ClinicalTrials.gov record
Terminated Phase 3 Interventional Results available

A Double-blind, Randomized Conversion to Monotherapy Study to Evaluate the Efficacy and Safety of Brivaracetam in Subjects (≥ 16 to 75 Years Old) With Partial Onset Seizures

ClinicalTrials.gov ID: NCT00698581

Public ClinicalTrials.gov record NCT00698581. 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 5, 2026, 12:22 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 International, Double-blind, Randomized, Multi-center, Parallel Group, Historical-control Conversion to Monotherapy Study to Evaluate the Efficacy and Safety of Brivaracetam in Subjects (≥ 16 to 75 Years Old) With Partial Onset Seizures With or Without Secondary Generalization

Study identification

NCT ID
NCT00698581
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
88 participants

Conditions and interventions

Conditions

Interventions

  • Brivaracetam Drug

Drug

Eligibility (public fields only)

Age range
16 Years to 75 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
Jul 31, 2008
Primary completion
Dec 31, 2009
Completion
Jan 31, 2010
Last update posted
Jul 10, 2018

2008 – 2010

United States locations

U.S. sites
26
U.S. states
19
U.S. cities
26
Facility City State ZIP Site status
Not listed Phoenix Arizona
Not listed Fresno California
Not listed Pasadena California
Not listed Denver Colorado
Not listed Miami Florida
Not listed Orlando Florida
Not listed Conyers Georgia
Not listed Macon Georgia
Not listed Peoria Illinois
Not listed Lexington Kentucky
Not listed Burlington Massachusetts
Not listed Las Vegas Nevada
Not listed Summit New Jersey
Not listed Mineola New York
Not listed New York New York
Not listed The Bronx New York
Not listed Hickory North Carolina
Not listed Kettering Ohio
Not listed Oklahoma City Oklahoma
Not listed Germantown Tennessee
Not listed Austin Texas
Not listed Dallas Texas
Not listed Houston Texas
Not listed Danville Virginia
Not listed Charleston West Virginia
Not listed Waukesha 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 27 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00698581, 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 10, 2018 · Synced May 5, 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 NCT00698581 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →