Rubraca Ovarian Cancer Maintenance Approval Brings PARP Inhibitor Parity On Broad Indication

US FDA approval of Rubraca's all-comers maintenance therapy for platinum-sensitive ovarian cancer continues model that Zejula and Lynparza used for a broad maintenance indication, with data broken out for germline BRCA mutation-positive patients in the clinical trials section of labeling.

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Clovis Oncology Inc.'s Rubraca (rucaparib) became the third of the three US FDA-approved PARP inhibitors indicated for maintenance therapy of platinum-sensitive ovarian cancer with the agency's April 6 approval.

The approval adds a second indication to Rubraca's labeling, for maintenance treatment of adult patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who are

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