Ball v. Baker

CourtDistrict Court, S.D. New York
DecidedDecember 19, 2022
Docket7:21-cv-06418
StatusUnknown

This text of Ball v. Baker (Ball v. Baker) 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
Ball v. Baker, (S.D.N.Y. 2022).

Opinion

USDC SDNY DOCUMENT ELECTRONICALLY FILED UNITED STATES DISTRICT COURT DOC #: SOUTHERN DISTRICT OF NEW YORK DATE FILED: 12/19/2022

DONALD A. BALL, derivatively on behalf of REGENERON PHARMACEUTICALS, INC., Plaintiff, -against-

CHARLES A. BAKER; MICHAEL S. BROWN; JOSEPH L. GOLDSTEIN; CHRISTINE A. POON; ARTHUR F. RYAN; LEONARD S. SCHLEIFER; GEORGE L. SING; MARC TESSIER-LAVIGNE; . P. ROY VAGELOS; GEORGE D. MO NON eR YANCOPOULOS; ROBERT TERIFAY; MURRAY GOLDBERG; ROBERT E. LANDRY; BONNIE L. BASSLER; N. ANTHONY COLES; and HUDA Y. ZOGHBI, Defendants. -and-

REGENERON PHARMACEUTICALS, INC., Nominal Defendant.

NELSON S. ROMAN, United States District Judge: Plaintiff Donald A. Ball (‘Plaintiff’) commenced the instant action, derivatively on behalf of nominal defendant Regeneron Pharmaceuticals, Inc. (“Regeneron”), in the Supreme Court of New York on June 29, 2021. Defendants Charles A. Baker, Michael S. Brown, Joseph L. Goldstein, Christine A. Poon, Arthur F. Ryan, Leonard S. Schleifer, George L. Sing, Marc Tessier- Lavigne, P. Roy Vagelos, George D. Yancopoulos, Robert Terifay, Murray Goldberg, Robert E. Landry, Bonnie L. Bassler, N. Anthony Coles, and Huda Y. Zoghbi (collectively, “Defendants’)

]

removed the action to this Court on July 28, 2021, under 28 U.S.C. §§ 1331 and 1441. (ECF Nos. 1-3.) Presently before the Court are (1) Plaintiff’s motion to remand (ECF No. 23); and (2) Defendants’ motion to dismiss or, in the alternative, to stay (ECF No. 27). For the following

reasons, Plaintiff’s motion to remand is DENIED. Defendant’s motion to stay is GRANTED. BACKGROUND1 The instant action is a shareholder derivative suit arising from the allegedly improper behavior of Regeneron. The allegations emanate from another lawsuit against Regeneron by the United States currently pending in the District Court of Massachusetts. See United States v. Regeneron Pharms., Inc., No. CV 20-11217-FDS, 2020 WL 7130004 (D. Mass. Dec. 4, 2020) (“DOJ action”). Regeneron, a pharmaceutical company, manufactures Eylea, a drug that treats neovascular age-related macular degeneration, or wet AMD. (Complaint” or “Compl.” at 1, ECF No. 1-1.) Wet AMD is a prevalent eye disease that affects older adults. (Compl. at 26.) Eylea is administered by

injection at the physician’s office once a month for the first 12 doses, and about 6 to 7 times per year thereafter. (Id.) Medicare, a federally funded insurance program, covers prescription drugs like Eylea. Medicare Part B covers 80 percent of Eylea’s cost for beneficiaries who have met their annual deductible. The beneficiaries themselves are responsible for the remaining 20 percent, known as a copay. The copay incentivizes patients to choose the most cost-effective treatment. Eylea has two main competitors, Avastin and Lucentis, both of which are made by Genentech. (Id.) All three drugs have similar efficacy but divergent prices. (Compl. at 27.) Eylea

1 The following facts are as alleged in the Complaint (ECF No. 1-1) unless otherwise noted. is priced at $1,850 per dose. (Id.) Lucentis costs approximately $2,000 per dose. (Id.) Avastin, when used off-label,2 costs approximately $55 per dose. (Id.) Physicians often prescribe Avastin for patients without insurance. (Id.) For patients with Medicare or other insurance, Eylea and Lucentis cost less than Avastin. (Id.)

On June 24, 2020, the United States initiated the DOJ action against Regeneron in the U.S. District Court for the District of Massachusetts. (Compl. at 7.; see also United States v. Regeneron Pharms., Inc., 2020 WL 7130004.) The core allegation in the DOJ action is that Regeneron improperly covered Eylea’s copay for Medicare beneficiaries through purported charitable donations, which the United States avers violated the federal Anti-Kickback Statute, 42 U.S.C. Section 1320a-7b (“AKS”), and False Claims Act, 31 U.S.C. Sections 3729 et seq (“FCA”). Specifically, the DOJ action alleges that Regeneron financed an “AMD fund” through a now- defunct non-profit foundation, The Chronic Disease Fund (“CDF”). 2020 WL 7130004, at *3. From 2011 through at least 2014, the AMD fund covered Eylea’s copays for physicians who submitted claims to CDF. Id. The United States avers in the DOJ action that “Regeneron

contributed tens of millions of dollars to the AMD fund” during the same period and that Regeneron “continuously communicated with CDF to ensure that it was donating enough to cover the Medicare copays of Eylea patients only.” 2020 WL 7130004, at *2. Regeneron’s funding of CDF allegedly “induced thousands of Medicare-reimbursed purchases of Eylea, resulting in tens of millions of dollars of Medicare claims.” 2020 WL 7130004, at *5 (internal quotations omitted). On December 4, 2020, Chief Judge F. Dennis Saylor of the District of Massachusetts denied Regeneron’s motion to dismiss the DOJ action pursuant to Rules 12(b)(6) and 9(b). 2020 WL 7130004, at *1.

2 According to the Complaint, “off-label prescription of a drug is for a condition or use other than that for which the drug has been officially approved.” (Compl. at 25, n.8.) Plaintiff avers that Medicare has spent $11.5 billion on Eylea since 2013. (Compl. at 7.) Citing the United States’ DOJ action complaint, Plaintiff maintains that before Regeneron began selling Eylea in late 2011, Regeneron internally considered a price range of $1,500 to $1,950. (Compl. at 7.) Plaintiff asserts that the individual Defendants chose the higher-end price of $1,850

knowing that Regeneron would cover patient co-pays through illicit donations to CDF, a “kickbacks” scheme which the individual Defendants understood to defy 42 U.S.C. § 1320-7b(b). (Compl. at 8.) Plaintiff additionally alleges that “many of the Individual Defendants, including a majority of the current Board members, collectively sold over $650 million in Regeneron stock (pursuant to the exercise of stock options) during this time.” (Compl. at 9.) Thus, “[t]his derivative action seeks to recover those damages for the benefit of the Company from the true wrongdoers – the officers and directors of Regeneron.” (Compl. ¶ 16.) On June 29, 2021, Plaintiff commenced the instant action in New York Supreme Court, Westchester County, alleging: (1) breach of fiduciary duty against all individual Defendants under

N.Y. Bus. Corp. Law § 717 and New York common law; and (2) breach of fiduciary duty for insider stock selling under New York common law against twelve of the fifteen individual Defendants. (Compl. at 62-64.) Plaintiff’s Complaint incorporates the DOJ action and alleges the same conduct by Regeneron in violation of AKS and FCA. (Compl. at 14-15). On July 28, 2021, Defendants timely removed the action to this Court. On September 23, 2021, Plaintiff moved to remand the action to state court. On September 27, 2021, Defendants moved to dismiss the Complaint for failure to state a claim or to stay the action pending the resolution of the DOJ action. LEGAL STANDARD I. Removal A “civil action” initially filed in state court may be removed by the defendant to the federal district court embracing the place where the state court action is pending, so long as the district

court has original subject matter jurisdiction over the plaintiff’s claim. See 28 U.S.C. § 1441; Lupo v.

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Ball v. Baker, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ball-v-baker-nysd-2022.