ClinicalTrials.gov record
Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study on Safety and Immune Response of Investigational RSV OA Vaccine in Combination With Herpes Zoster Vaccine in Healthy Adults

ClinicalTrials.gov ID: NCT05966090

Public ClinicalTrials.gov record NCT05966090. 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, 7:02 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 III, Open-label, Randomized, Controlled, Multi-country Study to Evaluate the Immune Response, Safety and Reactogenicity of RSVPreF3 OA Investigational Vaccine When Co-administered With Herpes Zoster Recombinant Subunit (HZ/su) Vaccine in Adults Aged 50 Years and Older

Study identification

NCT ID
NCT05966090
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
530 participants

Conditions and interventions

Interventions

  • HZ/su vaccine Biological
  • RSVPreF3 OA investigational vaccine Biological

Biological

Eligibility (public fields only)

Age range
50 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
Jul 27, 2023
Primary completion
Feb 18, 2024
Completion
Jul 28, 2024
Last update posted
Mar 31, 2025

2023 – 2024

United States locations

U.S. sites
11
U.S. states
9
U.S. cities
11
Facility City State ZIP Site status
GSK Investigational Site Daphne Alabama 36526
GSK Investigational Site Tempe Arizona 85281
GSK Investigational Site Corte Madera California 94925
GSK Investigational Site Aurora Colorado 80012
GSK Investigational Site North Miami Beach Florida 33162
GSK Investigational Site West Palm Beach Florida 33409
GSK Investigational Site Columbus Georgia 31904-8946
GSK Investigational Site Versailles Kentucky 40383
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site San Antonio Texas 78229

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05966090, 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 Mar 31, 2025 · Synced May 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05966090 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →