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

NCT05544058 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2024-08-02

No results posted yet for this study

Summary

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).

Conditions

Interventions

OTHER

Retrospective study

Retrospective study

Sponsors & Collaborators

  • Biocodex

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-27
Primary Completion
2024-06-28
Completion
2024-06-28

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05544058 on ClinicalTrials.gov