Overview

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

Status:
Not yet recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
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.
Phase:
Phase 1
Details
Lead Sponsor:
Shanghai Kechow Pharma, Inc.
Treatments:
Docetaxel