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Study to Evaluate Immunogenicity and Safety of a High-Dose Influenza Vaccine in Adults 50 Through 64 Years of Age

Completed · Phase 3 · NCT06641180

Conditions: Influenza

At a glance

Research payments reported, 2025
$2.8M
U.S. investigators named
21
Sites paid
13
Planned or actual enrollment
1,180

About the trial

Sponsor
Sanofi Pasteur, a Sanofi Company
Tested
High-Dose trivalent influenza vaccine (Split virion, Inactivated) (biological), Standard-dose trivalent influenza vaccine (Split virion, Inactivated) (biological)
Dates
Started 2024-11-04; completion 2025-06-24
Results posted
Not yet

The purpose of this study is to evaluate Immunogenicity and Safety of a High-Dose (HD) Influenza Vaccine (IV) in Adults 50 through 64 Years of Age.

From ClinicalTrials.gov, last updated 2025-12-03. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Sanofi Pasteur Inc. reported $2.8M in research payments for this study in 2025 (111 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Cr Services Acquisition Us Llc $556,026
  • Alliance for Multispecialty Research,llc $473,374
  • Research Centers of America $315,326
  • Cenexel Iresearch Llc $298,074
  • Collaborative Neuroscience Research (cenexel Cns) $265,222
  • Hassman Research Institute Llc $262,981
  • Lucas Research, Inc $207,637
  • Bb Holdings,llc Dba Jean Brown Research $183,521
  • Group Health Cooperative $67,899
  • Cbh Health Llc $56,286
  • Research Centers of America,llc $49,648
  • Emory University Hospital, GA $41,913
  • Kaiser Foundation Hospital-Santa Clara, CA $31,109

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.