Drug intelligence / Profile preview

fruquintinib + eribulin

Development stage
Unknown
Lead developer
HUTCHMED
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Fruquintinib + eribulin is a combination therapy currently under clinical investigation for the treatment of advanced malignancies, specifically triple-negative breast cancer (TNBC). Fruquintinib is a potent and highly selective oral tyrosine kinase inhibitor of vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, designed to inhibit tumor angiogenesis while minimizing off-target toxicities. Eribulin is a non-taxane microtubule dynamics inhibitor that disrupts mitotic spindles, causing cell cycle arrest in the G2/M phase and subsequent apoptosis. The combination is being explored to enhance therapeutic efficacy in patients with refractory breast cancer, with studies led by institutions such as Jiangsu Cancer Hospital evaluating its safety and anti-tumor activity.

Other names
fruquintinib and eribulineribulin and fruquintinib
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR-1 (Vascular endothelial growth factor receptor 1)TUBB (Tubulin (alpha and beta subunits))VEGFR3 (Vascular endothelial growth factor receptor 3)

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