Topical Ruxolitinib Evaluation in Vitiligo Study 2 (TRuE-V2)
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- Incyte Corporation
- Study ID
- NCT04057573
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 12 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 adolescent and adult participants with non-segmental vitiligo for whom total body involved vitiligo area (facial and nonfacial) does not exceed 10% body surface area (BSA).
Key Dates
- Start date
- Oct 3, 2019
- Status verified
- Aug 2025
- Primary completion
- Mar 15, 2021
- Completion
- Oct 1, 2021
Study Design
- Enrollment
- 344 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- TREATMENT
Arms
- Experimental: Double-Blind Period: Ruxolitinib cream 1.5% BIDParticipants applied ruxolitinib 1.5% cream twice daily (BID) for 24 weeks.
- Placebo Comparator: Double-Blind Period: Vehicle cream BIDParticipants applied matching vehicle cream BID for 24 weeks.
- Experimental: Treatment-Extension Period: Ruxolitinib cream 1.5% BIDParticipants who completed the Week 24 assessments with no safety concerns could continue into the 28-week Treatment-Extension Period. Participants who applied ruxolitinib cream 1.5% BID during the Double-Blind Period continued to apply ruxolitinib cream 1.5% BID for an additional 28 weeks in the Treatment-Extension Period.
- Experimental: Treatment-Extension Period: Vehicle cream to Ruxolitinib cream 1.5% BIDParticipants who completed the Week 24 assessments with no safety concerns could continue into the 28-week Treatment-Extension Period. Participants who applied vehicle cream BID during the Double-Blind Period applied ruxolitinib cream 1.5%m BID for 28 weeks in the Treatment-Extension Period.
Primary Outcome Measure
Percentage of Participants Achieving a ≥ 75% Improvement From Baseline in the Face Vitiligo Area Scoring Index (F-VASI75) Score at Week 24 [ Time Frame: Baseline; Week 24 ]
Locations (34)
Find similar trials in Gilbert, AZ
By research site
Desert Sky Dermatology· Gilbert, AZCenter For Dermatology Cosmetic and Laser Surgery· Fremont, CAUci Beckman Laser Institute and Medical Clinic· Irvine, CAUCI Health Beckman Laser Institute and Medical Center· Irvine, CADermatology Research Associates· Los Angeles, CAVitiligo & Pigmentation Institute of Southern California· Los Angeles, CA
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