JM Smith Corporation v. AstraZeneca Pharmaceuticals L P

CourtDistrict Court, S.D. New York
DecidedAugust 11, 2020
Docket1:19-cv-07233
StatusUnknown

This text of JM Smith Corporation v. AstraZeneca Pharmaceuticals L P (JM Smith Corporation v. AstraZeneca Pharmaceuticals L P) 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
JM Smith Corporation v. AstraZeneca Pharmaceuticals L P, (S.D.N.Y. 2020).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF NEW YORK

JM SMITH CORPORATION, d/b/a SMITH DRUG COMPANY, on behalf of itself and all others similarly situated,

Plaintiff, Dkt. No. 19 Civ. 7233 (CM)

-against-

ASTRAZENECA PHARMACEUTICALS L P, ASTRAZENECA L P, ASTRAZENECA UK LIMITED, HANDA PHARMACEUTICALS, LLC, and PAR PHARMACEUTICAL, INC.,

Defendants.

ORDER GRANTING DEFENDANTS’ MOTION TO TRANSFER

McMahon, C.J.:

J M Smith Corporation d/b/a, Smith Drug Company (“Smith”) brings this antitrust class action on behalf of itself and similarly situated direct purchaser plaintiffs (“DPPs”) against Defendants AstraZeneca Pharmaceuticals L.P. and AstraZeneca L.P. (collectively, “AstraZeneca”), AstraZeneca UK Ltd. (“AZ UK”), Handa Pharmaceuticals, LLC (“Handa”), and Par Pharmaceutical, Inc. (“Par”) (collectively, “Defendants”). All Defendants move to dismiss for lack of jurisdiction or improper venue; or in the alternative, to transfer pursuant to 28 U.S.C. § 1404. (Dkt. No. 68.) In a separate motion, they also moved to dismiss Smith’s Complaint for failure to state a claim. (Dkt. No. 69.) For the reasons stated below, Defendants’ motion to transfer is GRANTED. BACKGROUND A. Parties Smith is a South Carolina corporation headquartered in Spartanburg, South Carolina. (Dkt. No. 1 at ¶ 2 (“Compl.”).) Smith purchased branded and generic Seroquel XR from AstraZeneca

and Par, respectively, during the proposed Class Period: “from September 29, 2011 until the effects of Defendants’ conduct ceases.” (Id. ¶¶ 34, 41.) AstraZeneca and other generic competitors launched their own versions of generic Seroquel XR in or around early May 2017. (Id. ¶¶ 21-22.) AstraZeneca L.P. was a Delaware limited partnership headquartered in Wilmington, Delaware. It was dissolved on December 31, 2018, and all of its assets and liabilities were assumed by AstraZeneca Pharmaceuticals L.P. (Aff. of Matthew Bowden ¶¶ 4–5, Dkt. No. 68-7.) AstraZeneca Pharmaceuticals L.P. is a Delaware limited partnership headquartered in Wilmington, Delaware. (Compl. ¶ 35.) AZ UK is a U.K. company headquartered in London, United Kingdom. (Id. ¶ 37.) Handa is headquartered in San Jose, California. (Id. ¶ 38.) While Smith asserts that Handa

is a California LLC (id.), Handa explains that while it was previously a California LLC, in September 2016 Handa was registered as a Delaware LLC. (Aff. of Stephen D. Cary ¶¶ 3, 8, Dkt. No. 68-9.) Par is a Delaware corporation presently headquartered in Chestnut Ridge, New York. (Compl. ¶ 39.) Prior to March 2015, Par maintained its principal place of business in Woodcliff Lake, New Jersey. (See Decl. of Terrell T. Stevens, Dkt. No. 82-1.) B. The Alleged Conspiracies This case arises from alleged conspiracies between and among Defendants to delay and suppress competition for generic versions of AstraZeneca’s branded quetiapine fumarate extended-release tablets, Seroquel XR®. Specifically, AstraZeneca entered into allegedly anti- competitive patent settlement agreements with Handa (later assigned to Par) and non-party Accord Pharmaceuticals, Inc. (“Accord”). Before generic versions of Seroquel XR entered the market, AstraZeneca sold branded

Seroquel XR in the United States to the tune of $1 billion per year. (Compl. ¶ 2.) Handa, a generics manufacturer, was the first to file an Abbreviated New Drug Application (“ANDA”) for the 50, 150, 200, and 300mg strengths of generic Seroquel XR. (Id. ¶ 3.) It also filed an ANDA for the 400mg strength, but it was not the first to do so. Rather, Accord filed the first ANDA for the 400mg strength generic Seroquel XR. (Id.) Handa and Accord sent AstraZeneca Paragraph IV notice letters, each certifying that they would seek final FDA approval and intended to launch their generic Seroquel XR products prior to the expiration of AstraZeneca’s follow-on patent, U.S. Patent No. 5,948,437 (the “’437 Patent”). Handa and Accord claimed the ‘437 Patent was invalid or otherwise would not be infringed by their generic products. (Id. ¶ 4.) The ‘437 Patent expired on May 28, 2017, and its regulatory

exclusivities expired on November 28, 2017. (Id. ¶ 5.) In 2008 and early 2009, AstraZeneca initiated patent infringement lawsuits against Handa and Accord in the District of New Jersey, alleging that Handa and Accord’s respective ANDAs infringed the ‘437 Patent. (Id. ¶¶ 6–10.) Around October 1, 2011, AstraZeneca allegedly entered into two settlement agreements – one with Handa, the other with Accord – whereby the parties resolved the patent lawsuits; Handa and Accord agreed to delay their launches of generic Seroquel XR (in their respective strengths) until November 1, 2016; and AstraZeneca agreed not to launch an authorized generic (“AG”) Seroquel XR until May 1, 2017. (Id. ¶¶ 15, 18). On October 29, 2012, Par – another generics manufacturer – announced that it had acquired Handa’s ANDA. As part of the agreement, Handa assigned Par the settlement agreement with AstraZeneca – including the right to market generic Seroquel XR on November 1, 2016. Par was required to share a portion of its profits from the sale of the generic with Handa. (Id. ¶¶ 16–17.)

Smith and the putative class of DPPs were harmed by the allegedly unlawful settlement agreements because (a) no generic Seroquel XR was available until November 1, 2016 and (b) only one generic was available for six months thereafter, until May 1, 2017. Absent the settlement agreements, (a) generics would have entered the market sooner and (b) AstraZeneca’s AG would have launched at the time those generics entered the market – such that the DPPs could have acquired extended-release quetiapine fumarate at significantly lower prices substantially earlier. Smith asserts five causes of action under the Sherman Act: Counts I and II assert violations of Section 1 and Section 2, respectively, against AstraZeneca, Handa, and Par as to the 50, 150, 200, and 300mg strengths of Seroquel XR (Id. ¶¶ 185-201);

Counts III and IV assert violations of Section 1 and Section 2, respectively, against AstraZeneca as to the 400mg strength of Seroquel XR (Id. ¶¶ 202-16); and Count V asserts a violation of Section 2 against AstraZeneca for monopolization and monopolistic scheme (Id. ¶¶ 217-22). C. Relevant Contracts Defendants assert that two agreements cover Smith’s relationship with AstraZeneca: (1) a 2005 Wholesale Distribution Agreement (“Wholesale Agreement”) (Ex. 1 to Defs.’ Mot. to Dismiss, Dkt. No. 68-4) and (2) a 2011 Wholesale Distribution Services Agreement, amended in 2016 (“DS Agreements”) (Exs. 2 & 3 to Defs.’ Mot. to Dismiss, Dkt. Nos. 68-5, 68-6.) The Wholesale Agreement appoints Smith as a non-exclusive distributor for AstraZeneca’s products. The DS Agreements govern, inter alia, the level of inventory of Seroquel XR Smith must maintain. Defendants identify the specific sections of the DS Agreements that require Smith to maintain both target inventory levels and stable purchase quantities of AstraZeneca products every

month, including Seroquel XR in 50, 150, 200, 300, and 400mg strengths. (See Ex. 2 §§ 5.1, 11.2, Attach. G; Ex. 3 §§ 1.19, 3.2, 3.3, Attach. A-1.) Smith characterizes the DS Agreements as imposing an obligation on Smith “to provide data to AstraZeneca and to refrain from speculative buying, in order to assist AstraZeneca ‘to manage its product inventory,’ ‘minimize the potential of product unavailability,’ ‘better forecast future product demand,’ and ‘better manage inventory requirements from customers’; in exchange, AstraZeneca agreed to pay [Smith] certain monies.” (Opp’n to Defs.’ Mot. to Dismiss, Dkt. No. 73 at 21 (quoting Ex. 2 at 1; Ex. 3 at 1).) The DS Agreements contain the same forum selection clause: Jurisdiction.

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