Topical Ruxolitinib Evaluation in Chronic Hand Eczema
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Incyte Corporation
- Study ID
- NCT05906628
- Phase
- PHASE2
- Status
- Completed
Conditions
- Hand Eczema
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ruxolitinib cream — DRUGRuxolitinib cream is a topical formulation applied as a thin film to affected areas.
- Vehicle — DRUGVehicle cream is a topical formulation applied as a thin film to affected areas.
Study Details
The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in adult participants with diagnosis of chronic hand eczema (CHE) and moderate to severe disease activity (Investigator's Global Assessement (IGA) of CHE score 3 or 4).
Key Dates
- Start date
- Jul 31, 2023
- Status verified
- Jul 2025
- Primary completion
- Jul 15, 2024
- Completion
- Dec 13, 2024
Study Design
- Enrollment
- 186 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: RuxolitinibRuxolitinib cream 1.5% twice daily (BID) for 16 weeks followed by ruxolitinib cream 1.5% BID for an additional 16-week treatment extension period.
- Placebo Comparator: VehicleVehicle cream for 16 weeks followed by crossover to ruxolitinib cream 1.5% BID in a 16-week treatment extension period.
Primary Outcome Measure
Percentage of Participants With Investigator's Global Assessment-Chronic Hand Eczema Treatment Success (IGA-CHE-TS) at Week 16 [ Time Frame: Baseline; Week 16 ]
Locations (23)
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