UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d)

OF THE SECURITIES EXCHANGE ACT OF 1934

 

Date of Report (Date of Earliest Event Reported):  May 3, 2017

 

IMMUNOMEDICS, INC.

(Exact name of registrant as specified in its charter)

 

Delaware

 

000-12104

 

61-1009366

(State or other jurisdiction of incorporation)

 

(Commission File Number)

 

(I.R.S. Employer Identification No.)

 

300 The American Road
Morris Plains, New Jersey

 

07950

(Address of principal executive offices)

 

(Zip Code)

 

Registrant’s telephone number, including area code: ( 973) 605-8200

 

Not Applicable

(Former name or former address, if changed since last report.)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

 

o             Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

o             Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

o             Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

o             Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company o

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. o

 

 

 



 

Item 1.01 Entry into a Material Definitive Agreement.

 

The information contained below under Item 3.02 and under Item 1.02 is hereby incorporated by reference into this Item 1.01.

 

Settlement Term Sheet and Settlement Agreement

 

On May 3, 2017, Immunomedics, Inc., a Delaware corporation (the “ Company ”) entered into a binding settlement term sheet (the “ Term Sheet ”) by and among the Company, venBio Select Advisor LLC, a Delaware limited liability company (“ venBio ”), Dr. David M. Goldenberg, a director of the Company and the Company’s Chief Scientific Officer and Chief Patent Officer (“ Goldenberg ”), Ms. Cynthia L. Sullivan, a director of the Company and the Company’s President and Chief Executive Officer (“ Sullivan ”), and Mr. Brian A. Markison, a director of the Company (“ Markison ”, together with venBio, Goldenberg, Sullivan and the Company, the “ Parties ”) in order to resolve certain legal actions among the Parties, as described below. The Parties also agreed to cooperate and use their best efforts to reduce the Term Sheet to a definitive settlement agreement (the “ Settlement Agreement ”) and, to the extent necessary, obtain the approval of the Court of Chancery of the State of Delaware (the “ Court of Chancery ”).

 

Resolution of Litigation

 

Pursuant to the Term Sheet, the Parties submitted a stipulation and proposed order to the Court of Chancery lifting the Status Quo Order (as defined in Item 8.01 hereof) and confirming that the Status Quo Board (as defined in Item 8.01 hereof) is the lawful board of directors of the Company (provided however, if the 225 Action is not dismissed, the Parties will be restored to their positions in the 225 Action as of immediately prior to the execution of the Term Sheet).  The Court of Chancery entered the proposed order on the afternoon of May 4, 2017.  Pursuant to the Term Sheet, the Parties also agreed to submit a stipulation and proposed order to the Court of Chancery staying the venBio Action (as defined in Item 8.01 hereof)  and removing the trial dates from the calendar of the Court of Chancery.

 

The Company has further agreed to reimburse venBio for reasonable fees and expenses it incurred in connection with the proxy contest between venBio and the Company, the venBio Action, the 225 Action (as defined in Item 8.01 hereof) and the Federal Action (as defined in Item 8.01 hereof and, together with the venBio Action and the 225 Action, the “ Actions ”), and Goldenberg and Sullivan have agreed to not object to such reimbursement.

 

The Parties have agreed, immediately upon execution of the Settlement Agreement, to submit stipulations and proposed orders dismissing with prejudice both the 225 Action and the Federal Action. The Settlement Agreement will include (i) a mutual release of all claims that were or could have been asserted in the Federal Action or in the 225 Action and (ii) a comprehensive release of all direct and derivative claims that have been or could be asserted by or on behalf of (a) venBio or the Company, whether known or unknown, against Goldenberg, Sullivan and Markison and their affiliates and related persons, and (b) Goldenberg, Sullivan or Markison, whether known or unknown, against venBio or the Company and their affiliates and related persons, in both cases in connection with the claims alleged in the venBio Action, the Financing (as defined in Item 3.02 hereof), the settlement of the venBio Action, the Licensing Transaction (as defined in Item 1.02 hereof) and the Termination Agreement (both terms as defined in Item 1.02 hereof). The settlement of claims against Goldenberg, Sullivan and Markison in the venBio Action will be subject to approval of the Court of Chancery.  venBio and the Company have agreed to stay the venBio Action and submit the claims asserted against the remaining individual defendants (former directors Robert Forrester, Jason Aryeh, Geoff Cox and Bob Oliver) and Greenhill to non-binding

 

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mediation.  As part of the Termination Agreement, which is subject to the approval of the Court of Chancery, venBio will release Seattle Genetics from any claims in the venBio Action.

 

Financing and Termination of Seattle Genetics Transaction

 

Pursuant to the Term Sheet, Goldenberg and Sullivan have or will (i) vote to support the Financing, (ii) vote to terminate the Licensing Transaction pursuant to the terms of the Termination Agreement, (iii) vote to approve the Charter Amendment (as defined in Item 3.02 hereof), (iv) approve the submission of a stipulation in the 225 Action to permit the board of directors of the Company (the “ Board ”) to consummate and enter into both the Financing and the Termination Agreement, and (v) agree to not sell any shares of the Company (with certain exceptions) until the date which is the earlier of July 31, 2017 or the date on which the Charter Amendment is approved and the shares of common stock, par value $0.01 per share, of the Company (the “ Common Stock ”) issuable upon conversion of the Preferred Shares (as defined in Item 3.02 hereof) are registered and issued.

 

Indemnification

 

The Term Sheet provides that the Company will, to the extent not covered by the Company’s insurance policies, (i) indemnify Goldenberg, Sullivan and Markison from attorneys’ fees and expenses or other losses in connection with the Actions, and (ii) reimburse and indemnify Goldenberg and Sullivan for legal fees for actions taken with respect to the Actions and negotiation of the Settlement Agreement.  The Term Sheet provides that the indemnification agreements entered into between the Company and each of Goldenberg, Sullivan and Markison on or about February 9, 2017 shall be terminated and not apply to acts, transactions, legal fees or expenses incurred after approval of the Settlement Agreement by the Court of Chancery.

 

Intellectual Property Assignments

 

The Settlement Agreement shall provide that Goldenberg and Sullivan will assign global intellectual property rights, other than those subject to existing agreements with the Company and Goldenberg’s patent and related intellectual property relating to cyber space medicine, to the Company, and perform all acts reasonably requested by the Company to perfect title in and to all such assigned intellectual property.

 

Sullivan Resignation

 

Upon execution of the contemplated Settlement Agreement, Sullivan has agreed to resign from all director, officer and other positions of the Company and any of its affiliates, effective as of the date of the Settlement Agreement.  The Settlement Agreement will provide that Sullivan will abide by all post-termination covenants and obligations contemplated by her employment agreement with the Company (the “ Sullivan Agreement ”).    In exchange for a release of claims as required by the Sullivan Agreement and subject to compliance with the terms of the Settlement Agreement, Sullivan will be entitled to (i) termination payments in accordance with the Sullivan Agreement for a termination without Good Cause after a Change in Control, (ii) accelerated vesting or extension of the exercise period for equity awards already earned, pursuant to the Sullivan Agreement, and (iii) COBRA payments.  The foregoing cash payments accumulate to approximately $3.4 million (a portion of which remain in dispute).

 

Goldenberg Resignation

 

Upon execution of the Settlement Agreement, Goldenberg will remain a director of the Company, but has agreed to resign from all officer and other positions of the Company and all director, officer and other positions at any of the Company’s affiliates (other than Goldenberg’s position as a member of the board

 

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of directors of IBC Pharmaceuticals, the Company’s majority owned U.S. subsidiary), effective as of the date of the Settlement Agreement.  The Settlement Agreement will provide that Goldenberg will abide by all post-termination covenants and obligations contemplated by his employment agreement with the Company (the “ Goldenberg Agreement ”).    In exchange for a release of claims as required by the Goldenberg Agreement and subject to compliance with the terms of the Settlement Agreement, Goldenberg will be entitled to (i) termination payments in accordance with the Goldenberg Agreement for a termination without Good Cause after a Change in Control, (ii) accelerated vesting or extension of exercise period for equity awards already earned, pursuant to the Goldenberg Agreement, (iii) COBRA payments, (iv) royalties or payment in accordance with existing agreements. The foregoing cash payments accumulate to approximately $3.6 million (a portion of which remain in dispute).

 

Arbitration of Disputed Matters

 

The Parties have agreed to arbitrate disputes relating to Goldenberg’s claimed entitlement to certain equity awards and severance payments, and Goldenberg’s and Sullivan’s claimed rights to certain bonus payments, to the extent the Parties cannot reach agreement on such issues before execution of the Settlement Agreement. The Company has agreed to pay in full the arbitrator in such arbitration as well as reasonable attorneys’ fees and expenses incurred by Goldenberg and/or Sullivan in connection with any such arbitration, up to a cap of $650,000.

 

The description of the Term Sheet in this Current Report on Form 8-K does not purport to be complete and is qualified in its entirety by reference to the complete text of the contemplated Settlement Agreement, which is expected to be filed as an exhibit to the Company’s annual report on Form 10-K for the period ended June 30, 2017.

 

Item 1.02 Termination of a Material Definitive Agreement.

 

As previously disclosed on a current report on Form 8-K filed with the SEC on February 10, 2017, the Company entered into a Licensing and Development Agreement (the “ Licensing Agreement’ ) with Seattle Genetics, Inc., a Delaware corporation (“ Seattle Genetics ”), granting Seattle Genetics a worldwide, exclusive license, including the right to sublicense subject to the terms and conditions of the License Agreement, to develop, manufacture and commercialize sacituzumab govitecan (“ IMMU-132 ”), an antibody-drug conjugate comprising hRS7, SN-38 and the proprietary linker CL-2A, and any second generation antibody-drug conjugates binding to Trop-2 for all human therapeutic uses in all indications (the “ Licensing Transaction ”). In connection with the Licensing Agreement, the Company and Broadridge Corporate Issuer Solutions, Inc., a Pennsylvania corporation, as warrant agent for the benefit of Seattle Genetics, entered into a Warrant Agreement, dated as of February 16, 2017, pursuant to which the Company agreed to execute and deliver to, and in favor of, Seattle Genetics, warrants to acquire up to an aggregate of 8,655,804 shares of Common Stock at an initial exercise price of $4.90 per share (the “ SGEN Warrant ”).

 

On May 4, 2017, the Company and Seattle Genetics entered into a Termination Agreement (the “ Termination Agreement ”), pursuant to which the Company and Seattle Genetics relinquish their respective rights under the Licensing Agreement.  Pursuant to the terms of the Termination Agreement, the Company and Seattle Genetics also agreed to amend the terms of the SGEN Warrant to amend the expiration date from February 10, 2020 to the later of (i) December 31, 2017, and (ii) the date that is six (6) months following the date on which a sufficient number of shares of Common Stock are authorized and reserved for issuance to permit the full exercise of the SGEN Warrant.

 

The Termination Agreement constitutes an agreement to terminate the License Agreement and is not in any way an admission of liability or breach by either the Company or Seattle Genetics.  The Termination

 

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Agreement between the Company and Seattle Genetics and the settlement of the venBio lawsuit against Seattle Genetics remain subject to court approval of the dismissal of the venBio Action.  The termination of the Licensing Transaction will be effective as of the date of the court approval.  In the event the court declines to dismiss the venBio Action against Seattle Genetics, or if the effective date of the Termination Agreement does not occur on or before October 1, 2017, any party to the Termination Agreement may terminate the Termination Agreement upon written notice to such other party.

 

The description of the Termination Agreement in this Current Report on Form 8-K does not purport to be complete and is qualified in its entirety by reference to the complete text of the Termination Agreement, which is to be filed as an exhibit to the Company’s annual report on Form 10-K for the period ended June 30, 2017.

 

Item 3.02 Unregistered Sales of Equity Securities.

 

On May 4, 2017, the Company entered into a securities purchase agreement (the “ Purchase Agreement ”) with a select group of institutional purchasers, including venBio (the “ Purchasers ”), pursuant to which the Company, in a private placement, agreed to issue and sell to the Purchasers one million (1,000,000) shares (the “ Preferred Shares ”) of the Company’s newly-designated Series A-1 Convertible Preferred Stock, par value $0.01 per share (the “ Series A-1 Convertible Preferred Stock ”), at a price of $125 per share for gross proceeds to the Company of $125 million, before deducting fees and expenses (the “ Financing ”). Each Preferred Share will be convertible, subject to the terms of the Certificate of Designation (as defined below), into 23.10536 shares of Common Stock (or an aggregate of 23,105,360 shares of Common Stock).  The effective purchase price per share of Common Stock (assuming conversion) is $5.41, (the closing price per share of Common Stock as listed on NASDAQ on May 4, 2017).  The Financing is expected to close on or about May 10, 2017, subject to the satisfaction of customary closing conditions.

 

The Company currently does not have a sufficient number of authorized and unreserved shares of Common Stock to permit the conversion of the Preferred Shares.  Pursuant to the Purchase Agreement, the Company has agreed to use commercially reasonable efforts to seek stockholder approval of an amendment to the Company’s Amended and Restated Certificate of Incorporation, as amended, to increase the number of shares of authorized Common Stock by an aggregate number of shares of Common Stock to enable conversion of all of the Preferred Shares into shares of Common Stock (the “ Charter Amendment ”), and to continue, as necessary, to seek such stockholder approval until the Charter Amendment receives the requisite stockholder approval.  The Preferred Shares will automatically convert to shares of Common Stock upon stockholder approval of the Charter Amendment and subsequent filing of the Charter Amendment with the Secretary of State of the State of Delaware.  To the extent the Company is unsuccessful in obtaining stockholder approval for the Charter Amendment and the increase in authorized shares of Common Stock has not become effective by August 31, 2017, then a cash dividend shall accrue on each share of Series A-1 Convertible Preferred Stock at a rate per annum equal to 1.00% of the initial purchase price per share of Series A-1 Convertible Preferred Stock, with the rate of accrual to increase by an additional 1.00% for each month following August 31, 2017 during which the Preferred Conversion Event (as defined in the Certificate of Designation) has not occurred.

 

Included in the Purchase Agreement are provisions which require the Company to register the resale of the Preferred Shares and the Common Stock underlying the Preferred Shares. The Company is required to prepare and file a registration statement with the Securities and Exchange Commission within 30 days following approval by the Company’s stockholders of the Charter Amendment and the subsequent effectiveness of the Charter Amendment, and to use commercially reasonable efforts to have the registration statement declared effective within 90 days if there is no review by the Securities and Exchange Commission, and within 120 days in the event of such review.

 

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The Preferred Shares were offered and will be issued and sold in reliance upon the exemption from the registration requirements of the Securities Act of 1933, as amended (the “ Securities Act ”), set forth under Section 4(a)(2) of the Securities Act relating to sales by an issuer not involving any public offering and in reliance on similar exemptions under applicable state laws. Each Purchaser represented that it is an accredited investor and that it is acquiring the Preferred Shares for investment purposes only and not with a view to any resale, distribution or other disposition of such securities in violation of the United States federal securities laws. Neither this Current Report on Form 8-K, nor the exhibits attached hereto is an offer to sell or the solicitation of an offer to buy the securities described herein.

 

The Company expects to use the proceeds from the financing towards working capital and general corporate purposes, including the continued development of its lead product candidate, IMMU-132.

 

Cowen and Company, LLC is acting as the sole placement agent for the Financing.

 

The description of the Purchase Agreement in this Current Report on Form 8-K does not purport to be complete and is qualified in its entirety by reference to the complete text of the Purchase Agreement, which is to be filed as an exhibit to the Company’s annual report on Form 10-K for the period ended June 30, 2017.

 

Item 5.02 Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of Certain Officers.

 

The information set forth under Item 1.01 of this Current Report on Form 8-K is incorporated by reference in response to this Item 5.02.

 

In addition, the Company appointed Michael R. Garone to serve as interim Chief Executive Officer, effective upon the execution and effectiveness of the Settlement Agreement.  Mr. Garone joined the Company as Vice President, Finance and Chief Financial Officer in June 2016.  From August 2007 through June 2016, Mr. Garone was the Chief Financial Officer of Emisphere Technologies, Inc. (“ Emisphere ”), a commercial stage, specialty pharmaceutical company, where he also served as Corporate Secretary since October 2008 and as Interim Chief Executive Officer from February 2011 until September 2012. Before Emisphere, Mr. Garone served as Interim Chief Executive Officer and Chief Financial Officer of Astralis, Ltd.  Prior to that, Mr. Garone served 20 years at AT&T, where he held several positions, including Chief Financial Officer of AT&T Alascom.  Mr. Garone received an MBA from Columbia University and a BA in Mathematics from Colgate University.

 

There are no family relationships between Mr. Garone and any director or executive officer of the Company, and he has no direct or indirect material interest in any transaction required to be disclosed pursuant to Item 404(a) of Regulation S-K.

 

As a result of the leadership transitions set forth in Item 1.01 and Item 5.02 herein, the Board plans on deciding on a permanent CEO and filling out additional leadership positions within the Company.

 

Item 5.03 Amendments to Articles of Incorporation or Bylaws; Change in Fiscal Year.

 

In connection with the private placement described in Item 3.02, the Board approved the Certificate of Designation of Series A-1 Convertible Preferred Stock in the form attached hereto as Exhibit 3.1, which designates One Million (1,000,000) shares as Series A-1 Convertible Preferred Stock. The material terms of the Series A-1 Convertible Preferred Stock are described in Item 3.02 and are incorporated herein by reference. The Company expects to file the Certificate of Designation with the Secretary of State of the State of Delaware prior to the closing of the Financing, on or about May 5, 2017.

 

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Item 7.01 Regulation FD Disclosure.

 

The Company has made available on its website a slide presentation dated May 2017 that is intended to provide an update on the Company’s business.  The slide presentation is attached hereto as Exhibit 99.1 and is incorporated herein by reference.

 

The information in Item 7.01 of this Current Report on Form 8-K shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “ Exchange Act ”), or incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.

 

Item 8.01 Other Events.

 

Press Release

 

On May 5, 2017, the Company issued a press release announcing the Financing. The full text of the press release issued in connection with the announcement for the Financing is attached as Exhibit 99.2 to this Form 8-K and is incorporated herein by reference.

 

Neither the filing of the press release as an exhibit to this Current Report on Form 8-K nor the inclusion in the press release of a reference to the Company’s internet address shall, under any circumstances, be deemed to incorporate the information available at its internet address into this Current Report on Form 8-K. The information available at the Company’s internet address is not part of this Current Report on Form 8-K or any other report filed by the Company with the SEC.

 

Litigation Update

 

Stockholder Claim in the Court of Chancery of the State of Delaware

 

On February 13, 2017, venBio commenced an action captioned venBio Select Advisor LLC v. Goldenberg, et al. , C.A. No. 2017-0108-VCL (Del. Ch.) (the “ venBio Action ”), alleging that Company’s Board breached their fiduciary duties when the Board (i) rescheduled the Company’s 2016 Annual Meeting of Stockholders (the “ 2016 Annual Meeting ”) from December 14, 2016 to February 16, 2017, and then again to March 3, 2017, and (ii) agreed to the proposed Licensing Transaction with Seattle Genetics. venBio also named Seattle Genetics as a defendant and sought an injunction preventing the Company from closing the licensing transaction with Seattle Genetics.  On March 6, 2017, venBio amended its complaint, adding further allegations, including that the Company’s Board breached their fiduciary duties when the Board amended the Company’s Amended and Restated By-laws (the “ By-Laws ”) to call for a plurality voting regime for the election of directors instead of majority voting, and providing for mandatory advancement of attorneys’ fees and costs for the Company’s directors and officers.  The Court of Chancery entered a temporary restraining order on March 9, 2017, enjoining the closing of the Licensing Transaction.  venBio amended its complaint a second time on April 19, 2017, this time adding as an additional defendant the Company’s financial advisor on the Licensing Transaction, Greenhill & Co., LLC.  On May 3, 2017, venBio and the Company and individual defendants Goldenberg, Sullivan and Markison (collectively, the “ Individual Defendants ”) entered into the Term Sheet, which will be memorialized in a settlement agreement (“Settlement Agreement”), pursuant to which, among other things, venBio and the Company will release the Individual Defendants from all claims.  As to all other claims, the Parties stipulated to stay the venBio Action and submit the remaining claims to non-binding mediation.  Once the Parties execute the Settlement Agreement, it will be submitted to the Court of Chancery for approval.   As to all other claims, including those asserted against the remaining individual defendants (former directors Robert Forrester, Jason Aryeh, Geoff Cox

 

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and Bob Oliver) and Greenhill, the parties will stipulate to stay the action and venBio and the Company will submit the remaining claims to non-binding mediation.

 

Lawsuit Against venBio Select Advisor LLC in the U.S. District Court (Delaware)(the “ District Court ”)

 

On February 17, 2017, the Company commenced an action captioned Immunomedics, Inc. v. venBio Select Advisor LLC , No. 17-176-LPS (D. Del.) (the “ Federal Action ”), seeking for the District Court to invalidate the proxies solicited by venBio in furtherance of its contest for the election of directors of the Company.  The Company named as defendants venBio and its then-nominees, Behzad Aghazadeh, Scott Canute, Peter Barton Hutt, and Khalid Islam.  The Company alleged that venBio had conducted its proxy contest and solicited proxies in violation the federal securities laws and regulations, namely by failing timely file a Schedule 13D form indicating venBio’s intent to effectuate change at the Company, publishing early voting results of the Company’s annual election of directors, publishing improper statements about the then-incumbent Board, forming a “group” of like-minded stockholders without publicly disclosing the group, and soliciting proxies without disclosing the solicitations to the SEC.  On February 21, 2017, the Company sought an injunction preventing, among other things, the venBio nominees from benefiting from allegedly illegal shadow proxy contest, including, but not limited to, by asserting any claimed right to take office as a member of the Board until venBio made corrective disclosures and the stockholders were permitted time to consider them.  On March 2, 2017, the District Court denied the Company the requested relief.  On April 6, 2017, the District Court entered a stipulation and order pursuant to which the Company’s claims were voluntarily dismissed without prejudice.  On April 17, 2017, Dr. Goldenberg, the Company’s Chief Scientific Officer and Chief Patent Officer and director, notified the District Court that he may maintain the claims initially brought by the Company. On May 3, 2017, Goldenberg and venBio entered into the Term Sheet pending the Settlement Agreement, pursuant to which, among other things, the Parties have agreed to submit to the District Court a stipulation and proposed order dismissing all claims in the Federal Action with prejudice, including those against the individual defendants (the then-venBio nominees).  The Settlement Agreement will also include a mutual release of claims.

 

Lawsuit Challenging the Results of the 2016 Election of Directors

 

On March 3, 2017, six of the seven then-incumbent members of the Company’s Board commenced an action captioned Goldenberg, et al. vs Aghazadeh, et al. , C.A. No. 2017-0163-VCL (Del. Ch.) (the “ 225 Action ”), challenging the results of the election of directors at the 2016 Annual Meeting that took place on March 3, 2017, in which all four of venBio’s nominees won seats on the Company’s Board.  The director-plaintiffs named as defendants venBio and its then-nominees, Behzad Aghazadeh, Scott Canute, Peter Barton Hutt, and Khalid Islam.  The incumbent directors alleged the same underlying facts as the Company alleged in its lawsuit against venBio in federal court.  On March 13, 2017, the Court of Chancery entered an order (the “ Status Quo Order ”) seating all four venBio nominees (with the three incumbent directors who also won election (based on the plurality vote standard), the “ Status Quo Board ”) and limiting the Company’s Board to actions within the “ordinary course of business,” unless either waived by the parties on a case-by-case basis or ordered by the Court of Chancery.  On March 24, 2017, the defendants, venBio and its four nominees, moved to dismiss the action.  The plaintiffs in the action have opposed this motion to dismiss, which remains pending.  On April 7, 2017, three of the six plaintiffs voluntarily withdrew their claims, leaving Goldenberg, Sullivan and Markison as plaintiffs.  On April 20, 2017, the parties agreed to permit the Status Quo Board to explore a potential financing plan for the Company and negotiate a termination of the Licensing Transaction. On May 3, 2017, the Parties entered into the Term Sheet, pursuant to which, among other things, the Parties agreed to submit to the Court of Chancery a stipulation and proposed order lifting the Status Quo Order .  On May 4, 2017, the Parties submitted that stipulation, which confirmed that the Status Quo Board is the lawful Board of the Company.  Once the Settlement Agreement is executed, the Parties will submit to the Court of Chancery

 

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another stipulation and proposed order dismissing the 225 Action with prejudice, including those against the individual defendants (the then-venBio nominees).  The Settlement Agreement will also include a mutual release of all claims.

 

Regulatory Update

 

The recently-seated Immunomedics Board of Directors has conducted a review of the strategy of the Company, including a review of the projected timeline for submission of a Biologics License Applications (“ BLA ”) submission for IMMU-132.  These efforts to date have resulted in an updated timeline for the execution of delivering IMMU-132 to market, as well as the assessment of various deal structures and partnerships towards advancing and maximizing the Company’s full pipeline for metastatic triple negative breast cancer (“ mTNBC ”) and beyond.  The Company is targeting a BLA for IMMU-132 for approval in mTNBC cancer between late fourth quarter 2017 and first quarter 2018, subject to FDA input on the acceptance of the Company’s chemistry, manufacturing and controls filing plan.

 

Certain Financial Data

 

As of March 31, 2017, the Company had approximately $46 million in cash, cash equivalents and marketable securities.

 

Item 9.01.                                   Financial Statements and Exhibits.

 

The Exhibits to this Current Report on Form 8-K are listed in the Exhibit Index attached hereto.

 

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SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

Dated: May 5, 2017

IMMUNOMEDICS, INC.

 

By:

/s/ Michael R. Garone

 

Name:

Michael R. Garone

 

Title:

Vice President, Finance and

 

 

Chief Financial Officer

 

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EXHIBIT INDEX

 

Exhibit
No.

 

Description

 

 

 

3.1

 

Form of Certificate of Designation of Series A-1 Convertible Preferred Stock.

 

 

 

99.1

 

Investor Presentation, dated May 2017.

 

 

 

99.2

 

Press Release of Immunomedics, Inc., dated May 5, 2017.

 

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Exhibit 3.1

 

CERTIFICATE OF DESIGNATION
OF
SERIES A-1 CONVERTIBLE PREFERRED STOCK
(PAR VALUE $0.01 PER SHARE)
OF
IMMUNOMEDICS, INC.

 


 

Pursuant to Section 151 of the General Corporation Law of the State of Delaware

 


 

It is hereby certified that:

 

1.                                       The name of the corporation is Immunomedics, Inc., a Delaware corporation (the “ Corporation ”).

 

2.                                       The Amended and Restated Certificate of Incorporation of the Corporation authorizes the issuance of ten million (10,000,000) shares of preferred stock with a par value of $0.01 per share each and expressly vests in the board of directors (the “ Board ”) of the Corporation the authority provided therein to issue any or all of said shares remaining undesignated in one or more series by resolution or resolutions.

 

3.                                       The Board, pursuant to the authority expressly vested in it as aforesaid, has adopted the following resolutions, at a meeting of the Board held on May 4, 2017.

 



 

RESOLUTIONS OF THE BOARD OF DIRECTORS OF IMMUNOMEDICS, INC.

 


 

WHEREAS , in the judgment of the board of directors (the “ Board ”) of Immunomedics, Inc., a Delaware corporation (the “ Corporation ”), it is advisable and in the best interests of the Corporation to establish a series of preferred stock designated as “Series A-1 Convertible Preferred Stock,” the number of shares of which shall be 1,000,000.

 

NOW THEREFORE, BE IT RESOLVED , that pursuant to Article IV of the Corporation’s Amended and Restated Certificate of Incorporation, the Board hereby establishes a series of preferred stock of the Corporation designated as “Series A-1 Convertible Preferred Stock” (the “ Series A-1 Preferred ”) and the number of shares constituting such series shall be 1,000,000 with the following voting powers, designations, preferences, and relative, participating, optional, or other special rights, and qualifications, limitations or restrictions:

 

1.                                       Voting Rights .

 

(a)                                  Except as otherwise required by law or expressly provided herein, each share of Series A-1 Preferred shall entitle the holder thereof to vote on each matter submitted to a vote of the stockholders of the Corporation and to have the number of votes equal to the number (rounded down to the nearest whole share) of shares of common stock of the Corporation, par value $0.01 per share (the “ Common Stock ”), into which such share of Series A-1 Preferred is then convertible (without regard to whether the Corporation has sufficient authorized but otherwise unissued or unreserved shares of Common Stock to permit such conversion) pursuant to the provisions hereof at the record date for the determination of stockholders entitled to vote on such matter or, if no such record date is established, at the date such vote is taken or any written consent of stockholders becomes effective.  Except as otherwise required by law or expressly provided below or in the Amended and Restated Certificate of Incorporation of the Corporation (the “Certificate of Incorporation”), the holders of shares of Common Stock and Series A-1 Preferred shall vote together and not as separate classes on any matter presented to the stockholders of the Corporation.

 

(b)                                  For so long as any shares of Series A-1 Preferred remain outstanding, unless a greater percentage shall be required by law, the affirmative vote or consent of the holders representing a majority of the outstanding shares of Series A-1 Preferred, in person or by proxy, at an annual meeting of the stockholders of the Corporation or at a special meeting called for such purpose, or by written consent in lieu of such meeting, shall be required to alter, repeal or amend, whether by merger, consolidation, combination, reclassification or otherwise, any provisions of the Amended and Restated Certificate of Incorporation of the Corporation, this Certificate of Designation establishing the Series A-1 Preferred (this “ Certificate ”), or the Second Amended and Restated By-Laws of the Corporation, as

 

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amended, if the alteration, repeal or amendment would (i) amend, alter or affect this Certificate or any right or preference of the Series A-1 Preferred or (ii) disproportionately and adversely affect the holders of Series A-1 Preferred as compared to the holders of Common Stock generally.

 

2.                                       Liquidation Rights .  If the Corporation shall be voluntarily or involuntarily liquidated, dissolved or wound up, including (x) the sale of all or substantially all of the assets of the Corporation or (y) the merger or consolidation in which the Corporation is a constituent party or a subsidiary of the Corporation is a constituent party and the Corporation issues shares of its capital stock pursuant to such merger or consolidation, except any such merger or consolidation involving the Corporation or a subsidiary in which the shares of capital stock of the Corporation outstanding immediately prior to such merger or consolidation continue to represent, or are converted into or exchanged for shares of capital stock that represent, immediately following such merger or consolidation, at least a majority, by voting power, of the capital stock of (i) the surviving or resulting corporation; or (ii) if the surviving or resulting corporation is a wholly owned subsidiary of another corporation immediately following such merger or consolidation, the parent corporation of such surviving or resulting corporation, then the net assets of the Corporation available for distribution shall be distributed pro rata to the holders of Common Stock and Series A-1 Preferred (being treated as if converted into Common Stock without regard to whether the Corporation has sufficient authorized but otherwise unissued or unreserved shares of Common Stock to permit such conversion) in proportion to the number of shares of Common Stock held or deemed to be held by all holders.

 

3.                                       Conversion; Redemption; Additional Dividend .

 

(a)                                  Terms of Conversion .

 

(i)                                      Automatic Conversion .  As used herein, “ Preferred Conversion Event ” means the approval by the Corporation’s stockholders, and subsequent filing by the Corporation with the Secretary of State of the State of Delaware, of an amendment to the Corporation’s Certificate of Incorporation to increase the number of the Corporation’s authorized shares of Common Stock by an aggregate number of shares of Common Stock in a sufficient amount to enable conversion of all outstanding shares of Series A-1 Preferred into shares of Common Stock at the then effective Conversion Price (the “ Charter Amendment ”) and the effectiveness of the Charter Amendment (collectively, the “ Charter Approval ”); provided, however, notwithstanding the foregoing, in the event that the Corporation has not received the upfront payment (the “ Upfront Payment ”) contemplated by Section 8.1 of the Development and License Agreement, dated February 10, 2017, by and between the Corporation and Seattle Genetics, Inc. (the “ License Agreement ”) and such License Agreement has not yet

 

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been terminated, then, subject to the optional conversion right provided to holders of Series A-1 Preferred set forth in Section 3(a)(ii) below, the effective date of such Preferred Conversion Event shall be extended until the date that such License Agreement is terminated, or if the Corporation has received the Upfront Payment, then no such Preferred Conversion Event shall occur and such shares of Series A-1 Preferred shall be redeemed in accordance with Section 3(c) hereof.  Upon the occurrence of the Preferred Conversion Event and subject to prior payment in cash of any accrued and unpaid Additional Dividend, each share of Series A-1 Preferred shall be automatically converted, without cost, on the terms of this Section 3, into such number of fully paid and nonassessable shares of Common Stock as is equal to the quotient of (A) the Original Issue Price for the Series A-1 Preferred divided by (B) the Conversion Price for the Series A-1 Preferred in effect at the time of conversion.  The Original Issue Price per each share of Series A-1 Preferred shall equal $125.00 (the “ Original Issue Price ”), subject to appropriate adjustment in the event of any stock dividend, stock split, combination or other similar recapitalization with respect to the Series A-1 Preferred.  The “Conversion Price” for the Series A-1 Preferred means $5.41, which initial Conversion Price, and the rate at which shares of Series A-1 Preferred may be converted into shares of Common Stock, is subject to adjustment as provided in this Certificate of Designation.

 

(ii)                                   Optional Conversion .  So long as Charter Approval has occurred, and notwithstanding whether the License Agreement has been terminated or the Corporation has received the Upfront Payment, each share of Series A-1 Preferred shall be convertible at the option of the holder thereof without payment of additional consideration but subject to payment of any accrued and unpaid Additional Dividend, at any time and from time to time on or after January 1, 2018, into the number of fully paid and nonassessable shares of Common Stock as is determined by dividing (A) the Original Issue Price for the Series A-1 Preferred by (B) the Conversion Price in effect at the time of conversion.

 

(b)                                  Failure to Increase Authorized Common Stock .  In the event that, as of August 31, 2017, the Charter Approval has not occurred, during the period beginning on such date until such date as the Charter Approval occurs:

 

(i)                                      a cash dividend (“ Additional Dividend ”) shall accrue on each share of Series A-1 Preferred at a rate per annum equal to 1.00% of the Original Issue Price, with the rate of accrual to increase by an additional 1.00% for each month following August 31, 2017 during which the Preferred Conversion Event has not occurred; provided, however, that at no time shall the Additional Dividend

 

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exceed 8.00% per annum.  Any Additional Dividend payable pursuant to the terms hereof shall apply on a pro rated basis for any portion of a month in which a share of Series A-1 Preferred remains outstanding.  All pro rated calculations made pursuant to this paragraph shall be based upon the actual number of days in such pro rated month. The Additional Dividend shall be payable in cash by the Corporation quarterly in arrears on March 31, June 30, September 30 and December 31 of each year to the holders of record of such shares;

 

(ii)                                   with respect to the Additional Dividend payments set forth in Section 3(b)(i):

 

(A)                                the holders of record entitled to each such payment shall be determined on the 15 th  day of the month during which such payment occurs; and

 

(B)                                in the event the Charter Approval occurs on a day on which there is any accrued and unpaid Additional Dividend, all such accrued and unpaid Additional Dividend shall be payable immediately prior to the conversion of the Series A-1 Preferred as set forth in Section 3(a).

 

(c)                                   Redemption .

 

(i)                                      On or prior to the tenth (10th) business day following the receipt by the Corporation of the Upfront Payment, the Corporation shall redeem (the “ Redemption ”) from each holder of shares of Series A-1 Preferred, in cash, all of such holder’s outstanding shares of Series A-1 Preferred at a redemption price per share equal to the Original Issue Price plus any accrued and unpaid dividends, including any Additional Dividend, plus the Redemption Premium (as defined in Section 3(c)(ii)) (the “ Redemption Price ”).  The Corporation shall send written notice of the Redemption (the “ Redemption Notice ”) to each holder of record of Series A-1 Preferred not less than ten (10) days prior to the date of such redemption (the “ Redemption Date ”), which Redemption must occur and be effective no later than ten (10) business days following the Corporation’s receipt of the Upfront Payment.  On or before the Redemption Date, and subject to the optional conversion right provided to holders of Series A-1 Preferred pursuant to Section 3(a)(ii) above, each holder of shares of Series A-1 Preferred to be redeemed on the Redemption Date shall, if a holder of shares in certificated form, surrender the certificate or certificates representing such shares (or, if such registered holder alleges that such certificate has been lost, stolen or destroyed, a lost certificate affidavit and agreement reasonably acceptable to the

 

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Corporation to indemnify the Corporation against any claim that may be made against the Corporation on account of the alleged loss, theft or destruction of such certificate) to the Corporation, in the manner and at the place designated in the Redemption Notice, and thereupon the Redemption Price for such shares shall be payable to the order of the person whose name appears on such certificate or certificates as the owner thereof.  If the Redemption Notice shall have been duly given, and if on the Redemption Date the Redemption Price payable upon redemption of the shares of Series A-1 Preferred to be redeemed on such Redemption Date is paid or tendered for payment or deposited with an independent payment agent so as to be available therefor in a timely manner, then notwithstanding that any certificates evidencing any of the shares of Series A-1 Preferred so called for redemption shall not have been surrendered, dividends with respect to such shares of Series A-1 Preferred shall cease to accrue after such Redemption Date and all rights with respect to such shares shall forthwith after the Redemption Date terminate, except only the right of the holders to receive the Redemption Price without interest upon surrender of any such certificate or certificates therefor.  Notwithstanding anything set forth to the contrary herein, Redemption shall not occur at any time following (x)  the termination of the License Agreement and this Section 3(c) shall be null and void immediately upon such termination, or (y) with respect to any shares of Series A -1 Preferred as to which the holder has elected to convert such shares pursuant to Section 3(a)(ii) above, the date of such election.

 

(ii)                                   From and after the date of the issuance of any shares of Series A-1 Preferred, dividends at the rate per annum equal to 5.00% of the Original Issue Price shall accrue on such shares of Series A-1 Preferred (subject to appropriate adjustment in the event of any stock dividend, stock split, combination or other similar recapitalization with respect to the Series A-1 Preferred) (the “ Redemption Premium ”).  Notwithstanding any other provision herein, the Redemption Premium, which shall be payable in cash, shall only be payable by the Corporation to the holders of record of such shares upon the Redemption in accordance with Section 3(c)(i) and shall not be payable at any time other than upon the Redemption.  The Redemption Premium shall accrue from day to day, whether or not declared, and shall be cumulative.  The Corporation shall not declare, pay or set aside any dividends on shares of any other class or series of capital stock of the Corporation without the requisite consent of the holders of a majority of the Series A-1 Preferred then outstanding.

 

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(d)                                  Mechanics of Conversion .

 

(i)                                      With respect to Section 3(a)(i), the conversion of shares of Series A-1 Preferred shall take place upon the date of the occurrence of the Preferred Conversion Event and the payment of any accrued and unpaid Additional Dividend, whether or not the certificates representing such shares of Series A-1 Preferred shall have been surrendered or new certificates representing the shares of Common Stock into which such shares have been converted shall have been issued.  With respect to Section 3(a)(i), following the Preferred Conversion Event, the holders of shares so converted shall surrender the certificate or certificates therefor at the office of the Corporation or any transfer agent for the Series A-1 Preferred.  Upon such surrender, the Corporation shall issue and deliver to each holder, or to the nominee or nominees of such holder, a certificate or certificates for the number of shares of Common Stock to which such holder is entitled.  Any dividends or distributions, including any Additional Dividend, unpaid but accrued at the time of conversion with respect to a share of Series A-1 Preferred so converted shall be declared and payable as of the conversion date, ratably to the holders of the Common Stock issued upon such conversion.

 

(ii)                                   With respect to Section 3(a)(ii), in order for a holder of shares of Series A-1 Preferred to convert shares of Series A-1 Preferred into shares of Common Stock, such holder shall deliver a written notice to the Corporation that such holder elects to convert all or any number of the shares of the Series A-1 Preferred held by such holder (a “Notice of Conversion”).  Such notice shall state such holder’s name or the names of the nominees in which such holder wishes the certificate or certificates for shares of Common Stock to be issued.  Such shares of Series A-1 Preferred shall be deemed to have been converted and the person or persons entitled to receive the shares of Common Stock issuable upon such conversion shall be treated for all purposes as the record holder or holders of such shares of Common Stock as of the date such Notice of Conversion shall have been received by the Corporation, whether or not the certificates representing such shares of Series A-1 Preferred shall have been surrendered or new certificates representing the shares of Common Stock into which such shares have been converted shall have been issued.  With respect to Section 3(a)(ii), following the Notice of Conversion, the holders of shares so converted shall surrender the certificate or certificates for such shares of Series A-1 Preferred at the office of the Corporation or any transfer agent for the shares of Series A-1 Preferred The Corporation will, as soon as practicable after the surrender of such certificates, issue and deliver at such office to such holder of shares of Series A-1 Preferred, or to his or its nominees, a certificate or certificates for the number of shares of Common Stock to which such holder shall

 

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be entitled, together with cash in lieu of any fraction of a share.  Any dividends or distributions, including any Additional Dividend, unpaid but accrued at the time of conversion with respect to a share of Series A-1 Preferred so converted shall be payable, when declared, ratably to the holders of the Common Stock issued upon such conversion.  In the event less than all of the shares of Series A-1 Preferred represented by a certificate are converted, a new certificate, instrument, or book entry representing the unconverted shares of Series A-1 Preferred shall promptly be issued to such holder.  Notwithstanding anything to the contrary contained in this Certificate, any holder of Series A-1 Preferred shares may deliver one or more subsequent Notices of Conversion after a Notice of Conversion that requires the holder to return the original certificate for Series A-1 Preferred to the Corporation despite the fact that the Corporation may not have physically re-issued a replacement certificate for the unconverted shares of Series A-1 Preferred.

 

(e)                                   Adjustment of Conversion Price .

 

(i)                                      Subdivision or Combination of Shares .  If the Corporation at any time subdivides or combines the outstanding Common Stock, the Conversion Price shall be decreased, in the case of a subdivision, or increased, in the case of a combination, in the same proportions as the Common Stock is subdivided or combined, effective automatically as of the date of the Corporation shall take a record of the holders of its Common Stock for the purpose of the subdivision or combination (or if no such record is taken, as of the effectiveness of the subdivision or combination).

 

(ii)                                   Stock Dividends .  If the Corporation at any time pays a dividend, or makes any other distribution, to holders of Common Stock payable in shares of Common Stock, or fixes a record date for the determination of holders of Common Stock entitled to receive a dividend or other distribution payable in shares of Common Stock, the Conversion Price in effect immediately prior to the close of business on the record date for such dividend or other distribution shall be decreased by multiplying it by a fraction:

 

(A)                                the numerator of which shall be the total number of shares of Common Stock outstanding immediately prior to the close of business on the record date for such dividend or distribution, and

 

(B)                                the denominator of which shall be the total number of shares of Common Stock outstanding immediately after such dividend or distribution,

 

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effective automatically as of the date the Corporation shall take a record of the holders of its Common Stock for the purpose of receiving such dividend or distribution (or if no such record is taken, as of the effectiveness of such dividend or distribution).

 

(iii)                                Reclassification, Consolidation or Merger .  If at any time, as a result of a Fundamental Transaction, the Common Stock issuable upon the conversion of Series A-1 Preferred shall be changed into or exchanged for the same or a different number of shares of any class or classes of stock of the Corporation or any other corporation, or other securities convertible into such shares, then , as a part of such reorganization, reclassification, merger or consolidation, appropriate adjustments shall be made in the terms of Series A-1 Preferred (or of any securities into which Series A-1 Preferred is changed or for which Series A-1 Preferred is exchanged), so that:

 

(y)                                  the holders of Series A-1 Preferred or of such substitute securities shall thereafter be entitled to receive, upon conversion of Series A-1 Preferred or of such substitute securities, the kind and amount of shares of stock, other securities, money and property which such holders would have received at the time of such capital reorganization, reclassification, merger, or consolidation, if such holders had converted their Series A-1 Preferred immediately prior to such capital reorganization, reclassification, merger, or consolidation, and

 

(z)                                   Series A-1 Preferred, or such substitute securities shall thereafter be adjusted on terms as nearly equivalent as may be practicable to the adjustments theretofore provided in this Section 3.

 

The provisions of this Section 3(e)(iii) shall similarly apply to successive capital reorganizations, reclassifications, mergers, and consolidations.

 

“Fundamental Transaction” means that the Corporation shall, directly or indirectly, in one or more related transactions, (i) consolidate or merge with or into (whether or not the Corporation is the surviving corporation) another Person or Persons, if the holders of the Voting Stock (not including any shares of Voting Stock held by the Person or Persons making or party to, or associated or affiliated with the Persons making or party to, such consolidation or merger) immediately prior to such consolidation or merger shall hold or have the right to direct the voting of less than 50% of the Voting Stock or such voting securities of such

 

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other surviving Person immediately following such transaction, or (ii) sell, assign, transfer, convey or otherwise dispose of (including by exclusive license) all or substantially all of the properties or assets of the Corporation to another Person, or (iii) allow another Person to make a purchase, tender or exchange offer that is accepted by the holders of more than the 50% of the outstanding shares of Voting Stock (not including any shares of Voting Stock held by the Person or Persons making or party to, or associated or affiliated with the Persons making or party to, such purchase, tender or exchange offer), or (iv) consummate a stock purchase agreement or other business combination (including, without limitation, a reorganization, recapitalization, spin-off or scheme of arrangement) with another Person whereby such other Person acquires more than the 50% of the outstanding shares of Voting Stock (not including any shares of Voting Stock held by the other Person or other Persons making or party to, or associated or affiliated with the other Persons making or party to, such stock purchase agreement or other business combination), (v) reorganize, recapitalize or reclassify its Common Stock or (vi) any “person” or “group” (as these terms are used for purposes of Sections 13(d) and 14(d) of the Securities Exchange Act of 1934, as amended) is or shall become the “beneficial owner” (as defined in Rule 13d-3 under the Securities Exchange Act of 1934, as amended), directly or indirectly, of 50% of the aggregate ordinary voting power represented by issued and outstanding Common Stock.

 

“Voting Stock” of a Person means capital stock of such Person of the class or classes pursuant to which the holders thereof have the general voting power to elect, or the general power to appoint, at least a majority of the board of directors, managers or trustees of such Person (irrespective of whether or not at the time capital stock of any other class or classes shall have or might have voting power by reason of the happening of any contingency).

 

Any successor entity in a Fundamental Transaction will assume all of the Corporation’s obligations under this Certificate of Designation.

 

(iv)                               Other Action Affecting Common .  If at any time the Corporation takes any action affecting its Common Stock, other than an action described in any of Sections 3(e)(i) through 3(e)(iii) or, which, in the opinion of the Board, would have an adverse effect upon the Conversion Price or the kind of securities issuable upon the conversion of Series A-1 Preferred, the Conversion Price for Series A-1 Preferred shall be adjusted in such manner and at such time as the Board may in good faith determine to be equitable in the circumstances.

 

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(f)                                    Fractional Shares .  No fractional shares of Common Stock shall be issued upon conversion of Series A-1 Preferred.  If a single holder shall surrender more than one share of Series A-1 Preferred for conversion at the same time, the number of full shares of Common Stock issuable by the Corporation upon conversion thereof shall be computed on the basis of the aggregate number of shares of Series A-1 Preferred so surrendered.  In lieu of any fractional shares to which a holder would otherwise be entitled on conversion, such holder will be entitled to an amount in cash equal to the product of such fraction multiplied by the fair market value of one share of the Common Stock on the date of conversion, as determined in good faith by the Board.

 

(g)                                   Full Consideration .  All shares of Common Stock which shall be issued upon the conversion of any shares of Series A-1 Preferred will, upon conversion, be fully paid and non-assessable.

 

(h)                                  Notice of Adjustments .  Whenever the Conversion Price or the kind of securities issuable upon the conversion of Series A-1 Preferred shall be adjusted pursuant to Section 3, the Corporation shall prepare a certificate signed by its President or a Vice President and by its Chief Financial Officer, Secretary or Assistant Secretary, setting forth, in reasonable detail, the event requiring the adjustment, the amount of the adjustment, the method by which such adjustment was calculated (including a description of the basis on which the Board made any determination hereunder), and the Conversion Price and the kind of securities issuable upon the conversion of Series A-1 Preferred after giving effect to such adjustment, and shall cause copies of such certificate to be mailed (by first class mail postage prepaid) to each holder of Series A-1 Preferred, promptly after each adjustment.

 

4.                                       Distributions of Assets .  If the Corporation shall declare or make any dividend or other distributions of its assets (or rights to acquire its assets) to any or all holders of shares of Common Stock, by way of return of capital or otherwise (including without limitation, any distribution of cash, stock or other securities, property, options, evidence of indebtedness or any other by way of a dividend, spin off, reclassification, corporate rearrangement, scheme of arrangement or other similar transaction) (the “ Distributions ”), then each holder of Series A-1 Preferred will be entitled to such Distributions as if such holder had held the number of shares of Common Stock acquirable upon complete conversion of the Preferred Shares (without taking into account any limitations or restrictions on the convertibility of the Series A-1 Preferred) immediately prior to the date on which a record is taken for such Distribution or, if no such record is taken, the date as of which the record holders of Common Stock are to be determined for such Distributions.

 

5.                                       Purchase Rights . If at any time the Corporation grants, issues or sells any Options, Convertible Securities or rights to purchase stock, warrants, securities or other property pro rata to all or substantially all of the record holders of any class

 

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of Common Stock (the “ Purchase Rights ”), then each holder of Series A-1 Preferred will be entitled to acquire, upon the terms applicable to such Purchase Rights, the aggregate Purchase Rights which such holder could have acquired if such holder had held the number of shares of Common Stock acquirable upon complete conversion of all the Series A-1 Preferred (without taking into account any limitations or restrictions on the convertibility of the Series A-1 Preferred) held by such holder immediately prior to the date on which a record is taken for the grant, issuance or sale of such Purchase Rights, or, if no such record is taken, the date as of which the record holders of shares of Common Stock are to be determined for the grant, issue or sale of such Purchase Rights.

 

( Signature Page Follows )

 

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IN WITNESS WHEREOF , Immunomedics, Inc. has caused this Certificate to be duly executed in its name and on its behalf by its Vice President, Finance and Chief Financial Officer this 5th day of May, 2017.

 

By:

/s/ Michael R. Garone

 

Name:

Michael R. Garone

 

Title:

Vice President, Finance and Chief Financial Officer

 

 


Exhibit 99.1

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This presentation, in addition to historical information, may contain certain forward-looking statements made pursuant to the Private Securities Litigation Reform Act of 1995. Such statements, including statements regarding clinical trials (including the funding therefor, anticipated patient enrollment, trial outcomes, timing or associated costs), regulatory applications and related timelines, out-licensing arrangements, forecasts of future operating results, potential collaborations, and capital raising activities, involve significant risks and uncertainties and actual results could differ materially from those expressed or implied herein. Factors that could cause such differences include, but are not limited to, the Company’s dependence on business collaborations or availability of required financing from capital markets, or other sources on acceptable terms, if at all, in order to further develop our products and finance our operations, new product development (including clinical trials outcome and regulatory requirements/actions), the risk that we or any of our collaborators may be unable to secure regulatory approval of and market our drug candidates, risks associated with the outcome of pending litigation (including applicable court approval of pending settlements) and competitive risks to marketed products, and the Company’s ability to repay its outstanding indebtedness, if and when required, as well as the risks discussed in the Company’s filings with the Securities and Exchange Commission. The Company is not under any obligation, and the Company expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise. Forward-Looking Statements 2

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Business Update and Situation Overview 3

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Offering Summary 4 Confidential Issuer Immunomedics, Inc. (NASDAQ: IMMU) (the “Company”) Security Convertible preferred shares Amount ~$120 million Offering Structure 4(a)(2) private placement Effective Purchase Price for Common Stock underlying preferred shares Last bid price or negotiated premium to market price of common stock Conversion Converts into common equity at the later of: (i) termination of the licensing transaction or (ii) shareholder approval / authorization of additional shares Optional Conversion Should shareholder approval occur and the license agreement not have a resolution by January 1, 2018, an optional conversion right will be provided to shareholders. Callable If Seattle Genetics licensing transaction proceeds, the Company shall call the security Dividends The security shall bear dividends at a rate of 5% per annum (only applicable in the event the Seattle Genetics transaction is consummated and the Company calls the security) Registration Rights Company to file a registration statement as soon as practicable, and no later than 30 days from shareholder approval / authorization of additional shares Company to use commercially reasonable efforts to have registration statement declared effective as soon as practicable after filing, and not later than 90 days from closing, subject to a 30-day extension if reviewed by the SEC

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Start confirmatory Phase 3 clinical trial in mTNBC (Q3 2017) Execute CRO Agreement Site selection / trial initiation / patient enrollment (US & EU) Continue CMC preparations for commercial launch Begin transfer of manufacturing to large-scale CMO Pre-approval inspection activities continue Phase 2 and Phase 3 clinical trial materials manufactured Commercial drug manufacturing continues Submit BLA for Accelerated Approval in mTNBC Late 2017 / early 2018 (pending FDA input on process validation) Explore potential strategic partnerships to maximize the value of the pipeline, including regional partnerships for IMMU-132 Key Business Objectives for 2017 5 Confidential

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Key Updates Termination of Development and License Agreement with Seattle Genetics The mutually agreed upon termination of the licensing agreement between Immunomedics and Seattle Genetics is subject to court approval Immunomedics will retain all rights to IMMU-132 No payments or expense reimbursements will be made by either party Management Update Cynthia Sullivan has agreed to resign from all director, officer and other positions of the Company and any of its affiliates, upon execution of the contemplated Settlement Agreement, effective as of the date of the Settlement Agreement, which is to be entered into and is subject to court approval. Michael Garone was appointed interim CEO, effective upon the execution and effectiveness of the Settlement Agreement. The Board plans to retain an executive search firm to identify a permanent CEO for the Company Board to also evaluate additional senior management appointments Dr. David Goldenberg will remain a director of the Company, but has agreed to resign from all officer positions with the Company, including as chief scientific officer and chief patent officer, effective upon the execution of the settlement agreement. 6 Confidential

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The Status Quo Board Activities Deployed multiple workstreams to independently assess organizational baseline Led by independent consultants reporting directly to the Board Organization Manufacturing Clinical/Regulatory Initial focus on IMMU-132 Accelerated Approval filing preparedness in TNBC Commercial Manufacturing Additional workstreams planned Filing strategy in follow-on indications Pipeline prioritization Management succession (CEO and CSO) 7 Confidential

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Proposed Financing Allows Pivot Towards Execution if IMMU-132 Rights Regained 8 Proposed financing sufficient to reach Accelerated Approval by FDA Confidential Approval Needs Q3 2017 Q4 2017 Q1 2018 Q2 2018 CMC Clinical Regulatory Commercial CRO Phase III TNBC Start - up First patient dosed Phase III TNBC Enrollment Phase II TNBC Completion CSR ( assumed) 11/2017 BLA Master Plan TPP Type B Meeting 6/2017 Lock & Publish Antibody Second Source: CMO Selection to Commercial Scale - Up; sBLA anticipated early 2019 Validation by Spring - to - Summer 2018 Commercial planning, preparedness, staffing Inspection Readiness, PAI Facility Registration Proprietary Name BLA Submission Dec 2017 – Mar 2018 Accelerated Approval Jun 2018 – Sep 2018 Gating factor: CMC validation

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IMMU ADC Technology 9

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Unique approach to ADC therapeutics for cancer Highly cancer-specific antibodies based on 30 years of experience Utilize antibodies with dual activity Moderately potent payloads increased therapeutic index Proprietary linker designed for SN-38 High drug-to-antibody ratio (~7.6:1) Rapid payload release at or inside tumor SN-38 payload Active metabolite more potent than parent compound, irinotecan (a commonly used chemotherapeutic) ADCs’ unique chemistry avoids low solubility and selectively delivers SN-38 to the tumor What Makes IMMU’s ADCs Different? 10 Confidential

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IMMU-132 11

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Overview of IMMU-132 (Sacituzumab Govitecan) 12 Confidential Single-arm Phase 2 study Enrolled 100 assessable TNBC patients with at least 2 prior therapies required for BLA submission Patient follow-up ongoing Third-party “blinded” confirmation of response assessment ongoing Phase 3 confirmatory trial Enrollment planned to commence in mid-2017 Selected a CRO to run trial in U.S. and Europe BLA submission for accelerated approval Expected late 2017 / early 2018 Key Highlights Key Updates on Clinical Development for TNBC Breakthrough Therapy Designation granted in metastatic triple-negative breast cancer (mTNBC) Validated mechanism of action Binds Trop-2 Delivers enhanced SN-38 concentrations at or in the tumor Exploring treatment for multiple solid cancers Pursuing TNBC, UC, NSCLC and SCLC and additional solid cancer indications Strong results in Phase 2 study for TNBC 29% ORR in 85 patients treated Promising durable activity – achieved median PFS / OS of 6.0 / 18.8 months, respectively Acceptable safety profile in heavily pretreated patients Note: TNBC = triple-negative breast cancer, UC = urothelial cancer, NSCLC = non-small-cell lung cancer, SCLC = small-cell lung cancer.

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Cancer Type1 Number of Patients Confirmed % ORR2 Median PFS (months)3 PFS 95% CI Median OS (months)3 OS 95% CI TNBC 85 29% 6.0 5.0 – 7.1 18.8 11.5 – 20.6 UC 36 31% 7.2 6.7 – 11.7 15.5 8.9 – 17.2 NSCLC 47 19% 5.2 2.6 – 7.1 9.5 6.0 – 16.7 SCLC 43 16% 3.7 2.0 – 4.3 7.0 5.5 – 8.3 1 TNBC = triple-negative breast cancer, UC = urothelial cancer, NSCLC = non-small-cell lung cancer, SCLC = small-cell lung cancer. 2 Objective response rate (%ORR) = (complete response + partial response)/number of patients. 3 Based on number of intention-to-treat patients of 89, 41, 54 and 53 for TNBC, UC, NSCLC and SCLC, respectively. Patients with at least one post-treatment response evaluation IMMU-132: Active in a Number of Solid Cancers TNBC, NSCLC and SCLC results presented at Immunomedics Investor R&D Day in January 2017, UC results presented at 2017 ASCO-GU Cancers Symposium. 13 Confidential

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IMMU-132: Best Response from mTNBC Patients (N=85) Confirmed ORR (RECIST 1.1) = 29% Median # prior therapies = 5 (range, 2 – 12) Presented at Immunomedics Investor R&D Day in January 2017. 14 Confidential -100 -80 -60 -40 -20 0 20 40 60 80 B e s t R e s p o n s e B e s t % c h a n g e i n T L f r o m b a s e l i n e Complete response (confirmed) Partial response (confirmed) Partial response (pending) Partial response (unconfirmed) Stable disease Progression 79/85 response assessable pts who completed 1 treatment cycle are represented 3 progressed, but TL measurement unavailable 3 did not have a CT response assessment Overall response assessment descriptor

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Phase 3 Confirmatory Trial Design for IMMU-132: TNBC Designed to Replicate Success Primary endpoint is PFS Two arms: IMMU-132 vs physician’s choice of 1 from 4 chemotherapies 328 patients to be enrolled, 1:1 randomization Attention to Execution Trial will be conducted under a SPA and is expected to take ~3 years Key powering considerations: 99% powering for PFS Phase 3 Design Control Arm 164 patients to receive physician’s choice of 1 from 4 chemotherapies (Eribulin, Capecitabine, Gemcitabine and Vinorelbine) Primary Endpoint: PFS Treatment Arm 164 patients to receive IMMU-132 328 patients with mTNBC failed 2+ prior lines of treatment Randomized 1:1 15 Confidential

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IMMU-132: Best Response from mUC Patients (N=36) Presented at 2017 ASCO-GU Cancers Symposium. Confirmed ORR (RECIST 1.1) = 31% Median # prior therapies = 2 (range, 1 – 5) 16 Confidential -100 -80 -60 -40 -20 0 20 40 B e s t R e s p o n s e B e s t % c h a n g e i n T L f r o m b a s e l i n e P D S D Complete response Partial response Partial response (confirmation pending) Partial response (unconfirmed) Stable disease Progression l « l l « « « « « l 8 mg/kg (all others are 10 mg/kg) prior checkpoint inhibitor therapy « « « « « « « «

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IMMU-132: Best Response from mNSCLC Patients (N=47) Presented at Immunomedics Investor R&D Day in January 2017. Confirmed ORR (RECIST 1.1) = 19% Median # prior therapies = 3 (range, 1 – 7) 17 Confidential -80 -60 -40 -20 0 20 40 B e s t % c h a n g e i n t a r g e t l e s i o n s f r o m b a s e l i n e Partial response (confirmed) (PR) Unconfirmed PR (PRu) (stable disease) Stable disease Progression « Ä « « « « « « « « « « Ä Ä Ä Ä Ä « Squamous cell histology 8 mg/kg starting dose Prior checkpoint inhibitor Tx Ä Ä + + early CT assessment after 2 doses

 


IMMU-132: Best Response from mSCLC Patients (N=43) Confirmed ORR (RECIST 1.1) = 16% Median # prior therapies = 2 (range, 1 – 7) Presented at Immunomedics Investor R&D Day in January 2017. 18 Confidential -100 -80 -60 -40 -20 0 20 40 60 80 B e s t R e s p o n s e B e s t % c h a n g e i n T L f r o m b a s e l i n e l l l l l l l l l l l l l Partial response (confirmed) Partial response (unconfirmed) Stable disease Progression l 8 mg/mg (all others, 10 mg/kg)

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Starting Dose of 10 mg/kg (N=361 Patients) Interim Adverse Events (ranked by Grades 3+) Grade 3+ All Grades Neutropenia 25% 37% Anemia 8% 28% Diarrhea 7% 41% Fatigue 7% 32% Febrile neutropenia 5% 5% Nausea 4% 46% Vomiting 3% 28% Alopecia N/A 25% IMMU-132: Mild, Predictable and Manageable Toxicity Data on file. Camptosar (irinotecan) US Prescribing Information (USPI) “boxed warnings” Early and late forms of diarrhea can occur (Grades 3 & 4: 38%) Severe myelosuppression may occur (Neutropenia: Grades 3 & 4: 31%) 19 Confidential

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IMMU-132 Patent Portfolio 32 issued U.S. and 16 foreign patents covering composition of matter, synthesis and uses of IMMU-132 Company’s main composition of matter patents expire in 2023 in the U.S., and in 2029 in Europe In addition, IMMU-132 has patent coverage through 2033 for uses in various cancers at different dose schedules, and other proprietary features of the antibody-drug conjugate Patent applications are being prosecuted in all major countries, with patents issued in Australia, Canada, China, Europe, Israel, Japan and South Korea IMMU-132 has regulatory exclusivity of 12 years in the US and 10 years in Europe Moreover, the product has been granted Orphan Drug status in the US and EU for certain secondary indications 20 Confidential

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IMMU Pipeline 21

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Research/Preclinical Phase 1 Phase 2 Phase 3 Sacituzumab govitecan/IMMU-132 (anti-Trop-2-SN-38 ADC) Metastatic triple-negative breast cancer FDA granted BTD Epratuzumab (humanized anti-CD22) Labetuzumab govitecan/IMMU-130 (anti-CEACAM5-SN-38 ADC) Metastatic solid cancers (urothelial/lung/endometrial/prostate) Metastatic colorectal cancer Milatuzumab (anti-CD74) for autoimmune diseases IMMU-140 (anti-HLA-DR ADC) Veltuzumab (anti-CD20) for cancer and autoimmune diseases Other product candidates Broad Pipeline of Antibody-Based Therapies Pediatric acute lymphoblastic leukemia* * The International clinical trial on childhood relapsed acute lymphoblastic leukemia (IntReALL) is funded by the European Commission. Preclinical product candidates (E1)-3s (T-cell-redirecting bispecific antibody) IMMU-114 (anti-HLA-DR) for hematologic malignancies 22 Confidential

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Financial Highlights 23

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Financial Highlights Common Shares Authorized 155 million Shares outstanding 109 Shares reserved 461 Total outstanding and reserved 155 million Debt (convertible senior notes due Feb 2020)2 $100 million Cash3 $46 million Average monthly operating cash burn (YTD) $5.5 million 1. Does not include approx. 8.6 million shares issuable upon exercise of outstanding warrants. 2. Notes convertible at $5.11 per share. 3. As of March 31, 2017. 24 Confidential

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May 2017

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[LOGO]

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Exhibit 99.2

 

 

NEWS RELEASE

 

IMMUNOMEDICS DELIVERS BUSINESS UPDATES, ANNOUNCES PRIVATE PLACEMENT OFFERING AND OUTLINES STRATEGIC STEPS TO DRIVE STOCKHOLDER VALUE

 

Immunomedics and Seattle Genetics reach mutual agreement to dissolve previously agreed upon Exclusive Global Licensing Agreement, returning Sacituzumab Govitecan (IMMU-132) to Immunomedics

 

Unwinding of the deal releases both companies from all material obligations subject to Court approval; Seattle Genetics maintains its existing equity stake in the Company; Exercise period of IMMU warrants held by Seattle Genetics shortened substantially

 

Immunomedics announces completion of $125 million private placement of Series A-1 Convertible Preferred Stock to institutional investors; capital will support execution of plan to file for accelerated approval for IMMU-132

 

Immunomedics Board provides update on ongoing strategic review and clinical development timelines; targeting BLA submission for IMMU-132 in TNBC by late 2017 / early 2018

 

Current Immunomedics CFO Michael Garone to be named interim CEO once settlement agreement is finalized — Board in the process of considering candidates for permanent CEO

 

Morris Plains, N.J., May 5, 2017 -— Immunomedics, Inc., (NASDAQ: IMMU) (“Immunomedics” or “the Company”) today delivered several business and leadership updates and outlined a new strategic plan to drive long-term value for stockholders. These updates include the termination of the previously announced Exclusive Global Licensing Agreement with Seattle Genetics (NASDAQ: SGEN), returning full rights of Sacituzumab Govitecan (“IMMU-132”), the Company’s breakthrough therapy candidate to treat metastatic triple-negative breast cancer (mTNBC), to Immunomedics. Immunomedics also announced that it has raised $125 million in gross proceeds in a private placement of its Series A-1 Convertible Preferred Stock with institutional investors, and has taken a series of steps to drive positive organizational and operational changes.

 

Behzad Aghazadeh, Chairman of the Board of Immunomedics, stated: “We are pleased to announce these significant developments and to provide this new level of clarity regarding the progress that has been made at Immunomedics and the future direction of the Company. After conducting a full multi-faceted review of the organizational, operational, and clinical and regulatory capabilities, we are confident that Immunomedics can fully execute on a strategic plan over the next several years to become a recognized leader in the field of antibody-drug conjugates. We now have the financial ability to fully focus on taking the steps to ensure the Company has the right leadership, organizational structure and resources necessary to bring IMMU-132 to market and achieve our long-term objectives. The enthusiastic reception from institutional investors to invest in Immunomedics and IMMU-132 reflects the value the Company is poised to deliver to patients, employees and stockholders.”

 

~ more ~

 



 

Mutual Termination of Exclusive Global Licensing Agreement with Seattle Genetics

 

Under the termination agreement, the Company will retain all rights to IMMU-132. Seattle Genetics will maintain its existing equity investment in Immunomedics granted as part of the licensing agreement.  Further, the expiration date for the warrants has been shortened to the later of December 31, 2017 and the date that is six (6) months following the date on which a sufficient number of shares of the Company’s Common Stock are authorized and reserved for issuance to permit the full exercise of such warrants. In addition, the termination agreement provides that no payments or expense reimbursements shall be made by either party and each party has provided full releases to the other party.  Aspects of the mutually agreed upon termination of the licensing agreement between Immunomedics and Seattle Genetics are subject to court approval.

 

Business Updates

 

The newly elected Immunomedics Board of Directors has conducted a multifaceted review of the Company with initial emphasis on IMMU-132 in mTNBC, which had received Breakthrough Therapy Designation for this indication from the U.S. Food and Drug Administration in February 2016. The work streams have focused on the organizational, operational, and clinical and regulatory capabilities, with each being led by highly credentialed independent consultants with specific relevant expertise. These efforts have resulted in an updated timeline for the execution of delivering IMMU-132 to market, with the Company now targeting the submission of a BLA for IMMU-132 for approval in mTNBC between late fourth quarter 2017 and first quarter 2018, subject to FDA input on the acceptance of the CMC filing plan. Importantly, this review confirmed that the data generated in the ongoing 100-patient phase 2 study of IMMU-132 in 3 rd  line TNBC, which was fully enrolled in December 2016, can provide the basis for accelerated approval, subject to review by the FDA.

 

This review has furthermore led to detailed filing and manufacturing plans. Alongside the immediate focus on preparations for a BLA filing, the company will proceed with the final selection of a CRO to launch the confirmatory phase 3 study with the expectation of first patient enrolled in late Q3 2017, as well as executing on a manufacturing plan to build commercial inventory in preparation for a potential launch in the U.S. in 2018.

 

Over the course of the upcoming months, the scope of the ongoing strategic review will expand with the goal of executing on the following key initiatives:

 

·                   Develop plans for IMMU-132 beyond mTNBC

·                   Explore strategic opportunities for IMMU-132 with regional partners

·                   Execute an orderly management succession plan

 

The Board will provide additional updates to stockholders on these initiatives periodically.

 

Announcement of Private Placement

 

The Company has designated and agreed to sell 1,000,000 shares of Series A-1 Preferred Stock which are initially convertible into an aggregate of 23,105,360 shares of common stock, upon the approval by the Immunomedics stockholders of a charter amendment to increase the number of authorized shares of common stock to enable full conversion of the Series A-1 Preferred Stock.

 



 

The price per share of the Series A-1 Preferred Stock is $125.00, which equates to an underlying price per share of common stock $5.41 (the closing price of Immunomedics common stock at the close of trading on May 4, 2017).  The aggregate number of shares of Common Stock issuable upon conversion of the Preferred Stock is 23,105,360.  Immunomedics expects to use the net proceeds from the $125 million private placement to support the development of IMMU-132, including the goal of filing a BLA for Accelerated Approval from the FDA. The capital will also fund general corporate and operational enhancements. With this new capital and the Company’s current cash on hand, Immunomedics expects to have sufficient operating funds through the third quarter of 2018. As of March 31, 2017, cash and cash equivalents were $46 million. The charter amendment needed to effect the conversion to common stock is subject to a stockholder vote, for which the Company expects to file a proxy statement with the Securities Exchange Commission in the near future.  The authorization of additional shares is subject to a shareholder vote, which the company will seek in the near future.

 

The securities offered by the Company in the private placement have not been registered under the Securities Act of 1933, as amended (the “Securities Act”), or any state securities laws and may not be offered or sold in the United States absent such registration or an applicable exemption from registration requirements. This press release is being issued for informational purposes pursuant to Rule 135c of the Securities Act and shall not constitute an offer to sell or a solicitation of an offer to buy any securities, nor shall there be any sale of securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

 

Leadership Transition Update

 

Immunomedics also announced today that effective upon the execution of the settlement agreement memorializing the terms of the binding settlement term sheet, Cynthia L. Sullivan will be stepping down from all director and officer positions with the Company, including her role as president and chief executive officer. Michael R. Garone, the current chief financial officer of Immunomedics, will then assume the role of interim CEO.

 

In addition, Dr. David M. Goldenberg, founder of the Company, is stepping down from all officer positions with the Company, including as chief scientific officer and chief patent officer, effective upon the execution of the settlement agreement. Dr. Goldenberg will continue to serve as a director on Immunomedics’ Board.

 

“It has been a pleasure to lead Immunomedics to this pivotal stage in its growth,” commented Ms. Sullivan. “I am confident that the board and leadership team will continue the work of bringing IMMU-132 to patients as soon as possible.”

 

“On behalf of the entire Board, we would like to thank Cynthia and David for their contributions to the Company and the incredible scientific potential they have positioned Immunomedics to be able to realize,” added Dr. Aghazadeh. “We look forward to continuing to work with David in his capacity as a director moving forward.”

 

With these transition steps in place, the Board plans on deciding on a permanent CEO and filling out additional leadership positions within the Company.

 



 

Litigation Update

 

In addition to the Company’s resolution of its claims against Seattle Genetics, the Company entered into a binding term sheet with Goldenberg, Sullivan, Markison and venBio, which will be memorialized in a settlement agreement (the “Settlement Agreement”) that will be subject to court approval.  If approved, both the Federal Action(1) as well as the 225 Action(2) will be dismissed. Yesterday, in accordance with the term sheet, the Court of Chancery entered an order lifting the provisions of the Status Quo Order, and confirming that the Status Quo Board is the lawful Board of the Company (provided that if the 225 Action is not dismissed, the Parties shall be restored to their positions in the 225 Action as of immediately prior to the execution of the term sheet). Upon the execution of the Settlement Agreement, the Parties will immediately submit a stipulation and proposed order dismissing the 225 Action with prejudice. The Settlement Agreement will include a mutual release of all claims that were or could have been asserted in the 225 Action.

 

The Federal Action challenging the annual meeting will be dismissed. Upon execution of the Settlement Agreements, the Parties will immediately submit a stipulation and order dismissing the claims in the Federal Action with prejudice. The Settlement Agreement will include a mutual release of all claims that were or could have been asserted in the Federal Action.

 

Regarding the venBio Action(3), individual defendants Goldenberg, Sullivan and Markison will be released from all claims made by venBio.  Once the Parties execute the Settlement Agreement, it will be submitted to the Court of Chancery for approval. As to all other claims, including those asserted against the remaining individual defendants (former directors Robert Forrester, Jason Aryeh, Geoff Cox and Bob Oliver) and Greenhill, the parties will stipulate to stay the action and venBio and the Company will submit the remaining claims to non-binding mediation.

 

“Today’s announcements collectively represent an important milestone in the next phase of Immunomedics, and while there is significant work ahead, the Board looks forward to continuing to drive value for all stakeholders.  The Company has a strong pipeline that we look forward to evaluating and intend to leverage to maximize the value for stockholders.  We will be providing additional updates, including with our quarterly earnings release, as appropriate in the coming weeks and months,” concluded Dr. Aghazadeh.

 

Advisors

 

Cowen and Company, LLC acted as sole placement agent to Immunomedics in connection with the offering and DLA Piper LLP (US) is serving as legal advisor to the Company on the transaction.

 


(1)  “Federal Action” refers to the action captioned Immunomedics, Inc. v. venBio Select Advisor LLC, et al. , C.A. No. 17-176-LPS.

 

(2)  “225 Action” refers to the action captioned David M. Goldenberg et al. v. Behzad Aghazadeh et al. , C.A. No. 2017-0163-JTL (Del. Ch.)

 

(3)  “venBio Action” refers to the action captioned venBio Select Advisor LLC v. David M. Goldenberg et.al , C.A. No. 2017-0108-JTL (Del. Ch.).

 



 

About Immunomedics

 

Immunomedics (the “Company”) is a clinical-stage biopharmaceutical company developing monoclonal antibody-based products for the targeted treatment of cancer, autoimmune disorders and other serious diseases. Immunomedics’ advanced proprietary technologies allow the Company to create humanized antibodies that can be used either alone in unlabeled or “naked” form, or conjugated with radioactive isotopes, chemotherapeutics, cytokines or toxins. Using these technologies, Immunomedics has built a pipeline of eight clinical-stage product candidates. Immunomedics’ portfolio of investigational products includes antibody-drug conjugates (ADCs) that are designed to deliver a specific payload of a chemotherapeutic directly to the tumor while reducing overall toxicities that are usually found with conventional administration of these chemotherapeutic agents. Immunomedics’ most advanced ADCs are sacituzumab govitecan (IMMU-132) and labetuzumab govitecan (IMMU-130), which are in Phase 2 trials for a number of solid tumors and metastatic colorectal cancer, respectively. IMMU-132 has received Breakthrough Therapy Designation from the FDA for the treatment of patients with triple-negative breast cancer who have failed at least two prior therapies for metastatic disease. Immunomedics has a research collaboration with Bayer to study epratuzumab as a thorium-227-labeled antibody. Immunomedics has other ongoing collaborations in oncology with independent cancer study groups. The IntreALL Inter-European study group is conducting a large, randomized Phase 3 trial combining epratuzumab with chemotherapy in children with relapsed acute lymphoblastic leukemia at clinical sites in Australia, Europe, and Israel. Immunomedics also has a number of other product candidates that target solid tumors and hematologic malignancies, as well as other diseases, in various stages of clinical and preclinical development. These include combination therapies involving its antibody-drug conjugates, bispecific antibodies targeting cancers and infectious diseases as T-cell redirecting immunotherapies, as well as bispecific antibodies for next-generation cancer and autoimmune disease therapies, created using its patented DOCK-AND-LOCK® protein conjugation technology. The Company believes that its portfolio of intellectual property, which includes approximately 310 active patents in the United States and more than 400 foreign patents, protects its product candidates and technologies. For additional information on the Company, please visit its website at www.immunomedics.com. The information on its website does not, however, form a part of this press release.

 

Cautionary note regarding forward-looking statements

 

This release, in addition to historical information, may contain forward-looking statements made pursuant to the Private Securities Litigation Reform Act of 1995. Such statements, including statements regarding clinical trials (including the funding therefor, anticipated patient enrollment, trial outcomes, timing or associated costs), regulatory applications and related timelines, out-licensing arrangements, forecasts of future operating results, potential collaborations, and capital raising activities, involve significant risks and uncertainties and actual results could differ materially from those expressed or implied herein. Factors that could cause such differences include, but are not limited to, the Company’s dependence on business collaborations or availability of required financing from capital markets, or other sources on acceptable terms, if at all, in order to further develop our products and finance our operations, new product development (including clinical trials outcome and regulatory requirements/actions), the risk that we or any of our collaborators may be unable to secure regulatory approval of and market our drug candidates, risks associated with the outcome of pending litigation and competitive risks to marketed products, and the Company’s ability to

 



 

repay its outstanding indebtedness, if and when required, as well as the risks discussed in the Company’s filings with the Securities and Exchange Commission. The Company is not under any obligation, and the Company expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise.

 

For More Information:

Dr. Chau Cheng

Senior Director, Investor Relations & Corporate Secretary

(973) 605-8200, extension 123

ccheng@immunomedics.com

 

Media/Investor Contact:

Dan Zacchei / Jaimee Pavia

Sloane & Company

212-486-9500

Dzacchei@sloanepr.com

Jpavia@sloanepr.com