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Safety and Immunogenicity of 2 Formulations of an Intramuscular A/H5N1 Pandemic Influenza Vaccine in Children

Influenza Clinical Trial

Clinical Trial Summary

This is an open, randomized, multicenter clinical trial.

Objectives:

- To describe the safety profiles during the 21 days following each primary and booster injection.

- To describe the immune response 21 days after each primary and booster injection of each formulation.

- To describe the antibody persistence after the first vaccination

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00491985
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 2
Start date June 2007
Completion date June 2010
View Details
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