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Completed Phase 3 Interventional Results available

Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A

ClinicalTrials.gov ID: NCT01610414

Public ClinicalTrials.gov record NCT01610414. 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 21, 2026, 7:03 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

Observer-blind Study to Evaluate Efficacy, Safety, and Immunogenicity of GSK Biologicals' Herpes Zoster Vaccine GSK1437173A

Study identification

NCT ID
NCT01610414
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,877 participants

Conditions and interventions

Conditions

Interventions

  • Herpes Zoster vaccine GSK1437173A Biological
  • Placebo Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 12, 2012
Primary completion
Nov 3, 2016
Completion
Jan 31, 2017
Last update posted
Jan 22, 2018

2012 – 2017

United States locations

U.S. sites
23
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Duarte California 91010
GSK Investigational Site San Francisco California 94143
GSK Investigational Site Aurora Colorado 80045
GSK Investigational Site Westwood Kansas 66205
GSK Investigational Site Lexington Kentucky 40536
GSK Investigational Site Boston Massachusetts 02111
GSK Investigational Site Boston Massachusetts 02114
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Detroit Michigan 48201
GSK Investigational Site Minneota Minnesota 55455
GSK Investigational Site Rochester Minnesota 55905
GSK Investigational Site Hackensack New Jersey 07601
GSK Investigational Site New York New York 10021
GSK Investigational Site Syracuse New York 13210
GSK Investigational Site Chapel Hill North Carolina 27599
GSK Investigational Site Durham North Carolina 27705
GSK Investigational Site Cleveland Ohio 44195
GSK Investigational Site Philadelphia Pennsylvania 19104
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site Seattle Washington 98108
GSK Investigational Site Seattle Washington 98109-1024
GSK Investigational Site Marshfield Wisconsin 54449

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 155 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01610414, 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 Jan 22, 2018 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01610414 live on ClinicalTrials.gov.

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