NCT06872125Phase 3Recruiting

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

Study sponsor: Stoke Therapeutics, Inc · STOK

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

Primary completion2027-03Estimated
Enrollment · participants170Estimated
Source updated2026-08-24Last update listed in the registry record
Version history

Changes to this trial

Last 12 months
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· 1 field changed

Planned enrollment increased by 20 participants

− Before

150 participants (planned)

+ After

170 participants (planned)

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