Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BGB-16673 + mosunetuzumab is a combination of two agents under investigation for B-cell malignancies. **BGB-16673** is an orally available, small-molecule chimeric degradation activation compound that targets and degrades Bruton's tyrosine kinase (BTK), disrupting B-cell receptor signaling and overcoming resistance due to BTK mutations[4][7]. **Mosunetuzumab** is a humanized, bispecific monoclonal antibody that binds CD20 (on B cells) and CD3 (on T cells), redirecting T-cell cytotoxicity toward malignant B cells[2][5]. The drugs are in clinical trial settings for relapsed or refractory B-cell lymphomas, including chronic lymphocytic leukemia (CLL), Waldenström macroglobulinemia (WM), and follicular lymphoma. Mosunetuzumab is already approved as monotherapy for relapsed or refractory follicular lymphoma after two prior therapies[2][5].
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 BGB-16673 + mosunetuzumab.