Attention Deficit Hyperactivity Disorder (ADHD) Clinical Trial
Official title:
A 10-week Randomized, Multicenter, Double-blind, Parallel, Fixed-dose Study of MDX (Metadoxine Immediate-release/Slow-release, Bilayer Tablet) 1400 mg Compared With Placebo in Adults With Attention Deficit Hyperactivity Disorder (ADHD)
This study is a multi-center, randomized, double-blind, placebo-controlled, phase 3 study of
MDX (1400 mg daily) for 10 weeks compared with placebo in adults with ADHD.
The study will be comprised of Screening, Washout (if required), Treatment (total of 10
weeks) and Follow-up periods. Approximately 750 patients will be enrolled and undergo
initial eligibility assessments.
- A 10-week randomized, multi-center, double-blind, placebo-controlled, phase 3 study of
MDX (1400 mg daily) for 10 weeks compared with placebo in adults with ADHD.
- The study will be comprised of Screening, Washout (if required), Treatment (total of 10
weeks) and Follow-up periods. Approximately 750 patients will be enrolled and undergo
initial eligibility assessments.
- Subjects requiring a washout will undergo a Washout period where ADHD medication is
discontinued (21 days for atomoxetine, 14 days for other ADHD medications). These
subjects will have an Interim Visit (off drug) on or about Day -10 (Day -10 to Day -3)
for CAARS-Inv assessment at the end of the Washout period.
- Subjects will be randomly assigned to placebo/MDX for a total treatment duration of up
to ten weeks.
There will be a one week Follow-up period after the last dose of study treatment or early
termination.
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