Oleogel-S10 Phase 3 study "EASE" for epidermolysis bullosa: study design and rationale

Epidermolysis bullosa (EB) is a group of rare, genetic diseases that affect the integrity of epithelial tissues, most notably the skin. Patients experience recurrent skin wounding, with severity depending on type, sub-type, and mutation. Oleogel-S10, a formulation of birch bark extract, has demonstr...

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Veröffentlicht in:Current controlled trials in cardiovascular medicine 2019-06, Vol.20 (1), p.350-350, Article 350
Hauptverfasser: Kern, Johannes S, Schwieger-Briel, Agnes, Löwe, Sandra, Sumeray, Mark, Davis, Charles, Martinez, Anna E
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Sprache:eng
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Zusammenfassung:Epidermolysis bullosa (EB) is a group of rare, genetic diseases that affect the integrity of epithelial tissues, most notably the skin. Patients experience recurrent skin wounding, with severity depending on type, sub-type, and mutation. Oleogel-S10, a formulation of birch bark extract, has demonstrated efficacy in a Phase 2 trial assessing re-epithelialization of wounds in EB. EASE (NCT03068780, EudraCT 2016-002066-32) is a randomized, Phase 3, placebo-controlled study designed to determine the efficacy of Oleogel-S10 versus placebo in patients with EB. EASE is a Phase 3, two-phase study comprising a 90-day, double-blind, randomized, placebo-controlled phase, followed by 24 months of open-label, single-arm follow-up. Patients with junctional EB, dystrophic EB, or Kindler syndrome and target wounds (10 - 50cm ) present for > 21 days and
ISSN:1745-6215
1745-6215
DOI:10.1186/s13063-019-3362-z