RecruitingPhase 3NCT06872125

A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome

Studying Dravet syndrome

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Key facts

Sponsor
Stoke Therapeutics, Inc
Intervention
zorevunersen(drug)
Enrollment
170 enrolled
Eligibility
2-17 years · All sexes
Timeline
20252028

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06872125 on ClinicalTrials.gov

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