Clinical Trials Directory

Trials / Completed

CompletedNCT06831786

Immunogenicity of COVID-19 Vaccine Co-administration With Influenza Vaccine in Healthy Volunteers

Immunogenicity to SARS-CoV-2 of Co-administering Bivalent mRNA BNT162b2 Booster and Quadrivalent Influenza Vaccine Among Healthy Volunteers: A Pilot Study

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Prince of Songkla University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study, a pilot randomized controlled trial, single-blind (outcome assessor), evaluating the immune response (both humoral and cell-mediated) against SARS-CoV-2 and the safety of three different vaccine administration approaches: the SARS-CoV-2 mRNA vaccine alone, the influenza vaccine alone, and the co-administration of both vaccines.

Conditions

Interventions

TypeNameDescription
BIOLOGICALBivalent mRNA SARS-CoV-2 vaccineAdministering a booster dose of the bivalent mRNA vaccine BNT162b2
BIOLOGICALQuardrivalent influenza vaccineAdministering a VaxigripTetra™

Timeline

Start date
2024-03-01
Primary completion
2024-05-31
Completion
2024-05-31
First posted
2025-02-18
Last updated
2025-12-04
Results posted
2025-12-04

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT06831786. Inclusion in this directory is not an endorsement.