drugset / Trial / NCT05217303

HL-085 in NRAS-mutated Advanced Melanoma

NCT05217303

Phase 2 Completed 100 enrolled Shanghai Kechow Pharma, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This was an open-label, single-arm, multi-center phase II clinical study, aimed at investigating the efficacy and safety of HL-085 capsule in the treatment of advanced melanoma patients with NRAS mutation.

Timeline

Start
2020-11-02
Primary completion
2023-02-19
Completion
2023-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Tunlametinib Small molecule 12 mg Oral

Indications