Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Zuberitamab (MIL62) is a glycoengineered, humanized Type II anti-CD20 monoclonal antibody developed by Beijing Mabworks Biotech. It is designed to target the CD20 antigen on the surface of B-cells with enhanced antibody-dependent cellular cytotoxicity (ADCC) and potent pro-apoptotic activity compared to first-generation anti-CD20 antibodies like rituximab. By utilizing a fucose-deficient glycoengineering approach, zuberitamab exhibits increased affinity for the FcγRIIIa receptor on effector cells, thereby augmenting its immune-mediated cell-killing capabilities. Zuberitamab is currently being evaluated in clinical trials for various B-cell malignancies, including mantle cell lymphoma, follicular lymphoma, and diffuse large B-cell lymphoma, as well as autoimmune conditions such as primary membranous nephropathy.
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 zuberitamab (Beijing Tianguangshi Pharmaceutical Technology).