drugset / Trial / NCT00092521

Cervical Intraepithelial Neoplasm (CIN)-Warts Efficacy Trial in Women (Gardasil)(V501-013)(COMPLETED)

NCT00092521

Phase 3 Completed 5759 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindPrevention

Summary

The primary purpose of the study is to determine if GARDASIL (V501) with four components is able to prevent cervical cancer, cervical dysplasia, including Cervical Intraepithelial Neoplasia (CIN)(Any Grade) and Adenocarcinoma In Situ (AIS), and genital warts.

Timeline

Start
2001-12
Primary completion
2007-07
Completion
2009-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Gardasil Vaccine 0.5 ml Intramuscular
Subject Human Papillomavirus (HPV) 16 Monovalent Vaccine 0.5 ml Intramuscular