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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Bivalent mRNA SARS-CoV-2 vaccine | Administering a booster dose of the bivalent mRNA vaccine BNT162b2 |
| BIOLOGICAL | Quardrivalent influenza vaccine | Administering 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.