Drug intelligence / Profile preview

anlotinib + capecitabine + toripalimab

Development stage
Unknown
Lead developer
Affiliated Hospital of North Sichuan Medical College
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

This triplet combination therapy consists of anlotinib, a multi-target tyrosine kinase inhibitor; capecitabine, a cytotoxic fluoropyrimidine carbamate; and toripalimab, a humanized monoclonal antibody targeting the programmed cell death protein 1 (PD-1) receptor. Anlotinib exerts its effects by inhibiting tumor angiogenesis and growth through the blockade of VEGFR, FGFR, PDGFR, and c-Kit signaling pathways. Capecitabine acts as an oral prodrug of 5-fluorouracil, functioning as an antimetabolite that interferes with DNA synthesis by inhibiting thymidylate synthase. Toripalimab enhances the immune system's ability to detect and destroy cancer cells by preventing the interaction between PD-1 and its ligands, PD-L1 and PD-L2. The combination is primarily being investigated by the Affiliated Hospital of North Sichuan Medical College for the treatment of triple-negative breast cancer (TNBC), aiming to leverage the synergistic potential of anti-angiogenesis, chemotherapy, and immune checkpoint inhibition.

Brand names
FukanghuaTuoyi
Other names
Anlotinib hydrochlorideJS-001JS001JS 001TAB001TAB-001TAB 001
02

Targets

PDGFRB (Platelet-derived growth factor receptor beta)PDCD1 (Programmed cell death protein 1 receptor)VEGFR4 (Vascular endothelial growth factor Receptor-3)VEGFR-1 (Vascular endothelial growth factor receptor 1)FGFR1 (Fibroblast growth factor receptor 1)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)

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