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

NCT02736162 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 61

Last updated 2017-03-09

No results posted yet for this study

Summary

The primary objective of this study is to assess the retention rate of perampanel when given as secondary monotherapy in routine clinical care.

Conditions

  • Epilepsy
  • Partial-Onset Seizures
  • Primary Generalized Tonic-Clonic Seizures

Interventions

OTHER

No treatment (intervention) was administered

Sponsors & Collaborators

  • Eisai Inc.

    lead INDUSTRY

Principal Investigators

  • Karen Cartwright, PhD · Eisai Limited

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2016-06-30
Completion
2016-07-31

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02736162 on ClinicalTrials.gov