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Clovis Oncology's Rubraca gets U.S. FDA approval for prostate cancer

May 15 (Reuters) - Clovis Oncology Inc said on Friday the U.S. Food and Drug Administration has approved its drug Rubraca for the treatment of adult patients with castration-resistant prostate cancer, whose tumors have a genetic mutation. The approval is for the drug's use in patients whose tumors have a mutation called BRCA, and whose disease had advanced despite prior rounds of chemotherapy, the company said. (Reporting by Manojna Maddipatla in Bengaluru; Editing by Shailesh Kuber)