drugset / Trial / NCT00395174

Comparison of the Immunogenicity, Safety and Reactogenicity of FluBlok, To a Licensed Vaccine In Elderly Adults

NCT00395174 ↗

Phase 3 Completed 870 enrolled Protein Sciences Corporation
RandomizedFactorialDouble-blindPrevention

Summary

The purpose of this study were to obtain additional evidence in support of the safety and immunogenicity of a recombinant hemagglutinin (rHA) vaccine in an elderly population, and to establish non-inferiority of the immunogenicity of the rHA vaccine when compared with a licensed trivalent influenza vaccine (TIV). Another purpose was to provide a preliminary estimate of the relative efficacy of the two vaccines against culture-positive influenza-like illness during the subsequent epidemic.

Timeline

Start
2006-10
Primary completion
2007-05
Completion
2007-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Flublok Vaccine 135 ug Intramuscular
Subject Flublok Vaccine 0.5 ml Intramuscular
Subject Fluzone Vaccine 45 ug Intramuscular
Subject Fluzone Vaccine 0.5 ml Intramuscular

Indications