Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Raxibacumab is a fully human IgG1λ monoclonal antibody indicated for the treatment and prophylaxis of inhalational anthrax due to Bacillus anthracis, in combination with appropriate antibacterial drugs. It works by binding to the protective antigen (PA) component of B. anthracis toxin, thereby blocking its interaction with cellular receptors and preventing the entry of lethal factor and edema factor into cells. This neutralizes the pathogenic effects of anthrax toxin but does not have direct antibacterial activity. Raxibacumab was originally developed by Human Genome Sciences (HGS), later acquired by GlaxoSmithKline, and is currently manufactured by Emergent BioSolutions. The drug was approved by the FDA on December 14, 2012.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Raxibacumab.