zorevunersen (STK-001) - Stoke Therap
radiprodil (RGH-896) - AbbVie, GRIN Therap
elsunersen (PRAX-222) - RogCon, Praxis Precision Medicines
soticlestat (TAK-935) - Takeda
azetukalner (XEN1101) - Xenon
darigabat (CVL-865) - AbbVie
Xcopri (cenobamate) - SK Bio
Ztalmy (ganaxolone oral) - Marinus
vormatrigine (PRAX-628) - Praxis Precision Medicines
relutrigine (PRAX-562) - Praxis Precision Medicines
Antiseizure Medications in Development: Novel Mechanisms, Precision Therapy, and the Move Towards Disease Modification. (PubMed, Curr Issues Mol Biol) - Aug 28, 2026 - "Functional-state-selective sodium channel modulation has emerged as a leading conceptual advance supported by converging mechanistic and early clinical evidence, exemplified by relutrigine (PRAX-562), a preferential persistent-current inhibitor for which a regulatory decision is pending in SCN2A/SCN8A-DEEs, and vormatrigine (PRAX-628), whose large open-label effect was not reproduced in a controlled (blinded) trial...Parallel advances include the selective Kv7 opener azetukalner; the dual-mechanism benchmark cenobamate; cholesterol-24-hydroxylase inhibition (soticlestat); selective serotonergic agonism (bexicaserin); glutamatergic precision agents (radiprodil); subtype-selective GABAA modulators (darigabat, ganaxolone); and gene-directed therapies (zorevunersen, elsunersen)... The pipeline reflects an ongoing shift from broad symptomatic agents toward mechanism-led, genotype-matched, and potentially disease-modifying treatments. This shift is tempered by a..." 
Journal • Review • CNS Disorders • Epilepsy • SCN8A
http://www.ncbi.nlm.nih.gov/pubmed/42651828
 
William Alves Martins
 
Aug 28, 2026
 
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