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Clinical Trials/NCT00120848
NCT00120848
Completed
Phase 2

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

GlaxoSmithKline1 site in 1 country776 target enrollmentNovember 2003

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Infections, Papillomavirus
Sponsor
GlaxoSmithKline
Enrollment
776
Locations
1
Primary Endpoint
Incident cervical infection with HPV-16 and/or HPV-18
Status
Completed
Last Updated
9 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
November 2003
End Date
July 2007
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Participated in study 580299/001 and received all three doses of vaccine/placebo.
  • Written informed consent obtained from the subject prior to enrollment

Exclusion Criteria

  • Decoding of the subject's treatment allocation to either the subject or the investigator in study 580299/001.

Outcomes

Primary Outcomes

Incident cervical infection with HPV-16 and/or HPV-18

Secondary Outcomes

  • Persistent cervical infection (6-month definition) with HPV 16 and/or HPV 18.
  • Persistent cervical infection (6-month definition) with oncogenic HPV types.
  • Incident cervical infection with oncogenic HPV types.
  • Histopathologically-confirmed CIN 1+ or CIN 2+ associated with HPV 16 and/or HPV 18 detected within the lesional component of the cervical tissue specimen.
  • Histopathologically-confirmed CIN 1+ or CIN 2+ associated with oncogenic HPV types detected within the lesional component of the cervical tissue specimen.
  • Abnormal cytology associated with an HPV-16 and/or HPV-18 cervical infection.
  • Abnormal cytology associated with oncogenic HPV type cervical infection.

Study Sites (1)

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