Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
4SCAR123 is a fourth-generation chimeric antigen receptor (CAR) T-cell therapy targeting CD123, developed by the Shenzhen Geno-Immune Medical Institute. It is designed for the treatment of various hematological malignancies, including B-cell malignancies and acute myeloid leukemia. The therapy utilizes a lentiviral vector to engineer autologous T cells to express a CAR construct featuring CD28 and CD27 costimulatory domains, a CD3ζ signaling domain, and an inducible caspase 9 (iCasp9) safety switch. This safety switch allows for the rapid elimination of the CAR-T cells using a small molecule dimerizer in the event of severe adverse toxicities, such as cytokine release syndrome. In clinical settings for B-cell malignancies, 4SCAR123 is frequently evaluated in combination with other CAR-T products, such as 4SCAR19, to address antigen escape and reduce the risk of CD19-negative relapse.
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 4SCAR123.