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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of Different Formulations of Monovalent Influenza A/Astrakhan/3212/2020 Like (H5N8) Virus Vaccine With AS03 Adjuvant System in Medically Stable Adults

ClinicalTrials.gov ID: NCT05975840

Public ClinicalTrials.gov record NCT05975840. 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 19, 2026, 3:34 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 I/II Observer-blind, Randomized, Multi-center Trial to Evaluate the Safety and Immunogenicity of Different Formulations of Monovalent Influenza A/Astrakhan/3212/2020 Like (H5N8) Virus Vaccine With AS03 Adjuvant System (Referred to as Q-Pan H5N8), Given as a Two-dose Series to Adults 18 to 64 Years of Age and 65 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 immunogenicity of different formulations of monovalent Influenza A/Astrakhan/3212/2020-like virus vaccine with AS03 adjuvant system in adults greater than or equal to (\>=)18 years of age.

Study identification

NCT ID
NCT05975840
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
518 participants

Conditions and interventions

Interventions

Biological

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
Aug 3, 2023 (Actual)
Primary completion
May 21, 2024 (Actual)
Completion
Sep 19, 2024 (Actual)
Last update posted
Aug 19, 2025

2023 – 2024

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Tempe Arizona 85281 —
GSK Investigational Site Chula Vista California 91911 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Santa Ana California 92705 —
GSK Investigational Site Pembroke Pines Florida 33025 —
GSK Investigational Site Chamblee Georgia 30341 —
GSK Investigational Site Meridian Idaho 83642 —
GSK Investigational Site El Dorado Kansas 67042 —
GSK Investigational Site Lenexa Kansas 66219 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Anderson South Carolina 29621 —
GSK Investigational Site Knoxville Tennessee 37920 —
GSK Investigational Site Austin Texas 78745 —
GSK Investigational Site Boerne Texas 78006 —
GSK Investigational Site San Antonio Texas 78244 —
GSK Investigational Site Tomball Texas 77375 —
GSK Investigational Site Norfolk Virginia 23507 —

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 NCT05975840, 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 19, 2025 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05975840 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →