drugset / Trial / NCT00345878

Study to Evaluate the Immune Response and Safety of GSK Biologicals' HPV Vaccine in Healthy Women Aged 18-35 Years

NCT00345878

Phase 3 Completed 271 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindPrevention

Summary

Human papillomavirus infection has clearly been recognized as the cause of cervical cancer. The infection of the cervix by certain oncogenic types of HPV, if not cleared, can lead to cervical cancer in women. This study will evaluate the immunogenicity and safety of the HPV-16/18 L1 VLP AS04 vaccine. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Timeline

Start
2006-09-25
Primary completion
2007-12-21
Completion
2007-12-21

Drugs

EvaluationDrugModalityDoseRoute
Subject HPV 16/18 VLP AS04 Vaccine Intramuscular