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AMG 706 + panitumumab + gemcitabine + cisplatin

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

Overview

This is a four-drug combination regimen consisting of **AMG 706 (motesanib)**, **panitumumab**, **gemcitabine**, and **cisplatin**. - **AMG 706 (motesanib)** is an oral small-molecule multi-kinase inhibitor targeting vascular endothelial growth factor receptors (VEGFR1, VEGFR2, VEGFR3), platelet-derived growth factor receptor (PDGFR), and stem cell factor receptor (KIT). It primarily inhibits angiogenesis and tumor growth by blocking signaling pathways critical for tumor blood vessel formation and proliferation. - **Panitumumab** is a fully human monoclonal antibody that targets the epidermal growth factor receptor (EGFR), inhibiting cell growth and survival in EGFR-expressing tumors. - **Gemcitabine** is a nucleoside analog that interferes with DNA synthesis, resulting in apoptosis of rapidly dividing tumor cells. - **Cisplatin** is a platinum-containing DNA crosslinker, causing DNA damage and apoptosis in cancer cells. This combination was tested in a **Phase 1b clinical trial** to evaluate its safety and tolerability in patients with advanced cancer, particularly solid tumors[4].

Other names
motesanibpanitumumabgemcitabinecisplatin
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFR (PDGFR family)VEGFR-1 (Vascular endothelial growth factor receptor 1)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)RET (Rearranged during transfection receptor tyrosine kinase)

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