drug_type
RELEVANT_DRUG
intervention_type
CAR-T cell therapy (cellular immunotherapy)
drug_description
A fully human BCMA-targeted chimeric antigen receptor (CAR) autologous T-cell therapy. Patient T cells are engineered to express an anti-BCMA scFv linked to CD3ζ signaling and a 4-1BB (CD137) co-stimulatory domain to enhance activation, proliferation, persistence, and cytotoxic activity against BCMA-expressing multiple myeloma cells.
nci_thesaurus_concept_id
C185123
nci_thesaurus_preferred_term
Equecabtagene Autoleucel
nci_thesaurus_definition
A preparation of autologous T-lymphocytes that have been transduced with a lentiviral vector expressing a chimeric antigen receptor (CAR) with a fully human single chain variable fragment (scFv) targeting the human tumor-associated antigen (TAA) B-cell maturation antigen (BCMA; tumor necrosis factor receptor superfamily member 17; TNFRSF17), with potential immunostimulating and antineoplastic activities. Upon administration, equecabtagene autoleucel specifically recognize and induce selective toxicity in BCMA-expressing tumor cells. BCMA, a receptor for both a proliferation-inducing ligand (APRIL) and B-cell activating factor (BAFF), is a member of the tumor necrosis factor receptor superfamily (TNFRSF). BCMA is found on the surfaces of plasma cells, is overexpressed on malignant plasma cells, and plays a key role in plasma cell proliferation and survival.
drug_mesh_term
CT103A chimeric antigen receptor
drug_category
CAR T
drug_class
Cellular Therapy
drug_delivery_route
Intravenous
drug_mechanism_of_action
Autologous T cells engineered via lentiviral transduction to express a fully human anti-BCMA CAR with CD3ζ signaling and 4-1BB co-stimulation. Upon binding BCMA on myeloma cells, CAR signaling activates the T cells, enhancing proliferation and persistence and mediating cytotoxic killing (perforin/granzymes, cytokine release), also depleting normal BCMA+ plasma cells.
drug_name
CT103A
nct_id_drug_ref
NCT05698303