Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lesabelimab (BC-003) is a human monoclonal antibody targeting programmed death-ligand 1 (PD-L1), developed by Dragonboat Biopharmaceutical, a subsidiary of Guilin Sanjin Pharmaceutical. By binding to PD-L1, lesabelimab prevents its interaction with the PD-1 receptor on T cells, thereby inhibiting the immunosuppressive signaling that allows tumors to evade the immune system. It is currently under clinical investigation in Phase I and Phase II trials for the treatment of various advanced malignant solid tumors, including squamous cell carcinomas of the head and neck, esophagus, and penis, as well as lymphoma and several types of gynecological and urological cancers.
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 lesabelimab.