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Active, not recruiting Phase 2 Interventional

A Study to Evaluate Efficacy and Safety of Perampanel Administered as an Adjunctive Therapy in Pediatric Participants With Childhood Epilepsy

ClinicalTrials.gov ID: NCT04015141

Public ClinicalTrials.gov record NCT04015141. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 8, 2026, 11:07 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Study With Extension Phase to Evaluate the Efficacy and Safety of Perampanel Administered as an Adjunctive Therapy in Pediatric Subjects (Age 1 Month to Less Than 18 Years) With Childhood Epilepsy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to evaluate the efficacy of perampanel as measured by the 50 percent (%) responder rate during the maintenance period of the core study for seizure frequency in participants with pediatric epileptic syndrome (Cohort 1) and partial-onset seizures (POS) (Cohort 2).

Study identification

NCT ID
NCT04015141
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Month to 18 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 30, 2019
Primary completion
Apr 5, 2027
Completion
Dec 22, 2027
Last update posted
Jul 9, 2026

2019 – 2027

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
David Geffen School of Medicine at UCLA Los Angeles California 90095
Childrens Hospital Colorado Aurora Colorado 80045
Nicklaus Children's Hospital Miami Florida 33155
Pediatric Epilepsy and Neurology Specialists Tampa Florida 33607
Meridian Clinical Research-(Savannah Georgia) Savannah Georgia 31406
Children's Hospital of Michigan Detroit Michigan 48201
Northeast Regional Epilepsy Group Hackensack New Jersey 07601
Wake Forest Baptist Medical Center - PPDS Winston-Salem North Carolina 27157
University Hospitals Cleveland Medical Center Cleveland Ohio 44106
Dayton Children's Hospital Dayton Ohio 45404
Child Neurology Consultants of Austin Austin Texas 78731
Road Runner Research Ltd San Antonio Texas 78249
Children's Specialty Group Norfolk Virginia 23510
Children's Hospital of Richmond at VCU - CHoR-PIN Richmond Virginia 23298
Seattle Children's Hospital Seattle Washington 98105

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04015141, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 9, 2026 · Synced Sep 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04015141 live on ClinicalTrials.gov.

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