Eslicarbazepine Acetate Sodium channel blocker, Antiepileptic drug

被引:10
作者
Dulsat, C. [1 ]
Mealy, N. [1 ]
Castaner, R. [1 ]
Bolos, J. [1 ]
机构
[1] Prous Sci, Barcelona 08025, Spain
关键词
BIA-2-093; SEP-0002093; Exalief (R); Zebinix (R); Stedesa (TM); BIA; 2-093; PHARMACOKINETICS; ANTICONVULSANT; OXCARBAZEPINE; CARBAMAZEPINE; EPILEPSY; BIA-2-093;
D O I
10.1358/dof.2009.034.03.1352675
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eslicarbazepine acetate (BIA-2-093) is a prodrug of eslicarbazepine ([S]-licarbazepine), a third-generation drug belonging to the carbamazepine (CBZ) family and the active metabolite of oxcarbazepine (OXC) Eslicarbazepine acetate is currently being developed as a flew antiepileptic drug (AED), with the aim of improving the efficacy and tolerability profiles of CBZ and OXC Favorable phase III data from studies in patients with partial-onset seizures have indicated effective reductions in seizure frequency, good response rates, good safety and improvements in quality-of-life parameters when eslicarbazepine acetate is used as odd-on therapy These Studies hove resulted in the recent recommendation by the EMEA granting marketing authorization to BIAL - Portelo (Zebinix (R) Exalief (R) to be marketed in Europe by Eisai) Clinical development of eslicarbazepine acetate (Stedesa (TM)) is also under way in the U S and Canada by licensee Septocor
引用
收藏
页码:189 / 195
页数:7
相关论文
共 87 条
[1]   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
[2]  
ALMEIDA L, 2008, EPILEPSIA S7, V49
[3]  
ALMEIDA L, 2005, EPILEPSIA, V46
[4]  
ALMEIDA L, 2007, 36 ANN M AM COLL CLI
[5]  
ALMEIDA L, 2007, EPILEPSIA S6, V48
[6]   Pharmacokinetics of eslicarbazepine acetate in patients with moderate hepatic impairment [J].
Almeida, Luis ;
Potgieter, J. Hendrick ;
Maia, Joana ;
Potgieter, M. Alida ;
Mota, Fernando ;
Soares-da-Silva, P. .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 64 (03) :267-273
[7]   Disposition of eslicarbazepine acetate in the mouse after oral administration [J].
Alves, Gilberto ;
Figueiredo, Isabel ;
Castel-Branco, Margarida ;
Lourenco, Nulita ;
Falcao, Amilcar ;
Caramona, Margarida ;
Soares-da-Silva, Patricio .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2008, 22 (05) :529-536
[8]   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
[9]   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
[10]   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