Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
CD7-CART is a Chimeric Antigen Receptor (CAR) T-cell therapy designed to treat CD7-positive hematological malignancies. This therapy involves genetically engineering a patient's (autologous) or a donor's (allogeneic) T-cells to express a CAR that specifically targets the CD7 protein, a transmembrane glycoprotein highly expressed in over 95% of T-cell acute lymphoblastic leukemia (T-ALL) and T-lymphoblastic lymphoma (T-LBL) cells, as well as in a subset of peripheral T-cell lymphomas and natural killer (NK) cells. A significant challenge in developing CD7-CART is preventing "fratricide," where the CAR-T cells, which also express CD7, attack each other. To overcome this, various strategies are employed, such as genetic deletion of the CD7 gene in the CAR-T cells (e.g., using CRISPR/Cas9) or utilizing protein expression blockers (PEBL) to prevent CD7 from being expressed on the CAR-T cell surface. Once re-infused into the patient, these engineered T-cells are designed to seek out and destroy CD7-expressing cancer cells.
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 CD7-CART.