Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This combination regimen, abbreviated as PD-1i+RMO, is a multi-agent therapeutic approach being investigated by The First Affiliated Hospital with Nanjing Medical University. It is specifically designed for patients with newly diagnosed primary central nervous system lymphoma (ND-PCNSL) and secondary central nervous system lymphoma (SCNSL). The regimen integrates four distinct therapeutic modalities: a PD-1 inhibitor (a monoclonal antibody that blocks the PD-1/PD-L1 pathway to restore T-cell mediated anti-tumor immunity), rituximab (a chimeric monoclonal antibody targeting the CD20 antigen on B-lymphocytes), methotrexate (a high-dose antimetabolite chemotherapy that penetrates the blood-brain barrier), and orelabrutinib (a highly selective, second-generation Bruton's tyrosine kinase inhibitor). By combining immune checkpoint inhibition with targeted B-cell depletion and cytotoxic chemotherapy, the regimen aims to improve complete response rates and progression-free survival in aggressive CNS-localized B-cell malignancies.
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 PD-1 inhibitor + rituximab + methotrexate + orelabrutinib.