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Active, not recruiting Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT06212999

Public ClinicalTrials.gov record NCT06212999. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 31, 2026, 3:05 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Double-Blind Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 \[NCT05620836\]).

Study identification

NCT ID
NCT06212999
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Incyte Corporation
Industry
Enrollment
617 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 30, 2024 (Actual)
Primary completion
Dec 26, 2026 (Estimated)
Completion
Dec 26, 2026 (Estimated)
Last update posted
Aug 25, 2026

2024 – 2026

United States locations

U.S. sites
61
U.S. states
24
U.S. cities
54
Facility City State ZIP Site status
Investigative Site US303 Phoenix Arizona 85006 —
Investigative Site US240 Scottsdale Arizona 85255 —
Investigative Site US307 Fort Smith Arkansas 72916 —
Investigative Site US214 Rogers Arkansas 72758 —
Investigative Site US315 Laguna Niguel California 92677 —
Investigative Site US223 Los Angeles California 90033 —
Investigative Site US222 Oakland California 94611 —
Investigative Site US226 San Diego California 92103 —
Investigative Site US309 Clearwater Florida 33614 —
Investigative Site US317 Hialeah Florida 33012-3618 —
Investigative Site US306 Hollywood Florida 33021 —
Investigative Site US320 Hollywood Florida 33021 —
Investigative Site US316 Maitland Florida 32751 —
Investigative Site US227 Margate Florida 33063 —
Investigative Site US204 Miami Florida 33125 —
Investigative Site US236 Miami Florida 33173 —
Investigative Site US321 North Miami Beach Florida 33162-4708 —
Investigative Site US200 Ocala Florida 34470 —
Investigative Site US228 Tampa Florida 33609 —
Investigative Site US201 Tampa Florida 33613 —
Investigative Site US311 Marietta Georgia 30060 —
Investigative Site US220 West Dundee Illinois 60118 —
Investigative Site US206 Indianapolis Indiana 46250 —
Investigative Site US337 Indianapolis Indiana 46250 —
Investigative Site US341 Bowling Green Kentucky 42104 —
Investigative Site US209 Louisville Kentucky 40241 —
Investigative Site US305 Baton Rouge Louisiana 70809 —
Investigative Site US207 Metairie Louisiana 70006 —
Investigative Site US229 New Orleans Louisiana 70115 —
Investigative Site US224 Baltimore Maryland 21287 —
Investigative Site US325 Marriottsville Maryland 21104 —
Investigative Site US225 Boston Massachusetts 02115 —
Investigative Site US304 Boston Massachusetts 02215 —
Investigative Site US310 Brighton Massachusetts 02135 —
Investigative Site US221 Quincy Massachusetts 02169 —
Investigative Site US213 Fort Gratiot Michigan 48059 —
Investigative Site US217 Waterford Michigan 48328 —
Investigative Site US212 Minneapolis Minnesota 55455 —
Investigative Site US302 St Louis Missouri 63110 —
Investigative Site US318 Portsmouth New Hampshire 03801 —
Investigative Site US230 East Windsor New Jersey 08520 —
Investigative Site US324 Kew Gardens New York 11415 —
Investigative Site US202 New York New York 10028 —
Investigative Site US210 Rochester New York 14620 —
Investigative Site US205 Chapel Hill North Carolina 27516 —
Investigative Site US215 Bexley Ohio 43209 —
Investigative Site US339 Bexley Ohio 43209 —
Investigative Site US330 Boardman Ohio 44512 —
Investigative Site US314 Cincinnati Ohio 45219 —
Investigative Site US312 Cleveland Ohio 44106 —
Investigative Site US203 Gahanna Ohio 43230 —
Investigative Site US301 Portland Oregon 97201 —
Investigative Site US232 Murfreesboro Tennessee 37130 —
Investigative Site US235 Arlington Texas 76011 —
Investigative Site US218 Bellaire Texas 77401 —
Investigative Site US340 Bellaire Texas 77401 —
Investigative Site US238 Pflugerville Texas 78660 —
Investigative Site US300 Plano Texas 75025 —
Investigative Site US234 San Antonio Texas 78213 —
Investigative Site US313 Norfolk Virginia 23502 —
Investigative Site US308 Spokane Washington 99202 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06212999, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 25, 2026 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06212999 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →