A Phase 2 Study of TCP-25 Gel in Patients With Epidermolysis Bullosa, STEP-study
Condition(s) studied
Investigational drug(s) / intervention(s)
TCP-25 gel: Topical gel
Vehicle (placebo): Placebo gel
Study summary
This is a Phase 2, double-blind, randomized, vehicle-controlled study designed to evaluate efficacy, safety, and tolerability of topically applied TCP-25 gel in patients with confirmed DEB or JEB. The study will implement intrasubject randomization, ie, a pair of matching index wounds will be randomly assigned to be treated with a local application of either TCP 25 gel or vehicle gel.
Eligibility
Primary outcome measure(s)
- Open wound area — 56 days
Trial sites (10)
| Facility | City | Region | Status |
|---|---|---|---|
| Cincinnati Children's Hospital Medical Center | Cincinnati | Ohio | Recruiting |
| Hopital St Louis | Paris | France | Recruiting |
| Andreas Syngros Hospital of Veneral & Dermatological Diseases | Athens | Greece | Recruiting |
| Hospital Of Skin And Venereal Diseases of Thessaloniki | Thessaloniki | Greece | Recruiting |
| IDI Istituto Dermopatico dell'Immacolata IRCCS | Rome | Italy | Recruiting |
| San Joan de Deu, SJD Children's hospital Barcelona | Barcelona | Catalonia | Recruiting |
| Hospital Clinic de Barcelona | Barcelona | Spain | Recruiting |
| Hospital Univ La Paz | Madrid | Spain | Recruiting |
| University hospital | Lund | Skåne County | Recruiting |
| Akademiska sjukhuset | Uppsala | Sweden | Recruiting |
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 NCT06594393 on ClinicalTrials.gov ↗ ← All trials in Italy