A Safety and Efficacy Study of ABT-089 in Children With Attention-Deficit/Hyperactivity Disorder (ADHD)
Public ClinicalTrials.gov record NCT00528697. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Dose-Ranging Study of the Safety and Efficacy of ABT-089 in Children With Attention Deficit-Hyperactivity Disorder (ADHD)
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
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 identification
- NCT ID
- NCT00528697
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Enrollment
- 278 participants
Conditions and interventions
Conditions
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
- Aug 31, 2007
- Primary completion
- Mar 31, 2008
- Completion
- Mar 31, 2008
- Last update posted
- Jan 28, 2013
2007 – 2008
United States locations
- U.S. sites
- 20
- U.S. states
- 16
- U.S. cities
- 20
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Site Reference ID/Investigator# 5999 | Little Rock | Arkansas | 72205 | — |
| Site Reference ID/Investigator# 5979 | El Centro | California | 92243 | — |
| Site Reference ID/Investigator# 5986 | Boulder | Colorado | 80304 | — |
| Site Reference ID/Investigator# 5993 | Bradenton | Florida | 34208 | — |
| Site Reference ID/Investigator# 5995 | Jacksonville | Florida | 32216 | — |
| Site Reference ID/Investigator# 5977 | Orlando | Florida | 32806 | — |
| Site Reference ID/Investigator# 5981 | Northbrook | Illinois | 60062 | — |
| Site Reference ID/Investigator# 5982 | Overland Park | Kansas | 66212 | — |
| Site Reference ID/Investigator# 5992 | Omaha | Nebraska | 68198 | — |
| Site Reference ID/Investigator# 5997 | Las Vegas | Nevada | 89128 | — |
| Site Reference ID/Investigator# 5987 | Clementon | New Jersey | 08021 | — |
| Site Reference ID/Investigator# 5996 | Eugene | Oregon | 97401 | — |
| Site Reference ID/Investigator# 5984 | Portland | Oregon | 97210 | — |
| Site Reference ID/Investigator# 5980 | Salem | Oregon | 97301 | — |
| Site Reference ID/Investigator# 5994 | Charleston | South Carolina | 29405 | — |
| Site Reference ID/Investigator# 5976 | Memphis | Tennessee | 38119 | — |
| Site Reference ID/Investigator# 6000 | Austin | Texas | 78756 | — |
| Site Reference ID/Investigator# 5998 | Herndon | Virginia | 20170 | — |
| Site Reference ID/Investigator# 5978 | Bellevue | Washington | 98007 | — |
| Site Reference ID/Investigator# 5983 | 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 NCT00528697, 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 Jan 28, 2013 · Synced Sep 4, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00528697 live on ClinicalTrials.gov.