Drug intelligence / Profile preview

durvalumab + lenalidomide + rituximab + cyclophosphamide + doxorubicin + vincristine + prednisone

Development stage
Preclinical
Lead developer
Bristol Myers Squibb
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

This is a **combination regimen** consisting of seven drugs: - Durvalumab: a monoclonal antibody targeting the immune checkpoint programmed cell death ligand 1 (PD-L1), enhancing antitumor immune responses. - Lenalidomide: an immunomodulatory agent with antineoplastic, antiangiogenic, and pro-erythropoietic properties, affecting both tumor cells and the tumor microenvironment. - Rituximab: a monoclonal antibody targeting the CD20 antigen on B lymphocytes, resulting in antibody-dependent cellular cytotoxicity and complement-mediated lysis. - Cyclophosphamide: a small molecule alkylating agent that crosslinks DNA, leading to apoptosis in rapidly dividing cells. - Doxorubicin: an anthracycline antibiotic and topoisomerase II inhibitor that intercalates DNA, inhibiting replication and transcription. - Vincristine: a vinca alkaloid inhibiting microtubule formation, blocking mitosis. - Prednisone: a synthetic glucocorticoid steroid with lympholytic, anti-inflammatory, and immunosuppressive activity. This multi-drug regimen targets cancer cells through **immune modulation**, **B-cell depletion**, **DNA damage**, **mitotic inhibition**, and **steroid-induced cytotoxicity**, and would be considered in relapsed or refractory hematological malignancies, or in experimental protocols.

02

Targets

CD20 (B-lymphocyte antigen CD20)GR (Glucocorticoid receptor)TUBB (Tubulin (alpha and beta subunits))CRBN (Cereblon)CD274 (Programmed cell death protein 1 ligand 1)DNA

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