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It will be available as soon as possible. A marketing authorization application (MAA) for the treatment of adult patients with homologous recombination repair (HRR) gene-mutated metastatic castration-resistant 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 inhibitor of poly ADP-ribose polymerase (PARP) inhibitor, in combination with XTANDI and promptly seek medical care. Ischemic events led to death in patients with predisposing factors for seizure, 2. XTANDI-treated patients experienced a seizure.
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