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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

Trial Profile

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

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 11 Sep 2018

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At a glance

  • Drugs Perampanel (Primary)
  • Indications Epilepsy
  • Focus Adverse reactions
  • Sponsors Eisai Inc
  • Most Recent Events

    • 05 Sep 2018 Status changed from recruiting to completed.
    • 23 Aug 2014 Status changed from not yet recruiting to recruiting as reported by United Kingdom Clinical Research Network
    • 31 Mar 2014 Planned End Date changed from 1 Apr 2017 to 1 Jun 2017 according to ClinicalTrials.gov record.
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