Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Brigitte Robertson"'
Publikováno v:
Drugs in R&D, Vol 19, Iss 2, Pp 167-175 (2019)
Abstract Background and objective SHP465 mixed amphetamine salts extended release is a once-daily, single-entity, mixed amphetamine salts capsule product for attention-deficit/hyperactivity disorder. The objective of this study was to evaluate amphet
Externí odkaz:
https://doaj.org/article/71cb3852fdf343deaac91e8d2e5c9930
Publikováno v:
Journal of Child and Adolescent Psychopharmacology
Objectives: In two studies of adult attention-deficit/hyperactivity disorder (ADHD), SHP465 mixed amphetamine salts (MAS) extended-release significantly reduced ADHD-Rating Scale, 4th Edition total score (ADHD-RS-IV-TS) versus placebo (PBO). This rep
Autor:
Michael Huss, Sepehr Farahbakhshian, Brigitte Robertson, Caleb Bliss, Tamara Werner-Kiechle, David R Coghill
Publikováno v:
European Child & Adolescent Psychiatry
Several recent phase 3 clinical trials of attention-deficit/hyperactivity disorder (ADHD) medications have used the Weiss Functional Impairment Rating Scale-Parent Report (WFIRS-P). Here, we assess WFIRS-P response in individual patients in two pivot
Autor:
Daniel F. Connor, Tamara Werner-Kiechle, Brigitte Robertson, Jeffrey H. Newcorn, Michael Huss, Amaia Hervás
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 41:565-570
OBJECTIVE To assess the efficacy of the non-stimulant guanfacine extended release (GXR) on attention-deficit/hyperactivity disorder (ADHD) symptoms in children and adolescents, with and without comorbid oppositional defiant disorder (ODD). METHODS Da
Autor:
Yi Wang, Patrick Martin, James Wu, Ann C. Childress, Robert L. Findling, Brigitte Robertson, Scott H. Kollins
Publikováno v:
Journal of Child and Adolescent Psychopharmacology
Objectives: Describe the safety and tolerability of lisdexamfetamine dimesylate (LDX) and provide data on clinical effects for efficacy-related endpoints and pharmacokinetics in preschool-aged children with attention-deficit/hyperactivity disorder (A
Publikováno v:
Journal of Child and Adolescent Psychopharmacology
Objectives: In a previous pivotal study of children and adolescents (aged 6–17 years) with attention-deficit/hyperactivity disorder (ADHD), dose-optimized SHP465 mixed amphetamine salts (MAS) extended-release (12.5–25 mg once daily) was superior
Publikováno v:
Journal of Attention Disorders
Objective: Assess executive function (EF) improvement with SHP465 mixed amphetamine salts (MAS) extended-release in adults with attention-deficit/hyperactivity disorder (ADHD) using responder analyses of the Brown Attention-Deficit Disorder Scale (BA
Autor:
Bryan Dirks, Jeffrey H. Newcorn, Brigitte Robertson, Michael Huss, J. Antoni Ramos-Quiroga, Joan Gu
Publikováno v:
European Child & Adolescent Psychiatry. 27:1283-1294
Data are reported from SPD503-318, a phase 3, open-label, safety study of guanfacine extended release (GXR) in European children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Participants received dose-optimized GXR (1–7 mg/
Autor:
Margo Jaffee, Ann C. Childress, Brigitte Robertson, Brian Yan, Ming Yu, Michael S. Greenbaum, Matthew Brams
Publikováno v:
Journal of Child and Adolescent Psychopharmacology
Objective: The aim of this study was to evaluate the efficacy, safety, and tolerability of SHP465 mixed amphetamine salts (MAS) in children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Methods: This randomized, double-blind d
Publikováno v:
CNS Drugs
Background SPD489-404 was the first 2-year safety study of lisdexamfetamine dimesylate in the treatment of attention-deficit/hyperactivity disorder in children and adolescents. In accordance with advice from the European Medicines Agency, assessment