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Active, not recruiting Phase 3 Interventional Accepts healthy volunteers

An Extension and Crossover Vaccination Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus Given to Adults 60 Years of Age and Above Who Participated in RSV OA=ADJ-006 Study

ClinicalTrials.gov ID: NCT06534892

Public ClinicalTrials.gov record NCT06534892. 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 25, 2026, 1:26 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 3b, Randomized, Open Label, Multicountry, Multi-center, Extension and Crossover Vaccination Study to Evaluate the Immunogenicity and Safety of Different Revaccination Schedules and Persistence of a Single Dose of the RSVPreF3 OA Vaccine in Adults Aged 60 Years and Above Who Participated in the RSV OA=ADJ-006 Study

Brief summary

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

The purpose of this study is: * To investigate the optimal timing for revaccination after the initial RSVPreF3 OA vaccine dose, * To evaluate the long-term immune persistence and safety up to 5 consecutive RSV seasons (approximately 60 months) of a single dose of RSVPreF3 OA vaccine, * To give the opportunity to participants who received only placebo in the RSVOA=ADJ- 006 study, to receive a dose of the RSVPreF3 OA vaccine and collect additional safety information.

Study identification

NCT ID
NCT06534892
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
10,212 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
60 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 1, 2024 (Actual)
Primary completion
Sep 30, 2026 (Estimated)
Completion
Sep 30, 2026 (Estimated)
Last update posted
Oct 1, 2026

2024 – 2026

United States locations

U.S. sites
56
U.S. states
23
U.S. cities
53
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205 —
GSK Investigational Site Birmingham Alabama 35211 —
GSK Investigational Site Huntsville Alabama 35802 —
GSK Investigational Site Phoenix Arizona 85020 —
GSK Investigational Site Tucson Arizona 85741 —
GSK Investigational Site Cerritos California 90703 —
GSK Investigational Site Doral Florida 33172-2513 —
GSK Investigational Site Fort Myers Florida 33912-4316 —
GSK Investigational Site Jacksonville Florida 32205 —
GSK Investigational Site Lake City Florida 32055 —
GSK Investigational Site Melbourne Florida 32934-8172 —
GSK Investigational Site Miami Florida 33174 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Pinellas Park Florida 33781 —
GSK Investigational Site The Villages Florida 32162 —
GSK Investigational Site West Palm Beach Florida 33409 —
GSK Investigational Site Atlanta Georgia 30328 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Chicago Illinois 60602 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site Mishawaka Indiana 46544 —
GSK Investigational Site El Dorado Kansas 67042-2187 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Wichita Kansas 67205-1132 —
GSK Investigational Site Wichita Kansas 67226 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Rockville Maryland 20854 —
GSK Investigational Site Richfield Minnesota 55423 —
GSK Investigational Site Kansas City Missouri 64114 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Las Vegas Nevada 89113 —
GSK Investigational Site New York New York 10017 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site Hickory North Carolina 28601 —
GSK Investigational Site Mooresville North Carolina 28117 —
GSK Investigational Site Rocky Mount North Carolina 27804 —
GSK Investigational Site Salisbury North Carolina 28144 —
GSK Investigational Site Winston-Salem North Carolina 27103-3914 —
GSK Investigational Site Centerville Ohio 45459 —
GSK Investigational Site Cincinnati Ohio 45236 —
GSK Investigational Site Columbus Ohio 43212 —
GSK Investigational Site Erie Pennsylvania 16508 —
GSK Investigational Site Pittsburgh Pennsylvania 15236 —
GSK Investigational Site Anderson South Carolina 29621 —
GSK Investigational Site Mt. Pleasant South Carolina 29405 —
GSK Investigational Site Knoxville Tennessee 37938 —
GSK Investigational Site Memphis Tennessee 38119 —
GSK Investigational Site Dallas Texas 75234 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77008 —
GSK Investigational Site Keller Texas 76248 —
GSK Investigational Site San Antonio Texas 78229-6306 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Salt Lake City Utah 84106 —
GSK Investigational Site Norfolk Virginia 23502 —

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 195 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06534892, 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 Oct 1, 2026 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06534892 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →