.

Manufacture

6

 

 

 

1.45.

Marketing Application

6

 

 

 

1.46.

Net Sales

6

 

 

 

1.47.

Patent Rights

7

 



 

1.48.

Person

7

 

 

 

1.49.

Phase I Clinical Trial

7

 

 

 

1.50.

Phase II Clinical Trial

7

 

 

 

1.51.

Phase III Clinical Trial

7

 

 

 

1.52.

Product Data

8

 

 

 

1.53.

Promotion

8

 

 

 

1.54.

Recall

8

 

 

 

1.55.

Registrational Filing

8

 

 

 

1.56.

Regulatory Approval

8

 

 

 

1.57.

Regulatory Authority

8

 

 

 

1.58.

Regulatory Marketing Authorization

8

 

 

 

1.59.

Right of Reference

8

 

 

 

1.60.

Samples

9

 

 

 

1.61.

Sublicense

9

 

 

 

1.62.

Sublicensee

9

 

 

 

1.63.

Term

9

 

 

 

1.64.

Territory

9

 

 

 

1.65.

Third Party

9

 

 

 

1.66.

Trademark

9

 

 

 

1.67.

Valid Claim

9

 

 

 

1.68.

VGX Device Improvements

9

 

 

 

1.69.

VGX Know-How

9

 

 

 

1.70.

VGX Licensed Technology

9

 

 

 

1.71.

VGX Patent Rights

9

 

 

 

1.72.

VGX Product Data

10

 



 

1.73.

VGX Regulatory Approvals

10

 

 

 

1.74.

VGX Sublicensee

10

 

 

 

2.

LICENSE GRANTS

10

 

 

 

2.1.

Licenses to VGX

10

 

 

 

2.2.

Product Enhancements

11

 

 

 

2.3.

Direct Licenses to Affiliates

11

 

 

 

2.4.

Right of Reference

11

 

 

 

2.5.

No Other Rights

12

 

 

 

3.

COORDINATION

12

 

 

 

3.1.

Development Liaison Representative

12

 

 

 

3.2.

Responsibiloites of Development Liaison Representatives

12

 

 

 

4.

PRODUCT DEVELOPMENT AND COMMERCIALIZATION

12

 

 

 

4.1.

General

12

 

 

 

4.2.

Diligence

12

 

 

 

4.3.

Regulatory Responsibilities

13

 

 

 

4.4

Regulatory Documentation-Device

13

 

 

 

4.5

Commercialization Responsibilities

14

 

 

 

5.

MANUFACTURING AND SUPPLY

15

 

 

 

5.1.

General

15

 

 

 

5.2.

Diligence

15

 

 

 

5.3.

Genetic Construct Manufacture

15

 

 

 

5.4.

Device Manufacture

15

 

 

 

6.

CONSIDERATION

15

 

 

 

6.1.

Upfront Payment

15

 

 

 

6.2.

Development Payments

15

 

 

 

6.3.

Royalty Payments

16

 



 

6.4.

Reports and Payments

17

 

 

 

7.

MUTUAL COVENANTS

19

 

 

 

7.1.

Confidentiality

19

 

 

 

7.2.

Compliance with Law

20

 

 

 

8.

REPRESENTATIONS AND WARRANTIES

21

 

 

 

8.1.

Representations and Warranties of Each Party

21

 

 

 

8.2.

Additional Representations and Warranties of Genetronics

21

 

 

 

8.3.

Representation by Legal Counsel

21

 

 

 

8.4.

Disclaimer

22

 

 

 

9.

INTELLECTUAL PROPERTY

22

 

 

 

9.1.

Disclosure

22

 

 

 

9.2.

Ownership

22

 

 

 

9.3.

Prosecution and Maintenance of Patent Rights

23

 

 

 

9.4.

Trademarks

23

 

 

 

9.5.

Enforcement of Technology Rights

24

 

 

 

9.6.

Third Party Claims

25

 

 

 

9.7.

Patent Marking, Certification and Term Restoration

26

 

 

 

10.

GOVERNMENT APPROVALS

26

 

 

 

10.1.

Each Party’s Obligations

26

 

 

 

10.2.

Additional Approvals

26

 

 

 

11.

TERM AND TERMINATION

26

 

 

 

11.1.

Term

26

 

 

 

11.2.

Termination

27

 

 

 

11.3.

Insolvency

27

 

 

 

11.4.

Change of Control

29

 



 

11.5.

Accrued Rights

30

 

 

 

11.6.

Disposition of Inventory

30

 

 

 

11.7.

Survival

30

 

 

 

12.

INDEMNIFICATION AND INSURANCE

30

 

 

 

12.1.

Indemnification by VGX

30

 

 

 

12.2.

Indemnification by Genetronics

31

 

 

 

12.3.

Procedure

31

 

 

 

12.4.

Insurance

32

 

 

 

13.

MISCELLANEOUS

32

 

 

 

13.1.

Assignment

32

 

 

 

13.2.

Further Actions

32

 

 

 

13.3.

Force Majeure

32

 

 

 

13.4.

Correspondence and Notices

33

 

 

 

13.5.

Amendment

34

 

 

 

13.6.

Waiver

34

 

 

 

13.7.

Severability

34

 

 

 

13.8.

Descriptive Headings

34

 

 

 

13.9.

Governing Law; Venue

34

 

 

 

13.10.

Entire Agreement

35

 

 

 

13.11.

Independent Contractors

35

 

 

 

13.12.

Counterparts

35

 

 

 

13.13.

Future Relationships

35

 

 

 

13.14.

Interpretation

35

 

 

 

13.15.

No Third Party Rights or Obligations

35

 



 

SCHEDULES

 

 

 

 

 

Schedule 1.18

Existing Genetronics Patents

 

 

 

 

Schedule 5.4.1

Clinical Supply Terms

 

 

 

 

Schedule 6.1

Upfront Payments

 

 

 

 

Schedule 6.2

Development Payments

 

 

 

 

Schedule 6.3.2

Royalty Payments

 

 


 

LICENSE AND DEVELOPMENT AGREEMENT

 

This License and Development Agreement (the “ Agreement ”) is entered into this 9th day of November, 2006 (the “ Effective Date ”), by and between Genetronics, a corporation organized and existing under the laws of the State of California and having a principal place of business at 11494 Sorrento Valley Road, San Diego, California 92121 (“ Genetronics ”), and VGX Pharmaceuticals, Inc., a corporation organized and existing under the laws of the State of Delaware and having a principal place of business at 450 Sentry Parkway, Blue Bell, PA 19422 (“ VGX ”).  VGX and Genetronics may each be referred to herein individually as a “Party” and collectively as the “Parties.”

 

WHEREAS, Genetronics is engaged in the development and commercialization of human applications of electroporation and possesses rights to certain patents thereto; and

 

WHEREAS, VGX is engaged in the research, development and commercialization of human pharmaceutical and biologic products related to certain nucleic acid-based Genetic Constructs potentially useful in the treatment of cancer; and

 

WHEREAS, VGX and Genetronics wish to collaborate, on the terms and conditions set forth in this Agreement, on the development and commercialization of products combining those Genetic Constructs with Genetronics’s intratumoral electroporation delivery technology;

 

NOW THEREFORE, in consideration of the mutual promises and covenants set forth below and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties hereby agree as follows:

 

1.              DEFINITIONS.

 

Capitalized Terms not otherwise defined herein shall have the following meanings:

 

1.1.                Additional Third Party License .  “Additional Third Party License” shall have the meaning set forth in Section 9.6.2 hereof.

 

1.2.                Affiliate(s).   “Affiliate(s)” shall mean any legal entity directly or indirectly controlling, controlled by or under common control with VGX that has executed (a) this Agreement, or (b) a written joinder agreement, in a form reasonably satisfactory to Genetronics, agreeing to be bound by all of the terms and conditions of this Agreement, as if such Affiliate were an original party to this Agreement.  For purposes of this Agreement, “control” means the direct or indirect ownership of more than fifty percent (50%) of the outstanding voting securities of a legal entity, and/or the right to receive more than fifty (50%) of the profits or earnings of a legal entity, and/or the right to control the policy decisions of a legal entity.   Any reference to VGX Affiliates or VGX and its Affiliates shall mean Affiliate under this paragraph.   As for Genetronic’s Affiliates the following shall apply:   Affiliate shall mean, as, as of any point in time and for so long as such relationship continues to exist with respect to any Person (as defined below), any other Person which controls, is controlled by or is under common control with such Person.  A Person shall be regarded as in control of another Person if it owns or controls at least fifty percent (50%) of the equity securities of the subject Person entitled to vote in the election of directors (or, in

 



 

the case of a Person that is not a corporation, for the election of the corresponding managing authority); provided, however, that the term “Affiliate” shall not include subsidiaries or other entities in which a Person owns a majority of the ordinary voting power necessary to elect a majority of the board of directors or other governing board, but is restricted from electing such majority by contract or otherwise, until such time as such restrictions are no longer in effect.

 

1.3.                Applicator .  “Applicator” shall mean an existing 6-needle, high voltage (>800V/cm) Genetronics product designed for use solely with the Generator to deliver a Genetic Construct by means of intratumoral electroporation, and which product is intended to be disposed of after one administration to a patient of a Licensed Product, or after a defined number of such administrations of a Licensed Product.

 

1.4.                Calendar Quarter .  “Calendar Quarter” shall mean the respective periods of three (3) consecutive calendar months ending on March 31, June 30, September 30 or December 31 of each Calendar Year.

 

1.5.                Calendar Year .  “Calendar Year” shall mean any calendar year, for so long as this Agreement is in effect.

 

1.6.                Change of Control .  “Change of Control” shall mean a transaction in which VGX: (a) sells, conveys or otherwise disposes of all or substantially all of its property or business; or (b)(i) merges or consolidates with any other entity (other than an Affiliate of VGX); or (ii) effects any other transaction or series of transactions; in each case of clause (i) or (ii), such that the stockholders of VGX immediately prior thereto, in the aggregate, no longer own, directly or indirectly, beneficially or legally, at least fifty percent (50%) of the outstanding voting securities or capital stock of the surviving entity following the closing of such merger, consolidation, other transaction or series of transactions.

 

1.7.                Clinical Trial .  “Clinical Trial” shall mean a clinical study conducted by or for VGX on human subjects pursuant to a protocol approved by an appropriate regulatory authority, which study is designed to support the Marketing Application for the Licensed Product that is the subject of such study.

 

1.8.                Commercialize .  “Commercialize” or “Commercializing” shall mean to use, import, export, market, Promote, distribute, offer for sale, sell, have sold or otherwise commercialize or prepare to commercialize.  When used as a noun, “Commercialization” shall mean any and all activities involved in Commercializing.  “Commercialization” does not include Development or Manufacturing and to “Commercialize” does not include to Develop or to Manufacture.

 

1.9.                Confidential Information.   “Confidential Information” means, with respect to a Party, all information (and all tangible and intangible embodiments thereof), which is Controlled by such Party, including, without limitation, (i) scientific or medical information, material, results and data of any type whatsoever, in any tangible or intangible form whatsoever, including databases, inventions, practices, methods, techniques, specifications, formulations, formulae, cell lines, cell media, knowledge, know-how, skill,

 

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experience, manufacturing materials, financial data, test data including pharmacological, biological, chemical, biochemical, toxicological and clinical test data, analytical and quality control data, quality assurance data, stability data, and studies and procedures, (ii) all regulatory filings and communications or any kind, and patent and other legal information or descriptions and (iii) commercial information of any kind, including product forecasts and sales information, sales force information, marketing studies and marketing materials, comparative analysis of competing products, physician education materials, customer and distribution channel information, and any information regarding post-approval trials, adverse event reports, or other product information.  Notwithstanding the foregoing, Confidential Information of a Party which is disclosed by such Party to the other Party or otherwise received by the receiving Party shall not include information which the receiving Party can establish by written documentation (a) was publicly known prior to its disclosure to or receipt by the receiving Party, (b) became publicly known, without breach of this Agreement on the part of the receiving Party or an agent thereof, subsequent to its disclosure to or receipt by the receiving Party, (c) was received by the receiving Party at any time from a source, other than the disclosing Party, rightfully having possession of and the right to disclose such information free of confidentiality obligations, (d) was otherwise known by the receiving Party free of confidentiality obligations to the disclosing Party prior to its disclosure to or receipt by the receiving Party, or (e) was independently developed by employees or others on behalf of the receiving Party without the aid, application or use of the information disclosed to or received by the receiving Party.

 

1.10.              Control or Controlled .  “Control” or “Controlled” shall mean with respect to any material, item of information, or intellectual property right, the possession, whether by ownership, license or otherwise, of the right to grant a license or other right with respect thereto to the extent set forth herein.

 

1.11.              Develop .  “Develop” or “Developing” shall mean to discover, research, have researched, develop, have developed or use for development purposes, including conducting non-clinical and clinical research and development activities such as toxicology, pharmacology and other discovery efforts, test method development and stability testing, process development, formulation development, delivery system development, quality assurance and quality control development, statistical analysis, clinical studies (including pre- and post-approval studies), regulatory affairs, pharmacovigilance and Regulatory Approval and Clinical Trial regulatory activities (including regulatory activities directed to obtaining pricing and reimbursement approvals).  When used as a noun, “Development” shall mean any and all activities involved in Developing.  Development shall not include Manufacturing or Commercialization and to “Develop” does not include to Commercialize or to Manufacture.

 

1.12.              Development Term .  “Development Term” shall mean the period of time from the Effective Date until the First Commercial Sale of the first Licensed Product to be sold in any country in the Territory.

 

1.13.              Device .  “Device” shall mean a Generator or Applicator.  “Devices” shall mean Generators or Applicators, or both.

 

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1.14.              EP .  “EP” shall mean intratumoral electroporation.

 

1.15.              Existing EP Intellectual Property .  “Existing EP Intellectual Property” shall mean the Existing Genetronics Patent Rights and Existing Genetronics Know-How.

 

1.16.              Existing Genetronics Know-How .  “Existing Genetronics Know-How” shall mean any Genetronics Know-How Controlled by Genetronics or its Affiliates as of the Effective Date in the Licensed Field.

 

1.17.              Existing Genetronics Patent Rights .  “Existing Genetronics Patent Rights” shall mean any Genetronics Patent Rights Controlled by Genetronics or its Affiliates as of the Effective Date.

 

1.18.              Existing Genetronics Patents .  “Existing Genetronics Patents” shall mean the patents and patent applications listed on Schedule 1.18 attached hereto.

 

1.19.              FDA .  “FDA” shall mean the United States Food and Drug Administration or any successor agency thereto.

 

1.20.              FD&C Act .  “FD&C Act” shall mean the United States Federal Food, Drug, and Cosmetic Act, as amended from time to time, and the rules and regulations promulgated thereunder.

 

1.21.              First Commercial Sale .  “First Commercial Sale” shall mean, with respect to any Licensed Product and with respect to any country of the Territory, the first sale of such Licensed Product to a Third Party in such country after such Licensed Product has been granted Regulatory Marketing Authorization by a competent Regulatory Authority for such country.

 

1.22.              FTE .  “FTE” shall mean a full time equivalent scientific person year, consisting of a minimum of a total of one thousand eight hundred (1800) hours per year of scientific work by an appropriately educated, qualified and experienced employee of Genetronics or VGX directly related to activities under the Agreement.

 

1.23.              GAAP .  “GAAP” shall mean United States generally accepted accounting principles consistently applied.

 

1.24.              Genetic Construct .  “Genetic Construct” shall mean any pharmaceutical or biologic preparation comprising a nucleic acid sequence encoding a peptide or protein, including, but not limited to, antigen(s), adjuvant(s), expression vectors, and/or formulations that VGX Develops, Manufactures, or Commercializes in the Licensed Field.

 

1.25.              Generator .  “Generator” shall mean an intratumoral EP device, including any software that is not custom designed for use with a Genetic Construct, for which the manufacture and/or use with a Genetic Construct in the Licensed Field would infringe the Genetronics Patent Rights or utilize the Genetronics Licensed Technology, including but not limited to pulse generation equipment.

 

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1.26.              Genetronics Competitor .  “Genetronics Competitor” means any company (other than Genetronics or VGX) that is either (i) significantly engaged in the manufacturing, commercialization, and/or marketing of EP Applicators and/or Generators or (ii) is a Sublicensee of Genetronics or its parent company.

 

1.27.              Genetronics Costs .  “Genetronics Costs” means all fully burdened FTE costs incurred by Genetronics that are related to the performance by Genetronics of its assigned activities under this agreement that have been approved in writing in advance by VGX.

 

1.28.              Genetronics Product Enhancements .  “Genetronics Product Enhancements” shall mean any Genetronics Patent Rights or Genetronics Know-How Controlled by Genetronics or its Affiliates developed or obtained by Genetronics during the Term that enhances or technically improves a Licensed Product.

 

1.29.              Genetronics EP Technology .  “Genetronics EP Technology” shall mean Genetronics’s intratumoral EP delivery technology related to the Licensed Field, including but not limited to Devices and any other electroporation equipment, designs thereof, and methods of use thereof.

 

1.30.              Genetronics Know-How.  “Genetronics Know-How” shall mean all EP-related Know-How Controlled by Genetronics or its Affiliates, now or at any time during the Term, necessary for the Development, Manufacture, use, sale or importation of any Licensed Product in a Licensed Field and in the Territory (other than Genetronics’s interest in Joint IP).

 

1.31.              Genetronics Licensed Technology .  “Genetronics Licensed Technology” shall mean Genetronics’s rights in (i) Existing EP Intellectual Property, (ii) Genetronics’s interest in Genetronics Product Enhancements, and (iii) any other Genetronics Patent Rights and Genetronics Know-How (other than Genetronics’s interest in Joint IP) related to the Licensed Products in the Licensed Field and in the Territory.

 

1.32.              Genetronics Patent Rights .  “Genetronics Patent Rights” shall mean any EP-related Patent Rights Controlled by Genetronics or its Affiliates now or at any time during the Term, which would be infringed by the Development, Manufacture, use, sale or importation of any Licensed Product in the Licensed Field in the Territory (other than Genetronics’s interest in Joint IP).  Genetronics Patent Rights shall include Genetronics Existing Patent Rights.

 

1.33.              Genetronics Third Party Agreement .  “Genetronics Third Party Agreement” shall mean any agreement between Genetronics and any Third Party that involves a license by such Third Party to Genetronics that comprises Genetronics Licensed Technology.

 

1.34.              IND .  “IND” shall mean an Investigational New Drug Application, as defined in the FD&C Act, that is required to be filed with the FDA before beginning clinical testing in human subjects, or an equivalent foreign filing.

 

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1.35.              Indication .  “Indication” means, with respect to any Licensed Product, any indication for such Licensed Product in the Licensed Field for which Regulatory Marketing Authorization has been achieved or is being sought.

 

1.36.              Joint IP .  “Joint IP” shall mean the Joint Know-How and the Joint Patent Rights.

 

1.37.              Joint Know-How .  “Joint Know-How” shall mean any Know-How covering or embodied by or in any Joint Collaboration Technology.

 

1.38.              Joint Patent Right .  “Joint Patent Right” means any Patent Right covering any Joint Collaboration Technology.

 

1.39.              Joint Collaboration Technology .  “Joint Collaboration Technology” shall mean any invention, development or discovery, whether or not patentable, made or created jointly by (i) employees or agents of Genetronics or any of its Affiliates, and (ii) employees or agents of VGX or any of its Affiliates in the course of carrying out this Agreement.

 

1.40.              Know-How .  “Know-How” shall mean any confidential unpatented or unpatentable technology, compound, cell line or other biological material, probe, sequence, technical information, method, or other confidential information or material, in all cases to the extent, but only to the extent, not in the public domain.

 

1.41.              Licensed Field .  “Licensed Field” shall mean the delivery of HIV vpr gene sequences via DNA intratumoral electroporation at voltages greater than 800V/cm and less than 2000 V/cm to treat cancer in humans.

 

1.42.              Licensed Product .  “Licensed Product” shall mean any product where Therapeutic Genetic Constructs are used together with the Devices in administering treatments to patients in the Licensed Field.

 

1.43.              Major Market Country .  “Major Market Country” shall mean the United States, France, Germany, the United Kingdom, and Italy.

 

1.44.              Manufacture .  “Manufacture,” “Manufactured” or “Manufacturing” means all activities involved in the production, packaging and labeling of a Licensed Product to be Developed and/or Commercialized under this Agreement.  “Manufacturing” does not include Development or Commercialization.

 

1.45.              Marketing Application .  “Marketing Application” means a new drug application or product license application or its equivalent filed with and accepted by the FDA after completion of human clinical trials to obtain marketing approval for a Licensed Product, or any comparable application filed with and accepted by the Regulatory Authority of a country other than the United States, including, where applicable, any applications for governmental pricing and marketing approval.

 

1.46.              Net Sales .  “Net Sales” shall mean the gross amount invoiced for any sale of any Licensed Product by VGX, any VGX Affiliate or any VGX Sublicensee, as appropriate (a “Selling Person”), to a non-Affiliate in a bona fide arm’s length transaction, less the

 

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following deductions, in each case to the extent specifically related to the Licensed Product and taken by the Selling Person or otherwise paid for or accrued by the Selling Person (“Permitted Deductions”):

 

(i)                   trade, cash, promotional and quantity discounts and wholesaler fees;

 

(ii)                  taxes on sales (such as excise, sales or use taxes or value added taxes) to the extent imposed upon and paid directly with respect to the sales price (and excluding national, sales or local taxes based on income);

 

(iii)                 freight, insurance, packing costs and other transportation charges to the extent included in the invoice price to the buyer;

 

(iv)                amounts repaid or credits taken by reason of damaged goods, rejections, defects, expired dating, recalls, returns or because of retroactive price reductions;

 

(v)                 charge back payments and rebates granted to (a) managed healthcare organizations, (b) federal, state and/or provincial and/or local governments or other agencies, (c) purchasers and reimbursers, or (d) trade customers, including wholesalers and chain and pharmacy buying groups; and

 

(vi)                documented custom duties actually paid by the Selling Person.

 

1.47.              Patent Rights .  “Patent Rights” shall mean any and all (a) U.S. or foreign patents, (b) U.S. or foreign patent applications, including, without limitation, all provisional applications, substitutions, continuations, continuations-in-part, divisions, renewals, and all patents granted thereon, (c) all U.S. or foreign patents-of-addition, reissues, reexaminations and extensions or restorations by existing or future extension or restoration mechanisms, including, without limitation, patent term adjustments, patent term extensions, supplementary protection certificates or the equivalent thereof, and (d) any other form of government-issued right substantially similar to any of the foregoing.

 

1.48.              Person .  “Person” shall mean any individual or legal entity.

 

1.49.              Phase I Clinical Trial.   “Phase I Clinical Trial” shall mean a human Clinical Trial conducted on sufficient numbers of healthy human volunteers with the endpoint of determining initial tolerance, safety and/or pharmacokinetic information in single dose, single ascending dose, multiple dose and/or multiple ascending dose regimens, and to support its continued testing in Phase II Clinical Trials .

 

1.50.              Phase II Clinical Trial .  “Phase II Clinical Trial” shall mean a human Clinical Trial that is designed to determine initial efficacy and dose range findings and to define warnings, precautions and adverse reactions that may be associated with the product in such dosage range.

 

1.51.              Phase III Clinical Trial .  “Phase III Clinical Trial” shall mean a human Clinical Trial that is designed to establish that a treatment is safe and efficacious for its intended use, and to define warnings, precautions and adverse reactions that are associated with the

 

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product in the dosage range to be prescribed, and to support Regulatory Approval of such treatment or label expansion of such medicinal product.

 

1.52.              Product Data .  “Product Data” shall mean all pre-clinical data and results, clinical protocols, studies, clinical data and results, post-marketing data and results, manufacturing data and results, and other information necessary or useful for obtaining Regulatory Approval of a Licensed Product in the Licensed Field.

 

1.53.              Promotion .  “Promotion” shall mean those activities, including, without limitation, detailing and distributing Samples of Licensed Product, normally undertaken by a pharmaceutical company’s sales force to implement marketing plans and strategies aimed at encouraging the approved use of a particular Licensed Product.  When used as a verb, “Promote” means to engage in such activities.

 

1.54.              Recall .  “Recall” shall mean, with respect to any pharmaceutical product, a “recall” or a “product withdrawal” or a “stock recovery” or any similar term as utilized by any Regulatory Authority under such Regulatory Authority’s procedures regarding the recall of pharmaceutical products, as the same may be amended from time to time, and shall include any post-sale warning or mailing of information regarding such product, including any warnings or mailings described in the Regulatory Authority’s product recall procedures.

 

1.55.              Registrational Filing .  “Registrational Filing” shall mean an application submitted to the appropriate Regulatory Authority seeking a Regulatory Marketing Authorization.

 

1.56.              Regulatory Approval .  “Regulatory Approval” means any technical, medical, scientific or other license, registration, authorization or approval of any Regulatory Authority regarding the research, development, clinical testing, commercial manufacture, distribution, marketing, pricing, reimbursement, Promotion, offer for sale, use, import, export or sale of any pharmaceutical product, proposed pharmaceutical product, medical device, proposed medical device, or any combination thereof.

 

1.57.              Regulatory Authority .  “Regulatory Authority” shall mean, with respect to a country in the Territory, any national (e.g., the FDA), supra-national (e.g., the European Commission, the Council of the European Union, or the European Agency for the Evaluation of Medicinal Products), regional, state or local regulatory agency, department, bureau, commission, council or other governmental entity involved in the granting of a Regulatory Approval for such country or countries.

 

1.58.              Regulatory Marketing Authorization .  “Regulatory Marketing Authorization” shall mean, with respect to any Licensed Product in any country or region and in any indication, Regulatory Approval authorizing the marketing of such Licensed Product in such country or region for such indication.

 

1.59.              Right of Reference .  “Right of Reference” shall mean the right to reference, cross-reference, review, have access to, incorporate and use in any regulatory applications or filings, any patent filings, or for any research, development or commercialization purpose.

 

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1.60.              Samples .  “Samples” means a unit of Licensed Product that is not intended to be sold and is intended to Promote the sale of such Licensed Product.  When used as a verb “Sample” means to provide Samples to healthcare providers.

 

1.61.              Sublicense .  When used as a verb, “Sublicense” shall mean to, directly or indirectly, sublicense, or grant any other right with respect to, or agree not to assert, any intellectual property right granted to a Party under this Agreement.  When used as a noun, “Sublicense” shall mean any agreement to Sublicense.

 

1.62.              Sublicensee .  “Sublicensee” shall mean any VGX Sublicensee or any Genetronics Sublicensee.

 

1.63.              Term .  “Term” shall mean the period of time from the Effective Date until the expiration or earlier termination of this Agreement.

 

1.64.              Territory .  “Territory” shall mean worldwide.

 

1.65.              Third Party .  “Third Party” shall mean any Person other than VGX, Genetronics or their respective Affiliates.

 

1.66.              Trademark .  “Trademark” shall mean any trademark used by the Parties in connection with a Licensed Product, other than the Parties’ trade names and trademarks used by the Parties to identify their companies generally.

 

1.67.              Valid Claim .  “Valid Claim” shall mean a claim of an issued and unexpired Patent Right that has not been held permanently revoked, unenforceable or invalid by a decision of a court or other governmental agency of competent jurisdiction, unappealed or unappealable within the time allowed for appeal, and that has not been admitted to be invalid or unenforceable through reissue, disclaimer or otherwise.

 

1.68.              VGX Device Improvements .  “VGX Device Improvements” shall mean any invention, development or discovery, whether or not patentable, related solely to Devices and not related to any other subject matter (including, without limitation, Genetic Constructs) made solely by VGX or jointly by VGX and Genetronics and arising under this Agreement.

 

1.69.              VGX Know-How .  “VGX Know-How” shall mean all Know-How Controlled by VGX or its Affiliates, now or at any time during the term of this Agreement that relates to the Genetic Construct or to the use of the Genetic Construct in connection with the Development, Manufacture, or Commercialization of any Licensed Product.

 

1.70.              VGX Licensed Technology .  “VGX Licensed Technology” shall mean the VGX Patent Rights and VGX Know-How (other than VGX’s interest in Joint IP).

 

1.71.              VGX Patent Rights .  “VGX Patent Rights” shall mean any Patent Right (other than a Genetronics Patent Right) Controlled by VGX or its Affiliates, now or at any time during the term of this Agreement, that relate to the Genetic Construct or to the use of the

 

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Genetic Construct in connection with the Development, Manufacture, or Commercialization of any Licensed Product.

 

1.72.              VGX Product Data .  “VGX Product Data” shall mean all Product Data Controlled by VGX or its Affiliates at any time during the term of this Agreement.

 

1.73.              VGX Regulatory Approvals .  “VGX Regulatory Approvals” means those Regulatory Approvals Controlled by VGX or its Affiliates related to the Development or Commercialization of a Licensed Product.

 

1.74.              VGX Sublicensee .  “VGX Sublicensee” shall mean any Person to whom VGX has granted, directly or indirectly, any Sublicense of any right granted to VGX by Genetronics under this Agreement.

 

2.              LICENSE GRANTS.

 

2.1.                Licenses to VGX.

 

2.1.1.           Non-Exclusive License from Genetronics to VGX .   Subject to the terms and conditions of this Agreement, Genetronics hereby grants to VGX and its Affiliates a non-exclusive license, with the right to grant sublicenses pursuant to Section 2.1.3, under the Genetronics Licensed Technology to Develop, Manufacture, and Commercialize Licensed Products in the Licensed Field in the Territory.

 

2.1.2.           Trademark License from Genetronics to VGX .  Upon VGX’s written request at any time during the Term and subject to the terms and conditions of this Agreement, Genetronics shall grant to VGX and its Affiliates a non-exclusive, fully paid-up, royalty-free, non-transferable Trademark license, with the right to grant sublicenses, to use Genetronics’s Trademarks and/or trade names in connection with Genetronics Technology solely to Commercialize and Manufacture Licensed Products in the Licensed Field in the Territory.  If granted, such Trademark license shall become perpetual and irrevocable upon expiration of the Term, but shall remain non-transferable and solely useable by VGX in connection with Genetronics Technology solely to Manufacture, Commercialize and Sell Licensed Products in the Licensed Fields in the Territory The Trademark license will terminate with the Technology License in the event of early termination.

 

2.1.3.           VGX Sublicenses to Third Parties .  Subject to the payment and other provisions of Section 6, VGX may, upon written consent from Genetronics, which consent shall not be unreasonably withheld or delayed, Sublicense any rights licensed or otherwise granted to VGX under this Agreement to (i) VGX’s Affiliates; (ii) VGX’s distributors of Licensed Products pursuant to bona fide arm’s length distribution agreements; and (iii) any Third Party other than a Genetronics Competitor or sublicensee, in each case that enters into a bona fide license and/or collaboration agreement with VGX to Develop, Manufacture, or Commercialize Licensed Products in the Licensed Field in the Territory.  Any Sublicense by VGX shall be subject to the provisions of this Agreement and may, at Genetronics’ sole discretion, survive termination of the licenses or other rights granted to VGX under this Agreement in accordance with Section 

 

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11.2.2(iii) hereof; provided, however, that in no event shall Genetronics be required to accept any sublicense on terms less favorable to it than the terms of this Agreement, and provided, further, that VGX shall remain legally liable to Genetronics for the performance by each such sublicensee of its obligations thereunder.

 

2.1.4         VGX Sublicenses from Third Parties .  In the event that any of the rights licensed or otherwise granted by Genetronics to VGX under this Agreement comprise rights also licensed or otherwise granted by Genetronics to a Third Party, then neither VGX nor any VGX Affiliate shall enter into any arrangement with that Third Party whereby the Third Party would sublicense such rights to VGX or a VGX Affiliate on terms any different from those contained herein.

 

2.2.                Product Enhancements.

 

2.2.1.           Non-Exclusive License for Product Enhancements to VGX .  Subject to the terms and conditions of this Agreement, Genetronics hereby grants to VGX a non-exclusive, fully paid-up, royalty-free, non-sublicensable license to Genetronics Product Enhancements under the Genetronics Licensed Technology and Genetronics’ interest in the Joint IP solely for use by VGX with Licensed Products in the Licensed Field in the Territory.

 

2.2.2.           License for VGX Device Improvements .  Subject to the terms and conditions of this Agreement, VGX hereby grants to Genetronics an exclusive, fully paid-up, royalty-free, sublicensable license in the Territory under VGX’s rights in the VGX Device Improvements to Develop, Commercialize and Manufacture Devices and methods in any field.

 

2.3.                Direct Licenses to Affiliates .  VGX may at any time request and authorize Genetronics to grant licenses directly to Affiliates of VGX by giving written notice designating to whom a direct license is to be granted.  Upon receipt of any such notice, Genetronics shall enter into and sign a separate direct license agreement with such designated Affiliate of VGX.  All such direct license agreements shall be consistent with the terms and conditions of this Agreement, except for such modifications as may be required by the laws and regulations in the country in which the direct license will be exercised; provided, however , that Genetronics shall have no obligation to enter into any such direct license agreement if the effect of entering into such agreement (and continuing as a party to this Agreement) would be to increase the level of obligations owed by or risks assumed by Genetronics, or decrease the consideration owed to Genetronics, relative to the obligations owed by, risks assumed by, or consideration owed to Genetronics under this Agreement; and provided, further, that in no event shall a direct license of rights to a VGX Affiliate relieve VGX of its primary liability to Genetronics for all obligations (including but not limited to obligations of payment, confidentiality, and diligence) hereunder In countries where validity of the direct license agreement requires prior government approval or registration, such direct license agreement shall not become binding between the parties thereto until such approval or registration is granted, which approval or registration shall be obtained by VGX or its Affiliate.

 

2.4.                Right of Reference.  Genetronics hereby grants to VGX a Right of Reference to any Product Data, regulatory filings, and Regulatory Approvals Controlled by Genetronics or its Affiliates that relates to Licensed Products in the Licensed Field for VGX’s use in the Development, Manufacture, and Commercialization of Licensed Products, all to the extent that

 

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they are directly related to VGX’s obligations under the Agreement.  VGX hereby grants to Genetronics a Right of Reference to any Product Data, regulatory filings, and Regulatory Approvals Controlled by VGX or its Affiliates that relates to Licensed Products in the Licensed Field solely for Genetronics’s use in preparing regulatory filings related to any Device, required safety reporting to Regulatory Authorities, and any other internal purposes, all to the extent that they are directly related to Genetronics’s obligations under the Agreement.

 

2.5.                No Other Rights .  No rights, other than those expressly set forth in this Agreement, are granted to either Party hereunder, and no additional rights shall be deemed granted to either Party by implication, estoppel or otherwise.

 

3.              COORDINATION.

 

3.1.              Development Liaison Representative .   VGX and Genetronics shall designate one of its representatives to serve as Development Liaison Representative (“DLR”).  Each Party shall be free to change its DLR on written notice to the other Party.

 

3.2.              Responsibilities of the Development Liaison Representatives .  The DLR’s shall be responsible for the coordination of certain activities under the Collaboration, including

 

(i)          coordinating the supply of any Device under any Development Agreement along with any activities in support of obtaining Regulatory Approval in the Licensed Field for such Device;

 

(ii)         providing general oversight of the entire collaboration between VGX and Genetronics, including Development and Commercialization of each Licensed Product and determination of when milestones have been reached with respect to any Licensed Product;

 

(iii)        fostering the collaborative relationship between the Parties;

 

(iv)        facilitating all required technology transfer;

 

(v)         reaching mutual agreement as to termination of the Agreement due to failure of purpose or science; and

 

(vi)        such other matters as the Parties may assign to the DLR’s from time to time.

 

4.              PRODUCT DEVELOPMENT AND COMMERCIALIZATION.

 

4.1.              General .  Except as set forth in Section 4.3 (Regulatory Responsibilities), VGX shall be solely responsible for Developing and Commercializing Licensed Products in the Licensed Field during the Term.

 

4.2.              Diligence.  VGX shall use Commercially Reasonable Efforts to Develop, Manufacture and Commercialize a Licensed Product in the Licensed Field in the Major Market Countries.  In the event that VGX does not use commercially reasonable efforts to develop Licensed Product in the Field by failing to initiate a clinical study within two (2) years of the

 

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effective date or failure to initiate a pivotal Phase III clinical trial within six (6) years of the effective date, then, unless otherwise agreed by the Parties in writing, the License Grant shall terminate and all rights granted herein shall revert to Genetronics.

 

4.3.              Regulatory Responsibilities .  VGX shall have overall responsibility for developing a registration strategy for each Licensed Product and for coordinating all regulatory matters under the Collaboration.   Anything in this Section 4.3 notwithstanding, however, the Parties expressly agree that under no circumstances shall VGX make any regulatory filing, seek any Regulatory Approval, or otherwise communicate with or submit information to any Regulatory Authority regarding any regulatory filing or Regulatory Approval, in connection with any Device without the prior review and written approval of Genetronics.

 

4.4.              Regulatory Documentation-Device.   Genetronics shall provide all regulatory documentation and support related to the Device necessary for VGX to obtain approval of Licensed Product using such Device and any related enhancements or technical improvements or changes thereto.  In the event that VGX requires special documentation, testing or regulatory support not already existing at Genetronics or that can not be generated based on the IL-12 study currently carried out at the Moffitt Cancer Center, VGX shall reimburse Genetronics for the FTE cost associated with generating such documentation.

 

4.4.1.        Regulatory Filing and Approvals .  VGX shall file, in its own name (or the name of its designated Affiliate), all applications for any form of Regulatory Approval in the Licensed Field for each Licensed Product in all countries in the Territory and shall own all Regulatory Approvals resulting from such applications.  If VGX determines in its sole discretion that Regulatory Approval for a Device would be necessary or useful to the registration strategy for any Licensed Product in the Licensed Field, upon VGX ‘s written request Genetronics shall prepare and file, in its own name, applications for Regulatory Approval in the Licensed Field for such Device.  VGX shall have the opportunity to review and comment on all such filings prior to submission.  All Regulatory Approvals related to the device (e.g., CE mark, PMA or 510k) resulting from such applications shall be the property of Genetronics.  VGX or its designated Affiliate shall be the named sponsor of any Clinical Trial to be conducted during Development of the Licensed Products.

 

4.4.2.        Reporting .  VGX shall be responsible for filing all reports required to be filed in order to maintain any Regulatory Marketing Authorizations granted for Licensed Products in all countries of the Territory in the Licensed Field.  VGX shall be responsible for the adverse experience and safety reporting for all Licensed Products in compliance with the requirements of the FD&C Act and the regulations promulgated thereunder and the equivalent regulations in other countries in the world.  Genetronics shall cooperate with VGX in preparing and filing all such reports and, upon VGX’s request, provide VGX with any information in Genetronics’s possession or Control which VGX reasonably deems to be relevant to any such report.  Genetronics shall be responsible for filing all reports required to be filed in order to maintain any Regulatory Marketing Authorizations granted for Devices.  VGX shall cooperate with Genetronics in preparing and filing all such reports and, upon Genetronics’ request, provide Genetronics with any information in VGX’s possession or Control which Genetronics reasonably deems to be relevant to any such report.

 

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4.4.3.                               Communications with Regulatory Authorities; Genetronics Assistance .  VGX shall have the primary responsibility for communicating with any Regulatory Authority regarding any regulatory filing or any Regulatory Approval related to any Licensed Product prior to submission, during registration/review by a Regulatory Authority or post approval in the Territory in the Licensed Field.  At VGX’s written request, and at VGX’s expense pursuant to Section 5.4.6 below, Genetronics shall (a) provide VGX with advice and reasonable assistance in (i) developing a Regulatory Approval filing strategy for Licensed Products, (ii) reviewing study reports from Clinical Studies of Licensed Products, (iii) preparing applications for Regulatory Approval for Licensed Products, (iv) preparing supplements to applications for Regulatory Approval for Licensed Products, (v) responding to questions from Regulatory Authorities regarding applications for Regulatory Approval or any supplement thereto and (b) participate in interactions with Regulatory Authorities concerning the Licensed Products.

 

4.4.4.                               Product Recalls .  VGX shall be solely responsible for all contact with Regulatory Authorities relating to any Recall of any Licensed Product.  VGX shall be solely responsible for implementing, directing and administering any Recall of any such Licensed Product required or recommended by any Regulatory Authority or court of competent jurisdiction, or determined by VGX, in its sole discretion, to be necessary or advisable.  VGX shall bear the expense of any such recall except for those cases that are determined to be caused by Device malfunctions resulting from manufacturing defects.  Gentronics shall bear the expense of a recall of the Devices that malfunction due to manufacturing defects.

 

4.4.5.                               Inspections .  The Parties shall cooperate in good faith with respect to the conduct of any inspections by any Regulatory Authority of a Party’s site and facilities related to Licensed Products.

 

4.4.6.                               Expenses .  VGX shall be responsible for its own expenses (both internal expenses and out-of-pocket costs paid to a Third Party) incurred in performing its responsibilities in making any filing or otherwise seeking any Regulatory Approval for the Licensed Products in the Licensed Field or in responding to any Regulatory Authority including post approval commitments.  VGX shall reimburse Genetronics for its fully burdened FTE costs in performing its regulatory activities pursuant to Sections 4.4.1 and 4.4.3 including but not limited to reimbursement for FTE’s actually employed by Genetronics in such activities, as agreed in advance by VGX, at a rate of **** per FTE; provided, however , that such regulatory activities were approved in writing by VGX prior to being performed by Genetronics.

 

4.5.                                               Commercialization Responsibilities .

 

4.5.1.                               General .  VGX shall have sole responsibility and exclusive control over all matters relating to the Commercialization of Licensed Products.  Without limiting the generality of the foregoing, VGX (or its designated Affiliates) shall:

 

(i)                            be the exclusive distributor for Licensed Products in the Territory for its own account and risk;

 

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(ii)                         be responsible for invoicing and booking sales for, warehousing, and distributing all Licensed Products in the Territory and shall perform related distribution activities; and

 

(iii)                      have the right and responsibility for establishing and modifying the terms and conditions with respect to the sale of Licensed Products (including any Device sold as a part of a Licensed Product) in the Territory, including any terms and conditions relating to or affecting the price at which Licensed Products will be sold; discounts available to managed care providers; any discount attributable to payments on receivables; any conditions of local reimbursement; distribution of Licensed Products; and credits, price adjustments, other discounts, and allowances to be granted or refused.

 

5.                                        MANUFACTURING AND SUPPLY.

 

5.1.                                               General .  Except as set forth in Section 5.4, VGX (or its designated Affiliates or Third Parties) shall be responsible for the Manufacture and supply of Genetic Constructs and Licensed Products in the Licensed Field in the Territory.

 

5.2.                                               Diligence .  Genetronics shall use Commercially Reasonable Efforts to fulfill its obligations under any Clinical Supply Agreement and the Commercial Supply Agreement.

 

5.3.                                               Genetic Construct Manufacture .  VGX shall have sole responsibility and exclusive control over all matters relating to the Manufacture of Genetic Constructs for Licensed Products.  Without limiting the foregoing, VGX may contract with its Affiliates or Third Parties of its sole choice to perform any or all of the activities relating to the Manufacture of such Genetic Constructs.

 

5.4.                                               Device Manufacture .  Subject to execution of a Clinical Supply Agreement and Commercial Supply Agreements as set forth below, Genetronics shall be responsible for the Manufacture and supply of the quantities of each Device needed for Development and Commercialization of Licensed Products in the Field in the Territory as described below.

 

5.4.1.                               Clinical Supply .  For all clinical trials required to obtain regulatory approval of Licensed Product, Genetronics will supply electroporation applicators and generators and any technical advancements thereto, to VGX at the price indicated in Schedule 5.4.1.

 

5.4.2.                               Commercial Supply .  Upon reaching commercial level production volumes of its electroproation-assisted DNA delivery devices, Genetronics will enter good faith negotiations with regard to the per unit price to VGX, such per unit price to be established at commercially reasonable terms.

 

6.                                        CONSIDERATION.

 

6.1.                               Upfront Payment .  Within thirty (30) days of the Effective Date, VGX shall pay to Genetronics the sum indicated in Schedule 6.1.

 

6.2.                               Development Payments .  In partial consideration for Genetronics’s development of the Genetronics Technology and performance of Genetronics’s obligations under this

 

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Agreement, VGX shall pay to Genetronics the amounts set forth in Schedule 6.2  (each, a “ Development Payment ”) within thirty (30) days of the first occurrence of each event described below for any Licensed Product in the Licensed Field (each, a “ Development Event ”).  A Licensed Product shall be considered to have “entered” a Clinical Trial when, following all applicable Regulatory Approvals, the Licensed Product is first administered to a subject enrolled in such Clinical Trial.

 

For the avoidance of doubt, in the event that a Licensed Product bypasses an earlier Development Event and achieves a later Development Event, then upon achievement of the later Development Event, Development Payments shall be made at that time both for the Development Event achieved and any earlier Development Events bypassed.

 

6.2.1.                               Each of the Development Payments above shall be payable when the Development Event is achieved and shall be due in its entirety regardless of the number or configuration of the studies.

 

6.2.2.                               If one or more subsequent Licensed Product candidates replaces the first or subsequent Licensed Product candidate in Development, such replacement Licensed Product candidate(s) shall only be subject to those Development Payments that have not previously been achieved by the replaced Licensed Product candidate(s).

 

6.3.                                               Royalty Payments.

 

6.3.1.                               Patent Royalty Period .   The Patent Royalty Period will be, with respect to any particular Licensed Product in any country, the period of time beginning on the First Commercial Sale of such Licensed Product in such country and extending until the earlier of (i) the date when there is not any Valid Claim included in any Genetronics Patent Right in any country which would be infringed by the sale of the Licensed Product in any country but for a license granted by Genetronics to VGX hereunder, or (ii) ten (10) years from the date of First Commercial Sale of such Licensed Product in such country.  Thereafter, no further royalties shall be payable in respect of sales of such Licensed Product in such country and, thereafter, the license granted to VGX under Section 2.1 with respect to such Licensed Product in such country shall become fully paid-up, perpetual, irrevocable, non-exclusive, royalty-free licenses.

 

6.3.2.                               Royalties .  VGX, on a Licensed Product-by-Licensed Product and country-by-country basis, shall pay to Genetronics royalties in the amount of the Applicable Net Sales Percentage of the Net Sales obtained by VGX, its Affiliates or VGX Sublicensees from the sale of each Licensed Product in the Licensed Fields in the Territory in any Calendar Year during the Patent Royalty Period, as set forth in Schedule 6.3.2.

 

6.3.3.                                       Royalty Adjustments .  The following adjustments shall be made, on a Licensed Product-by-Licensed Product and country-by-country basis, to the royalties payable pursuant to Section 6.3.1 hereof.

 

No Patent Coverage .  In the case of any Net Sales of any Licensed Product in the Licensed Fields in any country where such Licensed Product is not covered by an issued Valid Claim of the Genetronics Licensed Technology, the royalty payable by VGX to Genetronics on such Net Sales shall be reduced to **** of the amount that would

 

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otherwise have been payable during the Patent Royalty Period with respect to such Net Sales pursuant to Section 6.3.1.

 

6.4.                                               Reports and Payments.

 

6.4.1.                               Cumulative Royalties .  The obligation to pay royalties under this Agreement shall be imposed only once with respect to any sale of any Licensed Product.

 

6.4.2.                               Royalty Statements and Payments .  Within sixty (60) days of the end of each Calendar Quarter, VGX shall deliver to Genetronics a report setting forth for such Calendar Quarter, the following information, on a Licensed Product-by-Licensed Product, country-by-country and worldwide basis: (a) the Net Sales of each Licensed Product, (b) the basis for any adjustments to the royalty payable for the sale of any such Licensed Product, and (c) the royalty due hereunder for the sale of each such Licensed Product.  No such reports shall be due for any such Licensed Product before the First Commercial Sale of such Licensed Product.  The total royalty due for the sale of all such Licensed Products during such Calendar Quarter shall be remitted at the time such report is made.

 

6.4.3.                               Taxes and Withholding .  All payments under this Agreement will be made without any deduction or withholding for or on account of any tax, duties, levies, or other charges unless such deduction or withholding is required by applicable laws or regulations to be assessed against Genetronics.  If VGX is so required to deduct or withhold, VGX will (i) promptly notify Genetronics of such requirement, (ii) pay to the relevant authorities the minimum amount actually required by law or treaty to be deducted or withheld promptly upon the earlier of determining that such deduction or withholding is required or receiving notice that such amount has been assessed against Genetronics, and (iii) promptly forward to Genetronics an official receipt (or certified copy) or other documentation reasonably acceptable to Genetronics evidencing such payment to such authorities.

 

6.4.4.                               Currency .  All amounts payable and calculations hereunder shall be in United States dollars.  As applicable, Net Sales and any royalty deductions shall be translated into United States dollars at the exchange rate used by VGX for public financial accounting purposes in accordance with generally accepted accounting principles.  If, due to restrictions or prohibitions imposed by national or international authority, payments cannot be made as provided in this Section 6.4.4, then VGX shall nonetheless remain fully liable to Genetronics for payment hereunder.

 

6.4.5.                               Record Keeping .  VGX shall keep and shall cause its Affiliates and Sublicensees to keep books and accounts of record in connection with the sale of Licensed Products, in accordance with GAAP and in sufficient detail to permit accurate determination of all figures necessary for verification of royalties to be paid hereunder.  VGX and its Affiliates shall maintain such records for a period of at least three (3) years after the end of the Calendar Quarter in which they were generated, provided, however, that if any records are in dispute and VGX has received written notice from Genetronics of the records which are in dispute, VGX shall keep such records until the dispute is resolved.

 

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6.4.6.                               Audits .  Upon thirty (30) days prior written notice from Genetronics, VGX shall permit an independent certified public accounting firm of nationally recognized standing selected by Genetronics and reasonably acceptable to VGX, to examine, at Genetronics’s sole expense, the relevant books and records of VGX and its Affiliates as may be reasonably necessary to verify the amounts reported by VGX in accordance with Section 6.4.2 and the payment of royalties hereunder.  An examination by Genetronics under this Section 6.4.6 shall occur not more than once in any Calendar Year and shall be limited to the pertinent books and records for any Calendar Year ending not more than three (3) years before the date of the request.  The accounting firm shall be provided access to such books and records at VGX’s facility(ies) where such books and records are normally kept and such examination shall be conducted during VGX’s normal business hours.  VGX may require the accounting firm to sign a standard non-disclosure agreement before providing the accounting firm access to VGX’s facilities or records.  Upon completion of the audit, the accounting firm shall provide both VGX and Genetronics a written report disclosing any discrepancies in the reports submitted by VGX or the royalties paid, and, in each case, the specific details concerning any discrepancies.  No other information shall be provided to Genetronics.

 

6.4.7.                               Underpayments/Overpayments .  If such accounting firm correctly concludes that additional royalties were due to Genetronics, VGX shall pay to Genetronics the additional royalties within forty-five (45) days of the date VGX receives such accountant’s written report.  Notwithstanding any other provision in this Section 6.4 to the contrary, if such underpayment exceeds three percent (3%) of the royalties that were to be paid to Genetronics, VGX also shall reimburse Genetronics for the out-of-pocket expenses incurred in conducting the audit.  Neither Genetronics nor VGX shall reveal to such accounting firm the conditions under which the audit expenses are to be reimbursed hereunder.  If such accounting firm correctly concludes that VGX over paid royalties to Genetronics, Genetronics will refund such overpayments to VGX, within forty-five (45) days of the date Genetronics receives such accountant’s report.

 

6.4.8.                               Confidentiality .  All reports and financial information of VGX which is subject to review under this Section 6 shall be deemed to be VGX’s Confidential Information subject to the provisions of Section 7.1 hereof, and Genetronics shall not disclose such Confidential Information to any Third Party or use such Confidential Information for any purpose other than verifying payments to be made by VGX to Genetronics hereunder; provided, however, that such Confidential Information may be disclosed by Genetronics to Third Parties only to the extent necessary to enforce Genetronics’s rights under this Agreement.

 

6.4.9.                               Disclaimer .  Genetronics acknowledges and agrees that nothing in this Agreement (including any exhibits or attachments hereto) shall be construed as representing an estimate or projection of either (a) the number of Licensed Products that will or may be successfully Developed or Commercialized or (b) anticipated sales or the actual value of any Licensed Product.  The foregoing disclaimer shall not mitigate VGX’s obligation to use Commercially Reasonable due diligence to develop the Licensed Products in the Licensed Field.

 

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7.                                        MUTUAL COVENANTS.

 

7.1.                                               Confidentiality.

 

7.1.1.                               Confidentiality .  During the term of this Agreement and for a period of five years following the expiration or earlier termination thereof, each Party shall maintain in confidence the Confidential Information of the other Party, and shall not disclose, use or grant to a Third Party the right to use any of the Confidential Information of the other Party except on a need-to-know basis to such Party’s directors, officers and employees, and to such Party’s consultants working on such Party’s premises, to the extent such disclosure is reasonably necessary in connection with such Party’s activities as expressly authorized by this Agreement.  To the extent that disclosure to any person is authorized by this Agreement, prior to disclosure, a Party shall obtain written agreement of such person to hold in confidence and not disclose, use or grant the use of the Confidential Information of the other Party except as expressly permitted under this Agreement.  Each Party shall notify the other Party promptly upon discovery of any unauthorized use or disclosure of the other Party’s Confidential Information.

 

7.1.2.                               Terms of Agreement .  Neither Party shall disclose any terms or conditions of this Agreement to any Third Party without the prior written consent of the other Party; provided, however, that a Party may disclose the terms or conditions of this Agreement, (a) on a need-to-know basis to its legal and financial advisors, who are obligated to maintain such information in confidence, and (b) to a Third Party (who is obligated to maintain such information in confidence) in connection with (i) an equity investment in Genetronics by such Third Party (so long as such investment is not by a pharmaceutical company the market capitalization of which makes it a competitor of VGX), (ii) a merger, consolidation or similar transaction by such Party, or (iii) the sale of all or substantially all of the assets of such Party relating to the subject matter of this Agreement.  Notwithstanding the foregoing, prior to execution of this Agreement, the Parties have agreed upon the substance of information that can be used to describe the terms and conditions of this transaction, and each Party may disclose such information, as modified by mutual written agreement of the Parties, without the consent of the other Party.

 

7.1.3.                               Permitted Disclosures .  The confidentiality obligations under this Section 7 shall not apply (a) to the extent that a Party is required to disclose information by applicable law, regulation or order of a governmental agency or a court of competent jurisdiction, or (b) to the extent necessary or desirable to allow either Party (where possible, with adequate safeguards for confidentiality) to defend against litigation or to file and prosecute patent applications; provided, however, in either such case that such Party shall provide written notice thereof to the other Party, consult with the other Party with respect to such disclosure and provide the other Party sufficient opportunity to object to any such disclosure or to request that the disclosing Party seek confidential treatment thereof, in which event, the disclosing Party shall use all reasonable efforts to accommodate the other Party’s requests.

 

7.1.4.                               Announcements .  Except as may be expressly permitted under Section 7.1.3, neither Party will make any public announcement regarding this Agreement without the prior written approval of the other Party.  For the sake of clarity, nothing in this Agreement shall prevent VGX from making any scientific publication or public announcement concerning VGX’s Commercialization activities with respect to any Licensed Product under this Agreement; provided, however, that VGX shall not disclose any of Genetronics’s Confidential Information in any such publication or announcement without obtaining Genetronics’s prior written consent to do so.  The Parties expressly agree that both parties may release a press release upon the execution of this Agreement subject to each other’s prior review and written approval.

 

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7.1.5.                               Publications .  During the term of this Agreement, each Party shall submit to the other Party for review and approval all proposed academic, scientific, and medical publications and public presentations relating to the Licensed Product for review in connection with preservation of Patent Rights and/or to determine whether Confidential Information of the other Party should be modified or deleted, provided, however that after the approval of an academic, scientific or medical publication and/or public presentation has been given, then such Party shall not have to resubmit any such information for re-approval should it be republished or publicly disclosed in another form.  The parties agree not to unreasonably withhold such consent. Written copies of such proposed publications and presentations shall be submitted to the other Party no later than 60 days before submission for publication or presentation and such other Party shall provide its comments with respect to such publications and presentations within 30 days following its receipt of such written copy; provided, however, that if it is determined by the reviewing Party that publication or presentation would jeopardize the intellectual property rights of such Party, then publication or presentation will be delayed for a period of time reasonably sufficient to allow the reviewing Party to apply for patent protection with respect to such intellectual property.  Genetronics and VGX shall each comply with standard academic practice regarding authorship of scientific publications and recognition of contribution of other parties in any publications relating to the development of the Licensed Products.

 

7.2.                                               Compliance with Law .  Each Party here covenants and agrees to comply with all laws and regulations applicable to its activities connected with the Development, Manufacture and Commercialization (as applicable) of Licensed Products.  Without limiting the generality of the foregoing:

 

7.2.1.                               Patient Information .  Each Party agrees to abide by all laws, rules, regulations, and orders of all applicable supranational, national, federal, state, provincial, and local governmental entities concerning the confidentiality or protection of patient identifiable information and/or patients’ protected health information, as defined by U.S. C.F.R. Part 160 or personal data as defined by EU Directive 95/46/EC or any other applicable legislation, in the course of their performance under this Agreement.

 

7.2.2.                               Export Controls .  This Agreement is made subject to any restrictions concerning the export of products or technical information from the United States or other countries which may be imposed upon or related to VGX or Genetronics from time to time.  Each Party agrees that it shall not export, directly or indirectly, any technical information acquired from the other Party under the Agreement or any products using such technical information to a location or in a manner that at the time of export requires an export license or other governmental approval, without first obtaining the written consent to do so from the appropriate agency or other governmental entity.

 

7.2.3.                               Debarment .  Each Party agrees that it shall not use, in any capacity, in connection with any of its obligations to be performed under the Agreement any individual who has been debarred under the FD&C Act or the Generic Drug Enforcement Act.

 

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8.                                        REPRESENTATIONS AND WARRANTIES.

 

8.1.                                               Representations and Warranties of Each Party .  As of the Effective Date, each of Genetronics and VGX hereby represents and warrants to the other Party hereto as follows:

 

(a)                                   it is a corporation or entity duly organized and validly existing under the laws of the state or other jurisdiction of its incorporation or formation;

 

(b)                                  the execution, delivery and performance of this Agreement by such Party has been duly authorized by all requisite corporate action and does not require any shareholder action or approval;

 

(c)                                   it has the power and authority to execute and deliver this Agreement and to perform its obligations hereunder;

 

(d)                                  the execution, delivery and performance by such Party of this Agreement and its compliance with the terms and provisions does not and shall not conflict with or result in a breach of any of the terms and provisions of or constitute a default under (i) a loan agreement, guaranty, financing agreement, agreement affecting a product or other agreement or instrument binding or affecting it or its property; (ii) the provisions of its charter or operative documents or bylaws; or (iii) any order, writ, injunction or decree of any court or governmental authority entered against it or by which any of its property is bound; and

 

(e)                                   it has the full right, power and authority to grant all of the right, title and interest in the licenses granted to the other Party under this Agreement.

 

8.2.                                               Additional Representations and Warranties of Genetronics .  Genetronics hereby represents, warrants, and covenants to VGX that:

 

(a)                                   it has the full right, power and authority to grant all of the right, title and interest in the licenses in Existing Genetronics Patents granted to VGX under this Agreement;

 

(b)                                  except as provided in the Genetronics Third Party Agreements, Genetronics is the owner of or otherwise Controls the Existing Genetronics Patents, all of which are free and clear of any liens, charges and encumbrances;

 

(c)                                   as of the Effective Date, there are no claims, judgments or settlements against or owed by Genetronics or, to the best of its knowledge, pending claims or litigation, in either case relating to the Existing Genetronics Patents.

 

8.3.                                               Representation by Legal Counsel .  Each Party hereto represents that it has been represented by legal counsel in connection with this Agreement and acknowledges that it has participated in the drafting.  In interpreting and applying the terms and provisions of this Agreement, the Parties agree that no presumption shall exist or be implied against the Party which drafted such terms and provisions.

 

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8.4.                                               Disclaimer .  THE FOREGOING WARRANTIES OF EACH PARTY ARE IN LIEU OF ANY OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING, WITHOUT LIMITATION, ANY IMPLIED WARRANTIES OF NONINFRINGEMENT, ANY IMPLIED WARRANTIES OF MERCHANTABILITY OR ANY IMPLIED WARRANTIES OF FITNESS FOR A PARTICULAR PURPOSE ALL OF WHICH ARE HEREBY SPECIFICALLY EXCLUDED AND DISCLAIMED.

 

9.                                        INTELLECTUAL PROPERTY.

 

9.1.                                               Disclosure .  During the Term, each Party shall promptly disclose to the other Party all Know-How Controlled by the first Party that is conceived, reduced to practice, or developed by any employee of the first Party (or its Affiliates), or by or on behalf of any Third Party retained by the first Party, in the course of fulfilling such Party’s obligations under the Collaboration (whether patentable or not) (“ Collaboration Know-How ”).  Any Patent Rights (“ Collaboration Patent Rights ”) derived from such Know-How, together with such Know-How, constitute “ Collaboration Technology ”.

 

9.2.                                               Ownership.

 

9.2.1.                               Genetic Constructs .  Notwithstanding any other provision of the Agreement, VGX shall own all interest in and to any Collaboration Technology which constitutes an improvement, modification, or enhancement to, or further development of, any Genetic Constructs Controlled by VGX, and such Collaboration Technology shall be deemed VGX Collaboration Technology.  Genetronics shall sign or have its employees and agents sign such documentation as may be necessary to obtain, perfect or maintain assignment of any such Collaboration Technology to VGX.

 

9.2.2.                               Collaboration Technology .  Subject to the license grants in Section 2, as between the Parties, VGX shall own all Collaboration Know-How (and related Collaboration Patent Rights) conceived, reduced to practice and developed either (a) solely by VGX, its Affiliates or any of their employees or consultants or (b) by VGX, its Affiliates or any of their employees or consultants together with a third party or a third party’s employees or consultants (“VGX Collaboration Technology ”), and Genetronics shall own all Collaboration Know-How (and related Collaboration Patent Rights) conceived, reduced to practice and developed either (a) solely by Genetronics, its Affiliates or any of their employees or consultants or (b) by Genetronics, its Affiliates or any of their employees or consultants together with a third party or a third party’s employees or consultants (“ Genetronics Collaboration Technology ”).  All Collaboration Know-How (and related Collaboration Patent Rights) conceived, reduced to practice or developed jointly by VGX, its Affiliates or any of their employees or consultants and by Genetronics, its Affiliates or any of their employees or consultants (“ Joint Collaboration Technology ”) shall be owned jointly by VGX and Genetronics except as set forth above in Section 9.2.1.

 

9.2.3.                               Non-Collaboration Technology .  Each Party shall retain all intellectual property owned or Controlled by such Party that is not Collaboration Technology, including without limitation, all intellectual property owned by a Party prior to the Execution Date and all

 

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intellectual property conceived, reduced to practice or developed by a Party outside of the scope of this Agreement (“ Non-Collaboration Technology ”).

 

9.2.4.                               Rights of Use to Joint Collaboration Technology .  Subject to the rights granted hereunder, either Party may use or license its interest in any Joint Collaboration Technology without accounting to the other Party.

 

9.2.5.                               Inventorship .  Determinations as to which Party has invented any Patent Right or Know-How shall be made in accordance with the standards of inventorship and conception under U.S. patent law.

 

9.3.                                               Prosecution and Maintenance of Patent Rights.

 

9.3.1.                               Each Party’s Own Patent Rights .

 

(i)                            Each Party shall have the initial right, but not the obligation, to file, prosecute, and maintain any Patent Right covering intellectual property owned by such Party, other than any Patent Right covering Joint Collaboration Technology (a “ Joint Patent Right ”), and to determine in which countries to do so, in all cases at its own expense.

 

9.3.2.                               Joint Patent Rights .  Upon the identification of Joint Collaboration Know-How, the Parties shall (i) promptly discuss such Joint Collaboration Know-How, (ii) promptly discuss the desirability of filing a United States patent application covering such Joint Collaboration Know-How, as well as any foreign counterparts, and (iii) make the final decision with respect to any such filings as soon as practicable, including the allocation of expenses therefore.

 

9.3.3.                               Costs and Expenses .  Each Party shall bear the costs and expenses of filing, prosecuting, and maintaining Patent Rights as provided for in this Section 9.3.

 

9.4.                                               Trademarks.

 

9.4.1.                               Licensed Product Trademarks .  All Licensed Products shall be sold in the Territory under Trademarks and trade dress selected by VGX.  Except with respect to Trademarks licensed by Genetronics to VGX pursuant to Section 2.1.2, VGX shall own such Trademarks, trade dress, domain names and copyrights, along with all goodwill associated therewith, and shall be responsible for the filing, prosecution and maintenance at its own expense of such Trademarks, trade dress and copyrights in the Territory.  VGX may select and use its own Trademarks and trade dress in connection with the Commercialization of Licensed Products under this Agreement.  Except with respect to Trademarks licensed by Genetronics to VGX pursuant to Section 2.1.2, Genetronics shall neither use nor seek to register, anywhere in the world, any trademarks which are confusingly similar to any Trademarks, trade names, trade dress or logos used by or on behalf of VGX, its Affiliates or Sublicensees in connection with any Licensed Product.  Except with respect to Trademarks licensed by Genetronics to VGX pursuant to Section 2.1.2, VGX shall neither use nor seek to register, anywhere in the world, any trademarks which are confusingly similar to any Trademarks, trade names, trade dress or logos used by or on behalf of Genetronics, its Affiliates or Sublicensees in connection with any Licensed Product.

 

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9.4.2.          Costs .  Except with respect to Trademarks licensed by Genetronics to VGX pursuant to Section 2.1.2, VGX shall bear the costs of obtaining and maintaining Trademarks and trade dress used in the Commercialization of Licensed Products.

 

9.4.3.          Party Names on Product Promotional Material .  VGX shall have sole control and sole regulatory responsibility over the packaging and labeling of Licensed Products, but shall provide for Genetronics to be appropriately identified in accordance with applicable law on all packaging, labels, packaging inserts and other promotional materials used in connection with any Licensed Product.

 

9.5.               Enforcement of Technology Rights.

 

9.5.1.          Notice .  If VGX or Genetronics becomes aware that any VGX Licensed Technology, Genetronics Licensed Technology or Joint IP is being infringed or misappropriated by a Third Party in the Licensed Field or is subject to a declaratory judgment action, nullity action or similar proceedings arising from such infringement (collectively, an “ Infringement ”), VGX or Genetronics, as the case may be, shall promptly notify the other Party thereof in writing reasonably detailing the Infringement.

 

9.5.2.          Enforcement by Genetronics.

 

(i)         Genetronics Licensed Technology in the Licensed Field and Joint IP Generally .   Genetronics shall have the first right (but not the obligation), at its sole expense, to enforce any Genetronics Licensed Technology in the Licensed Field or Joint IP inside or outside the Licensed Field against any Infringement; provided, however , that (i) VGX shall have the right to join such proceeding at any time at its own expense and shall do so at any time if it is deemed to be a necessary party, and (ii)  however, whether or not joined, VGX shall not admit the invalidity or unenforceability of any Genetronics Licensed Technology or Joint IP without Genetronics’s prior written consent.   Genetronics shall keep VGX reasonably informed prior to and during any such enforcement.  VGX agrees in any event to assist Genetronics, upon Genetronics’ request and at Genetronics’ expense, in taking any action to enforce such Joint IP or Genetronics Licensed Technology.

 

(ii)        Genetronics Licensed Technology Outside the Licensed Field .  Genetronics shall have the right (but not the obligation), at its sole expense, to enforce any Genetronics Licensed Technology outside the Licensed Field against any Infringement.

 

9.5.3.          Enforcement by VGX .

 

(i)         Genetronics Licensed Technology in the Licensed Field and Joint IP Generally .  If Genetronics fails to abate an Infringement of the Genetronics Licensed Technology in the Licensed Field or Joint IP inside the Licensed Field, or to file an action to abate such Infringement within six (6) months after a written request from VGX to do so (or earlier if delay will prejudice Genetronics’s rights to take action, or if Genetronics discontinues the prosecution of any such action, VGX at its expense shall have the right, in its discretion, to undertake such action as it determines appropriate to enforce such Joint IP or Genetronics Licensed Technology.  VGX shall keep Genetronics reasonably informed on a quarterly basis, in person or by telephone, prior to and during any such enforcement.  In such case, Genetronics shall assist VGX, upon VGX’s

 

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request and at VGX’s sole expense, in taking any action to enforce such Joint IP or Genetronics Licensed Technology.

 

9.5.4.          Recoveries .  All monies recovered upon the final judgment or settlement of any such action described in Section 9.5.2(i) shall be used first to reimburse the costs and expenses (including reasonable attorneys’ fees and costs) of Genetronics and VGX.  Thereafter, (a) to the extent that any final judgment, award or settlement payment is based on or specified as lost revenues or lost profits from sale of Licensed Products, such award or payment will be deemed Net Sales, and royalties will be paid pursuant to Section 6.3; and (b) to the extent that any final judgment or settlement is other than lost revenues or lost profits from sale of Licensed Products, the parties will share any such award or payment equally.

 

9.5.5.          No Liability for Unfavorable Outcome to Litigation .  Neither Party shall incur any liability to the other Party as a consequence of any litigation brought as provided above or any unfavorable decision resulting therefrom, including any decision holding any Patent Right invalid or unenforceable.

 

9.6.               Third Party Claims.

 

9.6.1.          Third Party Claims – Course of Action .  If the Development, Manufacture, use, sale or importation of a Licensed Product is alleged by a Third Party to infringe a Third Party’s Patent Right(s) or misappropriate a Third Party’s trade secret, the Party becoming aware of such allegation shall promptly notify the other Party thereof, in writing, reasonably detailing the claim.

 

9.6.2.          Additional Third Party Licenses .  If VGX is required or deems it is desirable to license one or more Patent Rights from one or more Third Parties in order to make, have made, use, sell, offer for sale, import or otherwise exploit a Licensed Product in the Licensed Field under the terms of this Agreement, VGX, after good faith consultation with Genetronics, and at VGX’s own expense, shall have the right, but not the obligation, to negotiate and obtain a license under such Patent Right(s) (each such Third Party license referred to herein as an “ Additional Third Party License ”).

 

9.6.3.          Third Party Suit .  If a Third Party sues a Party (the “ Sued Party ”) alleging that the Sued Party’s Development, Manufacture, or Commercialization of any Licensed Product infringes or would infringe such Third Party’s Patent Right(s) or misappropriates such Third Party’s trade secret(s), then upon the Sued Party’s request and in connection with the Sued Party’s defense of any such Third Party suit, the other Party shall provide reasonable assistance to the Sued Party for such defense and shall join such suit if deemed a necessary party, all at the Sued Party’s expense.  The Sued Party shall keep the other Party, if such other Party has not joined in such suit, reasonably informed prior to and during the pendency of any such suit.  The Sued Party shall not admit the invalidity of any patent within the VGX Patent Rights (if the Sued Party is Genetronics), Genetronics Patent Rights (if the Sued Party is VGX) or Joint Patent Rights, nor settle any such suit, without written consent of the other Party.

 

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9.7.               Patent Marking, Certification and Term Restoration.

 

9.7.1.          Patent Marking .  To the extent it is commercially feasible to do so, each Party agrees to mark and have its Affiliates and all Sublicensees mark all Licensed Products (or their containers or labels) sold pursuant to this Agreement in the country or countries of Manufacture and sale thereof where failure to mark adversely affects the recovery of damages, and taking into account manufacturing efficiencies in relation to non-U.S. markets.

 

9.7.2.          Patent Certifications .  Each Party shall immediately give written notice to the other that any certification of which it becomes aware has been filed pursuant to 21 U.S.C. § 355(b)(2)(A), or § 355(j)(2)(A)(vii) (or any amendment or successor statute thereto) claiming that the VGX Patent Rights, Genetronics Patent Rights, or Collaboration Patent Rights covering any Licensed Product are invalid or that infringement would not arise from the Development, Manufacture or Commercialization of such product by a Third Party.

 

9.7.3.          Patent Term Restoration .  The Parties shall cooperate with each other in obtaining patent term restoration or extension anywhere in the Territory, including under 35 U.S.C. § 156, where applicable to any Patent Right covering the Development, Manufacture, or Commercialization of any Licensed Product.  If any election with respect to obtaining such patent term restoration is to be made with respect to any such Patent Right, which election in VGX’s reasonable judgment would materially affect the Commercialization of such Licensed Product, then VGX shall make such election (after consultation with Genetronics).

 

10.           GOVERNMENT APPROVALS.

 

10.1.             Each Party’s Obligations .  Each of Genetronics and VGX shall use its good faith efforts to eliminate any concern on the part of any court or government authority regarding the legality of the proposed transaction, including, if required by federal or state antitrust authorities, promptly taking all steps to secure government antitrust clearance, including, without limitation, cooperating in good faith with any government investigation including the prompt production of documents and information demanded by a second request for documents and of witnesses if requested.

 

10.2.             Additional Approvals .  Genetronics and VGX shall cooperate and use respectively all reasonable efforts to make all other registrations, filings and applications, to give all notices and to obtain as soon as practicable all governmental or other consents, transfers, approvals, orders, qualifications authorizations, permits and waivers, if any, and to do all other things necessary or desirable for the consummation of the transactions as contemplated hereby.  Neither Party shall be required, however, to divest or out-license products or assets or materially change its business if doing so is a condition of obtaining approval under governmental approvals of the transactions contemplated by this Agreement.

 

11.           TERM AND TERMINATION.

 

11.1.             Term .  The term of this Agreement (“ Term ”) shall commence on the Effective Date and extend unless this Agreement is terminated earlier in accordance with this Section 11, until the last to expire of any Royalty Period for any Licensed Product.

 

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11.2.             Termination.

 

11.2.1.        Termination For Cause .  This Agreement may be terminated effective immediately by written notice by either Party at any time during the Term if the other Party materially breaches any provision of this Agreement, which breach remains uncured for sixty (60) days measured from the date written notice of such breach is given to the breaching Party, provided, however , that if such breach is not susceptible of cure within the stated period and the breaching Party uses diligent good faith efforts to cure such breach, the stated period shall be extended by an additional sixty (60) days.

 

11.2.2.        Effects of Termination .

 

(i)         Termination for Cause by Genetronics .  In the event Genetronics terminates this Agreement in its entirety or with respect to any Licensed Product for cause pursuant to Section 12.2.1, (i) the license for VGX Device Improvements granted by VGX to Genetronics under Section 2.2.2 shall become perpetual and irrevocable, and (ii) except as otherwise expressly provided herein, all rights and obligations of each Party hereunder in their entirety or with respect to such Licensed Product, as applicable, shall cease, including, all rights and licenses granted by either Party to the other Party hereunder.

 

(ii)        Termination for Cause by VGX  In the event of an uncured material breach by Genetronics, VGX may elect, at its discretion, (a) to terminate all or any portion of this Agreement for cause pursuant to Section 12.2.1, in which case licenses to those VGX Device Improvements granted by Genetronics to VGX under Section 2.2.2 shall become fully paid-up, perpetual, non-exclusive, irrevocable and royalty-free, except as otherwise expressly provided herein, all other rights and obligations of each Party so terminated shall cease; or (b) not to terminate, but to pay royalties reduced by fifty (50) percent on those Licensed Product(s) that are the subject of the breach for the remainder of the relevant Royalty Term.

 

(iii)       Effect of Termination on Sublicenses .  Upon any termination of this Agreement, all Sublicenses granted by VGX prior to such termination may, at Genetronics’ sole discretion on a case-by-case basis, be assumed by Genetronics in accordance with their terms, except that Genetronics shall not be required in connection with any such assumption to take on obligations greater than those of Genetronics under this Agreement.

 

(iv)       Effect of Termination on Manufacturing-Related Agreements .  Unless otherwise stated therein, a termination of this Agreement shall result in termination of any and all provisions of any Clinical Supply Agreement or the Commercial Supply Agreement between the parties herein and in effect at the time of termination of this Agreement.

 

11.3.             Insolvency.

 

11.3.1.        Termination for Insolvency .  This Agreement may be terminated by written notice by either Party at any time during the Term upon the declaration by a court of competent jurisdiction that the other Party is bankrupt and, pursuant to the U.S. Bankruptcy Code such other Party’s assets are to be liquidated, the filing or institution of bankruptcy, liquidation or receivership proceedings (other than reorganization proceedings under Chapter 11 of the U.S. Bankruptcy Code), or upon an assignment of a substantial portion of the assets for the benefit of creditors by the other Party, or in the event a receiver or custodian is appointed for such Party’s

 

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business, or if a substantial portion of such Party’s business is subject to attachment or similar process; provided, however , that in the case of any involuntary bankruptcy proceeding such right to terminate shall only become effective if the proceeding is not dismissed within 60 days after the filing thereof.

 

11.3.2.        Effect on Licenses .  All rights and licenses granted under or pursuant to this Agreement by one Party to the other Party are, for all purposes of Section 365(n) of Title 11 of the United States Code (“ Title 11 ”), licenses of rights to “intellectual property” as defined in Title 11.  Each Party agrees that the other Party, as licensee of such rights under this Agreement shall retain and may fully exercise all of its rights and elections under Title 11.  Each Party further agrees and acknowledges that the upfront payment and Development Payments, and all other payment by VGX to Genetronics hereunder, other than royalty payments pursuant to Section 6.3.1 (and subject to reduction pursuant to Section 6.3.3) do not constitute royalties within the meaning of Section 365(n) of Title 11 or relate to licenses of intellectual property hereunder.  Each Party agrees during the term of this Agreement to create and maintain current copies or, if not amenable to copying, detailed descriptions or other appropriate embodiments, to the extent feasible, of all such intellectual property.  If a case is commenced by or against a Party under Title 11 (the “ Title 11 Party ”), such Party (in any capacity, including debtor-in-possession) and its successors and assigns (including, without limitation, a Title 11 Trustee) shall,

 

(i)         as the other Party may elect in a written request, immediately upon such request:

 

(a)          perform all of the obligations provided in this Agreement to be performed by the Title 11 Party including, where applicable and without limitation, providing to the other Party portions of such intellectual property (including embodiments thereof) held by the Title 11 Party and such successors and assigns or otherwise available to them; or

 

(b)         provide to the other Party all such intellectual property (including all embodiments thereof) held by the Title 11 Party and such successors and assigns or otherwise available to them; and

 

(ii)        not interfere with the rights of the other Party under this Agreement, or any agreement supplemental hereto, to such intellectual property (including such embodiments), including any right to obtain such intellectual property (or such embodiments) from another entity.

 

11.3.3.        Rights to Intellectual Property .  If a Title 11 case is commenced by or against Genetronics, and this Agreement is rejected as provided in Title 11, and VGX elects to retain its rights hereunder as provided in Title 11, then Genetronics (in any capacity, including debtor-in-possession) and its successors and assigns (including, without limitation, a Title 11 Trustee) shall grant to VGX a non-exclusive right of access to, and the right to obtain possession of and to benefit from, each of the following, which the Parties expressly agree constitute “embodiments” of intellectual property licensed to VGX under the Agreement for the purposes of Section 365(n) of the Bankruptcy Code:  (i) copies of pre-clinical and clinical research data and results regarding Licensed Products, (ii) any tools, dyes, drawings, designs or specifications relating to Licensed Products customized by Genetronics at VGX’s request, (iii) copies of laboratory notes

 

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and notebooks related to any Licensed Product, (iv) Regulatory Filings and Regulatory Approvals related to any Licensed Product or its Manufacture, (vii) rights of reference in respect of Regulatory Filings and Regulatory Approvals, and (viii) all other embodiments of such intellectual property, in Genetronics’s possession or Control.  The Parties agree that (i) Genetronics’s obligations to Manufacture and supply any Device are supplementary rights to the intellectual property rights licensed to VGX under the Agreement and are entitled to the protection of Section 365(n) and (ii) only the payments specifically characterized as royalties under the Agreement, and no other obligations, constitute royalties within the meaning of Section  §365(n).

 

11.3.4.        Additional Rights .  All rights, powers and remedies of a Party provided herein are in addition to and not in substitution for any and all other rights, powers and remedies now or hereafter existing at law or in equity (including, without limitation, Title 11) in the event of the commencement of a Title 11 case by or against the Title 11 Party.  A non-Title 11 Party, in addition to the rights, power and remedies expressly provided herein, shall be entitled to exercise all other such rights and powers and resort to all other such remedies as may now or hereafter exist at law or in equity (including, without limitation, Title 11) in such event.  The Parties agree that they intend the foregoing rights to extend to the maximum extent permitted by law, including, without limitation, for purposes of Title 11:

 

(i)         the right of access to any intellectual property (including all embodiments thereof) of the Title 11 Party, or any Third Party with whom the Title 11 Party contracts to perform an obligation of the Title 11 Party under this Agreement, and, in the case of the Third Party, which is necessary for the Development, Manufacture and Commercialization of Licensed Products; and

 

(ii)        the right to contract directly with any Third Party described in Section 2.1.3 (Sublicensing to Third Parties) to complete the contracted work.

 

11.4.             Change of Control.

 

11.4.1.        Change of Control Notice .  Each Party shall notify the other Party in writing, referencing this Section of the Agreement, immediately upon any Change of Control, and shall provide such notice where possible at least sixty (60) days prior to the Change of Control.

 

11.4.2.        Right to Terminate if Confirmation of Continued Priority Not Received .  Genetronics may terminate this Agreement upon any Change of Control of VGX unless prior to sixty (60) days following such Change of Control, Genetronics has received from the other Party, and any Third Party who is acquiring or has acquired Control of VGX, written confirmation reasonably satisfactory to Genetronics to the effect that (i) after such Change of Control, the Development, Manufacture, and Commercialization of Licensed Products as contemplated by the Agreement will have a priority for the other Party following such Change of Control which is equal to or greater than the priority that such Development, Manufacture, and Commercialization had for VGX upon signing this Agreement; and (ii) that the other Party will continue to meet all of its obligations under the Agreement following such Change of Control.

 

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11.5.             Accrued Rights .  Expiration or termination of this Agreement for any reason shall be without prejudice to any right which shall have accrued to the benefit of either Party prior to such termination, including, without limitation, damages arising from any breach under this Agreement.  Expiration or termination of this Agreement shall not relieve either party from any obligation which is expressly indicated to survive such expiration or termination.

 

11.6.             Disposition of Inventory .  VGX shall have the right to continue to sell Licensed Product inventory Manufactured prior to the effective date of termination of this Agreement for a reasonable time after the effective date of such termination (not to exceed twelve (12) months), provided that VGX makes any required royalty payments with respect to such sales pursuant to Section 6.

 

11.7.             Survival .  Expiration or termination of this Agreement shall not relieve the Parties of any obligation accruing before such expiration or termination.  The provisions of this Agreement that must, by their nature, survive expiration or termination of this Agreement to give effect to their intent, shall so survive, including without limitation Section 6.4 (Reports and Payments), Section 7.1 (Confidentiality); Section 12 (Indemnification and Insurance) and Section 11 (Term and Termination).  Any expiration or early termination of this Agreement shall be without prejudice to the rights of either Party against the other accrued or accruing under this Agreement before termination.  In the event that either Party has license rights following termination that require the payment of royalties based on Net Sales of Licensed Products, the provisions of this Agreement regarding the calculation of Net Sales and the reporting and auditing of amounts payable with respect to such Net Sales shall apply, with appropriate substitution for Genetronics for VGX or vice versa if the royalties are payable by Genetronics to VGX.

 

12.           INDEMNIFICATION AND INSURANCE.

 

12.1.             Indemnification by VGX .  VGX shall indemnify, defend and hold harmless Genetronics, each of its Affiliates, and each of its and its Affiliates’ employees, officers, directors and agents (each, a “ Genetronics Indemnified Party ”) from and against any and all liability, loss, damage, expense (including reasonable attorneys’ fees and expenses) and cost (collectively, a “ Liability ”) that the Genetronics Indemnified Party may be required to pay to one or more Third Parties resulting from or arising out of:

 

(a)          any claims of any nature arising out of the Manufacture of Genetic Constructs pursuant to Section 5.3 by, on behalf of, or under the authority of VGX;

 

(b)         any claims of any nature arising out of the Development or Commercialization of any Licensed Product by, on behalf of, or under the authority of, VGX (other than claims by any Genetronics Indemnified Party), other than claims by Third Parties relating to patent infringement arising out of the exercise of rights under the Genetronics Licensed Technology ; or

 

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(c)          the breach by VGX of any of its representations, warranties or covenants set forth herein;

 

except, in each case, to the extent caused by the negligence or willful misconduct of Genetronics or any Genetronics Indemnified Party or is otherwise subject to indemnification by Genetronics.  Notwithstanding the foregoing, VGX shall have no obligation to defend, indemnify or hold harmless any Genetronics Indemnified Party from and against any Liability arising out of or resulting from the infringement of a Third Party patent.

 

12.2.             Indemnification by Genetronics .  Genetronics shall indemnify, defend and hold harmless VGX, each of its Affiliates, Sublicensees, distributors and each of its and their respective employees, officers, directors and agents (each, a “VGX Indemnified Party ”) from and against any and all Liabilities that the VGX Indemnified Party may be required to pay to one or more Third Parties resulting from or arising out of:

 

(a)          any claims of any nature arising out of the Manufacture of Devices pursuant to Section 5.4 by, on behalf of, or under the authority of Genetronics (except to the extent such claims relate to specifications for the Devices provided by VGX, which claims shall fall under VGX’s obligations under Section 13.1); or

 

(b)         the breach by Genetronics of any of its representations, warranties or covenants set forth herein;

 

except, in each case, to the extent caused by the negligence or willful misconduct of VGX or any VGX Indemnified Party or is otherwise subject to indemnification by VGX.  Notwithstanding the foregoing, Genetronics shall have no obligation to defend, indemnify or hold harmless any VGX Indemnified Party from and against any Liability arising out of or resulting from the infringement of a Third Party patent.

 

12.3.             Procedure .  Each Party shall notify the other in the event it becomes aware of a claim for which indemnification may be sought hereunder.  In case any proceeding (including any governmental investigation) shall be instituted involving any Party in respect of which indemnity may be sought pursuant to this Section 12, such Party (the “ Indemnified Party ”) shall promptly notify the other Party (the “ Indemnifying Party ”) in writing and the Indemnifying Party and Indemnified Party shall meet to discuss how to respond to any claims that are the subject matter of such proceeding.  The Indemnifying Party, upon request of the Indemnified Party, shall retain counsel reasonably satisfactory to the Indemnified Party to represent the Indemnified Party and shall pay the fees and expenses of such counsel related to such proceeding.  In any such proceeding, the Indemnified Party shall have the right to retain its own counsel, but the fees and expenses of such counsel shall be at the expense of the Indemnified Party unless (i) the Indemnifying Party and the Indemnified Party shall have mutually agreed to the retention of such counsel or (ii) the named parties to any such proceeding (including any impleaded parties) include both the Indemnifying Party and the Indemnified Party and representation of both Parties by the same counsel would be inappropriate due to actual or potential differing interests between them.  All such fees and expenses shall be reimbursed as they are incurred.  The Indemnifying Party shall not be liable for any settlement of any proceeding effected without

 

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its written consent, but if settled with such consent or if there be a final judgment for the plaintiff, the Indemnifying Party agrees to indemnify the Indemnified Party from and against any loss or liability by reason of such settlement or judgment.  The Indemnifying Party shall not, without the written consent of the Indemnified Party, effect any settlement of any pending or threatened proceeding in respect of which the Indemnified Party is, or arising out of the same set of facts could have been, a party and indemnity could have been sought hereunder by the Indemnified Party, unless such settlement includes an unconditional release of the Indemnified Party from all liability on claims to which the indemnity relates that are the subject matter of such proceeding.

 

12.4.             Insurance .  Each Party further agrees to obtain and maintain, [once the Licensed Product enters clinical trials], Commercial General Liability Insurance in the United States, including Products Liability coverage with carriers having A.M. Best rating of A-VII or better to cover its indemnification obligations under Sections 12.1 or 12.2, as applicable, with limits of not less than $1 million per occurrence and $3 million in the aggregate, or during any period in which such Party has a market capitalization of at least $500 million, a program of self-insurance.  In the event that clinical trials are to be conducted outside of the United States, the Parties shall discuss commercially reasonable and appropriate insurance coverage, which in any case shall not be unduly burdensome to the Parties.

 

13.           MISCELLANEOUS.

 

13.1.             Assignment .  Neither this Agreement, nor any right or obligation hereunder may be assigned or delegated, in whole or part, by either Party without the prior express written consent of the other (which consent shall not be unreasonably withheld or delayed) except as expressly set forth below in this Section 13.1.  Notwithstanding the foregoing, either Party may, without the written consent of the other Party, assign (i) any or all of this Agreement and its rights and delegate its obligations hereunder to any of its Affiliates or (ii) the Agreement as a whole to a Third Party in connection with the transfer or sale of all or substantially all of its business relating to the subject matter of this Agreement (provided that any such assignment by VGX to a Third Party shall be deemed a Change of Control of VGX for purposes of Section 11.4.  Each Party shall promptly notify the other Party of any assignment or transfer under the provisions of this Section.  This Agreement shall be binding upon the successors and permitted assigns of the Parties and the name of a Party appearing herein shall be deemed to include the names of such Party’s successors and permitted assigns to the extent necessary to carry out the intent of this Agreement.  Any assignment not in accordance with this Section 13.1 shall be void.

 

13.2.             Further Actions .  Each Party agrees to execute, acknowledge and deliver such further instruments, and to do all such other acts, as may be necessary or appropriate in order to carry out the purposes and intent of the Agreement.

 

13.3.             Force Majeure .  Nonperformance of a Party under this Agreement (other than for the payment of money) shall be excused to the extent that performance is rendered impossible by strike, fire, earthquake, flood, governmental acts or orders or restrictions, failure of suppliers, or any other reason where failure to perform, is beyond the reasonable control and not caused by the negligence, intentional conduct or misconduct of the

 

32



 

nonperforming Party.  The nonperforming Party shall notify the other Party promptly should such circumstances arise, giving an indication of the likely extent and duration thereof, and shall use all Commercially Reasonable Efforts to resume performance of its obligations as soon as practicable, provided, however, that neither Party shall be required to settle any labor dispute or disturbance.

 

13.4.             Correspondence and Notices.

 

13.4.1.        Ordinary Notices .  Correspondence, reports, documentation, and any other communication in writing between the Parties in the course of ordinary implementation of this Agreement shall be delivered by hand, sent by facsimile transmission (receipt verified), or by nationally recognized overnight delivery service to the employee or representative of the other Party who is designated by such other Party to receive such written communication.  In the absence of a specific designation, such notices shall be addressed as follows:

 

To Genetronics:                                                            Genetronics, Inc.
11494 Sorrento Valley Road
San Diego, California 92121
Attn: President

 

To VGX:                                                                                                   VGX Pharmaceuticals, Inc.
450 Sentry Parkway
Blue Bell, PA 19422

Attn: President

 

13.4.2.        Extraordinary Notices .  Extraordinary notices and communications (including, without limitation, notices of termination, force majeure, material breach, change of address) shall be in writing and delivered by hand or sent by nationally recognized overnight delivery service, prepaid registered or certified air mail, or by facsimile confirmed by prepaid first class, registered or certified mail letter, and shall be deemed to have been properly served to the addressee upon receipt of such written communication.

 

All correspondence to VGX shall be addressed as follows:

 

VGX Pharmaceuticals, Inc.

450 Sentry Parkway

Blue Bell, PA 19422

Attn:President
Fax: 267-440-4242

 

with a copy to:

 

VGX Pharmaceuticals, Inc.

450 Sentry Parkway

Blue Bell, PA 19422

Attn: Senior Vice President, Business Development
Fax:  267-440-4208

 

33



 

All correspondence to Genetronics shall be addressed as follows:

 

Genetronics, Inc.
11494 Sorrento Valley Road
San Diego, California 92121
Attn: President
Fax:  858-597-0451

 

with a copy to:

 

Genetronics, Inc.
11494 Sorrento Valley Road
San Diego, California 92121
Attn: Director, Intellectual Property
Fax:  858-597-0451

 

13.5.             Amendment .  No amendment, modification or supplement of any provision of this Agreement shall be valid or effective unless made in writing and signed by a duly authorized officer of each Party.

 

13.6.             Waiver .  No provision of the Agreement shall be waived by any act, omission or knowledge of a Party or its agents or employees except by an instrument in writing expressly waiving such provision and signed by a duly authorized officer of the waiving Party.

 

13.7.             Severability .  If any clause or portion thereof in this Agreement is for any reason held to be invalid, illegal or unenforceable, the same shall not affect any other portion of this Agreement, as it is the intent of the Parties that this Agreement shall be construed in such fashion as to maintain its existence, validity and enforceability to the greatest extent possible.  In any such event, this Agreement shall be construed as if such clause or portion thereof had never been contained in this Agreement, and there shall be deemed substituted therefor such provision as shall most nearly carry out the intent of the Parties as expressed in this Agreement to the fullest extent permitted by applicable law.

 

13.8.             Descriptive Headings .  The descriptive headings of this Agreement are for convenience only and shall be of no force or effect in construing or interpreting any of the provisions of this Agreement.

 

13.9.             Governing Law; Venue .  This Agreement, and all claims arising under or in connection therewith, shall be governed by and interpreted in accordance with the substantive laws of the State of Delaware, without regard to conflict of law principles thereof and without giving effect to the United Nations Convention on Contracts for the International Sale of Goods, the 1974 Convention on the Limitation Period in the

 

34



 

International Sale of Goods (the “1974 Convention”) and the Protocol amending the 1974 Convention, done at Vienna April 11, 1980, except for the interpretation of patent law, which shall be interpreted in accordance with the patent laws of each country in which a patent has been granted or patent application has been filed.  Venue for any action brought under this Agreement shall lie exclusively in the state courts of the State of Delaware, United States of America and both Parties hereby consent to such venue.

 

13.10.           Entire Agreement .  This Agreement constitutes and contains the complete, final and exclusive understanding and agreement of the Parties with respect to the subject matter hereof and cancels and supersedes any and all prior negotiations, correspondence, understandings and agreements, whether oral or written, between the Parties respecting the subject matter hereof.

 

13.11.           Independent Contractors .  Both Parties are independent contractors under this Agreement.  Nothing herein contained shall be deemed to create an employment, agency, joint venture or partnership relationship between the Parties hereto or any of their agents or employees, or any other legal arrangement that would impose liability upon one Party for the act or failure to act of the other Party.  Neither Party shall have any express or implied power to enter into any contracts or commitments or to incur any liabilities in the name of, or on behalf of, the other Party, or to bind the other Party in any respect whatsoever.

 

13.12.           Counterparts .  This Agreement may be executed in any number of counterparts, each of which need not contain the signature of more than one Party but all such counterparts taken together shall constitute one and the same agreement.

 

13.13.           Future Relationships .  Nothing contained in this Agreement shall be construed, by implication or otherwise, as an obligation of any Party hereto to enter into a further agreement regarding the subject matter of this Agreement.

 

13.14.           Interpretation .  The use of any gender herein shall be deemed to be or include the other genders and the use of the singular herein shall be deemed to include the plural (and vice versa), wherever appropriate. The words “include”, “includes” and “including” shall be deemed to be followed by the phrase “without limitation.” The word “will” shall be construed to have the same meaning and effect as the word “shall.” Unless the context requires otherwise (a) any definition of or reference to any agreement, instrument or other document herein shall be construed as referring to such agreement, instrument or other document as from time to time amended, supplemented or otherwise modified (subject to any restrictions on such amendments, supplements or modifications set forth herein), (b) any reference herein to any Person shall be construed to include the Person’s successors and assigns, (c) the words “herein”, “hereof” and “hereunder”, and words of similar import, shall be construed to refer to this Agreement in its entirety and not to any particular provision hereof, and (d) all references herein to Articles, Sections, or Schedules shall be construed to refer to Articles, Sections, and Schedules of this Agreement.

 

13.15.           No Third Party Rights or Obligations .  No provision of this Agreement shall be deemed or construed in any way to result in the creation of any rights or obligation in any Person not a Party to this Agreement.

 

35



 

IN WITNESS WHEREOF, duly authorized representatives of the Parties have duly executed this Agreement to be effective as of the Effective Date.

 

VGX PHARMACEUTICALS, INC.

 

GENETRONICS, INC.

 

 

 

 

 

 

By

 /s/ J. Joseph Kim

 

By

 /s/ Avtar Dillon

Name: J. Joseph Kim

 

Name: Avtar Dillon

Title: President & CEO

 

Title: President & CEO

 




Exhibit 10.66

 

OMB Approval 0990-0115

 

 

1.                THIS CONTRACT IS A RATED ORDER

RATING

PAGE OF PAGES

AWARD/CONTRACT

UNDER DPAS (15 CFR 350)                               

N/A

1

45

 

 

 

2.                CONTRACT (Proc. Inst. Ident.) NO.
HHSN272200800063C

3.                EFFECTIVE DATE
September 30, 2008

4.                REQUISITION/PURCHASE REQUEST/PROJECT NO.
750904

 

 

 

5.                ISSUED BY

CODE

 

6.                ADMINISTERED BY (If other than Item 6)

CODE

Office of Acquisitions, DEA
National Institute of Allergy and Infectious Diseases
National Institutes of Health, DHHS
6700-B Rockledge Dr., Room 3214, MSC 7612
Bethesda, Maryland 20892-7612

 

AIDS RCB

RFP NUMBER: NIH-NIAID-DAIDS-BAA-08-16
NIAID Contract # N01-AI-80063

 

 

7.                NAME AND ADDRESS OF CONTRACTOR (No. street, county, state and ZIP Code)

8.                DELIVERY

 

o   FOB ORIGIN

x   OTHER (See below)
FOB Destination

 

 

 

VGX Pharmaceuticals, Inc.

VIN#1150944

9.                DISCOUNT FOR PROMPT PAYMENT

450 Sentry Parkway East

N/A

Blue Bell, Pennsylvania 19422

 

 

10.          SUBMIT INVOICES

ITEM

 

 

 

CODE

FACILITY CODE

ADDRESS SHOWN IN:

Art. G.3.

 

 

 

 

11.  SHIP TO/MARK FOR

CODE

N/A

12.   PAYMENT WILL BE MADE BY

CODE

N/A

 

 

 

 

 

  Article F.1.

 

 

  See Article G.3.

 

 

 

 

 

 

13.          AUTHORITY FOR USING OTHER FULL AND OPEN COMPETITION:

14.          ACCOUNTING AND APPROPRIATION DATA

 

 

TIN# 51-0404886

SOC 25.55

DUNS 063784784

o   10 U.S.C. 2304(c)(     )

o   41 U.S.C. 253(c)(     )

CAN 8-8470035

$4,663,588

 

 

15A.           ITEM NO.

15B.            SUPPLIES/SERVICES

15C.  QUANTITY

15D.  UNIT

15E.  UNIT PRICE

15F.  AMOUNT

Title: HIV Vaccine Design and Development Teams project Entitled “Development of Improved DNA Vaccines and Electroporation Delivery Devices for HIV Prophylactic HIV Vaccines”

 

 

Period:  September 30, 2008 through September 29, 2015

Contract Type: Cost Reimbursement with Options (Completion)

 

 

FY 08 Base

FY 09 Option

FY 10 Option

FY 11 Option

FY 12 Option

FY 14 Option

FY 15 Option

$4,663,588

$6,573,776

$5,258,144

$2,717,534

$2,056,112

$1,193,230

$1,132,465

 

15G.     TOTAL AMOUNT OF CONTRACT        

$23,594,849

 

 

 

16.  TABLE OF CONTENTS

 

x

SEC.

DESCRIPTION

PAGE(S)

x

SEC.

DESCRIPTION

PAGE(S)

PART I - THE SCHEDULE

PART II - CONTRACT CLAUSES

x

A

SOLICITATION/CONTRACT FORM

1

x

I

CONTRACT CLAUSES

35

x

B

SUPPLIES OR SERVICES AND PRICE/COST

4

PART III - LIST OF DOCUMENTS, EXHIBITS AND OTHER ATTACH.

x

C

DESCRIPTION/SPECS./WORK STATEMENT

12

x

J

LIST OF ATTACHMENTS

44

x

D

PACKAGING AND MARKING

17

PART IV - REPRESENTATIONS AND INSTRUCTIONS

x

E

INSPECTION AND ACCEPTANCE

18

x

K

REPRESENTATIONS, CERTIFICATIONS AND

45

x

F

DELIVERIES OR PERFORMANCE

19

 

 

OTHER STATEMENTS OF OFFERORS

 

x

G

CONTRACT ADMINISTRATION DATA

22

o

L

INSTRS., CONDS., AND NOTICES TO OFFERORS

 

x

H

SPECIAL CONTRACT REQUIREMENTS

26

o

M

EVALUATION FACTORS FOR AWARD

 

 

CONTRACTING OFFICER WILL COMPLETE ITEM 17 OR 18 AS APPLICABLE

 

17.   x CONTRACTOR’S NEGOTIATED AGREEMENT (Contractor is required to sign this document and return            copies to issuing office.)  Contractor agrees to furnish and deliver all items or perform all the services set forth or otherwise identified above and on any continuation sheets for the consideration stated herein.  The rights and obligations of the parties to this contract shall be subject to and governed by the following documents:  (a) this award/contract, (b) the solicitation, if any, and (c) such provisions, representations, certifications, and specifications, as are attached or incorporated by reference herein.  (Attachments are listed herein.)

 

18.   o AWARD  ( Contractor is not required to sign this document.)   Your offer on Solicitation Number                                            , including the additions or changes made by you which additions or changes are set forth in full above, is hereby accepted as to the items listed above and on any continuation sheets.  This award consummates the contract which consists of the following documents:  (a) the Government’s solicitation and your offer, and (b) this award/contract.  No further contractual document is necessary.

 

 

19A.           NAME AND TITLE OF SIGNER   (Type or print)

20A.           NAME OF CONTRACTING OFFICER

NIRANJAN Y. SARDESAI, SR. VP, R&D

Eileen D. Webster-Cissel
Contracting Officer, Office of Acquisitions, DEA, NIAID, NIH, DHHS

 

 

19B.            NAME OF CONTRACTOR

19C.            DATE SIGNED

20B.            UNITED STATES OF AMERICA

20C.            DATE SIGNED

 

 

 

 

 

9/25/08

 

9/26/08

VGX Pharmaceuticals, Inc.   /S/Niranjan Y. Sardesai

 

BY

/s/ Eileen D. Webster-Cissel

 

(Signature of person authorized to sign)

 

(Signature of Contracting Officer)

 

 

NSN 7540-01-152-8069

26-107

STANDARD FORM 26 (REV. 4-85)

PREVIOUS EDITION UNUSABLE

Computer Generated

Prescribed by GSA

 

 

FAR (48 CFR) 53.214(a)

 




Exhibit 10.67

 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THIS AGREEMENT DATED AS OF [TODAY’S DATE] BETWEEN VGX PHARMACEUTICALS, INC. (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF THESE SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THESE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

WARRANT TO PURCHASE COMMON STOCK

 

OF

 

VGX PHARMACEUTICALS, INC.

 

No. VGXW- [NUMBER]                                                                                                      [TODAY’S DATE]

 

Void After [EXPIRATION DATE]

 

VGX PHARMACEUTICALS, INC., a Delaware corporation (the “Company”), hereby certifies that, FOR VALUE RECEIVED, [ GRANTEE ] (the “Holder”), or any registered assign of the Holder, is entitled to purchase from the Company, subject to the provisions of this Warrant, and from time to time within the Exercise Period (as such term is defined below), in whole or in part, up to that number of fully paid, validly issued and nonassessable shares of common stock, par value $0.0001 per share (“Common Stock”), of the Company, as is equal to the [NUMMBER OF SHARES] ( ###,### ) shares.  The actual number of shares of Common Stock to be issued to the Holder upon the exercise of this Warrant and the price to be paid for each share of Common Stock may be adjusted from time to time as hereinafter set forth.  The shares of Common Stock deliverable upon such exercise, and as adjusted from time to time, are hereinafter referred to as “Warrant Shares.”  The exercise price at which this Warrant may be exercised shall be [GRANT PRICE] ($ #.## ) price per share.

 



 

1.             EXERCISE OF WARRANT .

 

(a)           This Warrant may only be exercised, in whole or in part, at any time or from time to time on or after the closing of the Equity Financing and until 5:00 p.m. (Eastern Standard Time) on [EXPIRATION DATE] (the “Exercise Period”); provided , however , that if such day is a day on which banking institutions in the State of New York are authorized by law to close, then on the next succeeding day which shall not be such a day.  This Warrant may be exercised by presentation and surrender hereof to the Company at its principal office, or at the office of its stock transfer agent, if any, with the Purchase Form attached hereto as Exhibit A , duly executed and accompanied by payment of the purchase price which shall equal the product of the Exercise Price and the number of Warrant Shares specified on such Purchase Form (the “Purchase Price”).  The Holder shall pay the Purchase Price for the exercised Warrant Shares by: (i) delivering a certified check, bank draft or wire transfer of immediately available funds to the order of the Company; or (ii) a Cashless Exercise (as such term is defined below) whereby a certain number of Warrant Shares, to be determined in the manner set forth in Subsection 1(b) hereto, are retained by the Company as payment of the Purchase Price.  As soon as practicable after such exercise of the Warrant, but not later than seven days from the date of such exercise, the Company shall issue and deliver to the Holder a certificate or certificates for the Warrant Shares issuable upon such exercise, registered in the name of the Holder or his designee.  If this Warrant should be exercised in part only, the Company shall, upon surrender of this Warrant for cancellation, execute and deliver a new Warrant evidencing the rights of the Holder thereof to purchase the balance of the Warrant Shares purchasable thereunder.  Upon receipt by the Company of this Warrant at its principal office, or by the stock transfer agent of the Company at its office, if any, in proper form for exercise, the Holder shall be deemed to be the holder of record of the shares of Common Stock issuable upon such exercise, notwithstanding that the stock transfer books of the Company shall then be closed or that certificates representing such shares of Common Stock shall not then be physically delivered to the Holder.

 

(b)           At any time during the Exercise Period, the Holder may, at his option, convert this Warrant, in whole or in part, into the number of Warrant Shares determined in accordance with this Subsection 1(b) (a “Cashless Exercise”), by surrendering this Warrant at the principal office of the Company, or at the office of its stock transfer agent, if any, accompanied by a notice stating such Holder’s intent to effect such Cashless Exercise, the number of Warrant Shares to be exchanged and the date on which the Holder requests that such Cashless Exercise occur (the “Notice of Cashless Exchange”).  The Cashless Exercise shall take place on the date specified in the Notice of Cashless Exchange or, if later, the date the Notice of Cashless Exchange is received by the Company (the “Exchange Date”).  Certificates for the shares of Common Stock issuable upon such Cashless Exercise and, if applicable, a new warrant of like tenor evidencing the balance of the shares of Common Stock remaining subject to this Warrant, shall be issued as of the Exchange Date and delivered to the Holder within seven days following the Exchange Date.  In the event of a Cashless Exercise, the Holder shall receive that number of Warrant Shares (rounded to the next highest integer) equal to (i) the number of Warrant Shares specified by the Holder in his Notice of Cashless Exchange (the “Total Number”) less (ii) the number of Warrant Shares (the “Remaining Warrant Shares”) equal to the quotient obtained by dividing (A) the product of the Total Number and the existing Exercise Price by (B) the Fair Market Value.  The

 

2



 

Remaining Warrant Shares shall be retained by the Company as payment in full by the Holder of the Purchase Price.  “Fair Market Value” shall mean: (1) if the Common Stock is listed on a National Securities Exchange or admitted to unlisted trading privileges on such exchange or listed for trading on the Nasdaq National Market, the average of the last reported sale prices of the Common Stock on such exchange or system for the 20 business days ending on the last business day prior to the date for which the determination is being made; (2) if the Common Stock is not so listed or admitted to unlisted trading privileges, the average of the means of the last reported bid and asked prices reported by the National Quotation Bureau, Inc., for the 20 business days ending on the last business day prior to the date for which the determination is being made; or (3) if the Common Stock is not so listed or admitted to unlisted trading privileges and bid and asked prices are not so reported, an amount, not less than book value thereof as at the end of the most recent fiscal year of the Company ending prior to the Exchange Date, determined in such reasonable manner as may be prescribed by the Board of Directors of the Company.

 

2.             RESERVATION OF SHARES .  The Company shall at all times reserve for issuance and/or delivery upon exercise of this Warrant such number of shares of its Common Stock as shall be required for issuance and delivery upon exercise of this Warrant.

 

3.             FRACTIONAL SHARES .  No fractional shares or script representing fractional shares shall be issued upon the exercise of this Warrant.  With respect to any fraction of a share of Common Stock called for upon any exercise hereof, the Company shall pay to the Holder an amount in cash equal to such fraction multiplied by the Fair Market Value of a share of Common Stock.

 

4.             EXCHANGE, TRANSFER, ASSIGNMENT OR LOSS OF WARRANT .

 

(a)           This Warrant is exchangeable, without expense, at the option of the Holder, upon presentation and surrender hereof to the Company, or at the office of its stock transfer agent, if any, for other warrants of different denominations entitling the holder thereof to purchase in the aggregate the same number of shares of Common Stock purchasable hereunder.  Subject to the restrictions set forth in Subsection 4(b) below, and provided the conditions specified in the legend set forth at the front of this Warrant shall have been satisfied, upon surrender of this Warrant to the Company at its principal office, or at the office of its stock transfer agent, if any, with the Assignment Form attached hereto as Exhibit B , duly executed and funds sufficient to pay any transfer tax, the Company shall, without charge, execute and deliver a new Warrant in the name of the assignee named in such Assignment Form and this Warrant shall promptly be canceled.  This Warrant may be divided or combined with other warrants which carry the same rights upon presentation hereof at the principal office of the Company, or at the office of its stock transfer agent, if any, together with a written notice specifying the names and denominations in which new Warrants are to be issued and signed by the Holder hereof.  The term “Warrant” as used herein includes any Warrants into which this Warrant may be divided or exchanged.  Upon receipt by the Company of evidence satisfactory to the Company of the loss, theft, destruction or mutilation of this Warrant, and (in the case of loss, theft or destruction) of reasonably satisfactory indemnification, and upon surrender and cancellation of this Warrant, if mutilated, the Company will execute and deliver a new Warrant of like tenor and date.  Any such new Warrant executed and delivered shall constitute an additional contractual obligation on the part

 

3



 

of the Company, whether or not this Warrant so lost, stolen, destroyed or mutilated shall be at any time enforceable by anyone.

 

(b)           This Warrant and the shares of Common Stock issuable upon exercise hereof have not been registered under the Securities Act of 1933, as amended, or state securities laws by reason of an exemption therefrom.  The shares of Common Stock issuable upon exercise of this Warrant are not transferable except as provided in this Agreement.  Upon the written consent of the Company, and subject to applicable laws and the restriction on transfer set forth on this Warrant, this Warrant and all rights hereunder are transferable, by the Holder in person or by duly authorized attorney, upon delivery of this Warrant and the form of assignment attached hereto to any transferee designated by Holder.  The transferee shall sign an investment letter in form and substance satisfactory to the Company.  Shares of Common Stock issuable upon exercise of this Warrant will bear an appropriate legend to this effect.  The restrictions contained herein shall be binding on any transferee of the Common Stock issuable upon exercise of this Warrant and the Company may require any such transferee to execute an instrument agreeing in writing to be bound by these restrictions as a condition to transfer.

 

5.             RIGHTS OF THE HOLDER .  The Holder shall not be entitled to vote or receive dividends or be deemed the holder of Common Stock or any other securities of the Company that may at any time be issuable on the exercise hereof for any purpose, nor shall anything contained herein be construed to confer upon the Holder, as such, any of the rights of a stockholder of the Company or any right to vote for the election of directors or upon any matter submitted to stockholders at any meeting thereof, or to give or withhold consent to any corporate action (whether upon any recapitalization, issuance of stock, reclassification of stock, change of par value, or change of stock to no par value, consolidation, merger, conveyance or otherwise) or to receive notice of meetings, or to receive dividends or subscription rights or otherwise until the Warrant shall have been exercised as provided herein.  The rights of the Holder are limited to those expressed in this Warrant and are not enforceable against the Company except to the extent set forth herein.

 

6.             ADJUSTMENT PROVISIONS .  The Exercise Price in effect at any time and the number and kind of securities purchasable upon the exercise of the Warrant shall be subject to adjustment from time to time upon the happening of certain events as follows:

 

(a)           In case the Company shall (i) declare a dividend or make a distribution on its outstanding shares of Common Stock in shares of Common Stock, (ii) subdivide or reclassify its outstanding shares of Common Stock into a greater number of shares or (iii) combine or reclassify its outstanding shares of Common Stock into a smaller number of shares, the Exercise Price in effect at the time of the record date for such dividend or distribution or of the effective date of such subdivision, combination or reclassification shall be adjusted so that the Exercise Price equals the price determined by multiplying the Exercise Price by a fraction, the denominator of which shall be the number of shares of Common Stock outstanding after giving effect to such action, and the numerator of which shall be the number of shares of Common Stock outstanding immediately prior to such action.  Such adjustment shall be made successively whenever any event listed above shall occur.

 

4



 

(b)           Whenever the Exercise Price payable upon exercise of each Warrant is adjusted pursuant to Subsection 6(a) above, the number of Shares purchasable upon exercise of this Warrant shall simultaneously be adjusted by multiplying the number of Shares initially issuable upon exercise of this Warrant by the Exercise Price in effect on the date hereof and dividing the product so obtained by the Exercise Price, as adjusted.

 

(c)           No adjustment in the Exercise Price shall be required unless such adjustment would require an increase or decrease of at least 5% in such price; provided, however, that any adjustments which by reason of this Subsection 6(c) are not required to be made shall be carried forward and taken into account in any subsequent adjustment required to be made hereunder.  All calculations under this Section 6 shall be made to the nearest cent or to the nearest one-hundredth of a share, as the case may be.  Anything in this Section 6 to the contrary notwithstanding, the Company shall be entitled, but shall not be required, to make such changes in the Exercise Price, in addition to those required by this Section 6, as it shall determine, in its sole discretion, to be advisable in order that any dividend or distribution in shares of Common Stock, or any subdivision, reclassification or combination of Common Stock, hereafter made by the Company shall not result in any Federal Income tax liability to the holders of Common Stock or securities convertible into Common Stock (including Warrants).

 

(d)           Whenever the Exercise Price is adjusted, as herein provided, the Company shall promptly but no later than 10 days after any request for such an adjustment by the Holder, cause a notice setting forth the adjusted Exercise Price and adjusted number of Shares issuable upon exercise of each Warrant, and, if requested, information describing the transactions giving rise to such adjustments, to be mailed to the Holders at their last addresses appearing in the Warrant Register, and shall cause a certified copy thereof to be mailed to its transfer agent, if any.  The Company may retain a firm of independent certified public accountants selected by the Board of Directors (who may be the regular accountants employed by the Company) to make any computation required by this Section 6, and a certificate signed by such firm shall be conclusive evidence of the correctness of such adjustment.

 

(e)           In the event that at any time, as a result of an adjustment made pursuant to Subsection 6(a) above, the Holder of this Warrant thereafter shall become entitled to receive any shares of the Company, other than Common Stock, thereafter the number of such other shares so receivable upon exercise of this Warrant shall be subject to adjustment from time to time in a manner and on terms as nearly equivalent as practicable to the provisions with respect to the Common Stock contained in Subsection 6(a) through Subsection 6(d), inclusive above.

 

7.             OFFICER’S CERTIFICATE .  Whenever the Exercise Price shall be adjusted as required by the provisions of the foregoing Section, the Company shall forthwith file in the custody of its Secretary or an Assistant Secretary at its principal office and with its stock transfer agent, if any, an officer’s certificate showing the adjusted Exercise Price determined as herein provided, setting forth in reasonable detail the facts requiring such adjustment, including a statement of the number of additional shares of Common Stock, if any, and such other facts as shall be necessary to show the reason for and the manner of computing such adjustment.  Each such officer’s certificate shall be made available at all reasonable times for inspection by the holder or any holder of a Warrant executed and delivered pursuant to Section 1 and the Company shall,

 

5



 

forthwith after each such adjustment, mail a copy by certified mail of such certificate to the Holder or any such holder.

 

8.             NOTICES TO WARRANT HOLDERS .  So long as this Warrant shall be outstanding, (a) if the Company shall pay any dividend or make any distribution upon the Common Stock or (b) if the Company shall offer to the holders of Common Stock for subscription or purchase by them any share of any class or any other rights or (c) if any capital reorganization of the Company, reclassification of the capital stock of the Company, consolidation or merger of the Company with or into another corporation, sale, lease or transfer of all or substantially all of the property and assets of the Company to another corporation, or voluntary or involuntary dissolution, liquidation or winding up of the Company shall be effected, then in any such case, the Company shall cause to be mailed by certified mail to the Holder, at least 15 days prior to the date specified in (i) or (ii) below, as the case may be, a notice containing a brief description of the proposed action and stating the date on which (i) a record is to be taken for the purpose of such dividend, distribution or rights, or (ii) such reclassification, reorganization, consolidation, merger, conveyance, lease, dissolution, liquidation or winding up is to take place and the date, if any is to be fixed, as of which the holders of Common Stock or other securities shall receive cash or other property deliverable upon such reclassification, reorganization, consolidation, merger, conveyance, dissolution, liquidation or winding up.

 

9.             RECLASSIFICATION, REORGANIZATION OR MERGER .  In case of any reclassification, capital reorganization or other change of outstanding shares of Common Stock of the Company, or in case of any consolidation or merger of the Company with or into another corporation (other than a merger with a subsidiary in which merger the Company is the continuing corporation and which does not result in any reclassification, capital reorganization or other change of outstanding shares of Common Stock of the class issuable upon exercise of this Warrant) or in case of any sale, lease or conveyance to another corporation of the property of the Company as an entirety, the Company shall, as a condition precedent to such transaction, cause effective provisions to be made so that the Holder shall have the right thereafter by exercising this Warrant at any time prior to the expiration of the Warrant, to purchase the kind and amount of shares of stock and other securities and property receivable upon such reclassification, capital reorganization and other change, consolidation, merger, sale or conveyance by a holder of the number of shares of Common Stock which might have been purchased upon exercise of this Warrant immediately prior to such reclassification, change, consolidation, merger, sale or conveyance.  Any such provision shall include provision for adjustments which shall be as nearly equivalent as may be practicable to the adjustments provided for in this Warrant.  The foregoing provisions of this Section 9 shall similarly apply to successive reclassifications, capital reorganizations and changes of shares of Common Stock and to successive consolidations, mergers, sales or conveyances.  In the event that in connection with any such capital reorganization or reclassification, consolidation, merger, sale or conveyance, additional shares of Common Stock shall be issued in exchange, conversion, substitution or payment, in whole or in part, for a security of the Company other than Common Stock, any such issue shall be treated as an issue of Common Stock covered by the provisions of Subsection 6(a) hereof

 

[Signature page follows.]

 

6



 

IN WITNESS WHEREOF, the Company has duly caused this Warrant to be signed and attested by its duly authorized officers and as of the date as set forth below.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

ISSUED:

[TODAY’S DATE]

 

 

 

 

 

[Corporate Seal]

 

 

 

 

 

 

 

 

Attest:

 

 

 

 

 

 

 

 

 

 

 

 

Secretary

 

 

 



 

EXHIBIT A

 

PURCHASE FORM

 

                           , 200[   ]

 

o       The undersigned hereby irrevocably elects to exercise its rights pursuant to this Warrant to the extent of purchasing                   shares of Common Stock of VGX Pharmaceuticals, Inc., and hereby makes payment of $                           , in cash or in satisfaction of indebtedness, in payment of the exercise price thereof.

 

o       The undersigned hereby irrevocably elects to exercise its rights pursuant to this Warrant to the extent of purchasing            shares of Common Stock and hereby authorizes you to deliver such shares of Common Stock for sale to                       , and to retain from the proceeds of such sale $                         , in cash, in payment of the exercise price thereof and to remit to the undersigned the balance of such proceeds.

 

 

________________________________

 

 

INSTRUCTIONS FOR REGISTRATION OF STOCK

 

Name:________________________________________________________________________

  (Please typewrite or print in block letters)

 

Address:______________________________________________________________________

 

Signature:_____________________________________________________________________

 

Telephone Number:_____________________________________________________________

 

Facsimile Number:______________________________________________________________

 



 

EXHIBIT B

 

ASSIGNMENT FORM

 

 

FOR VALUE RECEIVED,                                                                   hereby sells, assigns and transfers unto:

 

Name:     ______________________________________________________________

  (Please typewrite or print in block letters)

 

Address:_____________________________________________________________

 

the right to purchase Common Stock of VGX Pharmaceuticals, Inc. (the “Company”), represented by this Warrant to the extent of                shares as to which such right is exercisable and does hereby irrevocably constitute and appoint                                  as Attorney, to transfer the same on the books of the Company with full power of substitution in the premises.

 

Date:                           , 200[    ]

 

Signature: ______________________________

 




EXHIBIT 10.68

 

VGX PHARMACEUTICALS, INC.

 

WARRANT PURCHASE AGREEMENT

 

THESE SECURITIES OF VGX PHARMACEUTICALS, INC. (THE “COMPANY”) ARE SUBJECT TO RESTRICTIONS ON TRANSFERABILITY AND RESALE AND MAY NOT BE TRANSFERRED OR RESOLD EXCEPT AS PERMITTED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), AND THE APPLICABLE STATE SECURITIES LAWS, PURSUANT TO REGISTRATION OR EXEMPTION THEREFROM.  THE BUYER SHOULD BE AWARE THAT HE MAY BE REQUIRED TO BEAR THE FINANCIAL RISKS OF THIS INVESTMENT FOR AN INDEFINITE PERIOD OF TIME.

 

AN INVESTMENT IN THESE SECURITIES IS SPECULATIVE AND INVOLVES A HIGH DEGREE OF RISK.  THE BUYER MUST BE ABLE TO BEAR THE ECONOMIC RISK OF HIS INVESTMENT FOR AN INDEFINITE PERIOD OF TIME AND BE ABLE TO SUSTAIN A LOSS OF HIS ENTIRE INVESTMENT.  THE BUYER WILL BE REQUIRED TO MAKE REPRESENTATIONS WITH RESPECT TO HIS NET WORTH OR INCOME AND HIS AUTHORITY TO MAKE SUCH INVESTMENT AND TO REPRESENT, AMONG OTHER THINGS, HE IS FAMILIAR WITH AND UNDERSTANDS THE TERMS OF THIS OFFERING.

 

IN MAKING AN INVESTMENT DECISION, THE BUYER MUST RELY ON HIS OWN EXAMINATION OF THE COMPANY AND THE TERMS OF THIS OFFERING, INCLUDING THE MERITS AND THE RISKS INVOLVED.  THESE SECURITIES HAVE NOT BEEN RECOMMENDED BY ANY FEDERAL OR STATE SECURITIES COMMISSION OR REGULATORY AUTHORITY.  FURTHERMORE, THE FOREGOING AUTHORITIES HAVE NOT CONFIRMED THE ACCURACY OR DETERMINED THE ADEQUACY OF THIS DOCUMENT.  ANY REPRESENTATION TO THE CONTRARY IS A CRIMINAL OFFENSE.

 

THE BUYER IS NOT TO CONSTRUE THE CONTENTS OF THIS AGREEMENT OR ANY PRIOR OR SUBSEQUENT COMMUNICATIONS FROM THE COMPANY OR ANY OF ITS OFFICERS, EMPLOYEES OR AGENTS AS INVESTMENT, LEGAL OR TAX ADVICE.  THE BUYER SHOULD CONSULT HIS OWN COUNSEL, ACCOUNTANT AND OTHER PROFESSIONAL ADVISORS AS TO INVESTMENT, LEGAL, TAX AND OTHER RELATED MATTERS CONCERNING THE BUYER’S PROPOSED INVESTMENT.

 

THE COMPANY EXTENDS TO THE BUYER THE OPPORTUNITY, PRIOR TO THE CONSUMMATION OF THE SALE OF THESE SECURITIES, TO ASK QUESTIONS OF, AND RECEIVE ANSWERS FROM, REPRESENTATIVES OF THE COMPANY CONCERNING THESE SECURITIES AND THE TERMS OF THIS OFFERING, AND TO OBTAIN ANY ADDITIONAL INFORMATION HE MAY CONSIDER NECESSARY IN MAKING AN INFORMED INVESTMENT DECISION OR IN ORDER TO VERIFY THE ACCURACY OF THE INFORMATION CONTAINED HEREIN, TO THE EXTENT THAT THE COMPANY POSSESSES SUCH INFORMATION OR CAN ACQUIRE SUCH INFORMATION WITHOUT UNREASONABLE EFFORT OR EXPENSE AND CAN MAKE SUCH INFORMATION AVAILABLE WITHOUT DIVULGING INFORMATION DEEMED BY THE COMPANY, IN ITS ABSOLUTE DISCRETION, TO BE PROPRIETARY AND CONFIDENTIAL .

 



 

THIS WARRANT PUCHASE AGREEMENT (the “Purchase Agreement”), dated this [ENTER TODAY’S DATE] , is by and between [ NAME OF BUYER ] , an individual (the “Buyer”), and VGX Pharmaceuticals, Inc. , a Delaware corporation (the “Company”).

 

WHEREAS, the Buyer wishes to purchase from the Company and the Company wishes to sell to the Buyer, upon the terms and subject to the conditions of this Purchase Agreement, a warrant to purchase common stock of the Company, and in connection with which the Company shall issue a warrant to the Buyer to purchase [###,###] shares of the Company’s common stock, par value $0.0001 per share (“Common Stock”), having a purchase price of $[#.##] per share in accordance with the terms, and subject to the conditions,

 

NOW THEREFORE, in consideration of the premises and the mutual covenants contained herein and other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the parties agree as follows:

 

1.             Sale and Issuance of Note and Warrant   Upon the terms and subject to the conditions of this Purchase Agreement, the Buyer agrees to purchase from the Company, and the Company agrees to sell and issue to the Buyer, a warrant to purchase common stock, in the form attached hereto as Exhibit A (the “Warrant”), to the Buyer to purchase, subject to the terms and conditions of the Warrant, in whole or in part, up to that number of fully paid, validly issued and nonassessable shares of Common Stock.

 

2.             Representations and Warranties of the Company .  By executing this Purchase Agreement, the Company makes the following representations, declarations, warranties and covenants to the Buyer, with the intent and understanding that the Buyer will rely thereon:

 

2.1           Organization of the Company; Authorization.

 

2.1.1        Good Standing .  The Company is a corporation duly organized, validly existing and in good standing under the laws of the State of Delaware and has all requisite corporate power and authority to own and lease its property, to carry on its business as presently conducted and as proposed to be conducted (as previously disclosed to the Buyer) and to execute and deliver, and to perform all of its obligations under, this Purchase Agreement, and Warrant (collectively, the “Company Documents”).

 

2.1.2        Enforceability .  The execution and delivery by the Company of the Company Documents and the consummation of the transactions contemplated thereby have been duly authorized by all requisite corporate action on the part of the Company, and this Purchase Agreement has been duly executed and delivered by the Company and constitutes the legal, valid and binding obligation of the Company, enforceable in accordance with its terms, in each case subject to bankruptcy, insolvency or similar laws relating to creditors rights and general equitable principles.

 



 

3.             Representations and Warranties of the Buyer .  By executing this Purchase Agreement, the Buyer makes the following representations, declarations, warranties and covenants to the Company, with the intent and understanding that the Company will rely thereon:

 

3.1           Investment Representations .  The Buyer has knowledge and experience in financial and business matters sufficient to enable him to evaluate the merits and risks of an investment in the Company.  The Buyer has assets sufficient to enable him to bear the economic risk of the Buyer’s investment in the Warrant and is an “accredited investor,” as defined in Rule 501 under the Securities Act of 1933, as amended (the “Securities Act”).  The Buyer is acquiring the Warrant for his own account, and not with a present view to, or for sale in connection with, any distribution thereof.  The Buyer understands that the Warrant and the Company’s securities issuable upon conversion of the Warrant have not been registered under the Securities Act by reason of their issuance in a transaction exempt from the registration requirements of the Securities Act pursuant to the exemption provided in Section 4(2) thereof, that the Warrant and the Company’s securities issuable upon conversion of the Warrant thereof have not been registered under applicable state securities laws by reason of their issuance in a transaction exempt from such registration requirements, and that the Warrant and the Company’s securities issuable upon conversion of the Warrant thereof may not be sold or otherwise disposed of unless registered under the Securities Act and applicable state securities laws (the Company being under no obligation to register such Warrant or securities issuable on conversion of the Warrant thereof) or exempted from registration.  The Buyer further acknowledges that the Warrant and the Company’s securities issuable upon conversion of the Warrant are subject to the restrictions on transfers set forth in the Company Documents, and that each transferee of the Warrant or the Company’s securities issuable upon conversion of the Warrant as a condition to such transfer may be required to agree in writing to be bound by such restrictions.

 

3.2           Buyer’s Acknowledgment as to Information.

 

3.2.1        The Buyer or representatives of the Buyer have received from the Company such information (including exhibits to this Purchase Agreement and of such documents referred to herein and therein as he or they have requested) with respect to the Company as the Buyer has deemed necessary and relevant in connection with the transactions contemplated by the Company Documents, and the Buyer has had the opportunity, directly or through such representatives, to ask questions of and receive answers from persons acting on behalf of the Company necessary to verify the information so obtained.

 

4.             Legend .  Each certificate evidencing the Warrant and the Company’s securities issuable upon conversion of the Warrant, and each certificate evidencing the Warrant and the Company’s securities issuable upon conversion of the Warrant held by subsequent transferees of any such certificate, shall be stamped or otherwise imprinted with a legend in substantially the following form:

 

THE SECURITIES REPRESENTED HEREBY HAVE BEEN ACQUIRED FOR INVESTMENT AND HAVE NOT BEEN REGISTERED UNDER THE SECURITIES ACT OF 1933, AS AMENDED (THE “SECURITIES ACT”), OR ANY APPLICABLE STATE SECURITIES LAWS.  ADDITIONALLY, THE TRANSFER OF

 

3



 

THESE SECURITIES IS SUBJECT TO CERTAIN CONDITIONS SPECIFIED IN THE WARRANT PURCHASE AGREEMENT DATED AS OF [ENTER TODAY’S DATE] , BETWEEN VGX PHARMACEUTICALS, INC. (THE “COMPANY”) AND THE SIGNATORY THERETO.  NO TRANSFER OF SUCH SECURITIES SHALL BE VALID OR EFFECTIVE UNTIL SUCH CONDITIONS HAVE BEEN FULFILLED.  COPIES OF SUCH AGREEMENT MAY BE OBTAINED AT NO COST BY WRITTEN REQUEST MADE BY THE HOLDER OF RECORD OF THIS CERTIFICATE TO THE SECRETARY OF THE COMPANY.  NEITHER THE SECURITIES NOR ANY INTEREST THEREIN MAY BE SOLD, TRANSFERRED, ASSIGNED, PLEDGED, HYPOTHECATED OR OTHERWISE DISPOSED OF UNLESS: (1) A REGISTRATION STATEMENT WITH RESPECT THERETO IS EFFECTIVE UNDER THE SECURITIES ACT AND ANY APPLICABLE STATE SECURITIES LAWS; OR (2) THE COMPANY RECEIVES AN OPINION OF COUNSEL, WHICH OPINION IS SATISFACTORY TO THE COMPANY, THAT REGISTRATION UNDER SUCH ACT AND APPLICABLE STATE SECURITIES LAWS IS NOT REQUIRED.

 

5.             Miscellaneous.

 

5.1           Legal Fees and Expenses .  Each party hereto agrees to pay its own legal fees and expenses incurred in connection with the transactions contemplated hereunder.

 

5.2           No Waiver .  The failure of a party to insist upon strict adherence to any term of this Purchase Agreement on any occasion shall not be considered a waiver or deprive that party of the right thereafter to insist upon strict adherence to that term or any other term of this Purchase Agreement.  Any waiver of any term of this Purchase Agreement must be in writing.

 

5.3           Entire Agreement; Amendment .  This Purchase Agreement and all Exhibits, Schedules and attachments hereto, along with the other Company Documents, set forth the entire agreement of the parties with respect to the subject matter hereof and supersede all prior agreements relating thereto, written or oral.  This Purchase Agreement may be amended or modified only by a written instrument executed by the Company and the Buyer.

 

5.4           Parties in Interest; Limitation on Assignment .  This Purchase Agreement shall inure to the benefit of and be binding upon the parties and their respective permitted successors and assigns; provided , however , that this Purchase Agreement shall not be assigned or assignable by either party without the prior written consent of the other party.

 

5.5           Counterparts .  This Purchase Agreement may be executed in any number of counterparts, each of which shall be considered an original, but all of which together shall constitute one and the same instrument.

 

5.6           Governing Law .  This Purchase Agreement shall be governed by, construed, interpreted and enforced in accordance with the laws of the Commonwealth of Pennsylvania as

 

4



 

applied to contracts entered into and performed entirely within the Commonwealth of Pennsylvania among Pennsylvania residents without regard to conflicts of laws principles.

 

5.7           Notices .  All notices, consents and other communications under this Purchase Agreement shall be in writing and shall be deemed to have been duly given when (a) delivered by hand, (b) sent by telex or telecopier (with receipt confirmed), provided that a copy is mailed by registered mail, return receipt requested, or (c) when received by the addressee, if sent by Express Mail, Federal Express or other express delivery service (receipt requested), in each case to the appropriate addresses, telex numbers and telecopier numbers set forth below (or to such other addresses, telex numbers and telecopier numbers as a party may designate as to itself by notice to the other party):

 

5.7.1        If to the Company:

 

VGX Pharmaceuticals, Inc.

450 Sentry Parkway E

Blue Bell, PA, 19422

Telecopier No. (267)440-4200

Attention:  Corporate Secretary

 

5.7.2        If to the Buyer:

 

5.8           Severability .  In the event that any court having jurisdiction shall determine that any provision contained in this Purchase Agreement shall be unreasonable or unenforceable in any respect, then such covenant or other provision shall be deemed limited to the extent that such court deems it reasonable and enforceable, and as so limited shall remain in full force and effect.  In the event that such court shall deem any such covenant or other provision wholly unenforceable, the remaining covenants and other provisions of this Purchase Agreement shall nevertheless remain in full force and effect.

 

5.9           Headings and Captions .  The headings and captions used herein to identify sections and subsections are for convenience only and shall not be used for interpretation of any provisions herein.

 

5.10         Specific Performance .  In addition to and not in limitation of any other legal or equitable remedies which it may have, the Company may enforce its rights hereunder by an action for specific performance.

 

5.11         Indemnity .  The representations, warranties and agreements made by the Buyer herein shall survive the execution of this Purchase Agreement.  The Buyer hereby agrees to indemnify and hold harmless the Company from and against any and all loss, liability, claim, damage and expense (including, without limitation, attorneys’ fees and disbursements) suffered or incurred as a result of a misrepresentation or breach of any warranty or agreement made by the Buyer in this Purchase Agreement.

 

5



 

[Signature Page Follows]

 

6



 

IN WITNESS WHEREOF , each of the parties has caused this Purchase Agreement to be executed on its behalf with the intent to be legally bound as of the day and year first above written.

 

 

VGX PHARMACEUTICALS, INC.

 

 

 

 

 

By:

 

 

 

J. Joseph Kim, Ph.D.

 

 

President and Chief Executive Officer

 

 

 

BUYER:

 

 

 

 

 

NAME OF BUYER

 

 

 

Address:

 

 

 

 

 

 

 



 

EXHIBIT A

 

FORM OF WARRANT

 

( see attached)

 




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Exhibit 23.3

Consent of Independent Registered Public Accounting Firm

        We consent to the reference to our firm under the caption "Experts" in the Registration Statement (Amendment No. 1 to Form S-4 No. 333-156035) and related joint proxy statement/prospectus of Inovio Biomedical Corporation and to the inclusion therein of our report dated March 12, 2008, with respect to the consolidated financial statements of Inovio Biomedical Corporation included in its Annual Report (Form 10-K) for the year ended December 31, 2007, filed with the Securities and Exchange Commission.

    /s/ Ernst & Young LLP

San Diego, California
January 20, 2009

 

 



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Exhibit 23.4

Consent of Independent Auditors

        We consent to the reference to our firm under the caption "Experts" and to the use of our report dated June 30, 2008 (except Note 3, as to which the date is January 19, 2009), with respect to the consolidated financial statements of VGX Pharmaceuticals, Inc. included in the Registration Statement (Amendment No. 1 to Form S-4 No. 333-156035) and related joint proxy statement/prospectus of Inovio Biomedical Corporation.

    /s/ Ernst & Young LLP

Philadelphia, Pennsylvania
January 19, 2009

 

 



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