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 pembrolizumab and rituximab and is being investigated for the treatment of relapsed or refractory Waldenström's macroglobulinemia. Pembrolizumab is a humanized monoclonal antibody that functions as an immune checkpoint inhibitor by targeting the programmed death-1 (PD-1) receptor. By blocking the interaction between PD-1 and its ligands (PD-L1 and PD-L2), it prevents the inhibition of T-cell activity, thereby enhancing the immune system's ability to attack malignant cells. Rituximab is a chimeric monoclonal antibody directed against the CD20 antigen found on the surface of B-lymphocytes. It induces B-cell depletion through antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), and apoptosis. The combination is currently being evaluated in the Phase II PembroWM trial led by University College London, marking the first investigation of checkpoint inhibition in this specific disease context.
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 pembrolizumab + rituximab.