Tagraxofusp, sold under the brand name Elzonris, is an anti-cancer medication described as a CD123-directed cytotoxin. It is a fusion protein combining interleukin-3 with diphtheria toxin, and it kills cultured plasmacytoid dendritic cells by binding to their interleukin-3 receptors, then blocking protein synthesis through the diphtheria toxin component, which inhibits the eukaryotic elongation factor 2. It treats blastic plasmacytoid dendritic cell neoplasm in patients aged two years and older and is given by intravenous injection. It received United States FDA approval in 2018, as a first-in-class medication with priority review, breakthrough therapy and orphan drug designations, and European Union approval in January 2021.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration First Approved / Isolated Year Sources
1. Tagraxofusp (Wikipedia)
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It was approved for medical use in the United States in 2018, and in the European Union in January 2021.
View the Source 2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Tagraxofusp (Wikipedia)
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Intravenous
View the Source 4. Drugs.com: Elzonris (tagraxofusp-erzs) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Elzonris (tagraxofusp-erzs) was first approved by the FDA on December 21, 2018
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