drugset / Trial / NCT03973151

Study of HL-085 in NRAS Mutant Advanced Melanoma

NCT03973151

Phase 1/2 Completed 42 enrolled Shanghai Kechow Pharma, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I/II, open-label, dose escalation study to evaluate tolerability, safety, pharmacokinetics and efficacy in patients with NRAS mutant advanced melanoma .

Timeline

Start
2017-09-01
Primary completion
2021-01-18
Completion
2021-01-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Tunlametinib Small molecule 0.5 mg Oral
Subject Tunlametinib Small molecule 12 mg Oral
Subject Tunlametinib Small molecule 18 mg Oral

Indications