Drug intelligence / Profile preview

ibritumomab tiuxetan + bortezomib

Development stage
Preclinical
Lead developer
IDEC
Modality
Small Molecules, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

A combination regimen of the radioimmunotherapy ibritumomab tiuxetan and the proteasome inhibitor bortezomib, investigated primarily for B-cell non-Hodgkin lymphoma. Ibritumomab tiuxetan is an anti-CD20 monoclonal antibody conjugated via the chelator tiuxetan to a radionuclide (commonly yttrium-90 for therapy; indium-111 for imaging), delivering targeted radiation to CD20-positive B cells and inducing cell death through beta emission and immune effector functions. Bortezomib is a reversible inhibitor of the 26S proteasome that disrupts protein degradation, leading to cell cycle arrest and apoptosis in malignant cells. The combination is intended to enhance antitumor activity by depleting CD20-positive B cells with radiotherapy while simultaneously sensitizing lymphoma cells to cytotoxic stress through proteasome inhibition.

Other names
Zevalin + bortezomibibritumomab tiuxetan radiolabeled + bortezomib
02

Targets

CD20 (B-lymphocyte antigen CD20)PSMB5 (Proteasome subunit beta Type-5)

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