| Literature DB >> 20589167 |
Giuseppe Astori1, Sabrina Soncin, Viviana Lo Cicero, Francesco Siclari, Daniel Sürder, Lucia Turchetto, Gianni Soldati, Tiziano Moccetti.
Abstract
Bone marrow derived stem cells administered after minimal manipulation represent an important cell source for cell-based therapies. Clinical trial results, have revealed both safety and efficacy of the cell reinfusion procedure in many cardiovascular diseases. Many of these early clinical trials were performed in a period before the entry into force of the US and European regulation on cell-based therapies. As a result, conflicting data have been generated on the effectiveness of those therapies in certain conditions as acute myocardial infarction. As more academic medical centers and private companies move toward exploiting the full potential of cell-based medicinal products, needs arise for the development of the infrastructure necessary to support these investigations. This review describes the regulatory environment surrounding the production of cell based medicinal products and give practical aspects for cell isolation, characterization, production following Good Manufacturing Practice, focusing on the activities associated with the investigational new drug development.Entities:
Keywords: Acute Myocardial Infarction; Advanced Therapy Medicinal Products; Cell Factory; Good Manufacturing Practice; Peripheral Vascular Disease; Stem Cells
Year: 2010 PMID: 20589167 PMCID: PMC2892405
Source DB: PubMed Journal: Am J Transl Res ISSN: 1943-8141 Impact factor: 4.060