Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CC-292 + rituximab is an investigational combination therapy evaluated for relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma. CC-292 (also known as AVL-292) is a potent, selective, covalent Bruton tyrosine kinase (BTK) inhibitor administered orally. Rituximab is an anti-CD20 monoclonal antibody targeting B lymphocytes. The combination is designed to synergistically inhibit B-cell receptor signaling and deplete malignant B cells. In phase 1 clinical studies, the doublet showed increased toxicity and insufficient efficacy improvement compared to other regimens. - CC-292 (AVL-292): small molecule, irreversible BTK inhibitor disrupting B-cell survival/proliferation - Rituximab: anti-CD20 chimeric monoclonal antibody mediating B-cell lysis via antibody-dependent cellular cytotoxicity and complement activation Developed for hematologic malignancies, particularly DLBCL and follicular lymphoma, the combination was investigated in a multicenter, phase Ib, dose-escalation trial (NCT02031419) but was not advanced due to safety/efficacy profile[1][2][3][4].
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 CC-292 + rituximab.