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首页> 外文期刊>Epilepsia: Journal of the International League against Epilepsy >Efficacy, safety, and tolerability of perampanel in Asian and non-Asian patients with epilepsy
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Efficacy, safety, and tolerability of perampanel in Asian and non-Asian patients with epilepsy

机译:亚洲和非亚洲癫痫患者Perampanel的疗效,安全性和耐受性

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摘要

People of different ethnic or racial backgrounds may experience variations in pharmacokinetic and pharmacodynamic responses to drug therapies. Our post hoc analysis evaluated the efficacy, safety, and tolerability of perampanel in Asian and non-Asian populations with refractory focal seizures with or without focal to bilateral tonic-clonic (FBTC) seizures. This analysis pooled data from 4 randomized, placebo-controlled, phase-3 studies involving patients aged >= 12 years who have focal seizures with or without FBTC seizures. Patients were receiving 2, 4, 8, or 12 mg perampanel (or placebo) by the end of a 6-week titration period and for a further 13 weeks during the maintenance phase. Efficacy endpoints included median percent change in seizure frequency per 28 days, and 50% and seizure-freedom responder rates relative to baseline. The median percent change in seizure frequency per 28 days from baseline was significantly greater than placebo for perampanel 8 and 12 mg (-31.1% and -38.1% change, respectively; each P < 0.0001) in the Asian population, and for perampanel 4, 8, and 12 mg (-21.1% [P = 0.0001], -26.3% [P < 0.0001], and -27.7% [P = 0.0001] change, respectively) in the non-Asian population. The 50% responder rate relative to baseline was significantly greater than placebo for perampanel 8 and 12 mg (40.1% and 43.8%, respectively; each P < 0.0001) in the Asian population, and for perampanel 4, 8, and 12 mg (29.4% [P = 0.0002], 32.8% [P < 0.0001] and 34.5% [P = 0.0001]), respectively, in the non-Asian population. Seizure-freedom rate among all patients was 4.9%-11.7% for perampanel 2, 4, 8, and 12 mg. The most frequently reported treatment-emergent adverse events (TEAEs) across both populations were dizziness, somnolence, irritability, headache, and fatigue. The most common psychiatric TEAEs were aggression and irritability. Perampanel demonstrated a favorable and similar risk-benefit profile in both Asian and non-Asian populations with refractory focal seizures.
机译:不同种族或种族背景的人可能会遇到药代动力学和药效学反应对药物治疗的变化。我们的后HOC分析评估了Perampanel在亚洲和非亚洲群体中的疗效,安全性和可耐受性,其中难核焦点癫痫发作有或没有焦点对双边滋补克隆(FBTC)癫痫发作。该分析从4名随机,安慰剂对照,第3期研究中汇集了数据,涉及年龄的患者> = 12岁的患者,他们在有或没有FBTC癫痫发作。患者在6周滴定期结束时接受2,4,8或12mg Perampanel(或安慰剂),在维持阶段期间进一步13周。功效终点包括每28天的癫痫发作频率的中位数百分比,以及相对于基线的50%和癫痫发作 - 自由响应率。从基线每28天的癫痫发作频率的中位数百分比显着大于Perampanel 8和12毫克的安慰剂(分别为12毫克(-31.1%和-38​​.1%),分别在亚洲人口中,并且对于Perampanel 4,在非亚亚人群中,8和12mg(-21.1%[p = 0.0001],-26.3%[p <0.0001],分别为-27.7%[p = 0.0001])。相对于基线的50%响应率明显大于Perampanel 8和12毫克的安慰剂(分别为40.1%和43.8%;每次P <0.0001),以及Perampanel 4,8和12毫克(29.4在非亚亚人群中,分别分别在非亚洲群体中[p = 0.0002],32.8%[P <0.0001]和34.5%[p = 0.0001])。所有患者的癫痫发作率为4.9%-11.7%,适用于Perampanel 2,4,8和12毫克。两种种群的最常报告的治疗紧急的不良事件(茶)是头晕,嗜睡,烦躁,头痛和疲劳。最常见的精神科茶是侵略性和烦躁。 Perampanel在亚洲和非亚洲人群中表现出有利和类似的风险福利概况,难以抵抗难忘的焦点癫痫发作。

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