Conditions
Metastatic Castration-resistant Prostate Cancer
The purpose of this study is to assess the safety and efficacy of pembrolizumab (MK-3475) combination therapy in participants with metastatic castration-resistant prostate cancer (mCRPC). There will be ten cohorts in this study: Cohort A will receive pembrolizumab + olaparib, Cohort B will receive pembrolizumab + docetaxel + prednisone, Cohort C will receive pembrolizumab + enzalutamide, Cohort D will receive pembrolizumab + abiraterone + prednisone, Cohort E will receive pembrolizumab+lenvatinib, Cohort F will receive pembrolizumab+lenvatinib, Cohort G will receive a pembrolizumab/vibostolimab co-formulation (MK-7684A), Cohort H will receive a pembrolizumab/vibostolimab co-formulation, Cohort I will receive pembrolizumab+carboplatin+etoposide in Arm 1 and carboplatin+etoposide in Arm 2 and Cohort J will receive belzutifan in Arm1 and Pembrolizumab+belzutifan in Arm 2. Outcome measures will be assessed individually for each cohort.
NATIONAL TRIAL REFERENCE NUMBER
NCT02861573
EudraCT
2016-002312-41
EU CT
2023-506987-15-00
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Conditions
Metastatic Castration-resistant Prostate Cancer
Age Range
All ages
Sex
Male
Tests the medicine or vaccine in a small group of 20 to 100 volunteers who are usually healthy, but not always. The trial often takes place in a hospital.
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