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奥匹卡朋治疗帕金森病的临床药理学综述

Clinical pharmacology review of opicapone for the treatment of Parkinson's disease.

作者信息

Fabbri Margherita, Rosa Mario M, Ferreira Joaquim J

机构信息

Clinical Pharmacology Unit, Instituto de Medicina Molecular, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.

Laboratory of Clinical Pharmacology & Therapeutics, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.

出版信息

Neurodegener Dis Manag. 2016 Oct;6(5):349-62. doi: 10.2217/nmt-2016-0022. Epub 2016 Sep 7.

Abstract

Two catechol-O-methyl transferase inhibitors are currently used as add-on therapy to levodopa for the amelioration of end-of-dose motor fluctuations in Parkinson's disease patients: entacapone, which has moderate efficacy and requires multiple dosing, and tolcapone, which has a poor safety profile. Opicapone (OPC) is a novel, long-acting, peripherally selective, once daily, third-generation catechol-O-methyl transferase inhibitor. Two Phase III clinical trials demonstrated OPC efficacy in reducing OFF-time by an average of about 60 min daily compared with placebo, without increasing ON-time with troublesome dyskinesias, with a good drug safety profile. In June 2016, the European Commission granted a marketing authorization valid throughout the European Union for OPC, indicated as adjunctive of levodopa decarboxylase inhibitors in adult patients with Parkinson's disease and end-of-dose motor fluctuations.

摘要

目前有两种儿茶酚-O-甲基转移酶抑制剂作为左旋多巴的附加疗法,用于改善帕金森病患者的剂末运动波动:恩他卡朋,疗效中等且需多次给药;托卡朋,安全性较差。奥匹卡朋(OPC)是一种新型、长效、外周选择性、每日一次的第三代儿茶酚-O-甲基转移酶抑制剂。两项III期临床试验表明,与安慰剂相比,OPC在减少每日“关”期时间方面疗效显著,平均每日减少约60分钟,且不会增加伴有麻烦异动症的“开”期时间,药物安全性良好。2016年6月,欧盟委员会授予OPC在整个欧盟的上市许可,用于帕金森病成年患者及剂末运动波动患者,作为左旋多巴脱羧酶抑制剂的辅助用药。

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