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Clinical Trial Summary

This study will evaluate the effectiveness and safety of an investigational drug, IV ganaxolone, as adjunctive therapy to standard of care to treat subjects with status epilepticus.


Clinical Trial Description

This is a double-blind, randomized, placebo-controlled study to evaluate the safety, tolerability, and efficacy of adjunctive IV ganaxolone in subjects with SE. Study drug will be added to standard of care before IV anesthetic during the treatment of SE. Subjects will be screened for inclusion/exclusion criteria prior to receiving study drug as adjunctive therapy by continuous IV. Subject's will be followed up for 3 weeks post-treatment. Subjects who are known to be at risk for SE may be consented and/or assented prior to an SE event. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03350035
Study type Interventional
Source Marinus Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date February 19, 2018
Completion date September 18, 2019

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