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Clinical Trials in the USA / NCT06594393
Recruiting Phase 2

A Phase 2 Study of TCP-25 Gel in Patients With Epidermolysis Bullosa, STEP-study

NCT06594393 · tracked via the Priya Life Science USA tracker
Sponsor
Xinnate AB
Phase
Phase 2
Started
2026-01-30
Last updated
2026-08-12

Condition(s) studied

Epidermolysis Bullosa (EB)Dystrophic Epidermolysis BullosaJunctional Epidermolysis Bullosa

Investigational drug(s) / intervention(s)

TCP-25 gelVehicle (placebo)

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

Sex
ALL
Min age
4 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Male or female patients with documented diagnosis of DEB or JEB, confirmed by genetic testing and/or by a skin biopsy with immunofluorescence mapping. * Patients ≥4 years old. Note: Initially, patients ≥12 years will be enrolled. Enrollment will be open to 4 to 11 year old pediatric patients (both inclusive), after a DMC reviews and provides a positive opinion regarding the safety and tolerability of the IMP in at least 3 patients 12 to 18 years old who have completed at least 4 weeks of IMP use. Exclusion Criteria: * The patient has any subtype of EB other than DEB or JEB. * The patient is currently being treated or planned to be treated with systemic antibiotics. Note: Use of preventive and/or anti-inflammatory antibiotic treatment, including doxycycline, on an established treatment regimen (stable dose for ≥6 weeks before the Baseline Visit) is permitted. Use of topical antibiotics on the index wounds within 7 days before the Baseline Visit is prohibited. • Use of systemic corticosteroids \>0.2 mg/kg prednisone dose equivalent per day within 30 days or use of topical corticosteroids on index wounds within 7 days before the Screening Visit. Note: Corticosteroids for inhalation, ophthalmic, or intranasal use are permitted. • The patient has a history of or current malignancy over the index wound, eg, basal cell carcinoma or squamous cell carcinoma.

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
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

Other trials for the same condition

Official registry record

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 the USA