In re Restasis (Cyclosporine Ophthalmic Emulsion) Antitrust Litig.

355 F. Supp. 3d 145
CourtDistrict Court, E.D. New York
DecidedNovember 8, 2018
Docket18-MD-2819 (NG) (LB)
StatusPublished
Cited by9 cases

This text of 355 F. Supp. 3d 145 (In re Restasis (Cyclosporine Ophthalmic Emulsion) Antitrust Litig.) is published on Counsel Stack Legal Research, covering District Court, E.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Restasis (Cyclosporine Ophthalmic Emulsion) Antitrust Litig., 355 F. Supp. 3d 145 (E.D.N.Y. 2018).

Opinion

NINA GERSHON, United States District Judge

TABLE OF CONTENTS

I. INTRODUCTION...150

II. PLAINTIFFS' ALLEGATIONS...150

III. LEGAL STANDARD...151

IV. ANALYSIS...151

A. Plaintiffs' State Law Antitrust Claims...151

1. Arkansas, Florida, Hawaii, Minnesota, and Missouri...151
Arkansas...152
Florida...154
Hawaii...154
Minnesota...156
Missouri...157
2. In-State Impact under Tennessee and Wisconsin Law...157

B. Plaintiffs' State Law Consumer Protection Claims...158

Arkansas...158
California...159
Colorado...159
Pennsylvania...160
Vermont...161

V. CONCLUSION...162 *150I. INTRODUCTION

This multi-district litigation arises out of defendant Allergan's alleged actions to improperly delay the market entry of generic competitors to its dry-eye medication Restasis ® (cyclosporine ophthalmic emulsion). There are two groups of plaintiffs: those that purchased Restasis ® directly from Allergan and End-Payor Plaintiffs ("EPPs"), health and welfare funds that purchased (or reimbursed members' purchases of) Restasis ® from distributors or retailers. Both groups contend that the price they paid for Restasis ® would have been lower if Allergan had faced competition from generic manufacturers and that they were also deprived of the opportunity to purchase lower-priced, generic versions of the drug.

The EPPs are precluded from asserting federal damages claims under Illinois Brick Co. v. Illinois , 431 U.S. 720, 97 S.Ct. 2061, 52 L.Ed.2d 707 (1977), which interpreted federal antitrust law to preclude indirect purchasers from recovering damages in order to avoid "a serious risk of multiple liability for defendants" and "whole new dimensions of complexity to treble-damages suits [which would] seriously undermine their effectiveness." Id. at 730, 737, 97 S.Ct. 2061. However, the Supreme Court has recognized that, although federal antitrust law does not permit indirect purchasers to recover damages, neither does it preempt state antitrust statutes that do so. California v. ARC Am. Corp. , 490 U.S. 93, 105-06, 109 S.Ct. 1661, 104 L.Ed.2d 86 (1989). In their Consolidated Complaint, EPPs seek injunctive relief under the Clayton Act, 15 U.S.C. § 26, and declaratory relief under 28 U.S.C. § 2201 for alleged violations of sections 1, 2, and 3 of the Sherman Act, 15 U.S.C. §§ 1 - 3. And plaintiffs bring their claims for monetary damages only under the antitrust and consumer protection laws of various states, Puerto Rico, and the District of Columbia.

Allergan now moves under Rule 12(b)(6) of the Federal Rules of Civil Procedure to dismiss certain claims brought under the laws of some of the jurisdictions. For the reasons set forth below, Allergan's motion is granted in part and denied in part.

II. PLAINTIFFS' ALLEGATIONS

For a full recitation of plaintiffs' factual allegations, I refer to my Opinion and Order dated September 18, 2018 denying defendant's motion to dismiss for failure to allege causation. (Docket No. 146.) Briefly, EPPs allege that Allergan took a number of improper actions to delay the Food and Drug Administration ("FDA") in approving generic competitors for Restasis ®, including: (1) filing sham citizen petitions with the FDA; (2) defrauding the U.S. Patent and Trademark Office ("USPTO") into issuing second-wave patents for Restasis ®; (3) using those patents to file baseless patent infringement lawsuits, further delaying the FDA's approval process for generic Restasis ® equivalents; and (4) when it appeared that its patents were likely to be invalidated, transferring those patents to the Saint Regis Mohawk Tribe, which licensed them back, in an effort to frustrate invalidation of the patents by renting the Tribe's sovereign immunity. As a result, EPPs allege that Allergan has maintained a monopoly for several years beyond what it would have had absent its wrongful conduct and has used that monopoly to charge an inflated price for Restasis ®. The EPPs assert that they have been injured because they overpaid for cyclosporine.

EPPs bring five claims, only two of which are at issue on this motion.1 The *151Second Claim challenges Allergan's monopolistic conduct and seeks damages under the laws of 22 jurisdictions on an antitrust theory. The Third Claim challenges Allergan's unfair, unconscionable, deceptive, and fraudulent conduct under the consumer protection laws of five states. For each claim, EPPs rely on the same factual allegations.

Allergan moves to dismiss the antitrust claims as to eight of the 22 jurisdictions,2 and moves to dismiss the consumer protection claims as to each of the five jurisdictions. In their opposition, EPPs voluntarily withdraw their claims brought under the laws of Puerto Rico, but they oppose dismissal of their other claims.

III. LEGAL STANDARD

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355 F. Supp. 3d 145, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-restasis-cyclosporine-ophthalmic-emulsion-antitrust-litig-nyed-2018.