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cenobamate 片剂治疗成人局灶性发作性癫痫。

Cenobamate tablets as a treatment for focal-onset seizures in adults.

机构信息

Kork Epilepsy Center, Kehl-Kork, Germany.

Department of Neurology, Albert-Ludwigs University of Freiburg, Freiburg, Germany.

出版信息

Expert Rev Clin Pharmacol. 2021 Feb;14(2):161-172. doi: 10.1080/17512433.2021.1879637. Epub 2021 Jan 26.

Abstract

: Despite the introduction of numerous new antiseizure medications (ASMs) still about one-third of epilepsies remain drug-resistant. Therefore, new compounds with advanced efficacy are urgently needed. Cenobamate (CNB) is a new ASM that has been recently introduced in the United States for the treatment of adults with focal-onset seizures. The approval in Europe is under way.: This review covers the pharmacological profile of CNB, the proof-of-concept trial, the two double-blind, placebo-controlled phase 2 trials investigating adjunct CNB in adults with focal-onset seizures, one open-label safety trial, and a variety of published abstract material that provided additional post hoc data.: In two placebo-controlled randomized multicenter phase 2 trials adjunct CNB showed unusually high efficacy with rates of seizure-free people with epilepsy (PWE) partially beyond 20%. However, during the clinical program cases of drug-related reactions with eosinophilia and systemic symptoms (DRESS syndrome) occurred. Therefore, an open-label safety study was performed in more than 1300 PWE with particularly slower titration schedules which did not add more cases with similar reactions. Taking into consideration the promising efficacy and the safety experience from the open-label trial, CNB applied according to the meanwhile recommended titration strategy, might offer a new prospect.

摘要

尽管有许多新的抗癫痫药物(ASMs)问世,但仍有约三分之一的癫痫患者对药物无反应。因此,迫切需要具有更高疗效的新化合物。苯妥英(CNB)是一种新的抗癫痫药物,最近已在美国获准用于治疗局灶性发作的成人癫痫。在欧洲,该药也正在审批中。

本文综述了 CNB 的药理学特性、概念验证试验、两项在局灶性发作成人中评估添加 CNB 的双盲、安慰剂对照的 2 期临床试验、一项开放标签安全性试验以及提供了额外事后数据的各种已发表的摘要材料。

在两项安慰剂对照的随机多中心 2 期临床试验中,添加 CNB 显示出异常高的疗效,癫痫患者(PWE)无癫痫发作的比例部分超过 20%。然而,在临床项目中,出现了药物相关性反应伴嗜酸性粒细胞增多和全身症状(DRESS 综合征)的病例。因此,对 1300 多名 PWE 进行了开放标签的安全性研究,采用了特别缓慢的滴定方案,没有增加类似反应的病例。考虑到该药的疗效前景和开放标签试验的安全性经验,如果按照目前推荐的滴定策略使用 CNB,可能会提供一个新的前景。

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