100
Participants
Start Date
July 2, 2007
Primary Completion Date
March 28, 2008
Study Completion Date
March 28, 2008
Cervarix™ (HPV-16/18 L1 VLP AS04)
Three doses of vaccine administered intramuscularly according to a 0, 1, 6-month schedule.
GSK Investigational Site, Saitama
GSK Investigational Site, Saitama
GSK Investigational Site, Tokyo
GSK Investigational Site, Tokyo
GSK Investigational Site
Lead Sponsor
GlaxoSmithKline
INDUSTRY