drugset / Trial / NCT03336593

Protectivity and Safety of Quadrivalent Influenza HA Vaccine in Indonesian Population

NCT03336593 ↗

Phase 2 Completed 810 enrolled PT Bio Farma
RandomizedParallel-groupDouble-blindPrevention

Summary

This study is to assess protectivity and safety of Quadrivalent Influenza Vaccine in Indonesian Population

Timeline

Start
2017-11-21
Primary completion
2018-03-14
Completion
2018-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Quadrivalent influenza vaccine Vaccine 0.25 ml —
Subject Quadrivalent influenza vaccine Vaccine 0.5 ml —
Comparator Trivalent Influenza Vaccine Vaccine 0.5 ml —

Indications

No indication recorded.