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isatuximab + lenalidomide + dexamethasone

Development stage
Unknown
Lead developer
Sanofi
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous (isatuximab), Oral (lenalidomide), Oral (dexamethasone)
01

Overview

Combination therapy of **isatuximab** (a monoclonal antibody targeting CD38), **lenalidomide** (an immunomodulatory agent), and **dexamethasone** (a synthetic glucocorticoid corticosteroid) is used primarily in the treatment of relapsed/refractory multiple myeloma. Isatuximab is a chimeric IgG1 monoclonal antibody that binds to a unique epitope on CD38, inducing several antitumor mechanisms, including direct induction of apoptosis, antibody-dependent cellular cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), complement-dependent cytotoxicity, and inhibition of CD38 ecto-enzymatic activity[1][2][4][6]. Lenalidomide enhances immune effector cell activity, especially natural killer and T cells, and exerts direct anti-proliferative effects on myeloma cells. Dexamethasone has anti-inflammatory and lympholytic properties, suppressing tumor cell proliferation and enhancing the effects of isatuximab and lenalidomide. This three-drug regimen, via synergistic immunostimulatory and cytotoxic mechanisms, results in increased efficacy in heavily pretreated multiple myeloma patients, with an overall favorable safety profile and significant objective response rates[1][5].

Other names
isatuximab + lenalidomide + dexamethasone
02

Targets

GR (Glucocorticoid receptor)CD38 (Cluster of Differentiation 38)CRBN (Cereblon)

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