drugset / Trial / NCT04895722

Evaluation of Co-formulated Pembrolizumab/Quavonlimab (MK-1308A) Versus Other Treatments in Participants With Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Stage IV Colorectal Cancer (CRC) (MK-1308A-008/KEYSTEP-008).

NCT04895722

Phase 2 Active not recruiting 302 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy and safety of co-formulated pembrolizumab/quavonlimab versus other treatments in participants with MSI-H or dMMR Metastatic Stage IV Colorectal Cancer.

Timeline

Start
2021-06-25
Primary completion
2025-05-21
Completion
2026-08-06

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-4830 Unknown 800 mg Intravenous
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous
Subject Pembrolizumab Monoclonal antibody 400 mg Intravenous
Subject Pembrolizumab/Favezelimab Unknown 200 mg Intravenous
Subject Pembrolizumab/Favezelimab Unknown 800 mg Intravenous
Subject Pembrolizumab/Quavonlimab Unknown 25 mg Intravenous
Subject Pembrolizumab/Quavonlimab Unknown 400 mg Intravenous
Subject Pembrolizumab/Vibostolimab Unknown 200 mg Intravenous

Indications