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Clinical Trial Summary

To evaluate the efficacy of open-label ganaxolone as adjunctive therapy for uncontrolled seizures in female children with PCDH19 mutation and other rare genetic epilepsies in an open-label proof-of-concept study.


Clinical Trial Description

The purpose of this proof-of-concept study is to evaluate ganaxolone as adjunctive therapy for uncontrolled seizures in female children with PCDH19 mutations and other rare genetic epilepsies. After establishing baseline seizure frequency, qualifying subjects will enter the study and be treated with open-label ganaxolone for up to six months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02358538
Study type Interventional
Source Marinus Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date November 6, 2015
Completion date January 4, 2019

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