Eslicarbazepine acetate (BIA 2-093)

被引:148
作者
Almeida, Luis [1 ]
Soares-da-Silva, Patricio [1 ]
机构
[1] BIAL, Dept Res & Dev, P-4745 Mamede, Portugal
关键词
eslicarbazepine; acetate; BIA; 2-093; antiepileptic drugs; drug therapy; epilepsy;
D O I
10.1016/j.nurt.2006.10.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Eslicarbazepine acetate ( ESL) [( S)-(-)-10-acetoxy-10,11- dihydro-5H-dibenz[b,f]azepine-5-carboxamide], formerly known as BIA 2-093, is a novel central nervous system ( CNS)-active compound with anticonvulsant activity. It behaves as a voltage-gated sodium channel ( VGSC) blocker and is currently under clinical development for the treatment of epilepsy and bipolar disorder. ESL shares with carbamazepine and oxcarbazepine the dibenzazepine nucleus bearing the 5-carboxamide substitute, but is structurally different at the 10,11- position. This molecular variation results in differences in metabolism, preventing the formation of toxic epoxide metabolites such as carbamazepine-10,11 epoxide. In pharmacokinetic studies in humans, ESL was rapidly and extensively metabolized to eslicarbazepine ( S-licarbazepine), which is responsible for pharmacological activity. ESL has been tested in patients with refractory partial-onset seizures and was found to be efficacious and well tolerated. Monotherapy studies in adult epileptic patients and add-on studies in epileptic children are in the planning process. The efficacy and safety data appear to be very promising considering the refractory nature of the epileptic population enrolled in studies to date. Results of ongoing phase III studies in adult epileptic patients are expected to be available in 2007 and are required to define the position of ESL in the therapy of patients with epilepsy.
引用
收藏
页码:88 / 96
页数:9
相关论文
共 25 条
[1]  
Almeida L, 2005, EPILEPSIA, V46, P167
[2]   Single-dose and steady-state pharmacokinetics of eslicarbazepine acetate (BIA 2-093) in healthy elderly and young subjects [J].
Almeida, L ;
Falcao, A ;
Maia, J ;
Mazur, D ;
Gellert, M ;
Soares-da-Silva, P .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (09) :1062-1066
[3]   Safety, tolerability, and pharmacokinetic profile of BIA 2-093, a novel putative antiepileptic, in a rising multiple-dose study in young healthy humans [J].
Almeida, L ;
Soares-da-Silva, P .
JOURNAL OF CLINICAL PHARMACOLOGY, 2004, 44 (08) :906-918
[4]   Safety, tolerability and pharmacokinetic profile of BIA 2-093, a novel putative antiepileptic agent, during first administration to humans [J].
Luis Almeida ;
Patrício Soares-da-Silva .
Drugs in R & D, 2003, 4 (5) :269-284
[5]   Inhibition of glutamate release by BIA 2-093 and BIA 2-024, two novel derivatives of carbamazepine, due to blockade of sodium but not calcium channels [J].
Ambósio, AF ;
Silva, AP ;
Malva, JO ;
Soares-da-Silva, P ;
Carvalho, AP ;
Carvalho, CM .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (10) :1271-1275
[6]   Neurotoxic/neuroprotective profile of carbamazepine, oxcarbazepine and two new putative antiepileptic drugs, BIA 2-093 and BIA 2-024 [J].
Ambrósio, AF ;
Silva, AP ;
Araújo, I ;
Malva, JO ;
Soares-da-Silva, P ;
Carvalho, AP ;
Carvalho, CM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 406 (02) :191-201
[7]   Neurotoxicity induced by antiepileptic drugs in cultured hippocampal neurons:: A comparative study between carbamazepine, oxcarbazepine, and two new putative antiepileptic drugs, BIA 2-024 and BIA 2-093 [J].
Araújo, IM ;
Ambrósio, AF ;
Leal, EC ;
Verdasca, MJ ;
Malva, JO ;
Soares-Da-Silva, P ;
Carvalho, AP ;
Carvalho, CM .
EPILEPSIA, 2004, 45 (12) :1498-1505
[8]   PHARMACOKINETIC DRUG-INTERACTIONS WITH ORAL-CONTRACEPTIVES [J].
BACK, DJ ;
ORME, MLE .
CLINICAL PHARMACOKINETICS, 1990, 18 (06) :472-484
[9]   Anticonvulsant and sodium channel-blocking properties of novel 10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide derivatives [J].
Benes, J ;
Parada, A ;
Figueiredo, AA ;
Alves, PC ;
Freitas, AP ;
Learmonth, DA ;
Cunha, RA ;
Garrett, J ;
Soares-da-Silva, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (14) :2582-2587
[10]   Progress report on new antiepileptic drugs: a summary of the Seventh Eilat Conference (EILAT VII) [J].
Bialer, M ;
Johannessen, SI ;
Kupferberg, HJ ;
Levy, RH ;
Perucca, E ;
Tomson, T .
EPILEPSY RESEARCH, 2004, 61 (1-3) :1-48