The purpose of this study is to determine what the safest dose of talazoparib plus temozolomide for participants with metastatic castration resistant prostate cancer. The purpose of Phase II is to test the efficacy (effectiveness) of talazoparib and temozolomide at the maximum tolerated dose, which was determined to be 1mg talazoparib and 75mg/m² temozolomide in the Phase Ib portion of this study.
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Phase I: Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability])
Timeframe: 30 days after last dose of study treatment (+/- 3 days)
Phase II: Overall Response Rate
Timeframe: 30 days after last dose of study treatment (+/- 3 days)