Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The combination of **acalabrutinib + obinutuzumab + venetoclax** is an investigational regimen combining three agents for the treatment of chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL)[1][3][4][5]. - **Acalabrutinib** is a second-generation small molecule inhibitor of Bruton's tyrosine kinase (BTK), which disrupts B-cell receptor signaling, inhibiting malignant B-cell growth and survival. - **Obinutuzumab** is a glycoengineered type II anti-CD20 monoclonal antibody that targets CD20 on B cells, mediating direct cell death and antibody-dependent cellular cytotoxicity. - **Venetoclax** is a selective inhibitor of the anti-apoptotic protein BCL2, inducing apoptosis specifically in B-cell malignancies. The combination is intended to achieve deep and durable remissions (including undetectable minimal residual disease, uMRD) by synergistically combining BCR signaling inhibition, immune-mediated cytotoxicity, and apoptosis induction. This regimen is being studied in both relapsed/refractory and treatment-naive CLL patients[1][3][4][5]. It is not approved by major regulatory bodies for routine clinical use as a triple regimen, but individual agents and doublets have received approvals.
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 + obinutuzumab + venetoclax.