Drug intelligence / Profile preview

lenvatinib + sorafenib

Development stage
Preclinical
Lead developer
Eisai
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Oral
01

Overview

Lenvatinib + sorafenib is a combination of two oral small molecule multikinase inhibitors, each approved individually for the treatment of advanced hepatocellular carcinoma (HCC) and other cancers. Both drugs act as tyrosine kinase inhibitors (TKIs), targeting multiple receptor tyrosine kinases involved in tumor angiogenesis, growth, and progression. Lenvatinib inhibits vascular endothelial growth factor receptors (VEGFR1-3), fibroblast growth factor receptors (FGFR1-4), platelet-derived growth factor receptor alpha (PDGFRα), KIT, and RET. Sorafenib targets VEGFR2/3, PDGFRβ, RAF kinases, KIT, FLT-3, and RET. The combination has been explored in clinical settings but is not an established or approved regimen; both are more commonly used as monotherapies or in combination with other agents such as immunotherapies or transarterial chemoembolization (TACE). Their mechanisms overlap but also complement each other by inhibiting a broader spectrum of signaling pathways critical to tumor vascularization and proliferation[6][10][8].

02

Targets

FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)RAF1 (c-Raf-1 (Y340D/Y341D))RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)

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