Khoja v. Orexigen Therapeutics, Inc.

District Court, S.D. California·Decided November 2, 2020·No. 3:15-cv-00540·Unknown

Opinion

KARIM KHOJA, on behalf of himself and Case No.: 15-CV-540 JLS (JLB) all others similarly situated, ORDER (1) GRANTING IN PART Plaintiff, AND DENYING IN PART MOVING v. DEFENDANTS’ REQUEST TO CONSIDER MATERIALS OREXIGEN THERAPEUTICS, INC., INCORPORATED BY REFERENCE, JOSEPH P. HAGAN, MICHAEL A. AND (2) GRANTING MOVING NARACHI, and PRESTON KLASSEN, DEFENDANTS’ PARTIAL MOTION Defendants. TO DISMISS

AND ALL CONSOLIDATED CASES (ECF No. 114)

Presently before the Court is Moving Defendants Joseph P. Hagan, Michael A. Narachi, and Preston Klassen, M.D., M.H.S.’s Partial Motion to Dismiss Consolidated Amended Complaint for Violation of the Federal Securities Laws (“Mot.,” ECF No. 114),1 as well as Lead Plaintiff Karim Khoja’s Opposition to (“Opp’n,” ECF No. 115) and Moving Defendants’ Reply in Support of (“Reply,” ECF No. 116) the Motion.

1 Defendant Orexigen Therapeutics, Inc., filed a voluntary petition for bankruptcy under Chapter 11, see In re Orexigen Therapeutics, Inc., No. 18-10518-KG (Bankr. D. Del. filed Mar. 12, 2018); consequently, pursuant to the automatic bankruptcy stay, see 11 U.S.C. § 362(a), Orexigen is not a party to this Motion, Also before the Court are Moving Defendants’ Request to Consider Documents Incorporated by Reference into the Consolidated Amended Complaint for Violation of the Federal Securities Laws in Support of Defendants’ Partial Motion to Dismiss (“Defs.’ Req.,” ECF No. 114-9), Lead Plaintiff’s Notice of Supplemental Authority in Support of Opposition to Defendants’ Partial Motion to Dismiss the Consolidated Amended Complaint (“1st Not. of Supp. Auth.,” ECF No. 118), Moving Defendants’ Response to Lead Plaintiff’s Notice of Supplemental Authorities (“Resp. to 1st Not. of Supp. Auth.,” ECF No. 119), Lead Plaintiff’s Notice of Supplemental Authorities in Support of Opposition to Defendants’ Partial Motion to Dismiss the Consolidated Amended Complaint (“2d Not. of Supp. Auth.,” ECF No. 126), Moving Defendants’ Response to Lead Plaintiff’s Notice of Supplemental Authorities (“Resp. to 2d Not. of Supp. Auth.,” ECF No. 127), Lead Plaintiff’s Third Notice of Supplemental Authorities in Support of Opposition to Defendants’ Partial Motion to Dismiss the Consolidated Amended Complaint (“3d Not. of Supp. Auth.,” ECF No. 128), Lead Plaintiff’s Notice of Recent Controlling Authority (“4th Not. of Supp. Auth.,” ECF No. 136), Moving Defendants’ Response to Lead Plaintiff’s Notice of Recent Controlling Authority (“Resp. to 4th Not. of Supp. Auth.,” ECF No. 137), and Lead Plaintiff’s Reply to Defendants’ Response to Lead Plaintiff’s Notice of Recent Controlling Authority (“Reply ISO 4th Not. of Supp. Auth.,” ECF No. 138). The Court vacated the hearing and took the Motion under submission without oral argument pursuant to Civil Local Rule 7.1(d)(1). See ECF No. 117. Having carefully considered Lead Plaintiff’s Consolidated Amended Complaint (“CAC,” ECF No. 111) and the material appropriately incorporated by reference, the Parties’ arguments, and the law, including the cases identified in Lead Plaintiff’s Notices of Supplemental Authority, the Court GRANTS IN PART AND DENIES IN PART Moving Defendants’ Request to Consider Documents Incorporated by Reference and GRANTS Moving Defendants’ Motion. / / / The factual and procedural background of this case was set forth in detail in this Court’s September 23, 2019 Order (1) Granting in Part and Denying in Part the Moving Defendants’ Request for Judicial Notice, (2) Denying Lead Plaintiff’s Request for Judicial Notice, and (3) Granting in Part and Denying in Part the Moving Defendants’ Motion to Dismiss. See ECF No. 110 at 2–14. To the extent relevant, the Court incorporates that recitation into this Order. Accordingly, the Court sets forth below only those facts relevant to the instant Motion3 and the procedural history since the issuance of this Court’s September 23, 2019 Order. I. Factual Background Orexigen, “a developmental stage biotechnology firm,” has a collaboration agreement with Takeda Pharmaceutical Company Limited (“Takeda”) to develop and commercialize Orexigen’s “primary product candidate,” a drug for the treatment of obesity called Contrave, in the United States, Canada, and Mexico. CAC ¶ 7. Phase III clinical trials have been completed, and Contrave “was being studied in a drug trial known as the

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Khoja v. Orexigen Therapeutics, Inc., (S.D. Cal. 2020).

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