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Completed Phase 2 Interventional Accepts healthy volunteers Results available

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)

ClinicalTrials.gov ID: NCT06508320

Public ClinicalTrials.gov record NCT06508320. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Observer-blind Study to Evaluate the Safety, Reactogenicity, and Immunogenicity in Relation to the Product Attributes of mRNA-1083 (SARS-CoV-2 and Influenza) Vaccine in Adults ≥50 to <65 Years of Age

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT06508320
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ModernaTX, Inc.
Industry
Enrollment
931 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
50 Years to 64 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 15, 2024 (Actual)
Primary completion
Sep 25, 2025 (Actual)
Completion
Sep 25, 2025 (Actual)
Last update posted
Oct 8, 2026

2024 – 2025

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
12
Facility City State ZIP Site status
Indago Research & Health Center, Inc. Hialeah Florida 33012 —
Cenexel RCA Hollywood Florida 33024 —
Suncoast Research Group, LLC DBA Flourish Research Miami Florida 33135 —
Cenexel IRA Decatur Georgia 30030 —
DM Clinical Research - River Forest River Forest Illinois 60305 —
JCCT Lenexa Kansas 66219 —
Hassman Research Institute - Berlin - CenExel - PPDS Marlton New Jersey 80530 —
DM Clinical Research - Philadelphia Philadelphia Pennsylvania 19107 —
DM Clinical Research - Cyfair Clinical Research Center - PPDS Houston Texas 77065-5685 —
Clinical Trials of Texas, LLC DBA Flourish Research San Antonio Texas 78229 —
DM Clinical Research - Sugarland Sugar Land Texas 77478 —
DM Clinical Research - Tomball MDC Tomball Texas 77375 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06508320, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 8, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06508320 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →