Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
cd38 chimeric antigen receptor t cells + cs1 chimeric antigen receptor t cells refers to a dual-targeted cellular immunotherapy approach designed for the treatment of relapsed or refractory multiple myeloma. This therapy involves autologous T cells that are genetically engineered to express chimeric antigen receptors (CARs) specific for two distinct antigens highly expressed on malignant plasma cells: CD38 and CS1 (also known as SLAMF7 or CD319). CD38 is a transmembrane glycoprotein with ectoenzymatic activity, while CS1 is a member of the Signaling Lymphocyte Activation Molecule (SLAM) family. By targeting both antigens simultaneously—either through the use of a single T cell expressing both receptors (dual/bispecific CAR) or a cocktail of separate CAR-T products—the therapy aims to enhance tumor recognition and prevent immune escape, which frequently occurs through the downregulation of a single target antigen. Clinical development is primarily centered in academic institutions and specialized biotech firms in China, demonstrating promising results in achieving deep clinical responses in patients with advanced plasma cell malignancies.
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 cd38 chimeric antigen receptor t cells + cs1 chimeric antigen receptor t cells.