CIGNA CORPORATION v. CELGENE CORPORATION

CourtDistrict Court, D. New Jersey
DecidedMay 24, 2021
Docket2:21-cv-11686
StatusUnknown

This text of CIGNA CORPORATION v. CELGENE CORPORATION (CIGNA CORPORATION v. CELGENE CORPORATION) 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
CIGNA CORPORATION v. CELGENE CORPORATION, (D.N.J. 2021).

Opinion

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

CIGNA CORPORATION, CIVIL ACTION

Plaintiff, NO. 21-90-KSM v.

CELGENE CORPORATION, et al.,

Defendants.

MEMORANDUM MARSTON, J. May 24, 2021 Plaintiff Cigna Corporation filed this action against Defendants Celgene Corporation and its parent company Bristol-Meyers Squibb Corporation (“BMS”) (collectively Defendants) alleging that Defendants violated federal and state antitrust laws by suppressing generic competition against Celgene’s Thalomid and Revlimid drugs. (Doc. No. 1.) Presently before the Court is the parties’ joint motion to transfer venue to the District of New Jersey pursuant to 28 U.S.C. § 1404(a). (Doc. No. 17.) Following a status conference with the Court, the parties filed a supplemental memorandum in support of their joint motion to transfer providing additional information related to BMS’s presence in the Eastern District of Pennsylvania.1 (Doc. No. 19.) For the reasons that are discussed below, the parties’ joint motion will be granted. I. Cigna’s complaint alleges six counts against Defendants: (I) violation of Section 2 of the Sherman Act; (II) a monopolization and monopolistic scheme under various state laws; (III) an

1 The parties also argued that if the Court were to find venue improper, transfer to the District of New Jersey would also be proper pursuant to 28 U.S.C. § 1406(a). (Doc No. 19 at 2–3.) attempted monopolization under state laws; (IV) unfair and deceptive trade practices under state laws; (V) unjust enrichment under state laws; and (VI) declaratory and injunctive relief under Section 16 of the Clayton Act for Celgene’s violations of Section 2 of the Sherman Act. (Id. at ¶¶ 448–89.) The facts of this action are complex, as evidenced by Cigna’s 131-page complaint. As relevant to this Memorandum, the facts are as follows.2

Cigna is a Delaware corporation with a principal place of business in Bloomfield, Connecticut. (Doc. No. 1 at ¶ 14.) Cigna is the parent company of or is otherwise affiliated with businesses that operate specialty pharmacies, health insurance plans, and prescription drug plans. (Id. at ¶¶ 15–16.) Celgene is a pharmaceutical company, incorporated in Delaware and with a principal place of business in Summit, New Jersey, that manufactures and markets Thalomid and Revlimid. (See id. at ¶ 19.) BMS is Celgene’s parent company and is incorporated in Delaware, with a principal place of business in New York City, New York. (Id. at ¶ 20.) BMS has owned Celgene since January 2, 2019. (Id.) According to the parties’ supplemental memorandum in support of their joint transfer motion, BMS also leases a storage facility in Falsington,

Pennsylvania, which is located within the Eastern District of Pennsylvania. (Doc. No. 19 at ¶ 4.) The prescription drug market is subject to a complex regulatory scheme designed to balance the intellectual property rights of pharmaceutical companies, patient health and safety, and the benefits of free-market competition. (See id. at ¶¶ 21–67.) Federal law requires companies that invent a new drug to obtain approval from the Food and Drug Administration

2 Unless otherwise noted, these facts are all drawn from Cigna’s complaint. At this stage of the litigation, we take the well-pleaded allegations in Cigna’s complaint as true. See Lewis v. Nat’l Bd. of Osteopathic Med. Exam’rs, Civil Action No. 20-4368, 2020 WL 7260747, at *1 n.1 (E.D. Pa. Dec. 10, 2020). (“FDA”) before they may sell the drug.3 (Id. at ¶ 28 (citing 21 U.S.C. § 355(b)).) At issue in this suit are the allegedly unlawful tactics that Defendants purportedly employed to protect two of Celgene’s name-brand drugs, Thalomid and Revlimid, from generic competition. (Id. at ¶ 1.) Cigna alleges that Celgene manipulated its Risk Evaluation and

Mitigation Strategy (“REMS”) programs for these drugs, abused the patent process related to them, and filed baseless citizen petitions, all to prevent generic manufacturers from producing generic versions of the drugs. (Id.) Cigna also alleges that when these efforts failed, Celgene paid off generic manufacturers to delay bringing their generic versions of the drugs to market. (Id. at ¶ 2. See generally id. at ¶¶ 77–417.) But for this alleged misconduct, Cigna claims that generic Thalomid would have been commercially available in early 2009, and generic Revlimid would have entered the market in or around 2010. (Id. at ¶¶ 419–420.) The result of Celgene’s conduct, Cigna says, was the illegal maintenance of a monopoly over the sale of Thalomid and Revlimid, allowing Celgene to artificially inflate the prices of these drugs without fear of lost sales. (Id. at ¶ 430.) Additionally,

Cigna asserts that it was personally injured by Celgene’s alleged misconduct in that the misconduct forced Cigna to spend more money on Thalomid and Revlemid than it would have otherwise had to if those drugs were subject to generic competition. (Id. at ¶ 425.) Cigna and its subsidiaries have purchased both Thalomid and Revlemid from Celgene in this District. (Id. at ¶ 12.) This is one of several cases that has been filed in federal and state courts across the country by various plaintiffs alleging the same basic violations against Defendants. (See Doc.

3 New drugs that are approved by the FDA become known as “brand-name drugs”; when these same drugs are manufactured and sold by other companies, they are known as “generic drugs.” See Generic Drug Facts, U.S. FOOD & DRUG ADMIN., https://www.fda.gov/drugs/generic-drugs/generic-drug-facts (last accessed May 6, 2021). No. 17 at ¶¶ 2, 10.) In this case, as well as at least three other cases, Defendants have filed motions to transfer to the District of New Jersey, where similar cases are pending.4 II. Although the parties have stipulated to a transfer of venue to the District of New Jersey,

the Court must independently evaluate whether transfer is appropriate. See White v. ABCO Eng’g Corp., 199 F.3d 140, 142 (1999) (“We conclude that § 1404(a) transfers may not be made simply by stipulation.”). “In addressing a motion to transfer, ‘all well-pleaded allegations in the complaint are generally taken as true unless contradicted by the defendant’s affidavits, and the Court may examine facts outside the complaint to determine proper venue.’” Lewis, 2020 WL 7260747, at *1 n.1 (quoting Holiday v. Bally’s Park Place, Inc., CV No. 06-4588, 2007 WL 2600877, at *1 (E.D. Pa. Sept. 10, 2007)). In federal court, venue transfers are governed by 28 U.S.C. §§ 1404(a) and 1406(a). Jumara v. State Farm Ins. Co., 55 F.3d 873, 878 (3d Cir. 1995). Section 1404(a) governs transfer when “both the original and the requested venue are proper.” Id. Under § 1404(a), a

district court may for the convenience of the parties and witnesses and if it is in the interest of justice “transfer any civil action to any other district or division where it may have been brought or to any district or division to which all parties have consented.” See 28 U.S.C. § 1404(a).

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CIGNA CORPORATION v. CELGENE CORPORATION, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cigna-corporation-v-celgene-corporation-njd-2021.