drugset / Trial / NCT01209780

Safety and Immunogenicity of Trivalent Subunit Inactivated Flu Vaccine Administered to Healthy Children and Adolescents 3 to 17 Years of Age

NCT01209780 ↗

Phase 3 Completed 3116 enrolled Novartis Vaccines
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study will evaluate the safety and immunogenicity in healthy children and adolescents after one or two IM dose(s) of trivalent subunit inactivated flu vaccine.

Timeline

Start
2010-09
Primary completion
2011-03
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Comparator TIV Vaccine — Intramuscular
Comparator Fluvirin Vaccine — Intramuscular
Subject TIV Vaccine — Intramuscular

Indications