Safety and tolerability of flexible dosages of prolonged-release OROS methylphenidate in adults with attention-deficit/hyperactivity disorder

JK Buitelaar, JA Ramos-Quiroga, M Casas… - Neuropsychiatric …, 2009 - Taylor & Francis
The osmotic release oral system (OROS) methylphenidate formulation is a prolonged-
release medication for the treatment of attention-deficit/hyperactivity disorder (ADHD) in …

Methylphenidate Controlled-Delivery Capsules (Equasym™ XL, Metadate CD™) A Review of its Use in the Treatment of Children and Adolescents with Attention …

VR Anderson, GM Keating - Pediatric Drugs, 2006 - Springer
Controlled-delivery methylphenidate (methylphenidate CD)[Equasym™ XL, Metadate
CD™], an oral stimulant, is approved in the US and EU to treat children aged≥ 6 years who …

Academic, Behavioral, and Cognitive Effects of OROS® Methylphenidate on Older Children with Attention-Deficit/Hyperactivity Disorder

SB Wigal, T Wigal, S Schuck, M Brams… - Journal of child and …, 2011 - liebertpub.com
Objective: To assess the effect of Osmotic-Release Oral System (OROS) methylphenidate
(MPH) on a variety of measures evaluating academic performance, cognition, and social …

12-month efficacy and safety of OROS® MPH in children and adolescents with attention-deficit/hyperactivity disorder switched from MPH

P Hoare, H Remschmidt, R Medori, C Ettrich… - European child & …, 2005 - Springer
Purpose The aim of this study was to evaluate long-term clinical treatment with OROS®
methylphenidate (MPH)(Concerta®) in children and adolescents with attention …

Efficacy and safety of a long-acting multilayer-release methylphenidate formulation (PRC-063) in the treatment of adolescent attention-deficit/hyperactivity disorder: a …

MD Weiss, AJ Cutler, SH Kollins… - Journal of child and …, 2021 - liebertpub.com
Objectives: To study the safety and efficacy of the long-acting methylphenidate formulation
PRC-063 in adolescents with attention-deficit/hyperactivity disorder (ADHD). Methods …

Single-and multiple-dose pharmacokinetics of methylphenidate administered as methylphenidate transdermal system or osmotic-release oral system methylphenidate …

D Pierce, A Katic, M Buckwalter… - Journal of clinical …, 2010 - journals.lww.com
This was a 1-month, multicenter, open-label, randomized study to determine single-and
multiple-dose pharmacokinetics of d, l-methylphenidate (MPH) after MPH transdermal …

[HTML][HTML] Methylphenidate hydrochloride modified-release in adults with attention deficit hyperactivity disorder: a randomized double-blind placebo-controlled trial

M Huss, Y Ginsberg, T Tvedten, T Arngrim… - Advances in …, 2014 - Springer
Introduction Treatment options for adults with attention deficit hyperactivity disorder (ADHD)
are limited. The study was conducted to confirm the clinically effective and safe dose of …

A single-dose, single-period pharmacokinetic assessment of an extended-release orally disintegrating tablet of methylphenidate in children and adolescents with …

A Childress, J Newcorn, JG Stark… - Journal of Child and …, 2016 - liebertpub.com
Objective: To determine the pharmacokinetic (PK) profile of a proprietary formulation of
methylphenidate (MPH) in children and adolescents with attention-deficit/hyperactivity …

Efficacy and safety of immediate-release methylphenidate treatment for preschoolers with ADHD

L Greenhill, S Kollins, H Abikoff, J McCracken… - Journal of the American …, 2006 - Elsevier
OBJECTIVE: The Preschool ADHD Treatment Study (PATS) was a NIMH-funded, six-center,
randomized, controlled trial to determine the efficacy and safety of immediate-release …

A randomized, double-blind, placebo-controlled study of HLD200, a delayed-release and extended-release methylphenidate, in children with attention-deficit …

AC Childress, AJ Cutler, A Marraffino… - Journal of child and …, 2020 - liebertpub.com
Objectives: HLD200, a once-daily, evening-dosed, delayed-release and extended-release
methylphenidate (DR/ER-MPH), was designed to provide therapeutic effect beginning upon …