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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 Nov 4, 2026, 8:48 AM EST

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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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The aim of this study is to demonstrate the immune response and to evaluate the safety of the RSVPreF3 OA investigational vaccine in non-immunocompromised adults 18-49 years of age (YOA), who are at increased risk (AIR) for RSV disease, compared to older adults (OA) 60 YOA and above.

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

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 29, 2024 (Actual)
Primary completion
Jul 29, 2024 (Actual)
Completion
Mar 18, 2025 (Actual)
Last update posted
Sep 25, 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 25, 2025 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06389487 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →