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simmitinib + irinotecan liposome (Shanghai Runshi Pharmaceutical Technology Co., Ltd.)

Development stage
Unknown
Lead developer
Shanghai Runshi Pharmaceutical Technology
Modality
Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Oral, Intravenous
01

Overview

Simmitinib + irinotecan liposome is a combination therapy being developed by Shanghai Runshi Pharmaceutical Technology for the treatment of advanced esophageal squamous cell carcinoma (ESCC). Simmitinib (also known as RS1805) is an orally bioavailable, multi-targeted small molecule tyrosine kinase inhibitor that primarily targets the vascular endothelial growth factor receptors (VEGFR1/2/3), platelet-derived growth factor receptors (PDGFRα/β), and c-Kit, thereby inhibiting tumor angiogenesis and proliferation. Irinotecan liposome is a nanoparticle-encapsulated formulation of the cytotoxic agent irinotecan, which acts as a topoisomerase I inhibitor to prevent DNA religation, leading to double-strand breaks and cell death. This combination is currently in Phase II clinical trials for patients with advanced ESCC who have progressed after first-line therapy, aiming to provide a more effective second-line treatment option by combining anti-angiogenic and cytotoxic mechanisms.

Other names
simmitinib plus irinotecan liposome
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)CSF1R (Macrophage colony-stimulating factor receptor)PDGFRB (Platelet-derived growth factor receptor beta)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)TOP1 (DNA Topoisomerase I)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)

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