Immunogenicity and Safety Study of GSK Biologicals' Human Papillomavirus 580299 Vaccine in Healthy Female Subjects

PHASE3CompletedINTERVENTIONAL
Enrollment

750

Participants

Timeline

Start Date

October 24, 2009

Primary Completion Date

December 8, 2010

Study Completion Date

December 8, 2010

Conditions
Infections, Papillomavirus
Interventions
BIOLOGICAL

CervarixTM

Subjects will receive three doses of the Cervarix vaccine intramuscularly according to a 0, 1, 6-month schedule.

OTHER

Control

Subjects will receive three doses of control intramuscularly according to a 0, 1, 6-month schedule.

Trial Locations (1)

225300

GSK Investigational Site, Taizhou

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT00996125 - Immunogenicity and Safety Study of GSK Biologicals' Human Papillomavirus 580299 Vaccine in Healthy Female Subjects | Biotech Hunter | Biotech Hunter