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Completed Phase 3 Interventional Accepts healthy volunteers

The Celljuvant Study: A Phase 3 Immunogenicity and Safety Study of aQIVc Vaccine in Adults Aged 50 Years and Older

ClinicalTrials.gov ID: NCT06015282

Public ClinicalTrials.gov record NCT06015282. 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, 12:10 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, Observer-Blind, Controlled, Multicenter, Clinical Study to Evaluate Immunogenicity and Safety of a MF59-Adjuvanted Quadrivalent Subunit Cell-derived Influenza Vaccine (aQIVc) in Comparison With Quadrivalent Influenza Vaccines, in Adults Aged 50 Years and Older.

Brief summary

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

This is a Phase 3, randomized, parallel-group, comparator-controlled, observer-blind, multicenter study of immunogenicity and safety in approximately 7700 male and female adults aged 50 years and older (approximately equally split between two age groups: 50-64 years; 65 years and older), who are healthy or have stable comorbidities that increase their risk of complications from influenza infection. Three lots of aQIVc will be evaluated for consistency and pooled for the comparison with the 2 control vaccines. Subjects will be randomly assigned to receive 1 of 3 lots of aQIVc, QIVr, or aQIV in a 1:1:1:2:2 ratio (for a 3:2:2 ratio for aQIVc, QIVr, and aQIV). The study will have a treatment period (Day 1 to Day 29) and a follow-up period (Day 30 up to Day 181); a subset of 770 subjects will be followed up up to Day 365.

Study identification

NCT ID
NCT06015282
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Seqirus
Industry
Enrollment
7,741 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
50 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
Nov 3, 2023 (Actual)
Primary completion
Mar 5, 2024 (Actual)
Completion
Jan 30, 2025 (Actual)
Last update posted
Apr 27, 2025

2023 – 2025

United States locations

U.S. sites
51
U.S. states
25
U.S. cities
50
Facility City State ZIP Site status
Alliance for Multispecialty Research (AMR) Phoenix Tempe Arizona 85281 —
Baptist Health Center for Clinical Research Little Rock Arkansas 72205 —
Marvel Clinical Research Huntington Beach California 92647 —
Paradigm Clinical Research Center, LLC Redding California 96001 —
Clinical Research Consulting, Inc. Milford Connecticut 06460 —
Chase Medical Research, LLC Waterbury Connecticut 06708 —
Innovative Research of West Florida, Inc. Clearwater Florida 33756 —
USA and International Research Inc. Doral Florida 33126 —
Velocity Clinical Research, New Smyrna Beach Edgewater Florida 32132 —
Health Awareness, Inc. Jupiter Florida 33458 —
ARS - Lake Oconee Largo Florida 33777 —
Global Health Research Center Miami Lakes Florida 33016 —
Precision Clinical Research Sunrise Florida 33351 —
Global Health Research center Tampa Florida 33615 —
Velocity Clinical Research- Boise Meridian Idaho 83642 —
Great Lakes Clinical Trials, LLC Ravenswood dba Flourish Research Chicago Illinois 60640 —
Great Lakes Clinical Trials, LLC. Ravenswood dba Flourish Research Gurnee Illinois 60031 —
Velocity Clinical Research Valparaoso Valparaiso Indiana 46383 —
Velocity Clinical Research, Sioux City Sioux City Iowa 51106 —
Velocity Clinical Research, Baton Rough Baton Rouge Louisiana 70809 —
Benchmark Research Metairie Louisiana 70006 —
IMA Evaluations LLC Monroe Louisiana 71201 —
Centennial Medical Group, PC Columbia Maryland 21075 —
Velocity Clinical Research Rockville Rockville Maryland 20854 —
Velocity Clinical Research Gulfport Gulfport Mississippi 39503 —
Alliance for Multispecialty Research, LLC Kansas City Missouri 64114 —
Sundance Clinical Research St Louis Missouri 63141 —
Velocity Clinical Research, Norfolk Norfolk Nebraska 68701 —
Velocity Clinical Research, Omaha Omaha Nebraska 68134 —
Alliance for Multispecialty Research (AMR) LLC, Las Vegas Las Vegas Nevada 89119 —
Velocity Clinical Research, Binghamton Binghamton New York 13905 —
Velocity Clinical Research, Syracuse East Syracuse New York 13057 —
Velocity Clinical Research, Vestal New York New York 13850 —
M3 Wake Research, Inc Raleigh North Carolina 27612 —
CTI Clinical Research Center Cincinnati Ohio 45212 —
Velocity Clinical Research Cincinnati Cincinnati Ohio 45242 —
Velocity Clinical Research, Cleveland Cleveland Ohio 44122 —
Velocity Clinical Research - Medford Medford Oregon 97504 —
Velocity Clinical Research-Providence East Greenwich Rhode Island 02818 —
Velocity Clinical Research, Gaffney Gaffney South Carolina 29340 —
Velocity Clinical Research, Spartanburg Spartanburg South Carolina 29303 —
AMR-Knoxville Knoxville Tennessee 37909 —
Clinical Research Associates, Inc. Nashville Tennessee 37203 —
Cedar Health Research, LLC Dallas Texas 75251 —
Benchmark Research Fort Worth Texas 76135 —
DM Clinical Research - Martin Diagnostic Clinic Houston Texas 77065 —
ACRC trials Parent HQ Plano Texas 75024 —
DM Clinical Research Tomball Texas 77375 —
BBCR Holdings LLC dba JBR Clinical Research - Midvale Campus Salt Lake City Utah 84107 —
Velocity Clinical Research, Salt Lake City West Jordan Utah 84088 —
Velocity Clinical Research, Suffolk Suffolk Virginia 23435 —

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06015282, 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 27, 2025 · 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 NCT06015282 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →