Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD138-specific CAR T cells are genetically engineered autologous T cells that express a chimeric antigen receptor (CAR) targeting CD138, a transmembrane proteoglycan (syndecan-1) highly expressed on both normal and malignant plasma cells, especially in multiple myeloma (MM). The CAR is typically constructed using a single-chain variable fragment (scFv) derived from an anti-CD138 antibody (for example, derived from BT062) fused to T cell signaling domains like CD3ζ and costimulatory domains such as CD28 or 4-1BB. Upon binding CD138 on myeloma cells, these CAR T cells become activated and mediate targeted cytotoxicity leading to tumor cell lysis. This immunotherapy shows promise for relapsed/refractory MM, with early-phase trials demonstrating manageable toxicity and signs of efficacy, although risks include antigen escape due to CD138 downregulation and on-target, off-tumor toxicity. CD138-specific CAR T cell therapy is under development in academic and clinical research settings for MM and being studied as monotherapy and in combination with other targets such as BCMA[1][3][4][6][7].
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 CD138-specific CAR T cells.