Diacerein orphan drug development for epidermolysis bullosa simplex: A phase 2/3 randomized, placebo-controlled, double-blind clinical trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze II, klinické zkoušky, fáze III, časopisecké články, randomizované kontrolované studie
PubMed
29410318
DOI
10.1016/j.jaad.2018.01.019
PII: S0190-9622(18)30130-0
Knihovny.cz E-zdroje
- Klíčová slova
- diacerein, epidermolysis bullosa, keratin, rare genodermatosis,
- MeSH
- adherence pacienta MeSH
- anthrachinony terapeutické užití MeSH
- antiflogistika MeSH
- aplikace lokální MeSH
- dítě MeSH
- dvojitá slepá metoda MeSH
- epidermolysis bullosa simplex diagnóza farmakoterapie MeSH
- hodnocení rizik MeSH
- lidé MeSH
- následné studie MeSH
- předškolní dítě MeSH
- rozvrh dávkování léků MeSH
- stupeň závažnosti nemoci MeSH
- výroba orphan drugs * MeSH
- výsledek terapie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze II MeSH
- klinické zkoušky, fáze III MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- anthrachinony MeSH
- antiflogistika MeSH
- diacerein MeSH Prohlížeč
BACKGROUND: Epidermolysis bullosa simplex (EBS) is a rare genetic, blistering skin disease for which there is no cure. Treatments that address the pathophysiology of EBS are needed. OBJECTIVE: Compare the impact of 1% diacerein cream with placebo in reducing the number of blisters in EBS. METHODS: In a randomized, placebo-controlled, phase 2/3 trial we used a 1% diacerein topical formulation to treat defined skin areas in 17 patients. In a 2-period crossover trial, patients were randomized to either placebo or diacerein for a 4-week treatment and a 3-month follow-up in period 1. After a washout, patients were crossed over during period 2. The prespecified primary end point was the proportion of patients with a reduction of number of blisters by more than 40% from baseline in selected areas over the treatment episode. RESULTS: Of the patients receiving diacerein, 86% in episode 1 and 37.5% in episode 2 met the primary end point (vs 14% and 17% with placebo, respectively). This effect was still significant after the follow-up. Changes in absolute blister numbers were significant for the diacerein group only. No adverse effects were observed. LIMITATIONS: Low patient numbers and no invasive data acquisition because of clinical burden in children. CONCLUSION: This trial provides evidence of the impact of 1% diacerein cream in the treatment of EBS.
Department of Laboratory Medicine Paracelsus Medical University Salzburg Austria
Department of Pediatric Dermatology Children's Hospital Brno Czech Republic
Landesapotheke Salzburg Department of Production Hospital Pharmacy Salzburg Austria
Research Office Biostatistics Paracelsus Medical University Salzburg Austria
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