Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Sitrelimab (HMPL-309) is a humanized IgG1 monoclonal antibody that targets programmed death-ligand 1 (PD-L1). Developed by HUTCHMED, it is designed to block the interaction between PD-L1 and its receptors, programmed cell death protein 1 (PD-1) and B7.1 (CD80). By inhibiting this checkpoint pathway, sitrelimab aims to restore and enhance T-cell-mediated anti-tumor immune responses, which are often suppressed in the tumor microenvironment. The drug has been investigated in Phase 1 clinical trials, specifically in China, for the treatment of patients with advanced malignant solid tumors to evaluate its safety, pharmacokinetics, and preliminary efficacy.
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 sitrelimab.