Development of new antiepileptic drugs: challenges, incentives, and recent advances

被引:293
作者
Perucca, Emilio
French, Cqueline
Bialer, Meir [6 ]
机构
[1] C Mondino Fdn, IRCCS, Neurol Inst, Pavia, Italy
[2] Univ Pavia, Clin Pharmacol Unit, I-27100 Pavia, Italy
[3] Univ Pavia, Dept Internal Med & Therapeut, I-27100 Pavia, Italy
[4] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[5] Hebrew Univ Jerusalem, Fac Med, David R Bloom Ctr Pharm, IL-91120 Jerusalem, Israel
[6] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, Dept Pharmaceut, IL-91120 Jerusalem, Israel
关键词
D O I
10.1016/S1474-4422(07)70215-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Despite the introduction of many second-generation antiepileptic drugs (AEDs) in the past 15 years, a third of patients with epilepsy remain refractory to available treatments, and newer and more effective therapies are needed. Although our understanding of the mechanisms of drug resistance is fragmented, novel AED targets have been identified, and models of refractory epilepsy have been developed that can help to select candidate compounds for development. There are more than 20 compounds with potential antiepileptic activity in various stages of clinical development, and for many of these promising clinical trial results are already available. Several incentives justify further investment into the discovery of newer and more effective AEDs. Moreover, developments in clinical trial methodology enable easier completion of proof-of-concept studies, earlier definition of the therapeutic potential of candidate compounds, and more efficient completion of trials for various epilepsy indications.
引用
收藏
页码:793 / 804
页数:12
相关论文
共 65 条
[1]   Topiramate reduces AMPA-induced Ca2+ transients and inhibits GluR1 subunit phosphorylation in astrocytes from primary cultures [J].
Ängehagen, M ;
Rönnbäck, L ;
Hansson, E ;
Ben-Menachem, E .
JOURNAL OF NEUROCHEMISTRY, 2005, 94 (04) :1124-1130
[2]  
Applebaum J, 2005, BIPOLAR DISORD, V7, P30
[3]   Correlation analysis between anticonvulsant ED50 values of antiepileptic drugs in mice and rats and their therapeutic doses and plasma levels [J].
Bailer, M ;
Twyman, RE ;
White, HS .
EPILEPSY & BEHAVIOR, 2004, 5 (06) :866-872
[4]   Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy [J].
Barton, ME ;
Klein, BD ;
Wolf, HH ;
White, HS .
EPILEPSY RESEARCH, 2001, 47 (03) :217-227
[5]   Efficacy and safety of Losigamone in partial seizures: a randomized double-blind study [J].
Baulac, M ;
Klement, S .
EPILEPSY RESEARCH, 2003, 55 (03) :177-189
[6]   Lacosamide:: A review of preclinical properties [J].
Beyreuther, Bettina K. ;
Freitag, Joachim ;
Heers, Cara ;
Krebsfaenger, Niels ;
Scharfenecker, Ute ;
Stoehr, Thomas .
CNS DRUG REVIEWS, 2007, 13 (01) :21-42
[7]   Progress report on new antiepileptic drugs: a summary of the fourth Eilat conference (EILAT IV) [J].
Bialer, M ;
Johannessen, SI ;
Kupferberg, HJ ;
Levy, RH ;
Loiseau, P ;
Perucca, E .
EPILEPSY RESEARCH, 1999, 34 (01) :1-41
[8]   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
[9]   New antiepileptic drugs currently in clinical trials: Is there a strategy in their development? [J].
Bialer, M .
THERAPEUTIC DRUG MONITORING, 2002, 24 (01) :85-90
[10]   Valproic acid: Second generation [J].
Bialer, Meir ;
Yagen, Boris .
NEUROTHERAPEUTICS, 2007, 4 (01) :130-137