UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 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):   June 28, 2016
 


SIGA TECHNOLOGIES, INC.
(Exact name of registrant as specified in its charter)

Delaware
0-23047
13-3864870
(State or other jurisdiction of incorporation or organization)
(Commission file number)
(I.R.S. employer identification no.)

660 Madison Avenue, Suite 1700
New York, New York
 
10065
(Address of principal executive offices)
 
(Zip code)

Registrant’s telephone number, including area code:  (212) 672-9100
 
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):
 
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
 
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
 
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
 
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
 


Item 1.01 Entry into a Material Definitive Agreement.

On June 28, 2016, SIGA Technologies, Inc. (“SIGA”), a Delaware corporation, entered into a modification (the “Modification”) of its 2011 procurement contract with the Biomedical Advanced Research and Development Authority (“BARDA”) of the United States Department of Health and Human Services (the “Contract”).

The total dollar value of the Contract is unchanged. Pursuant to the Modification, SIGA may receive up to $82 million earlier than anticipated. The changes to the Contract reflected in the Modification include:

·
An increase of $36.20 per course in the payment for the manufacture and delivery of 1.7 million courses of TPOXX™.  The increase in delivery payments will total $61.5 million and was accomplished by reducing the contractual holdback amount that is tied to FDA approval of TPOXX™ from $102.5 million to $41 million.

·
A change in the requirements for a $20.5 million (5% of contract price) milestone in the Contract.  For payment, this milestone now requires SIGA to submit documentation to BARDA indicating that data covering the first 100 subjects enrolled in the phase III pivotal safety study have been submitted to and reviewed by a Data & Safety Monitoring Board (“DSMB”) and that such DSMB recommends continuation of the safety study, as well as submission of the final pivotal rabbit efficacy study report to the United States Food & Drug Administration (the “FDA”).  Previously, this milestone required the successful submission to the FDA of a complete application for TPOXX™ regulatory approval.

The foregoing description is qualified in its entirety by reference to the text of the Modification, which is attached hereto as Exhibit 10.1.

Item 9.01. Financial Statements and Exhibits.
 
(c) Exhibits
 
Exhibit No.
Description
   
 
Amendment of Solicitation/Modification of Contract 0013, dated June 28, 2016, to Agreement, dated May 13, 2011, between the Biomedical Advanced Research and Development Authority of the United States Department of Health and Human Services and SIGA (portions of this exhibit have been omitted and separately filed with the Securities and Exchange Commission with a request for confidential treatment).
 

SIGNATURE
 
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.

 
SIGA TECHNOLOGIES, INC.
     
 
By:
 
  /s/ Daniel J. Luckshire
 
 
Name:
Daniel J. Luckshire
 
Title:
Chief Financial Officer
   
Date:
July 5, 2016
 
 
 


Exhibit 10.1
 
AMENDMENT OF SOLICATION/MODICATION OF CONTRACT
Contract id code
N/A
   Page of pages
1
9
2. Amendment/modification no.
Modification 0013
3. Effective date
See Block 16 C
4. Requisition/purchase req. No
N/A
5. Project no.   ( If applicable )
N/A
6. issued by
HHS/OS/ASPR/AMCG
330 Independence Avenue, SW,
Room G640,
Washington, DC 20201
 
code
N/A
7. Administered by   (If other than item 6)
code
N/A
   
   
   
   
8. NAME AND ADDRESS OF CONTRACTOR (No., street, county, State and ZIP Code)
 
 
9A. Amendment of solicitation no .
SIGA TECHNOLOGIES, INC.
35 E 62 nd Street
New York, NY 10065
 
 
 
 
9B. dated (see item 11)
 
 
10A. Modification of contract/order no .
 
HHSO100201100001C
CODE N/A
FACILITY CODE N/A
 
10B. DATED (SEE ITEM 13 )
05/13/2011
11. THIS ITEM ONLY APPLIES TO AMENDMENTS OF SOLICITATIONS
 
~ The above numbered solicitation is amended as set forth In Item 14. The hour and date specified for receipt of Offers ~ is extended, ~ not extended.
Offers must acknowledge receipt of this amendment prior to the hour and date specified in the solicitation or as amended by one of the following methods: (a) By completing Items 8 and 15, and returning ______________ copies of the amendment; (b) By acknowledging receipt of this amendment on each copy of the offer submitted; or (c) By separate letter or telegram which includes a reference to the solicitation and amendment numbers.   FAILURE OF YOUR ACKNOWLEDGEMENT TO BE RECEIVED AT THE PLACE DESIGNATED FOR THE RECEIPT OF OFFERS PRIOR TO THE HOUR AND DATE SPECIFIED MAY RESULT IN REJECTION OF YOUR OFFER.  If by virtue of this amendment, you desire to change an offer already submitted, such change may be made by telegram or letter, provided each telegram or letter makes reference to the solicitation and this amendment, and is received prior to the opening hour and date specified .
12. ACCOUNTING AND APPROPRIATION DATA (If required)
N/A
13.   THIS ITEM APPLIES ONLY TO MODIFICATIONS OF CONTRACTS/ORDERS, IT MODIFIES THAT CONTRACT/ORDER NO. AS DESCRIBED IN ITEM 14.
A.            THIS CHANGE ORDER IS ISSUED PURSUANT TO:  (Specify authority) THE CHANGES SET FORTH IN ITEM 14 ARE MADE IN THE CONTRACT ORDER NO. IN ITEM 10A.
 
 
B.            THE ABOVE NUMBERED CONTRACT/ORDER IS MODIFIED TO REFLECT THE ADMINISTRATIVE CHANGES (such as changes in paying office, appropriation date, etc.) SET FORTH IN ITEM 14, PURSUANT TO THE AUTHORITY OF FAR 43.103(b).
C.            THIS SUPPLEMENTAL AGREEMENT IS ENTERED INTO PURSUANT TO AUTHORITY OF:
FAR 52.243-2 –Changes – Cost Reimbursement and FAR 1.605-1 – Mutual Agreement of the Parties
 
D.            OTHER (Specify type of modification and authority)
E. IMPORTANT: Contractor [ ] is not, [X] is required to sign this document and return   1  copies to the issuing office.
14. DESCRIPTION OF AMENDMENT/MODIFICATION (Organized by UCF section headings, including solicitation/contract subject matter where feasible)
 
PURPOSE:
This modification is to change the criteria for milestone 0001AB and reduce the CLIN 0002 holdback amount
 
FUNDS ALLOTED PRIOR TO MOD #13
 
$470,314,469.00
FUNDS ALLOTTED WITH MOD #13
 
$                  0.00
TOTAL FUNDS ALLOTED TO DATE
 
$470,314,469.00 (Unchanged)
 
 
 
EXPIRATION DATE:
 
September 24, 2020 (Unchanged)
 
 
 
CONTRACT FUNDED THROUGH
 
September 24, 2020 (Unchanged)
 
Except as provided herein, all terms and conditions of the document referenced in Item 9A or 10A, as heretofore changed, remains unchanged and in full force and effect.
15A. NAME AND TITLE OF SIGNER (Type or print)
16A. NAME AND TITLE OF CONTRACTING OFFICER (Type or print)
 
Linda D. Luczak, Contracting Officer
Dennis E. Hruby
 
   
15B. CONTRACTOR/OFFEROR
15C. DATE SIGNED
16B. UNITED STATES OF AMERICA
16C. DATE SIGNED
       
/s/ Dennis E. Hruby  
28 Jun 2016
BY
/s/ Linda D. Luczak
 
6/28/2016
(Signature of person authorized to sign)
  (Signature of Contracting Officer)  
       
NSN 7540-01-152-8070       OMB No. 0990—0115 STANDARD FORM 30 (rev. 10-83)  
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 2 of 9
  A. The following CLINS 0001 (0001AA, 0001AB, 0001AC, and 0001AD) and 0002 under B.5 Price Schedule is hereby modified as follows:

B. 5 Price Schedule

BASE
         
CLIN#
Cost
Type
Supply or Service
U/I
Qty
Unit Price
Extended Price
0001
FFP
Manufacture and deliver 1,700,000 smallpox antiviral treatment courses (minimum 60 month stability from date of manufacture) to support appropriate regulatory filing submitted by CDC as described in Section C.1)
NOTE: The maximum amount payable for all 1,700,000 FDA approved treatment courses is $409,811,755.00 (inclusive of all advance payments, milestone payments and hold back)
EA
1,700,000
[redacted] *
$368,900,000.00
0001AA
 
Advance Payments
JOB
[redacted] *
[redacted] *
$40,981,175.00
0001AB
 
Milestone Payment 1:
Documentation to BARDA that data covering the first 100 subject enrolled in the phase III pivotal safety study have been submitted to and reviewed by a DSMB, and submission of the final pivotal rabbit efficacy study report to the FDA.
JOB
[redacted] *
[redacted] *
$20,490,587.00
0001AC
 
Milestone Payment 2A: Complete FDP Commercial Validation batches and report
JOB
[redacted] *
[redacted]*
$8,196,235.00
0001AD
 
Milestone Payment 2B:
Approved product labeling strategy
JOB
[redacted]*
[redacted]*
$12,294,352.00
0002
FFP
Payment upon FDA Approval for all treatment courses being provided under this contract (CLIN 0001 and CLIN 0022). This CLIN contains the lump sum amount of holdback from CLIN 0001 of approximately [redacted]*
LS
[redacted] *
[redacted] *
$40,911,755.00

NOTE: The overall total amount of the contract remains unchanged,

B. Based on FDA agreeing upon the treatment dose to allow phase III efficacy trials to proceed and the Contractor’s successful enrollment of [redacted]* of projected study subjects in these trials the total amount of FDA approval hold back is being reduced from [redacted]* to approximately [redacted]*. The language under paragraph B.6.1.2. and B.6.1.2.1 is revised as follows:

B.6.1.2             FDA Approval Hold Bank

B.6.1.2.1            The negotiated dollar amount equivalent to approximately [redacted]* will be withheld from payment under CLIN 0001 until such time as the Contractor achieves FDA approval. This pertains to FDP doses that are delivered to the SNS prior to approval.
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 3 of 9
After achieving FDA approval, the Contractor shall invoice under CLIN 0002 in the lump sum amount of $40,911,755.00 for all treatment courses required under this contract are delivered to the SNS.
 
C. By revising the language under paragraph H.16.2 and table as follows:
 
H. 16.2 Approvals for advance payments and or milestone payments have been agreed upon as follows:

· Advance Payment - [redacted]* of the total negotiated contract amount
· Milestone payment ([redacted]*): Upon documentation provided to BARDA that data covering the first 100 subject enrolled in the phase III pivotal safety study have been submitted to and reviewed by a DSMB, and submission of the final pivotal rabbit efficacy study report to the FDA.
· Milestone payment ([redacted]*): Completion of Final Drug Product (FDP) Commercial Validation batches and report. [redacted]* of the total negotiated contract amount for the completion of FDP Commercial Validation batches and report. ([redacted]*)
· Milestone payment ([redacted]*): Approved Product Labeling Strategy - [redacted]*  of the total negotiated contract amount for the approval of the product labeling strategy ([redacted]*)

1.
[redacted]* Project BioShield Advance Payment - $40,981,175.00

The HHS Secretary has determined that an advance payment is necessary to ensure success of this project, and has authorized a [redacted]* advance payment in accordance with 42 USC 247d-6b(c)(7)(C)(ii)(I) PAYMENT CONDITIONED ON DELIVERY. This [redacted]* advance payment equates to 40,981,175.00 and is required to be repaid if there is a failure to perform by the Contractor under the contract.

Nothing in the PAYMENT CONDITIONED UPON DELIVERY sub-clause shall be construed as affecting the rights of vendors under provisions of law or regulation (including the Federal Acquisition Regulation) relating to the termination of contracts for the convenience of the Government.

Upon notification of receipt and notification of approval of the Final Security Plan, the Contractor shall invoice for $5,000,000. The remaining balance of $35,981,175 shall be invoiced 90 days of performance (TBD).

1.  Milestone Payment at [redacted]* for a total of $20,490,587. (Upon documentation provided to BARDA that data covering the first 100 subject enrolled in the phase III pivotal safety study have been submitted to and reviewed by a DSMB, and submission of the final pivotal rabbit efficacy study report to the FDA.)

Nothing in the PAYMENT CONDITIONED UPON DELIVERY sub-clause shall be construed as affecting the rights of vendors under provisions of law or regulation (including the Federal Acquisition Regulation) relating to the termination of contracts for the convenience of the Government.

Completion of each individual milestone is required prior to the issuance of each respective milestone payment. The contractor shall submit the deliverable (See below) for each respective milestone to the Contracting Officer’s Representative and Contracting Officer for review by the appropriate date, and is subject to Government concurrence and approval. The Contractor shall invoice for the milestone payment $20,490,587) after Contracting Officer approval is provided.
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 4 of 9
2A.  1 Milestone Payment at [redacted]* for a total of $8,196,235.00 (Completion of Final Drug Product (FDP) Commercial Validation batches and report)

Nothing in the PAYMENT CONDITIONED UPON DELIVERY sub-clause shall be construed as affecting the rights of vendors under provisions of law or regulation (including the Federal Acquisition Regulation) relating to the termination of contracts for the convenience of the Government.

Completion of each individual milestone is required prior to the issuance of each respective milestone payment. The contractor shall submit the deliverable (See below) for each respective milestone to the Contracting Officer’s Representative and Contracting Officer for review by the appropriate date, and is subject to Government concurrence and approval. The Contractor shall invoice for the milestone payment $8,196,235.00 after Contracting Officer approval is provided.
2B.  1 Milestone Payment at [redacted]* for a total of $12,294,352.00 (Approved Product Labeling Strategy)

Nothing in the PAYMENT CONDITIONED UPON DELIVERY sub-clause shall be construed as affecting the rights of vendors under provisions of law or regulation (including the Federal Acquisition Regulation) relating to the termination of contracts for the convenience of the Government.

Completion of each individual milestone is required prior to the issuance of each respective milestone payment. The contractor shall submit the deliverable (See below) for each respective milestone to the Contracting Officer’s Representative and Contracting Officer for review by the appropriate date, and is subject to Government concurrence and approval. The Contractor shall invoice for the milestone payment $12,284,352.00 after Contracting Officer approval is provided.

D. By revising the following advanced payment and milestone from CLIN 0001 table as follows:
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission .
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 5 of 9
Advanced and Milestone Payments from CLIN-0001
#
Payment
Milestones
Deliverable
Date
Payment:
   
Advance Payment
   
1
[redacted]*
 
[redacted]*
 
[redacted]*
[redacted]*
   
Payment Milestones #1
 
1
[redacted]*
 
[redacted]*
 
[redacted]*
[redacted]*
2A
[redacted]*
 
[redacted]*
 
[redacted]*
[redacted]*
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 6 of 9
2B
[redacted]*
 
[redacted]*
 
[redacted]*
[redacted]*

3
[redacted]*
 
[redacted]*
 
[redacted]*
[redacted]*

E. By adding the following reporting requirement to the table under F.3.3 as follows:

F.3.3 — “Reporting Requirements”
#
Type of
Deliverable
Frequency/Time
Periods
Description of
Deliverable
Reporting Procedures
30
Notification and documentation of DSMB data submitted to the FDA following enrollment of the first 100 subjects in the ST-246- 008 pivotal phase III safety trial
At least 15 business days prior to
submission to FDA
The contractor shall provide BARDA the opportunity to review and comment upon all draft regulatory documents before submission to the FDA. Contractors shall provide BARDA with an electronic copy of the final FDA submission. All documents shall be duly marked as either ‘Draft’ or ‘Final’
 
The Contractor must address in writing all concerns raised by BARDA to the satisfaction of BARDA before FDA submission
·      Contractor will submit proposed FDA Meeting Briefing Packets to BARDA at least 15 business days prior to FDA submission.
·      If corrective action is required, the Contractor must address in writing all concerns raised by BARDA staff to the satisfaction of BARDA
·      Final FDA submissions shall be submitted to BARDA concurrently or no later than one (1) calendar day of its submission to CDER
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 7 of 9
F. By the addition of items under Table B, Section F.3, Contract Milestone and Go/No Go Decision Gates as follows:

Section F.3 — Table B: — "Contract Milestones and Go/NO GO Decision Gates
Mstn
#
Go/NO GO
Decision Gates
Go Criteria
No-Go Criteria
Deliverable
SOO/WBS #
16
 
[redacted]*
 
[redacted]*
[redacted]*
[redacted]*
[redacted]*
17
 
[redacted]*
 
[redacted]*
[redacted]*
[redacted]*
[redacted]*
18
 
[redacted]*
 
[redacted]*
[redacted]*
[redacted]*
[redacted]*

G. By revising the Project BioShield Specific Deliverables (Item 1 only) under Section F.3 of the contract to read as follows:

Project BioShield Specific Deliverables
#
Type of Deliverable
Frequency/Time Periods
Description of Deliverable
Reporting Procedures
Quantity/Form
1
Delivery of MCM
 
 
[redacted]*
 
 
 
 
[redacted]*
 
 
 
 
[redacted]*
 
 
 
 
[redacted]*
 
 
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 8 of 9
H. By revising the Project BioShield Delivery Schedule under F.6 Delivery Schedule (previously modified under Modification 0009) as follows:
 
Delivery
Number
Number of Bottles
(42 x 200mg
Capsules)
Number of Courses
Delivery Date
Batches
#1
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#2
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#3
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#4
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#5
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#6
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#7
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#8
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#9
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#10
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#11
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#12
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#13
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#14
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#15
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#16
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#17
[redacted]*
[redacted]*
[redacted]*
[redacted]*
#18
[redacted]*
[redacted]*
[redacted]*
[redacted]*
Total
[redacted]*
[redacted]*
   
 
* Certain material has been omitted pursuant to a request for confidential treatment.  Such omitted material has been filed separately with the Securities and Exchange Commission.
 

Contract No.
HHSO100201100001C
Modification No.0013
Continuation Sheet
Block 14
Page 9 of 9
I. By changing all references of Contracting Officer’s Technical Representative to read Contracting Officer’s Representative (COR)

J. All other terms and conditions of contract HHSO100201100001C remain unchanged.

END OF MODIFICATION 0013 to HHSO10020110001C