Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SNAP-CAR T cells are a universal, programmable chimeric antigen receptor (CAR) T-cell therapy platform designed to overcome the limitations of conventional single-antigen-targeting CAR-T therapies. Developed by researchers at the University of Pittsburgh and licensed to Coeptis Therapeutics, the platform utilizes T cells engineered with a universal receptor containing an extracellular self-labeling SNAP-tag enzyme (a modified O6-alkylguanine-DNA alkyltransferase). Instead of directly binding to tumor antigens, these SNAP-CAR T cells are co-administered with tumor-targeting antibody adaptors (such as monoclonal antibodies) conjugated to a benzylguanine (BG) tag. Upon administration, the BG-tagged antibodies form a highly stable, covalent bio-orthogonal bond with the SNAP-tag on the CAR-T cells, effectively fusing the targeting antibody to the T cell. This modular design allows for tunable dosing to control toxicity, simultaneous or sequential targeting of multiple tumor antigens (such as HER2, CD20, and EGFR) to prevent antigen-escape relapse, and applicability across various hematological and solid tumor malignancies.
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 SNAP-CAR T cells.