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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of EPX-100 as adjunctive therapy in children and adult participants with Dravet Syndrome.


Clinical Trial Description

This is a global, multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of EPX-100 as adjunctive therapy in children and adult participants with Dravet Syndrome. The study consists of a 4-week observational period, a 16-week double blind period and a 3-year open label extension. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04462770
Study type Interventional
Source Epygenix
Contact Lorianne Masuoka, M.D.
Phone (415) 933-0826
Email lm@epygenix.com
Status Recruiting
Phase Phase 2
Start date September 15, 2020
Completion date December 19, 2024

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