There are several new antiepileptic drugs undergoing extensive clinica
l investigation. Five new drugs - vigabatrin, lamotrigine, gabapentin,
felbamate and oxcarbazepine - appear to be the most widely tested and
promising agents. Vigabatrin is most effective in drug-resistant part
ial epilepsy. Vigabatrin is also effective in infantile spasms, but se
ems to have negative effects on myoclonic epilepsies and absence seizu
res. Lamotrigine and felbamate seem to be effective in partial epileps
y and in Lennox-Gastaut syndrome. In addition, lamotrigine and felbama
te seem to have efficacy in idiopathic generalised epilepsies. Oxcarba
zepine appears to be equally as effective as carbamazepine, but less t
oxic. Gabapentin has few adverse effects and has efficacy in some pati
ents with drug-resistant partial epilepsy. Some of the new antiepilept
ic drugs modify excitatory or inhibitory amino acid transmission, but
some of them may employ new, still unknown mechanisms of action. Depen
ding on the mechanism of action, the therapeutic effectiveness of the
antiepileptic drugs may differ in specific epileptic syndromes. Future
antiepileptic drugs may thus give us the possibility to design ration
al polypharmacy for individual patients by combining agents with diffe
rent spectra of effectiveness. Considering the goal of good tolerabili
ty in the development bf the new antiepileptic drugs, polypharmacy wit
h these agents is not expected to increase adverse effects significant
ly.