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
Comparator Influenza Virus Vaccine Vaccine 0.5 ml
Subject Quadrivalent influenza vaccine Vaccine 0.25 ml
Subject Quadrivalent influenza vaccine Vaccine 0.5 ml

Indications

No indication recorded.