drugset / Trial / NCT00524940

Trial to Describe the Safety and Immunogenicity of Fluzone®

NCT00524940

Phase 2 Completed 124 enrolled Sanofi Pasteur, a Sanofi Company
Non-randomizedSingle-groupOpen-labelPrevention

Summary

Objective 1:To describe the safety of the inactivated, split-virion influenza vaccine, Northern Hemisphere (NH) 2007-2008 formulation. Objective 2: To describe the immunogenicity, of Fluzone, inactivated, split virion influenza vaccine NH 2007-2008 formulation. Objective 3: Serum Collection - To submit remaining available sera to Center for Biologics Evaluation and research (CBER) for further analysis by the Food and Drug Administration (FDA), the Center for Disease Control and Prevention (CDC), and the World Health Organization (WHO) to support selection and recommendation of antigen strains for subsequent influenza vaccines.

Timeline

Start
2007-08
Primary completion
2007-09
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Inactivated, Split-Virion Influenza Virus Vaccine 0.5 ml Intramuscular

Indications