Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
c-Met + CD3 (also referred to as BS001) is a bispecific antibody (BsAb) designed to simultaneously target the c-Met receptor tyrosine kinase and the CD3 T-cell surface marker. Developed by researchers associated with RemeGen, this therapeutic candidate employs a dual mechanism of action: it redirects T-cell cytotoxicity to c-Met-overexpressing tumor cells by bridging the two cell types, and it acts as a c-Met antagonist by blocking the interaction between Hepatocyte Growth Factor (HGF) and c-Met. This blockade inhibits c-Met phosphorylation and downstream oncogenic signaling. The antibody incorporates a human IgG1 Fc region to enhance its pharmacokinetic profile and extend its circulatory half-life. Preclinical evidence has demonstrated its efficacy in inducing T cell-mediated killing of tumor cells in models of lung adenocarcinoma (LUAD), lung squamous cell carcinoma (LUSC), and ovarian cancer.
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 c-Met + CD3.