drugset / Trial / NCT00779766

Efficacy, Immunogenicity and Safety of GSK Biologicals' HPV GSK 580299 Vaccine in Healthy Chinese Female Subjects

NCT00779766

Phase 3 Completed 6081 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a multicenter study in which women are planned to receive either the HPV vaccine or control. Study participation will last approximately 72 months and involves a total of thirteen or fourteen scheduled visits. Originally, the study was planned for 24 months. It was then extended for 2 more years with 4 additional visits (study end at Month 48). The protocol posting has been updated as the study was extended by additional 2 years with two or three additional visits (study end at Month 72) for subjects who consent to participate in the extension.

Timeline

Start
2008-10-22
Primary completion
2011-09-06
Completion
2016-02-28

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cervarix Vaccine Intramuscular