Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Penpulimab is a humanized IgG1 monoclonal antibody that targets the programmed cell death 1 (PD-1) receptor on T cells, blocking its interaction with PD-L1 and PD-L2. This blockade restores T-cell-mediated immune responses against tumor cells, enhancing antitumor immunity. Penpulimab is engineered with Fc region modifications to eliminate Fcγ receptor binding and Fc-mediated effector functions, reducing the risk of immune-related adverse effects such as antibody-dependent cellular cytotoxicity (ADCC) or phagocytosis. It demonstrates a slower dissociation rate from PD-1 compared to other inhibitors, resulting in higher receptor occupancy and enhanced T-cell activity. Developed by Akeso Biopharma in collaboration with Chia Tai Tianqing Pharmaceutical Group, penpulimab is approved for relapsed or refractory classic Hodgkin's lymphoma, recurrent/metastatic nasopharyngeal cancer (NPC), and locally advanced/metastatic squamous non-small cell lung cancer (NSCLC). It is also under review for hepatocellular carcinoma and being studied in various other solid tumors.
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 penpulimab.