Federal Trade Commission v. Vyera Pharmaceuticals, LLC

CourtDistrict Court, S.D. New York
DecidedFebruary 4, 2022
Docket1:20-cv-00706
StatusUnknown

This text of Federal Trade Commission v. Vyera Pharmaceuticals, LLC (Federal Trade Commission v. Vyera Pharmaceuticals, LLC) 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
Federal Trade Commission v. Vyera Pharmaceuticals, LLC, (S.D.N.Y. 2022).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF NEW YORK -------------------------------------- X : FEDERAL TRADE COMMISSION, STATE OF NEW : 20cv00706 (DLC) YORK, STATE OF CALIFORNIA, STATE OF : OHIO, COMMONWEALTH OF PENNSYLVANIA, : OPINION AND ORDER STATE OF ILLINOIS, STATE OF NORTH : CAROLINA, and COMMONWEALTH OF : VIRGINIA, : : Plaintiffs, : -v- : : MARTIN SHKRELI, : : Defendant. : : -------------------------------------- X APPEARANCES: For plaintiff Federal Trade Commission: Markus H. Meier Bradley S. Albert Armine Black Daniel W. Butrymowicz J. Maren Haneberg Leah Hubinger Lauren Peay Neal J. Perlman James H. Weingarten Amanda Triplett Matthew B. Weprin Federal Trade Commission 600 Pennsylvania Avenue, NW Washington, DC 20580 For plaintiff State of New York: Elinor R. Hoffmann Bryan Bloom Jeremy R. Kasha Amy E. McFarlane Saami Zain Office of the New York Attorney General Antitrust Bureau 28 Liberty Street, 20th Floor New York, NY 10005

For plaintiff State of California: Michael D. Battaglia Office of the Attorney General of California 455 Golden Gate Avenue, Suite 11000 San Francisco, CA 94102

For plaintiff State of Illinois: Richard S. Schultz Office of the Attorney General of Illinois 100 W. Randolph Street, 11th Floor Chicago, IL 60601

For plaintiff State of North Carolina: Jessica V. Sutton North Carolina Dept. of Justice Consumer Protection Division 114 West Edenton Street Raleigh, NC 27603

For plaintiff State of Ohio: Beth A. Finnerty Office of the Ohio Attorney General 150 E. Gay Street, 22nd Floor Columbus, OH 43215

For plaintiff Commonwealth of Pennsylvania: Joseph S. Betsko Pennsylvania Office of Attorney General Strawberry Square, 14th Floor Harrisburg, PA 17120

For plaintiff Commonwealth of Virginia: Tyler T. Henry Office of the Attorney General of Virginia 202 North Ninth Street Richmond, VA 23219

For defendant Martin Shkreli: Christopher H. Casey Jeffrey S. Pollack Andrew J. Rudowitz Sarah Fehm Stewart Sean P. McConnell J. Manly Parks Duane Morris LLP 30 South 17th Street Philadelphia, PA 19103 DENISE COTE, District Judge: Following trial, on January 14, 2022, this Court ordered that Martin Shkreli (“Shkreli”) be banned for life from participating in the pharmaceutical industry in any capacity and pay $64.6 million in disgorgement. Fed. Trade Comm'n v. Shkreli, No. 20CV00706 (DLC), 2022 WL 135026 (S.D.N.Y. Jan. 14, 2022). Having considered the injunction proposed by the plaintiffs and Shkreli’s objections, an injunction and final

judgment has been issued today. This Opinion addresses Shkreli’s objections to the injunction. “[I]njunctive relief should be narrowly tailored to fit specific legal violations, [and] the court must mould each decree to the necessities of the particular case.” City of New York v. Mickalis Pawn Shop, LLC, 645 F.3d 114, 144 (2d Cir. 2011) (“Mickalis”) (citation omitted). Rule 65(d) of the Federal Rules of Civil Procedure further provides that “[e]very order granting an injunction . . . must: (A) state the reasons why it issued; (B) state its terms specifically; and (C) describe in reasonable detail -- and not by referring to the complaint or other document -- the act or acts restrained or

required.” Fed. R. Civ. P. 65(d). “Rule 65(d) reflects Congress' concern with the dangers inherent in the threat of a contempt citation for violation of an order so vague that an enjoined party may unwittingly and unintentionally transcend its bounds.” Sanders v. Air Line Pilots Ass'n, Int'l, 473 F.2d 244,

247 (2d Cir. 1972) (citing International Longshoremen's Assoc., Local 1291 v. Philadelphia Marine Trade Assoc., 389 U.S. 64, 76 (1967)); see also Corning Inc. v. PicVue Elecs., Ltd., 365 F.3d 156, 157–58 (2d Cir. 2004) (“Corning”). Rule 65(d) is satisfied only if the party enjoined can “ascertain from the four corners of the order precisely what acts are forbidden.” All. for Open Soc'y Int'l, Inc. v. United States Agency for Int'l Dev., 911 F.3d 104, 112 (2d Cir. 2018), rev'd on other grounds sub nom., Agency for Int'l Dev. v. All. for Open Soc'y Int'l, Inc., 140 S. Ct. 2082 (2020) (citation omitted). An injunction may be overbroad “when it seeks to restrain the defendants from engaging in legal conduct, or from

engaging in illegal conduct that was not fairly the subject of litigation.” Mickalis, 645 F.3d at 145. An order entering an injunction that refers to extrinsic documents or is not tailored to the specific facts of the case does not meet the standard of Rule 65(d). See, e.g., Corning, 365 F.3d at 157–58; Howard Opera House Assocs. v. Urb. Outfitters, Inc., 322 F.3d 125, 130 (2d Cir. 2003). The specificity requirement is satisfied, however, when the terms of an injunction cannot be drawn more narrowly without “unduly complicating its enforcement and impairing its effectiveness.” Peregrine Myanmar Ltd. v. Segal, 89 F.3d 41, 51 (2d Cir. 1996). Shkreli first objects to components of three of the

injunction’s definitions. The definitions are of the terms Development, FDA Authorization, and Pharmaceutical Company. The plaintiffs have agreed to remove the term Marketing Authorization Applications, which refers to procedures in the European Union and the United Kingdom, from the definition of FDA Authorization but otherwise oppose the Shkreli objections. Shkreli’s remaining objections are overruled. In addition to the reasons given by the plaintiffs for retaining the definitions, Shkreli’s objections are denied to the extent that they depend on a restrictive description of the trial record. Shkreli is wrong to suggest that pharmaceutical research and development activities and that conduct outside the

United States were not among the conduct at issue in this case. Shkreli and Vyera used the promise that Vyera would engage in research and development activities to recruit Vyera executives and to induce one of the restrictive supply agreements at issue here. At trial, Shkreli sought to justify his anticompetitive conduct by his need for supracompetitive profits to fund such research and development work. Vyera and its generic drug competitors depended on a global network of API suppliers and drug manufacturers to provide pyrimethamine to American distributors, medical providers, and patients. Thus, while Shkreli’s violation of our nation’s antitrust laws arose from his conduct and its anticompetitive impact within our borders,

it denies reality to suggest that that anticompetitive activity could have succeeded without a coordinated effort that reached into the global pharmaceutical market. Similarly, Shkreli’s objection to the definition of Pharmaceutical Company fails. He contends that the definition is vague and could prevent him from working, for example, at a university that is engaged in pharmaceutical research or at an advertising agency that assists in the marketing of drugs. The injunction defines Pharmaceutical Company as “any Entity engaged in the research, Development, manufacture, commercialization, or marketing of any Drug Product or API.”1 In response to this and a related objection, the plaintiffs

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Federal Trade Commission v. Vyera Pharmaceuticals, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/federal-trade-commission-v-vyera-pharmaceuticals-llc-nysd-2022.