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A Clinical Study to Investigate the Safety and Immunogenicity in Relation to Product Attributes of mRNA-1083 (Severe Acute Respiratory Syndrome Coronavirus 2 [SARS-CoV-2] and Influenza Vaccine)

Completed · Phase 2 · NCT06508320

Conditions: Influenza, SARS-CoV-2

At a glance

Research payments reported, 2025
$3.1M
U.S. investigators named
12
Sites paid
13
Planned or actual enrollment
931

About the trial

Sponsor
ModernaTX, Inc.
Tested
mRNA-1083 (biological)
Dates
Started 2024-07-15; completion 2025-09-25
Results posted
Yes

The purpose of this study is to evaluate the safety, reactogenicity, and immunogenicity in relation to the product attributes of mRNA-1083 vaccine when administered as a single intramuscular (IM) injection in adults ≥50 to \<65 years of age.

From ClinicalTrials.gov, last updated 2026-10-08. Full record, eligibility and contacts (opens in a new tab)

Industry funding

ModernaTX, Inc. reported $3.1M in research payments for this study in 2025 (98 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

  • Research Centers of America LLC $1.1M
  • Indago Research and Health Center Inc $442,048
  • Suncoast Research Group LLC $428,712
  • Cenexel Iresearch LLC $278,842
  • Research Centers of America $194,855
  • Dynamed Clinical Research LP $186,996
  • Johnson County Clintrials $171,393
  • Dynamed Chicago LLC $117,968
  • Dynamed Philadelphia LLC $110,897
  • Clinical Trials of Texas Inc. $57,763
  • Hassman Research Institute LLC $57,138
  • Indago Research and Health $15,090
  • Clinical Trials of Texas Inc $2,500

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