drugset / Trial / NCT01736709

The Immunogenicity and Safety of 2012-2013 Trivalent Seasonal Influenza Vaccine

NCT01736709 ↗

Phase 4 Completed 202 enrolled Sinovac Biotech Co., Ltd
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the immunogenicity and safety of 2012-2013 trivalent seasonal influenza vaccine in 60 healthy infants aged 6-35 months old, 60 healthy adults aged 18-60 years old, and 60 healthy older people aged \> 60 years.

Timeline

Start
2012-11
Primary completion
2013-04
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject 2012-2013 trivalent seasonal influenza vaccine Vaccine 0.25 ml —
Subject 2012-2013 trivalent seasonal influenza vaccine Vaccine 0.5 ml —

Indications