Drug intelligence / Profile preview

R-EPOCH + ibrutinib

Development stage
Unknown
Lead developer
Pharmacyclics
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Recombinant Proteins and Enzymes, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

R-EPOCH + ibrutinib is a combination regimen used primarily in the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL), including AIDS-related lymphomas. The R-EPOCH regimen consists of rituximab (a monoclonal antibody targeting CD20), etoposide (a topoisomerase II inhibitor), prednisone (a corticosteroid), vincristine (a microtubule inhibitor), cyclophosphamide (an alkylating agent), and doxorubicin (an anthracycline antibiotic). Ibrutinib is a small molecule Bruton’s tyrosine kinase inhibitor that blocks B-cell receptor signaling pathways critical for the survival and proliferation of malignant B cells. The addition of ibrutinib to R-EPOCH aims to enhance antitumor activity by combining cytotoxic chemotherapy with targeted inhibition of B-cell signaling[1][3][5][6].

Brand names
RituxanToposarOncovinCytoxanAdriamycin
Other names
dose-adjusted EPOCH-R plus rituximab and ibrutinib
02

Targets

ITK (Interleukin 2-inducible T-cell kinase)CD20 (B-lymphocyte antigen CD20)TOP2A (DNA topoisomerase II)BMX (Bone Marrow Tyrosine Kinase X-linked)GR (Glucocorticoid receptor)DNATUBB (Tubulin (alpha and beta subunits))BTK (Bruton tyrosine kinase)

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