Drug intelligence / Profile preview

anlotinib + docetaxel

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Anlotinib + docetaxel is a combination therapy used primarily in the treatment of advanced non-small cell lung cancer (NSCLC) and small-cell lung cancer (SCLC), particularly as a second-line or later option after failure of first-line treatments. Anlotinib is an oral, novel multitarget tyrosine kinase inhibitor that inhibits angiogenesis and tumor progression by targeting multiple kinases including VEGFR, PDGFR, FGFR-2, and c-Kit. It blocks tumor growth by inhibiting new blood vessel formation (angiogenesis) and has demonstrated antitumor effects in several cancers. Docetaxel is a semisynthetic taxoid antineoplastic agent that stabilizes microtubules by promoting their assembly from tubulin dimers and preventing depolymerization, thereby disrupting mitosis and inducing apoptosis in cancer cells. The combination has shown improved clinical effectiveness over monotherapy with either agent alone, with enhanced survival rates and manageable safety profiles[1][4][5].

02

Targets

TUBB (Tubulin (alpha and beta subunits))PDGFRB (Platelet-derived growth factor receptor beta)VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR (FGFR family)MYC (MYC proto-oncogene protein)

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