Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Nadunolimab + mFOLFOX is an investigational combination regimen comprising nadunolimab, a human monoclonal antibody targeting Interleukin-1 Receptor Accessory Protein (IL1RAP), and mFOLFOX, a modified standard-of-care chemotherapy regimen. - Nadunolimab (CAN04) inhibits IL1RAP, thereby blocking IL-1 mediated pro-inflammatory signaling critical for tumor progression and the tumor microenvironment. - mFOLFOX is a chemotherapy regimen that combines folinic acid (leucovorin), fluorouracil (5-FU), and oxaliplatin. These agents exert cytotoxic effects by interfering with DNA synthesis and repair in dividing tumor cells. This combination has shown early evidence of anti-tumor activity and a potential to reduce chemotherapy-induced peripheral neuropathy (CIPN), representing a possible dual benefit for patients, particularly in advanced pancreatic ductal adenocarcinoma (PDAC) and potentially other solid tumors. Clinical development is ongoing to validate efficacy and neuroprotection[1][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 nadunolimab + mFOLFOX.