Drug intelligence / Profile preview

SHR-1701 + bevacizumab + capecitabine + oxaliplatin

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

Overview

A **combination regimen** consisting of SHR-1701 (a bifunctional fusion protein targeting PD-L1 and TGF-β), **bevacizumab** (a monoclonal antibody against VEGF-A), **capecitabine** (an oral prodrug of fluorouracil), and **oxaliplatin** (a platinum-based chemotherapeutic agent) used primarily for the first-line treatment of **unresectable metastatic colorectal cancer**. SHR-1701 exerts dual antagonism—blocking PD-L1 to unleash antitumor immunity and sequestering TGF-β via the extracellular domain of TGFβ receptor II, mitigating immunosuppressive tumor microenvironment effects. Bevacizumab inhibits angiogenesis by blocking VEGF-A; capecitabine is metabolized to 5-fluorouracil, inhibiting thymidylate synthase, and oxaliplatin forms DNA crosslinks resulting in cytotoxicity. The combination demonstrates a **manageable safety profile and potent antitumor activity** with objective response rates approaching 60% in phase 2 studies for metastatic colorectal cancer[3].

Brand names
XELOX
Other names
SHR-1701 + BP102 + XELOX
02

Targets

TS (Thymidylate synthase)TGFB (GARP–latent transforming growth factor beta 1 complex)VEGFA (Vascular endothelial growth factor A)CD274 (Programmed cell death protein 1 ligand 1)DNA

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