Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Emergent BioSolutions
With
Department of Health and Human Services
BioThrax® (also called Anthrax Vaccine Adsorbed or AVA) is the only FDA-licensed vaccine for the prevention of anthrax infection. This study will evaluate the immunogenicity of the vaccine using a post-exposure vaccination schedule. Correlations will be drawn to immunogenicity and survival data from animal models to demonstrate that BioThrax® can elicit a protective immune response for PEP.
Age
18–65
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Be between 18 and 65 years of age, inclusive, at the time of enrollment.
Be in good health as determined by the investigator from medical history and a physical examination.
If a pre-menopausal female, must be using acceptable methods of birth control.
Have all hematology and chemistry parameters (measured at Screening) within the laboratory's normal range.
Be willing and able to return for all visits and blood collections for the duration of the study.
Have read, understood and signed an informed consent form.
You may not be if
Prior immunization with anthrax vaccine or known exposure to anthrax organisms.
Intend to enlist in the military during the study.
Have a known allergy to aluminum hydroxide, formaldehyde, benzethonium chloride, or latex.
Plan to receive experimental products at any time during the study.
Have received a live vaccine in the 30 days before study entry.
Plan to receive a live vaccine at any time during the study.
Have ongoing drug abuse/dependence (including alcohol) issues and/or test positive in a urine drug screen for amphetamines, barbiturates, cocaine or opiates;
Have received immunosuppressive therapy (including systemic steroids) within 3 months prior to study entry.
Have a condition known to produce or be associated with immunosuppression.
Have received cytotoxic therapy in the previous 5 years.
A medical condition that, in the opinion of the Principal Investigator (PI), could adversely impact the subject's participation, safety, or conduct of the study.
Clareo Health | Immunogenicity and Safety Study of a Three-Dose BioThrax® Regimen for Post-Exposure Prophylaxis in Healthy Adults
