A Study to Evaluate the Efficacy and Safety of Povorcitinib (INCB054707) in Participants With Moderate to Severe Hidradenitis Suppurativa
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Incyte Corporation
- Study ID
- NCT05620823
- Phase
- PHASE3
- Status
- Completed
Conditions
- Hidradenitis Suppurativa (HS)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Povorcitinib — DRUGOral; Tablet
- Placebo — DRUGOral; Tablet
Study Details
The purpose of this study is to evaluate the efficacy and safety of Povorcitinib (INCB054707) in participants with moderate to severe Hidradenitis Suppurativa (HS) over a 12-week placebo controlled period, followed by a 42-week extension period.
Key Dates
- Start date
- Dec 19, 2022
- Status verified
- Feb 2026
- Primary completion
- Feb 3, 2025
- Completion
- Dec 23, 2025
Study Design
- Enrollment
- 608 participants (actual)
- Allocation
- 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.
- Placebo Comparator: PlaceboParticipants will receive Placebo for 12 weeks, followed by Povorcitinib (Dose A or Dose B) for 42 weeks.
Primary Outcome Measure
Proportion of participants who achieve Hidradenitis Suppurativa Clinical Response (HiSCR) [ Time Frame: Week 12 ]
Locations (37)
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