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Clinical Trial Active — Not Recruiting Phase III NCT06212999

A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa

A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa — Active Not Recruiting • Phase III • NCT06212999.

📅 25 Aug 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase III
NCT ID
NCT06212999
Start
2024-01-30
Completion
2026-12-26
ClinicaliQ Trial Snapshot
  • A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa — Active Not Recruiting • Phase III • NCT06212999.
  • Long-term safety and effectiveness study of povorcitinib for moderate to severe hidradenitis suppurativa in patients completing earlier trials.

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What This Trial Is Studying

The purpose of this study is to evaluate long-term safety and efficacy of povorcitinib in participants with moderate to severe hidradenitis suppurativa who completed the 54 weeks of study treatment within the originating parent Phase 3 studies (INCB 54707-301 [NCT05620823] or INCB 54707-302 [NCT05620836]). Conditions: Hidradenitis Suppurativa (HS) Interventions: Povorcitinib Lead Sponsor: Incyte Corporation Planned Enrollment: 617 participants

Full Trial Details
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Eligibility criteria, protocol, and results when available
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