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A Study to Evaluate Adrixetinib (Q702) in Adults With Active Chronic Graft-Versus-Host Disease
Sponsor: Qurient Co., Ltd.
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
Conditions
Interventions
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