Drug intelligence / Profile preview

motesanib + paclitaxel

Development stage
Discontinued
Lead developer
Takeda
Modality
Small Molecules
Administration
Oral (motesanib), Intravenous (paclitaxel)
01

Overview

**Motesanib (AMG 706) + paclitaxel** is an investigational combination therapy evaluated in several phase II and III trials for advanced cancers, including non-small cell lung cancer and breast cancer. Motesanib is an orally administered small molecule that acts as an antagonist to multiple receptor tyrosine kinases, including **vascular endothelial growth factor receptors 1, 2, and 3 (VEGFR1/2/3)**, **platelet-derived growth factor receptors (PDGFR)**, and **stem cell factor receptor (c-KIT)**. Paclitaxel is a chemotherapy drug that stabilizes microtubules, thereby inhibiting cell division. Motesanib is developed to target tumor angiogenesis, while paclitaxel targets cell proliferation. The combination was not shown to significantly improve progression-free survival or overall survival compared to chemotherapy alone, and development has been discontinued for multiple indications following lack of efficacy and safety concerns, including serious adverse events like posterior reversible encephalopathy syndrome[1][2][3][5][6][7].

Brand names
None
Other names
motesanib + paclitaxelAMG 706 + paclitaxel
02

Targets

TUBB (Tubulin (alpha and beta subunits))VEGFR3 (Vascular endothelial growth factor receptor 3)PDGFR (PDGFR family)VEGFR2 (Vascular endothelial growth factor receptor 2)ABCB1 (P-glycoprotein)VEGFR-1 (Vascular endothelial growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)

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