The purpose of this study is to test if the investigational medication ABT-089 is a safe and effective treatment for adults with Attention-Deficit/Hyperactivity Disorder (ADHD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
160
Site Reference ID/Investigator# 7546
Lafayette, California, United States
Site Reference ID/Investigator# 7551
Jacksonville, Florida, United States
Site Reference ID/Investigator# 7553
Orlando, Florida, United States
CAARS: Inv Total Score
Time frame: Screening, Day -1, Day 7, Day 14, Day 28, Day 42 and Day 56
CAARS Inattentive and Hyperactive/Impulsivity Sub-scale scores, CAARS ADHD Index, CGI-ADHD-S, AISRS, CAARS:Self
Time frame: Screening, Day -1, Day 7, Day 14, Day 28, Day 42 and Day 56
TASS, AAQoL, WPAI
Time frame: Day -1, Day 28, Day 56
BRIEF-A, FTND
Time frame: Day-1, Day 56
QSU-Brief, Number of Cigarettes smoked per day
Time frame: Day -1, Day 7, Day 14, Day 28, Day 42, Day 56
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Site Reference ID/Investigator# 7545
Overland Park, Kansas, United States
Site Reference ID/Investigator# 7552
Farmington Hills, Michigan, United States
Site Reference ID/Investigator# 7548
Troy, Michigan, United States
Site Reference ID/Investigator# 7554
Eugene, Oregon, United States
Site Reference ID/Investigator# 7547
Portland, Oregon, United States
Site Reference ID/Investigator# 7555
Memphis, Tennessee, United States
Site Reference ID/Investigator# 7549
Virginia Beach, Virginia, United States
...and 2 more locations