Drug intelligence / Profile preview

axitinib + gemcitabine + cisplatin

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

Overview

Axitinib + gemcitabine + cisplatin is a combination regimen of three pharmaceutical agents used in oncology, particularly for the treatment of advanced or metastatic cancers such as biliary tract cancer and non-small cell lung cancer. Axitinib is a potent and selective small molecule inhibitor of vascular endothelial growth factor receptors (VEGFR) 1, 2, and 3, thereby inhibiting angiogenesis required for tumor growth[1]. Gemcitabine is a nucleoside analog that interferes with DNA synthesis by incorporating into DNA during replication, leading to masked chain termination and apoptosis[2]. Cisplatin is a platinum-based alkylating agent that cross-links DNA strands, preventing replication and transcription which results in cell death[5][6]. This combination leverages complementary mechanisms—antiangiogenic effects from axitinib with cytotoxic effects from gemcitabine and cisplatin—to enhance antitumor efficacy.

Other names
axitinib + gemcitabine + cisplatin
02

Targets

RNR (Ribonucleotide reductase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)

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