Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
5E5-CD2z CAR T cells are an experimental chimeric antigen receptor (CAR) T-cell therapy designed to target the tumor-associated glycoform of Mucin 1 (Tn-MUC1), which is frequently overexpressed in various adenocarcinomas, including pancreatic cancer. The construct features the 5E5 scFv for high-specificity binding to the Tn-MUC1 epitope and incorporates a novel signaling architecture using the human CD2 cytoplasmic tail as a costimulatory domain in tandem with the CD3ζ activation motif. Developed by researchers at the University of Pennsylvania, this design aims to overcome the limitations of traditional CD28- or 4-1BB-based CARs by providing a balanced signaling profile that supports both rapid tumor debulking and sustained T-cell persistence. Preclinical evidence indicates that CD2 costimulation promotes an early effector-memory phenotype, enhances metabolic fitness through mTORC1 and glycolytic pathways, and reduces T-cell exhaustion, leading to superior in vivo tumor control in orthotopic pancreatic cancer models compared to standard second-generation CAR designs.
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 5E5-CD2z CAR T cells.