drugset / Trial / NCT00652938

Evaluation of Immunogenicity and Safety of Human Papillomavirus (HPV) Vaccine Co-administered With Another Vaccine in Healthy Female Subjects

NCT00652938

Phase 3 Completed 744 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

Infection with human papillomavirus (HPV) has been clearly established as the necessary cause of cervical cancer. Vaccination of pre-teens and adolescents, ideally before sexual debut and thus before exposure to oncogenic HPV, is a rational strategy for prevention of cervical cancer. Thus, HPV vaccination could complement the existing pre-adolescent/adolescent vaccination programs. This Phase IIIb study is designed to evaluate the immunogenicity and safety of co-administering a commercially available vaccine with GSK Biologicals' HPV-16/18 L1 VLP AS04 (Cervarix TM) vaccine as compared to the administration of either vaccine alone.

Timeline

Start
2008-04-09
Primary completion
2009-08-28
Completion
2010-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Cervarix Vaccine Intramuscular
Comparator Engerix-B Vaccine Intramuscular