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RECRUITING
NCT07138196
PHASE1

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

Sponsor: Qurient Co., Ltd.

View on ClinicalTrials.gov

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).

Official title: A Phase 1b, Open-label Dose Escalation Study to Evaluate the Safety, Pharmacodynamic, Pharmacokinetic and Preliminary Efficacy of Q702 in Subjects With Relapsed or Refractory Active Chronic Graft-versus-Host Disease (cGVHD)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2025-12-23

Completion Date

2029-10-31

Last Updated

2025-12-30

Healthy Volunteers

No

Interventions

DRUG

Adrixetinib

Administered orally

Locations (8)

Hospital Clinic de Barcelona

Barcelona, Spain

Hospital General Universitario Gregorio Maranon

Madrid, Spain

Hospital Universitario Puerta de Hierro Majadahonda

Majadahonda, Spain

Hospital Universitario Virgen de la Arrixaca

Murcia, Spain

Clinica Universidad de Navarra

Pamplona, Spain

Hospital Universitario Marques de Valdecilla

Santander, Spain

Hospital Universitario Virgen del Rocio

Seville, Spain

Instituto de Investigacion Sanitaria

Valencia, Spain