Cited by 13Attention Deficit Hyperactivity DisorderPharmacology and Obesity TreatmentNeurotransmitter Receptor Influence on Behavior

Lisdexamfetamine Dimesylate: In Attention-Deficit Hyperactivity Disorder in Adults

Weber, Juliane, Siddiqui, M. Asif A.·2009·CNS Drugs

Abstract

Lisdexamfetamine dimesylate is a long-acting amfetamine prodrug that requires in vivo hydrolysis to gradually release active d-amfetamine. It is approved in the US for the treatment of attention-deficit hyperactivity disorder (ADHD) in adults and in children aged 6-12 years. In a study in adult stimulant abusers, oral lisdexamfetamine 50 or 100 mg showed less 'likability' response than immediate-release d-amfetamine 40 mg on the Drug Rating Questionnaire-Subject (DRQS) Liking scale. However, there was no significant difference between lisdexamfetamine 150 mg and d-amfetamine 40 mg. In a randomized, double-blind, phase III trial in adult patients with ADHD, oral lisdexamfetamine 30, 50 or 70 mg/day for 4 weeks caused a significantly greater improvement in ADHD-Rating Scale (ADHD-RS) total score than placebo; significant between-group differences favouring lisdexamfetamine were evident after 1 week. Lisdexamfetamine was generally well tolerated in adult patients with ADHD, with most treatment-emergent adverse events being of mild to moderate severity and consistent with the known effects of psychostimulants.

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Crossref · 10.2165/00023210-200923050-00005

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5 of 5 references verified0 citation errors · 0 not checkable

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  • Study subjects on lisdexamfetamine have been reported to have low scores on drug likability scales, even with intravenous use.

    “Study subjects on LDX have been reported to have low scores on drug likability scales, even with intravenous use”
  • In that study, lisdexamfetamine 50 mg and 100 mg were similar to placebo on liking, but lisdexamfetamine 150 mg was equivalent to 40 mg dextroamphetamine.

    “The 50 mg and 100 mg doses of lisdexamfetamine were similar to placebo; however, the 150 mg dose was equivalent to the 40 mg dose of dextroamphetamine.”
  • In Weber et al randomized six-step crossover Phase I study in individuals with a history of stimulant abuse, compared with placebo, dextroamphetamine and diethylpropion produced significant differences on the Drug Rating Questionnaire-Subject Liking Scale.

    “A randomized, six-step, crossover Phase I study43 in individuals with a history of stimulant abuse using placebo, lisdexamfetamine 50 mg, 100 mg, and 150 mg, immediate-release dextroamphetamine 40 mg, diethylpropion 200 mg, and placebo showed that, compared with placebo, dextroamphetamine and diethylpropion produced significant differences on the Drug Rating Questionnaire-Subject Liking Scale.”

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Authors
Weber, J., & Siddiqui, M. A. A.
Affiliations
Wolters Kluwer Health (NZ)
Corresponding author
Siddiqui, M. Asif A.
Venue
CNS Drugs
Published
2009-05
Volume
23
Issue
5
Pages
419-425
ISSN
1172-7047 (ISSN-L)
OpenAlex
W1981797096
Cited by
13
References
5
Citations by year
2020: 1 · 2018: 1 · 2016: 1 · 2014: 2 · 2013: 3
FWCI
0.82
Type
journal article
Language
en
Open access
closed
Locations
  • CNS Drugs (publishedVersion)
  • PubMed (publishedVersion)
Funders
University of Illinois at Urbana-Champaign
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
  • Health Sciences › Medicine › Pharmacology › Pharmacology and Obesity Treatment
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Keywords
lisdexamfetamine dimesylate, attention deficit hyperactivity disorder, ADHD treatment, stimulant abuse, drug liking, drug tolerability, psychostimulants, ADHD Rating Scale
MeSH terms
Lisdexamfetamine Dimesylate, Adult, Central Nervous System Stimulants, Attention Deficit Disorder with Hyperactivity, Child, Dextroamphetamine, Dose-Response Relationship, Drug, Drug Evaluation, Female, Humans, Male, Surveys and Questionnaires, Clinical Trials, Phase III as Topic, Young Adult

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