Drug intelligence / Profile preview

MEDI-573 + sorafenib

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

Overview

MEDI-573 + sorafenib is a **combination regimen** under investigation for the treatment of unresectable or metastatic hepatocellular carcinoma (HCC). MEDI-573 is a human immunoglobulin G2 lambda (IgG2λ) monoclonal antibody that simultaneously neutralizes both insulin-like growth factor I (IGF-I) and insulin-like growth factor II (IGF-II) ligands, thereby inhibiting their interaction with the insulin-like growth factor-1 receptor (IGF-1R) and insulin receptor. Sorafenib is a small molecule multikinase inhibitor that targets serine/threonine and tyrosine kinases including RAF kinases (CRAF, BRAF), vascular endothelial growth factor receptors (VEGFR-2, VEGFR-3), and platelet-derived growth factor receptor beta (PDGFR-β), exerting antitumor and anti-angiogenic effects. The combination is administered as intravenous MEDI-573 every 21 days with continuous oral sorafenib. The drug was developed primarily for HCC that is unresectable or metastatic, and is being studied for safety and efficacy in phase 1 and 2 clinical trials[2][4][5][7].

Brand names
Nexavar
02

Targets

BRAF (B-Raf proto-oncogene, serine/threonine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)RAF1 (c-Raf-1 (Y340D/Y341D))PDGFRB (Platelet-derived growth factor receptor beta)IGF-1R (Insulin-like growth factor 1 receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)IGF2 (Insulin-like growth factor 2)

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