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Completed Phase 2 Interventional Accepts healthy volunteers

A Study to Evaluate the Immune Response and Safety of an Influenza Vaccine in Adults 18 Years of Age and Above

ClinicalTrials.gov ID: NCT07204964

Public ClinicalTrials.gov record NCT07204964. 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 21, 2026, 9:24 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, 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 reactogenicity, safety and immune response of GlaxoSmithKline's (GSK) messenger RNA (mRNA)-based multivalent seasonal influenza vaccine candidates administered in healthy younger and older adults.

Study identification

NCT ID
NCT07204964
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
971 participants

Conditions and interventions

Interventions

Biological · Combination Product

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
Oct 7, 2025 (Actual)
Primary completion
Aug 24, 2026 (Actual)
Completion
Aug 24, 2026 (Actual)
Last update posted
Sep 18, 2026

2025 – 2026

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
GSK Investigational Site Guntersville Alabama 35976-2206 —
GSK Investigational Site Canoga Park California 91303 —
GSK Investigational Site Walnut Creek California 94598 —
GSK Investigational Site Hialeah Florida 33012 —
GSK Investigational Site Miami Florida 33186 —
GSK Investigational Site Pembroke Pines Florida 33025 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Carson City Nevada 89706 —
GSK Investigational Site Las Vegas Nevada 89109 —
GSK Investigational Site Greensboro North Carolina 27408 —
GSK Investigational Site North Charleston South Carolina 29405 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Garland Texas 75043 —
GSK Investigational Site Newport News Virginia 23606 —
GSK Investigational Site Seattle Washington 98104-2725 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07204964, 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 Sep 18, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07204964 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →