drugset / Trial / NCT00196937

Human Papilloma Virus (HPV) Vaccine Immunogenicity and Safety Trial in Young and Adult Women With GSK Biologicals' HPV-16/18

NCT00196937

Phase 3 Completed 667 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelPrevention

Summary

Infection with human papillomavirus (HPV) has been clearly established as the central cause of cervical cancer. Indeed, certain oncogenic types of HPV can infect the cervix (part of the uterus or womb). This infection may go 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. This study will evaluate the immunogenicity and safety of GSK Biologicals HPV-16/18 vaccine over 12 months, in women up to 55 years of age at study start. Approximately 660 study subjects will receive the HPV vaccine administered intramuscularly according to a 0-1-6 month schedule. The study will be extended to assess long-term safety and immunogenicity of the HPV-16/18 vaccine.

Timeline

Start
2004-10-07
Primary completion
2005-12-15
Completion
2005-12-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cervarix Vaccine Intramuscular