Obiltoxaximab

Obiltoxaximab, sold under the brand name Anthim, is a monoclonal antibody medication designed for the treatment of exposure to Bacillus anthracis spores (etiologic agent of anthrax).[2][1]

Obiltoxaximab
Monoclonal antibody
TypeWhole antibody
SourceChimeric (mouse/human)
TargetBacillus anthracis anthrax
Clinical data
Trade namesAnthim
Other namesETI-204
AHFS/Drugs.comMonograph
License data
Routes of
administration
Intravenous
ATC code
Legal status
Legal status
Identifiers
CAS Number
DrugBank
ChemSpider
  • none
UNII
KEGG
Chemical and physical data
FormulaC6444H9994N1734O2022S44
Molar mass145521.59 g·mol−1

This drug was developed by Elusys Therapeutics, Inc.[1][3]

Society and culture

On 17 September 2020, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization under exceptional circumstances for obiltoxaximab, intended for the treatment or post-exposure prophylaxis of inhalational anthrax.[4] The applicant for this medicinal product is SFL Pharmaceuticals Deutschland GmbH.[4] It was approved for medical use in the European Union in November 2020.[5]

References

  1. "Anthim- obiltoxaximab solution". DailyMed. 9 December 2019. Retrieved 21 September 2020.
  2. Statement On A Nonproprietary Name Adopted By The USAN Council - Obiltoxaximab, American Medical Association.
  3. "Anthim (obiltoxaximab) Injection". U.S. Food and Drug Administration (FDA). 26 April 2016. Retrieved 18 October 2020. Lay summary (PDF).
  4. "Obiltoxaximab SFL: Pending EC decision". European Medicines Agency (EMA). 17 September 2020. Retrieved 21 September 2020. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  5. "Obiltoxaximab EPAR". European Medicines Agency (EMA). 15 September 2020. Retrieved 27 November 2020.
  • "Obiltoxaximab". Drug Information Portal. U.S. National Library of Medicine.
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