drugset / Trial / NCT06008119

Efficacy and Safety of Tunlametinib Plus Vemurafenib in Patients With BRAF V600E-mutant Metastatic Colorectal Cancer

NCT06008119

Phase 3 Recruiting 165 enrolled Shanghai Kechow Pharma, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, randomized, open-label, Phase 3 study

Timeline

Start
2023-10-25
Primary completion
2026-12-24
Completion
2026-12-24

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody
Comparator Cetuximab Monoclonal antibody
Subject Tunlametinib Small molecule 12 mg
Subject Vemurafenib Small molecule 720 mg

Indications