Blue Cross and Blue Shield of Massachusetts, Inc. v. Regeneron Pharmaceuticals, Inc.

CourtDistrict Court, D. Massachusetts
DecidedSeptember 27, 2022
Docket1:21-cv-12094
StatusUnknown

This text of Blue Cross and Blue Shield of Massachusetts, Inc. v. Regeneron Pharmaceuticals, Inc. (Blue Cross and Blue Shield of Massachusetts, Inc. v. Regeneron Pharmaceuticals, Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Blue Cross and Blue Shield of Massachusetts, Inc. v. Regeneron Pharmaceuticals, Inc., (D. Mass. 2022).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF MASSACHUSETTS

_______________________________________ ) BLUE CROSS AND BLUE SHIELD OF ) MASSACHUSETTS, INC., and ) BLUE CROSS AND BLUE SHIELD OF ) MASSACHUSETTS HMO BLUE, INC., ) ) Plaintiffs, ) ) Civil Action No. v. ) 21-12094-FDS ) REGENERON ) PHARMACEUTICALS, INC., ) ) Defendant. ) _______________________________________)

MEMORANDUM AND ORDER ON DEFENDANT’S MOTION TO TRANSFER, STAY, OR DISMISS SAYLOR, C.J. This is an action alleging a kickback scheme arising out of a pharmaceutical company’s donations to a charity. Plaintiffs Blue Cross and Blue Shield of Massachusetts, Inc., and Blue Cross and Blue Shield of Massachusetts HMO Blue, Inc., have sued defendant Regeneron Pharmaceuticals, Inc., alleging that Regeneron used an illegal kickback scheme to boost sales of Eylea, its signature eye-disease drug. Plaintiffs assert claims under 18 U.S.C. § 1962 and Mass. Gen. Laws ch. 93A, § 9. Plaintiffs also contend that Regeneron’s actions amount to fraudulent concealment, fraud, tortious interference with contract, and unjust enrichment.1 Regeneron has moved to transfer, stay, or dismiss the complaint. It asks that the Court

1 In two separate actions, Horizon Healthcare Services and Medical Mutual of Ohio have made essentially identical allegations against Regeneron. (See Compl. ¶¶ 5-12, Horizon Healthcare Servs., Inc. v. Regeneron Pharm., Inc., No. 1:22-cv-10493-FDS (D. Mass. Apr. 4, 2022); Compl. ¶¶ 5-12, Medical Mut. of Ohio v. Regeneron Pharm., Inc., No. 1:22-cv-10302-FDS (D. Mass. Feb. 23, 2022). either transfer the case to the Southern District of New York or stay the case pending resolution of a Department of Justice civil action against Regeneron in this court. In addition, Regeneron has moved to dismiss the complaint on two grounds: that the claims are time-barred and for failure to plead fraud with particularity under Fed. R. Civ P. 9(b). For the following reasons, the motion to transfer will be denied and the motion to stay

will be granted. The motion to dismiss will remain pending during the period the stay is in force. I. Background A. Factual Background Unless otherwise noted, the facts are stated as set forth in the complaint. Blue Cross and Blue Shield of Massachusetts, Inc., and Blue Cross and Blue Shield of Massachusetts HMO Blue., Inc., (collectively, “Blue Cross”) are health-insurance companies headquartered in Boston, Massachusetts. (Compl. ¶ 1). Among other services, Blue Cross, through contracts with the Centers for Medicare and Medicaid Services, provides Medicare benefits to Medicare Part C and Medicare Part D recipients. (Id. ¶ 2). Blue Cross also provides private commercial health-plan benefits. (Id.). Blue Cross covers prescription-drug costs under both Medicare and private health plans. (Id.).

Regeneron Pharmaceuticals, Inc., is a pharmaceutical company based in Tarrytown, New York. (Id. ¶ 4). Regeneron sells Eylea, a treatment for wet age-related macular degeneration, an eye disease. (Id. ¶ 12). In 2020, Eylea sales generated $4.9 billion for Regeneron, more than half of its sales revenue for that year. (Id. ¶ 113). According to the complaint, Regeneron used the Chronic Disease Foundation (“CDF”) to boost sales of Eylea, making it the dominant treatment for wet age-related macular degeneration. CDF is a charity headquartered in Texas that relies on donations from drug manufacturers to assist patients with their cost-sharing obligations for drugs, including Eylea. (Def. Mem. at 13; Compl. ¶ 64). The complaint alleges that from 2013 to 2020, Regeneron coordinated its donations with CDF by contributing exactly enough money to cover CDF’s Eylea co-pay assistance, with no funds left over to pay for any other drug. (Compl. ¶¶ 77, 84). This alleged kickback scheme allowed Regeneron to directly subsidize Eylea treatments, encouraging patients

to pick Eylea over competing products such as Lucentis and Avastin. (Id. ¶¶ 82-83). CDF profited from this arrangement by taking a portion of Regeneron’s funding as a fee. (Id. ¶ 85). According to the complaint, Regeneron enlisted the Lash Group to advertise the CDF co- pay assistance program. The Lash Group is a pharmaceutical-industry consulting firm headquartered in South Carolina. (Id. ¶ 93; Def. Mem. at 13). Lash created an advertising program that referred physicians to CDF, assuring physicians that patients to whom they prescribed Eylea would receive co-pay assistance through CDF. (Compl. ¶¶ 98-100). Lash’s advertisements represented that CDF was an independent charity. (Id. ¶ 96). Blue Cross alleges that it has paid more than $100 million to cover the cost of providing

Eylea to patients. (Id. ¶ 115). According to the complaint, its contract with CMS to provide Medicare benefits requires it to comply with 42 U.S.C. § 1320a-7b, the federal anti-kickback statute. (Id. ¶ 92). It contends that the scheme violated the anti-kickback statute by causing healthcare providers to submit Eylea treatment claims that were ultimately subsidized by a drug manufacturer. (Id. ¶¶ 54-55). In addition, it contends that both its Medicare and private commercial plans contain cost provisions that require patients to pay a portion of drug costs, and that CDF’s co-pay assistance violated these contract provisions. (Id. ¶ 43). According to the complaint, the kickback scheme first came to light in 2020, when the Department of Justice filed a civil action against Regeneron in this court. (Id. ¶ 57). The DOJ action is based on the same alleged kickback scheme. (See Am. Compl. ¶¶ 1-5, United States v. Regeneron Pharm., Inc., No. 1:20-cv-11217-FDS (D. Mass. Aug. 24, 2021)). As in this case, the complaint in the DOJ action alleges that Regeneron violated the anti-kickback statute. (Id. ¶¶ 91-96). The DOJ action is currently in the discovery stage. Four other similar civil actions based on Regeneron’s alleged kickback scheme are

pending in the federal courts. Two actions in the Southern District of New York have been stayed pending resolution of the DOJ action. See UnitedHealthcare Ins. Co. v. Regeneron Pharm., 2021 WL 6137097, at *1 (S.D.N.Y. Dec. 29, 2021). The other two actions are before this court, and Regeneron has filed essentially identical motions to transfer, stay, or dismiss in both. (See Def. Mem. at 1, Horizon Healthcare Servs., Inc. v. Regeneron Pharm., Inc., No. 1:22- cv-10493-FDS (D. Mass. June 13, 2022); Def. Mem. at 1, Medical Mut. of Ohio v. Regeneron Pharm., Inc., No. 1:22-cv-10302-FDS (D. Mass. May 31, 2022)). B. Procedural Background On December 20, 2021, Blue Cross filed this action against Regeneron. The complaint asserts six claims: violation of 18 U.S.C. § 1962; conspiracy to violate 18 U.S.C. § 1962;

violation of Mass. Gen. Laws ch. 93A, § 9; fraudulent concealment and fraud; tortious interference with contract; and unjust enrichment. Regeneron has moved to transfer this case to the Southern District of New York under 28 U.S.C. § 1404(a), and has also moved to stay the action pending resolution of the DOJ action. In addition, it has moved to dismiss the complaint for failure to state a claim pursuant to Fed. R. Civ. P.

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Blue Cross and Blue Shield of Massachusetts, Inc. v. Regeneron Pharmaceuticals, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/blue-cross-and-blue-shield-of-massachusetts-inc-v-regeneron-mad-2022.