drug_type
RELEVANT_DRUG
intervention_type
Biological (Cellular Gene Therapy)
drug_description
Allogeneic, multiplex base-edited anti-CD7 CAR-T cell therapy with edits in TRAC, CD7, PDCD1 (PD-1), and CD52 to target CD7+ malignant T cells, reduce GVHD and fratricide, resist alemtuzumab, and enhance antitumor activity.
nci_thesaurus_concept_id
C200791
nci_thesaurus_preferred_term
Allogeneic Anti-CD7 CAR-T Cells BEAM-201
nci_thesaurus_definition
A preparation of off-the-shelf (OTS) donor-derived T-lymphocytes that have been multiplex base-edited and transduced with a lentiviral vector to express a chimeric antigen receptor (CAR) directed against the tumor-associated antigen (TAA) CD7, with potential immunostimulating and antineoplastic activities. Upon administration, allogeneic anti-CD7 CAR-T cells BEAM-201 specifically target and kill CD7-expressing tumor cells. CD7 is a transmembrane glycoprotein expressed by T-cells and natural killer (NK) cells and their precursors. It is expressed in the majority of lymphoblastic T-cell leukemias and lymphomas and in a subset of peripheral T-cell lymphomas.
drug_mesh_term
Chimeric Antigen Receptor T-Cell Therapy
drug_category
CAR T
drug_class
Cellular Therapy
drug_delivery_route
Intravenous
drug_mechanism_of_action
Allogeneic, multiplex base-edited anti-CD7 CAR T cells that bind CD7 on malignant T cells and mediate targeted cytotoxicity. Edits knock out TRAC (removes TCR to reduce GVHD), CD7 (prevents fratricide), PDCD1/PD-1 (limits checkpoint inhibition to enhance activity), and CD52 (confers resistance to alemtuzumab during conditioning), enabling effective killing of CD7+ T-cell malignancies.
drug_name
BEAM-201
nct_id_drug_ref
NCT05885464