Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD33 CAR-T is an investigational chimeric antigen receptor (CAR) T-cell therapy developed by the Shenzhen Geno-Immune Medical Institute for the treatment of relapsed or refractory acute myeloid leukemia (AML). The therapy involves the genetic modification of a patient's T cells using a lentiviral vector to express a CAR that specifically recognizes CD33 (also known as Siglec-3), a transmembrane glycoprotein highly expressed on the surface of AML blasts and myeloid progenitors. Upon intravenous infusion, these engineered T cells bind to CD33-positive cells, triggering T-cell activation and subsequent lysis of the leukemic cells. In clinical trials, this therapy is often evaluated as part of a multi-target strategy, combined with other CAR-T products targeting antigens like CLL-1 or CD123, to improve therapeutic efficacy and mitigate the risk of antigen-escape-mediated 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 CD33 CAR-T (Shenzhen Geno-Immune Medical Institute).