Live30 webinars are thirty-minute presentations designed to update you on the latest innovations, applications, and data in a fast yet interactive format.
Discover the potential of transposon and genome editing technologies to develop next-generation, cost-effective single-domain antibody (sdAb) CAR-T therapies. This webinar will explore how non-viral delivery of CAR constructs using a transposon system enhances manufacturing efficiency, improves cell viability through optimized electroporation methods, and enables the creation of universal allogenic CAR-T cells. Attendees will gain insight into how combining genome editing tools such as CRIPSR/Cas9 and base editing with transposon systems supports the rapid, scalable production of therapeutic-grade CAR-T cells.
The speakers will demonstrate key pre-clinical findings showcasing the comparable in vitro and in vivo antitumor efficacy of transposon-based CAR-T cells relative to conventional CAR-T therapies. They will highlight the development of robust, GMP-compliant manufacturing protocols that have previously supported the initiation of clinical trials for patients with relapsed or refractory lymphoma. Lastly, they will delve into how a streamlined, one-step process for the generation of universal CAR-T cells can reduce costs and accelerate clinical translation, while maintaining potency and durability in hematological malignancy models.
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