Dose Escalation Trial of a Plague Vaccine, Flagellin/F1/V, in Healthy Adult Volunteers

Inclusion Criteria:

Inclusion criteria that must met prior to the initial vaccination:

• At least 18 and less than or equal to 45 years of age at the time of first vaccination.
• Never had plague or disease caused by Yersinia pestis.
• Able to provide informed consent.
• Read, signed, and dated informed consent document.
• Available for follow-up for the planned duration of the study.
• Satisfactory medical assessment with no clinically significant and relevant abnormalities as established by medical history and physical examination at screening.
• If the subject is female and of childbearing potential, negative serum pregnancy test at screening and negative urine or serum pregnancy test within 24 hours prior to each vaccination.
• If the subject is female and of childbearing potential, she agrees to use acceptable contraception and remain on the same method during the study as they were using prior to entering the study, and not become pregnant for 28 days following the last vaccination. A woman is considered of childbearing potential unless post-menopausal or surgically sterilized. Acceptable contraception methods are restricted to effective devices [e.g., intrauterine device (IUD), NuvaRing®] or licensed hormonal products with use of method for a minimum of 30 days prior to vaccination, a monogamous relationship with a vasectomized partner and abstinence from sexual intercourse with men.
• Negative enzyme-linked immunosorbent assay (ELISA) for human immunodeficiency virus (HIV).
• Negative hepatitis B surface antigen and negative antibody to hepatitis C virus.
• Safety labs have to be within institutional normal limits, or as otherwise specified.
• Weight: greater than or equal to 110 pounds.
• Body Mass Index (BMI) of greater than or equal to 19 and less than 33.
• Subject agrees not to donate blood for the duration of their study participation.

Inclusion criteria that must be met prior to the second vaccination:

• Never had plague or disease caused by Yersinia pestis.
• Satisfactory medical assessment with no clinically significant and relevant abnormalities as established by medical history.
• If the subject is female and of childbearing potential, negative urine or serum pregnancy test within 24 hours prior to vaccination.
• If the subject is female and of childbearing potential, she has remained on the same contraception method as used prior to entering the study, and not become pregnant for 28 days following the last vaccination. A woman is considered of childbearing potential unless post-menopausal or surgically sterilized. Acceptable contraception methods are restricted to effective devices (e.g., IUDs, NuvaRing®) or licensed hormonal products with use of method for a minimum of 30 days prior to vaccination, a monogamous relationship with a vasectomized partner and abstinence from sexual intercourse with men.
• Post dose one safety labs (Day 14) have to be within institutional normal limits, or as otherwise specified at the Day 14 post the initial vaccination or any observed laboratory toxicities have to be resolved prior to the second vaccination.

Exclusion Criteria:

Exclusion criteria prior to 1st vaccination:

• History of immunodeficiency or suspected impairment of immunologic functioning.
• Known or suspected history of plague vaccination.
• Pregnant women or women that are breastfeeding.
• Uncontrolled hypertension (defined as systolic blood pressure >140 mm Hg and/or diastolic blood pressure > 90 mm Hg).
• Subject is on statin therapy.
• 10% or greater risk of developing a myocardial infarction or coronary death within the next 10 years using the National Cholesterol Education Program's risk assessment tool (http://hin.nhlbi.nih.gov/atpiii/calculator.asp). NOTE that this criterion applies only to subjects 20 years of age and older AND only if at least one of the following apply: have smoked a cigarette in the past month, have hypertension (defined as systolic blood pressure >140 mm Hg) or are on antihypertensive medication and/or have a family history of coronary heart disease in male first-degree relative (father or brother) \<55 years of age or a female first-degree relative (mother or sister) \<65 years of age.
• Current use or use within 30 days of screening of immunosuppressive medication or corticosteroids (use of topical or nasal corticosteroids is allowed). Persons who are using a topical steroid can be enrolled after their therapy is completed. Inhaled steroids for asthma are not permissible.
• Chronic use of non-steroidal anti-inflammatory drug therapy
• Malignancy not including squamous cell skin cancer or basal cell skin cancer unless at the vaccination site or history of skin cancer at the vaccination site.
• Active autoimmune disease [Persons with vitiligo or thyroid disease (e.g., taking thyroid hormone replacement) are not excluded].
• Receipt of any vaccine 14 days prior to vaccination.
• Receipt of live attenuated vaccine within 30 days prior to vaccination.
• Planned receipt of any vaccine including allergy shots during the 28 day vaccination period and through 14-days post the second vaccination (Visit 7).
• Receipt of blood products or immunoglobulin within six months prior to vaccination.
• Medical or psychiatric condition or occupational responsibilities that preclude subject compliance with the protocol.
• Use of any other experimental agent (i.e. chemical or biological entity not registered for clinical use) within 30 days prior to vaccination and for the duration of the study
• Donation of a unit of blood within 56 days prior to vaccination.
• Acute febrile illness (>100.2 degrees F) on the day of vaccination.
• Any condition that, in the opinion of the investigator, might interfere with study objectives or would make administration of the study vaccine hazardous or make it difficult to monitor adverse effects.
• Study personnel.
• Current abuse of alcohol or drug addiction that in the opinion of the Investigator may interfere with the subject's ability to comply with trial procedures.

Exclusion criteria that apply prior to second vaccination:

• Subject that were discontinued due to meeting individual halting rule after the first vaccination.
• History of immunodeficiency or suspected impairment of immunologic functioning.
• Known or suspected history of plague vaccination, excluding the vaccine received as part of this study.
• Pregnant women or women that are breastfeeding.
• Uncontrolled hypertension (defined as systolic blood pressure >140 mm Hg and/or diastolic blood pressure > 90 mm Hg).
• Subject is on statin therapy
• Current use or use since initial vaccination of immunosuppressive medication or corticosteroids (use of topical or nasal corticosteroids is allowed). Persons who are using a topical steroid can be enrolled after their therapy is completed. Inhaled steroids for asthma are not permissible.
• Malignancy not including squamous cell skin cancer or basal cell skin cancer unless at the vaccination site or history of skin cancer at the vaccination site.
• Active autoimmune disease [Persons with vitiligo or thyroid disease (e.g., taking thyroid hormone replacement) are not excluded].
• Receipt of any vaccine 14 days prior to vaccination.
• Receipt of live attenuated vaccine within 30 days prior to vaccination.
• Receipt of blood products or immunoglobulin since initial vaccination.
• Medical or psychiatric condition or occupational responsibilities that preclude subject compliance with the protocol.
• Use of any other experimental agent (i.e. chemical or biological entity not registered for clinical use) within 30 days prior to vaccination and for the duration of the study.
• Donation of a unit of blood within 56 days prior to vaccination.
• Subject experienced a Grade 2 or higher fever (equal or greater than 101.6 °F) within the first 24 hours following the initial study vaccination.
• Acute febrile illness (>/= 100.0 °F) on the day of vaccination.
• Any condition that, in the opinion of the investigator, might interfere with study objectives or would make administration of the study vaccine hazardous or make it difficult to monitor adverse effects.
• Study personnel.
• Current abuse of alcohol or drug addiction that in the opinion of the Investigator may interfere with the subject's ability to comply with trial procedures.