Drug intelligence / Profile preview

gemcitabine + oxaliplatin + lenvatinib + PD-1 inhibitor

Development stage
Preclinical
Lead developer
Eli Lilly
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a multi-agent combination regimen consisting of four drugs with distinct mechanisms of action, used primarily in oncology research and clinical trials. - **Gemcitabine** is a nucleoside analog (antimetabolite) that inhibits DNA synthesis, leading to apoptosis in rapidly dividing tumor cells. - **Oxaliplatin** is a platinum-based chemotherapeutic agent that forms DNA adducts, disrupting DNA replication and transcription. - **Lenvatinib** is an oral small molecule tyrosine kinase inhibitor targeting multiple receptors including VEGFR, FGFR, PDGFRα, RET, and KIT; it inhibits angiogenesis and tumor cell proliferation. - **PD-1 inhibitors** are monoclonal antibodies that block the programmed death 1 (PD-1) immune checkpoint on T cells (such as pembrolizumab or nivolumab), enhancing anti-tumor immune responses. This combination leverages cytotoxic chemotherapy (gemcitabine/oxaliplatin), targeted therapy (lenvatinib), and immunotherapy (PD-1 inhibitor) for synergistic anti-cancer effects. It has been explored in various advanced solid tumors but does not have a unique brand name or established fixed-dose formulation.

02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDCD1 (Programmed cell death protein 1 receptor)RNR (Ribonucleotide reductase)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)DNA polymerase familyFGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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