Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Cadonilimab is a first-in-class, humanized IgG1 tetrameric bispecific monoclonal antibody that targets both programmed cell death protein 1 (PD-1) and cytotoxic T lymphocyte antigen 4 (CTLA-4). By binding to PD-1 and CTLA-4 on tumor-infiltrating T lymphocytes, cadonilimab blocks their interaction with respective ligands (PD-L1/PD-L2 for PD-1; B7.1/B7.2 for CTLA‑4), thereby inhibiting immunosuppressive signaling pathways and promoting the activation of tumor-specific T-cell immunity. Its Fc-null design reduces cellular phagocytosis and antibody-mediated toxicity compared to traditional combination checkpoint blockade, resulting in improved efficacy with lower toxicity. Cadonilimab has demonstrated clinical benefit across multiple solid tumors, including cervical cancer and gastric cancer, where it is approved or under regulatory review. It is being investigated in numerous other cancers as monotherapy or in combination regimens[3][5][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 cadonilimab.