drugset / Trial / NCT03330899

Safety and Immunogencity of H7N9 Influenza Antigen With 2 Adjuvant Formulations in Healthy Adults in Brazil

NCT03330899 ↗

Phase 1 Completed 432 enrolled Butantan Institute
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The overall aim of this study is to evaluate the safety, immunogenicity and dose sparing effects of H7N9 influenza antigen formulated with 2 different adjuvants .

Timeline

Start
2018-09-24
Primary completion
2020-01-30
Completion
2020-08-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator H7N9 antigen Vaccine 3.75 ug —
Comparator H7N9 antigen Vaccine 7.5 ug —
Comparator H7N9 antigen Vaccine 15 ug —
Comparator IB160 Other / unclassified — —
Comparator SE Other / unclassified — —

Indications