Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Conversion to Monotherapy Study With Keppra XR for Partial Seizures

ClinicalTrials.gov ID: NCT00419094

Public ClinicalTrials.gov record NCT00419094. 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 12, 2026, 8:55 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

A Multi-center, Double-blind, Historical Control, Randomized Conversion to Monotherapy Study With Keppra XR for Treatment of Partial Onset Seizures

Brief summary

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

The primary objective of this study is to assess the efficacy of two doses of Keppra XR compared with a historical control as the placebo, in the monotherapy treatment of partial onset seizures.

Study identification

NCT ID
NCT00419094
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
228 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 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, 2007
Primary completion
Aug 31, 2009
Completion
Aug 31, 2009
Last update posted
Sep 4, 2014

2007 – 2009

United States locations

U.S. sites
24
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
Not listed Dothan Alabama
Not listed Northport Alabama
Not listed Phoenix Arizona
Not listed Little Rock Arkansas
Not listed Bakersfield California
Not listed Jacksonville Florida
Not listed Loxahatchee Groves Florida
Not listed Atlanta Georgia
Not listed Suwanee Georgia
Not listed Winfield Illinois
Not listed Witchita Kansas
Not listed Shreveport Louisiana
Not listed Bethesda Maryland
Not listed Detroit Michigan
Not listed Camden New Jersey
Not listed New Brunswick New Jersey
Not listed Buffalo New York
Not listed Cedarhurst New York
Not listed Toledo Ohio
Not listed Tulsa Oklahoma
Not listed Bend Oregon
Not listed Monaca Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Beaufort South Carolina

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00419094, 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 Sep 4, 2014 · Synced Sep 12, 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 NCT00419094 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →