Joaquim J. Ferreira, Olivier Rascol, Fabrizio Stocchi, Angelo Antonini, Joana Moreira, Guillermo Castilla-Fernández, José-Francisco Rocha, Joerg Holenz, Werner Poewe, the Epsilon Study investigators
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The primary efficacy endpoint was the mean change from baseline to week 24 in Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III) total score.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 355 patients were randomized (opicapone 50 mg <i>n</i> = 177, placebo <i>n</i> = 178) and 322 (91%) completed the double-blind period. The adjusted mean [95% CI] change from baseline to week 24 in MDS-UPDRS-III subscore was −6.5 [−7.9, −5.2] in the opicapone group versus −4.3 [−5.7, 3.0] in the placebo group resulting in a significant difference of −2.2 [−3.9, −0.5] favoring opicapone (<i>p</i> = 0.010). There was no difference in the incidence of patients who developed motor complications (5.5% with opicapone vs. 9.8% with placebo) and the incidence of adverse events considered related to study medication was similar between groups (opicapone 10.2% vs. placebo 13.5%).</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Treatment with once-daily adjunct opicapone was well tolerated, improved motor severity, and did not induce the development of motor complications. 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引用次数: 0
摘要
背景:儿茶酚- o -甲基转移酶(COMT)抑制剂通常用于控制帕金森病(PD)的运动波动。我们评估了阿匹卡朋对左旋多巴治疗的无运动并发症患者运动症状严重程度的影响。方法:这是一项随机、双盲、24周、安慰剂对照的研究,阿picapone 50 mg辅助左旋多巴(NCT04978597)。左旋多巴治疗的无运动并发症的患者被随机分配到24周的双盲治疗中,并辅以50毫克的阿匹卡朋或匹配的安慰剂。主要疗效终点是运动障碍学会统一帕金森病评定量表第三部分(MDS-UPDRS-III)总分从基线到第24周的平均变化。结果:随机抽取355例患者(奥picapone 50 mg n = 177,安慰剂n = 178), 322例(91%)完成双盲期。从基线到第24周,MDS-UPDRS-III亚评分的调整平均[95% CI]变化在阿匹卡酮组为-6.5[-7.9,-5.2],而安慰剂组为-4.3[-5.7,3.0],导致阿匹卡酮优势显著差异为-2.2 [-3.9,-0.5](p = 0.010)。发生运动并发症的患者发生率没有差异(奥匹卡彭组为5.5%,安慰剂组为9.8%),与研究药物相关的不良事件发生率在两组之间相似(奥匹卡彭组为10.2%,安慰剂组为13.5%)。结论:每日1次辅助奥匹卡彭治疗耐受性良好,改善了运动严重程度,且未引起运动并发症的发生。这些结果支持阿匹卡朋在治疗无运动并发症的PD患者中的临床应用。
Opicapone as adjunct to levodopa in treated Parkinson's disease without motor complications: A randomized clinical trial
Background
Catechol-O-methyl transferase (COMT) inhibitors are routinely used to manage motor fluctuations in Parkinson's disease (PD). We assessed the effect of opicapone on motor symptom severity in levodopa-treated patients without motor complications.
Methods
This was a randomized, double-blind, 24-week, placebo-controlled study of opicapone 50 mg as adjunct to levodopa (NCT04978597). Levodopa-treated patients without motor complications were randomized to 24 weeks of double-blind treatment with adjunct opicapone 50 mg or matching placebo. The primary efficacy endpoint was the mean change from baseline to week 24 in Movement Disorder Society-Unified Parkinson's Disease Rating Scale Part III (MDS-UPDRS-III) total score.
Results
A total of 355 patients were randomized (opicapone 50 mg n = 177, placebo n = 178) and 322 (91%) completed the double-blind period. The adjusted mean [95% CI] change from baseline to week 24 in MDS-UPDRS-III subscore was −6.5 [−7.9, −5.2] in the opicapone group versus −4.3 [−5.7, 3.0] in the placebo group resulting in a significant difference of −2.2 [−3.9, −0.5] favoring opicapone (p = 0.010). There was no difference in the incidence of patients who developed motor complications (5.5% with opicapone vs. 9.8% with placebo) and the incidence of adverse events considered related to study medication was similar between groups (opicapone 10.2% vs. placebo 13.5%).
Conclusions
Treatment with once-daily adjunct opicapone was well tolerated, improved motor severity, and did not induce the development of motor complications. These results support the clinical usefulness of opicapone in the management of PD patients without motor complications.
期刊介绍:
The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).