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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study on the Immune Response and Safety of the Shingles Vaccine and the Influenza Vaccine When Either is Given to Healthy Adults at the Same Time or Following a COVID-19 Booster Vaccine

ClinicalTrials.gov ID: NCT05047770

Public ClinicalTrials.gov record NCT05047770. 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 20, 2026, 3:54 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 III, Randomized, Open-label, Controlled, Multicenter Study to Evaluate the Immune Response and Safety of Both Herpes Zoster Subunit Vaccine in Healthy Adults Aged 50 Years and Older AND the Influenza Virus Vaccine in Healthy Adults Aged 18 Years and Older When Administered Sequentially or Coadministered With mRNA-1273 Booster Vaccination

Brief summary

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

The aim of this study was to evaluate the immune response and safety of both GlaxoSmithKline Biologicals SA's (GSK's) herpes zoster (HZ) subunit (su) vaccine in healthy adults 50 years of age (YOA) and older and quadrivalent seasonal influenza (Flu D-QIV) vaccine in healthy adults 18 YOA and older, when administered sequentially or co-administered with Moderna's mRNA-1273 booster vaccination against COVID-19.

Study identification

NCT ID
NCT05047770
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
2,013 participants

Conditions and interventions

Conditions

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, 2021 (Actual)
Primary completion
Aug 29, 2022 (Actual)
Completion
Aug 31, 2022 (Actual)
Last update posted
Nov 13, 2023

2021 – 2022

United States locations

U.S. sites
46
U.S. states
20
U.S. cities
43
Facility City State ZIP Site status
GSK Investigational Site Tempe Arizona 85283 —
GSK Investigational Site Oxnard California 93030-5841 —
GSK Investigational Site San Diego California 92103-6204 —
GSK Investigational Site San Diego California 92103 —
GSK Investigational Site Atlantis Florida 33462 —
GSK Investigational Site Fort Myers Florida 33912 —
GSK Investigational Site Jacksonville Florida 32256 —
GSK Investigational Site Lake Worth Florida 33461 —
GSK Investigational Site Miami Florida 33135 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Ocala Florida 34471 —
GSK Investigational Site Orlando Florida 32801 —
GSK Investigational Site Sarasota Florida 34243-2878 —
GSK Investigational Site Atlanta Georgia 30308 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Meridian Idaho 83642 —
GSK Investigational Site El Dorado Kansas 67042 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Topeka Kansas 66606 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Biloxi Mississippi 39531 —
GSK Investigational Site Fremont Nebraska 68025-2592 —
GSK Investigational Site Omaha Nebraska 68114 —
GSK Investigational Site Berlin New Jersey 08009 —
GSK Investigational Site Albuquerque New Mexico 87102 —
GSK Investigational Site Columbus Ohio 43213 —
GSK Investigational Site Norman Oklahoma 73072 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Yukon Oklahoma 73099 —
GSK Investigational Site Grants Pass Oregon 97527 —
GSK Investigational Site Anderson South Carolina 29621 —
GSK Investigational Site Columbia South Carolina 29204 —
GSK Investigational Site Greenville South Carolina 29615 —
GSK Investigational Site Memphis Tennessee 38119 —
GSK Investigational Site Beaumont Texas 77706 —
GSK Investigational Site Cedar Park Texas 78613 —
GSK Investigational Site Houston Texas 77090 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Tomball Texas 77375 —
GSK Investigational Site Salt Lake City Utah 84107 —
GSK Investigational Site West Jordan Utah 84088 —
GSK Investigational Site Norfolk Virginia 23502 —
GSK Investigational Site Cheney Washington 99204 —
GSK Investigational Site Tacoma Washington 98405 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05047770, 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 Nov 13, 2023 · Synced Oct 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 public registry record, listed eligibility criteria, and available contact information for NCT05047770 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →