drugset / Trial / NCT01277042

Study to Assess Immune Responses and Safety of the GSK-580299 Vaccine in Healthy Women (26 to 45 Years)

NCT01277042

Phase 3 Completed 1212 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

This study is designed to evaluate the immunogenicity and safety of GSK Biologicals' human papillomavirus (HPV) vaccine in adult female subjects aged 26-45 years. One group of subjects will receive the HPV vaccine and the other group will receive an active control (GSK Biologicals' hepatitis B vaccine). Immunogenicity data of the HPV group will be compared with those from the HPV group included in the NCT00779766 study (aged 18-25 years).

Timeline

Start
2011-02-17
Primary completion
2011-09-26
Completion
2012-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Cervarix Vaccine Intramuscular
Comparator Engerix-BTM Unknown Intramuscular