Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AK117 + cetuximab is a combination therapy consisting of ligufalimab (AK117), a humanized monoclonal antibody targeting CD47, and cetuximab, a chimeric monoclonal antibody targeting the epidermal growth factor receptor (EGFR). Ligufalimab is designed to block the CD47-SIRPα "don't eat me" signaling pathway, which is often overexpressed by tumor cells to evade immune surveillance; by blocking this interaction, ligufalimab enhances macrophage-mediated phagocytosis of cancer cells. Cetuximab inhibits EGFR-mediated downstream signaling pathways involved in cell proliferation and survival, while also promoting antibody-dependent cellular cytotoxicity (ADCC). The combination is being evaluated as a second-line treatment for patients with recurrent or metastatic head and neck squamous cell carcinoma (R/M HNSCC) who have failed prior platinum-based chemotherapy or PD-1/PD-L1 inhibitors, aiming to leverage the synergistic potential of dual innate and adaptive immune activation.
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 ligufalimab + cetuximab.