Drug intelligence / Profile preview

anlotinib + gemcitabine + cisplatin

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

Anlotinib + gemcitabine + cisplatin is a combination regimen consisting of three drugs used primarily in oncology. Anlotinib is a small molecule multi-targeted tyrosine kinase inhibitor that blocks angiogenesis and tumor cell proliferation by inhibiting receptors such as VEGFR, FGFR, PDGFR, and c-Kit. Gemcitabine is a nucleoside analog that inhibits DNA synthesis, leading to apoptosis in rapidly dividing cells. Cisplatin is a platinum-based chemotherapeutic agent that causes DNA crosslinking and subsequent cell death. This combination has been investigated as first-line therapy for recurrent or metastatic nasopharyngeal carcinoma (R/M NPC) and advanced biliary tract cancer (BTC), showing promising efficacy with manageable safety profiles[1][2][4]. The regimen leverages the antiangiogenic effects of anlotinib alongside the cytotoxic actions of gemcitabine and cisplatin.

02

Targets

DNA polymerase familyFGFR (FGFR family)KIT (c-KIT proto-oncogene receptor tyrosine kinase)RNR (Ribonucleotide reductase)PDGFRB (Platelet-derived growth factor receptor beta)DNAVEGFR3 (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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