Overview

TGRX-678 Chinese Phase I in Chronic Myelogenous Leukemia (CML) Patients

Status:
Recruiting
Trial end date:
2022-12-31
Target enrollment:
Participant gender:
Summary
The purpose of this single- arm, open-lable, dose escalation + dose expansion study is to evalulate the safety, tolerability, pharmacokinetic and preliminary efficacy of TGRX-678 in Chronic Myelogenous Leukemia patients who had failure with or are intolerant to TKI treatments.
Phase:
Phase 1
Details
Lead Sponsor:
Shenzhen TargetRx, Inc.
Collaborator:
Peking University People's Hospital