Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination therapy consists of the PD-1 inhibitor tislelizumab and water-filtered infrared A (WIRA) whole-body hyperthermia. Tislelizumab is a humanized IgG4 monoclonal antibody developed by BeiGene that binds to the Programmed cell death protein 1 (PD-1) receptor, blocking its interaction with PD-L1 and PD-L2 to enhance anti-tumor immune responses. In this specific regimen, WIRA whole-body hyperthermia (using the HECKEL 3000MT-4T device) is employed as a sensitizing agent to modulate the tumor microenvironment and improve the efficacy of immune checkpoint inhibition. This approach is particularly targeted at advanced gastrointestinal tumors with a microsatellite-stable (MSS) or proficient mismatch repair (pMMR) phenotype, which typically show poor responses to monotherapy with checkpoint inhibitors. The regimen is currently being evaluated in a Phase 2 clinical trial led by Pengyuan Liu.
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 tislelizumab + water-filtered infrared A whole-body hyperthermia.