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A/H1N1 Immunogenicity and Safety in Infants, Children and Adolescents

2014-08-27 03:19:23 | BioPortfolio

Summary

The purpose of this study is to determine the preferred dose of H1N1 pandemic influenza vaccine in a pediatric population, aged 6 months to 17 years, based upon assessments of immunogenicity and safety.

Study Design

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

Conditions

Influenza

Intervention

H1N1 pandemic influenza vaccine (whole virion, Vero Cell-derived, inactivated)

Location

General Practice
Eferding
Upper Austria
Austria
4070

Status

Completed

Source

Baxter Healthcare Corporation

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:19:23-0400

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