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1 Indications And Usage Rubraca Is A Poly (Adp-Ribose) Polymerase (Parp) Inhibitor Indicated: Ovarian Cancer For The Maintenance Treatment Of Adult Patients With Recurrent Epithelial Ovarian, Fallopian Tube, Or Primary Peritoneal Cancer Who Are In A Complete Or Partial Response To Platinum-Based Chemotherapy. ( 1.1 ) For The Treatment Of Adult Patients With A Deleterious Brca Mutation (Germline And/or Somatic)-Associated Epithelial Ovarian, Fallopian Tube, Or Primary Peritoneal Cancer Who Have Been Treated With Two Or More Chemotherapies. Select Patients For Therapy Based On An Fda-Approved Companion Diagnostic For Rubraca. ( 1.1 , 2.1 ) Prostate Cancer For The Treatment Of Adult Patients With A Deleterious Brca Mutation (Germline And/or Somatic)-Associated Metastatic Castration-Resistant Prostate Cancer (Mcrpc) Who Have Been Treated With Androgen Receptor-Directed Therapy And A Taxane-Based Chemotherapy. ( 1.2 , 2.1 ) This Indication Is Approved Under Accelerated Approval Based On Objective Response Rate And Duration Of Response. Continued Approval For This Indication May Be Contingent Upon Verification And Description Of Clinical Benefit In Confirmatory Trials. ( 1.2 ) 1.1 Ovarian Cancer Rubraca Is Indicated For The Maintenance Treatment Of Adult Patients With Recurrent Epithelial Ovarian, Fallopian Tube, Or Primary Peritoneal Cancer Who Are In A Complete Or Partial Response To Platinum-Based Chemotherapy. Rubraca Is Indicated For The Treatment Of Adult Patients With A Deleterious Brca Mutation (Germline And/or Somatic)-Associated Epithelial Ovarian, Fallopian Tube, Or Primary Peritoneal Cancer Who Have Been Treated With Two Or More Chemotherapies. Select Patients For Therapy Based On An Fda-Approved Companion Diagnostic For Rubraca [See Dosage And Administration ( 2.1 )]. 1.2 Metastatic Castration-Resistant Prostate Cancer With Brca Mutations Rubraca Is Indicated For The Treatment Of Adult Patients With A Deleterious Brca Mutation (Germline And/or Somatic)-Associated Metastatic Castration-Resistant Prostate Cancer (Mcrpc) Who Have Been Treated With Androgen Receptor-Directed Therapy And A Taxane-Based Chemotherapy [See Dosage And Administration ( 2.1 )]. This Indication Is Approved Under Accelerated Approval Based On Objective Response Rate And Duration Of Response [See Clinical Studies ( 14.2 )] . Continued Approval For This Indication May Be Contingent Upon Verification And Description Of Clinical Benefit In Confirmatory Trials.
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