drugset / Trial / NCT00566345

Efficacy Study of an Investigational Influenza Vaccine (Vero Cell Derived) to Prevent Culture Confirmed Influenza Infection (CCII)

NCT00566345 ↗

Phase 3 Completed 3670 enrolled Alachua Government Services, Inc.
RandomizedParallel-groupDouble-blindPrevention

Summary

The primary purpose of this study is to demonstrate the efficacy of an investigational Vero-cell derived influenza vaccine to prevent infection in an adult population with an influenza virus that is antigenically similar to one of the three strains in the vaccine. All subjects will be randomized to receive a single 0.5 ml intramuscular injection from one of three lots of seasonal Vero-cell derived influenza vaccine or saline placebo. Subjects will be monitored for 180 days following vaccination for occurrence of adverse events. For determining antibody response, subjects will have one blood draw before and one blood draw 21 days after vaccination.

Timeline

Start
2007-11
Primary completion
2008-06
Completion
2008-06

Outcome

Met primary endpoint

paper Overall protective efficacy for antigenically matched influenza infection was 78·5% (95% CI 60·8-88·2). PMID 21329971 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Inactivated seasonal influenza vaccine (split virus, Vero cell-derived) Vaccine 0.5 ml Intramuscular

Indications