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Multi-target CAR-T cells (Second Affiliated Hospital of Guangzhou Medical University)

Development stage
Unknown
Lead developer
Second Affiliated Hospital of Guangzhou Medical University
Modality
Gene Editing → Gene Therapies, Gene Addition/Replacement → Gene Therapies, Gene Silencing → Gene Therapies, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies
Administration
Parenteral
01

Overview

These third-generation chimeric antigen receptor (CAR) T-cell therapies are developed by the Second Affiliated Hospital of Guangzhou Medical University for the treatment of advanced lung cancer and other solid tumors. The program utilizes CAR-T cells engineered to target thirteen different tumor-associated antigens: GPC3, Mesothelin, Claudin18.2, GUCY2C, B7-H3, PSCA, PSMA, MUC1, TGFβ, HER2, Lewis-Y, AXL, and EGFR. These candidates are being evaluated in Phase I clinical trials to assess their safety, tolerability, and preliminary efficacy, either as monotherapies or in combination, to address the challenge of tumor heterogeneity in solid malignancies. The third-generation CAR construct typically includes multiple costimulatory domains to enhance T-cell persistence and anti-tumor activity.

Other names
GPC3/Mesothelin/Claudin18.2/GUCY2C/B7-H3/PSCA/PSMA/MUC1/TGFβ/HER2/Lewis-Y/AXL/EGFR-CAR-T cellsCAR-T cells-Second Affiliated Hospital of Guangzhou Medical University-lung cancer-advanced solid tumors
02

Targets

GUCY2C (Guanylate cyclase C receptor)MesothelinLeY (Lewis Y antigen)PSCA (Prostate stem cell antigen)ERBB2 (Erb-b2 receptor tyrosine kinase 2)Claudin 18.2TGFB (GARP–latent transforming growth factor beta 1 complex)GPC3 (Glypican-3)B7-H3MUC (Mucin family)

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