drugset / Trial / NCT01381575

Evaluation of Immunogenicity and Safety of Two 2-dose Human Papillomavirus (HPV) Vaccine Schedules in 9-14 Year Old Girls

NCT01381575

Phase 3 Completed 1447 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

This study has been designed to evaluate the immunogenicity and safety of GSK Biologicals' HPV-16/18 vaccine when administered according to alternative 2-dose schedules (0,6 months and 0,12 months) in healthy 9-14 year old females as compared to the standard 3-dose schedule (0,1,6 months) in 15-25 year old females.

Timeline

Start
2011-06-29
Primary completion
2012-06-28
Completion
2014-11-13

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject 580299 Vaccine Intramuscular