Skip to content
Trial Eligibility
Menu

Safety and Efficacy of Roflumilast Foam 0.3% in Adolescent and Adult Subjects With Hidradenitis Suppurativa

NCT07689188

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

This study investigates the efficacy of topical roflumilast foam in patients with HS.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Hidradenitis Suppurativa (HS)

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
12 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Harrison Dermatology
Last updated on ClinicalTrials.gov
October 13, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Texas · 1

  • Harrison Institute for Clinical Research at Harrison Dermatology · Missouri City, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.