Echo Bay Pharmaceuticals, LLC v. Torrent Pharma, Inc.

CourtDistrict Court, S.D. New York
DecidedJune 14, 2022
Docket1:20-cv-06345
StatusUnknown

This text of Echo Bay Pharmaceuticals, LLC v. Torrent Pharma, Inc. (Echo Bay Pharmaceuticals, LLC v. Torrent Pharma, Inc.) is published on Counsel Stack Legal Research, covering District Court, S.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Echo Bay Pharmaceuticals, LLC v. Torrent Pharma, Inc., (S.D.N.Y. 2022).

Opinion

| USDC SDNY | DOCUMENT UNITED STATES DISTRICT COURT p ELECTRONICALLY FILED SOUTHERN DISTRICT OF NEW YORK FO eirestcintmeion DATE FILED:_ 6/14/22 ECHO BAY PHARMACEUTICALS, LLC, Plaintiff, 20-CV-6345 (BCM) -against- OPINION AND ORDER TORRENT PHARMA, INC., Defendant.

In this diversity action between two pharmaceutical companies, plaintiff Echo Bay Pharmaceuticals, LLC (Echo Bay) alleges that defendant Torrent Pharma, Inc. (Torrent) breached both the express terms of the parties’ Co-Development Settlement Agreement (CSA) and the covenant of good faith and fair dealing implied therein. Now before the Court is defendant's motion (Dkt. No. 94) to dismiss the Second Amended Complaint (SAC) (Dkt. No. 91) pursuant to Fed. R. Civ. P. 12(b)(6). For the reasons that follow: (1) the motion to dismiss will be granted; and (11) Echo Bay will be given leave to replead, limited to its claim that Torrent breached the implied covenant by withdrawing its Abbreviated New Drug Application (ANDA) for a pharmaceutical product known as Fluocinonide without notice to Echo Bay. I. BACKGROUND A. Factual Allegations On January 18, 2018, Echo Bay entered into the CSA with Torrent's predecessor, Bio-Farm Incorporated (BFI), for the purpose of developing and commercializing certain generic pharmaceutical products (the Products). SAC 4 20-21. Concurrently with the execution of the CSA, Torrent acquired BPI through a stock purchase agreement, obtained an assignment of BPI's rights and obligations under the CSA, and undertook to perform under the contract. /d. Jj 26-28, 32. Torrent also became the owner of BPI's manufacturing facility in Levittown, Pennsylvania (the Levittown Facility), where the Products were to be developed. /d. {J 26, 32. Thereafter, BPI was

merged into Torrent and ceased to exist. Id. ¶ 29. Thus, "at all times from January 18, 2018 through the present, Torrent, as assignee of and/or successor in interest to BPI, was obligated to perform under the CSA." Id. ¶ 31. Echo Bay is a citizen of Illinois, while Torrent is a citizen of Delaware and New Jersey. SAC ¶¶ 2-4.

1. The CSA Under the terms of the CSA, as amended on December 15, 2018 (SAC Exs. A, B), Echo Bay granted Torrent "the sole and exclusive worldwide rights" to "Commercialize each of the Products" specified in the contract, CSA § 2.2.1 To that end, Torrent was "responsible to the Regulatory Authorities for carrying out Development activities," as well as "post-approval maintenance, prosecution, and fees." Id. § 3.3.2 Echo Bay, for its part, was to "provide all reasonable assistance to [Torrent] regarding Development activities, including answering questions from the FDA [the U.S. Food and Drug Administration] or any other Regulatory Authority, regarding any Product." Id. § 3.4. It was also required to supply all necessary materials developed for product labels, packaging materials, and inserts. Id. § 4.2. No generic drug can be sold to the public until the FDA approves the manufacturer's

ANDA, which must show that the generic "has the 'same active ingredients as,' and is 'biologically equivalent' to, the already-approved brand-name drug." F.T.C. v. Actavis, Inc., 570 U.S. 136, 142

1 The CSA defines "Commercialization" as: "the commercial exploitation of any Product, directly or indirectly through Affiliates, including manufacturing, distribution, promotion, marketing, selling, or offering for sale, of any Product." CSA § 1.2. 2 The CSA defines "Development" as: "all preclinical and clinic drug activities, including test method development and stability testing, toxicology, bioequivalency, formulation, process development, manufacturing scale-up, development-stage manufacturing, quality assurance/ quality control development, statistical analysis and report writing, and conducting clinical trials for the purpose of obtaining any and all approvals, licenses, registrations or authorizations from any Regulatory Authority necessary for the manufacture, use, storage, import, export, transport, promotion, marketing and sale of any product." CSA § 1.5. (2013) (quoting Caraco Pharm. Lab'ys, Ltd. v. Novo Nordisk A/S, 566 U.S. 399, 405 (2012). "[T]his process is designed to speed the introduction of low-cost generic drugs to market." Caraco, 566 U.S. at 405. The parties were to share equally the "Development Expenses" incurred by Torrent. CSA

§§ 1.6, 3.1, 3.2. Echo Bay was required to pay its share on a quarterly basis upon receipt of an invoice from Torrent. Id. §§ 3.1, 3.2. In return, once a Product was Commercialized, Echo Bay would be entitled to 50% of the Net Revenue generated by that Product, less a Marketing Allocation. CSA §§ 1.7, 1.12, 2.4. However, "[n]othing contained in this Agreement is a warranty by the Company [Torrent] that any Commercialization in connection with this Agreement will achieve its aims or any other results." CSA § 2.5. The CSA specifically gave "either Party" the right to "cease contributing Development expenses" with respect to a Product, at any time prior to the FDA's approval of the ANDA for that Product, "by notifying the other Party in writing[.]" CSA § 8.4(a). In addition, Torrent would be "deemed to have ceased Development of the Product," whether or not it provided "such written

notice," if "no significant Development activities with regard to a Product have occurred over a given successive twelve (12) month period and such inactivity is not due to actions or omissions of a Third Party or events outside of the control of the Company." Id. In such an event, "the other Party . . . may choose to continue to develop [the Product] and initially incur one hundred percent (100%) of the remaining Development Expenses for such Product." Id. 2. The Active Products The referenced Products are set out in Exhibit A of the CSA, and include the following Active Products: • Fluocinolone (fluocinolone acetonide solution .01%); • Fluocinonide (fluocinonide solution 5%); • Pyridostigmine (pyridostigmine oral syrup); and • Gabapentin (gabapentin solution).3

The FDA never approved an ANDA for any of the Active Products, SAC ¶¶ 56-76, 105, meaning that they could not be Commercialized. According to Echo Bay, this occurred because – despite its "reasonable expectation" that Torrent would "take prudent and necessary steps to develop such products in a timely manner so as to enjoy the revenue from the Commercialization of such products," id. ¶ 41 – Torrent failed adequately to "complete the remaining Development" of the Active Products. Id. ¶ 43. In particular, Echo Bay alleges that Torrent "botched" the development of the four Active Products, SAC ¶¶ 56-85, due largely to problems with its Levittown Facility, as follows: Pyridostigmine. Torrent submitted an ANDA for Pyridostigmine on April 27, 2018. SAC ¶ 57. On February 20, 2019, the FDA determined that it could not "approve this ANDA in its

present form" because of "major" deficiencies in "pharmaceutical quality, drug substance, drug product, and facilities inspection deficiencies." Id. ¶ 66 & Ex. G. The facilities inspection deficiencies stemmed from an FDA inspection of the Levittown Facility, "in which the FDA field investigator observed objectionable conditions that were conveyed to the facility representative." Id. Ex. G, ¶ 11. The FDA advised Torrent that "[s]atisfactory resolution of the observations is

3 Echo Bay lists a fifth Active Product, known as Felbamate (felbamate suspension). SAC ¶ 44. However, as Torrent points out, Felbamate was "assigned to Echo Bay in December 2018" when the parties amended their contract. Def. Mem. in Supp. of Mtn. to Dismiss SAC (Dkt. No. 95) at 3 n.2; Compl. Ex. B, ¶ 2.8.

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