Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

Cross-vaccination Study of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine (GSK 1437173A) in Subjects Who Previously Received Placebo in ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229) Studies.

NCT02690207 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to cross-vaccinate and collect safety data in terms of unsolicited Adverse Events (AEs), Serious Adverse Events (SAEs) and potential Immune Mediated Disease (pIMD) from subjects \>= 50 Years of age (YOA) who previously received placebo in ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229).

Conditions Studied

Interventions

  • BIOLOGICAL Herpes Zoster Vaccine GSK1437173A

Study Locations (20)

Arizona

  • GSK Investigational Site — Mesa
  • GSK Investigational Site — Phoenix
  • GSK Investigational Site — Phoenix
  • GSK Investigational Site — Phoenix
  • GSK Investigational Site — Tucson

Florida

  • GSK Investigational Site — Clearwater
  • GSK Investigational Site — DeLand
  • GSK Investigational Site — Jacksonville
  • GSK Investigational Site — Jacksonville
  • GSK Investigational Site — West Palm Beach

Maryland

  • GSK Investigational Site — Columbia
  • GSK Investigational Site — Elkridge

North Carolina

  • GSK Investigational Site — Cary
  • GSK Investigational Site — Charlotte

California

  • GSK Investigational Site — Spring Valley

Idaho

  • GSK Investigational Site — Meridian

Kansas

  • GSK Investigational Site — Wichita

Missouri

  • GSK Investigational Site — Kansas City

Trial Details

FieldValue
Enrollment Target 8,687 participants
Start Date 2016-03-16
Est. Completion 2019-03-15
Phase Phase 3

Sponsor

GlaxoSmithKline

558 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02690207

The ClinicalTrials.gov registry entry for NCT02690207 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8,687 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Herpes Zoster appearing as the primary indexed condition, and to 1 intervention — of which Herpes Zoster Vaccine GSK1437173A is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02690207 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Arizona, Florida, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02690207 about?

NCT02690207 is a clinical study titled "Cross-vaccination Study of GSK Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine (GSK 1437173A) in Subjects Who Previously Received Placebo in ZOSTER-006 (NCT01165177) and ZOSTER-022 (NCT01165229) Studies.". The purpose of this study is to cross-vaccinate and collect safety data in terms of unsolicited Adverse Events (AEs), Serious Adverse Events (SAEs) and potential Immune Mediated Disease (pIMD) from subjects \>= 50 Years of age (YOA) who previously received placebo in ZOSTER-006 (NCT01165177) and ZOS...

What is the current status of trial NCT02690207?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 8,687 participants. The study started on 2016-03-16. Estimated completion is 2019-03-15.

What conditions does trial NCT02690207 study?

This clinical trial studies the following conditions: Herpes Zoster. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02690207?

The interventions under investigation include: Herpes Zoster Vaccine GSK1437173A (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02690207?

This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02690207 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Idaho, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial