Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is a combination regimen consisting of **BGB-A445** (a humanized IgG1 monoclonal antibody agonist of OX40), **tislelizumab** (a humanized IgG4 anti-PD-1 monoclonal antibody), and standard **chemotherapy** (agents such as cisplatin, gemcitabine, or docetaxel—exact chemotherapy varies by trial). BGB-A445 activates OX40 (TNFRSF4) on T cells, promoting T cell survival, proliferation, and depleting regulatory T cells via ADCC. Tislelizumab blocks the PD-1 immune checkpoint, enhancing T cell antitumor activity. The regimen is under investigation for advanced solid tumors, especially nasopharyngeal carcinoma (NPC), non-small cell lung cancer (NSCLC), and head and neck squamous cell carcinoma (HNSCC). It is being developed and studied primarily by BeiGene. Early clinical data show the triple regimen is generally well tolerated and has preliminary antitumor activity, particularly in advanced NPC, NSCLC, and HNSCC.[1][3][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 BGB-A445 + tislelizumab + chemotherapy.