Safety and tolerability of different titration rates of retigabine (ezogabine) in patients with partial-onset seizures

被引:10
作者
Biton, Victor [1 ]
Gil-Nagel, Antonio [2 ]
Brodie, Martin J. [3 ]
DeRossett, Sarah E. [4 ]
Nohria, Virinder [5 ]
机构
[1] Arkansas Epilepsy Program, Little Rock, AR 72205 USA
[2] Hosp Ruber Int, Madrid 28034, Spain
[3] Univ Glasgow, Western Infirm, Epilepsy Unit, Glasgow G11 6NT, Lanark, Scotland
[4] GlaxoSmithKline, Res Triangle Pk, NC 27709 USA
[5] Valeant Pharmaceut Int, Durham, NC 27701 USA
关键词
Epilepsy; Retigabine; Ezogabine; Titration rates; Safety; Adverse events; ANTICONVULSANT RETIGABINE; ANTIEPILEPTIC DRUGS; PARTIAL EPILEPSY; CONTROLLED TRIAL; HUMAN LIVER; CHANNEL; GLUCURONIDATION; ACTIVATION; INITIATION; CURRENTS;
D O I
10.1016/j.eplepsyres.2013.08.021
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Retigabine (RTG; international nonproprietary name)/ezogabine (EZG; US adopted name) is an antiepileptic drug (AED) that prolongs neuronal voltage-gated potassium-channel KCNQ2-5 (K-v 7.2-7.5) opening. This double-blind study evaluated different RTG/EZG dose-titration rates. Patients (N = 73) with partial-onset seizures receiving concomitant AEDs were randomized to one of three titration groups, all of which were initiated at RTG/EZG 300 mg/day divided into three equal doses. Fast-, medium-, and slow-titration groups received dose increments of 150 mg/day every 2, 4, and 7 days, respectively, achieving the target dose of 1200 mg/day after 13, 25, and 43 days, respectively. Safety assessments were performed throughout. Discontinuation rates due to treatment-emergent adverse events (TEAEs) were numerically higher in the fast- (10/23) and medium- (7/22) titration groups than in the slow-titration group (3/23) but statistical significance was achieved only for the high-titration group compared with the tow-titration group (p = 0.024). Stratified analysis, with concomitant AEDs divided into enzyme inducers (carbamazepine, phenytoin, oxcarbazepine) or noninducers, showed that the risk of discontinuation due primarily to TEAEs was significantly higher in the fast- (p = 0.010) but not in the medium-titration group (p = 0.078) when compared with the slow-titration group. Overall, the slow-titration rate appeared to be best tolerated and was used in further efficacy and safety studies with RTG/EZG. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
相关论文
共 23 条
[1]  
Biton V, 2001, ANN PHARMACOTHER, V35, P173
[2]   N-Glucuronidation of the antiepileptic drug retigabine: results from studies with human volunteers, heterologously expressed human UGTs, human liver, kidney, and liver microsomal membranes of Crigler-Najjar type II [J].
Borlak, Jurgen ;
Gasparic, Antje ;
Locher, Mathias ;
Schupke, Hubert ;
Hermann, Robert .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2006, 55 (06) :711-721
[3]   Efficacy and safety of adjunctive ezogabine (retigabine) in refractory partial epilepsy [J].
Brodie, M. J. ;
Lerche, H. ;
Gil-Nagel, A. ;
Elger, C. ;
Hall, S. ;
Shin, P. ;
Nohria, V. ;
Mansbach, H. .
NEUROLOGY, 2010, 75 (20) :1817-1824
[4]   Retigabine for the Adjunctive Treatment of Adults with Partial-Onset Seizures in Epilepsy with and without Secondary Generalization [J].
Craig, Dawn ;
Rice, Stephen ;
Paton, Fiona ;
Fox, David ;
Woolacott, Nerys .
PHARMACOECONOMICS, 2013, 31 (02) :101-110
[5]   Adverse effects of antiepileptic drugs: a brief overview of important issues [J].
Cramer, Joyce A. ;
Mintzer, Scott ;
Wheless, James ;
Mattson, Richard H. .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2010, 10 (06) :885-891
[6]   Concerns with antiepileptic drug initiation: Safety, tolerability and efficacy [J].
Ferrendelli, JA .
EPILEPSIA, 2001, 42 :28-30
[7]   Rapid initiation of gabapentin - A randomized, controlled trial [J].
Fisher, RS ;
Sachdeo, RC ;
Pellock, J ;
Penovich, PE ;
Magnus, L ;
Bernstein, P .
NEUROLOGY, 2001, 56 (06) :743-748
[8]   Randomized, double-blind, placebo-controlled trial of ezogabine (retigabine) in partial epilepsy [J].
French, J. A. ;
Abou-Khalil, B. W. ;
Leroy, R. F. ;
Yacubian, E. M. T. ;
Shin, P. ;
Hall, S. ;
Mansbach, H. ;
Nohria, V. .
NEUROLOGY, 2011, 76 (18) :1555-1563
[9]  
GlaxoSmithKline, 2012, POTIGA EZ TABL PRESC
[10]  
Gueler Nevzat, 2008, Ther Umsch, V65, P633, DOI 10.1024/0040-5930.65.10.633