Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**SUV39H1-deficient (SJ25C1)1XX CAR-T cells** are an advanced chimeric antigen receptor (CAR) T-cell therapy where patient-derived T cells are genetically engineered to express the (SJ25C1)1XX CAR, targeting CD19 on B-cell malignancies, and additionally edited to knock out SUV39H1, a histone-3 lysine-9 methyltransferase. This epigenetic modification sustains stem/memory gene expression, enhances metabolic fitness (glycolysis and oxidative phosphorylation), promotes a memory phenotype, increases expansion after repeated stimulations, reduces inhibitory receptors like PD1 and TIM3, limits exhaustion, and improves long-term persistence and tumor rejection upon rechallenge in both hematologic (e.g., NALM-6 leukemia) and solid tumor (e.g., A549 lung) models. Developed through research at Institut Curie, it shows superior effector function compared to standard 4-1BB/CD3ζ CAR-T cells and supports planned clinical trials in liquid and solid cancers.[1][3][5]
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 SUV39H1-deficient (SJ25C1)1XX CAR-T cells.