Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**eprenetapopt + venetoclax + rituximab** is a combination therapy studied primarily for relapsed or refractory hematologic malignancies, particularly chronic lymphocytic leukemia (CLL) and other lymphoid cancers. - **Eprenetapopt (APR-246, PRIMA-1MET)** is a small molecule that restores the normal function of mutant p53 protein, inducing cancer cell apoptosis. - **Venetoclax (ABT-199, Venclexta)** is a small molecule inhibitor of B-cell lymphoma-2 (BCL-2), promoting programmed cell death in malignant lymphocytes. - **Rituximab (IDEC-C2B8, Rituxan)** is a monoclonal antibody targeting CD20 on B cells, leading to immune-mediated B cell depletion. This combination aims to synergistically induce apoptosis in malignant B cells by targeting different apoptotic pathways and surface antigens. Eprenetapopt is being developed by Aprea Therapeutics, venetoclax by AbbVie/Genentech, and rituximab by Roche/Genentech/Biogen. The combination is under clinical investigation, and current development in the US is on *clinical hold* due to pending data and safety review by the FDA. In at least one reported CLL patient treated with this combination, a complete remission was achieved[2][7].
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 eprenetapopt + venetoclax + rituximab.