drugset / Trial / NCT01494740

Immunogenicity and Safety of an Inactivated Split-virion 2009 Pandemic Influenza A H1N1 Vaccine in Infants

NCT01494740 ↗

Phase 2 Completed 312 enrolled Shanghai Institute Of Biological Products
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The aim of this study is to investigate the immunogenicity and safety of the inactivated split-virion vaccine in infants.

Timeline

Start
2009-12
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject split-virion, non-adjuvanted H1N1 vaccine Vaccine 7.5 ug —
Subject split-virion, non-adjuvanted H1N1 vaccine Vaccine 15 ug —
Subject split-virion, non-adjuvanted seasonal influenza vaccine Vaccine — —

Indications