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dc.contributor.authorErickson, Craig A.
dc.contributor.authorVeenstra-Vanderweele, Jeremy M.
dc.contributor.authorMelmed, Raun D.
dc.contributor.authorMcCracken, James T.
dc.contributor.authorGinsberg, Lawrence D.
dc.contributor.authorSikich, Linmarie
dc.contributor.authorScahill, Lawrence
dc.contributor.authorCherubini, Maryann
dc.contributor.authorZarevics, Peter
dc.contributor.authorWalton-Bowen, Karen
dc.contributor.authorCarpenter, Randall L.
dc.contributor.authorWang, Paul P.
dc.contributor.authorKing, Bryan H.
dc.contributor.authorBear, Mark
dc.date.accessioned2015-03-03T21:25:15Z
dc.date.available2015-03-03T21:25:15Z
dc.date.issued2013-11
dc.identifier.issn0162-3257
dc.identifier.issn1573-3432
dc.identifier.urihttp://hdl.handle.net/1721.1/95779
dc.description.abstractSTX209 (arbaclofen), a selective GABA-B agonist, is hypothesized to modulate the balance of excitatory to inhibitory neurotransmission, and has shown preliminary evidence of benefit in fragile X syndrome. We evaluated its safety, tolerability, and efficacy in non-syndromic autism spectrum disorders, in an 8-week open-label trial enrolling 32 children and adolescents with either Autistic Disorder or Pervasive Developmental Disorder—Not Otherwise Specified, and a score ≥17 on the Aberrant Behavior Checklist (ABC)—Irritability subscale. STX209 was generally well-tolerated. The most common adverse events were agitation and irritability, which typically resolved without dose changes, and were often felt to represent spontaneous variation in underlying symptoms. Improvements were observed on several outcome measures in this exploratory trial, including the ABC-Irritability (the primary endpoint) and the Lethargy/Social Withdrawal subscales, the Social Responsiveness Scale, the CY-BOCS-PDD, and clinical global impression scales. Placebo-controlled study of STX209 is warranted.en_US
dc.description.sponsorshipSeaside Therapeutics Inc.en_US
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.relation.isversionofhttp://dx.doi.org/10.1007/s10803-013-1963-zen_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceBear via Courtney Crummetten_US
dc.titleSTX209 (Arbaclofen) for Autism Spectrum Disorders: An 8-Week Open-Label Studyen_US
dc.typeArticleen_US
dc.identifier.citationErickson, Craig A., Jeremy M. Veenstra-Vanderweele, Raun D. Melmed, James T. McCracken, Lawrence D. Ginsberg, Linmarie Sikich, Lawrence Scahill, et al. “STX209 (Arbaclofen) for Autism Spectrum Disorders: An 8-Week Open-Label Study.” Journal of Autism and Developmental Disorders 44, no. 4 (November 23, 2013): 958–964.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentPicower Institute for Learning and Memoryen_US
dc.contributor.approverBear, Marken_US
dc.contributor.mitauthorBear, Marken_US
dc.relation.journalJournal of Autism and Developmental Disordersen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsErickson, Craig A.; Veenstra-Vanderweele, Jeremy M.; Melmed, Raun D.; McCracken, James T.; Ginsberg, Lawrence D.; Sikich, Linmarie; Scahill, Lawrence; Cherubini, Maryann; Zarevics, Peter; Walton-Bowen, Karen; Carpenter, Randall L.; Bear, Mark F.; Wang, Paul P.; King, Bryan H.en_US
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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