| Literature DB >> 28501294 |
Johanna H van der Lee1, Jonathan Morton2, Heather R Adams3, Lorne Clarke4, Berendine Johanne Ebbink5, Maria L Escolar6, Roberto Giugliani7, Paul Harmatz8, Melissa Hogan9, Simon Jones10, Shauna Kearney11, Joseph Muenzer12, Stewart Rust13, Margaret Semrud-Clikeman14, Frits A Wijburg15, Zi-Fan Yu16, Darren Janzen17, Elsa Shapiro18.
Abstract
The design and conduct of clinical studies to evaluate the effects of novel therapies on central nervous system manifestations in children with neuronopathic mucopolysaccharidoses is challenging. Owing to the rarity of these disorders, multinational studies are often needed to recruit enough patients to provide meaningful data and statistical power. This can make the consistent collection of reliable data across study sites difficult. To address these challenges, an International MPS Consensus Conference for Cognitive Endpoints was convened to discuss approaches for evaluating cognitive and adaptive function in patients with mucopolysaccharidoses. The goal was to develop a consensus on best practice for the design and conduct of clinical studies investigating novel therapies for these conditions, with particular focus on the most appropriate outcome measures for cognitive function and adaptive behavior. The outcomes from the consensus panel discussion are reported here.Entities:
Keywords: Adaptive behavior; Clinical trial; Cognitive; Mucopolysaccharidoses; Neurological; Protocol
Mesh:
Year: 2017 PMID: 28501294 DOI: 10.1016/j.ymgme.2017.05.004
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797