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Clinical Trial Summary

To allow open-label extension to patients who have completed Protocol 1042-0500


Clinical Trial Description

Patient should have completed all scheduled clinical study visits in the double blind, controlled trial (Protocol 1042-0500) and have been deemed eligible (had a response to treatment) by the Investigator. Male or female, with a diagnosis of IS with a video EEG (vEEG) recording confirming the diagnosis. There will be a total of 14 visits over 99(+or-1)week. A 24-hr vEEG is only required if the subject has been spasm-free for more than 24-hrs. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00442104
Study type Interventional
Source Marinus Pharmaceuticals
Contact
Status Terminated
Phase Phase 2
Start date January 2007
Completion date March 2009

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