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NCT00640185 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by AbbVie (prior sponsor, Abbott).

Completed
Registry status
Phase 2
Development phase
160
Enrollment target

NCT00640185: Completed Phase 2 study, sponsored by AbbVie (prior sponsor, Abbott).

NCT00640185 is a Phase 2 study that has completed, run by AbbVie (prior sponsor, Abbott). The registered enrollment target is 160 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00640185, a Phase 2 study, has completed, sponsored by AbbVie (prior sponsor, Abbott).

COMPLETED
Registry status
Phase 2
Development phase
160 participants
Enrollment target

Study Summary

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).

Interventions

  • DRUG Placebo
  • DRUG ABT-089

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2008-03
Est. Completion 2008-08
Phase Phase 2
AbbVie (prior sponsor, Abbott)

88 total trials

What the finished NCT00640185 record still lists

NCT00640185 is an interventional study that assigns participants to a tested intervention. The registered 160 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (20% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00640185 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00640185 about?

NCT00640185 is a clinical study titled "Safety, Tolerability and Efficacy Study of ABT-089 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)". 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).

What is the current status of trial NCT00640185?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 160 participants. The study started on 2008-03. Estimated completion is 2008-08.

What interventions are being tested in trial NCT00640185?

The interventions under investigation include: Placebo (DRUG), ABT-089 (DRUG).

Who is sponsoring clinical trial NCT00640185?

This trial is sponsored by AbbVie (prior sponsor, Abbott), which has 88 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00640185's enrollment target sits among peer trials

160 422nd of 2000 higher than 1,559 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00640185, the US trial registry maintained by the National Library of Medicine. NCT00640185 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.