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Phase 3 Completed N=336 Randomized Quadruple-blind Treatment

Randomized, Double-blind Safety and Efficacy Study of Lisdexamfetamine Dimesylate (LDX) in Children and Adolescents Aged 6-17

Source: ClinicalTrials.gov NCT00763971 ↗
Enrolled (actual)
336
Serious AEs
2.4%
Results posted
Mar 2012
Primary outcomePrimary: Change From Baseline in Attention Deficit Hyperactivity Disorder Rating Scale-fourth Edition (ADHD-RS-IV) Total Score at up to 7 Weeks — -24.3; -18.7; -5.7 Scores on a scale — p=<0.001

Summary

The main aim of this study is to see if giving LDX to children and adolescents aged 6-17 years with ADHD decreases symptoms of ADHD.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Attention Deficit Hyperactivity Disorder Rating Scale-fourth Edition (ADHD-RS-IV) Total Score at up to 7 Weeks
-24.3; -18.7; -5.7 <0.001 sig
SECONDARY
Percentage of Participants With Improvement on Clinical Global Impression-Improvement (CGI-I) Scores
78.0; 60.6; 14.4 <0.001 sig
SECONDARY
Change From Baseline in Conner's Parent Rating Scale - Revised (CPRS-R) Total Score at up to 7 Weeks
-24.5; -18.4; -3.2 <0.001 sig
SECONDARY
Health Utilities Index-2 (HUI-2) Scores at up to 7 Weeks
0.811; 0.822; 0.806; 0.878; 0.887; 0.843
SECONDARY
Change From Baseline in the Child Health and Illness Profile, Child Edition: Parent Report Form (CHIP-CE:PRF) Global T-score at up to 7 Weeks
8.6; 7.1; -0.2 <0.001 sig
SECONDARY
Change From Baseline in Weiss Functional Impairment Rating Scale - Parent Report (WFIRS-P) Global Score at up to 7 Weeks
-0.3; -0.3; 0.0 <0.001 sig
SECONDARY
Change From Baseline in Brief Psychiatric Rating Scale for Children (BPRS-C) Total Score at up to 7 Weeks
-9.15; -9.71; -2.59
SECONDARY
Columbia-Suicide Severity Rating Scale (C-SSRS)
1; 0; 0; 1; 0; 0

Eligibility Criteria

Inclusion Criteria

  • Subject is a male or female aged 6-17 years inclusive at the time of consent.
  • Subject must meet Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition - Text Revision (DSM-IV-TR) criteria for a primary diagnosis of ADHD based on a detailed psychiatric evaluation.
  • Subject must have a Baseline ADHD-RS-IV total score ≥28.
  • Subject has blood pressure measurements within the 95th percentile for age, gender, and height at Screening and Baseline.
  • Subject is able to swallow a capsule.

Exclusion Criteria

  • Subject has failed to respond to more than one adequate course (dose and duration) of stimulant therapy. One course must have been a long-acting formulation.
  • Subject has a conduct disorder. Oppositional Defiant Disorder is not exclusionary.
  • Subject is currently considered a suicide risk, has previously made a suicide attempt or has a prior history of, or is currently, demonstrating active suicidal ideation.
  • Subject has glaucoma.
  • Subject weighs less than 22.7kg (50lbs).
  • Subject is significantly overweight based on Centre for Disease Control and Prevention Body Mass Index (BMI)-for-age gender specific charts at Screening. Significantly overweight is defined as a BMI >97th percentile for this study.
  • Subject has a documented allergy, hypersensitivity, or intolerance to amphetamine or methylphenidate.
  • Subject has a documented allergy, hypersensitivity, or intolerance to any excipients in the test or reference products.
  • Subject has a history of seizures (other than infantile febrile seizures), a tic disorder, or a current diagnosis and/or a known family history of Tourette's Disorder.
  • Subject has a known history of symptomatic cardiovascular disease, advance arteriosclerosis, structural cardiac abnormality, cardiomyopathy, serious heart rhythm abnormalities, coronary artery disease, or other serious cardiac problems that may place them at increased vulnerability to the sympathomimetic effects of a stimulant drug.
  • Subject has a known family history of sudden cardiac death or ventricular arrhythmia.
  • Subject is well controlled on their current ADHD medication with acceptable tolerability.
  • Subject has a pre-existing severe gastrointestinal tract narrowing (pathologic or iatrogenic).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00763971). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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