Evaluation of Safety of a Vaccine Against Cervical Cancer in Healthy Korean Females

CompletedOBSERVATIONAL
Enrollment

3,091

Participants

Timeline

Start Date

July 1, 2010

Primary Completion Date

February 20, 2014

Study Completion Date

February 20, 2014

Conditions
Infections, Papillomavirus
Interventions
BIOLOGICAL

Cervarix.

Subjects will receive three doses of the Cervarix vaccine administered intramuscularly according to a 0, 1, 6 month vaccination schedule in routine clinical practice settings.

OTHER

Data collection

All adverse events will be recorded by all subjects or the subject's parents/guardians using diary cards.

Trial Locations (2)

602-702

GSK Investigational Site, Busan

138-736

GSK Investigational Site, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01101542 - Evaluation of Safety of a Vaccine Against Cervical Cancer in Healthy Korean Females | Biotech Hunter | Biotech Hunter