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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Long-Term Immunogenicity of the Norovirus GI.1/GII.4 Bivalent Virus-like Particle (VLP) Vaccine (NoV Vaccine) in Adults

ClinicalTrials.gov ID: NCT03039790

Public ClinicalTrials.gov record NCT03039790. 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 24, 2026, 1:27 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 2, Long-Term Immunogenicity Follow-up Trial of Adult and Elderly Subjects Who Have Previously Received an Intramuscular Injection of Norovirus GI.1/GII.4 Bivalent Virus-Like Particle Vaccine

Study identification

NCT ID
NCT03039790
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
528 participants

Conditions and interventions

Interventions

  • NoV Vaccine Biological

Biological

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
Feb 20, 2017
Primary completion
Jul 21, 2021
Completion
Jul 21, 2021
Last update posted
Nov 8, 2022

2017 – 2021

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Simon-Williamson Clinic/Synexus Clinical Research US, Inc Birmingham Alabama 35211
Synexus Clinical Research US, Inc./Fountain Hills Family Practice, P.C. Fountain Hills Arizona 85268
Synexus Clinical Research US, Inc/Southwest Family Medicine Littleton Colorado 80127
Miami Research Associates Miami Florida 33143
Johnson County Clin-Trials Lenexa Kansas 66219
St. Louis University, School of Medicine St Louis Missouri 63106
Regional Clinical Research Inc. Endwell New York 13760
University of Rochester Rochester New York 14642
Benchmark Research Austin Austin Texas 78705

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03039790, 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 8, 2022 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03039790 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →