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
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
- lead INDUSTRY
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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