Drug intelligence / Profile preview

EGFR bispecific antibody armed activated T-cells

Development stage
Unknown
Lead developer
Memorial Sloan Kettering Cancer Center
Modality
Allogeneic CAR-T → CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Autologous CAR-T → CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, TCR-Engineered T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Tumor-Infiltrating Lymphocytes (TILs) → Native Immune Cells → Adoptive Cell Transfer → Cell Therapies, Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

EGFR bispecific antibody armed activated T-cells (EGFR BATs) is an autologous cell-based immunotherapy developed by Memorial Sloan Kettering Cancer Center for the treatment of advanced pancreatic adenocarcinoma. The production process involves harvesting a patient's peripheral blood mononuclear cells, which are then activated and expanded ex vivo using anti-CD3 monoclonal antibodies and interleukin-2 (IL-2). These activated T cells (ATC) are subsequently "armed" by coating them with a bispecific antibody (BiAb) that targets both CD3 on the T cells and the epidermal growth factor receptor (EGFR) overexpressed on pancreatic cancer cells. This approach effectively turns the T cells into targeted cytotoxic effectors that can recognize and kill EGFR-positive tumor cells without requiring MHC restriction. Early clinical studies have evaluated the safety and efficacy of these cells in patients who have progressed on standard chemotherapy.

Other names
Anti-CD3 x Anti-EGFR-bispecific antibody armed activated T-cellsAnti-CD-3 x Anti-EGFR-bispecific antibody armed activated T-cellsAnti-CD 3 x Anti-EGFR-bispecific antibody armed activated T-cellsEGFRBi-armed activated T cellsEGFR-bispecific antibody armed activated T-cells
02

Targets

CD3 (T-cell surface glycoprotein CD3)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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