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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Phase 3 Safety and Immunogenicity Study of aQIV in Elderly Adults

ClinicalTrials.gov ID: NCT03314662

Public ClinicalTrials.gov record NCT03314662. 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, 10:25 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 3, Randomized, Double-Blind, Controlled, Multicenter, Clinical Study to Evaluate Safety and Immunogenicity of an MF59-Adjuvanted Quadrivalent Subunit Influenza Vaccine in Comparison With an MF59-Adjuvanted Trivalent Subunit Influenza Vaccine and an MF59-Adjuvanted Trivalent Subunit Influenza Vaccine Containing the Alternate B Strain, in Adults Aged 65 Years and Above

Study identification

NCT ID
NCT03314662
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Seqirus
Industry
Enrollment
1,778 participants

Conditions and interventions

Interventions

  • MF59-adjuvanted Quadrivalent Subunit Inactivated Egg-derived Influenza Vaccine (aQIV) Biological
  • Licensed MF59-adjuvanted Trivalent Subunit Inactivated Egg-derived Influenza Vaccine (aTIV-1) Biological
  • MF59-adjuvanted Trivalent Subunit Inactivated Egg-derived Influenza Vaccine Containing the Alternate B Strain (aTIV-2) Biological

Biological

Eligibility (public fields only)

Age range
65 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 16, 2017
Primary completion
Dec 10, 2017
Completion
May 16, 2018
Last update posted
Jul 21, 2020

2017 – 2018

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Coastal Clinical Research, Inc. Mobile Alabama 36608
Anaheim Clinical Trials Anaheim California 92801
Paradigm clinical Research Centers, Inc Redding California 96001
Clinical Research of South Florida, an AMR Company Coral Gables Florida 33134
Meridan Clinical Research, LLC Savannah Georgia 31406
Advanced Clinical Research Meridian Idaho 83642
Johnson County Clin-Trials Lenexa Kansas 66219
Heartland Research Associates, LLC - An AMR Company Newton Kansas 67114
Heartland Research Associates, LLC - An AMR Company Wichita Kansas 67207
Center for Pharmaceutical Research, LLC Kansas City Missouri 64114
Sundance Clinical Research, LLC St Louis Missouri 63141
Meridian Clinical Research, LLC Omaha Nebraska 68134
United Medical Associates Binghamton New York 13901
Rapid Medical Research, Inc. Cleveland Ohio 44122
Medical Research South Charleston South Carolina 29407
New Orleans Center for Clinical Research Knoxville Tennessee 37920
Benchmark Research Fort Worth Texas 76135
Benchmark Research San Angelo Texas 76904
Martin Diagnostic Clinic Tomball Texas 77375
Advanced Clinical Research West Jordan Utah 84088

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 NCT03314662, 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 Jul 21, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03314662 live on ClinicalTrials.gov.

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