Recruiting
Phase 2

TCP-25

Sponsor:

Xinnate AB

Code:

NCT06594393

Conditions

Epidermolysis Bullosa (EB)

Dystrophic Epidermolysis Bullosa

Junctional Epidermolysis Bullosa

Eligibility Criteria

Sex: All

Age: 4+

Healthy Volunteers: Not accepted

Interventions

TCP-25 gel

Vehicle (placebo)

Study Details

Brief 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.

Conditions

Epidermolysis Bullosa (EB)

Dystrophic Epidermolysis Bullosa

Junctional Epidermolysis Bullosa

Study ID

NCT06594393

Start date

Jan 30, 2026

Status verified date

Aug, 2026

Completion date

Jun 30, 2027

Anticipated

Primary completion date

Jun 30, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 4+

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

32 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: TCP-25

Topical gel

placebo comparator: Vehicle

Placebo gel

Interventions

TCP-25 gel

Topical gel

Vehicle (placebo)

Placebo gel

Primary outcome measure

  • Open wound area [ Time Frame: 56 days ]

Central Contacts and Locations

Central contacts

Head of Clinical Development

46462756000info@xinnate.com

Locations

Cincinnati Children's Hospital Medical Center

Recruiting

Cincinnati, Ohio, United States, 45229

Contacts

Dr. Kalyani Marathe, PI, MD

kalyani.marathe@cchmc.org

More Information

Sponsor

Xinnate AB

Last update posted

Aug 12, 2026

Last verified

Aug, 2026

Keywords

  • epidermolysis bullosa
  • topical treatment

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Xinnate AB on 2026-08-12.