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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Investigate the Safety and Immunogenicity of the Quadrivalent Influenza mRNA Vaccines in Adults Aged 18 Years and Above

ClinicalTrials.gov ID: NCT06361875

Public ClinicalTrials.gov record NCT06361875. 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 Sep 1, 2026, 9:33 PM 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 I/II Study to Investigate the Safety and Immunogenicity of Quadrivalent Influenza mRNA Vaccines MRT5421, MRT5424, and MRT5429 in Healthy Participants Aged 18 Years and Above

Brief summary

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

The purpose of this study was to evaluate the safety and immunogenicity of a single intramuscular (IM) injection of different formulations of Quadrivalent Influenza Vaccine (QIV) messenger ribonucleic acid (mRNA) (MRT5421, MRT5424, and MRT5429) compared to an active control (QIV- standard dose (SD), QIV- high dose (HD) \[adults ≥ 65 years of age only\], or quadrivalent recombinant influenza vaccine (RIV4)) in adults 18 years of age and older.

Study identification

NCT ID
NCT06361875
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Enrollment
908 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 31, 2024
Primary completion
Jun 8, 2025
Completion
Jun 8, 2025
Last update posted
Aug 3, 2026

2024 – 2025

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
California Research Foundation Site Number : 8400038 San Diego California 92123-1881
Indago Research and Health Center- Site Number : 8400032 Hialeah Florida 33012
Cenexel Research Centers of America- Site Number : 8400037 Hollywood Florida 33024
Brengle Family Medicine Site Number : 8400045 Indianapolis Indiana 46260
AMR Lexington- Site Number : 8400042 Lexington Kentucky 40509
Velocity Clinical Research- New Orleans Site Number : 8400053 New Orleans Louisiana 70119
The Alliance for Multispecialty Research - KCM, LLC- Site Number : 8400034 Kansas City Missouri 64114
Velocity Clinical Research Norfolk- Site Number : 8400046 Norfolk Nebraska 68701
AMR Knoxville- Site Number : 8400043 Knoxville Tennessee 37909
Clinical Trials of Texas, Inc. - PPDS- Site Number : 8400029 San Antonio Texas 78229
Cenexel JBR- Site Number : 8400051 Salt Lake City Utah 84107

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06361875, 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 Aug 3, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06361875 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →