drugset / Trial / NCT03777163

Safety and Immunogenicity of the Butantan Institute Influenza Vaccine Compared to Sanofi Pasteur Influenza Vaccine

NCT03777163 ↗

Phase 4 Completed 632 enrolled Butantan Institute
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The overall aim of this study is to evaluate the safety and immunogenicity of Butantan Institute Trivalent Seasonal Influenza Vaccine in comparison with the Sanofi Trivalent Seasonal Influenza Vaccine.

Timeline

Start
2019-04-22
Primary completion
2020-01-15
Completion
2020-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Butantan Institute Trivalent Seasonal Influenza Vaccine Vaccine 0.5 ml Intramuscular
Subject Sanofi Trivalent Seasonal Influenza Vaccine Vaccine 0.5 ml Intramuscular

Indications