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Terminated Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT00554385

Public ClinicalTrials.gov record NCT00554385. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 9:57 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Long-term Safety and Tolerability of ABT-089 in Children With Attention-Deficit/Hyperactivity Disorder (ADHD): An Open-Label Extension Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to evaluate the long-term safety and tolerability of ABT-089 in children with ADHD.

Study identification

NCT ID
NCT00554385
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Abbott
Industry
Enrollment
283 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Years to 12 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2007
Primary completion
Jul 31, 2008
Completion
Not listed
Last update posted
Aug 22, 2011

Started 2007

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
22
Facility City State ZIP Site status
Site Ref #/Investigator 6800 Little Rock Arkansas 72205
Site Ref #/Investigator 6812 Boulder Colorado 80304
Site Ref #/Investigator 8366 Bradenton Florida 34208
Site Ref #/Investigator 6808 Jacksonville Florida 32216
Site Ref #/Investigator 6827 Orlando Florida 32806
Site Ref #/Investigator 8383 Libertyville Illinois 60048
Site Ref #/Investigator 6802 Northbrook Illinois 60062
Site Ref #/Investigator 6824 Overland Park Kansas 66212
Site Ref #/Investigator 8428 Troy Michigan 48085
Site Ref #/Investigator 6902 Omaha Nebraska 68198
Site Ref #/Investigator 6856 Las Vegas Nevada 89128
Site Ref #/Investigator 6683 Clementon New Jersey 08021
Site Ref #/Investigator 8297 Oklahoma City Oklahoma 73103
Site Ref #/Investigator 6682 Eugene Oregon 97401
Site Ref #/Investigator 6811 Portland Oregon 97210
Site Ref #/Investigator 8701 Portland Oregon 97210
Site Ref #/Investigator 6681 Salem Oregon 97301
Site Ref #/Investigator 6799 Charleston South Carolina 29405
Site Ref #/Investigator 7955 Memphis Tennessee 38119
Site Ref #/Investigator 6836 Austin Texas 78756
Site Ref #/Investigator 6835 Herndon Virginia 20170
Site Ref #/Investigator 6791 Bellevue Washington 98007
Site Ref #/Investigator 6838 Middleton Wisconsin 53562

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00554385, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 22, 2011 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00554385 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →