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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome
by
Schneider, Andrea
, Ceulemans, Berten
, Bickel, Erika S.
, Nguyen, Danh V.
, Hagerman, Randi J.
, Tassone, Flora
, Van Dijck, Anke
, Kooy, R. Frank
, Lozano, Reymundo
, Chen, Yanjun
, Hessl, David
, Angkustsiri, Kathleen
, Ligsay, Andrew
in
Adolescents
/ Allosteric properties
/ Anxiety
/ Autism
/ Behavior
/ Binding sites
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Clinical trial
/ Clinical trials
/ Cognitive ability
/ Complications and side effects
/ Design
/ Double-blind studies
/ Drug therapy
/ Epilepsy
/ Fragile X syndrome
/ Ganaxolone
/ Human Genetics
/ Hyperactivity
/ Intellectual disabilities
/ Intelligence tests
/ Males
/ Motivation
/ Neurology
/ Neuropsychology
/ Neurosciences
/ Pediatrics
/ Population studies
/ Psychiatry
/ Psychological aspects
/ Psychopharmacology
/ Quantitative psychology
/ Rodents
/ Statistical analysis
/ Teenagers
/ γ-Aminobutyric acid A receptors
2017
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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome
by
Schneider, Andrea
, Ceulemans, Berten
, Bickel, Erika S.
, Nguyen, Danh V.
, Hagerman, Randi J.
, Tassone, Flora
, Van Dijck, Anke
, Kooy, R. Frank
, Lozano, Reymundo
, Chen, Yanjun
, Hessl, David
, Angkustsiri, Kathleen
, Ligsay, Andrew
in
Adolescents
/ Allosteric properties
/ Anxiety
/ Autism
/ Behavior
/ Binding sites
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Clinical trial
/ Clinical trials
/ Cognitive ability
/ Complications and side effects
/ Design
/ Double-blind studies
/ Drug therapy
/ Epilepsy
/ Fragile X syndrome
/ Ganaxolone
/ Human Genetics
/ Hyperactivity
/ Intellectual disabilities
/ Intelligence tests
/ Males
/ Motivation
/ Neurology
/ Neuropsychology
/ Neurosciences
/ Pediatrics
/ Population studies
/ Psychiatry
/ Psychological aspects
/ Psychopharmacology
/ Quantitative psychology
/ Rodents
/ Statistical analysis
/ Teenagers
/ γ-Aminobutyric acid A receptors
2017
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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome
by
Schneider, Andrea
, Ceulemans, Berten
, Bickel, Erika S.
, Nguyen, Danh V.
, Hagerman, Randi J.
, Tassone, Flora
, Van Dijck, Anke
, Kooy, R. Frank
, Lozano, Reymundo
, Chen, Yanjun
, Hessl, David
, Angkustsiri, Kathleen
, Ligsay, Andrew
in
Adolescents
/ Allosteric properties
/ Anxiety
/ Autism
/ Behavior
/ Binding sites
/ Biomedical and Life Sciences
/ Biomedicine
/ Children
/ Children & youth
/ Clinical trial
/ Clinical trials
/ Cognitive ability
/ Complications and side effects
/ Design
/ Double-blind studies
/ Drug therapy
/ Epilepsy
/ Fragile X syndrome
/ Ganaxolone
/ Human Genetics
/ Hyperactivity
/ Intellectual disabilities
/ Intelligence tests
/ Males
/ Motivation
/ Neurology
/ Neuropsychology
/ Neurosciences
/ Pediatrics
/ Population studies
/ Psychiatry
/ Psychological aspects
/ Psychopharmacology
/ Quantitative psychology
/ Rodents
/ Statistical analysis
/ Teenagers
/ γ-Aminobutyric acid A receptors
2017
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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome
Journal Article
A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome
2017
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Overview
Background
Gamma-aminobutyric acid (GABA) system deficits are integral to the pathophysiologic development of fragile X syndrome (FXS). Ganaxolone, a GABA
A
receptor positive allosteric modulator, is hypothesized to improve symptoms such as anxiety, hyperactivity, and attention deficits in children with FXS.
Methods
This study was a randomized, double-blind, placebo-controlled, crossover trial of ganaxolone in children with FXS, aged 6–17 years.
Results
Sixty-one participants were assessed for eligibility, and 59 were randomized to the study. Fifty-five participants completed at least the first arm and were included in the intention-to-treat analysis; 51 participants completed both treatment arms. There were no statistically significant improvements observed on the primary outcome measure (Clinical Global Impression-Improvement), the key secondary outcome measure (Pediatric Anxiety Rating Scale-R), or any other secondary outcome measures in the overall study population. However, post-hoc analyses revealed positive trends in areas of anxiety, attention, and hyperactivity in participants with higher baseline anxiety and low full-scale IQ scores. No serious adverse events (AEs) occurred, although there was a significant increase in the frequency and severity of AEs related to ganaxolone compared to placebo.
Conclusions
While ganaxolone was found to be safe, there were no significant improvements in the outcome measures in the overall study population. However, ganaxolone in subgroups of children with FXS, including those with higher anxiety or lower cognitive abilities, might have beneficial effects.
Trial registration
ClinicalTrials.gov,
NCT01725152
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Anxiety
/ Autism
/ Behavior
/ Biomedical and Life Sciences
/ Children
/ Complications and side effects
/ Design
/ Epilepsy
/ Males
/ Rodents
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