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 Influenza Virus Vaccine Vaccine 45 ug Intramuscular
Subject Influenza Virus Vaccine Vaccine 0.5 ml Intramuscular

Indications