Pfizer Inc, Groton, Connecticut, U.S.A.
Epilepsia. 2014 Dec;55(12):1934-43. doi: 10.1111/epi.12830. Epub 2014 Nov 6.
To evaluate the safety, tolerability, and pharmacokinetics (PK) of pregabalin as adjunctive therapy in children with refractory partial seizures.
This was a phase 1, randomized, placebo-controlled, parallel-group, escalating-dose, multiple-dose study comprising a 7-day, double-blind treatment period and a single-blind, single dose of pregabalin administered to all children on day 8. Children in four age cohorts (1-23 months, 2-6, 7-11, and 12-16 years) received one of four doses of pregabalin (2.5, 5, 10, or 15 mg/kg/day) or placebo. Safety and tolerability were assessed throughout the study. Steady-state and single-dose PK parameters on day 8 were analyzed using standard noncompartmental procedures.
Sixty-five children received at least one dose of treatment. Four pregabalin-treated children discontinued treatment, three of whom received 15 mg/kg/day. Two children experienced serious adverse events, one of whom received pregabalin 15 mg/kg/day. During double-blind treatment, the most common adverse events reported in the pregabalin-treated population were somnolence (27.1%) and dizziness (12.5%). Steady-state pregabalin peak and total exposure in each age cohort appeared to increase linearly with dose. Apparent oral clearance (CL/F) was directly related to creatinine clearance, consistent with adults. CL/F normalized for body weight was 43% higher in patients weighing <30 kg. Steady-state and single-dose PK were consistent.
Pregabalin at doses up to 10 mg/kg/day in children aged 1 month to 16 years, and at doses up to 15 mg/kg/day in those aged <6 years, demonstrated acceptable safety and tolerability. For children weighing <30 kg, a dose increase of 40% (mg/kg dosing) is required to achieve comparable exposure with adults or children weighing ≥30 kg. These data will inform dose selection in phase 3 trials of the efficacy and safety of adjunctive pregabalin in children with refractory partial seizures.
评估普瑞巴林作为辅助治疗药物用于治疗耐药性部分性癫痫发作儿童的安全性、耐受性和药代动力学(PK)。
这是一项 1 期、随机、安慰剂对照、平行分组、递增剂量、多次剂量研究,包括 7 天的双盲治疗期和所有儿童在第 8 天接受单次单盲普瑞巴林剂量。四个年龄组(1-23 个月、2-6 岁、7-11 岁和 12-16 岁)的儿童分别接受四种剂量的普瑞巴林(2.5、5、10 或 15mg/kg/天)或安慰剂。整个研究过程中评估安全性和耐受性。第 8 天使用标准非房室药代动力学程序分析稳态和单次剂量 PK 参数。
65 名儿童至少接受了一剂治疗。四名接受普瑞巴林治疗的儿童停止治疗,其中三名儿童接受 15mg/kg/天的治疗。两名儿童出现严重不良事件,其中一名儿童接受 15mg/kg/天的普瑞巴林治疗。在双盲治疗期间,接受普瑞巴林治疗的人群中报告的最常见不良事件是嗜睡(27.1%)和头晕(12.5%)。每个年龄组的稳态普瑞巴林峰浓度和总暴露似乎与剂量呈线性增加。口服清除率(CL/F)与肌酐清除率直接相关,与成人一致。根据体重归一化的 CL/F 在体重<30kg 的患者中高 43%。稳态和单次剂量 PK 一致。
在 1 个月至 16 岁的儿童中,普瑞巴林剂量高达 10mg/kg/天,在<6 岁的儿童中,普瑞巴林剂量高达 15mg/kg/天,具有可接受的安全性和耐受性。对于体重<30kg 的儿童,需要增加 40%(mg/kg 剂量)的剂量,以达到与成人或体重≥30kg 的儿童相似的暴露水平。这些数据将为普瑞巴林辅助治疗耐药性部分性癫痫发作儿童的疗效和安全性的 3 期试验提供剂量选择信息。