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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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
18 and up
Critères de participation
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.
Lieu de l'étude
Investigative Site CA202
Investigative Site CA202Calgary, Alberta
Canada
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Investigative Site CA205
Investigative Site CA205Fredericton, New Brunswick
Canada
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Investigative Site CA206
Investigative Site CA206St-jérôme, Quebec
Canada
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Investigative Site CA207
Investigative Site CA207Mississauga, Ontario
Canada
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Investigative Site CA301
Investigative Site CA301Winnipeg, Manitoba
Canada
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Investigative Site CA303
Investigative Site CA303London, Ontario
Canada
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Investigative Site CA307
Investigative Site CA307Montreal, Quebec
Canada
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Investigative Site CA204
Investigative Site CA204Edmonton, Alberta
Canada
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Investigator Site CA304
Investigator Site CA304Barrie, Ontario
Canada
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Investigative Site CA302
Investigative Site CA302Peterborough, Ontario
Canada
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Investigative Site CA200
Investigative Site CA200Surrey, British Columbia
Canada
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Investigative Site CA308
Investigative Site CA308Hamilton, Ontario
Canada
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Investigator Site CA208
Investigator Site CA208Richmond Hill, Ontario
Canada
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- Étude parrainée par
- Incyte Corporation
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06212999