
Treatment for inhalational anthrax approved
FDA has approved Anthrax Immune Globulin Intravenous (Human) (Anthrasil, Emergent BioSolutions) also known as AIGIV, for treatment of inhalational anthrax in combination with appropriate antibacterial drugs.
FDA has approved Anthrax Immune Globulin Intravenous (Human) (Anthrasil,
Anthrasil is a sterile solution of purified human immune globulin G (IgG) containing polyclonal antibodies that targets the anthrax toxins of Bacillus anthracis, the bacteria that causes anthrax disease. It is prepared using plasma collected from healthy, screened donors who have been immunized with Emergent's
The product qualifies for 7 years of market exclusivity.
To support the nation’s preparedness against a possible anthrax attack, the U.S. Department of Health and Human Services’
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The efficacy of Anthrasil was studied in animals because it was not feasible or ethical to conduct adequately controlled efficacy studies in humans. Rabbits and monkeys were exposed to a lethal aerosolized dose of B anthracis spores, then treated with Anthrasil or a placebo, and evaluated for survival. Survival in anthrax-infected monkeys treated with Anthrasil ranged from 36% to 70% compared to 0% survival in the placebo group with a trend toward increased survival at higher doses of Anthrasil. Rabbits treated with a moderate dose of Anthrasil after infection exhibited 26% survival compared to 2% survival in the placebo group. Another study in rabbits showed that a combination of Anthrasil and antibiotics resulted in 71% survival compared to 25% survival in animals treated with
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