Overview

A Study to Evaluate Adrixetinib (Q702) in Adults With Active Chronic Graft-Versus-Host Disease

Status:
NOT_YET_RECRUITING
Trial end date:
2029-10-31
Target enrollment:
Participant gender:
Summary
Open-label, dose escalation study to evaluate safety, tolerability pharmacokinetic and pharmacodynamic activity, and efficacy of Adrixetinib (Q702) in subjects with relapsed or refractory active chronic graft-versus-host disease (cGVHD).
Phase:
PHASE1
Details
Lead Sponsor:
Qurient Co., Ltd.