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Clinical Trial Summary

The objective is to assess the effect of a booster vaccination on immunogenicity of IC51 in terms of seroconversion rate.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00595309
Study type Interventional
Source Valneva Austria GmbH
Contact
Status Completed
Phase Phase 3
Start date December 2007
Completion date October 2009

See also
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