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Best Practices in Fragile X Syndrome Treatment Development

Preclinical studies using animal models of fragile X syndrome have yielded several agents that rescue a wide variety of phenotypes. However, translation of these treatments to humans with the disorder has not yet been successful, shedding light on a variety of limitations with both animal models and...

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Autores principales: Erickson, Craig A., Kaufmann, Walter E., Budimirovic, Dejan B., Lachiewicz, Ave, Haas-Givler, Barbara, Miller, Robert M., Weber, Jayne Dixon, Abbeduto, Leonard, Hessl, David, Hagerman, Randi J., Berry-Kravis, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315698/
https://www.ncbi.nlm.nih.gov/pubmed/30558274
http://dx.doi.org/10.3390/brainsci8120224
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author Erickson, Craig A.
Kaufmann, Walter E.
Budimirovic, Dejan B.
Lachiewicz, Ave
Haas-Givler, Barbara
Miller, Robert M.
Weber, Jayne Dixon
Abbeduto, Leonard
Hessl, David
Hagerman, Randi J.
Berry-Kravis, Elizabeth
author_facet Erickson, Craig A.
Kaufmann, Walter E.
Budimirovic, Dejan B.
Lachiewicz, Ave
Haas-Givler, Barbara
Miller, Robert M.
Weber, Jayne Dixon
Abbeduto, Leonard
Hessl, David
Hagerman, Randi J.
Berry-Kravis, Elizabeth
author_sort Erickson, Craig A.
collection PubMed
description Preclinical studies using animal models of fragile X syndrome have yielded several agents that rescue a wide variety of phenotypes. However, translation of these treatments to humans with the disorder has not yet been successful, shedding light on a variety of limitations with both animal models and human trial design. As members of the Clinical Trials Committee of the National Fragile X Foundation, we have discussed a variety of recommendations at the level of preclinical development, transition from preclinical to human projects, family involvement, and multi-site trial planning. Our recommendations are made with the vision that effective new treatment will lie at the intersection of innovation, rigorous and reproducible research, and stakeholder involvement.
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spelling pubmed-63156982019-01-11 Best Practices in Fragile X Syndrome Treatment Development Erickson, Craig A. Kaufmann, Walter E. Budimirovic, Dejan B. Lachiewicz, Ave Haas-Givler, Barbara Miller, Robert M. Weber, Jayne Dixon Abbeduto, Leonard Hessl, David Hagerman, Randi J. Berry-Kravis, Elizabeth Brain Sci Commentary Preclinical studies using animal models of fragile X syndrome have yielded several agents that rescue a wide variety of phenotypes. However, translation of these treatments to humans with the disorder has not yet been successful, shedding light on a variety of limitations with both animal models and human trial design. As members of the Clinical Trials Committee of the National Fragile X Foundation, we have discussed a variety of recommendations at the level of preclinical development, transition from preclinical to human projects, family involvement, and multi-site trial planning. Our recommendations are made with the vision that effective new treatment will lie at the intersection of innovation, rigorous and reproducible research, and stakeholder involvement. MDPI 2018-12-15 /pmc/articles/PMC6315698/ /pubmed/30558274 http://dx.doi.org/10.3390/brainsci8120224 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Commentary
Erickson, Craig A.
Kaufmann, Walter E.
Budimirovic, Dejan B.
Lachiewicz, Ave
Haas-Givler, Barbara
Miller, Robert M.
Weber, Jayne Dixon
Abbeduto, Leonard
Hessl, David
Hagerman, Randi J.
Berry-Kravis, Elizabeth
Best Practices in Fragile X Syndrome Treatment Development
title Best Practices in Fragile X Syndrome Treatment Development
title_full Best Practices in Fragile X Syndrome Treatment Development
title_fullStr Best Practices in Fragile X Syndrome Treatment Development
title_full_unstemmed Best Practices in Fragile X Syndrome Treatment Development
title_short Best Practices in Fragile X Syndrome Treatment Development
title_sort best practices in fragile x syndrome treatment development
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315698/
https://www.ncbi.nlm.nih.gov/pubmed/30558274
http://dx.doi.org/10.3390/brainsci8120224
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