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This combination therapy is an investigational regimen consisting of irinotecan hydrochloride liposome, anlotinib, and enlonstobart. **Irinotecan hydrochloride liposome** is a liposomal formulation of the cytotoxic topoisomerase I inhibitor irinotecan, designed to provide sustained drug release and improved tumor penetration. **Anlotinib** is a multi-target small molecule tyrosine kinase inhibitor that primarily targets VEGFR1/2/3, FGFR1-4, PDGFR alpha/beta, and c-Kit, thereby inhibiting tumor angiogenesis and proliferation. **Enlonstobart** (also known as SG001) is a humanized monoclonal antibody that acts as a checkpoint inhibitor by targeting the programmed cell death protein 1 (PD-1) receptor, enhancing the immune system's anti-tumor response. The combination is being evaluated for its synergistic potential in treating advanced solid tumors, particularly colorectal cancer, by simultaneously attacking the tumor through cytotoxic, anti-angiogenic, and immunotherapeutic pathways.
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