A Study to Evaluate Vimseltinib in Adults With Active Chronic Graft-Versus-Host Disease (cGVHD)
Part of paid clinical trials in Duarte, California.
- Sponsor
- Deciphera Pharmaceuticals, LLC
- Study ID
- NCT06619561
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Chronic Graft-Versus-Host Disease (cGVHD)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Vimseltinib — DRUGAdministered orally
Study Details
The purpose of this study is to determine if vimseltinib is safe, tolerable and works effectively to treat adults with active moderate to severe cGVHD. Participants will be treated with vimseltinib in 28-day treatment cycles for approximately 2 years.
Key Dates
- Start date
- Nov 21, 2024
- Status verified
- Dec 2025
- Primary completion
- Oct 31, 2029
- Completion
- Oct 31, 2029
Study Design
- Enrollment
- 48 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: VimseltinibEscalating doses of vimseltinib in 28 day cycles.
Primary Outcome Measure
Number of Participants with Dose-Limiting Toxicities (DLTs) [ Time Frame: Cycle 1 (28 Days) ]
Central Contacts
- Clinical Team888-724-3274
Locations (26)
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