A Phase I Trial to Evaluate the Safety, Reactogenicity, and Immunogenicity of MVA-BN Yellow Fever Vaccine With and Without Montanide ISA-720 Adjuvant in 18-45 Year Old Healthy Volunteers

This study is a multi-center, double-blind, placebo-controlled, Phase I study to evaluate the
safety, reactogenicity, tolerability, and immunogenicity of MVA-BN-YF in Flavivirus-naïve
healthy male and non-pregnant female adult subjects. There are six dose groups in this study.
Subjects who have never received a licensed or investigational smallpox vaccine will be
randomized to Groups 1-5 and vaccine administration and follow-up will be conducted in a
double-blinded fashion. Subjects who have previously received two, 1 x 108 TCID50 doses of
MVA-BN between 19 and 45 days apart by SC or IM routes will be enrolled in Group 6 and will
be dosed open-label. Since this is a first in human, phase I study, a sentinel cohort will be
utilized. The first two subjects (1st sentinel group) one at each clinical site will be
randomized to Group 2 or 3 and vaccinated with MVA-BN-YF with or without ISA 720. Subjects
and study personnel will be blinded as to whether ISA 720 was administered. Subjects will be
monitored for safety for one day, and if no pre-defined halting rule is met (Section 9.5.1)
then two additional subjects (2nd sentinel group) one at each clinical site will be assigned
to the group the previous subject was not assigned to. These subjects will be vaccinated and
monitored as above. A total of 4 sentinel subjects will be vaccinated. Primary objectives are
assessment of the safety, tolerability, and reactogenicity of MVA-BN-YF vaccine administered
with or without ISA 720; comparison of the safety, tolerability, and reactogenicity of
MVA-BN-YF vaccine administered with or without ISA 720 with YF-VAX and MVA-BN. Secondary
objectives are: assessment of the immunogenicity against the MVA-BN backbone and Yellow Fever
virus (YF) antigen insert of MVA-BN-YF with and without ISA 720 as assessed by kinetics of
the immune responses, seroconversion rates, and peak Geometric Mean Titer (GMT); assessment
of the impact of previous MVA-BN vaccination on peak immune responses to YF antigen in
MVA-BN-YF; comparison of the peak immunogenicity against YF antigen of 1 or 2 doses of
MVA-BN-YF with or without ISA 720 with YF-VAX; comparison of the peak immunogenicity against
the MVA-BN backbone of 1 or 2 doses of MVA-BN-YF with or without ISA 720 with MVA-BN;
assessment of durability of immune response to YF antigen and MVA-BN at 6 months after 2nd
vaccination or placebo administration.

Inclusion Criteria:

1. Must be a male or female at least 18 to
2. Must be able to read and provide written consent and complete the Informed Consent.

3. Must have a body mass index (BMI) >/=18.5 and <35.0 kg/m2.

4. Must be in good health on the basis of physical examination, vital signs, medical
history, safety laboratories, and the investigator's clinical judgment. Safety
laboratory normal ranges will be those used by the reference clinical lab.
Protocol-specific criteria for individual subjects are listed in criteria #6 -The
clinical laboratory evaluations that will be graded as laboratory AEs and be
considered for the Study or Individual Halting Rules are those which are included in
the laboratory toxicity grading scales (Section 9.2.3). -Vital signs must be in normal
ranges as per Sections 9.2.2 and 9.2.3. If a subject has elevated systolic or
diastolic blood pressure, subject may rest for 10 minutes in a quiet room and then the
blood pressure may be retaken once.

5. For Group 6: subjects must have documented previous vaccination with MVA-BN. In order
to be enrolled, a subject has to have received two 1 x 10^8 TCID50 doses of MVA-BN
19-45 days apart SC or IM as part of participation in DMID vaccine trials 11-0021 or
09-0002. First dose must have been administered no earlier than 2010.

6. Must have acceptable laboratory criteria within 28 days before enrollment. Acceptable
lab parameters include: -Hemoglobin: women: >11.0 g/dL; men >12.5 g/dL -White blood
cell count: >3,700 cells/mm3 but <11,000 cells/mm3 -Platelets: >125,000 but <375,000
per mm3 -Urine dipstick (clean urine sample): protein <1+, glucose negative -Alanine
aminotransferase and aspartate aminotransferase (ALT, AST) <1.25 x institutional upper
limit of normal -Blood urea nitrogen (BUN) -Total bilirubin <1.25x institutional upper limit of normal. Serum creatinine institutional upper limit of normal -If laboratory screening tests are out of range,
repeat of screening tests is permitted once, provided there is an alternative
explanation for the out of range value.

7. Women of childbearing potential must have a negative serum pregnancy test at screening
and negative urine pregnancy tests prior to each vaccination.

8. Women of childbearing potential must have an acceptable method of contraception from
28 days prior to the 1st vaccination until at least 60 days after the 2nd vaccination.
Acceptable methods of contraception include the following: -Prescription oral
contraceptives, contraceptive injections, intrauterine device (IUD), implants, vaginal
ring, double-barrier method, contraceptive patch, male partner sterilization,
abstinence (defined as refraining from heterosexual intercourse during participation
in the study [from 28 days before the first vaccination until at least 60 days after
the last vaccination]). Women of non-childbearing potential, defined as postmenopausal
(any age with amenorrhea for = / >12 months without other known or suspected cause for
amenorrhea, or surgically sterile (hysterectomy, bilateral tubal ligation, obilateral
oophorectomy, or successful Essure® placement (permanent, non-surgical, non-hormonal
sterilization) with documented confirmation test at least 3 months after the
procedure), are not required to use the birth control methods.

9. Female subjects must agree to not donate eggs (ova, oocytes) from the start of
screening onwards until at least 60 days after the last vaccination.

10. Male subjects who have not had a vasectomy and is sexually active with a woman of
childbearing potential must agree to use an acceptable measure of birth control from
28 days prior to 1st vaccination until at least 60 days after the last vaccination.
Acceptable methods of birth control include the following: - Abstinence (defined as
refraining from heterosexual intercourse with a female partner of childbearing
potential during participation in the study [from 28 days before the first vaccination
until at least 60 days after the last vaccination]. -A double-barrier method of birth
control, such as condom with spermicidal foam/gel/film/cream/suppository and partner
with occlusive cap (diaphragm, cervical/vault caps). -In case the female partner is
using an acceptable method of birth control (see Inclusion Criterion #8), a
single-barrier method of birth control for the male subject is acceptable.

11. Male subjects must agree to not donate sperm from the start of screening onwards until
at least 60 days after the last vaccination.

12. Must be available and willing to participate for the duration of the study visits and
follow-up.

13. Must have a means to be contacted by telephone.

Exclusion Criteria:

1. Was ever vaccinated with a licensed or investigational YF vaccine or was diagnosed
with YF infection or disease. Includes YF-VAX, Stamaril, or Bio-Manguinhos yellow
fever vaccine. Subject's verbal history will suffice.

2. Was ever vaccinated with a licensed or investigational Flavivirus vaccine. Including
Japanese encephalitis virus (JEV) vaccine or an investigational Flavivirus vaccine
including dengue virus (DENV) or West Nile virus vaccine, or has been diagnosed with
an illness caused by a Flavivirus including DENV, West Nile virus (WNV), JEV, St.
Louis encephalitis, or tick-borne encephalitis virus (TBEV). Subject's verbal history
will suffice.

3. Positive serology for HIV, Hepatitis C virus, or Hepatitis B surface antigen.

4. Positive serology to Dengue, Yellow Fever, or West Nile virus.

5. Plans to travel to a Yellow-Fever endemic area during the course of the study or
travel to a Yellow-Fever endemic area within 30 days of screening. Subjects who have a
recent travel to a Yellow Fever endemic area may screen if they have returned to the
U.S. 30 or more days prior to the screening visit. Refer to the CDC Yellow Fever map
for countries/regions at risk for Yellow Fever virus infection.
http://www.cdc.gov/yellowfever/maps/

6. Was ever vaccinated with a licensed or investigational smallpox vaccine with the
exception of subjects in Group 6. Includes Dryvax, Acam2000, LC 16 m8, MVA-based
vaccine candidate or licensed vaccines, and Imvamune or Imvanex. EXCEPTION: Group 6
should have had two 1 x 10^8 TCID 50 doses of MVA-BN 19 - 45 days apart SC or IM as
part of participation in DMID vaccine trials 11-0021 or 09-0002. First dose must have
been administered no earlier than 2010.

7. Has known allergy or history of anaphylaxis or other serious adverse reaction to a
vaccine or vaccine products. Including egg products, aminoglycosides, gelatin,
sorbitol, tris (hydroxymethyl)-amino methane (THAM), or any of the constituents of the
study vaccines.

8. Has severe allergy or anaphylaxis to latex. Participants in Group 6 will not be
exposed to latex and so may have history of severe allergy or anaphylaxis to latex.

9. Has an acute illness or temperature > / =38.0ºC on Day 1 or Day 29. Subjects with
fever or acute illness on the Day of vaccination may be re-assessed and enrolled if
healthy or only minor residual symptoms remain within 3 days.

10. Female subjects who are pregnant or breast-feeding, or planning to become pregnant
while enrolled in the study.

11. Has history of chronic or acute severe neurologic condition. Including history of
seizure disorder or epilepsy, history of Guillain-Barre syndrome, Bell's palsy,
meningitis, or disease with any focal neurologic deficits.

12. Has history of thymus disorder including myasthenia gravis, thymoma or prior
thymectomy.

13. Has history of autoimmune disease or or clinically significant cardiac, pulmonary,
hepatic, rheumatologic, or renal disease by history, physical examination, and/or
laboratory studies. Includes the conditions and diagnoses defined as AESI in Section
9.3.4.

14. Has history of malignancy other than squamous cell or basal cell skin cancer, unless
there has been surgical excision that is considered to have achieved cure. Subjects
with a history of skin cancer must not be vaccinated at the previous tumor site.

15. Has known or suspected congenital or acquired immunodeficiency, or recent history or
current use of immunosuppressive therapy. Anti-cancer chemotherapy or radiation
therapy within the preceding 6 months, or long-term (at least 2 weeks within the
previous 3 months) systemic corticosteroids therapy (at a dose of at least 0.5
mg/kg/day). Intranasal or topical prednisone (or equivalent) are allowed.

16. Is post-organ and/or stem cell transplant whether or not on chronic immunosuppressive
therapy.

17. Had major surgery (per the investigator's judgment) within the 4 weeks prior to study
entry or planned major surgery during the course of the study.

18. Has personal history of recurring migraines (every 6 months or more often) or on
prescription medication for treatment of recurring headaches or migraines.

19. Has history of cardiac disease. Myocarditis, pericarditis, cardiomyopathy, transient
ischemic attack or stroke, myocardial infarction, angina, coronary artery disease,
congestive heart failure, clinically significant arrhythmia. Includes any arrhythmia
requiring medication, treatment, or clinical follow-up.

20. Has electrocardiogram (ECG) with clinically significant findings, or features that
would interfere with the assessment of myocarditis/pericarditis. Including any of the
following: -Conduction disturbance (complete left or complete right bundle branch
block or nonspecific intraventricular conduction disturbance with QRS = / >120 ms, PR
interval >219 ms, any second-or third-degree atrioventricular block, or prolongation
of the QT interval corrected according to Bazett's formula [QTcB] [>450 ms])
-Significant repolarization (ST-segment or T-wave) abnormality. -Significant atrial or
ventricular arrhythmia; frequent atrial or ventricular ectopy (e.g., frequent
premature atrial contractions, 2 premature ventricular contractions in a row).
-ST-elevation consistent with ischemia or evidence of past or evolving myocardial
infarction.

21. Has history of diabetes mellitus type 1 or type 2, including cases controlled with
diet alone. Note: history of isolated gestational diabetes is not an exclusion
criterion.

22. Has history of thyroidectomy, or thyroid disease requiring medication during the last
12 months.

23. Has history of hypertension even if medically controlled. Note: Vital signs must be
normal by protocol toxicity grading scale or determined to be normal-variant by
investigator. In the event of an abnormal heart rate or blood pressure due to
physiological variation or activity, the subject may rest for 10 minutes in a quiet
room, and then blood pressure and/or heart rate may be re-measured. Repeated vital
signs may be used to determine eligibility.

24. Received live attenuated vaccines from 30 days before Day 1 until 30 days after the
2nd vaccination.

25. Received killed or inactivated vaccines from 14 days before Day 1 until 14 days after
the 2nd vaccination.

26. Received experimental therapeutic agents within 3 months prior to the first study
vaccination or plans to receive any experimental therapeutic agents during the course
of the study.

27. Is currently participating or plans to participate in another clinical study which
would involve receipt of the following: An investigational product, blood drawing, or
an invasive medical procedure that would require administration of anesthetics or
intravenous dyes or removal of tissue during the study. -Includes endoscopy,
bronchoscopy, or administration of IV contrast.

28. Received blood products or immunoglobulin in the 3 months before study entry or
planned use during the course of the study.

29. Donated a unit of blood within 8 weeks before Day 1 or plans to donate blood during
the course of the study.

30. Has major psychiatric illness during the past 12 months that in the opinion of the
investigator would preclude participation.

31. Has current alcohol use or current or past abuse of recreational or narcotic drugs by
history as judged by the investigator to potentially interfere with study adherence.

32. Has a history of chronic urticaria (recurrent hives).

33. Has tattoos, scars, or other marks on both deltoid areas which would, in the opinion
of the investigator, interfere with assessment of the vaccination site.

34. Is a study site employee or staff who are paid entirely or partially by/through the
OCRR contract for the trial, or staff who are supervised by the PI or
Sub-Investigators. Including the Principal Investigator (PI), sub-Investigators listed
in Form FDA 1572 or Investigator of Record Form.

35. In the opinion of the investigator cannot communicate reliably, is unlikely to adhere
to the requirements of the study, or has any condition which would limit the subject's
ability to complete the study.