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179 Dasotraline in Children With Attention Deficit Hyperactivity Disorder: Results of a Randomized, Double-Blind, Placebo-Controlled Study

Published online by Cambridge University Press:  15 June 2018

Robert Goldman
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
Lenard Adler
Affiliation:
New York University Langone Medical Center, New York, NY
Thomas Spencer
Affiliation:
Massachusetts General Hospital, Boston, MA
Robert Findling
Affiliation:
Kennedy Krieger Institute/Johns Hopkins University, Baltimore, MD
Seth C. Hopkins
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
Kenneth K. Koblan
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
Kaushik Sarma
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
Jay Hsu
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
Antony Loebel
Affiliation:
Sunovion Pharmaceuticals Inc., Marlborough, MA
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Abstract

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Objectives

Once-daily dosing with dasotraline, a novel dopamine and norepinephrine reuptake inhibitor, achieves stable plasma concentrations over 24 hours with once-daily dosing. This study evaluated dasotraline in children aged 6–12 years (NCT02428088).

Methods

Patients were randomized 1:1:1 to 6 weeks of once-daily, fixed-dose dasotraline 2 or 4 mg/day, or placebo. The primary efficacy endpoint was change from baseline (CFB) at Week 6 in ADHD Rating Scale Version IV – Home Version (ADHD RS-IV HV) total score, using a mixed model for repeated measures (MMRM) in the intent-to-treat (ITT) population. Secondary endpoints included Clinical Global Impression-Severity (CGI-S) score and safety endpoints.

Results

The mean age of 342 randomized patients was 9.1 [SD: 1.9] years; 66.7% were male. Overall, 79% of patients completed the study. In the ITT population (N=336), ADHD RS-IV HV total score improved significantly with dasotraline 4 mg/day vs placebo(least squares [LS] mean [SE] CFB at Week 6: –17.53 [±1.31] vs –11.36 [±1.29], respectively, p<0.001; effect size [ES]: 0.48). Inattentiveness and hyperactivity/impulsivity subscale scores significantly improved with 4 mg/day vs placebo at Week 6 (p=0.001, p=0.003, respectively). Improvement in CGI-S score was statistically significant with dasotraline 4 mg/day vs placebo(LS mean [SE] CFB at Week 6: –1.39 [±0.12] vs –1.04 [±0.12], respectively, p=0.040; ES: 0.29). No significant improvement was observed on the ADHD RS-IV HV total score and the CGI-S score for dasotraline 2 mg/day vs placebo. The most frequent treatment-emergent AEs (≥5% and higher than placebo) were (2 mg/day; 4 mg/day; placebo): insomnia (15.3%; 21.7%; 4.3%, all terms combined), decreased appetite (12.6%; 21.7%; 5.2%), weight loss (5.4%; 8.7%; 0%), irritability (3.6%; 7.0%; 6.0%), nasopharyngitis (0.9%; 5.2%; 0.9%), and nausea (0%; 5.2%; 2.6%).

Conclusions

Compared with placebo, dasotraline 4 mg/day significantly improved ADHD symptoms in children, as assessed by ADHD RS-IV HV total score and inattentiveness and hyperactivity/impulsivity subscale scores. Dasotraline was generally well tolerated; most common AEs were insomnia, decreased appetite, weight loss and irritability.

Funding Acknowledgements

Study sponsored by Sunovion Pharmaceuticals Inc.

Type
Abstracts
Copyright
© Cambridge University Press 2018