Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CS1 chimeric antigen receptor T-cell therapy is an autologous cell therapy targeting the CS1 (also known as SLAMF7 or CD319) antigen. CS1 is a cell surface glycoprotein that is highly and consistently expressed on malignant plasma cells in multiple myeloma, while its expression on normal tissues is restricted to natural killer cells, some subsets of T cells, and mature B cells. The therapy involves the genetic modification of a patient's own T cells to express a chimeric antigen receptor (CAR) specific for CS1, enabling the T cells to recognize and eliminate CS1-expressing tumor cells. This specific clinical program, led by Tongji Hospital of Huazhong University of Science and Technology, is investigating the safety and efficacy of CS1 CAR-T cells in patients with relapsed or refractory CS1-positive hematological malignancies, including multiple myeloma, systemic light-chain amyloidosis, and POEMS syndrome.
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 CS1 chimeric antigen receptor T-cell.