Active Ingredient(s): Tagraxofusp-erzs
FDA Approved: * December 21, 2018

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Elzonris Overview

Tagraxofusp, sold under the brand name Elzonris, is an anti-cancer medication for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN).[3][4] It was approved for use in the United States in 2018,[5] and after a second review, in the EU in January 2021.[2] The U.S. Food and Drug Administration (FDA) considers it to be a first-in-class medication.[6] Tagraxofusp is a fusion protein consisting of i...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Tagraxofusp-erzs

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Possible Dosages for this and Related Drugs:

  • Solution: 1000mcg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Elzonris: (1 result)

Sorted by National Drug Code
  • 72187-0401 Elzonris 1000 ug/ml Intravenous Injection, Solution by Stemline Therapeutics, Inc.

Other drugs which contain Tagraxofusp-erzs or a similar ingredient: (1 result)