Workshop
Advancing AAV Gene Therapies: Insights from CURE Epilepsy-Funded Research
About
This investigators workshop examines adeno-associated virus gene therapies for epilepsy from design and animal testing through clinical translation. Research examples concern Lafora disease, SCN1B-related Dravet syndrome and SLC6A1-related neurodevelopmental disorder. The panel considers treatment efficacy, seizure-associated adverse effects and AAV toxicity, alongside strategies for overcoming current limitations. Discussion also covers biomarkers, scalability and the evidence needed to advance candidates beyond preclinical studies.
Sunday 6 December, 14:00–15:30 Mountain Standard Time (America/Denver). Part of the 2026 American Epilepsy Society Annual Meeting. In-person meeting registration and a free myAES account are required. Standard full-meeting rates are USD 800 for member scientists and USD 1,075 for non-member scientists; student rates are USD 250 and USD 360, respectively. Other professional and one-day categories are available. Seating priority goes to registered attendees.
Topics
- adeno-associated virus gene therapies, search World Wide
- epilepsy
- Lafora disease
- SCN1B-related Dravet syndrome, broader topic: Dravet syndrome
- SLC6A1-related neurodevelopmental disorder, broader topic: neurodevelopmental disorder
- seizure-associated adverse effects, search World Wide
- AAV toxicity, broader topic: toxicity
- biomarkers
- preclinical studies
- clinical translation
Guest speakers
- Priya Balasubramanian, CURE Epilepsy
- Beverly Davidson
- Henry Lee, Boston Children's Hospital
- Lori Isom, University of Michigan
- Mayank Verma, SBSI/UTSW
Details
Location
39.74314, -104.99556Colorado Convention Center, Denver, Colorado, USA
Organisations
American Epilepsy Society and CURE Epilepsy
Host