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NCT00485407 · ClinicalTrials.gov registry record · Phase 3
Guiding Dose Increases in Patients Incompletely Responsive to Usual Doses of Atomoxetine
A Phase 3 study, sponsored by Eli Lilly and Company.
- Completed
- Registry status
- Phase 3
- Development phase
- 377
- Enrollment target
NCT00485407: Completed Phase 3 study, sponsored by Eli Lilly and Company.
NCT00485407 is a Phase 3 study that has completed, run by Eli Lilly and Company. The registered enrollment target is 377 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (51% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00485407, a Phase 3 study, has completed, sponsored by Eli Lilly and Company.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 377 participants
- Enrollment target
Study Summary
The purpose of this trial is to test the value of dose increases in patients with residual ADHD symptoms after treatment with the usual target dose of atomoxetine
Interventions
- DRUG Atomoxetine Hydrochloride
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 377 participants |
| Start Date | 2003-07 |
| Est. Completion | 2005-06 |
| Phase | Phase 3 |
What the finished NCT00485407 record still lists
NCT00485407 is an interventional study that assigns participants to a tested intervention. The registered 377 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (51% lower).
The record links to 0 conditions, and to 1 intervention - of which Atomoxetine Hydrochloride is the first listed.
NCT00485407 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00485407 about?
NCT00485407 is a clinical study titled "Guiding Dose Increases in Patients Incompletely Responsive to Usual Doses of Atomoxetine". The purpose of this trial is to test the value of dose increases in patients with residual ADHD symptoms after treatment with the usual target dose of atomoxetine
What is the current status of trial NCT00485407?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 377 participants. The study started on 2003-07. Estimated completion is 2005-06.
What interventions are being tested in trial NCT00485407?
The interventions under investigation include: Atomoxetine Hydrochloride (DRUG).
Who is sponsoring clinical trial NCT00485407?
This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00485407's enrollment target sits among peer trials
377 988th of 2000 higher than 1,013 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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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