This study is a first-in-human, Phase 1, open-label, multicenter study to assess the safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD), and the preliminary efficacy of JANX007 in adults with metastatic castration-resistant prostate cancer (mCRPC).
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Incidence of Dose Limiting Toxicities (DLT)
Timeframe: 3 years
Incidence of Adverse Events (AE) and Serious Adverse Events (SAE)
Timeframe: 3 years