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A Study of mRNA-1345 Following a Primary Dose of a Licensed Protein Subunit Respiratory Syncytial Virus (RSV) Vaccine in Adult Participants ≥60 Years of Age

Completed · Phase 3 · NCT07117487

Conditions: Respiratory Syncytial Virus

At a glance

Research payments reported, 2025
$1.6M
U.S. investigators named
11
Sites paid
2
Planned or actual enrollment
507

About the trial

Sponsor
ModernaTX, Inc.
Tested
mRNA-1345 (biological)
Dates
Started 2025-08-05; completion 2026-03-27
Results posted
Not yet

The purpose of this study is to evaluate safety, tolerability and immunogenicity of mRNA-1345 in participants who have been previously vaccinated with either Arexvy or Abrysvo at least 12 months prior to enrollment, are medically stable and aged ≥60 years.

From ClinicalTrials.gov, last updated 2026-05-04. Full record, eligibility and contacts (opens in a new tab)

Industry funding

ModernaTX, Inc. reported $1.6M in research payments for this study in 2025 (90 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

  • Velocity Clinical Research Inc $1.1M
  • Indago Research and Health $550,103

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