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Study identifier: NCT07077902 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study for Evaluating Safety & Efficacy of Topical Roflumilast 0.3% Foam in Hidradenitis Suppurativa

Condition: Hidradenitis Suppurativa  ·  Sponsor: Tulane University

PhasePhase 2
Planned participants10
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

This is a phase 2a, open label study. As psoriasis and Hidradenitis Suppurativa (HS) share multiple inflammatory pathways, the investigators hypothesize that the use of topical roflumilast 0.3% foam is a safe and efficacious option as a monotherapy for patients with mild disease and as add-on therapy for maintenance and flares in patients with moderate to severe disease. The study will include correlative analysis to study gene expression profiling before and after therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Carole Bitar, MD  ·  504-988-5114  ·  cbitar@tulane.edu

Edward Coleman, MS  ·  504-988-5135  ·  ecoleman@tulane.edu

Always discuss trial participation with your own doctor first.

Locations (4)

Lakeview HospitalCovington, Louisiana, United StatesRecruiting
Lakeside HospitalNew Orleans, Louisiana, United StatesRecruiting
LCMC Multi-speciality ClinicNew Orleans, Louisiana, United StatesRecruiting
University Medical CenterNew Orleans, Louisiana, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07077902