Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD19 t-haNK + rituximab is an investigational combination immunotherapy for relapsed or refractory B-cell non-Hodgkin lymphoma (NHL) and Waldenstrom macroglobulinemia. The therapy consists of two components: - **CD19 t-haNK**: an allogeneic, off-the-shelf, engineered natural killer (NK) cell line that expresses a CD19-specific chimeric antigen receptor (CAR) and a high-affinity CD16 (FcγRIIIa) receptor, enabling dual anti-tumor mechanisms: direct CAR-mediated cytotoxicity against CD19+ lymphoma cells and augmented antibody-dependent cellular cytotoxicity (ADCC) when combined with monoclonal antibodies[5]. - **Rituximab**: a monoclonal antibody targeting CD20, used as standard therapy for B-cell NHL and promoting tumor cell death both directly and via ADCC. In clinical trials, patients receive a cycle of CD19 t-haNK monotherapy followed by CD19 t-haNK in combination with rituximab, targeting both CD19+ and CD20+ lymphoma cells[1][4][5]. The combination aims to increase anti-lymphoma efficacy by leveraging both CAR-NK cytotoxicity and ADCC through antibody engagement.
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 CD19 t-haNK + rituximab.