Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination regimen including **encorafenib**, a BRAF kinase inhibitor; **binimetinib**, a MEK kinase inhibitor; and **nivolumab**, an immune checkpoint inhibitor (PD-1 inhibitor). Encorafenib targets BRAF V600E/K mutant proteins in malignant cells, blocking cell proliferation driven by aberrant MAPK signaling. Binimetinib inhibits MEK1/2, further suppressing the MAPK/ERK signaling axis. Nivolumab is a human monoclonal antibody that binds PD-1 on T cells, preventing its interaction with PD-L1/PD-L2, thereby enhancing anti-tumor immune responses. This triple combination is under investigation for patients with advanced or metastatic melanoma with BRAF V600E or V600K mutations, aiming to leverage both targeted therapy against the MAPK pathway and immunotherapy to achieve deeper and more durable clinical responses[4][5][6][7].
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 encorafenib + binimetinib + nivolumab.