drugset / Trial / NCT04363359

Clinical Trial of Quadrivalent Influenza Virus Split Vaccine

NCT04363359

Phase 2 Completed 1980 enrolled Shanghai Institute Of Biological Products
RandomizedParallel-groupDouble-blindPrevention

Summary

To evaluate the immunogenicity and safety of 2 doses of quadrivalent influenza virus split vaccine in healthy population aged 6-35 month., so as to provide a data support for phase III clinical trials.

Timeline

Start
2020-01-15
Primary completion
2021-09-14
Completion
2021-09-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Quadrivalent influenza vaccine Vaccine 0.25 ml
Subject Quadrivalent influenza vaccine Vaccine 0.5 ml
Comparator Trivalent influenza vaccine(B/V) Vaccine 0.25 ml
Comparator Trivalent influenza vaccine(B/Y) Vaccine 0.25 ml

Indications