Drug intelligence / Profile preview

fruquintinib + toripalimab + SOX

Development stage
Unknown
Lead developer
HUTCHMED
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Oral, Intravenous
01

Overview

Fruquintinib + toripalimab + SOX is a combination regimen under clinical investigation for the first-line treatment of advanced or metastatic gastric cancer (GC) and gastroesophageal junction cancer (GEJC). The regimen consists of three components: - **Fruquintinib** is an oral, highly selective small molecule inhibitor targeting vascular endothelial growth factor receptors 1, 2, and 3 (VEGFR1/2/3), thereby inhibiting tumor angiogenesis. - **Toripalimab** is a monoclonal antibody that targets programmed cell death protein 1 (PD-1), functioning as an immune checkpoint inhibitor to enhance anti-tumor immune responses. - **SOX** refers to a chemotherapy doublet comprising S-1 (an oral fluoropyrimidine derivative) and oxaliplatin (a platinum-based chemotherapeutic agent). This combination aims to leverage the synergistic effects of antiangiogenic therapy, immunotherapy, and cytotoxic chemotherapy. Early-phase clinical trials have shown that this regimen is well tolerated with encouraging antitumor activity in patients with advanced GC/GEJC[2][9]. The trial NCT05024812 specifically evaluates this triplet as first-line therapy in HER2-negative patients.

02

Targets

PDCD1 (Programmed cell death protein 1 receptor)VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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