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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa (TRuE-HS1)

ClinicalTrials.gov ID: NCT06959225

Public ClinicalTrials.gov record NCT06959225. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 7:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Double-Blind, Randomized, Vehicle-Controlled, Efficacy and Safety Study of Ruxolitinib Cream in Participants With Hidradenitis Suppurativa

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the efficacy and safety of ruxolitinib cream in participants with hidradenitis suppurativa.

Study identification

NCT ID
NCT06959225
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Incyte Corporation
Industry
Enrollment
580 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 23, 2025 (Actual)
Primary completion
Oct 9, 2026 (Estimated)
Completion
Jul 11, 2027 (Estimated)
Last update posted
Jul 28, 2026

2025 – 2027

United States locations

U.S. sites
59
U.S. states
26
U.S. cities
54
Facility City State ZIP Site status
Investigative Site US020 Phoenix Arizona 85008 —
Investigative Site US033 Scottsdale Arizona 85259 —
Investigative Site US054 Tempe Arizona 85282 —
Investigative Site US002 Fayetteville Arkansas 72703 —
Investigative Site US055 Brea California 92821 —
Investigative Site US004 Laguna Niguel California 92677 —
Investigative Site US007 Los Angeles California 90033 —
Investigative Site US013 San Diego California 92103 —
Investigative Site US060 San Diego California 92120 —
Investigative Site US038 San Diego California 92121 —
Investigative Site US059 Aurora Colorado 80045 —
Investigative Site US045 Boynton Beach Florida 33437 —
Investigative Site US028 Fort Myers Florida 33912 —
Investigative Site US016 Miami Florida 33142 —
Investigative Site US027 Sanford Florida 32771 —
Investigative Site US057 Sweetwater Florida 33172 —
Investigative Site US029 Tampa Florida 33609 —
Investigative Site US061 Atlanta Georgia 30322 —
Investigative Site US053 Atlanta Georgia 30331 —
Investigative Site US019 Marietta Georgia 30060 —
Investigative Site US026 Chicago Illinois 60657 —
Investigative Site US049 Clarksville Indiana 47129 —
Investigative Site US052 West Lafayette Indiana 47906 —
Investigative Site US001 Bowling Green Kentucky 42104 —
Investigative Site US022 Louisville Kentucky 40241 —
Investigative Site US050 Baton Rouge Louisiana 70809 —
Investigative Site US046 Glenn Dale Maryland 20769 —
Investigative Site US003 Boston Massachusetts 02115 —
Investigative Site US030 Boston Massachusetts 02215 —
Investigative Site US010 Quincy Massachusetts 02169 —
Investigative Site US051 Novi Michigan 48377 —
Investigative Site US006 Minneapolis Minnesota 55455 —
Investigative Site US021 New Brighton Minnesota 55112 —
Investigative Site US036 Saint Joseph Missouri 64506 —
Investigative Site US034 New City New York 10956 —
Investigative Site US018 New York New York 10003 —
Investigative Site US017 New York New York 10023 —
Investigative Site US023 Rochester New York 14623 —
Investigative Site US014 Chapel Hill North Carolina 27516 —
Investigative Site US025 Fargo North Dakota 58103 —
Investigative Site US015 Bexley Ohio 43209 —
Investigative Site US044 Cincinnati Ohio 45219 —
Investigative Site US008 Columbus Ohio 43230 —
Investigative Site US031 Mason Ohio 45040 —
Investigative Site US048 Oklahoma City Oklahoma 73118 —
Investigative Site US043 Danville Pennsylvania 17822 —
Investigative Site US056 Philadelphia Pennsylvania 19107 —
Investigative Site US024 Charleston South Carolina 29425 —
Investigative Site US041 Myrtle Beach South Carolina 29788 —
Investigative Site US047 Nashville Tennessee 37215 —
Investigative Site US062 Dallas Texas 75390 —
Investigative Site US035 El Paso Texas 79902 —
Investigative Site US032 Frisco Texas 75033 —
Investigative Site US012 Plano Texas 75025 —
Investigative Site US011 San Antonio Texas 78213 —
Investigative Site US040 Layton Utah 84041 —
Investigative Site US037 Murray Utah 84107 —
Investigative Site US039 Ogden Utah 84405 —
Investigative Site US058 Seattle Washington 98195 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06959225, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 28, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06959225 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →