Research

We look to you as our partners as we collectively learn more about SCN2A and its effects on patients and their families. We will regularly share new studies, new information, and potential opportunities to get involved.

SCN2A Parent Survey

We want to learn from parents of children with mutations in the SCN2A gene. By taking our 15-minute anonymous survey, you will help inform our research efforts to develop novel therapies for SCN2A. The results will be shared with the SCN2A community.

Take the Survey

SCN2A Natural History Study

Learn how you can make a significant difference in the SCN2A community and help focus future drug development.

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Drug Development Programs

Praxis is currently developing potential new treatments for children with genetic epilepsies caused by gain-of-function mutations in SCN2A, SCN8A, and other indications.

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SCN2A Observational Study

Find out about a study to help researchers understand more about SCN2A and help you to consolidate and organize your child’s medical records.

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