Study of Fluzone® Quadrivalent, Fluzone® Intradermal, and Fluzone® High-Dose, Influenza Vaccines in Adults

Adults 18 to < 65 years of age will be randomly assigned in a 1:1 ratio to receive either
Fluzone® Quadrivalent or Fluzone® Intradermal vaccine. Adults ≥ 65 years of age will also be
randomly assigned in a 1:1 ratio to receive either Fluzone® Quadrivalent or Fluzone®
High-Dose vaccine.

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 2014-2015 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, 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 an 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 an Investigator or employee with
direct involvement in the proposed study.