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

Last updated:
2026-09-26
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View trial details

Overview

Official protocol title:

SELECTIVE TREATMENT OF ORAL POVORCITINIB IN HIDRADENITIS SUPPURATIVA LONG-TERM EXTENSION STUDY (STOP-HS LTE) - A PHASE 3, DOUBLE-BLIND STUDY TO EVALUATE THE LONG-TERM SAFETY AND EFFICACY OF POVORCITINIB IN PARTICIPANTS WITH MODERATE TO SEVERE HIDRADENITIS SUPPURATIVA

Intervention/treatment:
POVORCITINIB (INCB054707)
Medical condition:
HIDRADENITIS SUPPURATIVA
Protocol code:
INCB 54707-312
Control number:
278970
Status:
Active, not recruiting
Approved:
December 05, 2023
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT06212999
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Incyte Corporation Call Center (US)
Role
CONTACT
Phone:
1.855.463.3463
Name
Incyte Corporation Call Center (ex-US)
Role
CONTACT
Phone:
+800 00027423
Sponsor
INCYTE CORPORATION

Locations

Alberta

Investigative Site CA202
Calgary, Alberta, T3E 0B2
Investigative Site CA204
Edmonton, Alberta, T6G 1C3

British Columbia

Investigative Site CA200
Surrey, British Columbia, V3V 0C6

Manitoba

Investigative Site CA301
Winnipeg, Manitoba, R3M 3Z4

New Brunswick

Investigative Site CA205
Fredericton, New Brunswick, E3B 1G9

Ontario

Investigative Site CA203
St. John's, Ontario, A1A 4Y3
Investigative Site CA207
Mississauga, Ontario, L4W 0C2
Investigative Site CA208
Richmond Hill, Ontario, L4B 1L1
Investigative Site CA302
Peterborough, Ontario, K9J 5K2
Investigative Site CA303
London, Ontario, N6H 5L5
Investigative Site CA304
Barrie, Ontario, L4M 7G1
Investigative Site CA308
Hamilton, Ontario, L8L 3C3

Quebec

Investigative Site CA206
Saint-Jérôme, Quebec, J7Z 7E2
Investigative Site CA307
Montreal, Quebec, H2X 2V1
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