Drug intelligence / Profile preview

F520 + lenvatinib

Development stage
Unknown
Lead developer
Eisai
Modality
Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

F520 + lenvatinib is a combination therapy under investigation for advanced solid tumors. **F520** is a recombinant, humanized monoclonal antibody targeting programmed death receptor-1 (PD-1); it inhibits the interaction of PD-1 with its ligands PD-L1 and PD-L2, resulting in immune checkpoint blockade and promotion of anti-tumor T-cell activity. **Lenvatinib** is an orally available small molecule inhibitor of multiple receptor tyrosine kinases, including vascular endothelial growth factor receptors (VEGFR1, VEGFR2, VEGFR3), fibroblast growth factor receptors (FGFR1-4), platelet-derived growth factor receptor alpha (PDGFRα), KIT, and RET. The combination is being studied for enhanced antitumor effects in tumors, particularly endometrial and cervical cancer, by simultaneously blocking immune checkpoints and angiogenic pathways[1][2][3].

Brand names
Lenvima
02

Targets

FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR4 (Vascular endothelial growth factor Receptor-3)FGFR2 (Keratinocyte growth factor receptor)PDCD1 (Programmed cell death protein 1 receptor)PDGFRA (Platelet-derived growth factor receptor alpha)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)

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