Drug intelligence / Profile preview

lenvatinib + rAd-p53

Development stage
Unknown
Lead developer
Eisai
Modality
Viral Vectors → Gene Addition/Replacement → Gene Therapies, Small Molecules
Administration
Oral, Intratumoral
01

Overview

Lenvatinib + rAd-p53 is a combination therapy consisting of lenvatinib, a small molecule multi-kinase inhibitor, and rAd-p53 (recombinant adenoviral p53 gene therapy). Lenvatinib targets multiple receptor tyrosine kinases involved in tumor angiogenesis and proliferation, including vascular endothelial growth factor receptors (VEGFR), fibroblast growth factor receptors (FGFR), and platelet-derived growth factor receptor beta (PDGFR-β). rAd-p53 delivers the wild-type p53 gene to tumor cells via an adenoviral vector, aiming to restore normal p53 function and induce apoptosis in cancer cells with dysfunctional or mutated p53. The combination has been studied for its synergistic anti-tumor effects in cancers such as non-small cell lung cancer (NSCLC) and renal cell carcinoma (RCC), showing enhanced inhibition of tumor growth, migration, invasion, and increased apoptosis compared to either agent alone. Common adverse events include hypertension, diarrhea, nausea, proteinuria, body weight loss for the combination; fever is more common with gene therapy components[1][2][3].

02

Targets

CXADR (Coxsackievirus and adenovirus receptor)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)TP53 (Cellular Tumor Antigen p53 R175H)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)

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