Skip to content
Trial Eligibility
Menu

The Safety and Efficacy of Roflumilast Foam in HS

NCT07263230

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
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Beth Israel Deaconess Medical Center
Last updated on ClinicalTrials.gov
July 9, 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

Massachusetts · 1

  • Beth Israel Deaconess Medical Center · Boston, MA

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