Anthrax Monoclonal Antibody Therapeutic – Product Candidate
Bacillus anthracis are naturally occurring, spore-forming bacteria found in soil throughout the world.
B. anthracis spores can withstand extreme heat, cold and drought for long periods without nutrients or air.
Anthrax infections occur if the spores enter the body through one of three possible routes: 1) a cut, abrasion
or open sore (cutaneous anthrax), 2) ingestion of the spores (gastrointestinal anthrax), or 3) inhalation of
the spores (inhalational anthrax). Once inside the body, the spores germinate into bacteria that then multiply.
B. anthracis bacteria secrete three proteins, protective antigen (PA), lethal factor (LF), and edema factor (EF).
Individually these proteins are non-toxic, but they can become highly toxic if allowed to be combined in a binary
fashion (PA + LF or PA + EF) on the surface of human or animal cells.
Cutaneous anthrax, although rare in the United States, is the most common type of naturally acquired anthrax.
Cutaneous anthrax typically occurs through contact with contaminated animals and animal products. The fatality
rate for untreated cases of cutaneous anthrax is estimated to be approximately 20%.
Inhalational anthrax is the most lethal form of anthrax, and consequently aerosolized anthrax spores are the most
likely method to be used in a potential anthrax bioterrorism attack. Inhalational anthrax has been reported to
occur from one to 43 days after exposure to aerosolized spores. Initial symptoms of inhalational anthrax are
non-specific and may include sore throat, mild fever, cough, achiness or weakness, lasting up to a few days.
After a brief period of improvement, the release of anthrax toxins may cause an abrupt deterioration of the
infected person, with the sudden onset of symptoms including fever, shock and respiratory failure. Hemorrhagic
meningitis is common. Death often occurs within 24 hours of the onset of advanced respiratory complications. The
fatality rate for inhalational anthrax is estimated to be between 45% and 90%, depending on whether aggressive,
early treatment is provided.
Currently, there are no approved products for the treatment of anthrax disease that specifically target
anthrax toxins that have been released into the body. Because early symptoms of anthrax disease are
non-specific, a delay between exposure to anthrax and diagnosis of disease may occur and may render current
post-exposure treatments less effective. As observed in the 2001 letter attacks, by the time individuals with
inhalation anthrax were symptomatic, antibiotics prevented death in only 6 of 11 cases.
In August 2004, the U.S. Department of Health and Human Services (HHS) issued a request for proposal (RFP) seeking
between 10,000 and 200,000 courses of treatment of products to treat inhalational anthrax disease, including
monoclonal antibodies, polyclonal antibodies (such as human immune globulin), and other protein therapeutic
products. To date, HHS has awarded two procurement contracts for anthrax therapeutics for placement in the Strategic
National Stockpile (SNS) to: 1) a Canadian-based company for 10,000 therapeutic courses of treatment of an anthrax immune
globulin and 2) a U.S.-based company for 20,000 therapeutic courses of treatment of a monoclonal antibody.
We are developing AVP-21D9, a monoclonal anthrax therapeutic for use against symptomatic anthrax infection.
This product is a fully human monoclonal antibody that appears to be highly active as a therapeutic for anthrax
based on laboratory and experimental animal studies conducted to date. These studies suggest that AVP-21D9 could
have the potential to be a life-saving medical countermeasure and to fill an important unmet need. This product
candidate is being developed with funding support from NIAID that totals over $24.3 million. The addition of an
anthrax monoclonal therapeutic to the company’s portfolio would broaden Emergent’s anthrax countermeasure program
and reflects the company’s ongoing commitment to develop a full portfolio of countermeasures to strengthen national
preparedness in the event of future anthrax attacks.
Emergent BioSolutions Acquires Monoclonal Anthrax Product Candidate
Emergent BioSolutions Receives $24 Million Development Contract from the Department of Health and Human Services to Fund Continued Development of Anthrax Monoclonal Antibody
Emergent BioSolutions IND for Anthrax Monoclonal Antibody Therapeutic Clears FDA Review
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Target Indication
• Treatment of patients with symptoms of anthrax disease
Intended Market
• Stockpile
• Military
Target Product
Characteristics
• Intravenous monoclonal antibody
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