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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 Jul 23, 2026, 4:37 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 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

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

  • F2G22B/DL001Z Biological
  • F2H23D/DL001Z-NH Biological
  • F2H23B/DL001Z-NH Biological
  • F2H23H/DL001Z Biological
  • FDQ23A-NH (Flu D-QIV) Combination Product
  • GSK5800544A Biological
  • Flu D-TIV Combination Product
  • F2H23A/DL001Z-NH Biological
  • F2H23G/DL001Z Biological
  • Fluzone HD Quadrivalent Combination Product
  • Fluzone HD Combination Product

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 22, 2024
Primary completion
Dec 26, 2024
Completion
Jun 3, 2025
Last update posted
Mar 9, 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 9, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06431607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →