Drug intelligence / Profile preview

epcoritamab + ibrutinib + venetoclax

Development stage
Unknown
Lead developer
Genmab
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Subcutaneous, Oral
01

Overview

This is a **combination therapy** under clinical investigation for the treatment of chronic lymphocytic leukemia (CLL) and potentially related lymphoid malignancies. The regimen comprises: - **Epcoritamab:** a bispecific monoclonal antibody that targets both CD3 (on T cells) and CD20 (on B cells), facilitating T-cell mediated cytotoxicity of malignant B cells. - **Ibrutinib:** an oral small molecule inhibitor of Bruton's tyrosine kinase (BTK), interrupting B-cell receptor signaling and reducing proliferation and survival of B-cell malignancies. - **Venetoclax:** a selective small molecule inhibitor of BCL-2, promoting apoptosis in malignant B cells. This combination is designed to target malignant B cells with complementary mechanisms: direct immune-mediated cytotoxicity (epcoritamab), inhibition of survival/proliferation pathways (ibrutinib), and induction of apoptosis (venetoclax). Early-phase clinical and preclinical research supports superior cytotoxicity against CLL cells, including in settings with BTKi resistance. It is not an approved regimen but is under clinical investigation, most notably for relapsed/refractory CLL and high-risk cases[1][4][6].

Other names
epcoritamab + ibrutinib + venetoclax
02

Targets

CD20 (B-lymphocyte antigen CD20)CD3 (T-cell surface glycoprotein CD3)BTK (Bruton tyrosine kinase)

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