Drug intelligence / Profile preview

donafenib

Development stage
Phase 4
Lead developer
Suzhou Zelgen Biopharmaceuticals
Modality
Small Molecules
Administration
Oral
01

Overview

Donafenib is an orally available small molecule multikinase inhibitor developed for the treatment of various cancers, most notably unresectable hepatocellular carcinoma. It is a deuterated derivative of sorafenib with improved pharmacokinetic properties. Donafenib inhibits multiple kinases, including Raf kinase and several receptor tyrosine kinases such as vascular endothelial growth factor receptor (VEGFR), platelet-derived growth factor receptor (PDGFR), and fibroblast growth factor receptor (FGFR). By blocking these targets, donafenib disrupts key signaling pathways involved in tumor cell proliferation and survival. The drug was first approved in China in June 2021 for patients with unresectable hepatocellular carcinoma who have not previously received systemic therapy[1][2][4][7][8].

Brand names
ZepsunZeprosenZeprosyn
Other names
Sorafenib-d3Sorafenib-d-3Sorafenib-d 3Donafenib tosylate
02

Targets

RAF1 (c-Raf-1 (Y340D/Y341D))VEGFR1/2/3 (Vascular endothelial growth factor receptor 1 (VEGFR1) / Vascular endothelial growth factor receptor 2 (VEGFR2) / Vascular endothelial growth factor receptor 3 (VEGFR3))KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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