Molina Healthcare, Inc. v. Celgene Corporation

District Court, N.D. California·Decided January 18, 2022·No. 3:21-cv-05483·Unknown

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF CALIFORNIA

Case No. 21-cv-05483-JCS Plaintiff,

v. ORDER GRANTING MOTION TO REMAND CELGENE CORPORATION, et al., Re: Dkt. No. 14 Defendants. This is one of many cases filed against Defendant Celgene Corporation and its parent Defendant Bristol-Myers Squibb Company (“BMS”) regarding Celgene’s1 efforts to protect the market for two of its prescription drugs, Thalomid and Revlimid, from generic competitors. After opting out of an earlier class action and having been dismissed from a case in Minnesota, Plaintiff Molina Healthcare, Inc. (“Molina”) brought this action in the California Superior Court for the County of San Francisco,2 asserting claims under the laws of twenty-three states, including California’s Unfair Competition Law (the “UCL”). Defendants removed the case to this Court and move to transfer to the District of New Jersey or dismiss for lack of personal jurisdiction. Molina moves to remand. The Court finds the matter suitable for resolution without oral argument and VACATES the hearing previously set for January 28, 2022. For the reasons discussed below, Molina’s motion to remand is GRANTED. The Court does not reach Defendants motions.3 1 For simplicity, this order generally attributes the alleged conduct at issue to Celgene. Such references should not be construed as rejecting or otherwise addressing the contention that BMS can be held responsible for that conduct on a theory of agency or alter ego liability 2 In state court, this action was assigned case number CGC-21-592178. A. Allegations of the Complaint Molina, a corporation registered in Delaware and headquartered in Long Beach, California is the parent company of a number of regional subsidiaries that provide health insurance, including subsidiaries with names indicating they are based in or focused on California, Florida, Illinois, Kentucky, Michigan, Mississippi, Missouri, New Mexico, New York, Ohio, Puerto Rico, South Carolina, Texas, Utah, Idaho, Virginia, Washington, and Wisconsin. Compl (dkt. 1-1) ¶ 14.4 Those subsidiaries assigned Molina their claims arising from reimbursing plan members’ purchases of Thalomid and Revlimid in Alabama, Arizona, Colorado, Florida, Georgia, Illinois, Kansas, Michigan, Missouri, Mississippi, North Carolina, New Mexico, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin, and—of particular note for the purpose of the present motions—California and New Jersey. Id. ¶¶ 14–15. They asserted proper venue in the California Superior Court, where this case was filed, based on purchases in San Francisco. Id. ¶ 21. Molina contends that Celgene has used a number of different strategies to prevent competitors from developing and selling generic versions of Thalomid and Revlimid.5 First, Molina alleges that Celgene misused the FDA’s “REMS” program, a regulatory mechanism for ensuring the safe distribution of prescription drugs, to prevent generic competitors from obtaining samples of Thalomid and Revlimid, in violation of the Food and Drug Administration Amendments Act of 2007 (the “FDAAA”). Id. ¶¶ 95–105. According to Molina, Celgene pretextually cited FDA approval and other safety concerns to avoid selling samples, or in some cases refused sales without explanation, to potential generic competitors including Mylan (which later obtained a $62 million settlement from Celgene), id.

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Molina Healthcare, Inc. v. Celgene Corporation, (N.D. Cal. 2022).

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