The purpose of this study is to evaluate the safety, pharmacokinetics (PK), and preliminary activity of GDC-1261 in participants with advanced or metastatic prostate cancer. It's also to identify a recommended dose(s) and regimen for GDC-1261 for subsequent studies.
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Percentage of Participants With Adverse Events (AEs)
Timeframe: Up to approximately 24 months
Incidence and Nature of DLTs Dose-limiting Toxicities (DLTs)
Timeframe: From Day 1-28 of Cycle 1 (1 Cycle = 28 days)
Reference Study ID Number: GO46445 https://forpatients.roche.com/