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Benmelstobart (TQB2450) is a humanized IgG1 monoclonal antibody that targets programmed death-ligand 1 (PD-L1). It acts as an immune checkpoint inhibitor by blocking the interaction between PD-L1 and its receptors, PD-1 and B7.1, thereby restoring T-cell mediated antitumor immune responses. Developed by Chia Tai Tianqing Pharmaceutical Group, benmelstobart is being investigated across a broad range of solid tumors, including non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), esophageal squamous cell carcinoma (ESCC), triple-negative breast cancer (TNBC), and endometrial cancer. It is frequently evaluated in combination with anlotinib, a multi-targeted tyrosine kinase inhibitor, to enhance therapeutic efficacy through synergistic modulation of the tumor microenvironment and immune response.
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