Preclinical quality, safety, and efficacy of a human embryonic stem cell-derived product for the treatment of Parkinson's disease, STEM-PD

التفاصيل البيبلوغرافية
العنوان: Preclinical quality, safety, and efficacy of a human embryonic stem cell-derived product for the treatment of Parkinson's disease, STEM-PD
المؤلفون: Kirkeby, Agnete, Nelander, Jenny, Hoban, Deirdre B., Rogelius, Nina, Bjartmarz, Hjálmar, Storm, Petter, Fiorenzano, Alessandro, Adler, Andrew F., Vale, Shelby, Mudannayake, Janitha, Zhang, Yu, Cardoso, Tiago, Mattsson, Bengt, Landau, Anne M., Glud, Andreas N., Sørensen, Jens C., Lillethorup, Thea P., Lowdell, Mark, Carvalho, Carla, Bain, Owen, van Vliet, Trinette, Lindvall, Olle, Björklund, Anders, Harry, Bronwen, Cutting, Emma, Widner, Håkan, Paul, Gesine, Barker, Roger A., Parmar, Malin
المصدر: Cell Stem Cell StemTherapy: National Initiative on Stem Cells for Regenerative Therapy MultiPark: Multidisciplinary research focused on Parkinson´s disease. 30(10):1299-1314
مصطلحات موضوعية: ATMP, clinical trial, dopamine, minipig, neurosurgery, neurosurgical, Parkinson's, pluripotent, regulatory, stem cell therapy, transplantation, Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology
الوصف: Cell replacement therapies for Parkinson's disease (PD) based on transplantation of pluripotent stem cell-derived dopaminergic neurons are now entering clinical trials. Here, we present quality, safety, and efficacy data supporting the first-in-human STEM-PD phase I/IIa clinical trial along with the trial design. The STEM-PD product was manufactured under GMP and quality tested in vitro and in vivo to meet regulatory requirements. Importantly, no adverse effects were observed upon testing of the product in a 39-week rat GLP safety study for toxicity, tumorigenicity, and biodistribution, and a non-GLP efficacy study confirmed that the transplanted cells mediated full functional recovery in a pre-clinical rat model of PD. We further observed highly comparable efficacy results between two different GMP batches, verifying that the product can be serially manufactured. A fully in vivo-tested batch of STEM-PD is now being used in a clinical trial of 8 patients with moderate PD, initiated in 2022.
URL الوصول: https://lup.lub.lu.se/record/c071c5b6-e718-44d9-b75e-68e25cdd16f7
http://dx.doi.org/10.1016/j.stem.2023.08.014
قاعدة البيانات: SwePub
الوصف
تدمد:19345909
DOI:10.1016/j.stem.2023.08.014