Efficacy, Immunogenicity and Safety of GSK Biologicals' HPV GSK 580299 Vaccine in Healthy Chinese Female Subjects

PHASE3CompletedINTERVENTIONAL
Enrollment

6,081

Participants

Timeline

Start Date

October 22, 2008

Primary Completion Date

September 6, 2011

Study Completion Date

February 28, 2016

Conditions
Infections, Papillomavirus
Interventions
BIOLOGICAL

HPV GSK 580299 vaccine

Subjects were planned to receive three doses of the study vaccine administered intramuscularly according to a 0, 1, 6 month vaccination schedule.

BIOLOGICAL

Placebo control

Subjects were planned to receive three doses of the placebo control administered intramuscularly according to a 0, 1, 6 month vaccination schedule.

Trial Locations (4)

213200

GSK Investigational Site, Jintan

221006

GSK Investigational Site, Xuzhou

224500

GSK Investigational Site, Yancheng

Unknown

GSK Investigational Site, Lianshui

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY