drugset / Trial / NCT00365378

Study of Human Papillomavirus (HPV) 16 Vaccine in the Prevention of HPV 16 Infection in 16- to 23-Year-Old Females (V501-005)

NCT00365378 ↗

Phase 2 Completed 2409 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindPrevention

Summary

Subjects received HPV 16 L1 VLP vaccine or placebo (1:1 ratio). Endpoints included efficacy, immunogenicity, and safety.

Timeline

Start
1999-09
Primary completion
2004-03
Completion
2009-07

Outcome

Met primary endpoint

registry NUMBER HPV 16 L1 VLP (Group 1): 0.3 Incidence per 100 person-years NCT00365378 ↗

registry NUMBER Placebo (Group 2): 4.9 Incidence per 100 person-years NCT00365378 ↗

registry Vaccine Efficacy 94.3 (95% CI 87.8 to 97.7) NCT00365378 ↗

registry NUMBER HPV 16 L1 VLP (Group 1): 0.0 Incidence per 100 person-years NCT00365378 ↗

registry NUMBER Placebo (Group 2): 1.0 Incidence per 100 person-years NCT00365378 ↗

registry Vaccine Efficacy 100.0 (95% CI 84.0 to 100.0) NCT00365378 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject HPV 16 L1 Vaccine Vaccine — Intramuscular