A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Pediatric Participants With Nonsegmental Vitiligo
Purpose
The purpose of this study is to to evaluate the safety and efficacy of ruxolitinib cream in pediatric participants with nonsegmental vitiligo.
Condition
- NonSegmental Vitiligo
Eligibility
- Eligible Ages
- Between 2 Years and 11 Years
- Eligible Genders
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Clinical diagnosis of nonsegmental vitiligo with depigmented area including ≥ 0.5% BSA on the face, ≥ 0.5 F-VASI, ≥ 3% BSA on nonfacial areas, ≥ 3 T-VASI. - Total body vitiligo area does not exceed 10% BSA. - Pigmented hair within some of the areas of vitiligo on the face. - Must agree to discontinue all agents used to treat vitiligo from screening through the final safety follow-up visit. - For sexually active participants (except participants who are prepubescent) willingness to avoid pregnancy or fathering a child from screening through 30 days after the last application of study cream.
Exclusion Criteria
- Diagnosis of other forms of vitiligo (eg, segmental). - Other differential diagnosis of vitiligo or other skin depigmentation disorders (eg, piebaldism, pityriasis alba, leprosy, postinflammatory hypopigmentation, progressive macule hypomelanosis, nevus anemicus, chemical leukoderma, and tinea versicolor). - Any other skin disease that, in the opinion of the investigator, would interfere with the study drug application or study assessments. - Prior or current use of depigmentation treatments (eg, monobenzone). - Any serious illness or medical, physical, or psychiatric condition(s) that, in the investigator's opinion, would interfere with full participation in the study, including application of study cream and attending required study visits; pose a significant risk to the participant; or interfere with interpretation of study data. - Use of protocol-defined treatments within the indicated washout period before baseline. - Current or previous use of JAK inhibitors, systemic or topical. - Protocol-defined clinically significant abnormal laboratory values at screening. - BMI-for-age < 5th percentile or ≥ 85th percentile according to the CDC BMI Percentile Calculator for Child and Teen. - Pregnant or lactating participants or those considering pregnancy during the period of their study participation. - In the opinion of the investigator, unable or unlikely to comply with the application schedule and study evaluations. - Living with anyone participating in any current Incyte-sponsored ruxolitinib cream study. - Employees of the sponsor or investigator or are otherwise dependents of them. - Known allergy or reaction to any component of the study cream formulation. Other protocol-defined Inclusion/Exclusion Criteria may apply.
Study Design
- Phase
- Phase 3
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Treatment
- Masking
- Triple (Participant, Investigator, Outcomes Assessor)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Ruxolitinib 1.5 % Cream |
Participants received ruxolitinib 1.5% cream, applied topically to the affected area as defined in the protocol. |
|
|
Placebo Comparator Vehicle Cream |
Participants received vehicle cream, applied topically to the affected area as defined by the protocol. |
|
Recruiting Locations
The University of Texas Health Science Center At Houston
Bellaire, Texas 77401
Bellaire, Texas 77401
More Details
- Status
- Recruiting
- Sponsor
- Incyte Corporation