HPV Vaccine Study

A Phase IIIb open-label, randomised, multi-centre primary immunization study to evaluate the immunogenicity and safety of GSK Biologicals’ HPV-16/18 L1 VLP AS04 vaccine when administered intramuscularly according to alternative 2-dose schedules in 9 – 14 year old healthy females compared to the standard 3-dose schedule for GSK Biologicals’ HPV-16/18 L1 VLP AS04 vaccine in 15 – 25 year ol.

Register Today!

Trial Information

StatusCompleted
Trial Duration4 years
Number of Visits10-12
Lead CRCChantelle Jacklin

For additional information
on this trial contact:

Phone705-566-0005