drugset / Trial / NCT00328107

Immunogenicity and Safety of Trivalent Recombinant Hemagglutinin Influenza Vaccine in Healthy Adults

NCT00328107

Phase 2/3 Completed 459 enrolled Protein Sciences Corporation
RandomizedSingle-groupDouble-blindPrevention

Summary

The purpose of this study was to determine the dose-related safety, immunogenicity, and protective efficacy of a trivalent recombinant hemagglutinin influenza vaccine in healthy adults.

Timeline

Start
2004-11
Primary completion
2005-08
Completion
2005-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Flublok Vaccine 75 ug Intramuscular
Subject Flublok Vaccine 135 ug Intramuscular

Indications