Assess the Long Term Efficacy and Safety of Ruxolitinib Cream in Participants With Vitiligo
Part of paid clinical trials in Hoover, Alabama.
- Sponsor
- Incyte Corporation
- Study ID
- NCT04530344
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 12 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- ruxolitinib — DRUGruxolitinib cream is a topical formulation applied as a thin film to affected areas BID.
- 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 duration of response following withdrawal of ruxolitinib cream (Cohort A vehicle group), safety and maintenance of response with continued use of ruxolitinib cream in participants who have completed either Study NCT04052425 or NCT04057573 (parent studies) in which the participants will have been using ruxolitinib cream BID for the previous 28 to 52 weeks depending on their initial randomization in the parent study.
Key Dates
- Start date
- Sep 24, 2020
- Status verified
- Aug 2025
- Primary completion
- Nov 14, 2022
- Completion
- Nov 14, 2022
Study Design
- Enrollment
- 458 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort A : ruxolitinib creamParticipants who achieve complete or almost complete facial repigmentation (achieve ≥ F VASI90) at Week 52 in the parent study will be assigned to Cohort A and will be randomized 1:1 to ruxolitinib cream.
- Placebo Comparator: Cohort A : VehicleParticipants who achieve complete or almost complete facial repigmentation (ie, achieve ≥ F VASI90) at Week 52 in the parent study will be assigned to Cohort A and will be randomized 1:1 to vehicle cream.
- Experimental: Cohort B : roxolitinib creamParticipants who did not achieve ≥ F-VASI90 at Week 52 of the parent studies will be assigned to Cohort B and will continue ruxolitinib cream.
Primary Outcome Measure
Time to Relapse (Defined as <F-VASI75) [ Time Frame: from Week 52 (first visit of this Treatment Extension study) to Week 104 (end of treatment in this Treatment Extension study) ]
Locations (44)
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