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Recruiting Phase 3 Interventional Accepts healthy volunteers

A Study to Evaluate the Immune Response and Safety of a Vaccine Against Influenza in Adults 18-64 Years of Age

ClinicalTrials.gov ID: NCT07851246

Public ClinicalTrials.gov record NCT07851246. 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 12, 2026, 9:51 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 3 Randomized, Observer-Blind, Controlled Study to Evaluate the Immunogenicity, Reactogenicity and Safety of an mRNA-based Seasonal Influenza Vaccine, in Adults 18-64 Years of Age

Brief summary

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

This clinical trial will study an investigational seasonal influenza vaccine in adults 18 to 64 years of age. The vaccine is based on messenger ribonucleic acid, also called mRNA. The main goals of the study are to learn how well the vaccine helps the body make an immune response against influenza and what medical problems participants may have after vaccination. Researchers will also compare immune responses in adults 18 to 64 years of age from this study, with immune responses in adults 65 years of age and older from another study. Participants will receive 1 injection into the upper arm muscle and will be followed for about 6 months.

Study identification

NCT ID
NCT07851246
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
3,000 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 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
Oct 1, 2026 (Actual)
Primary completion
Jul 9, 2027 (Estimated)
Completion
Jul 9, 2027 (Estimated)
Last update posted
Oct 9, 2026

2026 – 2027

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Glendale Arizona 85308 Recruiting
GSK Investigational Site Tucson Arizona 85711 Recruiting
GSK Investigational Site San Diego California 92123 Recruiting
GSK Investigational Site Miami Florida 33186 Recruiting
GSK Investigational Site Miami Lakes Florida 33016 Recruiting
GSK Investigational Site Meridian Idaho 83642-3154 Recruiting
GSK Investigational Site Valparaiso Indiana 46383 Recruiting
GSK Investigational Site Lenexa Kansas 66219 Recruiting
GSK Investigational Site Hartsdale New York 10530 Recruiting
GSK Investigational Site Spartanburg South Carolina 29303 Recruiting
GSK Investigational Site DeSoto Texas 75115 Recruiting
GSK Investigational Site Fort Worth Texas 76135 Recruiting

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07851246, 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 9, 2026 · Synced Oct 12, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07851246 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →