Safety and Immunogenicity of a Monovalent Inactivated Influenza H3N2 Variant (H3N2v) Vaccine in Adult and Elderly Populations

This is a Phase II open-label study in approximately 200 (up to 240) healthy males and
non-pregnant females, aged 18 years and older. This study is designed to assess the safety,
reactogenicity, and immunogenicity of an unadjuvanted subvirion monovalent inactivated
influenza H3N2 variant (H3N2v) vaccine (MIV) manufactured by Sanofi Pasteur. Subjects will
be stratified by age (approximately 100 (up to 120) subjects 18-64 years old and
approximately 100 (up to 120) subjects >/= 65 years old) to receive two doses of H3N2v MIV,
delivered intramuscularly as 15 micrograms (mcg) of hemagglutinin (HA)/0.5 milliliter (mL)
dose, 21 days apart (see Table 1). Subjects may receive licensed seasonal influenza vaccine
prior to (2 weeks if given the inactivated vaccine or 4 weeks if given the live, attenuated
vaccine) the first H3N2v vaccination. Alternatively, subjects may receive licensed seasonal
influenza vaccine at any time after completion of the Day 42 visit or following an early
termination visit. Safety will be measured by the occurrence of solicited injection site and
systemic reactogenicity on the day of each H3N2v vaccination through 7 days after each H3N2v
vaccination, adverse events through 42 days after the first H3N2v vaccination, and serious
adverse events (SAEs) and new-onset chronic medical conditions through 7 months after the
first H3N2v vaccination. Immunogenicity testing will include performing hemagglutination
inhibition (HAI) and neutralizing (Neut) antibody assays on serum obtained on the day of and
prior to each H3N2v vaccination (Days 0 and 21), approximately 8 days after each H3N2v
vaccination (Days 8 and 29), and approximately 21 days after the second H3N2v vaccination
(Day 42).

From a subset of healthy adult subjects (up to 30 volunteers 18-64 years old enrolled at the
Emory VTEU site who consent to blood donation for the immunology exploratory assays), an
additional volume of venous blood will be drawn on Days 0, 8, 21, 29 and 42 to determine the
specificity/cross reactivity of antibodies from H3N2v-reactive B cells with other influenza
subtypes (e.g., 2009 H1N1 pandemic HA) and most recent H3 seasonal HA to define the
molecular profile of antibody repertoire changes in circulating B cells after H3N2v
vaccination, and to characterize the antibody-secreting cell (ASC), monoclonal antibody
(mAb), and CD4+ T cell responses to H3N2v vaccination. The duration of the study for each
subject will be approximately 7 months.

Inclusion Criteria:

1. Provide written informed consent prior to initiation of any study procedures.

2. Are able to understand and comply with planned study procedures and be available for
all study visits.

3. Are males or non-pregnant females, aged 18 years or older, inclusive.

4. Are in good health, as determined by vital signs (oral temperature, pulse and blood
pressure), medical history and targeted physical examination based on medical history
to ensure any existing medical diagnoses or conditions are stable (Stable chronic
medical condition - no change in prescription medication, dose, or frequency of
medication in the last 3 months and health outcomes of the specific disease are
considered to be within acceptable limits in the last 6 months. Any change that is
due to change of health care provider, insurance company etc., or that is done for
financial reasons, as long as in the same class of medication, will not be considered
a violation of this inclusion criterion. Any change in prescription medication due
to improvement of a disease outcome will not be considered a violation of this
inclusion criterion.) Subjects may be on chronic or as needed (prn) medications if,
in the opinion of the site principal investigator or appropriate sub-investigator,
they pose no additional risk to subject safety or assessment of reactogenicity and
immunogenicity. Note: Topical, nasal, and inhaled medications; vitamins; and
contraceptives are permitted with the exception of high dose inhaled steroids (see
exclusion criteria #13).

5. Oral temperature is less than 100.4°F.

6. Pulse is 50 to 100 bpm.

7. Systolic blood pressure is 90 to 150 mm Hg.

8. Diastolic blood pressure is 60 to 100 mmHg.

9. Women of childbearing potential (not surgically sterile via tubal ligation, bilateral
oophorectomy or hysterectomy or who are not postmenopausal for greater than or equal
to 1 year) must agree to practice adequate contraception (abstinence from sexual
intercourse with men, monogamous relationship with a vasectomized partner who was
vasectomized at least 6 months prior to the subject receiving the first H3N2v
vaccination, barrier methods such as condoms or diaphragms with spermicide or foam,
effective intrauterine devices NuvaRing®, successful Essure® placement (permanent,
non-surgical, non-hormonal sterilization) with documented confirmation test at least
3 months after the procedure), licensed hormonal methods such as implants,
injectables or oral contraceptives (the pill), and any other Food and Drug
Administration (FDA) approved birth control method) for at least 30 days prior to the
first H3N2v vaccination through at least 30 days after the last H3N2v vaccination .
Method of contraception will be captured on the appropriate data collection form.

10. Women of childbearing potential must have a negative urine or serum pregnancy test
within 24 hours prior to each H3N2v vaccination.

Exclusion Criteria:

1. Have an acute illness, including an oral temperature greater than or equal to
100.4°F, within 3 days prior to each H3N2v vaccination.

2. Have any condition that, in the opinion of the site principal investigator or
appropriate sub-investigator, would place the subject at an unacceptable risk of
injury, render them unable to meet the requirements of the protocol or confound the
interpretation of results.

3. Have immunosuppression as a result of an underlying illness or treatment, or use of
anticancer chemotherapy or radiation therapy (cytotoxic) within the preceding 36
months.

4. Have known active neoplastic disease or a history of any hematologic malignancy.

5. Have known HIV, hepatitis B, or hepatitis C infection.

6. Have a known allergy to eggs, egg or chicken protein, or other components of the
H3N2v MIV (including octylphenol ethoxylate (Triton® X-100), gelatin, formaldehyde,
and phosphate buffered saline).

7. Have a history of severe reactions following previous immunization with licensed
influenza virus vaccines.

8. Have a history of Guillain-Barre Syndrome.

9. Have a history of alcohol or drug abuse in the last 5 years.

10. Have any diagnosis, current or past, of schizophrenia, bipolar disease, or other
major psychiatric diagnosis.

11. Have been hospitalized for psychiatric illness, history of suicide attempt, or
confinement for danger to self or others, within the past 10 years.

12. Have taken high dose oral or parenteral glucocorticoids for 2 weeks or more in total
at any time during the past 2 months. High dose defined as prednisone greater than
or equal to 20mg total daily dose, or equivalent dose of other glucocorticoids.

13. Have taken high-dose inhaled steroids within the past 4 weeks. High dose defined as
>800mcg/day of beclomethasone dipropionate or equivalent.

14. Have taken systemic corticosteroids of any dose within the past 4 weeks.

15. Received any licensed live vaccine within 4 weeks or any licensed inactivated vaccine
within 2 weeks prior to the first H3N2v vaccination or planned receipt of any vaccine
within 42 days after the first H3N2v vaccination. This is inclusive of licensed
seasonal influenza vaccines.

16. Received immunoglobulin or other blood products (with exception of Rho D
immunoglobulin) within the 3 months prior to each H3N2v vaccination.

17. Received an experimental agent (vaccine, drug, biologic, device, blood product, or
medication) within 1 month prior to the first H3N2v vaccination.

18. Are participating or plan to participate in another clinical trial with an
interventional agent (licensed or unlicensed vaccine, drug, biologic, device, blood
product, or medication) during the 7-month study period.

19. Are enrolled or plan to enroll in another clinical trial that has a study
intervention such as a drug, biologic, device, blood product, or medication that
could interfere with the safety assessment of the investigational product at any time
during the 7-month study period.

20. Participated in an influenza A/H3N2v vaccine study in the past in a group receiving
vaccine (does not apply to documented placebo recipients) or have a history of
A/H3N2v infection prior to enrollment.

21. Plan to travel outside the U.S. (continental U.S., Hawaii and Alaska) in the time
between the first H3N2v vaccination and 42 days after the first H3N2v vaccination.

22. Women who are breastfeeding or plan to breastfeed at any given time during the
7-month study period.

23. Occupational exposure to or direct physical contact with pigs in the past year.

24. Blood donation within 30 days prior to enrollment (only for a subset of healthy adult
subjects - up to 30 volunteers 18-64 years old enrolled at the Emory VTEU site who
consent to blood donation for the immunology exploratory assays).