A Study to Assess Safety and Efficacy of Perampanel in Indian Participants as an Adjunctive Treatment in Partial Onset Seizures With or Without Secondary Generalized Seizures in Participants With Epilepsy Aged 12 Years or Older

NCT03836924 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2021-02-18

No results posted yet for this study

Summary

The purpose of this study is to assess the safety of perampanel in the treatment of partial onset seizures in participants of age 12 years and older with epilepsy.

Conditions

Interventions

DRUG

Perampanel

Perampanel tablets.

Sponsors & Collaborators

  • Eisai Pharmaceuticals India Pvt. Ltd

    lead INDUSTRY

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-18
Primary Completion
2020-03-01
Completion
2020-03-01

Countries

  • India

Study Locations

More Related Trials

Entities

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 NCT03836924 on ClinicalTrials.gov