drugset / Trial / NCT00170443

Trivalent rHA Dose Escalation Study in Elderly Subjects

NCT00170443 ↗

RandomizedParallel-groupDouble-blindPrevention

Summary

This study will compare the safety and immunogenicity of three different dose levels of an experimental recombinant influenza HA protein vaccine to a standard inactivated influenza vaccine in heallthy elderly subjects ages 65-80. Blood and nasal secretions for assessment of antibody responses will be obtained from all subjects prior to and one month after vaccination.

Timeline

Start
—
Primary completion
—
Completion
2004-06

Drugs

EvaluationDrugModalityDoseRoute
Subject rHAO Trivalent Influenza Vaccine Vaccine — Intramuscular

Indications