Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of the PD-1 inhibitor toripalimab, the EGFR-targeted monoclonal antibody cetuximab, and the chemotherapy agents cisplatin and fluorouracil (5-FU). It is being evaluated by the First Affiliated Hospital of Zhejiang University as a conversion therapy for patients with initially unresectable locally advanced oral cavity squamous cell carcinoma (OCSCC). Toripalimab (JS001) is a humanized IgG4 monoclonal antibody that blocks the PD-1 receptor on T cells, preventing its interaction with PD-L1 and PD-L2 to restore anti-tumor immune responses. Cetuximab is a chimeric monoclonal antibody that binds to the extracellular domain of the epidermal growth factor receptor (EGFR), inhibiting downstream signaling pathways involved in cell proliferation and survival. Cisplatin is a platinum-based chemotherapeutic that forms DNA cross-links, while fluorouracil is an antimetabolite that inhibits thymidylate synthase, both leading to DNA damage and apoptosis in rapidly dividing cancer cells.
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 toripalimab + cetuximab + cisplatin + fluorouracil.