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Cartesian Therapeutics is developing circular RNA (circRNA) engineered CAR-T cells targeting B-cell maturation antigen (BCMA). This platform utilizes circular RNA templates to drive transient CAR expression in T cells, avoiding the permanent genomic modification associated with viral vectors. Circular RNA is inherently more stable than linear mRNA due to its resistance to exonucleolytic degradation, which results in more sustained CAR expression and enhanced therapeutic potency. Preclinical studies in multiple myeloma models have demonstrated that the circular RNA format allows for deeper tumor regression and improved pharmacokinetics compared to linear mRNA-based CAR-T cells (such as Descartes-08). The therapy is being explored for both oncology and autoimmune indications, such as myasthenia gravis, and does not require lymphodepletion.
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