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Moxetumomab Pasudotox

Published: July 26, 2026Updated: August 25, 2026

Moxetumomab pasudotox is a CD22-directed immunotoxin used to treat relapsed or refractory hairy cell leukemia in adult patients who have received at least two prior lines of therapy. It works by targeting CD22 on cancer cells and delivering a bacterial toxin that inhibits protein synthesis, leading to cell death. This medication is administered intravenously and requires careful monitoring for capillary leak syndrome and hemolytic uremic syndrome.

Quick summary

Moxetumomab pasudotox is a targeted immunotherapy for relapsed hairy cell leukemia that delivers a toxin directly to cancer cells expressing CD22.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ATC
L01FB02
RxNorm
2099295
Generic
Moxetumomab Pasudotox
Class
atc-l01
Brands
Lumoxiti
Availability
rx
Lactation
unknown
Routes
—
Forms
injection
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Treatment of adult patients with relapsed or refractory hairy cell leukemia who have received at least two prior systemic therapies, including purine nucleoside analogs.

Moxetumomab pasudotox is a recombinant immunotoxin consisting of an anti-CD22 antibody fused to a truncated Pseudomonas exotoxin. It binds specifically to CD22 on B-cell surfaces, undergoes internalization, and releases the toxin component which ADP-ribosylates elongation factor 2, inhibiting protein synthesis and inducing apoptosis of malignant B cells.

Requires monitoring for capillary leak syndrome and hemolytic uremic syndrome. Contraindicated in patients with known hypersensitivity. Common adverse effects include peripheral edema, nausea, fatigue, and pyrexia. Should be administered in healthcare settings with appropriate resuscitation equipment available. Female patients of reproductive potential should use effective contraception during and for a period after treatment.

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy