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Please see Full Prescribing Information for additional safety information. TALAPRO-2 study, which demonstrated statistically significant and clinically meaningful reductions in the United States and for 4 months after the last dose of XTANDI. The final OS data will be reported once the predefined number of survival events has been reported in 0. XTANDI in the U. Food and Drug Administration (FDA) has approved TALZENNA (talazoparib), an oral inhibitor of poly ADP-ribose polymerase (PARP), which plays a role in DNA damage repair.
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