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Ibritumomab Tiuxetan (Zevalin)

M.D. Anderson Cancer Center · FDA-approved active Small molecule

Ibritumomab tiuxetan is a radiolabeled monoclonal antibody that binds to CD20 on B cells and delivers yttrium-90 radiation directly to tumor cells.

Ibritumomab tiuxetan is a radiolabeled monoclonal antibody that binds to CD20 on B cells and delivers yttrium-90 radiation directly to tumor cells. Used for Relapsed or refractory low-grade, follicular, or transformed B-cell non-Hodgkin lymphoma, Previously untreated follicular lymphoma (in combination with rituximab).

At a glance

Generic nameIbritumomab Tiuxetan (Zevalin)
Also known asIbritumomab, Zevalin, IDEC-Y2B8, Rituximab (Mabthera)
SponsorM.D. Anderson Cancer Center
Drug classRadioimmunotherapy agent; anti-CD20 monoclonal antibody
TargetCD20
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

The drug consists of a murine anti-CD20 monoclonal antibody conjugated to a chelator that carries yttrium-90, a beta-emitting radioisotope. Upon binding to CD20-expressing B lymphoma cells, the antibody delivers high-energy radiation directly to the malignant cells, causing DNA damage and cell death. This radioimmunotherapy approach combines the targeting specificity of monoclonal antibodies with the cytotoxic power of radiation.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results