Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 3

A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Pediatric Participants With Nonsegmental Vitiligo

NCT06548360 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to to evaluate the safety and efficacy of ruxolitinib cream in pediatric participants with nonsegmental vitiligo.

Conditions Studied

Interventions

  • DRUG Ruxolitinib Cream
  • DRUG Vehicle Cream

Study Locations (20)

California

  • Axon Clinical Research — Inglewood
  • University of California Irvine — Irvine
  • Vitiligo & Pigmentation Institute of Southern California — Los Angeles
  • Dermatology Research Associates — Los Angeles
  • La Universal Research Center, Inc — Los Angeles
  • Stanford School of Medicine — Palo Alto
  • Empire Clinical Research — Pomona
  • Norcal Clinical Research — Rocklin
  • Peninsula Research Associates Pra — Rolling Hills Estates
  • Integrative Skin Science and Research — Sacramento
  • Rady Children'S Hospital-San Diego — San Diego

Arizona

  • Phoenix Children'S Hospital — Phoenix
  • Omni Dermatology — Phoenix
  • Affiliated Dermatology — Scottsdale
  • Banner - University Medicine Multispecialty Services Clinic — Tucson

Arkansas

  • Premier Dermatology Clinical Trials Institute At Northwest Arkansas — Fayetteville
  • Burke Pharmaceutical Research — Hot Springs

Colorado

  • Children'S Hospital Colorado — Aurora
  • Paradigm Clinical Research Centers, Inc. — Wheat Ridge

Alabama

  • University of Alabama At Birmingham-School of Medicine — Birmingham

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2025-01-24
Est. Completion 2027-03-13
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 NCT06548360

The ClinicalTrials.gov registry entry for NCT06548360 describes a study currently listed as 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 180 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 Ruxolitinib Cream 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: NCT06548360 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Arizona, Arkansas. 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 NCT06548360 about?

NCT06548360 is a clinical study titled "A Study to Evaluate the Safety and Efficacy of Ruxolitinib Cream in Pediatric Participants With Nonsegmental Vitiligo". The purpose of this study is to to evaluate the safety and efficacy of ruxolitinib cream in pediatric participants with nonsegmental vitiligo.

What is the current status of trial NCT06548360?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 180 participants. The study started on 2025-01-24. Estimated completion is 2027-03-13.

What conditions does trial NCT06548360 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 NCT06548360?

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

Who is sponsoring clinical trial NCT06548360?

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 NCT06548360 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. 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