Clinical trial
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
NCT02033902 is registered in ClinicalTrials.gov with Eisai Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- 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
- Lead sponsor
- Eisai Inc.
- Phase
- Observational
- Overall status
- Completed
- Start date
- June 6, 2014
- Completion date
- January 31, 2018
- Enrollment
- 500 (actual)
- Sites
- 42
Conditions
As the registry lists them; a condition with its own page is linked.