Chauhan v. Intercept Pharmaceuticals, Inc.

CourtDistrict Court, S.D. New York
DecidedJanuary 25, 2021
Docket1:21-cv-00036
StatusUnknown

This text of Chauhan v. Intercept Pharmaceuticals, Inc. (Chauhan v. Intercept Pharmaceuticals, Inc.) 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
Chauhan v. Intercept Pharmaceuticals, Inc., (S.D.N.Y. 2021).

Opinion

USDC SDNY DOCUMENT SOUTHERN DISTRICT OF NEW YORK DOC #: annonces nana nna sansa nnscn KK DATE FILED:_ 1/25/2021 RAKESH CHAUHAN, individually and on behalf of all: others similarly situated, : Plaintiff, : 21-cv-00036 (LJL) -V- : OPINION AND ORDER INTERCEPT PHARMACEUTICALS, et al., : Defendants. :

LEWIS J. LIMAN, United States District Judge: Before the Court are competing motions from movants seeking to be appointed lead plaintiff pursuant to the Private Securities Litigation Reform Act of 1995 (“PSLRA”).' 15 U.S.C. § 78u—4(a)(3)(B). Each movant also proposes its respective retained counsel as class counsel. The Court appoints Richard Rice as Trustee of the Richard E. and Melinda Rice Revocable Family Trust 5/9/90 as lead plaintiff and appoints his counsel, Glancy Prongay & Murray LLP, as class counsel. BACKGROUND Plaintiffs bring claims under Sections 10(b) and 20(a) of the Securities Exchange Act of 1934 and Rule 10b—5 promulgated thereunder against Intercept Pharmaceuticals, Inc. (“Intercept” or the “Company’’), Intercept’s president, chief executive officer, and director Mark

' Movants are defined to include Peidong Wu (“Wu”), Trustees of Teamsters Union No. 142 Pension Fund (“Teamsters Union”) and City of Cape Coral Municipal General Employees’ Retirement Plan (“Cape Coral”), Margaret Neale (“Neale”), Paul Weller (“Weller”), City of Fort Lauderdale Police and Fire Retirement System (“Fort Lauderdale”), Paul Sapan (““Sapan’’) and Rony Awaida (“Awaida”), and Richard Rice (“‘Rice” or ““Trustee”) as Trustee of the Richard E. and Melinda Rice Revocable Family Trust 5/9/90 (“Trust”).

Pruzanski, and Intercept’s chief financial officer Sandip Kapadia (collectively, “Defendants”). The action is brought on behalf of all persons and entities other than Defendants that purchased or otherwise acquired Intercept securities between September 28, 2019 and October 7, 2020, inclusive (the “Class Period”). Intercept is a biopharmaceutical company that focuses on the development and

commercialization of therapeutics to treat progressive non-viral liver diseases in the United States. Dkt. No. 1 (“Complaint” or “Compl.”) ¶ 2. Its lead product candidate is Ocaliva (obeticholic acid (“OCA”)), used for the treatment of primary biliary cholangitis (“PBC”), a rare and chronic liver disease. Id. ¶ 3. Intercept is also developing OCA for various other indications, including nonalcoholic steatohepatitis (“NASH”). Id. In 2016, the U.S. Food and Drug Administration (“FDA”) granted accelerated approval of Ocaliva for treating PBC. Id. ¶ 4. In late 2017, both Intercept and the FDA issued warnings concerning the risk of overdosing patients with the drug and multiple reports of severe liver injuries and deaths linked with its use. Id. ¶ 5. The Complaint alleges that, despite these

concerns, Defendants continued to tout Ocaliva sales and purported benefits and its potential indication for treating various other medical conditions. Id. ¶ 6. For example, just two years later, in September 2019, Intercept submitted a New Drug Application (“NDA”) to the FDA for OCA to treat patients with liver fibrosis due to NASH. Id. Specifically, the Complaint alleges that during the Class Period, Defendants made false and/or misleading statements and/or failed to disclose that: (i) Defendants downplayed the true scope and severity of safety concerns associated with Ocaliva’s use in treating PBC; (ii) the foregoing increased the likelihood of an FDA investigation into Ocaliva’s development, thereby jeopardizing Ocaliva’s continued marketability and the sustainability of its sales; (iii) any purported benefits associated with OCA’s efficacy in treating NASH were outweighed by the risks of its use; (iv) as a result, the FDA was unlikely to approve the Company’s NDA for OCA in treating patients with liver fibrosis due to NASH; and (v) as a result of all the foregoing, the Company’s public statements were materially false and misleading at all relevant times. Id. ¶ 7. The trading price of Intercept’s common stock fell substantially in the wake of partial

disclosures made on May 22, 2020, June 29, 2020, and October 8, 2020. Id. ¶¶ 8-13. PROCEDURAL HISTORY The Complaint in this action was filed by Plaintiff Rakesh Chauhan (“Chauhan”) in the Eastern District of New York on November 5, 2020 under the caption Chauhan v. Intercept Pharmaceuticals, Inc., No. 20-cv-5377 (E.D.N.Y.). It was transferred to the Southern District of New York, and this Court specifically, on January 4, 2021 after a joint motion to transfer filed by the parties on December 29, 2020. Dkt. Nos. 9, 10. On January 4, 2021, seven parties timely moved for appointment of lead plaintiff under the PSLRA. Dkt. Nos. 12, 15, 17, 20, 25, 29, 33. On the same day, counsel for Plaintiff Chauhan informed the Court that he had made the requisite notice of the pendency of the action

under the PSLRA on November 5, 2020 by press release in PRNewswire, a national business- oriented wire service. Dkt. No. 28-2; see 15 U.S.C. § 78u–4(a)(3)(A)(i). On January 5, 2021, the Court entered a scheduling order that provided for opposition to any motion for appointment of lead plaintiff to be filed by January 13, 2021. Dkt. No. 36. That order also scheduled a hearing on the motions for January 15, 2021. Id. Four movants, Neale, Fort Lauderdale, Teamsters Union and Cape Coral, and Weller, withdrew their motions for lead plaintiff. Dkt. Nos. 39-41, 45. Movants Wu, Sapan and Awaida, and Rice submitted opposition briefs on January 13, 2021. Dkt. Nos. 46-48. The Court held a hearing on the motions on January 15, 2021. LEGAL STANDARD The PSLRA establishes the framework courts use to select a lead plaintiff in class actions brought under the federal securities laws. First, the PSLRA requires any prospective lead plaintiff to file a motion for appointment as lead plaintiff within sixty days of the publication of notice of the securities class action. 15 U.S.C. § 78u–4(a)(3)(B)(iii)(I)(aa); id. § 78u–

4(a)(3)(A)(i). Next, the PSLRA lays out standards for choosing one lead plaintiff from among the candidates who file motions. The PSLRA provides that: the court shall adopt a presumption that the most adequate plaintiff in any private action arising under this chapter is the person or group of persons that— (aa) has either filed the complaint or made a motion in response to a notice [of the complaint within sixty days of the publication of this notice]; (bb) in the determination of the court, has the largest financial interest in the relief sought by the class; and (cc) otherwise satisfies the requirements of Rule 23 of the Federal Rules of Civil Procedure. Id. § 78u–4(a)(3)(B)(iii)(I). Once the Court identifies a presumptive lead plaintiff, this presumption: may be rebutted only upon proof by a member of the purported plaintiff class that the presumptively most adequate plaintiff— (aa) will not fairly and adequately protect the interests of the class; or (bb) is subject to unique defenses that render such plaintiff incapable of adequately representing the class. Id. § 78u–4(a)(3)(B)(iii)(II). If the Court finds that the movant with the largest financial interest in the class action is otherwise ineligible for appointment as lead plaintiff, the Court applies the criteria of the PSLRA to the movant with the second-highest financial interest. This investigation continues until the Court identifies a suitable lead plaintiff.

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Bluebook (online)
Chauhan v. Intercept Pharmaceuticals, Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/chauhan-v-intercept-pharmaceuticals-inc-nysd-2021.