Next-generation anti-seizure therapy
Epilepsy affects around 70 million people worldwide, and roughly a third do not respond to existing medications. The developmental and epileptic encephalopathies — Dravet and Lennox-Gastaut syndromes among them — remain severely undertreated in children.
Cannabidiol proved the mechanism is real but carries practical limits: low oral bioavailability, variable exposure, liver signals and drug–drug interactions. Our lead series was designed against exactly those liabilities, and shows anti-seizure activity in zebrafish and mouse models of Dravet syndrome without the sedation and motor impairment that limit current options.
- Discovery
- Lead selected
- Preclinical validation
- IND-enabling
- Clinic