Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
UCARTCLL1 is an allogeneic, "off-the-shelf" chimeric antigen receptor (CAR) T-cell therapy candidate developed by Cellectis. It is engineered to target C-type lectin-like molecule 1 (CLL1, also known as CLEC12A), a cell surface antigen highly expressed on leukemic stem cells and myeloid blasts in acute myeloid leukemia (AML), while being absent on healthy hematopoietic stem cells. Unlike traditional autologous CAR-T therapies, UCARTCLL1 is derived from healthy donor T-cells. It utilizes TALEN gene-editing technology to knock out the T-cell receptor alpha constant (TRAC) gene to minimize the risk of graft-versus-host disease (GvHD) and the CD52 gene to enable the use of anti-CD52 antibodies for selective lymphodepletion. The primary indication is relapsed or refractory AML.
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 UCARTCLL1.