750
Participants
Start Date
October 24, 2009
Primary Completion Date
December 8, 2010
Study Completion Date
December 8, 2010
CervarixTM
Subjects will receive three doses of the Cervarix vaccine intramuscularly according to a 0, 1, 6-month schedule.
Control
Subjects will receive three doses of control intramuscularly according to a 0, 1, 6-month schedule.
GSK Investigational Site, Taizhou
Lead Sponsor
GlaxoSmithKline
INDUSTRY