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CNS Drugs. 2020 Feb;34(2):207-218. doi: 10.1007/s40263-020-00703-x.
Pitolisant (Wakix), an orally available, first-in-class antagonist/inverse agonist of the histamine 3 receptor, is approved in the EU (as of March 2016) for the treatment of narcolepsy with or without cataplexy in adults and in the USA (as of August 2019) for the treatment of excessive daytime sleepiness (EDS) in adults with narcolepsy. Pitolisant was demonstrated to have minimal risk of abuse in preclinical and clinical studies, and is the only anti-narcoleptic drug not scheduled as a controlled substance in the USA. The totality of evidence from pivotal and supportive phase III trials suggests that pitolisant administered at up to the recommended maximum dose of 36 mg once daily reduces EDS and cataplexy in adults with narcolepsy relative to placebo. Noninferiority of pitolisant to modafinil in the management of EDS was not demonstrated. Pitolisant was generally well tolerated in clinical trials. Consistent with its mechanism of action, the most common treatment-emergent adverse events included headache, insomnia and anxiety. With minimal abuse potential and offering the convenience of oral, once-daily administration, pitolisant extends the range of approved treatment options available to adult patients with narcolepsy with or without cataplexy.
皮替拉生(Wakix),一种口服的、组胺 3 受体的首创型拮抗剂/反向激动剂,在欧盟获批(截至 2016 年 3 月)用于治疗成人伴有或不伴有猝倒的发作性睡病,以及在美国获批(截至 2019 年 8 月)用于治疗成人发作性睡病的日间过度嗜睡(EDS)。在临床前和临床研究中,皮替拉生显示出极小的滥用风险,并且是唯一一种未被美国列为管制物质的抗嗜睡药物。关键性和支持性 III 期试验的全部证据表明,与安慰剂相比,每日一次最高推荐剂量为 36mg 的皮替拉生可降低伴有猝倒的成人发作性睡病患者的 EDS 和猝倒。皮替拉生在 EDS 管理方面并不优于莫达非尼。皮替拉生在临床试验中总体耐受性良好。与作用机制一致,最常见的治疗中出现的不良事件包括头痛、失眠和焦虑。由于潜在滥用风险极小,且具有口服、每日一次的给药便利,皮替拉生为伴有或不伴有猝倒的发作性睡病成年患者提供了更多已获批的治疗选择。