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

Study Identifier
M10-345
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
  • 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 (ADHD).

    Study Locations

    Location
    Status
    Location
    Site Reference ID/Investigator# 7536
    Little Rock, Arkansas, United States, 72205
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 7954
    Bradenton, Florida, United States, 34208
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 7543
    Jacksonville, Florida, United States, 32216
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 7542
    Orlando, Florida, United States, 32806
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 7537
    Libertyville, Illinois, United States, 60048
    Status
    Not applicable
    Location
    Site Reference ID/Investigator# 7561
    Overland Park, Kansas, United States, 66212
    Status
    Not applicable
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