A Study of Ruxolitinib in Patients With Graft-Versus Host Disease
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT07594587
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 0 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
This study aims to evaluate the safety and effectiveness of Jakavi® (ruxolitinib) in patients with acute graft-versus host disease (GVHD) and chronic GVHD in clinical practice.
Key Dates
- Start date
- May 11, 2026
- Status verified
- Jun 2026
- Primary completion
- May 15, 2030
- Completion
- May 15, 2030
Study Design
- Enrollment
- 395 participants (estimated)
Arms
- Arm: Ruxolitinib CohortPatients with acute and chronic GVHD treated with ruxolitinib.
Primary Outcome Measure
Number and Percentage of Patients With Common Terminology Criteria for Adverse Event (CTCAE) Grade ≥ 3 Infections [ Time Frame: Up to 1 year ]
Central Contacts
- Novartis Pharmaceuticals+41613241111
- Novartis Pharmaceuticals
Related Studies
- Improved Methods of Cell Selection for Bone Marrow Transplant AlternativesRecruiting · National Heart, Lung, and Blood Institute (NHLBI) · Bethesda, Maryland
- Post-Transplant Cyclophosphamide, Bortezomib and Abatacept for the Prevention of Graft-versus-Host-Disease (GvHD)PHASE1/PHASE2 · Recruiting · Northwell Health · New Hyde Park, New York
- A Study of Photobiomodulation (PBM) Therapy in People With Oral Graft-Versus-Host Disease (GVHD) After Stem Cell TransplantPHASE2 · Recruiting · Memorial Sloan Kettering Cancer Center · Bethesda, Maryland
- Multidisciplinary Intervention for Adults With Chronic Graft-versus-host DiseaseRecruiting · Massachusetts General Hospital · Miami, Florida