Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents.
Ontology highlight
ABSTRACT: Fragile X syndrome (FXS) is the most common monogenic cause of inherited intellectual and developmental disabilities. Mavoglurant, a selective metabotropic glutamate receptor subtype-5 antagonist, has shown positive neuronal and behavioral effects in preclinical studies, but failed to demonstrate any behavioral benefits in two 12-week, randomized, placebo-controlled, double-blind, phase IIb studies in adults and adolescents with FXS. Here we report the long-term safety (primary endpoint) and efficacy (secondary endpoint) results of the open-label extensions. Adolescent (n = 119, aged 12-19 years) and adult (n = 148, aged 18-45 years) participants received up to 100 mg bid mavoglurant for up to 34 months. Both extension studies were terminated prematurely due to lack of proven efficacy in t
SUBMITTER: Hagerman R
PROVIDER: S-EPMC6242849 | biostudies-literature | 2018 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA