Filsuvez® (Birch Triterpenes) Topical Gel.

Skinmed Pub Date : 2024-12-31 eCollection Date: 2024-01-01
Aditya K Gupta, Avantika Mann, Kimberly Vincent, William Abramovits
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Abstract

Filsuvez® (birch triterpenes) topical gel received approval in 2023 for the treatment of epidermolysis bullosa (EB) in pediatric patients (aged ≥6 months) and adults. It promotes wound healing by modulating inflammation, encouraging new tissue formation, and maintaining the skin barrier. In a randomized, double-blind, controlled, parallel-group, phase III trial (EASE, NCT03068780), 223 patients were randomly assigned to two groups: the first group received treatment with birch triterpenes topical gel (study gel, n = 109), and the second group received treatment with vehicle gel (n = 114). The study gel or vehicle gel was applied as a 1-mm layer to the affected wound surface once every 4 days for 90 days. The primary efficacy endpoint, defined as the first complete closure of the EB target wound by day 45, was achieved at a higher proportion in the study gel group (41.3% [45/109]), compared to the vehicle gel group (28.9% [33/114]). Application site reactions were reported in 7.3% (8/109) of patients in the study gel group and 6.1% (7/114) of patients in the vehicle gel group. It is recommended to apply as a 1-mm layer to the affected wound surface only.

Filsuvez®(桦木三萜)外用凝胶。
Filsuvez®(桦木三萜)外用凝胶于2023年获得批准,用于治疗儿童(年龄≥6个月)和成人的大疱性表皮松解症(EB)。它通过调节炎症、促进新组织形成和维持皮肤屏障来促进伤口愈合。在一项随机、双盲、对照、平行组的III期试验(EASE, NCT03068780)中,223例患者随机分为两组:第一组接受桦木三萜外用凝胶(研究凝胶,n = 109)治疗,第二组接受载体凝胶(n = 114)治疗。将研究凝胶或载体凝胶作为1毫米的层涂抹在患处创面,每4天一次,共90天。主要疗效终点,定义为第45天EB靶创面首次完全闭合,研究凝胶组达到的比例(41.3%[45/109])高于载体凝胶组(28.9%[33/114])。研究凝胶组和载体凝胶组分别有7.3%(8/109)和6.1%(7/114)的患者出现了应用部位反应。建议仅在受影响的伤口表面涂抹1毫米厚的一层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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