Pharmacokinetics, Safety, and Efficacy of Povorcitinib in Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Incyte Corporation
- Study ID
- NCT07213973
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Hidradenitis Suppurativa (HS)
Eligibility Criteria
- Sex
- ALL
- Age
- 12 Years - 17 Years
- Healthy Volunteers
- Not accepted
Interventions
- Povorcitinib — DRUGOral; Tablet
Study Details
The purpose of this study is to evaluate the pharmacokinetics, safety, and efficacy of povorcitinib in adolescent participants with moderate to severe hidradenitis suppurativa over a 54-week open-label treatment period.
Key Dates
- Start date
- Feb 2, 2026
- Status verified
- May 2026
- Primary completion
- Mar 25, 2028
- Completion
- Mar 25, 2028
Study Design
- Enrollment
- 40 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Povorcitinib Dose AParticipants will receive povorcitinib dose A for 54 weeks.
- Experimental: Povorcitinib Dose BParticipants will receive povorcitinib dose B for 54 weeks.
Primary Outcome Measure
Proportion of participants with Treatment-Emergent Adverse Events (TEAEs) [ Time Frame: Baseline through Week 54 ]
Central Contacts
- Incyte Corporation Call Center (US)1.855.463.3463
- Incyte Corporation Call Center (ex-US)+800 00027423
Locations (25)
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