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Search / Trial NCT02736162

Study to Investigate Dosage, Efficacy, and Safety of Perampanel Given as Monotherapy in Patients With Epilepsy

Launched by EISAI INC. · Apr 7, 2016

Trial Information

Current as of June 22, 2025

Completed

Keywords

Perampanel E2007 Phase 4 Fycompa

ClinConnect Summary

This study is a retrospective study of participants who received perampanel as primary or secondary monotherapy at approximately 40 centers in Europe, Asia, and Australia. Primary monotherapy is defined as the administration of perampanel in the absence of any concomitant antiepileptic drugs (AEDs). Secondary (conversion) monotherapy is defined as the conversion of perampanel from adjunctive therapy to monotherapy by withdrawing concomitant AEDs.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Diagnosis of epilepsy
  • Received perampanel as primary or secondary monotherapy at any time between 1 Jan 2013 and 15 Oct 2015
  • Provided written informed consent by the participant or the participant's legally authorized representative signed for the use of medical records per local requirements
  • Exclusion Criteria:
  • Not applicable

About Eisai Inc.

Eisai Inc. is a global pharmaceutical company committed to providing innovative solutions for patients with unmet medical needs. With a strong focus on neurology and oncology, Eisai leverages cutting-edge research and development to advance therapeutics that enhance patient outcomes and quality of life. The company emphasizes a patient-centric approach, fostering collaboration with healthcare professionals and stakeholders to ensure the effective delivery of its products. Eisai Inc. is dedicated to upholding the highest ethical standards in clinical trials, driving scientific excellence, and contributing to the advancement of healthcare worldwide.

Locations

Patients applied

0 patients applied

Trial Officials

Karen Cartwright, PhD

Study Director

Eisai Limited

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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