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

RecruitingPhase 2Ages 4 Years - anyAllXinnate AB
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
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 โ‰ฅ4 years old. Note: Initially, patients โ‰ฅ12 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 โ‰ฅ6 weeks before the Baseline Visit) is permitted. Use of topical antibiotics on the index wounds within 7 days before the Baseline Visit is prohibited. โ€ข 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. โ€ข The patient has a history of or current malignancy over the index wound, eg, basal cell carcinoma or squamous cell carcinoma.
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What it tests

  • TCP-25 gel
  • Vehicle (placebo)
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Where

13 sites
Cincinnati Children's Hospital Medical Center
Cincinnati, United States
Hopital St Louis
Paris, France
Andreas Syngros Hospital of Veneral & Dermatological Diseases
Athens, Greece
Hospital Of Skin And Venereal Diseases of Thessaloniki
Thessaloniki, Greece
Hospital
Modena, Italy
IDI Istituto Dermopatico dell'Immacolata IRCCS
Rome, Italy
University hospital
Gdansk, Poland
Dermoklinika Centrum Medyczne
Lodz, Poland

โ€ฆand 5 more on ClinicalTrials.gov.

๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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