Cerovene, Inc. v. Fukuzyu Pharmaceutical Co., Ltd.

CourtDistrict Court, S.D. New York
DecidedMarch 10, 2025
Docket1:24-cv-00464
StatusUnknown

This text of Cerovene, Inc. v. Fukuzyu Pharmaceutical Co., Ltd. (Cerovene, Inc. v. Fukuzyu Pharmaceutical Co., Ltd.) 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
Cerovene, Inc. v. Fukuzyu Pharmaceutical Co., Ltd., (S.D.N.Y. 2025).

Opinion

UNITED STATES DISTRICT COURT SOUTHERN DISTRICT OF NEW YORK

CEROVENE, INC. and DR. REDDY’S LABORATORIES, INC.,

Plaintiffs, No. 24-CV-464 (RA) v. MEMORANDUM FUKUZYU PHARMACEUTICAL CO., OPINION & ORDER LTD., Defendant.

RONNIE ABRAMS, United States District Judge: On January 22, 2024, Plaintiffs Cerovene, Inc. and Dr. Reddy’s Laboratories, Inc. initiated this antitrust action against Defendant Fukuzyu Pharmaceutical, Co. (“Fukuzyu”), alleging that Defendant violated Sections 1 and 2 of the Sherman Act by entering an illegal agreement in restraint of trade and a conspiracy to monopolize the U.S. market for the pharmaceutical drug Daraprim. Before this Court is Defendant’s motion to dismiss the Complaint for lack of personal jurisdiction and failure to state a claim. Defendant also moves for this Court to take judicial notice of a prior motion for, and an order approving, a settlement agreement between Plaintiffs and non- parties Vyera Pharmaceuticals, LLC (“Vyera”) and its parent company. Plaintiffs oppose both motions. For the reasons that follow, the Court orders jurisdictional discovery and denies Defendant’s motions without prejudice to renew. BACKGROUND The Court assumes the parties’ familiarity with the underlying facts and recites here only the facts pertinent to the Court’s instant opinion and order.1 Defendant is a Japanese company that manufactures pyrimethamine, the key active pharmaceutical ingredient (“API”) in Daraprim—a medication used in the treatment of acute parasitic infections for individuals with HIV infections. Am. Compl. ¶¶ 1–2, 4, 15, 36–37, ECF No. 30 (“AC”). Plaintiffs allege that Defendant conspired

with the pharmaceutical company Vyera to preserve its monopoly position over Daraprim in the U.S. market by refusing to supply pyrimethamine to Vyera’s potential market competitors, thereby preventing generic versions of Daraprim from entering the market. Id. ¶¶ 3–5. As a result of the anticompetitive conspiracy, Plaintiffs were delayed in entering the market. Id. ¶ 6. In 2013, two years before Vyera’s acquisition of Daraprim, Cerovene had begun developing a generic version of Daraprim and had partnered with Dr. Reddy’s Laboratories to market and sell the generic once approved. Id. ¶¶ 12–14. During the drug development phase for the generic in 2015, Cerovene attempted to purchase pyrimethamine from Defendant, the only supplier of Daraprim API approved by the U.S. Federal Drug Administration (“FDA”) at that time. Id. ¶¶ 4, 45, 55, 56. Negotiations took place through Sumitomo Corporation of Americas (“Sumitomo”), a

New York-based company, and its Japanese subsidiary Summit Pharmaceutical International. Id. ¶¶ 21, 55, 57. According to Plaintiffs, negotiations with Defendant proceeded “smoothly” until Cerovene sought to place an order in late 2016. Id. ¶ 55. On October 4, 2016, Sumitomo emailed Cerovene a letter from Defendant, which advised that Defendant would no longer sell pyrimethamine to Plaintiff. Id. ¶ 66 (citing Ex. I). Plaintiffs allege that Defendant sent this letter because Vyera, with whom Defendant had reached an exclusive supply agreement, id. ¶¶ 70–73, instructed Defendant to discontinue negotiations with

1 Unless otherwise noted, the Court draws the following facts from the Amended Complaint, “credit[ing] . . . plaintiff’s averments of jurisdictional facts as true.” In re Magnetic Audiotape Antitrust Litig., 334 F.3d 204, 206 (2d Cir. 2003). Cerovene, id. ¶¶ 67–68. Plaintiffs contend that Defendant ended negotiations with knowledge of and intent to maintain Vyera’s U.S. monopoly as to Daraprim. Id. ¶¶ 72–73. As a threshold matter, Defendant disputes that this Court has personal jurisdiction to hear this action. Accordingly, a key issue before the Court is the nature and extent of the contacts that

Defendant has had with New York. It is undisputed that Defendant is a Japanese company, incorporated under the laws of Japan with its principal place of business in Japan. Id. ¶ 15. In support of its motion to dismiss, however, Defendant submitted the Declaration of Teruo Kosugi, President and CEO of Fukuzyu, which disputes many of Plaintiffs’ factual allegations. Kosugi’s Declaration discusses the nature of Defendant’s negotiations with Cerovene, disclaims Sumitomo as a representative, speaks to Defendant’s contacts in the United States, and contends that Defendant’s negotiations with Vyera took place entirely in Japan. See generally Kosugi Decl., ECF No. 60. Defendant has moved to dismiss the Amended Complaint pursuant to Federal Rules of Civil Procedure 12(b)(2) and 12(b)(6) and moved for the Court to take judicial notice of a prior

motion for, and order granting, a settlement agreement between Plaintiffs, Vyera, and Vyera’s parent company. Plaintiffs oppose both motions. DISCUSSION “In order to survive a motion to dismiss for lack of personal jurisdiction, a plaintiff must make a prima facie showing that jurisdiction exists.” Licci ex rel. Licci v. Lebanese Canadian

Bank, SAL, 732 F.3d 161, 167 (2d Cir. 2013) (quoting Thomas v. Ashcroft, 470 F.3d 491, 495 (2d Cir. 2006)).2 “Determining personal jurisdiction over a foreign defendant in a federal-question case

2 Unless otherwise indicated, case quotations omit all internal citations, quotation marks, footnotes and omissions, and adopt alterations. such as this requires a two-step inquiry.” Id. at 168. The Court examines first whether there is “a statutory basis for personal jurisdiction.” PharmacyChecker.com, LLC v. Nat’l Ass’n of Bds. of Pharmacy, 530 F. Supp. 3d 301, 321 (S.D.N.Y. 2021). “If jurisdiction lies, [the Court] consider[s] whether the district court’s exercise of personal jurisdiction over a foreign defendant comports

with due process protections established under the United States Constitution.” Licci, 732 F.3d at 168. Plaintiffs assert that Section 12 of the Clayton Act as well as three provisions of New York’s long-arm statute, N.Y. C.P.L.R. § 302(a)(1)–(3), provide independent bases for personal jurisdiction over Defendant. The parties’ briefing, and the affidavits submitted in support, however, indicate that determination of the Court’s personal jurisdiction depends on certain facts in dispute. The parties disagree, for instance, as to whether Sumitomo was Defendant’s agent or representative, whether Defendant has solicited business in the United States or New York, the translation of a letter Sumitomo sent to Plaintiffs, and whether Defendant employs a U.S.-based agent to file materials with the FDA. See Def.’s Mem. of Law in Supp. of Mot. to Dismiss 8, 13–

14; see also Kosugi Decl. ¶¶ 6–10, 13–17. The Court thus concludes that jurisdictional discovery is appropriate. See In re Bernard L. Madoff Inv. Sec. LLC, 525 B.R. 871, 881 (S.D.N.Y. 2015) (ordering jurisdictional discovery before deciding 12(b)(2) motion to dismiss); Daventree Ltd. v. Republic of Azerbaijan, 349 F. Supp. 2d 736, 761 (S.D.N.Y. 2004) (ordering jurisdictional discovery); Luke v. Sunwing Travel Grp., No. 20-CV-6141 (PKC) (CLP), 2022 WL 595133, at *5 (E.D.N.Y. Feb. 28, 2022) (same). Defendant argues that Plaintiffs have not made out a prima facie case of personal jurisdiction.

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