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Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments
Finding new therapies for Parkinson’s disease (PD) is a slow process. We assembled an international committee of experts to examine drugs potentially suitable for repurposing to modify PD progression. This committee evaluated multiple drugs currently used, or being developed, in other therapeutic ar...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318242/ https://www.ncbi.nlm.nih.gov/pubmed/24018336 http://dx.doi.org/10.3233/JPD-139000 |
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author | Brundin, Patrik Barker, Roger A. Conn, P. Jeffrey Dawson, Ted M. Kieburtz, Karl Lees, Andrew J. Schwarzschild, Michael A. Tanner, Caroline M. Isaacs, Tom Duffen, Joy Matthews, Helen Wyse, Richard K.H. |
author_facet | Brundin, Patrik Barker, Roger A. Conn, P. Jeffrey Dawson, Ted M. Kieburtz, Karl Lees, Andrew J. Schwarzschild, Michael A. Tanner, Caroline M. Isaacs, Tom Duffen, Joy Matthews, Helen Wyse, Richard K.H. |
author_sort | Brundin, Patrik |
collection | PubMed |
description | Finding new therapies for Parkinson’s disease (PD) is a slow process. We assembled an international committee of experts to examine drugs potentially suitable for repurposing to modify PD progression. This committee evaluated multiple drugs currently used, or being developed, in other therapeutic areas, as well as considering several natural, non-pharmaceutical compounds. The committee prioritized which of these putative treatments were most suited to move immediately into pilot clinical trials. Aspects considered included known modes of action, safety, blood-brain-barrier penetration, preclinical data in animal models of PD and the possibility to monitor target engagement in the brain. Of the 26 potential interventions, 10 were considered worth moving forward into small, parallel ‘learning’ clinical trials in PD patients. These trials could be funded in a multitude of ways through support from industry, research grants and directed philanthropic donations. The committee-based approach to select the candidate compounds might help rapidly identify new potential PD treatment strategies for use in clinical trials. |
format | Online Article Text |
id | pubmed-4318242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-43182422015-02-05 Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments Brundin, Patrik Barker, Roger A. Conn, P. Jeffrey Dawson, Ted M. Kieburtz, Karl Lees, Andrew J. Schwarzschild, Michael A. Tanner, Caroline M. Isaacs, Tom Duffen, Joy Matthews, Helen Wyse, Richard K.H. J Parkinsons Dis Article Finding new therapies for Parkinson’s disease (PD) is a slow process. We assembled an international committee of experts to examine drugs potentially suitable for repurposing to modify PD progression. This committee evaluated multiple drugs currently used, or being developed, in other therapeutic areas, as well as considering several natural, non-pharmaceutical compounds. The committee prioritized which of these putative treatments were most suited to move immediately into pilot clinical trials. Aspects considered included known modes of action, safety, blood-brain-barrier penetration, preclinical data in animal models of PD and the possibility to monitor target engagement in the brain. Of the 26 potential interventions, 10 were considered worth moving forward into small, parallel ‘learning’ clinical trials in PD patients. These trials could be funded in a multitude of ways through support from industry, research grants and directed philanthropic donations. The committee-based approach to select the candidate compounds might help rapidly identify new potential PD treatment strategies for use in clinical trials. 2013-01-01 /pmc/articles/PMC4318242/ /pubmed/24018336 http://dx.doi.org/10.3233/JPD-139000 Text en © 2013 – IOS Press and the authors. All rights reserved http://creativecommons.org/licenses/by/3.0/ This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License. |
spellingShingle | Article Brundin, Patrik Barker, Roger A. Conn, P. Jeffrey Dawson, Ted M. Kieburtz, Karl Lees, Andrew J. Schwarzschild, Michael A. Tanner, Caroline M. Isaacs, Tom Duffen, Joy Matthews, Helen Wyse, Richard K.H. Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title | Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title_full | Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title_fullStr | Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title_full_unstemmed | Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title_short | Linked Clinical Trials – The Development of New Clinical Learning Studies in Parkinson’s Disease Using Screening of Multiple Prospective New Treatments |
title_sort | linked clinical trials – the development of new clinical learning studies in parkinson’s disease using screening of multiple prospective new treatments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318242/ https://www.ncbi.nlm.nih.gov/pubmed/24018336 http://dx.doi.org/10.3233/JPD-139000 |
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