This study is being conducted to learn more about the safety, tolerability, and effectiveness of an experimental treatment for metastatic prostate cancer called AZD8359. The study is split into different modules which will look at AZD8359 delivered by different methods. The study is also further split into 2 parts, Part A which will test different dose levels and dosing schedules of AZD8359 to determine which doses are the best in terms of safety and side effects (dose escalation), and Part B will further test at least two AZD8359 doses in a larger group of participants (dose expansion).
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Number of participants with adverse events (AE), adverse events of special interest (AESI), and serious adverse events (SAE)
Timeframe: From time of Informed Consent to 90 days post last dose of study intervention (up to 3 years)
Number of participants with dose-limiting toxicity (DLT), as defined in the protocol (Part A only)
Timeframe: From first study dose to 21 OR 28 days post first dose based on schedule
PSA response rate (Part B only)
Timeframe: Up to 3 years
AstraZeneca Clinical Study Information Center