drugset / Trial / NCT07445022

RWS of Tunlametinib in NRAS-Mutant Advanced Melanoma

NCT07445022

Phase 4 Recruiting 110 enrolled Fudan University
NaSingle-groupOpen-labelTreatment

Summary

This study is a prospective, open-label, multicenter, real-world clinical study to evaluate the efficacy and safety of tunlametinib in patients with NRAS-mutant advanced melanoma who have failed prior anti-PD-1/PD-L1 therapy.

Timeline

Start
2026-01-28
Primary completion
2028-09-30
Completion
2029-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tunlametinib Small molecule 12 mg Oral

Indications