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Study details
Enrolling now

The Safety and Efficacy of Roflumilast Foam in HS

Beth Israel Deaconess Medical Center
NCT IDNCT07263230ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

20

Study length

about 2.8 years

Ages

18+

Locations

1 site in MA

What this study is about

Researchers are testing the safety and effectiveness of a new treatment called roflumilast foam for people with hidradenitis suppurativa (HS). The trial will last 1005 days and involve applying the foam to affected areas. It is investigating whether this treatment can help improve symptoms associated with HS.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Roflumilast 0.3% topical foam

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
topical

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

DERMATOLOGICALS

Drug routes

topical

Endpoints

Primary: Mean Change from Baseline in Abscess and Inflammatory Nodule (AN) Count at Week 16.