Drug intelligence / Profile preview

bortezomib + bendamustine

Development stage
Preclinical
Lead developer
Teva Pharmaceutical Industries
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

Bortezomib + bendamustine is a chemotherapy combination used primarily in multiple myeloma and certain non-Hodgkin lymphomas. Bortezomib is a reversible 26S proteasome inhibitor that disrupts proteasomal degradation, leading to accumulation of pro-apoptotic proteins and apoptosis in malignant plasma and lymphoma cells. Bendamustine is a bifunctional alkylating agent (nitrogen mustard with benzimidazole ring) that induces DNA crosslinks and strand breaks, inhibiting DNA replication and triggering apoptosis. The combination has been investigated in newly diagnosed and relapsed/refractory multiple myeloma, and in indolent and mantle cell lymphomas, often with corticosteroids or rituximab in extended regimens. It is not a fixed-dose co-formulation; it is administered as two separate injectable drugs within a regimen.

Other names
BVDbendamustine + bortezomib
02

Targets

PSMB5 (Proteasome subunit beta Type-5)DNAPSMB6 (Proteasome 20S subunit beta 6)

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