Retrospective Non-interventional Study of Stiripentol Use in Dravet Patients in the USA

Retrospective Non-interventional Study of Stiripentol Use in Dravet Patients in the USA

The present study aims to collect data regarding the history of the disease, previous and current treatments, and the clinical status of Dravet patients during the 3 months prior to stiripentol initiation, the first 3 months on stiripentol and the last 3 months on stiripentol (irrespective of stiripentol discontinuation).

Inclusion Criteria:

• Patients diagnosed with Dravet syndrome
• Treated with stiripentol for a minimum of 3 months in routine practice

Exclusion Criteria:

• NA