Clinical Trials in the USA / NCT07049575
Recruiting
Phase 1
Study to Evaluate the Maximal Use of Ruxolitinib Cream in Adult and Adolescent Participants With Hidradenitis Suppurativa
NCT07049575 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Hidradenitis Suppurativa
Investigational drug(s) / intervention(s)
Ruxolitinib Cream: Ruxolitinib cream applied topically to the affected area as a thin film twice daily.
Study summary
The purpose of this study is to evaluate the maximal use of ruxolitinib cream in adult and adolescent participants with hidradenitis suppurativa.
Eligibility
Inclusion Criteria:
* Diagnosis of HS for at least 6 months before screening visit.
* Diagnosis of HS (Hurley Stage I, II, III) with a total abscess and inflammatory nodule count of at least 4 and affecting at least 3 distinct anatomical areas at screening and Day 1 visits.
* Total estimated treatment BSA \> 20% at screening and baseline.
* Agreement to not use topical or systemic antibiotics for treatment of HS during the Maximal Use Treatment Period.
* Willingness to avoid pregnancy or fathering children based on the criteria defined in the protocol.
* Further inclusion criteria apply.
Exclusion Criteria:
* Current or history of skin condition(s) other than HS that might confound the evaluation of HS; clinically uncontrolled cardiovascular disease; thrombosis; certain cancers; certain infections; severe anemia, thrombocytopenia, or neutropenia; other medical conditions at the discretion of the investigator.
* Laboratory values outside of the protocol-defined ranges.
* Further exclusion criteria apply.
Primary outcome measure(s)
- Number of participants with Treatment-emergent Adverse Events (TEAEs) — Up to 24 weeks
Defined as adverse events reported for the first time or worsening of a pre-existing event after the first application of study drug. - Number of participants with TEAEs leading to treatment interruption, discontinuation — Up to 24 weeks
Number of participants with TEAEs leading to dose interruption or discontinuation
Trial sites (21)
| Facility | City | Region | Status |
|---|---|---|---|
| Saguaro Dermatology | Phoenix | Arizona | Recruiting |
| First Oc Dermatology | Fountain Valley | California | Completed |
| Amicis Research Center Valencia | Northridge | California | Recruiting |
| Children'S Hospital of Orange County | Orange | California | Recruiting |
| Clinical Trials Research Institute | Thousand Oaks | California | Recruiting |
| Clarity Dermatology | Castle Rock | Colorado | Completed |
| International Clinical Research Tennessee Llc | Sanford | Florida | Recruiting |
| Lenus Research Medical Group, Llc | Sweetwater | Florida | Recruiting |
| Trueblue Clinical Research | Tampa | Florida | Recruiting |
| Lane Dermatology and Dermatologic Surgery | Columbus | Georgia | Recruiting |
| Options Research Group, Llc | West Lafayette | Indiana | Recruiting |
| Equity Medical, Llc | Bowling Green | Kentucky | Recruiting |
| Delricht Research | Baton Rouge | Louisiana | Recruiting |
| Revival Research Institute, Llc Troy | Troy | Michigan | Completed |
| Red River Research Partners | Bolivar | Missouri | Recruiting |
| Dr Bobby Buka, Md Greenwich Village | New York | New York | Recruiting |
| Equity Medical, Llc | New York | New York | Recruiting |
| Red River Research Partners | Fargo | North Dakota | Recruiting |
| Centricity Research Columbus | Columbus | Ohio | Completed |
| Unity Clinical Research | Oklahoma City | Oklahoma | Recruiting |
| Paddington Testing Co Inc | Philadelphia | Pennsylvania | Completed |
More Incyte Corporation trials in the USA
Other trials for the same condition
A Phase 3 Study to Assess Efficacy Safety and Tolerability of Remibrutinib in Adult and Adolescent Patients With Moderate to Severe Hidradenitis Suppurativa
Active, not recruiting
A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadacitinib in Adult and Adolescent Participants With Moderate to Severe Hidradenitis Suppurativa Who Have Failed Anti-TNF Therapy
Active, not recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07049575 on ClinicalTrials.gov ↗ ← All trials in the USA