Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Anti-CD7 UCART is an allogeneic chimeric antigen receptor (CAR) T-cell therapy engineered to target CD7, a transmembrane glycoprotein highly expressed on the surface of malignant T cells and some acute myeloid leukemia (AML) cells. Upon administration, these genetically modified T cells specifically recognize and bind to CD7-expressing tumor cells, leading to targeted cytotoxicity and tumor cell lysis. Anti-CD7 CAR-T therapies are being developed primarily for hematologic malignancies such as relapsed or refractory T-cell acute lymphoblastic leukemia (T-ALL), other aggressive T-cell lymphomas, and AML with high CD7 expression. The approach leverages the immune system’s ability to selectively eliminate cancerous cells while sparing normal myeloid populations due to their lack of CD7 expression[1][2][4][5].
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 anti-CD7 UCART.