Human Papillomavirus Vaccine Immunogenicity and Safety Trial in Young Adult Women With GSK Biologicals Novel HPV Vaccine

PHASE2CompletedINTERVENTIONAL
Enrollment

383

Participants

Timeline

Start Date

September 12, 2006

Primary Completion Date

January 30, 2007

Study Completion Date

January 30, 2007

Conditions
Infections, PapillomavirusPapillomavirus Vaccines
Interventions
BIOLOGICAL

CervarixTM

Subjects were administered three doses of HPV vaccine

BIOLOGICAL

HPV investigational vaccine GSK568893A, different formulations

Subjects were administered three doses of HPV investigational vaccine

Trial Locations (10)

1070

GSK Investigational Site, Brussels

2610

GSK Investigational Site, Wilrijk

3000

GSK Investigational Site, Leuven

3300

GSK Investigational Site, Tienen

4000

GSK Investigational Site, Liège

9000

GSK Investigational Site, Ghent

80262

GSK Investigational Site, Denver

80401

GSK Investigational Site, Golden

84109

GSK Investigational Site, Salt Lake City

84121

GSK Investigational Site, Salt Lake City

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY