drugset / Trial / NCT01863849

Tolerability and Immunogenicity Study of Fluval AB Suspension for Injection

NCT01863849 ↗

Phase 4 Completed 120 enrolled Fluart Innovative Vaccine Ltd, Hungary
Non-randomizedParallel-groupOpen-labelPrevention

Summary

To assess immunogenicity of a single intramuscular injection of Fluval AB suspension for injection (trivalent, seasonal influenza vaccine, active ingredient content: 15 μgHA/0.5mL of seasonal A/H1N1, A/H3N2 and B influenza antigens each), as measured by haemagglutination inhibition (HI) test.

Timeline

Start
2013-08-22
Primary completion
2013-09-17
Completion
2013-09-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluval AB Vaccine 0.5 ml Intramuscular

Indications

No indication recorded.