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. 2022 Oct 17;75(Suppl 3):S441–S450. doi: 10.1093/cid/ciac593

Table 1.

Antitoxins Evaluated in the United States Government–Funded Pre- and Postlicensure Studies

Generic Name Study Sponsora Product Name/Brand Name Also Known As FDA Approval Manufacturer Description Mechanism of Action
Raxibacumab NIH/BARDA 2012 Emergent Biosolutions Prevents binding of PA to anthrax toxin receptor, disrupting formation of the PA heptamer plasma membrane pore, impeding internalization of LT and ET [13]
Obiltoxaximab NIH/BARDA Anthim 2016 Elusys Therapeutics Prevents binding of PA to anthrax toxin cellular receptors, preventing formation of the PA plasma membrane pore and blocking internalization of lethal factor and edema factor [14]
AIGIV BARDA Anthrasil 2015 Emergent Biosolutions Purified human immune globulin from BioThrax-vaccinated donors Toxin-neutralizing antibodies directed at PA; act by preventing or impeding internalization of LT and ET [15, 16]
AIGIV NIH Anthrivig Emergent Biosolutions Purified human immune globulin from BioThrax-vaccinated donors Toxin-neutralizing antibodies directed at PA; act by preventing or impeding internalization of LT and ET [15, 16]
... NIH Valortim MDX-1303 Pharmathene, Inc. Tethers PA, free or bound, to a cell surface receptor, impeding attachment to the anthrax toxin receptor and internalization [17]
... NIH AVP-21D9 Emergent Biosolutions Binds to PA63 and disrupts formation of the heptamer pore [18, 19]

Abbreviations: AIGIV, anthrax immunoglobulin intravenous; BARDA, Biomedical Advanced Research and Development Authority; ET, edema toxin; FDA, United States Food and Drug Administration; LT, lethal toxin; NIH, National Institutes of Health; PA, protective antigen.

a

The NIH sponsored the prelicensure studies and BARDA sponsored the postlicensure studies.