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Clinical Trials associated with TranspoCART19(Instituto de Investigación Biomédica de Salamanca)Multicentre Phase I/IIa Study of Infusion of Autologous Peripheral Blood T Lymphocytes Expanded and Genetically Modified Using Sleeping Beauty Family Transposons to Express a Chimeric Antigenic Receptor With Anti-CD19 Specificity Conjugated to the 4-1BB Co-stimulatory Region and CD3z and huEGFRt Signal Transmission (TranspoCART19) in Patients With Relapsed or Refractory B-cell Lymphoma
The goal of this clinical trial is to to evaluate the safety and efficacy of TranspoCART19 in patients with relapsed/refractory B-lymphoma. The main questions it aims to answer are:
Maximum tolerated dose (MTD) Response rates Participants will be treated with the investigational medicinal product and will be followed for 36 months.
Phase I/IIa multicentre phase I/IIa study of infusion of autologous peripheral blood T lymphocytes expanded and genetically modified using Sleeping Beauty family transposons to express a chimeric antigenic receptor with anti-CD19 specificity conjugated to the 4-1BB co-stimulatory and signal-transduction region CD3z and huEGFRt (TranspoCART19) in patients with relapsed or refractory B-cell lymphoma.
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100 Clinical Results associated with TranspoCART19(Instituto de Investigación Biomédica de Salamanca)
100 Translational Medicine associated with TranspoCART19(Instituto de Investigación Biomédica de Salamanca)
100 Patents (Medical) associated with TranspoCART19(Instituto de Investigación Biomédica de Salamanca)
100 Deals associated with TranspoCART19(Instituto de Investigación Biomédica de Salamanca)