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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Find the Dose and Assess the Immune Response and Safety of a Vaccine Against Influenza in Healthy Younger and Older Adults

ClinicalTrials.gov ID: NCT06431607

Public ClinicalTrials.gov record NCT06431607. 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 24, 2026, 8:13 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 2a Randomized, Observer-blind, Dose-finding Study to Evaluate the Immunogenicity and Safety of mRNA-based Multivalent Seasonal Influenza Vaccine Candidates in Adults 18 Years of Age and Older

Brief summary

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

The purpose of this study is to assess the safety and immune response of GlaxoSmithKlines (GSK) messenger RNA (mRNA)-based multivalent vaccine (GSK4382276A) candidate against influenza, administered in healthy younger adults (YA) and older adults (OA).

Study identification

NCT ID
NCT06431607
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
845 participants

Conditions and interventions

Interventions

Biological · Combination Product

Eligibility (public fields only)

Age range
18 Years to 85 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
May 23, 2024 (Actual)
Primary completion
Dec 27, 2024 (Actual)
Completion
Jun 4, 2025 (Actual)
Last update posted
Mar 10, 2026

2024 – 2025

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
GSK Investigational Site Hialeah Florida 33012 —
GSK Investigational Site Miami Florida 33147 —
GSK Investigational Site Miami Florida 33186 —
GSK Investigational Site Chicago Illinois 60640 —
GSK Investigational Site Valparaiso Indiana 46383 —
GSK Investigational Site El Dorado Kansas 67042 —
GSK Investigational Site Lenexa Kansas 66219 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site Greensboro North Carolina 27408 —
GSK Investigational Site Knoxville Tennessee 37909 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Fort Worth Texas 76135 —
GSK Investigational Site Tomball Texas 77375 —
GSK Investigational Site Newport News Virginia 23606 —
GSK Investigational Site Norfolk Virginia 23502 —

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 NCT06431607, 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 Mar 10, 2026 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06431607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →