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Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder.

Publication ,  Journal Article
Adler, LA; Goodman, DW; Kollins, SH; Weisler, RH; Krishnan, S; Zhang, Y; Biederman, J; 303 Study Group,
Published in: J Clin Psychiatry
September 2008

OBJECTIVE: To evaluate the efficacy and safety of 30, 50, and 70 mg/day lisdexamfetamine dimesylate compared with placebo in adults with attention-deficit/hyperactivity disorder (ADHD). METHOD: Following a 7- to 28-day washout, 420 adults aged 18 to 55 years with moderate to severe ADHD (DSM-IV-TR criteria) were treated with 30, 50, or 70 mg/day lisdexamfetamine or placebo, respectively, for 4 weeks (N = 119, 117, 122, and 62, respectively). The 50- and 70- mg/day groups underwent forced-dose titration. The primary efficacy measure was the clinician-determined ADHD Rating Scale (ADHD-RS) total score. The study was conducted from May 2006 to November 2006. RESULTS: Treatment groups were well matched at baseline, including in ADHD-RS scores. At endpoint, changes in ADHD-RS scores were significantly greater for each lisdexamfetamine dose than for placebo (placebo = -8.2, 30 mg/day lisdexamfetamine = -16.2, 50 mg/day lisdexamfetamine = -17.4, 70 mg/day lisdexamfetamine = -18.6; all p < .0001 vs. placebo), with no differences between doses. Significant differences relative to placebo were observed in each lisdexamfetamine group, beginning at week 1 and for each week throughout. The percentage of subjects who improved (Clinical Global Impressions-Improvement scale rating < or = 2) was significantly greater for each lisdexamfetamine dose than for placebo at each week and at endpoint (placebo = 29%, 30 mg/day lisdexamfetamine = 57%, 50 mg/day lisdexamfetamine = 62%, 70 mg/day lisdexamfetamine = 61%; all p < .01). Adverse events were generally mild and included dry mouth, decreased appetite, and insomnia. CONCLUSION: All 3 lisdexamfetamine doses were significantly more effective than placebo in the treatment of adults with ADHD, with improvements noted within 1 week. Lisdexamfetamine was generally well tolerated by these patients.

Duke Scholars

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Published In

J Clin Psychiatry

DOI

EISSN

1555-2101

Publication Date

September 2008

Volume

69

Issue

9

Start / End Page

1364 / 1373

Location

United States

Related Subject Headings

  • Young Adult
  • Psychiatry
  • Personality Assessment
  • Middle Aged
  • Male
  • Lisdexamfetamine Dimesylate
  • Humans
  • Female
  • Double-Blind Method
  • Dose-Response Relationship, Drug
 

Citation

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Chicago
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Adler, L. A., Goodman, D. W., Kollins, S. H., Weisler, R. H., Krishnan, S., Zhang, Y., … 303 Study Group, . (2008). Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder. J Clin Psychiatry, 69(9), 1364–1373. https://doi.org/10.4088/jcp.v69n0903
Adler, Lenard A., David W. Goodman, Scott H. Kollins, Richard H. Weisler, Suma Krishnan, Yuxin Zhang, Joseph Biederman, and Joseph 303 Study Group. “Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder.J Clin Psychiatry 69, no. 9 (September 2008): 1364–73. https://doi.org/10.4088/jcp.v69n0903.
Adler LA, Goodman DW, Kollins SH, Weisler RH, Krishnan S, Zhang Y, et al. Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder. J Clin Psychiatry. 2008 Sep;69(9):1364–73.
Adler, Lenard A., et al. “Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder.J Clin Psychiatry, vol. 69, no. 9, Sept. 2008, pp. 1364–73. Pubmed, doi:10.4088/jcp.v69n0903.
Adler LA, Goodman DW, Kollins SH, Weisler RH, Krishnan S, Zhang Y, Biederman J, 303 Study Group. Double-blind, placebo-controlled study of the efficacy and safety of lisdexamfetamine dimesylate in adults with attention-deficit/hyperactivity disorder. J Clin Psychiatry. 2008 Sep;69(9):1364–1373.

Published In

J Clin Psychiatry

DOI

EISSN

1555-2101

Publication Date

September 2008

Volume

69

Issue

9

Start / End Page

1364 / 1373

Location

United States

Related Subject Headings

  • Young Adult
  • Psychiatry
  • Personality Assessment
  • Middle Aged
  • Male
  • Lisdexamfetamine Dimesylate
  • Humans
  • Female
  • Double-Blind Method
  • Dose-Response Relationship, Drug