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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study on the Immune Response and Safety of Vaccine Against Respiratory Syncytial Virus (RSV) Given to Adults 18 to 49 Years of Age at Increased Risk for Respiratory Syncytial Virus Disease, Compared to Older Adults 60 Years of Age and Above

ClinicalTrials.gov ID: NCT06389487

Public ClinicalTrials.gov record NCT06389487. 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 May 20, 2026, 1:31 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 3b, Open-label Study to Evaluate the Non-inferiority of the Immune Response and to Evaluate the Safety of the RSVPreF3 OA Investigational Vaccine in Adults 18-49 Years of Age at Increased Risk for Respiratory Syncytial Virus Disease, Compared to Older Adults >=60 Years of Age

Study identification

NCT ID
NCT06389487
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,459 participants

Conditions and interventions

Interventions

  • RSVPreF3 OA investigational vaccine Biological

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
Apr 28, 2024
Primary completion
Jul 28, 2024
Completion
Mar 17, 2025
Last update posted
Sep 24, 2025

2024 – 2025

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
GSK Investigational Site Glendale Arizona 85308
GSK Investigational Site Phoenix Arizona 85284
GSK Investigational Site North Hollywood California 91606-3287
GSK Investigational Site Oakland California 94610
GSK Investigational Site Walnut Creek California 94598
GSK Investigational Site Hialeah Florida 33012
GSK Investigational Site North Miami Florida 33173
GSK Investigational Site Orlando Florida 32806
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Silver Spring Maryland 20904
GSK Investigational Site Rochester New York 14609
GSK Investigational Site Oklahoma City Oklahoma 73111
GSK Investigational Site Knoxville Tennessee 37909
GSK Investigational Site DeSoto Texas 75115
GSK Investigational Site Charlottesville Virginia 22911
GSK Investigational Site Wenatchee Washington 98801

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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06389487, 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 24, 2025 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06389487 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →