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Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic–clonic seizures: A double‐blind, randomized, placebo‐controlled trial

机译:左乙拉西坦辅助治疗患有广泛性强直-阵挛性癫痫的中国和日本成年人:一项双盲,随机,安慰剂对照试验

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Objective To assess the efficacy, safety, and tolerability of adjunctive levetiracetam (LEV) in Chinese and Japanese adults with generalized tonic–clonic (GTC) seizures (N01159; NCT01228747). Methods This double‐blind, randomized, placebo‐controlled, multicenter phase III trial comprised: 4‐week retrospective and 4‐week prospective baseline, 12‐week dose‐adjustment, and 16‐week evaluation periods. Chinese and Japanese patients ≥16?years old with idiopathic generalized, symptomatic generalized, or undetermined epilepsy with GTC seizures received a single‐blind placebo during the prospective baseline, and then were randomized 1:1 to placebo or LEV 1,000?mg/day administered twice daily. Patients reporting GTC seizures up to week 8 had the LEV dosage increased to 3,000?mg/day. The primary efficacy variable was percent reduction from combined baseline in GTC seizures/week during the 28‐week treatment period. Results Overall, 251 patients were randomized (208 from China; 43 from Japan); 141 (56.2%) completed the 28‐week treatment period. Least‐squares mean percent reduction from combined baseline in GTC seizures/week (treatment period) was placebo 12.6% versus LEV 68.8% (95% confidence interval, 44.0–68.2; p? Significance In this trial, adjunctive LEV 1,000–3,000?mg/day was effective in reducing GTC seizure frequency in Chinese and Japanese patients ≥16?years old with GTC seizures. Seizure reduction occurred in both patients with idiopathic and symptomatic generalized epilepsy. LEV was well tolerated in this population.
机译:目的评估左乙拉西坦(LEV)辅助治疗在中国和日本成年人中广泛性强直-阵挛(GTC)发作的疗效,安全性和耐受性(N01159; NCT01228747)。方法该双盲,随机,安慰剂对照的多中心III期临床试验包括:4周回顾性和4周前瞻性基线,12周剂量调整和16周评估期。 ≥16岁的特发性,症状性或不确定性癫痫伴GTC癫痫发作的中国和日本患者在前瞻性基线期间接受单盲安慰剂治疗,然后以1:1的比例随机分配至安慰剂或LEV 1,000?mg /天每天两次。在第8周之前报告GTC癫痫发作的患者LEV剂量增加至3,000?mg /天。主要疗效变量是在28周的治疗期内,每周GTC癫痫发作合并基线的降低百分比。结果总共251例患者被随机分组​​(中国208例;日本43例)。 141(56.2%)人完成了28周的治疗期。 GTC癫痫发作/周(治疗期)与合并基线相比的最小二乘平均减少率为安慰剂12.6%,而LEV为68.8%(95%置信区间为44.0-68.2; p?显着性)在该试验中,辅助LEV 1,000-3,000?mg /天可有效降低≥16岁的中国和日本患者的GTC癫痫发作频率,特发性和症状性全身性癫痫患者均发生癫痫发作减少,该人群对LEV的耐受性良好。

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