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Clinical Trial Summary

A Phase 2 study of SEP-225289 in adults with attention deficit hyperactivity disorder (ADHD).


Clinical Trial Description

This is a Phase 2, randomized, double-blind, parallel-group, multicenter, outpatient study evaluating the efficacy and safety of SEP 225289 in adults with ADHD using 2 oral dosages (4 or 8 mg SEP 225289 once daily [QD]) versus placebo over a 4 week treatment period. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Adult Attention Deficit Hyperactivity Disorder
  • Attention Deficit Disorder with Hyperactivity
  • Hyperkinesis

NCT number NCT01692782
Study type Interventional
Source Sunovion
Contact
Status Completed
Phase Phase 2
Start date December 2012
Completion date December 2013

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