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ACTIVE NOT RECRUITING Phase 3

A Study to Evaluate Efficacy and Safety of Povorcitinib in Participants With Nonsegmental Vitiligo (STOP-V2)

NCT06113471 · View on ClinicalTrials.gov ↗

Study Summary

This study is being conducted to determine the efficacy and safety of povorcitinib in participants with nonsegmental vitiligo.

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

FieldValue
Enrollment Target 450 participants
Start Date 2023-11-27
Est. Completion 2027-03-16
Phase Phase 3

Sponsor

Incyte Corporation

163 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06113471

The ClinicalTrials.gov registry entry for NCT06113471 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 450 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 163 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with NonSegmental Vitiligo appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06113471 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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: NonSegmental Vitiligo. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06113471?

The interventions under investigation include: Placebo (DRUG), Povorcitinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06113471?

This trial is sponsored by Incyte Corporation, which has 163 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial