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SHR-1210 + bevacizumab + oxaliplatin + capecitabine
- Development stage
- Unknown
- Lead developer
- Jiangsu Hengrui Medicine
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
A combination regimen consisting of **SHR-1210 (camrelizumab)**, a humanized anti-PD-1 monoclonal antibody; **bevacizumab**, a humanized monoclonal antibody targeting vascular endothelial growth factor A (VEGF-A); **oxaliplatin**, a platinum-based small molecule chemotherapeutic agent that forms DNA crosslinks; and **capecitabine**, an oral prodrug of 5-fluorouracil that inhibits DNA synthesis in proliferating tumor cells. This combination is explored primarily in oncology settings, leveraging immune checkpoint inhibition (SHR-1210), antiangiogenic blockade (bevacizumab), DNA damage (oxaliplatin), and antimetabolite chemotherapeutic activity (capecitabine), with focus on solid tumors such as metastatic colorectal and hepatocellular cancer. The regimen aims to exploit additive or synergistic effects on tumor control through immune modulation, antiangiogenesis, and cytotoxicity[2][3][4][7].
- Other names
- camrelizumab + bevacizumab + oxaliplatin + capecitabine
02
Targets
TS (Thymidylate synthase)PDCD1 (Programmed cell death protein 1 receptor)VEGFA (Vascular endothelial growth factor A)DNA
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