drugset / Trial / NCT03834506

Study of Pembrolizumab (MK-3475) Plus Docetaxel Versus Placebo Plus Docetaxel in Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer (mCRPC) (MK-3475-921/KEYNOTE-921)

NCT03834506 ↗

Phase 3 Completed 1030 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the efficacy and safety of the combination of pembrolizumab (MK-3475) and docetaxel in the treatment of men with metastatic castration-resistant prostate cancer (mCRPC) who have not received chemotherapy for mCRPC but have progressed on or are intolerant to Next Generation Hormonal Agent (NHA). There are two primary study hypotheses. Hypothesis 1: The combination of pembrolizumab plus docetaxel plus prednisone is superior to placebo plus docetaxel plus prednisone with respect to Overall Survival (OS). Hypothesis 2: The combination of pembrolizumab plus docetaxel plus prednisone is superior to placebo plus docetaxel plus prednisone with respect to Radiographic Progression-free Survival (rPFS) per Prostate Cancer Working Group (PCWG)-modified Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) as assessed by blinded independent central review.

Timeline

Start
2019-05-02
Primary completion
2022-06-20
Completion
2023-07-18

Outcome

Mixed primary results

registry analysis (superiority test); Pembrolizumab + Docetaxel vs Placebo + Docetaxel; p = 0.1677; Hazard Ratio (HR) 0.92 (95% CI 0.78 to 1.09) NCT03834506 ↗

registry analysis (superiority test); Pembrolizumab + Docetaxel vs Placebo + Docetaxel; p = 0.0335; Hazard Ratio (HR) 0.85 (95% CI 0.71 to 1.01) NCT03834506 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Background Dexamethasone Small molecule 8 mg Oral
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Prednisone Other / unclassified 5 mg Oral

Indications