drugset / Trial / NCT00380367

Safety, Tolerability and Immunogenicity of HPV (Human Papilloma Virus) Vaccine in Healthy Females 9 to 15 Years of Age in India (V501-029)

NCT00380367

Phase 3 Completed 110 enrolled Merck Sharp & Dohme LLC
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the safety and tolerability of the Quadrivalent Human Papilloma Virus (HPV) vaccine in healthy females 9 to 15 years of age in India. Quadrivalent HPV Vaccine is composed of L1 virus-like particles (VLPs) from HPV types 6, 11, 16, and 18.

Timeline

Start
2007-05-03
Primary completion
2008-02-04
Completion
2008-02-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil Vaccine Intramuscular