Drug intelligence / Profile preview

anlotinib + bevacizumab + pyrotinib

Development stage
Unknown
Lead developer
Hengrui Therapeutics
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

This is a combination therapy consisting of three anti-cancer agents: anlotinib, bevacizumab, and pyrotinib. Pyrotinib is an irreversible dual pan-ErbB receptor tyrosine kinase inhibitor that targets EGFR (HER1), HER2, and HER4. It works by binding competitively to the ATP binding domain of the EGFR family, inhibiting phosphorylation of tyrosine kinase and blocking downstream RAS/RAF/MEK/MAPK and PI3K/AKT signaling pathways, thereby inhibiting tumor cell growth. Pyrotinib was developed in China and received conditional approval there for use in combination with capecitabine for HER2-positive advanced or metastatic breast cancer in patients previously treated with anthracycline or taxane chemotherapy.

Other names
BLTNIrenePyrotinib maleatePyrroltinib maleate
02

Targets

EGFR (Epidermal growth factor receptor)ERBB2 (Erb-b2 receptor tyrosine kinase 2)ERBB4 (Erb-b2 receptor tyrosine kinase 4)FGFR (FGFR family)VEGFR4 (Vascular endothelial growth factor Receptor-3)VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)VEGFA (Vascular endothelial growth factor A)

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