Lumoxiti OverviewMoxetumomab pasudotox is an anti-CD22 immunotoxin designed for the treatment of cancer. 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. In Sept 2018 the US FDA approved it (as Lumoxiti) for some cases of relapsed or refractory hairy cell leukemia (HCL). Discovery and Ownership Background On ...
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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/Moxetumomab_pasudotox
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Possible Dosages for this and Related Drugs:
- Injection: 1mg/vial
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