drugset / Trial / NCT00700193

A Study of the Safety, Tolerability & Immunogenicity of CSL Limited's Influenza Virus Vaccine In a Paediatric Population

NCT00700193

Phase 3 Completed 298 enrolled Seqirus
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to determine the Safety, Tolerability \& Immunogenicity of CSL Limited's Influenza Virus Vaccine in a two dose primary vaccination series, with a 12-month booster vaccination, in a paediatric population equal to or greater than 6 months to less than 9 years old.

Timeline

Start
2005-03
Primary completion
2006-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Influenza Virus Vaccine Vaccine 0.25 ml
Subject Influenza Virus Vaccine Vaccine 0.5 ml

Indications