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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Safety Study of GSK Biologicals' Human Papillomavirus Vaccine in 580299/008 Subjects From Canada or the US

ClinicalTrials.gov ID: NCT00799825

Public ClinicalTrials.gov record NCT00799825. 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 Oct 20, 2026, 9:54 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

Safety Study of GSK Biologicals' Human Papillomavirus Vaccine (GSK580299) in Female American and Canadian Subjects Who Had Received Control Vaccine in Study 580299/008

Brief summary

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

This phase 3b study is designed to assess the safety of GlaxoSmithKline Biological's HPV vaccine GSK580299 in female subjects who took part in study 580299/008 and received the control vaccine (Hepatitis A vaccine).

Study identification

NCT ID
NCT00799825
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
346 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Jan 1, 2009 (Type not available)
Primary completion
Aug 2, 2012 (Actual)
Completion
Aug 2, 2012 (Actual)
Last update posted
Jul 12, 2018

2009 – 2012

United States locations

U.S. sites
39
U.S. states
22
U.S. cities
37
Facility City State ZIP Site status
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site San Francisco California 94115 —
GSK Investigational Site Denver Colorado 80218 —
GSK Investigational Site Louisville Colorado 80027 —
GSK Investigational Site Clearwater Florida 33759 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site West Palm Beach Florida 33409 —
GSK Investigational Site Augusta Georgia 30912-3500 —
GSK Investigational Site Honolulu Hawaii 96826 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Arkansas City Kansas 67005 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Minneapolis Minnesota 55455 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Lebanon New Hampshire 03756 —
GSK Investigational Site Morristown New Jersey 07962 —
GSK Investigational Site Albuquerque New Mexico 87131 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site Poughkeepsie New York 12601 —
GSK Investigational Site Chapel Hill North Carolina 27514 —
GSK Investigational Site New Bern North Carolina 28562 —
GSK Investigational Site Cleveland Ohio 44109 —
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 Philadelphia Pennsylvania 19114 —
GSK Investigational Site Pleasant Hills Pennsylvania 15236 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Webster Texas 77598 —
GSK Investigational Site Charlottesville Virginia 22903 —
GSK Investigational Site Spokane Washington 99202 —
GSK Investigational Site Wenatchee Washington 98801 —

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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00799825, 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 12, 2018 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00799825 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →