Active Ingredient(s): Moxetumomab Pasudotox-tdfk
FDA Approved: * September 13, 2018
Pharm Company: * ASTRAZENECA AB
Category: Cancer

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

Lumoxiti Overview

Moxetumomab pasudotox is an anti-CD22 immunotoxin designed for the treatment of cancer.[1] Moxetumomab pasudotox is currently being developed by the biologics division of AstraZeneca, MedImmune. On 16 May 2013, the first dose in a Phase III trial was administered.[2][3] In Sept 2018 the US FDA approved it (as Lumoxiti) for some cases of relapsed or refractory hairy cell leukemia (HCL).[4] Discovery and ownership background On ...

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Possible Dosages for this and Related Drugs:

Moxetumomab Pasudotox-tdfk
  • Injection: 1mg/vial
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Lumoxiti: (1 result)

Sorted by National Drug Code
  • 0310-4700 Lumoxiti 1 mg/ml Intravenous Injection, Powder, Lyophilized, for Solution by Astrazeneca Pharmaceuticals Lp

Other drugs which contain Moxetumomab Pasudotox-tdfk or a similar ingredient: (1 result)

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