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The Aastrom experience
Aastrom Biosciences has developed a proprietary cell-processing technology that enables the manufacture of ixmyelocel-T, a patient-specific multicellular therapy expanded from a small sample of a patient's own bone marrow. Ixmyelocel-T is produced under current good manufacturing practices (cGM...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580464/ https://www.ncbi.nlm.nih.gov/pubmed/22776246 http://dx.doi.org/10.1186/scrt117 |
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author | Bartel, Ronnda L Cramer, Caryn Ledford, Kelly Longcore, Amy Parrish, Christopher Stern, Theresa Watling, Sharon Zeigler, Frank |
author_facet | Bartel, Ronnda L Cramer, Caryn Ledford, Kelly Longcore, Amy Parrish, Christopher Stern, Theresa Watling, Sharon Zeigler, Frank |
author_sort | Bartel, Ronnda L |
collection | PubMed |
description | Aastrom Biosciences has developed a proprietary cell-processing technology that enables the manufacture of ixmyelocel-T, a patient-specific multicellular therapy expanded from a small sample of a patient's own bone marrow. Ixmyelocel-T is produced under current good manufacturing practices (cGMP) in a fully closed, automated system that expands mesenchymal stem cells (MSCs) and macrophages. While the cell types in ixmyelocel-T are the same as those found in the bone marrow, the numbers of MSCs and alternative macrophages are greater in ixmyelocel-T. We propose that the mixture of expanded MSCs and alternatively activated macrophages promote long-term tissue repair of ischemic tissue. The multiple cell types in ixmyelocel-T have a range of biological activities that are likely to contribute to a complex mechanism of action. Clinical trial data collected to date support the potential for ixmyelocel-T as an efficacious and safe treatment for ischemic cardiovascular indications, including critical limb ischemia (CLI) and a severe form of heart failure, dilated cardiomyopathy (DCM). The CLI clinical program has completed phase 2 and has reached concurrence with the Food and Drug Administration (FDA) on a phase 3 study (REVIVE) through the Special Protocol Assessment (SPA) process. The phase 3 study began screening patients in February 2012. The DCM clinical program will initiate phase 2b in 2012. |
format | Online Article Text |
id | pubmed-3580464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35804642013-07-09 The Aastrom experience Bartel, Ronnda L Cramer, Caryn Ledford, Kelly Longcore, Amy Parrish, Christopher Stern, Theresa Watling, Sharon Zeigler, Frank Stem Cell Res Ther Review Aastrom Biosciences has developed a proprietary cell-processing technology that enables the manufacture of ixmyelocel-T, a patient-specific multicellular therapy expanded from a small sample of a patient's own bone marrow. Ixmyelocel-T is produced under current good manufacturing practices (cGMP) in a fully closed, automated system that expands mesenchymal stem cells (MSCs) and macrophages. While the cell types in ixmyelocel-T are the same as those found in the bone marrow, the numbers of MSCs and alternative macrophages are greater in ixmyelocel-T. We propose that the mixture of expanded MSCs and alternatively activated macrophages promote long-term tissue repair of ischemic tissue. The multiple cell types in ixmyelocel-T have a range of biological activities that are likely to contribute to a complex mechanism of action. Clinical trial data collected to date support the potential for ixmyelocel-T as an efficacious and safe treatment for ischemic cardiovascular indications, including critical limb ischemia (CLI) and a severe form of heart failure, dilated cardiomyopathy (DCM). The CLI clinical program has completed phase 2 and has reached concurrence with the Food and Drug Administration (FDA) on a phase 3 study (REVIVE) through the Special Protocol Assessment (SPA) process. The phase 3 study began screening patients in February 2012. The DCM clinical program will initiate phase 2b in 2012. BioMed Central 2012-07-09 /pmc/articles/PMC3580464/ /pubmed/22776246 http://dx.doi.org/10.1186/scrt117 Text en Copyright ©2012 BioMed Central Ltd |
spellingShingle | Review Bartel, Ronnda L Cramer, Caryn Ledford, Kelly Longcore, Amy Parrish, Christopher Stern, Theresa Watling, Sharon Zeigler, Frank The Aastrom experience |
title | The Aastrom experience |
title_full | The Aastrom experience |
title_fullStr | The Aastrom experience |
title_full_unstemmed | The Aastrom experience |
title_short | The Aastrom experience |
title_sort | aastrom experience |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580464/ https://www.ncbi.nlm.nih.gov/pubmed/22776246 http://dx.doi.org/10.1186/scrt117 |
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