Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SLAMF-7 BBz CAR is a second-generation chimeric antigen receptor (CAR) T-cell therapy designed to target Signaling Lymphocytic Activation Molecule Family member 7 (SLAMF7), also known as CS1 or CD319. The construct consists of an extracellular single-chain variable fragment (scFv) specific for SLAMF7, linked to a 4-1BB (CD137) costimulatory domain and a CD3-zeta signaling subunit. SLAMF7 is a surface glycoprotein highly expressed on malignant plasma cells in multiple myeloma, as well as on natural killer (NK) cells and some activated T cells. By redirecting T cells to recognize SLAMF7, this therapy facilitates the targeted destruction of myeloma cells. A significant challenge with SLAMF7-targeted CAR-T cells is fratricide (self-killing), as T cells can express the target; this is often addressed through gene editing to knock out endogenous SLAMF7 in the therapeutic T cells. In the context of current research, SLAMF-7 BBz CAR is frequently utilized as a standard benchmark for evaluating the efficacy of next-generation multispecific or hybrid receptor platforms.
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 SLAMF-7 BBz CAR.