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.
The study will include a Screening Period, a Treatment Period (Days 1 to 56, with study visits conducted every 2 weeks, including the baseline \[Day 1\], Day 14, Day 28, Day 42, and Day 56 visits) and a Safety Follow-up conducted via a telephone/video call at approximately 14 days after the last dose of the IMP. Patients will undergo efficacy, safety, tolerability, and PK assessments at scheduled visits. For evaluation of the primary efficacy endpoint, a trained clinician will take the images of the index wounds at all scheduled visits from baseline through Day 56 (Visit 6) using 3D digital photography and software for wound measurement.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
32
Topical gel
Placebo gel
Hopital St Louis
Paris, France
RECRUITINGAndreas Syngros Hospital of Veneral & Dermatological Diseases
Athens, Greece
RECRUITINGHospital Of Skin And Venereal Diseases of Thessaloniki
Thessaloniki, Greece
Open wound area
Time frame: 56 days
Frequency, intensity, and seriousness of Adverse Events in all treated patients until end of treatment
Time frame: 56 days
Change in procedural pain using the Wong Baker FACES® Pain Rating Scale (0 min -10 max)
Wong Baker FACES pain rating scale uses 6 graphically or cartoon-depicted faces with varying facial expressions that represent no pain (no hurt) (Face 0) to worst pain/hurt that can be imagined (Face 10).
Time frame: 56 days
Change from baseline in clinical impression of overall treatment area
Time frame: 56 days
TCP-25 plasma concentrations
Time frame: 56 days
Number of participants with treatment-related local tolerability assessment at the area of IMP application assessed on a 4-point scale
Time frame: 56 days
Clinically significant changes from baseline in blood pressure until end of treatment
Time frame: 56 days
Number of patients with clinically significant changes from baseline in pulse rate until end of treatment
Time frame: 56 days
Number of patients with clinically significant changes from baseline in physical examination findings until end of treatment
Time frame: 56 days
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Hospital Clinic de Barcelona
Barcelona, Spain
RECRUITINGHospital Univ La Paz
Madrid, Spain
RECRUITINGUniversity hospital
Lund, Skåne County, Sweden
NOT_YET_RECRUITING