SIGA Technologies, Inc. v. PharmAthene, Inc.

67 A.3d 330, 2013 WL 2303303, 2013 Del. LEXIS 265
CourtSupreme Court of Delaware
DecidedMay 24, 2013
DocketNo. 314, 2012
StatusPublished
Cited by133 cases

This text of 67 A.3d 330 (SIGA Technologies, Inc. v. PharmAthene, Inc.) is published on Counsel Stack Legal Research, covering Supreme Court of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
SIGA Technologies, Inc. v. PharmAthene, Inc., 67 A.3d 330, 2013 WL 2303303, 2013 Del. LEXIS 265 (Del. 2013).

Opinion

STEELE, Chief Justice:

A Delaware corporation appeals from the Vice Chancellor’s finding that it breached a contractual obligation to negotiate in good faith and is liable under the doctrine of promissory estoppel. We reaffirm that where parties agree to negotiate in good faith in accordance with a term sheet, that obligation to negotiate in good [334]*334faith is enforceable. Where a trial judge makes a factual finding, supported by the record, that the parties would have reached an agreement but for the defendant’s bad faith negotiation, we hold that a trial judge may award expectation damages. We reverse the Vice Chancellor’s promissory estoppel holding because a promise expressed in a fully enforceable contract cannot give rise to a promissory estoppel claim. We also reverse the Vice Chancellor’s equitable damages award based on his factual conclusion that the parties would have reached an agreement, so that he may reconsider the award in light of this opinion.

I. FACTUAL AND PROCEDURAL HISTORY1

A. Facts

Plaintiff-Appellee PharmAthene, Inc., and Defendant-Appellant SIGA Technologies, Inc., are both Delaware corporations engaged in biodefense research and development. In 2004, SIGA acquired an antiviral drug for the treatment of smallpox, ST-246. At that time, the drug’s viability, potential uses, safety, and efficacy were all unknown, but the drug had enormous potential.

By late 2005, SIGA had experienced difficulty developing the drug and was running out of money. NASDAQ threatened to delist SIGA’s shares and SIGA’s largest shareholder, MacAndrews & Forbes (MAF), was unwilling to invest additional money. SIGA estimated it needed approximately $16 million to complete the development process.2

As a result of SIGA’s difficulties, SIGA’s management began discussing a possible collaboration with PharmAthene. Thomas Konatich, SIGA’s Chief Financial Officer, contacted Eric Richman, PharmAthene’s Vice President of Business Development and Strategies. Richman desired a merger between the two companies, but SIGA resisted because of its past experience with PharmAthene.3 According to Rich-man’s contemporaneous notes, SIGA insisted on framing a license agreement before discussing a merger because of that past experience and because SIGA needed an immediate cash infusion to stabilize its financial situation. By the end of 2005, both SIGA’s and PharmAthene’s conservative estimates valued ST-246 at approximately $1 billion.

In late 2005 and early 2006, Konatich and Richman outlined the terms of a license agreement. Konatich kept Donald Drapkin, Chairman of SIGA’s Board of Directors and MAF’s Vice Chairman, well informed about the negotiations.4 Kona-[335]*335tich and Richman also assembled negotiation teams on behalf of their companies. On January 3, 2006, Richman sent Kona-tich and Dr. Dennis Hruby, SIGA’s Chief Scientific Officer, a proposed term sheet based on his discussions with SIGA about a license agreement for ST-246. On January 4, Hruby replied: “Thanks for the prompt response. We are most interested in trying to make this a mutually agreeable term sheet and moving on to the next step.”

Konatich and Richman continued to exchange draft term sheets. Much of the negotiation focused on upfront cash payments and funding guarantees. On January 16, Richman sent Konatich a revised term sheet that provided for a total deal size of $16 million, an increased upfront payment of $6 million, and significant cash milestone payments. When Konatich forwarded this' term sheet to Drapkin, he recommended that Drapkin speak directly to Richman to present SIGA’s Board of Directors’ position on PharmAthene’s proposal.

On January 17, the Vice Chancellor found that Drapkin and Richman discussed the term sheet during a telephone call and Drapkin requested that Richman make two changes.5 Richman testified that Drapkin told him that if the changes were acceptable to PharmAthene, then “[w]e have got a deal on the term sheet, and it’s ready to present to your board for approval.” At a January 18 PharmAthene board meeting, Richman presented the January 16 term sheet and explained Drapkin’s proposed changes.6 Jeffrey Baumel, Phar-mAthene’s outside counsel, drafted the minutes for that board meeting. The term sheet was not signed, however, and the minutes do not state that the board approved the term sheet.7

On January 19, Richman again spoke with Drapkin and told him that the Phar-mAthene board had approved the license agreement term sheet with Drapkin’s two proposed changes. While PharmAthene alleges that by this time, the parties had “a deal” and could move on to discussing a merger, Richman did not send a copy of the revised term sheet to Drapkin until February 10, 2006.8

On January 26, a clean copy was made of the two-page license agreement term sheet incorporating Drapkin’s two changes (the LATS). The LATS recites that the parties intended to “establish a partnership to further develop & commercialize [ST-246] for the treatment of [s]mallpox and orthopox related infections and to develop other orthopox virus therapeutics.” The LATS also sets forth terms relating to, among other things, patents covered, licenses, license fees, and royalties. How[336]*336ever, the LATS was not signed, and a footer on both pages states, “Non Binding Terms.”

The Vice Chancellor summarized the LATS in his posttrial opinion:

Without attempting to cover all the details, the LATS contemplates a license agreement along the following lines to support the further development and commercialization of ST-246 for the treatment of smallpox. First, SIGA would grant to PharmAthene “a worldwide exclusive license and [sic] under the Patents, Know-How and Materials to use, develop, make, have made, sell, export and import Products in Field. The right to grant sublicenses shall be specifically included in the license.” Second, the license would cover ST-246 and all other related products worldwide covered by the patents and know-how relating to ST-246 and its development and manufacture. Third, the LATS described the makeup of a research and development committee, which would include representatives from both Phar-mAthene and SIGA. The parties identified twelve categories of tasks relevant to that committee and assigned responsibility for each one to either SIGA or PharmAthene. In addition, PharmAth-ene agreed to fund the research and development based on a defined budget.
Fourth, the LATS included economic terms. PharmAthene was scheduled to pay a “License Fee” of $6 million in total, which consisted of $2 million cash upfront, $2.5 million as a deferred license fee to be paid twelve months after execution of a license agreement if certain events occurred, and $1.5 million after SIGA obtained financing in excess of $15 million. In addition, the LATS contained a provision under which Phar-mAthene would pay an additional $10 million based on the achievement of specific milestones relating to certain sales targets and regulatory approvals. The LATS also provided for PharmAthene to make annual royalty payments of 8% on “yearly net sales of Patented Products” of less than $250 million, 10% on sales greater than $250 million, and 12% on sales greater than $1 billion.

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Bluebook (online)
67 A.3d 330, 2013 WL 2303303, 2013 Del. LEXIS 265, Counsel Stack Legal Research, https://law.counselstack.com/opinion/siga-technologies-inc-v-pharmathene-inc-del-2013.