A Safety and Efficacy Study of ABT-089 in Children With Attention-Deficit/Hyperactivity Disorder (ADHD)

Study Identifier
M06-888
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Study Details

Medical Condition
  • Attention-Deficit/Hyperactivity Disorder (ADHD)
  • Study Drug
  • ABT-089
  • atomoxetine
  • placebo
  • Phase
    Phase 2
    Sex
    Female & Male
    Age
    6 - 12 Years

    Protocol Summary

    The purpose of this study is to test if the investigational medication ABT-089 is a safe and effective treatment for children with Attention-Deficit/Hyperactivity Disorder or ADHD.

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 5999
    Little Rock, Arkansas, United States, 72205
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 5979
    El Centro, California, United States, 92243
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 5986
    Boulder, Colorado, United States, 80304
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 5993
    Bradenton, Florida, United States, 34208
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 5995
    Jacksonville, Florida, United States, 32216
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 5977
    Orlando, Florida, United States, 32806
    Status
    Not applicable
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