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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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Detalles Bibliográficos
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
Descripción
Sumario: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.