Drug intelligence / Profile preview

capecitabine + camrelizumab + apatinib

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Allosteric Modulators → Classical Binding Small Molecules → Small Molecules, Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Oral, Intravenous
01

Overview

The combination of capecitabine, camrelizumab, and apatinib is an investigational regimen evaluated for the treatment of advanced biliary tract cancer (BTC). Capecitabine is an oral prodrug of 5-fluorouracil (5-FU) and acts as a chemotherapy agent by inhibiting DNA synthesis in rapidly dividing cells. Camrelizumab is a monoclonal antibody that targets the programmed cell death protein 1 receptor (PD-1) on T cells, functioning as an immune checkpoint inhibitor to enhance antitumor immune responses. Apatinib is a small molecule tyrosine kinase inhibitor that selectively inhibits vascular endothelial growth factor receptor 2 (VEGFR-2), thereby blocking angiogenesis required for tumor growth and metastasis. This triple combination leverages cytotoxic chemotherapy, immunotherapy, and antiangiogenic therapy to improve outcomes in patients with advanced BTC who have limited treatment options[1][2][6].

02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)PDCD1 (Programmed cell death protein 1 receptor)TS (Thymidylate synthase)

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