drugset / Trial / NCT02214225

A Study to Evaluate the Immunogenicity and Safety of bioCSL Quadrivalent Influenza Vaccine (QIV) in Adults Aged 18 Years and Above.

NCT02214225

Phase 3 Completed 3484 enrolled Seqirus
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a study to assess the immune (antibody) response and safety of a bioCSL split virion, inactivated quadrivalent influenza vaccine, in comparison with a US licensed 2014/2015 trivalent influenza vaccine (bioCSL TIV-1), and a trivalent influenza vaccine containing the alternate B strain (bioCSL TIV-2), in healthy adult volunteers aged 18 years and above.

Timeline

Start
2014-08
Primary completion
2014-11
Completion
2015-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Influvactetra Vaccine 0.5 ml Intramuscular
Comparator Trivalent Influenza Vaccine (TIV-1) Vaccine 0.5 ml Intramuscular
Comparator Trivalent Influenza Vaccine (TIV-2) Vaccine 0.5 ml Intramuscular

Indications