Drug intelligence / Profile preview

andamertinib + anlotinib

Development stage
Unknown
Lead developer
Jiangsu Aosaikang Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Andamertinib + anlotinib is a combination therapy consisting of a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) and a multi-targeted receptor tyrosine kinase inhibitor. Andamertinib (ASK120067) is an irreversible inhibitor that selectively targets EGFR sensitizing mutations and the T790M resistance mutation while sparing wild-type EGFR, thereby reducing skin and gastrointestinal toxicities. Anlotinib is a potent small-molecule inhibitor of vascular endothelial growth factor receptors (VEGFR 1-3), fibroblast growth factor receptors (FGFR 1-4), platelet-derived growth factor receptors (PDGFR alpha/beta), and c-Kit. By combining these two agents, the therapy aims to provide dual inhibition of oncogenic signaling pathways and tumor angiogenesis, potentially overcoming resistance to prior EGFR-TKI treatments. This combination is currently being evaluated in clinical trials for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who have progressed after treatment with third-generation EGFR-TKIs.

Brand names
FukanghuaFocus V
Other names
ASK120067 + AL3818andamertinib + anlotinib
02

Targets

RET (Rearranged during transfection receptor tyrosine kinase)BTK (Bruton tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)ITK (Interleukin 2-inducible T-cell kinase)

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