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Trials / Completed

CompletedNCT00157950

Human Papillomavirus (HPV) Registration Study (Gardasil)(V501-023)(COMPLETED)

An Immunogenicity and Safety Study of Gardasil (V501 (Human Papillomavirus [Types 6, 11, 16, 18] Recombinant Vaccine)) in Females 9 to 23 Years of Age in Korea

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
176 (actual)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
Female
Age
9 Years – 23 Years
Healthy volunteers
Accepted

Summary

This is an immunogenicity and safety study of Gardasil (V501) in females 9 to 23 years of age in Korea.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGardasil™Gardasil™ 3 dose regimen (Day 1, Month 2 and Month 6)
BIOLOGICALPlaceboGardasil™ matching placebo 3 dose regimen (Day 1, Month 2 and Month 6)

Timeline

Start date
2005-10-01
Primary completion
2006-06-01
Completion
2006-06-01
First posted
2005-09-12
Last updated
2016-02-04
Results posted
2010-09-14

Source: ClinicalTrials.gov record NCT00157950. Inclusion in this directory is not an endorsement.

Human Papillomavirus (HPV) Registration Study (Gardasil)(V501-023)(COMPLETED) (NCT00157950) · Clinical Trials Directory