Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Nivolumab + lirilumab is a combination of two monoclonal antibodies used in cancer immunotherapy. Nivolumab is an immune checkpoint inhibitor that targets the programmed cell death protein 1 (PD-1) receptor on T cells, blocking its interaction with PD-L1 and PD-L2 ligands, thereby enhancing T-cell-mediated anti-tumor responses[3][8]. Lirilumab targets killer-cell immunoglobulin-like receptors (KIRs) on natural killer (NK) cells, blocking inhibitory signals from HLA-C ligands and promoting NK cell activation and tumor cell killing[6]. This combination has been investigated in clinical trials for squamous cell carcinoma of the head and neck, showing enhanced objective response rates compared to nivolumab alone[5]. Nivolumab was developed by Bristol Myers Squibb; lirilumab was developed by Innate Pharma.
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 nivolumab + lirilumab.