Novel Therapies for Severe Acute GVHD (Graft-versus-host Disease)
- Sponsor
- Daihong Liu
- Study ID
- NCT07509749
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- GVHD, Acute
- Stem Cell Transplant Complications
Eligibility Criteria
- Sex
- ALL
- Age
- 14 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ruxolitinib and Methylprednisolone — DRUGParticipants began oral administration of ruxolitinib at 5 mg QD; Methylprednisolone (1mg/kg)
- Methylprednisolone — DRUGMethylprednisolone 2mg/kg/d , iv or iv gtt for at least 1 week, then taper according to the clinical response.
Study Details
The purpose of this study is to determine the efficacy and safety of combined Ruxolitinib With Corticosteroids as First Line Therapy for the severe acute GVHD (graft-versus-host disease )
Key Dates
- Start date
- Jun 30, 2025
- Status verified
- Mar 2026
- Primary completion
- Dec 30, 2027
- Completion
- Dec 30, 2027
Study Design
- Enrollment
- 54 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Ruxolitinib ArmRuxolitinib(5mg/d) combined with Methylprednisolone(1mg/kg)
- Active Comparator: Comparator armMethylprednisolone (2mg/kg)
Primary Outcome Measure
Overall response rate (ORR) at Day 28 [ Time Frame: Day 28 after treatment ]
Central Contacts
- Daihong Liu01066937079
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