Evaluate the Safety and Efficacy of Quadrivalent Influenza in Real-world Situations.

CompletedOBSERVATIONAL
Enrollment

4,900

Participants

Timeline

Start Date

November 17, 2021

Primary Completion Date

January 20, 2023

Study Completion Date

March 28, 2023

Conditions
GCP
Interventions
BIOLOGICAL

One dose of quadrivalent influenza virus split vaccine was administered

"Safety observation: All 4900 vaccine recipients participated in the safety observation after vaccination, and were followed up for adverse events (AE) within 30 minutes and 0-30 days after vaccination, and SAEs within 6 months after vaccination.~In addition to 1050 recipients aged 18-59 years who were included in the first layer test, 350 recipients aged 3-17 years and 350 recipients aged ≥60 years were randomly selected from each group. Blood samples were collected before and 30 days after vaccination for influenza virus HI antibody detection."

Trial Locations (1)

250000

Kou Zengqiang, Jinan

All Listed Sponsors
lead

Hualan Biological Bacterin Co. Ltd.

INDUSTRY

NCT06334510 - Evaluate the Safety and Efficacy of Quadrivalent Influenza in Real-world Situations. | Biotech Hunter | Biotech Hunter