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).
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |