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Clovis Transitions To Commercial Stage On Rubraca Approval

 
• By Jessica Merrill

FDA granted accelerated approval to PARP inhibitor Rubraca for treatment with BRCA-mutation positive ovarian cancer patients treated with two or more chemotherapies.

Clovis Oncology Inc. will launch its first commercial drug, Rubraca (rucaparib), this week at a wholesale acquisition cost of $13,740 for a 30-day supply, or $164,880 for a year of treatment.

The company announced the FDA approval of Rubraca under an accelerated approval Dec

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