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NCT06113471 · ClinicalTrials.gov registry record · Phase 3
A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)
A Phase 3 study of Non-segmental Vitiligo, sponsored by Incyte Corporation.
- Active
- Registry status
- Phase 3
- Development phase
- 450
- Enrollment target
- 20
- Study locations
NCT06113471: Active Phase 3 study of Non-segmental Vitiligo, sponsored by Incyte Corporation.
NCT06113471 is a Phase 3 study of Non-segmental Vitiligo that is active but no longer recruiting, run by Incyte Corporation. The registered enrollment target is 450 participants, above the 220-participant average among 9 other Non-segmental Vitiligo trials with a reported enrollment target (105% higher). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06113471, a Phase 3 study of Non-segmental Vitiligo, is active but no longer recruiting, sponsored by Incyte Corporation.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 3
- Development phase
- 450 participants
- Enrollment target
- 20
- Study locations
Study Summary
This study is being conducted to determine the efficacy and safety of povorcitinib in participants with nonsegmental vitiligo.
Primary Outcome
≥75% improvement in facial Vitiligo Area Scoring Index.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Povorcitinib
Study Locations (20)
California
- First Oc Dermatology Research Inc - Fountain Valley
- Center For Dermatology Clinical Research, Inc - Fremont
- Marvel Clinical Research Llc - Huntington Beach
- Vitiligo & Pigmentation Institute of Southern California - Los Angeles
- Dermatology Research Associates - Los Angeles
- Clinical Trials Research Institute - Thousand Oaks
Florida
- Skin Care Research, Llc - Boca Raton
- Total Vein and Skin Llc - Boynton Beach
- Driven Research Llc - Coral Gables
- Florida Academic Centers Research and Education Llc - Coral Gables
- Pediatric Skin Research Llc - Coral Gables
- Metabolic Research Institute Inc - West Palm Beach
Alabama
- University of Alabama At Birmingham Hospital-Whitaker Clinic - Birmingham
- C2 Research Center, Llc - Montgomery
Georgia
- Dermatology and Surgery Specialists of North Atlanta - Marietta
- Advanced Medical Research Pc - Sandy Springs
Illinois
- Dundee Dermatology - West Dundee
Indiana
- Indiana University School of Medicine Iusm Indianapolis - Indianapolis
Louisiana
- Delricht Research - Baton Rouge
Maryland
- Callender Dermatology and Cosmetic Center - Glenn Dale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 450 participants |
| Start Date | 2023-11-27 |
| Est. Completion | 2027-03-16 |
| Phase | Phase 3 |
What the registry record for NCT06113471 still lists
NCT06113471 is an interventional study that assigns participants to a tested intervention. The registered 450 participants enrollment target is mid-sized for trials with a published cap, above the 220-participant average among 9 other Non-segmental Vitiligo trials with a reported enrollment target (105% higher).
The record links to 1 condition, with Non-segmental Vitiligo appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT06113471 names 20 study sites across 8 states, led by California, Florida, Alabama.
Frequently Asked Questions
What is clinical trial NCT06113471 about?
NCT06113471 is a clinical study titled "A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)". This study is being conducted to determine the efficacy and safety of povorcitinib in participants with nonsegmental vitiligo.
What is the current status of trial NCT06113471?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 450 participants. The study started on 2023-11-27. Estimated completion is 2027-03-16.
What conditions does trial NCT06113471 study?
This clinical trial studies the following conditions: Non-segmental Vitiligo.
What interventions are being tested in trial NCT06113471?
The interventions under investigation include: Placebo (DRUG), Povorcitinib (DRUG).
Who is sponsoring clinical trial NCT06113471?
This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06113471 being conducted?
This trial has 20 study locations across Alabama, California, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Non-segmental Vitiligo
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06113471's enrollment target sits among peer trials
450 2nd of 9 the highest of 9 other Non-segmental Vitiligo trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Non-segmental Vitiligo trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Pediatric Participants With Nonsegmental Vitiligo
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A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V1)
ACTIVE NOT RECRUITING · Phase 3
-
Topical Ruxolitinib Evaluation in Vitiligo Study 1 (TRuE-V1)
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Phase 2 Study to Evaluate EI-001 in Non-segmental Vitiligo Patients
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