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

Hidradenitis Suppurativa (HS)

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 \[NCT05620836\]).

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Completion of the study treatment period of the originating parent study (INCB 54707-301 or INCB 54707-302).
* Agreement to use contraception.
* Willing and able to comply with the study protocol and procedures.
* Further inclusion criteria apply.

Exclusion Criteria:

* Participation in the extension study could expose the participant to an undue safety risk.
* Women who are pregnant (or who are considering pregnancy) or breastfeeding.
* Further exclusion criteria apply.

Study Location

Investigative Site CA202
Investigative Site CA202
Calgary, Alberta
Canada

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Investigative Site CA205
Investigative Site CA205
Fredericton, New Brunswick
Canada

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Investigative Site CA206
Investigative Site CA206
St-jérôme, Quebec
Canada

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Investigative Site CA207
Investigative Site CA207
Mississauga, Ontario
Canada

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Investigative Site CA301
Investigative Site CA301
Winnipeg, Manitoba
Canada

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Investigative Site CA303
Investigative Site CA303
London, Ontario
Canada

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Investigative Site CA307
Investigative Site CA307
Montreal, Quebec
Canada

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Investigative Site CA204
Investigative Site CA204
Edmonton, Alberta
Canada

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Investigator Site CA304
Investigator Site CA304
Barrie, Ontario
Canada

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Investigative Site CA302
Investigative Site CA302
Peterborough, Ontario
Canada

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Investigative Site CA200
Investigative Site CA200
Surrey, British Columbia
Canada

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Investigative Site CA308
Investigative Site CA308
Hamilton, Ontario
Canada

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Investigator Site CA208
Investigator Site CA208
Richmond Hill, Ontario
Canada

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Study Sponsored By
Incyte Corporation
Participants Required
More Information
Study ID: NCT06212999