Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Anti-CD20-CAR-transduced T cells are genetically engineered autologous or allogeneic human T lymphocytes that express a chimeric antigen receptor (CAR) specific for the B-cell surface protein CD20. The CAR construct typically consists of an extracellular single-chain variable fragment (scFv) derived from an anti-CD20 monoclonal antibody (such as Leu16), fused to intracellular signaling domains like 4-1BB and CD3ζ. These modified T cells recognize and kill malignant or pathogenic B-cells expressing CD20 through direct cytotoxicity and cytokine release. Anti-CD20-CAR-transduced T cell therapy is being developed primarily for the treatment of relapsed or refractory B-cell malignancies such as non-Hodgkin lymphoma and chronic lymphocytic leukemia, as well as being explored in solid tumors like melanoma where a subset of tumor stem-like cells express CD20[2][4][5][6]. The product can be manufactured using lentiviral transduction methods in either autologous or allogeneic settings.
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 anti-CD20-CAR-transduced T cells.