UnknownPhase 2NCT03016715
Using Topical Sirolimus 2% for Patients With Epidermolysis Bullous Simplex (EBS) Study
Studying Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Premier Specialists, Australia
- Principal Investigator
- Dedee F Murrell, MDUniversity of New South Wales
- Intervention
- Sirolimus 2%(drug)
- Enrollment
- 8 enrolled
- Eligibility
- 5 years · All sexes
- Timeline
- 2016
Study locations (1)
- Premier Specialists, Sydney, New South Wales, Australia
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT03016715 on ClinicalTrials.govOther trials for Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
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- ACTIVE NOT RECRUITINGPHASE2, PHASE3NCT06073132An International, Multicenter, Randomized, Double-Blind, Parallel Group, Vehicle-Controlled, Phase 2/3 Study With Open-Label Extension Evaluating the Efficacy and Safety of Diacerein 1% Ointment for the Treatment of Generalized Epidermolysis Bullosa Simplex (EBS)TWi Biotechnology, Inc.
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