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卡比多巴/左旋多巴缓释胶囊(息宁控释片(Rytary(®)),Nuient™):帕金森病治疗综述

Carbidopa/Levodopa ER Capsules (Rytary(®), Numient™): A Review in Parkinson's Disease.

作者信息

Greig Sarah L, McKeage Kate

机构信息

Springer, Private Bag 65901, Mairangi Bay, 0754, Auckland, New Zealand.

出版信息

CNS Drugs. 2016 Jan;30(1):79-90. doi: 10.1007/s40263-015-0306-3.

Abstract

A new extended-release (ER) capsule formulation of carbidopa/levodopa (Rytary(®), Numient™, IPX066) is available for the treatment of Parkinson's disease (PD). Carbidopa/levodopa ER capsules contain beads of carbidopa and levodopa, designed to release the drugs at different rates in the gastrointestinal tract and provide constant therapeutic levodopa concentrations that are maintained for 4-5 h (after an initial peak at ≈ 1 h). In randomized phase III trials, oral carbidopa/levodopa ER was significantly more effective than placebo with regard to improving motor symptoms and activities of daily living in patients with early PD after 30 weeks' treatment, and provided significantly greater reductions in daily 'off-time' in patients with advanced PD than immediate-release (IR) carbidopa/levodopa or carbidopa/levodopa IR plus entacapone after a treatment period of 13 and 2 weeks, respectively, without increasing troublesome dyskinesia. The efficacy of carbidopa/levodopa ER was maintained during a 9-month open-label extension in patients with early or advanced PD. Carbidopa/levodopa ER was generally well tolerated in clinical trials, with the most common adverse events in the extension study being nausea and insomnia in patients with early PD and falls and dyskinesia in patients with advanced PD. Thus, carbidopa/levodopa ER is an effective and generally well-tolerated treatment option for the motor symptoms of PD, reducing periods of 'off-time' compared with carbidopa/levodopa IR without increasing troublesome dyskinesia.

摘要

一种新的卡比多巴/左旋多巴缓释(ER)胶囊制剂(息宁控释片(Rytary®)、Nuient™、IPX066)可用于治疗帕金森病(PD)。卡比多巴/左旋多巴ER胶囊含有卡比多巴和左旋多巴微丸,其设计目的是在胃肠道以不同速率释放药物,并提供持续4 - 5小时(在约1小时出现初始峰值后)的治疗性左旋多巴浓度。在随机III期试验中,口服卡比多巴/左旋多巴ER在治疗30周后,对于改善早期PD患者的运动症状和日常生活活动方面显著优于安慰剂,并且在分别治疗13周和2周后,与速释(IR)卡比多巴/左旋多巴或卡比多巴/左旋多巴IR加恩他卡朋相比,晚期PD患者的每日“关期”时间显著缩短,且未增加令人烦恼的异动症。在早期或晚期PD患者的9个月开放标签延长期内,卡比多巴/左旋多巴ER的疗效得以维持。在临床试验中,卡比多巴/左旋多巴ER总体耐受性良好,在延长期研究中,早期PD患者最常见的不良事件是恶心和失眠,晚期PD患者是跌倒和异动症。因此,卡比多巴/左旋多巴ER是治疗PD运动症状的一种有效且总体耐受性良好的选择,与卡比多巴/左旋多巴IR相比,可减少“关期”时间,且不增加令人烦恼的异动症。

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