The purpose of this substudy is to assess the efficacy and safety of ifinatamab deruxtecan (I-DXd), given alone or with other treatments in participants with metastatic castration-resistant prostate cancer (mCRPC). The goals of this study are to learn about: * The safety of the study treatment and if people tolerate it. * A safe dose level of I-DXd that can be used with other treatments. * Participant levels of prostate specific antigen (PSA) during treatment.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Efficacy Phase: Number of Participants Who Experience One or More Dose-Limiting Toxicities (DLTs) - Combination Arms Only
Timeframe: Up to approximately 21 days
Efficacy Phase: Number of Participants Who Experienced an Adverse Event (AE)
Timeframe: Up to approximately 54 months
Efficacy Phase: Number of Participants Who Discontinued Study Intervention Due to an AE
Timeframe: Up to approximately 24 months
Efficacy Phase: Prostate-Specific Antigen (PSA) response rate
Timeframe: Up to approximately 54 months
Safety Lead-in Phase: Number of Participants Who Experience One or More Dose-Limiting Toxicities (DLTs) - Combination Arms Only
Timeframe: Up to approximately 21 days
Safety Lead-in Phase: Number of Participants Who Experienced an Adverse Event (AE) - Combination Arms Only
Timeframe: Up to approximately 21 days
Safety Lead-in Phase: Number of Participants Who Discontinued Study Intervention Due to an AE - Combination Arms Only
Timeframe: Up to approximately 21 days