Safety Study of an Oral Vaccine to Prevent Avian Influenza
Launched by VAXART · Apr 12, 2011
Trial Information
Current as of May 17, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • In good health as established by medical history, physical examination and laboratory testing at the time of enrollment.
- Exclusion Criteria:
- • Has had any other vaccines within the past 8 weeks.
- • Has had prior H5 avian influenza investigational vaccine.
- • Current history of chronic alcohol consumption and/or illicit and/or recreational drug use.
- • History of autoimmune related disease.
- • History of any confirmed or suspected immunodeficient or immunosuppressive condition (no congenital or acquired condition that impedes normal immune response, no concurrent immunosuppressive therapy).
- • Positive serology for HIV, HCV, or HBV.
- • Previous serious reactions to vaccination such as anaphylaxis, respiratory problems, hives or abdominal pain.
- • History of irritable bowel disease or other inflammatory digestive or gastrointestinal conditions that could affect the intended distribution or safety evaluation of an orally administered vaccine targeting the mucosa of the small intestine.
- • Use of proton pump inhibitors (Nexium, Prilosec) that substantially increases stomach pH.
- • Stool sample with occult blood at baseline exam
About Vaxart
Vaxart is a biotechnology company focused on developing and commercializing innovative oral vaccines using its proprietary oral vaccine platform. With a commitment to addressing unmet medical needs, Vaxart leverages its expertise in molecular biology and immunology to create effective vaccines against a range of infectious diseases, including influenza and norovirus. The company aims to enhance patient compliance and broaden vaccine accessibility through its unique delivery method, which facilitates a robust immune response without the need for injections. By prioritizing safety and efficacy, Vaxart is dedicated to advancing public health and improving global vaccine strategies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Diego, California, United States
San Diego, California, United States
Patients applied
Trial Officials
Sean N Tucker, PhD
Study Director
Vaxart
Martin Kabongo, MD, PhD
Principal Investigator
Accelovance
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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