ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Perampanel as Adjunctive Therapy in Pediatrics With Partial Onset Seizures or Primary Generalized Tonic Clonic Seizures

ClinicalTrials.gov ID: NCT02849626

Public ClinicalTrials.gov record NCT02849626. 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 May 20, 2026, 6:21 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, Multicenter Study With an Extension Phase to Evaluate the Safety, Tolerability, and Exposure-Efficacy Relationship of Perampanel Oral Suspension When Administered as an Adjunctive Therapy in Pediatric Subjects (Age 4 to Less Than 12 Years) With Inadequately Controlled Partial-Onset Seizures or Primary Generalized Tonic Clonic Seizures

Study identification

NCT ID
NCT02849626
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eisai Inc.
Industry
Enrollment
180 participants

Conditions and interventions

Interventions

  • Perampanel Drug

Drug

Eligibility (public fields only)

Age range
4 Years to 12 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
Nov 15, 2016
Primary completion
Feb 4, 2019
Completion
Dec 5, 2021
Last update posted
Oct 27, 2022

2016 – 2021

United States locations

U.S. sites
29
U.S. states
22
U.S. cities
28
Facility City State ZIP Site status
Facility #1 Little Rock Arkansas
Facility #1 Palo Alto California
Facility #1 Aurora Colorado
Facility #1 Gulf Breeze Florida
Facility #1 Loxahatchee Groves Florida
Facility #1 Orlando Florida
Facility #1 Atlanta Georgia
Facility #1 Savannah Georgia
Facility #1 Boise Idaho
Facility #1 Chicago Illinois
Facility #1 Urbana Illinois
Facility #1 Ames Iowa
Facility #1 Wichita Kansas
Facility #1 Lexington Kentucky
Facility #2 Lexington Kentucky
Facility #1 New Orleans Louisiana
Facility #1 Duluth Minnesota
Facility #1 Kansas City Missouri
Facility #1 Henderson Nevada
Facility #1 Hackensack New Jersey
Facility #1 Voorhees Township New Jersey
Facility #1 Brooklyn New York
Facility #1 Winston-Salem North Carolina
Facility #1 Cleveland Ohio
Facility #1 Memphis Tennessee
Facility #1 Austin Texas
Facility #1 San Antonio Texas
Facility #1 Tacoma Washington
Facility #1 Milwaukee Wisconsin

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 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02849626, 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 Oct 27, 2022 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02849626 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →