Trials / Completed
CompletedNCT05858450
This Study Intends to Describe the Characteristics of Patients Given the Pfizer-BioNTech Bivalent mRNA COVID-19 Vaccine and Any Commercially Available Influenza Vaccines at the Same Time Versus at Different Times.
Investigating Uptake and Subsequent Health Outcomes Associated With Pfizer-BioNTech Bivalent COVID-19/Influenza Vaccine Concomitant Administration Using a Claims-based Real-world Data Source in the US
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 3,442,996 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study intends to describe the characteristics of patients given the Pfizer-BioNTech bivalent mRNA COVID-19 vaccine and any commercially available influenza vaccines at the same time versus at different times.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | Comirnaty | COMIRNATY is an active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 12 years of age and older. |
| BIOLOGICAL | Quadrivalent Influenza Vaccine | Quadrivalent Influenza Vaccine is a class of vaccines indicated for active immunization for the prevention of influenza disease caused by influenza A subtype viruses and type B viruses contained in the vaccines |
Timeline
- Start date
- 2023-05-05
- Primary completion
- 2023-05-12
- Completion
- 2023-05-12
- First posted
- 2023-05-15
- Last updated
- 2024-09-20
- Results posted
- 2024-09-20
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05858450. Inclusion in this directory is not an endorsement.