Drug intelligence / Profile preview

daratumumab + ixazomib + dexamethasone

Development stage
Unknown
Lead developer
Johnson & Johnson
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous, Oral
01

Overview

The combination of daratumumab, ixazomib, and dexamethasone is used as a second-line therapy for patients with relapsed or refractory multiple myeloma, particularly those previously treated with lenalidomide-based regimens. Daratumumab is a monoclonal antibody that targets CD38 on myeloma cells, inducing cell death through direct cytotoxicity and immune-mediated mechanisms. Ixazomib is an oral small molecule proteasome inhibitor that disrupts protein degradation in cancer cells, leading to apoptosis. Dexamethasone is a synthetic glucocorticoid corticosteroid that exerts anti-inflammatory and immunosuppressive effects and enhances the efficacy of antimyeloma agents. This combination has demonstrated rapid responses and acceptable safety profiles in clinical studies for relapsed/refractory multiple myeloma[1][2][3][4][5].

Other names
Dara-Ixa-dex
02

Targets

CD38 (Cluster of Differentiation 38)GR (Glucocorticoid receptor)PSMB5 (Proteasome subunit beta Type-5)

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