Clinical Trials Directory

Trials / Completed

CompletedNCT00120848

Follow-up Study of GSK Biologicals' Human Papilloma Virus (HPV) Vaccine to Prevent Cervical Infection in Young Adults

Study of the Efficacy of Candidate HPV 16/18 VLP Vaccine in the Prevention of HPV-16 and/or HPV-18 Cervical Infection in Adolescent & Young Adult Women in North America and Brazil Vaccinated in Primary Study 580299/001

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
776 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
Female
Age
20 Years – 30 Years
Healthy volunteers
Accepted

Summary

Human Papilloma virus (HPV) are viruses that cause a common infection of the skin and genitals in men and women. Several types of HPV infection are transmitted by sexual activity and, in women, can infect the cervix (part of the uterus or womb). This infection often goes away by itself, but if it does not go away (this is called persistent infection), it can lead in women over a long period of time to cancer of the cervix. If a woman is not infected by HPV, it is very unlikely that she will get cervical cancer. This is an observer blind follow up study of the study HPV-001, which evaluated the ability of the HPV vaccine to prevent HPV infection. The current study invites all of the 1113 subjects in the HPV-001 study that received all three doses of vaccine/placebo to be enrolled and followed-up for several additional years to see if the HPV vaccine prevents HPV-16 and HPV-18 infections and to evaluate the safety of the vaccine. Subjects will remain in the same study group as in the primary study. No vaccine or placebo will be administered in this study. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHPV 16/18 VLP AS04

Timeline

Start date
2003-11-01
Primary completion
2007-07-01
Completion
2007-07-01
First posted
2005-07-19
Last updated
2016-11-04

Locations

27 sites across 3 countries: United States, Brazil, Canada

Source: ClinicalTrials.gov record NCT00120848. Inclusion in this directory is not an endorsement.