(RC) 2 Pharma Connect, LLC v. Mission Pharmacal Company

District Court, S.D. New York·Decided July 5, 2022·No. 1:21-cv-11096·Unknown

Opinion

USDC SDNY DOCUMENT SOUTHERN DISTRICT OF NEW YORK DOC #: Sone □□□ DR DATE FILED:_07/05/2022 (RC) 2 PHARMA CONNECT, LLC, : Plaintiff, : : 21-cv-11096 (LJL) -V- : : OPINION AND ORDER MISSION PHARMACAL COMPANY, : Defendant. :

LEWIS J. LIMAN, United States District Judge: Defendant Mission Pharmacal Company (“Defendant” or “Mission”) moves, pursuant to Federal Rule of Civil Procedure 12(b)(6), for an order dismissing the first amended complaint (“Complaint”) against it or, in the alternative, pursuant to Federal Rule of Civil Procedure 12(f), to strike portions of the complaint. Dkt. No. 34. For the following reasons, the motion to dismiss is granted. BACKGROUND The Court accepts as true the well-pleaded allegations of the Complaint and the documents incorporated by reference. Plaintiff (RC) Pharma Connection, LLC (“(RC) 2” or “Plaintiff’) is a pharmaceutical broker that specializes in sourcing and developing chemicals, pharmaceutical ingredients, and pharmaceutical products in cooperation with manufacturing partners that operate manufacturing facilities all over the world. Dkt. No. 8 4] 1. Its members are Dwight E. Raff I, Jason G. Raff, and William T. Cain. Jd. §] 18. Mission is a pharmaceutical company involved in, inter alia, the development and manufacture of pharmaceuticals as a contract partner for third parties. Id. 4 2. Its general counsel is Thomas James, who joined the company in 2020. Dkt. No. 8 {ff 3, 20, 23.

I. The Parties’ Initial Relationship Defendant was retained by Plaintiff to assist in the development of a generic version of a topical medication used to treat a common virus that causes cold sores. The medication is known under the brand name “Abreva,” and the generic version is docosanol 10% cream. The relationship between Plaintiff and Defendant is governed by two agreements.

A. The NDA In January 2019, Plaintiff and Defendant executed a non-disclosure agreement (“NDA”), effective January 2019, related to the development of docosanol 10% cream. Id. ¶¶ 29–32. The NDA permitted the parties to each share confidential information with the other and required the recipient “to protect and safeguard the confidentiality” of that information and not to use the disclosing party’s confidential information for any purpose other than “discussions regarding docosanol 10% cream” (defined as the “Purpose”) “or any related transactions between the Parties.” Dkt. No. 8-1 § 3(a), (b). It defined “Confidential Information” to include “the Disclosing Party’s unpatented inventions, ideas, methods and discoveries, trade secrets, know- how, unpublished patent applications and other confidential intellectual property.” Id. § 1(b). B. The Proposal Agreement

In March 2019, Plaintiff signed a Proposal Agreement dated March 13, 2019 for Defendant to perform activities to “support the development of a formulation and process for, preparation of and submission of an ANDA1 for, and commercial launch of Docosanol 10%

1 An ANDA is an Abbreviated New Drug Application. It contains data and is submitted to the FDA for the review and potential approval of a generic drug product. See Abbreviated New Drug Application (ANDA), FDA, https://www.fda.gov/drugs/types-applications/abbreviated- new-drug-application-anda (last visited July 5, 2022); see also In re Bystolic Antitrust Litig., 2022 WL 594534, at *3 (S.D.N.Y. Jan. 31, 2022), redacted opinion issued, 2022 WL 323945 (S.D.N.Y. Feb. 2, 2022) (describing ANDA process). cream,” subject to a successful facility visit on April 10, 2019; after the visit, (RC) 2 re-executed the agreement on May 17, 2019. Dkt. No. 8 ¶¶ 47–48; Dkt. No. 8-2. The Proposal Agreement contains a scope of work for Mission “to perform activities required to support the validation and production of launch stocks for Docosanol 10% cream” in five phases: Initial Development, Method Development, Technical Transfer, ANDA Preparation, and Commercialization and

Validation. As relevant here, Phase 3 (Technical Transfer) requires Mission to manufacture three batches of the product at scales identified in the agreement and to conduct stability testing and leachable and extractable testing and to test for “contact elemental impurities.” Dkt. No. 8-2 § 2.3. The Proposal Agreement explicitly contemplates that certain of the work (extractables/leachables and polymorph analysis) will be “outsourced.” Id. §§ 3.2, 3.4. It provides that (RC) 2 would be charged at an hourly rate of $250 an hour for Mission internal resources time spent on investigations and that “[c]osts of items sent to our Pharmacovigilance third party provider and cost for any external testimony required as part of an investigation” would be billed at cost. Id. § 3.7.2. The Proposal Agreement contemplates that work will be

done in phases. The first phase would be initiation followed by initial development and method development before technical transfer of materials, and then preparation of an ANDA, and finally commercialization and validation. Phase 4, which follows Phase 3, requires Mission to complete a development report, to compile all data and review as necessary, and to compose and file an ANDA. Finally, Phase 5 is commercialization and validation. In calculating an estimated unit pricing, the Proposal Agreement assumes that Mission would procure all required ingredients and packaging materials, that (RC) 2 would supply the docosanol active pharmaceutical ingredient, and that the parties would reach a five-year manufacturing agreement. The Proposal Agreement has a provision with respect to Project Management which requires Mission to conduct the work detailed under the supervision of an Account Manager, who would be the primary point of contact between the parties. Dkt. No. 8-2 § 5. On May 23, 2019, Mission sent (RC) 2 an undated proposed supply agreement, which contained New York personal jurisdiction, venue, and choice of law provisions. Dkt. No. 8-4; Dkt. No. 8 ¶ 52. Plaintiff never signed the agreement.

II. The Parties’ Disagreement over the Technology Transfer Agreement The relationship between the parties apparently began smoothly. Beginning soon after they entered into the Proposal Agreement, the parties held regular—typically bi-weekly—phone calls to discuss upcoming technical issues and deadlines. Mission provided an agenda before each of these phone calls. Dkt. No. 8 ¶ 59; see also, e.g., Dkt. No. 8-5 (containing minutes of a meeting held on July 15, 2021 that reflect the parties’ discussion of stability testing on the three batches, 39X21, 40X21, and 41X21, and the parties’ discussion that, with respect to the extractable leaching study, legal was requesting that a Technology Transfer Agreement be completed first). However, the relationship between the parties shifted after Mission’s General Counsel, James, became more actively involved in Mission’s relationship with (RC) 2. Dkt. No.

8 ¶ 60. On or about December 23, 2020, Mission sent (RC) 2 a proposed Technology Transfer Agreement (“TTA”) and stated that Mission’s “Legal Dept. is instituting Technical Transfer agreements for all existing and new projects.” Id. ¶ 67. The proposed TTA provided that Mission would perform a number of technology transfer activities, including manufacturing registration batches of the product and successfully completing stability testing of the six-month timepoint samples, with test results to be submitted to the FDA for product approval and registration. It also contemplated that thereafter (RC) 2 would enter into a manufacturing and supply agreement with Mission for the delivery of the commercial product. The draft TTA contained a section for the fees Mission would receive.

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