Drug intelligence / Profile preview

camrelizumab + anti-angiogenic tyrosine kinase inhibitors

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

Overview

This combination therapy involves the programmed cell death protein 1 (PD-1) inhibitor camrelizumab (Airuika) administered alongside anti-angiogenic tyrosine kinase inhibitors (TKIs) such as fruquintinib, regorafenib, or apatinib, often in conjunction with chemotherapy (e.g., irinotecan). It is being investigated in a Phase II clinical trial led by Zhejiang Cancer Hospital specifically for the treatment of metastatic colorectal mucinous adenocarcinoma (MAC), a subtype of colorectal cancer known for poor prognosis and resistance to standard therapies. Camrelizumab, developed by Jiangsu Hengrui Medicine, works by blocking the PD-1/PD-L1 pathway to restore T-cell antitumor activity, while the TKIs inhibit vascular endothelial growth factor receptors (VEGFR) to suppress tumor angiogenesis and potentially modulate the tumor microenvironment to enhance immunotherapy efficacy.

Brand names
Airuika
Other names
carilizumab + anti-angiogenic tkiscamrelizumab + fruquintinibcamrelizumab + regorafenibcamrelizumab + apatinibcamrelizumab + VEGFR TKIs
02

Targets

VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR1 (Fibroblast growth factor receptor 1)PDGFR (PDGFR family)VEGFR2 (Vascular endothelial growth factor receptor 2)PDCD1 (Programmed cell death protein 1 receptor)VEGFR-1 (Vascular endothelial growth factor receptor 1)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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