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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Efficacy of the Human Papillomavirus Vaccine in Healthy Adult Women of 26 Years of Age and Older

ClinicalTrials.gov ID: NCT00294047

Public ClinicalTrials.gov record NCT00294047. 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 Jul 23, 2026, 8:49 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 Study to Evaluate Safety, Immunogenicity and Efficacy of GSK Biologicals HPV-16/18 L1/AS04 Vaccine Administered Intramuscularly According to a Three-dose Schedule (0, 1, 6 Month) in Healthy Adult Female Subjects Aged 26 Years and Above

Study identification

NCT ID
NCT00294047
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
5,752 participants

Conditions and interventions

Interventions

  • Cervarix Biological
  • Placebo control Biological

Biological

Eligibility (public fields only)

Age range
26 Years and older
Sex
Female
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Feb 15, 2006
Primary completion
Jan 28, 2014
Completion
Jan 28, 2014
Last update posted
Jan 1, 2020

2006 – 2014

United States locations

U.S. sites
36
U.S. states
21
U.S. cities
32
Facility City State ZIP Site status
GSK Investigational Site Fountain Valley California 92708
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Golden Colorado 80401
GSK Investigational Site Coral Gables Florida 33134
GSK Investigational Site Miami Florida 33136
GSK Investigational Site Augusta Georgia 30912
GSK Investigational Site Iowa City Iowa 52242
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Bardstown Kentucky 40004
GSK Investigational Site Louisville Kentucky 40202
GSK Investigational Site Chaska Minnesota 55318
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site Lebanon New Hampshire 03756
GSK Investigational Site Albuquerque New Mexico 87131
GSK Investigational Site Syracuse New York 13057
GSK Investigational Site Chapel Hill North Carolina 27514
GSK Investigational Site New Bern North Carolina 28562
GSK Investigational Site Akron Ohio 44311
GSK Investigational Site Cleveland Ohio 44122
GSK Investigational Site Tulsa Oklahoma 74105
GSK Investigational Site Portland Oregon 97210
GSK Investigational Site Carnegie Pennsylvania 15106
GSK Investigational Site Erie Pennsylvania 16507
GSK Investigational Site Erie Pennsylvania 16508
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Pittsburgh Pennsylvania 15213
GSK Investigational Site Pittsburgh Pennsylvania 15236
GSK Investigational Site Wexford Pennsylvania 15090
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Houston Texas 77004
GSK Investigational Site Houston Texas 77030
GSK Investigational Site Salt Lake City Utah 84109
GSK Investigational Site Salt Lake City Utah 84121
GSK Investigational Site South Jordan Utah 84095
GSK Investigational Site Wenatchee Washington 98801
GSK Investigational Site La Crosse Wisconsin 54601

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 39 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00294047, 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 1, 2020 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00294047 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →