drugset / Trial / NCT00485732

A Study to Evaluate the Immune Response and Safety of GSK Biologicals' HPV-16/18 L1 VLP AS04 Vaccine/Cervarix TM Vaccine in Healthy Females Aged 15-25 Years

NCT00485732

Phase 3 Completed 225 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 GSK Biologicals' HPV-16/18 L1 VLP AS04 vaccine (Cervarix TM) vaccine. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Timeline

Start
2007-06-11
Primary completion
2008-03-30
Completion
2008-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject HPV 16/18 VLP AS04 Vaccine Intramuscular