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A Phase 2, Double-Blind, Randomized, 16-Week, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream Followed by an Open-Label Extension Period in Adults With Chronic Hand Eczema
The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in adult participants with diagnosis of chronic hand eczema (CHE) and moderate to severe disease activity (Investigator's Global Assessement (IGA) of CHE score 3 or 4).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Southwest Skin Specialists Phoenix Biltmore
Phoenix, Arizona, United States
First Oc Dermatology
Fountain Valley, California, United States
Marvel Clinical Research Llc
Huntington Beach, California, United States
Dermatology Research Associates
Los Angeles, California, United States
Skin Research of South Florida, Llc
Miami, Florida, United States
Well Pharma Medical Research Corporation
Miami, Florida, United States
Forcare Clinical Research
Tampa, Florida, United States
Midwest Allergy Sinus Asthma, Sc
Normal, Illinois, United States
The Indiana Clinical Trials Center Ictc
Plainfield, Indiana, United States
Delricht Research
Baton Rouge, Louisiana, United States
Start Date
July 31, 2023
Primary Completion Date
July 15, 2024
Completion Date
December 13, 2024
Last Updated
July 31, 2025
186
ACTUAL participants
Ruxolitinib cream
DRUG
Vehicle
DRUG
Lead Sponsor
Incyte Corporation
NCT06884163
NCT06997393
NCT05471934
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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