MLI RX LLC v. GLAXOSMITHKLINE LLC

CourtDistrict Court, D. New Jersey
DecidedMay 30, 2023
Docket2:23-cv-02960
StatusUnknown

This text of MLI RX LLC v. GLAXOSMITHKLINE LLC (MLI RX LLC v. GLAXOSMITHKLINE LLC) is published on Counsel Stack Legal Research, covering District Court, D. New Jersey primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
MLI RX LLC v. GLAXOSMITHKLINE LLC, (D.N.J. 2023).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE EASTERN DISTRICT OF PENNSYLVANIA

MLI RX, LLC, CIVIL ACTION AMERISOURCEBERGEN CORP., AMERISOURCEBERGEN DRUG CORP., H.D. SMITH, LLC, VALLEY WHOLESALE DRUG CO., LLC, (Subsidiary of H.D. Smith, LLC), NO. 23-429 CARDINAL HEALTH, INC., CARDINAL HEALTH P.R. 120, INC., THE HARVARD DRUG GROUP, L.L.C., CARDINAL HEALTH 110 LLC, McKESSON CORPORATION, BURLINGTON DRUG COMPANY, INC., DAKOTA DRUG, INC., NORTH CAROLINA MUTUAL WHOLESALE DRUG COMPANY, J.M. SMITH CORPORATION, doing business as “SMITH DRUG COMPANY,” VALUE DRUG COMPANY, and PRESCRIPTION SUPPLY, INC., Plaintiffs,

v.

GLAXOSMITHKLINE LLC, formerly known as “SMITHKLINE BEECHAM CORPORATION,” and doing business as “GLAXOSMITHKLINE,” TEVA PHARMACEUTICAL INDUSTRIES LTD., and TEVA PHARMACEUTICALS USA, INC., Defendants.

MEMORANDUM

HODGE, K. May 30, 2023

Plaintiffs MLI RX, LLC, AmerisourceBergen Corp., AmerisourceBergen Drug Corp., H.D. Smith, LLC, Valley Wholesale Drug Co. LLC, Cardinal Health, Inc., Cardinal Health P.R. 120, Inc., The Harvard Drug Group, L.L.C., Cardinal Health 110 LLC, McKesson Corporation, Burlington Drug Company, Inc., Dakota Drug, Inc., North Carolina Mutual Wholesale Drug Company, J.M. Smith Corporation, Value Drug Company, Prescription Supply, Inc. (collectively “Plaintiffs”) brought this antitrust action against Defendants GlaxoSmithKline LLC, Teva Pharmaceutical Industries LTD., and Teva Pharmaceuticals USA, Inc. (collectively

“Defendants”) alleging violations of Sections 1 and 2 of the Sherman Antitrust Act, 15 U.S.C §§ 1-2. Presently before the Court is Defendants’ Motion to Transfer (ECF Nos. 28 & 44)1 requesting that pursuant to Section 28 U.S.C. § 1404(a) and the “first-to-file” doctrine2 this matter be transferred to the United States District Court for the District of New Jersey (“District of New Jersey”) where a similar case, In re: Lamictal Direct Purchaser Antitrust Litig., No. 2:12-cv-00995 (D.N.J.) (the “New Jersey Action”), has been ongoing since February 17, 2012. Contemporaneously, Defendants also filed a Motion to Stay (ECF Nos. 30 & 44) this case pending the outcome of their Motion to Transfer. Plaintiffs do not dispute that the present matter is substantially similar to the New Jersey Action. Nor do they argue the District of New Jersey

lacks a connection to this matter, or that venue and jurisdiction would be improper there. Rather, Plaintiffs contend that this case should not be transferred to the District of New Jersey because of the “history of long delays” in that court. (ECF No. 40 at 9.) Citing the public and private interest factors under 28 U.S.C 1404(a) that weigh for and against a change of venue, Plaintiffs argue that transferring this action to the District of New Jersey would be improvident because it would “exacerbate the judicial burdens clearly facing that district.” (Id. at 10.) Plaintiffs also

1 The Motion to Transfer and Motion to Stay were filed only by Defendants GlaxoSmithKline LLC and Teva Pharmaceuticals USA, Inc. on March 2, 2023, but Defendant Teva Pharmaceutical Industries Ltd. subsequently joined these motions on March 16, 2023. (ECF No. 44.) 2 The “first-to-file” doctrine is sometimes referred to as the “first-filed” rule, and therefore, the Court uses these terms interchangeably. emphasize that three of the sixteen Plaintiffs and one of the Defendants have a nexus to Pennsylvania. (Id.) After reviewing the New Jersey Action, the Complaint in this matter, and the parties’ briefing, the Court agrees with the Defendants. The Court finds that the first-to-file rule applies

and supports a venue transfer to the District of New Jersey. The Court also finds that a venue transfer is warranted under Section 1404(a). Therefore, for the reasons more fully set forth below, the Court grants Defendants’ Motion to Transfer and, thereby, denies the Motion to Stay as moot. I. BACKGROUND On February 2, 2023 – a day after the District of New Jersey issued a ruling denying Plaintiff’s motion for class-certification in the New Jersey Action – Plaintiffs filed suit before this Court against the same defendants, GlaxoSmithKline LLC (“GSK”), Teva Pharmaceutical Industries LTD., and Teva Pharmaceuticals USA, Inc. (jointly “Teva”) alleging that they violated antitrust laws through their settlement agreement to end a patent suit over GSK’s brand-name

drug Lamictal and Teva’s generic form, lamotrigine. (ECF No. 1); see also In re: Lamictal Direct Purchaser Antitrust Litig., No. 2:12-cv-00995 (D.N.J.) (ECF Nos. 553 & 554.) The basis of this litigation stems from the Hatch-Waxman Act of 1984 that allows drug manufacturers to bring generics to market for a 180-day exclusivity period by piggybacking off a brand-name drug’s safety and efficacy studies and Food and Drug Administration (“FDA”) approval, through what is known as an Abbreviated New Drug Application (“ANDA”). (Id. at 3.) To do so, the generic manufacturer certifies in its ANDA that the brand-name drug’s patent is invalid, but if the brand-name manufacturer challenges that designation, FDA approval for the generic is enjoined for a certain time-period. (Id. at 4.) And that is exactly what occurred: GSK challenged Teva in patent litigation which delayed Teva’s generic version of lamotrigine from getting FDA approval and coming to market. Yet in that time, GSK, under the relevant regulatory framework, could have launched or licensed its own generic form of Lamictal, known as an “Authorized Generic (AG).” (Id. at 51-53.) Though Teva was successful in the patent litigation bench trial as

to one infringement claim, the judge informed the parties that he would subsequently deliberate as to the remaining claims whereupon GSK and Teva decided, instead, to settle.3 (Id. at 7.) As part of the settlement, GSK agreed not to launch an AG in exchange for Teva selling generic lamotrigine later than it otherwise would have been able to. (Id. at 9-14.) Plaintiffs, all purchasers of Defendants’ drugs, claim that the settlement agreement amounts to an antitrust violation as it caused them to pay more than they otherwise would have, had market competition not been delayed. (Id. at 45.) The New Jersey Action, originally filed on February 17, 2012, has resulted in a lengthy and complicated litigation history with numerous appeals and stays issued by the court. In re: Lamictal Direct Purchaser Antitrust Litig., No. 2:12-cv-00995 (D.N.J.) (ECF No. 1.) Originally,

the District of New Jersey granted Defendants’ motion to dismiss the putative class action complaint. In re: Lamictal Direct Purchaser Antitrust Litig., No. 2:12-cv-00995, 2012 U.S. Dist. LEXIS 183627 (D.N.J. Dec. 6, 2012). On appeal, however, the United States Court of Appeals for the Third Circuit held that the complaint sufficiently alleged an antitrust violation under the Supreme Court’s precedent in FTC v. Actavis, 133 S. Ct. 2223 (2013). See King Drug Co. of Florence, Inc. v. SmithKline Beecham Corp., 791 F.3d 388 (3d Cir. 2015) (ruling that the Actavis

3 In August of 2002, GSK filed a patent infringement suit against Teva in the District of New Jersey alleging that Teva’s ANDA for generic lamotrigine infringed GSK’s patent for Lamictal. See Smithkline Beecham Corp. v. Teva Pharm. USA, Inc., No. 02-3779 (D.N.J. Aug. 5, 2002) (ECF No. 1).

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Smith v. McIver
22 U.S. 532 (Supreme Court, 1824)
Van Dusen v. Barrack
376 U.S. 612 (Supreme Court, 1964)
Stewart Organization, Inc. v. Ricoh Corp.
487 U.S. 22 (Supreme Court, 1988)
Handy v. Shaw, Bransford, Veilleux & Roth
325 F.3d 346 (D.C. Circuit, 2003)
Kerotest Mfg. Co. v. C-O-Two Fire Equipment Co.
189 F.2d 31 (Third Circuit, 1951)
F.T.C. v. Actavis, Inc.
133 S. Ct. 2223 (Supreme Court, 2013)
Crosley Corporation v. Hazeltine Corporation
122 F.2d 925 (Third Circuit, 1941)
United States v. H & R Block, Inc.
789 F. Supp. 2d 74 (District of Columbia, 2011)
Lawrence v. Xerox Corp.
56 F. Supp. 2d 442 (D. New Jersey, 1999)
Fuller v. Abercrombie & Fitch Stores, Inc.
370 F. Supp. 2d 686 (E.D. Tennessee, 2005)
White v. Peco Foods, Inc.
546 F. Supp. 2d 339 (S.D. Mississippi, 2008)
In re: Lamictal Direct Purchas v.
957 F.3d 184 (Third Circuit, 2020)
MaxLite, Inc. v. ATG Electronics, Inc.
193 F. Supp. 3d 371 (D. New Jersey, 2016)
Unlimited Technology, Inc. v. Leighton
266 F. Supp. 3d 787 (E.D. Pennsylvania, 2017)

Cite This Page — Counsel Stack

Bluebook (online)
MLI RX LLC v. GLAXOSMITHKLINE LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/mli-rx-llc-v-glaxosmithkline-llc-njd-2023.