Drug intelligence / Profile preview

lisocabtagene maraleucel + ibrutinib

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Small Molecules, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Intravenous, Oral
01

Overview

Lisocabtagene maraleucel + ibrutinib is a combination therapy under investigation for the treatment of relapsed or refractory B-cell malignancies, particularly chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL). Lisocabtagene maraleucel (liso-cel) is an autologous, CD19-directed chimeric antigen receptor (CAR) T cell therapy that genetically modifies a patient's own T cells to express a CAR targeting the CD19 antigen on B cells. This enables the immune system to recognize and destroy malignant B cells[1][4][5]. Ibrutinib is an oral small molecule Bruton’s tyrosine kinase inhibitor that blocks signaling pathways essential for cancer cell proliferation and survival[2][3]. The combination aims to enhance anti-tumor efficacy by leveraging both direct cytotoxicity from CAR-T cells and disruption of tumor-supportive signaling by ibrutinib. Clinical studies have shown promising response rates in heavily pretreated CLL/SLL patients, including those previously treated with BTK inhibitors like ibrutinib[6][8].

Brand names
Imbruvica
Other names
lisocabtagene maraleucel + ibrutinib
02

Targets

BTK (Bruton tyrosine kinase)CD19 (B lymphocyte antigen CD19)ITK (Interleukin 2-inducible T-cell kinase)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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