2017
DOI: 10.1002/cpdd.366
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Effect of Food Intake on the Pharmacokinetics of a Novel Methylphenidate Extended‐Release Oral Suspension for Attention Deficit Hyperactivity Disorder

Abstract: We conducted an open-label, single-dose, randomized, crossover study in healthy adults to assess the impact of food on the bioavailability of 60 mg methylphenidate extended-release oral suspension (MEROS; Quillivant XR™)-a long-acting stimulant for the treatment of attention deficit hyperactivity disorder-by comparing the pharmacokinetic parameters under fed and fasting conditions. When MEROS 60 mg was administered under fed conditions compared with fasting conditions, the exposure of methylphenidate (d enanti… Show more

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Cited by 4 publications
(3 citation statements)
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“…Quillivant XR Ò (MPH). Quillivant XR was approved for use in 2012 (Childress and Berry 2010;FDA 2012aFDA , 2012bChildress and Sallee 2013;Robb et al 2017;Sallee et al 2017). It is a powder containing dl-MPH microparticles, which are proportioned as *20% uncoated (IR) microparticles and 80% film coated (for ER).…”
Section: Solutionsmentioning
confidence: 99%
“…Quillivant XR Ò (MPH). Quillivant XR was approved for use in 2012 (Childress and Berry 2010;FDA 2012aFDA , 2012bChildress and Sallee 2013;Robb et al 2017;Sallee et al 2017). It is a powder containing dl-MPH microparticles, which are proportioned as *20% uncoated (IR) microparticles and 80% film coated (for ER).…”
Section: Solutionsmentioning
confidence: 99%
“…En las formulaciones de liberación inmediata, el medicamento se absorbe casi completamente, alcanzando un pico plasmático de 1 a 3 horas de su administración (Challman & Lipsky, 2000). La absorción se puede ver acelerada si se administra el medicamento junto con comidas, efecto que no se observa significativamente en formulaciones de liberación prolongada (Sallee et al, 2017). La biodisponibilidad es del 30% aproximadamente (Freese et al, 2012).…”
Section: Farmacocinéticaunclassified
“…En las formulaciones de liberación inmediata, el medicamento se absorbe casi completamente, alcanzando un pico plasmático de 1 a 3 horas de su administración (Challman & Lipsky, 2000). La absorción se puede ver acelerada si se administra el medicamento junto con comidas, efecto que no se observa significativamente en formulaciones de liberación prolongada (Sallee et al, 2017). La biodisponibilidad es del 30% aproximadamente (Freese et al, 2012).…”
Section: Farmacocinéticaunclassified