Drug intelligence / Profile preview

axitinib + gemcitabine

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

Overview

**Axitinib + gemcitabine** is a combination therapy comprised of axitinib, an oral small molecule inhibitor of vascular endothelial growth factor receptors 1, 2, and 3 (VEGFR-1, -2, -3), and gemcitabine, a nucleoside analog chemotherapeutic agent that inhibits DNA synthesis. Axitinib targets angiogenesis by blocking VEGFR tyrosine kinases, while gemcitabine acts as an antimetabolite interfering with DNA replication. This combination has been investigated in phase I–III trials for advanced pancreatic cancer. Clinical studies show the combination is generally well tolerated, without significant pharmacokinetic interactions, but does not provide a survival benefit over gemcitabine alone in advanced pancreatic cancer[1][2][3][4][5].

Other names
axitinib and gemcitabine
02

Targets

DNA polymerase familyBCR-ABL1 T315I (Bcr-Abl T315I mutant protein)RNR (Ribonucleotide reductase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)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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