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 is a chemoimmunotherapy approach being evaluated for the treatment of relapsed or refractory aggressive non-Hodgkin lymphoma (NHL). The therapy involves the administration of an FDA-approved anti-CD19 chimeric antigen receptor (CAR) T-cell therapy followed by a consolidation phase using mosunetuzumab and polatuzumab vedotin. Polatuzumab vedotin is an antibody-drug conjugate (ADC) targeting CD79b that delivers the cytotoxic microtubule inhibitor monomethyl auristatin E (MMAE) directly to B cells. Mosunetuzumab is a bispecific monoclonal antibody that targets both CD20 on B cells and CD3 on T cells, facilitating T-cell mediated killing of malignant B cells. The anti-CD19 CAR-T therapy provides a direct cellular immune response against CD19-expressing lymphoma cells. This multi-targeted approach aims to improve durable response rates in patients who have failed prior lines of therapy.
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 anti-CD19 CAR-T therapy + mosunetuzumab + polatuzumab vedotin.