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Clinical Trial Summary

To further characterize the immune responses induced after an influenza vaccination performed either via the ID or the IM routes in two clearly distinct populations.

Objectives:

- To describe the immune response per age group and vaccine group after vaccination.

- To describe the safety of the vaccines per age group and per vaccine group after 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


NCT number NCT00776438
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 2
Start date September 2007
Completion date April 2009

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