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ANTHIM® (obiltoxaximab) is a Medical Countermeasure to Mitigate the Effect of Anthrax Exposure
Elusys has been awarded over $400 million in procurement and development contracts by the Biomedical Advanced Research and Development Authority (BARDA), the National Institute of Allergy and Infectious Disease (NIAID) and the Department of Defense (DoD). Working closely with these agencies, Elusys has been able to advance ANTHIM® to the commercial stage providing a therapeutic for inclusion in the Strategic National Stockpile to strengthen US biosecurity against a potential anthrax attack. Elusys was also contracted as of 2022 to deliver ANTHIM® to the Public Health Agency of Canada. Obiltoxaximab was first licensed for commercial use by the FDA in 2016, in Canada in 2020, and in Great Britain in 2021.
Obiltoxaximab is a monoclonal anthrax antitoxin licensed as ANTHIM® in the United States and Canada and as NYXTHRACIS® in Great Britain. Details including Indications and Usage and Important Safety Information can be found by visiting the website below.
Visit Anthim.com
US/CA:
ANTHIM® (obiltoxaximab)
US/CA:
ANTHIM® (obiltoxaximab)
US Prescribing Information
Canadian Monograph (English)
Canadian Monograph (French)
GB*:
NYXTHRACIS® (obiltoxaximab)
GB Summary of Product Characteristics (SmPC) (EN)
*SFL Pharmaceuticals Deutschland GmbH is the GB Marketing Authorization Holder