Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Y101D is a recombinant humanized bispecific antibody that simultaneously targets and inhibits both programmed death-ligand 1 (PD-L1) and transforming growth factor beta (TGF-β). By blocking these two immunosuppressive pathways, Y101D aims to enhance anti-tumor immune responses in the tumor microenvironment. Preclinical studies have shown that dual blockade of PD-L1 and TGF-β with agents like YM101 (a related molecule) can promote T cell infiltration into tumors, normalize the immune microenvironment, and produce superior anti-tumor effects compared to monotherapies targeting either pathway alone. The drug is being developed primarily for the treatment of advanced solid tumors including hepatocellular carcinoma and pancreatic cancer. It is under clinical investigation in China by Wuhan YZY Biopharma[1][3][4][5][8].
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 Y101D.