- Direct purchasers alleged biopharma company blocked generics
- $75 million in attorneys’ fees; $2.9 million in costs approved
Judge
The direct purchasers alleged the biopharmaceutical company used anticompetitive tactics to keep cheaper, generic drugs from the market.
The settlement, reached last September on the eve of trial, covers two classes of direct purchasers—entities or persons that purchased branded or generic Truvada and Atripla or generic Atripla over a five-year period. Each claimant will receive a pro rata share of the net settlement based on total unit volume of applicable purchases, depending which drugs were bought.
Before settlement, the plaintiffs’ economist estimated certified classes damages of $2.08 billion, the motion said. The $246.75 million from Gilead amounts to 11.9% of the possible damages.
The settlement follows a California jury finding in June that Gilead and
The unanimous verdict in litigation, brought by end payors, individual health plans, and United Healthcare Services Inc., affirmed that a 2014 patent settlement between Foster City, Calif.-based Gilead and Israel-based Teva didn’t violate antitrust law.
Kirkland & Ellis LLP and Proskauer Rose LLP represented Gilead. Law Offices of Francis O. Scarpulla are liaison counsel for the class. Roberts Law Firm US PC and NastLaw LLC are co-lead counsel for direct purchaser plaintiffs. Hausfeld LLP is counsel for the class.
The case is In re HIV Antitrust Litig., N.D. Cal., No. 3:19-cv-02573, 1/19/24.
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