Drug intelligence / Profile preview

Cimetinib

Development stage
Phase 3
Lead developer
Chinese Academy of Sciences
Modality
Small Molecules
Administration
Oral
01

Overview

Cimetinib (SOMCL-15-290) is a novel, orally administered small molecule tyrosine kinase inhibitor developed as a Class 1 anti-tumor drug. It is designed to selectively and potently inhibit Fibroblast Growth Factor Receptor (FGFR), Colony Stimulating Factor 1 Receptor (CSF1R), and Kinase Insert Domain Receptor (KDR, also known as VEGFR2). This multi-targeted mechanism aims to synergistically suppress tumor cell proliferation, remodel the tumor microenvironment, and overcome drug resistance, particularly cross-resistance to FGFR/KDR inhibitors. The drug also seeks to mitigate the severe clinical toxicities often associated with traditional multi-target inhibitors that primarily target KDR. Cimetinib was developed by the Chinese Academy of Sciences Institute of Drug Innovation / Shanghai Institute of Materia Medica, with clinical trials approved in China and an IND application being prepared for the US.

Brand names
simmitinib
Other names
希美替尼盐酸希美替尼
02

Targets

CSF1R (Macrophage colony-stimulating factor receptor)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR (Fibroblast growth factor receptor)

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