ClinicalTrials.gov record
Terminated Phase 3 Interventional Results available

Efficacy And Safety Study Of Pregabalin (Lyrica) As Monotherapy In Patients With Partial Seizures

ClinicalTrials.gov ID: NCT00524030

Public ClinicalTrials.gov record NCT00524030. 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 4, 2026, 3:20 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 Double-Blind, Randomized, Multicenter Efficacy And Safety Study Of Pregabalin (Lyrica) As Monotherapy In Patients With Partial Seizures

Study identification

NCT ID
NCT00524030
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Enrollment
161 participants

Conditions and interventions

Interventions

  • pregabalin 150 mg/day Drug
  • pregabalin 600 mg/day Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 31, 2007
Primary completion
Mar 31, 2011
Completion
May 31, 2011
Last update posted
Jan 19, 2021

2007 – 2011

United States locations

U.S. sites
63
U.S. states
26
U.S. cities
53
Facility City State ZIP Site status
Pfizer Investigational Site Northport Alabama 35476
Pfizer Investigational Site Phoenix Arizona 85003
Pfizer Investigational Site Phoenix Arizona 85013
Pfizer Investigational Site Sun City Arizona 85351
Pfizer Investigational Site Fayetteville Arkansas 72703
Pfizer Investigational Site Fullerton California 92835
Pfizer Investigational Site Long Beach California 90806
Pfizer Investigational Site Modesto California 95355
Pfizer Investigational Site Murrieta California 92562
Pfizer Investigational Site Newport Beach California 92660
Pfizer Investigational Site Temecula California 92591
Pfizer Investigational Site Denver Colorado 80204
Pfizer Investigational Site Jacksonville Florida 32209
Pfizer Investigational Site Melbourne Florida 32901
Pfizer Investigational Site Miami Florida 33126
Pfizer Investigational Site Miami Florida 33136
Pfizer Investigational Site Sarasota Florida 34232
Pfizer Investigational Site Sarasota Florida 34233
Pfizer Investigational Site Atlanta Georgia 30309
Pfizer Investigational Site Atlanta Georgia 30342
Pfizer Investigational Site Decatur Georgia 30033
Pfizer Investigational Site Lawrenceville Georgia 30045
Pfizer Investigational Site Suwanee Georgia 30024
Pfizer Investigational Site Anderson Indiana 46016
Pfizer Investigational Site Danville Indiana 46122
Pfizer Investigational Site Fort Wayne Indiana 46805
Pfizer Investigational Site Kansas City Kansas 66160
Pfizer Investigational Site Bowling Green Kentucky 42101
Pfizer Investigational Site Lexington Kentucky 40536-0284
Pfizer Investigational Site Lexington Kentucky 40536
Pfizer Investigational Site Houma Louisiana 70363
Pfizer Investigational Site Shreveport Louisiana 71105-5634
Pfizer Investigational Site Pikesville Maryland 21208
Pfizer Investigational Site Worcester Massachusetts 01605
Pfizer Investigational Site Worcester Massachusetts 01608
Pfizer Investigational Site Detroit Michigan 48202
Pfizer Investigational Site Minneapolis Minnesota 55422
Pfizer Investigational Site Flowood Mississippi 39232
Pfizer Investigational Site Hattiesburg Mississippi 39401-7246
Pfizer Investigational Site Great Falls Montana 59405
Pfizer Investigational Site Cedarhurst New York 11516
Pfizer Investigational Site Charlotte North Carolina 28207
Pfizer Investigational Site Charlotte North Carolina 28209
Pfizer Investigational Site Rocky Mount North Carolina 27804
Pfizer Investigational Site Cleveland Ohio 44195
Pfizer Investigational Site Columbus Ohio 43210-1250
Pfizer Investigational Site Columbus Ohio 43210
Pfizer Investigational Site Oklahoma City Oklahoma 73112
Pfizer Investigational Site Oklahoma City Oklahoma 73120
Pfizer Investigational Site Altoona Pennsylvania 16602
Pfizer Investigational Site Indiana Pennsylvania 15701
Pfizer Investigational Site Philadelphia Pennsylvania 19140
Pfizer Investigational Site Memphis Tennessee 38120
Pfizer Investigational Site Memphis Tennessee 38163
Pfizer Investigational Site Nashville Tennessee 37232
Pfizer Investigational Site Dallas Texas 75230
Pfizer Investigational Site Houston Texas 77074-2906
Pfizer Investigational Site San Antonio Texas 78258
Pfizer Investigational Site Temple Texas 76508
Pfizer Investigational Site Murray Utah 84107
Pfizer Investigational Site Salt Lake City Utah 84107
Pfizer Investigational Site West Jordan Utah 84088
Pfizer Investigational Site Milwaukee Wisconsin 53226

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00524030, 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 Jan 19, 2021 · Synced May 4, 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 NCT00524030 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →