drugset / Trial / NCT03784885

A Phase 2, Double-blind Study to Evaluate Intranasal Trivalent Influenza Virus Vaccine in Healthy Adult

NCT03784885

Phase 2 Completed 345 enrolled Advagene Biopharma Co. Ltd.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The objectives of this phase 2 study are to evaluate immunogenicity, safety and tolerability of AD07030, a trivalent influenza virus antigens vaccine, given intranasally in 2 doses in healthy adult volunteers.

Timeline

Start
2017-09-01
Primary completion
2018-01-07
Completion
2018-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject AD07010 Protein / enzyme biologic 30 ug Intranasal
Subject AD07010 Protein / enzyme biologic 45 ug Intranasal
Subject Inactivated Trivalent Influenza Vaccine Vaccine 22.5 ug Intranasal

Indications