Trial intelligence / Profile preview

Optimizing Time of Day of Influenza Vaccine Administration in Adults Aged 60-85 Years

2024-513558-30-00Phase 4Completed

Sponsor
National Institute for Public Health and the Environment
Start
Aug 2024
Modality
Vaccines & Immunotherapeutics, Recombinant Proteins and Enzymes, Split/Subunit Vaccines → Inactivated Vaccines → Prophylactic Vaccines → Vaccines & Immunotherapeutics
Countries
1
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Overview

Phase 4, randomised trial of quadrivalent influenza vaccine, Influenza A virus A/Texas/50/2012 X-223A (H3N2) hemagglutinin antigen and 23-valent pneumococcal polysaccharide vaccine in influenza and pneumococcal disease (2 arms), sponsored by National Institute for Public Health and the Environment. Primary endpoint: Increase in influenza vaccine strain-specific serum antibody titers. Started Aug 2024; status: completed.

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Drugs

quadrivalent influenza vaccineInfluenza A virus A/Texas/50/2012 X-223A (H3N2) hemagglutinin antigen23-valent pneumococcal polysaccharide vaccine
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Conditions

influenzapneumococcal disease

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