TCP-25 gel
DrugTopical gel
NCT Number: NCT06594393
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.
Interested in participating?
Request Info4 year and older
All sexes
Interventional
Phase 2
Hopital St Louis, Paris, France
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Note: Corticosteroids for inhalation, ophthalmic, or intranasal use are permitted.
Topical gel
Placebo gel
Time frame: 56 days
Time frame: 56 days
Time frame: 56 days
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
Time frame: 56 days
Time frame: 56 days
Time frame: 56 days
Time frame: 56 days
Time frame: 56 days
Contact information is provided by the study sponsor or research team.
Xinnate AB
Industry
A Randomized, Double-blind, Vehicle-controlled Phase 2 Study to Evaluate Efficacy, Safety, and Tolerability of Topically Applied TCP-25 in Patients With Epidermolysis Bullosa
Acronym: STEP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06713434
Collagen Diseases, Congenital Abnormalities
Santiago, Huechuraba, Chile
View Trial DetailsNCT03472287
Collagen Diseases, Congenital Abnormalities
Palo Alto, California, United States
View Trial DetailsNCT07011589
Collagen Diseases, Congenital Abnormalities
Redwood City, California, United States
View Trial DetailsNCT07717736
Collagen Diseases, Congenital Abnormalities
View Trial Details