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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine in Participants ≥65 Years in the US

ClinicalTrials.gov ID: NCT03282240

Public ClinicalTrials.gov record NCT03282240. 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 Oct 24, 2026, 10:35 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

Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine Administered by Intramuscular Route in Participants Aged 65 Years and Older

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, modified double-blind, active-controlled, multi-center trial assessed the safety and immunogenicity of the high-dose quadrivalent influenza vaccine (QIV-HD) compared to either the licensed or investigational high-dose trivalent influenza vaccine (TIV-HD) in adults.

Study identification

NCT ID
NCT03282240
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
2,670 participants

Conditions and interventions

Conditions

Interventions

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
Sep 8, 2017 (Actual)
Primary completion
Nov 2, 2017 (Actual)
Completion
Apr 19, 2018 (Actual)
Last update posted
Apr 7, 2022

2017 – 2018

United States locations

U.S. sites
36
U.S. states
24
U.S. cities
32
Facility City State ZIP Site status
Sanofi Pasteur Investigational Site 037 Anaheim California 92801 —
Sanofi Pasteur Investigational Site 029 Redding California 96001 —
Sanofi Pasteur Investigational Site 003 San Diego California 92117 —
Sanofi Pasteur Investigational Site 016 Colorado Springs Colorado 80920 —
Sanofi Pasteur Investigational Site 035 Milford Connecticut 06460 —
Sanofi Pasteur Investigational Site 031 Hollywood Florida 33024 —
Sanofi Pasteur Investigational Site 009 Jacksonville Florida 32205 —
Sanofi Pasteur Investigational Site 017 Jacksonville Florida 32216 —
Sanofi Pasteur Investigational Site 030 Stockbridge Georgia 30281 —
Sanofi Pasteur Investigational Site 010 Boise Idaho 83712 —
Sanofi Pasteur Investigational Site 034 Meridian Idaho 83642 —
Sanofi Pasteur Investigational Site 021 Council Bluffs Iowa 51501 —
Sanofi Pasteur Investigational Site 023 Wichita Kansas 67205 —
Sanofi Pasteur Investigational Site 028 Wichita Kansas 67207 —
Sanofi Pasteur Investigational Site 012 Bardstown Kentucky 40004 —
Sanofi Pasteur Investigational Site 018 Metairie Louisiana 70427 —
Sanofi Pasteur Investigational Site 026 Biloxi Mississippi 39531 —
Sanofi Pasteur Investigational Site 014 St Louis Missouri 63104 —
Sanofi Pasteur Investigational Site 011 Omaha Nebraska 68134 —
Sanofi Pasteur Investigational Site 024 Las Vegas Nevada 89104 —
Sanofi Pasteur Investigational Site 008 Rochester New York 14609 —
Sanofi Pasteur Investigational Site 005 Wilmington North Carolina 28401 —
Sanofi Pasteur Investigational Site 036 Winston-Salem North Carolina 27045 —
Sanofi Pasteur Investigational Site 004 Cleveland Ohio 44122 —
Sanofi Pasteur Investigational Site 015 Oklahoma City Oklahoma 73112 —
Sanofi Pasteur Investigational Site 013 Warwick Rhode Island 02886 —
Sanofi Pasteur Investigational Site 033 Mt. Pleasant South Carolina 29464 —
Sanofi Pasteur Investigational Site 001 Nashville Tennessee 37212 —
Sanofi Pasteur Investigational Site 002 Dallas Texas 75234 —
Sanofi Pasteur Investigational Site 025 Tomball Texas 77375 —
Sanofi Pasteur Investigational Site 027 Salt Lake City Utah 84109 —
Sanofi Pasteur Investigational Site 006 Salt Lake City Utah 84121 —
Sanofi Pasteur Investigational Site 019 Salt Lake City Utah 84123 —
Sanofi Pasteur Investigational Site 020 South Jordan Utah 84095 —
Sanofi Pasteur Investigational Site 022 West Jordan Utah 83642 —
Sanofi Pasteur Investigational Site 038 Norfolk Virginia 23507 —

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 NCT03282240, 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 7, 2022 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03282240 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →