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首页> 外文期刊>Drug Design, Development and Therapy >Review of deutetrabenazine: a novel treatment for chorea associated with Huntington's disease
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Review of deutetrabenazine: a novel treatment for chorea associated with Huntington's disease

机译:氘苯丁嗪的评论:一种与亨廷顿舞蹈病相关的舞蹈病的新疗法

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Deutetrabenazine was recently approved for the treatment of chorea in Huntington’s disease (HD) and is the first deuterated medication that has been US Food and Drug Administration (FDA)-approved for therapeutic use. In this article, we review deutetrabenazine’s drug design, pharmacokinetics, drug interactions, efficacy, adverse events, comparison with tetrabenazine, dosage, and administration. Deutetrabenazine is a deuterated form of tetrabenazine and is a vesicular monoamine transporter 2 (VMAT2) inhibitor. The substitution of deuterium for hydrogen at key positions in the tetrabenazine molecule allows a longer drug half-life and less frequent daily dosing. Deutetrabenazine is administered twice daily up to a maximum daily dose of 48?mg, which corresponds to a similar daily dose of 100?mg of tetrabenazine. In a Phase III clinical trial (First-HD), there was a statistically significant improvement of chorea in HD subjects, as well as improvements in global impression of change as assessed by both patients and clinicians. This improvement was seen without significant adverse effects as the overall tolerability profile of deutetrabenazine was similar to placebo. Somnolence was the most commonly reported symptom in the deutetrabenazine group. In a study where subjects converted from tetrabenazine to deutetrabenazine in an open-label fashion (ARC-HD) and indirect comparison studies between tetrabenazine and deutetrabenazine, there is a suggestion that while efficacy for chorea is similar, the data may slightly favor tetrabenazine, but adverse effects and tolerability strongly favor deutetrabenazine. These data have not been replicated in true head-to-head studies. Current evidence supports that deutetrabenazine is an effective therapeutic treatment option for chorea in HD and may provide a more favorable adverse effect profile than tetrabenazine. However, more data are needed, particularly in the form of head-to-head studies between deutetrabenazine and other treatment options as well as longer term clinical experience with deutetrabenazine.
机译:氘苯丁嗪最近被批准用于治疗亨廷顿舞蹈病(HD)的舞蹈病,并且是美国食品药品监督管理局(FDA)批准用于治疗用途的第一种氘代药物。在本文中,我们回顾了氘苯丁嗪的药物设计,药代动力学,药物相互作用,疗效,不良事件,与丁苯那嗪的比较,剂量和给药方式。氘苯丁嗪是氘苯丁嗪的氘化形式,是水泡单胺转运蛋白2(VMAT2)抑制剂。用丁苯那嗪分子中关键位置的氢置换氘,可以延长药物半衰期,并减少每日给药的频率。氘苯丁嗪每天两次给药,最大每日剂量为48?mg,相当于每天100mg的丁苯那嗪的相似剂量。在一项III期临床试验(First-HD)中,HD患者的舞蹈病在统计学上有显着改善,并且患者和临床医生都评估了总体变化印象。观察到这种改善没有明显的不利影响,因为氘苯丁嗪的总体耐受性与安慰剂相似。在氘苯丁嗪组中,嗜睡是最常见的症状。在一项研究中,受试者以开放标签方式(ARC-HD)从丁苯那嗪转换为氘苯丁那嗪,并对丁苯那嗪和氘苯丁那嗪进行了间接比较研究,这表明尽管对舞蹈症的疗效相似,但数据可能会偏向于丁苯那嗪,但不良反应和耐受性强烈支持氘苯特那嗪。这些数据尚未在真正的头对头研究中复制。当前证据支持氘苯丁嗪是HD舞蹈病的有效治疗选择,并且可能比丁苯那嗪提供更有利的不良反应。但是,还需要更多数据,尤其是以氘苯丁嗪和其他治疗方案之间的头对头研究形式以及氘苯他嗪的长期临床经验。

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