Drug intelligence / Profile preview

ningetinib

Development stage
Phase 2
Lead developer
HEC Pharm
Modality
Small Molecules
Administration
Oral
01

Overview

Ningetinib is a potent, orally bioavailable small molecule tyrosine kinase inhibitor (TKI) that targets multiple receptor tyrosine kinases implicated in tumor growth and resistance mechanisms. Its primary targets include c-Met (hepatocyte growth factor receptor), vascular endothelial growth factor receptor 2 (VEGFR2), Axl, Mer, RON, and Fms-like tyrosine kinase 3 (FLT3). By inhibiting these kinases, ningetinib disrupts signaling pathways essential for tumor cell proliferation, survival, angiogenesis, invasion, and metastasis. It has demonstrated antitumor activity in preclinical models of acute myeloid leukemia with FLT3 mutations as well as various solid tumors. Ningetinib is under clinical investigation primarily for non-small cell lung cancer (NSCLC), hepatocellular carcinoma (liver cancer), and renal cell carcinoma[1][2][3][4][6][8].

Other names
ningetinib-tosylateningetinib toluenesulfonate1394820-69-9
02

Targets

MET (Mesenchymal-epithelial transition factor receptor)AXL (AXL receptor tyrosine kinase)MST1R (Recepteur d'origine nantais)VEGFR2 (Vascular endothelial growth factor receptor 2)FLT3 (Fms related receptor tyrosine kinase 3)

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