Tolerability, safety, and efficacy of adjunctive brivaracetam for focal seizures in older patients: A pooled analysis from three phase III studies

被引:30
作者
Brodie, Martin J. [1 ]
Whitesides, John [2 ]
Schiemann, Jimmy [2 ]
D'Souza, Joseph [3 ]
Johnson, Martin E. [2 ]
机构
[1] Univ Glasgow, Glasgow, Lanark, Scotland
[2] UCB Pharma, Raleigh, NC USA
[3] UCB Pharma, Smyrna, GA USA
关键词
Epilepsy; Brivaracetam; Elderly; Safety; Tolerability; Efficacy; PLACEBO-CONTROLLED TRIAL; NEWLY-DIAGNOSED EPILEPSY; PARTIAL-ONSET SEIZURES; DOUBLE-BLIND; ANTIEPILEPTIC DRUGS; HEALTHY-SUBJECTS; CARBAMAZEPINE; PHARMACOKINETICS; LAMOTRIGINE; MULTICENTER;
D O I
10.1016/j.eplepsyres.2016.08.018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: This analysis was conducted to assess the tolerability, safety, and efficacy of brivaracetam (BRV) for adjunctive treatment of focal (partial-onset) seizures in patients aged >= 65 years. Methods: Safety/tolerability and efficacy data for patients aged >= 65 years were pooled from three randomized, double-blind, placebo-controlled, fixed-dose Phase III studies (NCT00490035, NCT00464269, and NCT01261325). Data were pooled by treatment group: placebo or the proposed therapeutic dose range of 50-200 mg/day: BRV 50, 100, 200 mg/day. Results: Thirty-two patients aged >= 65 years were randomized to placebo or BRV 50-200 mg/day. Of these, 30 patients (93.8%) completed their respective study. In the safety population (n = 32), 87.5% placebo-vs 73.3% BRV-treated patients reported treatment-emergent adverse events (TEAEs) during the treatment period; most commonly, headache (25.0% vs 12.5%), paresthesia (0% vs 12.5%), and somnolence (50.0% vs 12.5%) for placebo-vs BRV-treated patients, respectively. During the treatment period, drug-related TEAEs were reported by 62.5% of placebo-vs 53.3% of BRV-treated patients, and serious TEAEs (SAEs) were reported by 0% of placebo-and 4.2% of BRV-treated patients; there were no drug-related SAEs and no deaths. Three SAEs (placebo 1/8; BRV 2/24) and two deaths (placebo 1/8; BRV 1/24) occurred in the post-treatment period. In the efficacy population (n = 31), median percent reduction from baseline in focal seizure frequency/28 days was 14.0% for placebo vs 25.5%, 49.6%, and 74.9% for BRV 50, 100, and 200 mg/day, respectively. The >= 50% responder rate was 14.3% for placebo vs 25.0%, 50.0%, and 66.7% for BRV 50, 100, and 200 mg/day, respectively. Conclusions: Safety/tolerability and efficacy findings in this small subgroup of older patients treated with adjunctive BRV are consistent with those observed in the much larger overall pooled population. BRV may be a suitable adjunctive treatment for older patients with uncontrolled focal seizures. Further larger studies in this population are warranted. (C) 2016 The Authors. Published by Elsevier B.V.
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收藏
页码:114 / 118
页数:5
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