drugset / Trial / NCT03990077

Study of HL-085 Plus Docetaxel in Patients With KRAS Mutant NSCLC

NCT03990077

Phase 1 Terminated 2 enrolled Shanghai Kechow Pharma, Inc.
NaSequentialOpen-labelTreatment

Summary

This is a phase I, open label, dose escalation study to evaluate tolerability, safety , pharmacokinetics and efficacy in patients with KRAS mutant NSCLC by using HL-085 and Docetaxel.

Timeline

Start
2020-05-21
Primary completion
2021-07-20
Completion
2021-07-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Tunlametinib Small molecule
Background Docetaxel Small molecule 75 mg/m2 Intravenous