A Phase 1 Ascending Dose Study to Assess the Safety and Immunogenicity of Adenovirus Anthrax Vector Candidate Vaccines

This is an interventional prevention trial for Anthrax Infection focused on measuring Anthrax vaccine Read More

Inclusion Criteria:

• Able to understand the study and give written informed consent.
• Healthy men or women aged 18-40 years old,
• BMI between 18 to 36 kg/m2
• Women of child bearing potential must have a negative serum pregnancy test at screening and a negative urine pregnancy test prior to vaccination on all vaccination days; they must also be willing to use adequate birth control for the duration of the study and have additional pregnancy tests if indicated.
• Intact upper arms with sufficient muscular tissue in the deltoid region for IM vaccine administration.
• Subject must be available for the study duration
• Subject must avoid strenuous exercise for at least 72 hours prior to each study vaccine administration.

Exclusion Criteria:

• Subject is a healthcare worker who has direct contact with patients or has an household contact (HHC) who is immunodeficient or HIV-positive, pregnant, has an unstable medical condition, or is under the age of 18.
• Subject is a childcare worker or a parent who has direct contact with children 5 years old and younger.
• Subject directly prepares food in the food industry.
• Pregnant or breastfeeding throughout the duration of the study until the final visit
• Military service between 1971 and 1999, or after 2012 when Ad4 vaccine was/is routinely given
• Employment in an industry involved in contact with ruminant animals, veterinary sciences, or other potential exposure to B. anthracis
• Received previous Ad4 vaccination or experimental Ad4 vector vaccines
• Received previous anthrax vaccine
• Received or plans to receive any other approved or investigational vaccines from 30 days prior to the first study vaccination until 30 days after the final study vaccination for live attenuated vaccines and from 15 days prior to the first study vaccination until 15 days after the final study vaccination for inactivated vaccines
• HIV or Hepatitis B or C positive
• Immunodeficient or has an unstable medical condition including psychiatric conditions
• Active or past history of acute or chronic gastrointestinal conditions
• Active or past history of cancer except basal cell carcinoma
• Recipient of bone marrow or solid organ transplant
• Received or plans to receive systemic antiviral medication, within 30 days prior to the first study vaccination
• Known allergy to any component of the study vaccine
• Known allergy to, or known medical condition that precludes use of any systemic antiviral medication
• Received or plans to receive medications indicated for decreasing acidity of stomach including:
• Proton pump inhibitors or antacids or histamine 2-receptor antagonists
• Received or plans to receive immunoglobulin or other blood products within 60 days prior to the first study vaccination
• Received or plans to receive other investigational drugs within 30 days prior to the first study vaccination
• Received or plans to receive systemic immunosuppressive therapy, radiation therapy, or inhaled steroids within 30 days prior to the first study vaccination
• Asthmatic or requires asthmatic medications on a daily basis
• Use of systemic chemotherapy within 5 years prior to study
• Body temperature >38.1°C or acute illness within 3 days prior to vaccination
• History of excessive alcohol consumption, drug abuse, or significant psychiatric illness
• History of Guillain-Barré Syndrome
• Blood donation within 2 months prior to first study vaccination
• Expected to be noncompliant with study visits or plans to move away or be living with different HHCs during the next 8 months
• Drinks more than 1200 mL of tea/coffee/cocoa/cola or other caffeinated beverage per day.
• Any condition or finding that in the view of the primary investigator would impede full study participation