Postmarketing Surveillance Study for Quadrivalent Influenza Vaccine (VaxigripTetra Inj.) in Subjects Aged 3 Years Old and Above

NCT05406180 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 675

Last updated 2022-06-06

No results posted yet for this study

Summary

The objective is to describe the safety profile after 1 dose of VaxigripTetra inj. administered in subjects aged 3 years old and above under routine clinical practice.

The planned duration of each subject's participation in the study will be 21 to 28 days.

Conditions

Interventions

BIOLOGICAL

VaxigripTetra inj.

Suspension for injection in a pre-filled syringe Injection intramuscular

Sponsors & Collaborators

Eligibility

Min Age
3 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-10-10
Primary Completion
2019-12-27
Completion
2019-12-27

Countries

  • South Korea

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05406180 on ClinicalTrials.gov