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LauT-1 is an autologous T-cell receptor (TCR) engineered T-cell therapy designed to target the cancer-testis antigen New York Esophageal Squamous Cell Carcinoma-1 (NY-ESO-1). The therapy utilizes the affinity-enhanced, Human Leukocyte Antigen - A2 (HLA-A2) restricted I53F TCR, which recognizes the 157-165 epitope of the NY-ESO-1 protein. To produce LauT-1, a patient's own T lymphocytes are isolated via leukapheresis, genetically modified to express the I53F TCR, and expanded *ex vivo*. The drug is administered intravenously following a conditioning regimen of non-myeloablative lymphodepleting chemotherapy and low-dose tumor irradiation, which is intended to facilitate T-cell expansion and enhance infiltration into the tumor microenvironment. LauT-1 is primarily being investigated for the treatment of NY-ESO-1-positive advanced melanoma and various sarcomas.
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