Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
uCD7 chimeric antigen receptor T cells represent an advanced form of immunotherapy, specifically a cell and gene therapy, designed to combat CD7-positive malignancies and potentially autoimmune diseases. This therapy involves genetically engineering a patient's or a healthy donor's T cells to express a chimeric antigen receptor (CAR) that precisely targets the CD7 protein, a cell surface marker prevalent on malignant T cells in conditions like T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) and certain acute myeloid leukemia (AML) cases, as well as on normal T and NK cells. A critical challenge in developing CD7-targeting CAR T cells is preventing "fratricide," where the engineered T cells attack each other due to their own CD7 expression. This is overcome through genetic modifications, such as CRISPR/Cas9 or base editing, to knock out CD7 expression in the CAR T cells, rendering them fratricide-resistant. These modified T cells are then expanded ex vivo and infused into the patient, where they recognize and eliminate CD7-expressing cancer cells through T-cell mediated cytotoxicity. The goal is to provide an "off-the-shelf" allogeneic treatment option, reducing manufacturing complexities and improving accessibility.
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 uCD7 chimeric antigen receptor T cells.