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Clinical Trial Summary

The primary purpose of this study is to assess the retention rate of perampanel as a reliable proxy for overall effectiveness and tolerability in participants aged at least 12 years who are prescribed perampanel (for partial onset seizures [POS] with or without secondary generalization [SG] or for primary generalized tonic-clonic seizures [PGTCS] associated with idiopathic generalized epilepsy [IGE] as first adjunctive to antiepileptic drug (AED) monotherapy as part of their routine clinical care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04252846
Study type Observational
Source Eisai Inc.
Contact
Status Completed
Phase
Start date July 20, 2020
Completion date January 12, 2023

See also
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No longer available NCT01871233 - An Extended Access Program for Perampanel