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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Safety Evaluation of the GSK-580299 Vaccine in Women From the Control Group in the Primary NCT00294047 Study

ClinicalTrials.gov ID: NCT01190189

Public ClinicalTrials.gov record NCT01190189. 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 6, 2026, 11:51 PM 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 (GSK-580299) in Healthy Female Control Subjects From the Primary NCT00294047 Study

Brief summary

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

This extension study is designed to assess the safety of GSK Biological's human papillomavirus (HPV) vaccine GSK580299 in female subjects who took part in the primary study NCT00294047 and received the control vaccine in countries for which the licensed GSK HPV vaccine is not indicated for the subject's age group (26 years and older). This study is thus conducted to enable all women who received the control placebo in the primary NCT00294047 study to receive the GSK580299 vaccine.

Study identification

NCT ID
NCT01190189
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
137 participants

Conditions and interventions

Interventions

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
Mar 31, 2011
Primary completion
Nov 22, 2017
Completion
Nov 22, 2017
Last update posted
Jun 18, 2019

2011 – 2017

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
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 Omaha Nebraska 68131
GSK Investigational Site Lebanon New Hampshire 03756
GSK Investigational Site New Bern North Carolina 28562
GSK Investigational Site Cleveland Ohio 44122
GSK Investigational Site Carnegie Pennsylvania 15106
GSK Investigational Site Erie Pennsylvania 16507
GSK Investigational Site Erie Pennsylvania 16508
GSK Investigational Site Pittsburgh Pennsylvania 15236
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 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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01190189, 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 Jun 18, 2019 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01190189 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →