Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This investigational combination therapy regimen is being evaluated for the first-line treatment of advanced pancreatic ductal adenocarcinoma (PDAC). The regimen employs a sequential chemotherapy strategy, beginning with nab-paclitaxel and gemcitabine (AG) followed by modified FOLFOX (mFOLFOX, comprising oxaliplatin, leucovorin, and 5-fluorouracil). This cytotoxic backbone is integrated with serplulimab, a monoclonal antibody targeting the Programmed cell death protein 1 (PD-1) receptor, and bevacizumab (specifically the biosimilar HLX04), a monoclonal antibody targeting Vascular endothelial growth factor (VEGF). By combining sequential chemotherapy with immune checkpoint inhibition and anti-angiogenic therapy, the regimen aims to enhance therapeutic efficacy in the typically immunosuppressive and poorly vascularized microenvironment of pancreatic cancer. It is currently under investigation in Phase II and Phase III clinical trials led by Zhejiang Cancer Hospital.
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 nab-paclitaxel + gemcitabine + oxaliplatin + leucovorin + 5-fluorouracil + serplulimab + bevacizumab-Zhejiang Cancer Hospital-pancreatic ductal adenocarcinoma.