Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Acalabrutinib + rituximab + lenalidomide is a combination regimen for treating relapsed or refractory B-cell non-Hodgkin lymphoma, including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL)[1][3][4][5]. - **Acalabrutinib** is a second-generation Bruton tyrosine kinase (BTK) inhibitor that selectively inhibits BTK, blocking B-cell receptor signaling and downstream pathways critical for lymphoma cell survival and proliferation. - **Rituximab** is a monoclonal antibody targeting CD20 on B cells, inducing cell death via direct apoptosis, antibody-dependent cell-mediated cytotoxicity (ADCC), and complement-dependent cytotoxicity (CDC). - **Lenalidomide** is an immunomodulatory drug that exerts antitumor activity by enhancing immune responses, inhibiting angiogenesis, and direct cytotoxic effects on lymphoma cells. This combination, sometimes referred to as the R2A regimen, has shown potential synergism by combining complementary mechanisms: BTK pathway blockade, CD20-directed immunotherapy, and immunomodulation, with clinical studies reporting promising efficacy and manageable toxicity, particularly in relapsed/refractory aggressive B-cell lymphomas[1][3].
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 acalabrutinib + rituximab + lenalidomide.