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lisocabtagene maraleucel + venetoclax
- 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 is a CD19-directed, genetically modified autologous CAR-T cell therapy. It involves collecting a patient's T cells, engineering them to express a chimeric antigen receptor (CAR) targeting the CD19 antigen on B cells, and infusing them back into the patient to attack and kill malignant B cells. Venetoclax is an oral small molecule inhibitor of B-cell lymphoma 2 (BCL2), a protein that helps cancer cells survive by inhibiting apoptosis. The combination of these two drugs is being investigated for relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL), particularly in patients who have failed prior therapies including BTK inhibitors and venetoclax monotherapy[5][8]. Lisocabtagene maraleucel was developed by Juno Therapeutics/Bristol Myers Squibb; venetoclax was developed by AbbVie/Genentech.
- Other names
- lisocabtagene maraleucel + venetoclax
02
Targets
BCL-2 (BCL-2 family)CD19 (B lymphocyte antigen CD19)
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