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

COMPLETED Phase 3

A Study to Evaluate the Efficacy, and Safety Study of Ruxolitinib Cream in Adults With Moderate Atopic Dermatitis

NCT06238817 · View on ClinicalTrials.gov ↗

Study Summary

This study is being conducted to establish the efficacy of ruxolitinib cream in participants with moderate AD who had an inadequate response to, or are intolerant to, or contraindicated to topical corticosteroid (TCS)s and topical calcineurin inhibitor (TCI)s.

Conditions Studied

Interventions

  • DRUG Ruxolitinib Cream
  • DRUG Vehicle Cream

Study Locations (20)

California

  • First Oc Dermatology — Fountain Valley
  • Center For Dermatology Cosmetic and Laser Surgery — Fremont
  • Medderm Associates, Inc — San Diego

Texas

  • Center For Clinical Studies Webster — Houston
  • Texas Dermatology Research Center — Plano
  • Rainey and Finklea Dermatology — San Antonio

Florida

  • Encore Medical Research, Llc Hollywood — Hollywood
  • Entrust Clinical Research — Miami

Georgia

  • Lane Dermatology and Dermatologic Surgery — Columbus
  • Marietta Dermatology the Skin Cancer Center Marietta — Marietta

Illinois

  • Arlington Dermatology — Rolling Meadows
  • Northshore University Healthsystem — Skokie

Michigan

  • Oakland Hills Dermatology Pc — Auburn Hills
  • Revival Research Institute, Llc Troy — Troy

New South Wales

  • Premier Specialists Pty Ltd — Kogarah
  • Australian Clinical Research Network — Maroubra

Arkansas

  • Lynn Institute of the Ozarks — Little Rock

Trial Details

FieldValue
Enrollment Target 241 participants
Start Date 2024-04-26
Est. Completion 2025-10-17
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 NCT06238817

The ClinicalTrials.gov registry entry for NCT06238817 describes a study currently listed as completed. 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 241 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 Atopic Dermatitis 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: NCT06238817 reports 20 study locations spanning 11 distinct geographic areas — top geographies include California, Texas, Florida. 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 NCT06238817 about?

NCT06238817 is a clinical study titled "A Study to Evaluate the Efficacy, and Safety Study of Ruxolitinib Cream in Adults With Moderate Atopic Dermatitis". This study is being conducted to establish the efficacy of ruxolitinib cream in participants with moderate AD who had an inadequate response to, or are intolerant to, or contraindicated to topical corticosteroid (TCS)s and topical calcineurin inhibitor (TCI)s.

What is the current status of trial NCT06238817?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 241 participants. The study started on 2024-04-26. Estimated completion is 2025-10-17.

What conditions does trial NCT06238817 study?

This clinical trial studies the following conditions: Atopic Dermatitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06238817?

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 NCT06238817?

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 NCT06238817 being conducted?

This trial has 20 study locations across Arkansas, 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