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

Biocodex

Status: Completed

Conditions: Dravet Syndrome

Treatments: Other: Retrospective study

Study type: Observational

Funder types: Industry

Identifiers

NCT05544058

STIRUS (STP228)

Details and patient eligibility

About

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).

Enrollment: 100 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• NA