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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers

A Study to Find and Confirm the Dose and Assess Safety, Reactogenicity and Immune Response of a Vaccine Against Pandemic H5N1 Influenza Virus in Healthy Younger and Older Adults

ClinicalTrials.gov ID: NCT06382311

Public ClinicalTrials.gov record NCT06382311. 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, 1:23 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 1/2, RANDOMIZED, PARTIALLY-BLIND, DOSE-FINDING/DOSE-CONFIRMATION STUDY TO EVALUATE THE SAFETY, REACTOGENICITY AND IMMUNOGENICITY OF THE MRNA-BASED INVESTIGATIONAL PANDEMIC H5 INFLUENZA VACCINE CANDIDATE ADMINISTERED IN HEALTHY YOUNGER AND OLDER ADULTS

Study identification

NCT ID
NCT06382311
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
991 participants

Conditions and interventions

Interventions

  • Flu Pandemic mRNA_Dose level 1 Biological
  • Flu Pandemic mRNA_Dose level 2 Biological
  • Flu Pandemic mRNA_ Dose level 3. Biological
  • Flu Pandemic mRNA_ Dose level 4 Biological
  • Flu Pandemic mRNA_Dose level 5 Biological
  • Flu Pandemic mRNA_Dose level 6 Biological
  • Influenza virus vaccine Biological
  • Placebo Drug

Biological · Drug

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
Apr 17, 2024
Primary completion
Jan 12, 2026
Completion
Jan 12, 2026
Last update posted
Feb 4, 2026

2024 – 2026

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207
GSK Investigational Site Little Rock Arkansas 72204
GSK Investigational Site Fort Collins Colorado 80525
GSK Investigational Site Fort Myers Florida 33912
GSK Investigational Site West Palm Beach Florida 33409
GSK Investigational Site Chamblee Georgia 30043
GSK Investigational Site El Dorado Kansas 67042
GSK Investigational Site Lenexa Kansas 66219
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Kansas City Missouri 64114
GSK Investigational Site Omaha Nebraska 68144
GSK Investigational Site Las Vegas Nevada 89102
GSK Investigational Site Rochester New York 14609
GSK Investigational Site Greensboro North Carolina 27405
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Edmond Oklahoma 73013
GSK Investigational Site Yukon Oklahoma 73099
GSK Investigational Site Philadelphia Pennsylvania 19111
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Norfolk Virginia 23502
GSK Investigational Site Seattle Washington 98104

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 NCT06382311, 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 Feb 4, 2026 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06382311 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →