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A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Efficacy and Safety Study of Povorcitinib (INCB054707) in Participants With Moderate to Severe Hidradenitis Suppurativa

Trial Profile

A Phase 3, Double-Blind, Randomized, Placebo-Controlled, Efficacy and Safety Study of Povorcitinib (INCB054707) in Participants With Moderate to Severe Hidradenitis Suppurativa

Status: Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 28 Mar 2025

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At a glance

  • Drugs Povorcitinib (Primary)
  • Indications Hidradenitis suppurativa
  • Focus Registrational; Therapeutic Use
  • Acronyms STOP-HS1
  • Sponsors Incyte Corporation

Most Recent Events

  • 17 Mar 2025 According to Incyte media release, data from this study will be submitted for presentation at upcoming scientific meetings.
  • 17 Mar 2025 According to Incyte media release, primary endpoint (Proportion of participants who achieve Hidradenitis Suppurativa Clinical Response (HiSCR)) has been met, at both tested doses (45 mg and 75 mg).
  • 17 Mar 2025 According to Incyte media release, data from this study will support planned regulatory submission for povorcitinib in hidradenitis suppurativa (HS) worldwide.

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