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NCT06212999 · ClinicalTrials.gov registry record · Phase 3
A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa
A Phase 3 study of Hidradenitis Suppurativa (HS), sponsored by Incyte Corporation.
- Active
- Registry status
- Phase 3
- Development phase
- 617
- Enrollment target
- 20
- Study locations
NCT06212999 is a Phase 3 study of Hidradenitis Suppurativa (HS) that is active but no longer recruiting, run by Incyte Corporation. The registered enrollment target is 617 participants, above the 129-participant average among 12 other Hidradenitis Suppurativa (HS) trials with a reported enrollment target (378% higher). The trial reports 20 study locations across 4 states.
The verdict
NCT06212999, a Phase 3 study of Hidradenitis Suppurativa (HS), is active but no longer recruiting, sponsored by Incyte Corporation.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 3
- Development phase
- 617 participants
- Enrollment target
- 20
- Study locations
Study Summary
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 \[NCT05620836\]).
Conditions Studied
Interventions
- DRUG Povorcitinib
Study Locations (20)
Florida
- Investigative Site US309 - Clearwater
- Investigative Site US317 - Hialeah
- Investigative Site US306 - Hollywood
- Investigative Site US320 - Hollywood
- Investigative Site US316 - Maitland
- Investigative Site US227 - Margate
- Investigative Site US204 - Miami
- Investigative Site US236 - Miami
- Investigative Site US321 - North Miami Beach
- Investigative Site US200 - Ocala
- Investigative Site US228 - Tampa
- Investigative Site US201 - Tampa
California
- Investigative Site US315 - Laguna Niguel
- Investigative Site US223 - Los Angeles
- Investigative Site US222 - Oakland
- Investigative Site US226 - San Diego
Arizona
- Investigative Site US303 - Phoenix
- Investigative Site US240 - Scottsdale
Arkansas
- Investigative Site US307 - Fort Smith
- Investigative Site US214 - Rogers
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 617 participants |
| Start Date | 2024-01-30 |
| Est. Completion | 2026-12-26 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06212999
The ClinicalTrials.gov registry entry for NCT06212999 describes a study currently listed as active not recruiting, categorized as Phase 3. The registered enrollment target is 617 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 129-participant average among 12 other Hidradenitis Suppurativa (HS) trials with a reported enrollment target (378% higher). The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Hidradenitis Suppurativa (HS) appearing as the primary indexed condition, and to 1 intervention - of which Povorcitinib is the first listed.
NCT06212999 reports 20 study locations spanning 4 distinct geographic areas - top geographies include Florida, California, Arizona.
Frequently Asked Questions
What is clinical trial NCT06212999 about?
NCT06212999 is a clinical study titled "A Study to Evaluate the Long-Term Safety and Efficacy of Povorcitinib in Participants With Moderate to Severe Hidradenitis Suppurativa". 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 \[NCT0...
What is the current status of trial NCT06212999?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 617 participants. The study started on 2024-01-30. Estimated completion is 2026-12-26.
What conditions does trial NCT06212999 study?
This clinical trial studies the following conditions: Hidradenitis Suppurativa (HS).
What interventions are being tested in trial NCT06212999?
The interventions under investigation include: Povorcitinib (DRUG).
Who is sponsoring clinical trial NCT06212999?
This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06212999 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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