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QLS5132 + platinum + bevacizumab is an investigational combination therapy regimen being developed by Qilu Pharmaceutical for the treatment of advanced solid tumors, including gastric, non-small cell lung, endometrial, and ovarian cancers. The regimen consists of QLS5132, an antibody-drug conjugate (ADC) targeting Claudin-6 (CLDN6), combined with platinum-based chemotherapy and bevacizumab, an anti-angiogenic monoclonal antibody. QLS5132 utilizes a humanized anti-CLDN6 IgG1 antibody conjugated to a proprietary topoisomerase-1 inhibitor payload (QLS6916) via a hydrophilic cleavable linker. The combination is designed to provide synergistic anti-tumor activity by combining the targeted cytotoxicity of the ADC, the DNA-crosslinking effects of platinum agents, and the inhibition of vascular endothelial growth factor (VEGF) by bevacizumab to disrupt tumor blood supply.
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