Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Purtolimab (HX008) is a humanized monoclonal antibody targeting the programmed cell death protein 1 (PD-1) receptor. Developed by Lepu Biopharma, it acts as an immune checkpoint inhibitor by blocking the interaction between PD-1 and its ligands, PD-L1 and PD-L2. This blockade prevents the inhibitory signaling that typically suppresses T-cell activity in the tumor microenvironment, thereby restoring the immune system's ability to identify and destroy cancer cells. Purtolimab is approved in China for the treatment of patients with unresectable or metastatic melanoma who have failed previous systemic therapy, as well as for patients with advanced solid tumors that are microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) who have progressed following prior treatment.
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 purtolimab.