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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6315698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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