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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 Sep 7, 2026, 2:49 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 22, 2025
Primary completion
Oct 8, 2026
Completion
Jul 10, 2027
Last update posted
Jul 27, 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 27, 2026 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06959225 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →