A Long-term Extension Study of E2007 in Patients With Refractory Partial Seizures Uncontrolled With Other Anti-Epileptic Drugs (AEDs)
Completed
Eisai Co., Ltd.
Phase 2
2009-06-17
The purpose of this trial is to investigate the safety and tolerability of perampanel in
long- term treatment in the patients with refractory partial epilepsy (uncontrolled with
other anti-epileptic drugs) who completed Week 10 of Phase II Study E2007-J081-231 study.
A Global, Postmarketing Observational Safety Study to Evaluate the Safety and Tolerability of Fycompa (Perampanel) as Add-on Therapy in Epilepsy Patients Aged Greater Than or Equal to 12 Years
Completed
Eisai Inc.
2014-06-06
The purpose of this study is to evaluate the safety and tolerability of Fycompa (Perampanel)
as an add-on therapy in epilepsy patients aged greater than or equal to 12 years.
To Evaluate the Effect of Perampanel on Objective and Subjective Sleep in Subjects With Insomnia and Partial Onset Seizures
Withdrawn
Eisai Inc.
Phase 4
2015-03-01
This will be a multi-center, randomized, double-blind, placebo-controlled, crossover study to
evaluate the effects of 2007/Fycompa (perampanel) on sleep, in subjects with well controlled
partial onset seizures (on an antiepileptic drug [AED] monotherapy) who are experiencing
sleep onset insomnia.
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