Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**BC001 + sintilimab + oxaliplatin + capecitabine** is a combination regimen under clinical investigation, particularly for advanced or metastatic solid tumors including gastric and colorectal cancers. The regimen combines several active agents: - **BC001** is a fully human IgG1 monoclonal antibody targeting vascular endothelial growth factor receptor 2 (VEGFR2). It inhibits VEGF-mediated angiogenesis, thereby limiting tumor vascularization and growth. - **Sintilimab (Tyvyt, IBI308)** is a recombinant human monoclonal antibody against programmed cell death protein 1 (PD-1), acting as a checkpoint inhibitor to enhance T-cell mediated anti-tumor immunity. - **Oxaliplatin** is a platinum-based chemotherapeutic that creates DNA crosslinks and inhibits DNA synthesis, leading to tumor cell apoptosis. - **Capecitabine** is an oral prodrug of 5-fluorouracil (5-FU), an antimetabolite cytotoxic agent that inhibits thymidylate synthase and interferes with DNA synthesis. The combination of targeted anti-VEGFR2 therapy, immune checkpoint inhibition, and cytotoxic chemotherapy is being explored for potential synergistic efficacy in solid tumors, especially gastrointestinal cancers[1][2][3][4].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on BC001 + sintilimab + oxaliplatin + capecitabine.