Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Adebrelimab + cetuximab is an investigational combination regimen consisting of a PD-L1 inhibitor and an EGFR inhibitor. Adebrelimab (also known as SHR-1316) is a humanized monoclonal antibody that targets programmed death-ligand 1 (PD-L1), acting as an immune checkpoint inhibitor to restore T-cell mediated anti-tumor activity. Cetuximab is a chimeric monoclonal antibody that targets the epidermal growth factor receptor (EGFR), inhibiting downstream signaling pathways involved in cell growth and survival. This combination, often administered alongside chemotherapy (such as FOLFOX6 or FOLFIRI), is being evaluated for the treatment of RAS/BRAF wild-type unresectable liver metastases from colorectal cancer. The goal of this triplet approach is to convert initially unresectable liver metastases into resectable ones, thereby improving the prognosis and overall survival of patients with metastatic colorectal cancer.
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 adebrelimab + cetuximab.