Official Title: MK-2400-01A Substudy: A Phase 1/2, Open-label Umbrella Substudy of MK-2400-U01 Master Protocol to Evaluate the Safety and Efficacy of Ifinatamab Deruxtecan-based Treatment Combinations or Ifinatamab Deruxtecan Alone in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) (IDeate-Prostate02)
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.
Study Type:
Interventional
Study Phase:
Phase 1/Phase 2
Study Start Date:
July 2025
Estimated Study Completion Date:
February 2030
Estimated Primary Completion Date:
February 2030