Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study to Assess the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine (GSK1437173A) When Co-administered With GSK Biologicals' Diphtheria, Tetanus and Pertussis Vaccine (Boostrix®) in Adults Aged 50 Years and Older

ClinicalTrials.gov ID: NCT02052596

Public ClinicalTrials.gov record NCT02052596. 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 Jul 22, 2026, 7:43 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

Immunogenicity and Safety Study of GSK Biologicals' Herpes Zoster Vaccine GSK1437173A When Co-administered With Boostrix® in Adults Aged 50 Years and Older

Study identification

NCT ID
NCT02052596
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
935 participants

Conditions and interventions

Conditions

Interventions

  • Herpes Zoster vaccine GSK 1437173A Biological
  • Boostrix 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
Feb 6, 2014
Primary completion
Jun 15, 2015
Completion
Apr 20, 2016
Last update posted
Apr 23, 2018

2014 – 2016

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85704
GSK Investigational Site Tucson Arizona 85712
GSK Investigational Site San Diego California 92108
GSK Investigational Site Stockbridge Georgia 30281
GSK Investigational Site Meridian Idaho 83642
GSK Investigational Site Lewiston Maine 04240
GSK Investigational Site Las Vegas Nevada 89104
GSK Investigational Site Charlotte North Carolina 28209
GSK Investigational Site Salisbury North Carolina 28114
GSK Investigational Site Uniontown Pennsylvania 15401
GSK Investigational Site Warwick Rhode Island 02886
GSK Investigational Site Greer South Carolina 29650
GSK Investigational Site Richmond Virginia 23294

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 NCT02052596, 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 Apr 23, 2018 · Synced Jul 22, 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 NCT02052596 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →