Study of Fluzone® Quadrivalent, Fluzone® Intradermal, and Fluzone® High-Dose Influenza Virus Vaccines in Adults
This trial is active, not recruiting.
|Treatments||fluzone® quadrivalent, influenza virus vaccine (2013-2014 formulation),, fluzone® intradermal influenza virus vaccine (2013-2014 formulation),, fluzone® high dose influenza virus vaccine (2013-2014 formulation)|
|Sponsor||Sanofi Pasteur, a Sanofi Company|
|Start date||September 2013|
|End date||December 2013|
|Trial size||208 participants|
|Trial identifier||NCT01946438, GRC52, U1111-1127-7587|
The aim of the study is describe the safety and immunogenicity of Fluzone Quadrivalent and Fluzone Intradermal vaccines in adults 18 to < 65 years of age, and to describe the safety and immunogenicity of Fluzone Quadrivalent and Fluzone High-Dose vaccines in adults ≥ 65 years of age.
- To describe the safety of the 2013-2014 formulations of Fluzone Quadrivalent and Fluzone Intradermal vaccines in adults 18 to < 65 years of age and the safety of the 2013-2014 formulations of Fluzone Quadrivalent and Fluzone High-Dose vaccines in adults ≥ 65 years of age.
- To describe the immunogenicity of the 2013-2014 formulations of Fluzone Quadrivalent and Fluzone Intradermal vaccines in adults 18 to < 65 years of age and the immunogenicity of the 2013-2014 formulations of Fluzone Quadrivalent and Fluzone High-Dose vaccines in adults ≥ 65 years of age.
- To evaluate the compliance, in terms of immunogenicity, of each study vaccine (Fluzone Quadrivalent, Fluzone Intradermal, and Fluzone High-Dose) in the applicable age group with the requirements of the Committee for Human Medicinal Products (CHMP) Note for Guidance (NfG) CPMP/BWP/214/96.
- To submit sera from selected subjects to the Center for Biologics Evaluation and Research (CBER) for further analysis by the World Health Organization (WHO), the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA) to support formulation recommendations for subsequent influenza vaccines.
|United States||No locations recruiting|
|Other Countries||No locations recruiting|
|Santa Rosa, CA 95405, CA 95405||not available||no longer recruiting|
|Council Bluffs, IA 51503||not available||no longer recruiting|
|Metairie, LA 70006||not available||no longer recruiting|
|Cincinnati, OH 45249||not available||no longer recruiting|
|Endpoint classification||safety/efficacy study|
|Intervention model||parallel assignment|
|Masking||double blind (subject, caregiver, investigator, outcomes assessor)|
Number of participants reporting solicited injection site and systemic events and unsolicited adverse events following vaccination with Fluzone® influenza virus vaccines
time frame: Day 0 up to 21 Days post vaccination
Geometric mean titers of antibodies to vaccine antigens following vaccination with Fluzone® Quadrivalent, or Fluzone Intradermal, or Fluzone High Dose vaccine
time frame: Day 0 and Day 21 post vaccination
Seroprotection and seroconversion to vaccine antigens following vaccination with Fluzone® influenza virus vaccines
time frame: Day 0 and Day 21 post vaccination
Male or female participants at least 18 years old.
Inclusion Criteria: - Subject is ≥ 18 years of age on the day of inclusion - Informed consent form has been signed and dated - Able to attend all scheduled visits and to comply with all trial procedures. Exclusion Criteria: - History of serious adverse reaction to any influenza vaccine - Receipt of any vaccine within 30 days before receiving study vaccine, or plans to receive another vaccine before Visit 2. - Participation in another interventional clinical trial investigating a vaccine, drug, medical device, or medical procedure in the 30 days preceding the first study vaccination or during the course of the study, unless no intervention for the other study occurred within the 30 days prior to the first study vaccination and none are planned before the subject would complete safety surveillance for the present study - Thrombocytopenia, which may be a contraindication for intramuscular vaccination, at the discretion of the Investigator - Prior vaccination with any 2013-2014 formulation of influenza vaccine - Known systemic hypersensitivity to eggs, chicken proteins, or any of the vaccine components, or a history of a life-threatening reaction to Fluzone Quadrivalent, Fluzone Intradermal, or Fluzone High-Dose vaccine or to a vaccine containing any of the same substances (the complete list of vaccine components is included in the Prescribing Information) - Receipt of immune globulins, blood, or blood-derived products in the past 3 months - Bleeding disorder or receipt of anticoagulants in the 3 weeks preceding inclusion, which may be a contraindication for intramuscular vaccination, at the discretion of the Investigator - Subject is pregnant, or lactating, or of childbearing potential (to be considered of non-childbearing potential, a female must be pre-menarche or post-menopausal for at least 1 year, surgically sterile, or using an effective method of contraception or abstinence from at least 4 weeks prior to vaccination and until at least 4 weeks after vaccination) - Any condition that in the opinion of the Investigator would pose a health risk to the subject if enrolled or could interfere with the evaluation of the vaccine - Personal history of Guillain-Barré syndrome - Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months) - Chronic illness that, in the opinion of the Investigator, is at a stage where it might interfere with trial conduct or completion - Seropositivity for human immunodeficiency virus (HIV), hepatitis B, or hepatitis C, as reported by the subject - Deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized involuntarily - Current alcohol or drug addiction that, in the opinion of the Investigator, might interfere with the ability to comply with trial procedures - Moderate or severe acute illness/infection (according to Investigator judgment) or febrile illness (temperature ≥ 100.4°F]) on the day of vaccination. A prospective subject should not be included in the study until the condition has resolved or the febrile event has subsided - Identified as an Investigator or employee of the Investigator or study center with direct involvement in the proposed study, or identified as an immediate family member (i.e., parent, spouse, natural or adopted child) of the Investigator or employee with direct involvement in the proposed study.
|Official title||Safety and Immunogenicity Among Adults of Fluzone® Quadrivalent, Fluzone® Intradermal, and Fluzone® High-Dose Influenza Virus Vaccines, 2013-2014 Formulations|
|Description||Participants 18 to < 65 years of age on enrollment will be randomized to receive either Fluzone Quadrivalent or Fluzone Intradermal vaccine. Participants ≥ 65 years of age at enrollment will be randomized to receive either Fluzone Quadrivalent or Fluzone High-Dose vaccine. Solicited adverse event (AE) information will be collected for 7 days after each vaccination, unsolicited AE and Serious adverse event information will be collected from Visit 1 to Visit 2. Total duration of participation in the study is approximately 21 days.|
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