Drug intelligence / Profile preview

avelumab + lenvatinib

Development stage
Unknown
Lead developer
Merck KGaA
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Avelumab + lenvatinib is a combination therapy consisting of avelumab, a fully human IgG1 monoclonal antibody that targets programmed death-ligand 1 (PD-L1), and lenvatinib, an oral small molecule multiple receptor tyrosine kinase (RTK) inhibitor. **Avelumab** inhibits the interaction between PD-L1 and PD-1, thus preventing immune evasion by tumor cells and activating T cell-mediated antitumor responses, while also enabling antitumor activity through natural killer (NK) cell-mediated antibody-dependent cellular cytotoxicity (ADCC). **Lenvatinib** targets and inhibits the kinase activities of several RTKs implicated in tumor growth and angiogenesis, including vascular endothelial growth factor receptors VEGFR1, VEGFR2, VEGFR3, fibroblast growth factor receptors FGFR1, FGFR2, FGFR3, FGFR4, platelet-derived growth factor receptor alpha (PDGFRα), KIT, and RET. This combination is under investigation in advanced solid tumors, including metastatic renal cell carcinoma and other cancers, generally aiming to enhance both immune-mediated and anti-angiogenic antineoplastic effects[1][2][5][6].

Brand names
BavencioLenvima
Other names
avelumab plus lenvatinib
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)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)CD274 (Programmed cell death protein 1 ligand 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FcγR (Low affinity immunoglobulin gamma Fc region receptor II-c)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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