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NCT06213831 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Safety and Tolerability of Maximal Use Ruxolitinib Cream

A Phase 1 study of Prurigo Nodularis, sponsored by Incyte Corporation.

Completed
Registry status
Phase 1
Development phase
23
Enrollment target
20
Study locations

NCT06213831 is a Phase 1 study of Prurigo Nodularis that has completed, run by Incyte Corporation. The registered enrollment target is 23 participants, below the 228-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (90% lower). The trial reports 20 study locations across 13 states.

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The verdict

NCT06213831, a Phase 1 study of Prurigo Nodularis, has completed, sponsored by Incyte Corporation.

COMPLETED
Registry status
Phase 1
Development phase
23 participants
Enrollment target
20
Study locations

Study Summary

This study is being conducted to determine the safety and tolerability of ruxolitinib 1.5% cream under maximal use conditions in participants with Prurigo Nodularis (PN).

Conditions Studied

Interventions

  • DRUG Ruxolitinib Cream 1.5%

Study Locations (20)

California

  • First Oc Dermatology - Fountain Valley
  • Amicis Research Center Valencia - Northridge
  • Clinical Science Institute Clinical Research Specialists Inc - Santa Monica

Florida

  • Advanced Pharma Cr, Llc - Miami
  • Sullivan Dermatology North Miami Beach Office - North Miami Beach
  • Olympian Clinical Research - Tampa

Arizona

  • Saguaro Dermatology - Phoenix
  • Affiliated Dermatology - Scottsdale

Michigan

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

Texas

  • Dermresearch, Inc. - Austin
  • North Texas Center For Clinical Research Ntccr - Frisco

Idaho

  • St Lukes Clinic Dermatology Ketchum - Ketchum

Indiana

  • Dawes Fretzin Clinical Research Group Llc - Indianapolis

Kentucky

  • Equity Medical - Bowling Green

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2024-02-27
Est. Completion 2025-07-17
Phase Phase 1

Sponsor

Incyte Corporation

239 total trials

What the Registry Record Tells You About NCT06213831

The ClinicalTrials.gov registry entry for NCT06213831 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 228-participant average among 14 other Prurigo Nodularis trials with a reported enrollment target (90% lower). The listed sponsor is Incyte Corporation, which has 239 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prurigo Nodularis appearing as the primary indexed condition, and to 1 intervention - of which Ruxolitinib Cream 1.5% is the first listed.

NCT06213831 reports 20 study locations spanning 13 distinct geographic areas - top geographies include California, Florida, Arizona.

Frequently Asked Questions

What is clinical trial NCT06213831 about?

NCT06213831 is a clinical study titled "A Study to Evaluate the Safety and Tolerability of Maximal Use Ruxolitinib Cream". This study is being conducted to determine the safety and tolerability of ruxolitinib 1.5% cream under maximal use conditions in participants with Prurigo Nodularis (PN).

What is the current status of trial NCT06213831?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2024-02-27. Estimated completion is 2025-07-17.

What conditions does trial NCT06213831 study?

This clinical trial studies the following conditions: Prurigo Nodularis.

What interventions are being tested in trial NCT06213831?

The interventions under investigation include: Ruxolitinib Cream 1.5% (DRUG).

Who is sponsoring clinical trial NCT06213831?

This trial is sponsored by Incyte Corporation, which has 239 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06213831 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Idaho, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.