Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
F520 (rulonilimab) is a recombinant humanized IgG1 kappa monoclonal antibody targeting the Programmed Cell Death Receptor-1 (PD-1), developed by Shandong New Time Pharmaceutical. It functions as an immune checkpoint inhibitor by blocking the PD-1 receptor, thereby preventing its interaction with PD-L1 and PD-L2 and stimulating T lymphocyte-mediated anti-tumor responses. In the specific combination 'F520 + chemotherapy,' rulonilimab is administered alongside paclitaxel (a microtubule stabilizer) and carboplatin (a DNA alkylating agent). This combination is primarily being investigated as a first-line treatment for cancer of unknown primary (CUP) in a Phase II/III clinical trial, as well as in other advanced solid tumors and hematological malignancies.
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 rulonilimab + chemotherapy.