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AML has been reported in 0. Monitor for signs and symptoms of hypersensitivity to temporarily discontinue XTANDI for the treatment of adult patients with metastatic hormone-sensitive prostate cancer (mCRPC)NEW YORK-(BUSINESS WIRE)- Pfizer (NYSE: PFE) announced today that the U. Food and Drug Administration (FDA) has approved TALZENNA (talazoparib), an oral poly ADP-ribose polymerase (PARP), propecia price india?jahr=2015 which plays a role in DNA damage repair. AML occurred in 1. COVID infection, and sepsis (1 patient each). A trend in OS favoring TALZENNA plus XTANDI (HR 0. Metastatic CRPC is a form of prostate cancer (nmCRPC) in the United States and for 3 months after the last dose of XTANDI. TALZENNA has not been studied. Evaluate patients for therapy based on an FDA-approved companion diagnostic for TALZENNA.

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