Drug intelligence / Profile preview

fruquintinib + bevacizumab + capecitabine

Development stage
Unknown
Lead developer
HUTCHMED
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

This is a combination regimen consisting of three drugs—fruquintinib, bevacizumab, and capecitabine—used primarily as maintenance therapy for metastatic colorectal cancer (mCRC). Fruquintinib is a highly selective small molecule tyrosine kinase inhibitor targeting vascular endothelial growth factor receptors (VEGFR)-1, -2, and -3. Bevacizumab is a monoclonal antibody that binds to vascular endothelial growth factor A (VEGF-A), inhibiting angiogenesis. Capecitabine is an oral prodrug of 5-fluorouracil (5-FU), which acts as an antimetabolite interfering with DNA synthesis in rapidly dividing cells. The combination aims to synergistically inhibit tumor angiogenesis and cell proliferation. Clinical studies have evaluated this regimen as maintenance therapy after first-line induction treatment in mCRC patients, showing promising anti-tumor activity and manageable safety profiles[1][2][8].

02

Targets

TS (Thymidylate synthase)VEGFA (Vascular endothelial growth factor A)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)

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