Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A combination treatment regimen consisting of camrelizumab and gemcitabine-based chemotherapy. Camrelizumab is a humanized monoclonal antibody that targets the programmed cell death protein 1 (PD-1) receptor, acting as an immune checkpoint inhibitor to restore and enhance T-cell mediated anti-tumor activity. Gemcitabine is a pyrimidine nucleoside analog that functions as a cytotoxic chemotherapy agent by inhibiting DNA synthesis. This specific regimen is being evaluated by the Eye & ENT Hospital of Fudan University as a neoadjuvant and adjuvant therapy in conjunction with endoscopic surgery for patients with recurrent nasopharyngeal carcinoma. The protocol typically involves neoadjuvant cycles of the combination followed by surgical intervention and subsequent maintenance therapy with camrelizumab.
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 camrelizumab + gemcitabine.