A Study of INCB018424 Phosphate Cream in Subjects With Vitiligo
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Incyte Corporation
- Study ID
- NCT03099304
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ruxolitinib cream — DRUGRuxolitinib cream is a topical formulation applied as a thin film to affected areas.
- Vehicle cream — DRUGVehicle cream is matching in appearance to ruxolitinib cream and is to be applied in the same manner as ruxolitinib cream.
Study Details
The purpose of this study will be to examine the efficacy, safety, and tolerability of ruxolitinib cream in subjects with vitiligo.
Key Dates
- Start date
- Jun 7, 2017
- Status verified
- Oct 2022
- Primary completion
- Sep 12, 2018
- Completion
- Sep 8, 2021
Study Design
- Enrollment
- 157 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Ruxolitinib cream 1.5% twice daily (BID)Ruxolitinib cream 1.5% BID for 52 weeks, followed by ruxolitinib cream 1.5% BID in a 104-week open-label extension.
- Experimental: Ruxolitinib cream 1.5% once daily (QD)Ruxolitinib cream 1.5% QD in the morning (vehicle cream in the evening) for 52 weeks, followed by ruxolitinib cream 1.5% BID in a 104-week open-label extension.
- Experimental: Ruxolitinib cream 0.5% QDRuxolitinib cream 0.5% QD in the morning (vehicle cream in the evening) for 52 weeks, followed by ruxolitinib cream 1.5% BID in a 104-week open-label extension.
- Experimental: Ruxolitinib cream 0.15% QDRuxolitinib cream 0.15% QD in the morning (vehicle cream in the evening) for 52 weeks (opportunity for re-randomization to a higher dose at Week 24 if \< 25% improvement in F-VASI score), followed by ruxolitinib cream 1.5% BID in a 104-week open-label extension.
- Placebo Comparator: Vehicle BIDVehicle cream BID for 24 weeks, followed by re-randomization to ruxolitinib cream 1.5% BID, 1.5% QD, or 0.5% QD for Weeks 24 to 52, followed by ruxolitinib cream 1.5% BID in a 104-week open-label extension.
Primary Outcome Measure
Percentage of Participants Treated With Ruxolitinib Cream Who Achieved a ≥ 50% Improvement From Baseline in Facial Assessment of the Vitiligo Area and Severity Index Score (F-VASI50) Compared With Participants Treated With Vehicle at Week 24 [ Time Frame: Baseline; Week 24 ]
Locations (26)
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By research site
UNIVERSITY OF ALABAMA AT BIRMINGHAM (UAB), 1802 6th Ave S· Birmingham, ALBURKE PHARMACEUTICAL RESEARCH LLC, 3633 Central Ave· Hot Springs, ARNORTHWEST AR CLINICAL TRIALS CENTER, PLLC/HULL DERMATOLOGY, PA, 500 S 52nd Street· Rogers, ARDERMATOLOGY RESEARCH ASSOCIATES- LOS ANGELES, 8930 S Sepulveda Blvd· Los Angeles, CATHE VITILIGO & PIGMENTATION INSTITUE OF SOUTHERN CALIFORNIA, 5670 Wilshire Boulevard· Los Angeles, CADERMATOLOGY SPECIALISTS, 3629 Vista Way· Oceanside, CA
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