Drug intelligence / Profile preview

lenvatinib + paclitaxel

Development stage
Unknown
Lead developer
Eisai
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

Lenvatinib + paclitaxel is a combination regimen of two pharmaceutical agents used primarily in oncology. Lenvatinib is an oral, small molecule, multitargeted tyrosine kinase inhibitor that blocks the activity of several receptors involved in tumor angiogenesis and proliferation, including vascular endothelial growth factor receptors (VEGFR1-3), fibroblast growth factor receptors (FGFR1-4), platelet-derived growth factor receptor alpha (PDGFRα), RET proto-oncogene, and KIT proto-oncogene. Paclitaxel is a microtubule-stabilizing chemotherapeutic agent that inhibits cell division by promoting tubulin polymerization and preventing microtubule depolymerization. The combination has been investigated for synergistic antitumor effects in patients with recurrent endometrial cancer and platinum-resistant epithelial ovarian cancer. Clinical studies have shown encouraging response rates and manageable toxicity profiles for this regimen[1][2][5].

02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)TUBB (Tubulin (alpha and beta subunits))FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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