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NCT00707980 · ClinicalTrials.gov registry record · Phase 3
Safety and Tolerability of Vortioxetine (Lu AA21004) in Adults With Major Depressive Disorder
A Phase 3 study, sponsored by Takeda.
- Completed
- Registry status
- Phase 3
- Development phase
- 836
- Enrollment target
NCT00707980: Completed Phase 3 study, sponsored by Takeda.
NCT00707980 is a Phase 3 study that has completed, run by Takeda. The registered enrollment target is 836 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00707980, a Phase 3 study, has completed, sponsored by Takeda.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 836 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the long-term efficacy and safety of vortioxetine, once daily (QD), in adults with major depressive disorder.
Primary Outcome
Physical examination consisted of the following body systems: (1) appearance; (2) extremities; (3) skin; (4) head and neck; (5) eyes, ears, nose, and throat; (6) lungs and chest; (7) heart and cardiovascular system; (8) abdomen; and (9) musculoskeletal system. An assessment of the nervous system was conducted; any findings were captured under the appropriate body area. Each system was assessed as normal or abnormal.
Interventions
- DRUG Vortioxetine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 836 participants |
| Start Date | 2008-06 |
| Est. Completion | 2010-08 |
| Phase | Phase 3 |
What the finished NCT00707980 record still lists
NCT00707980 is an interventional study that assigns participants to a tested intervention. The registered 836 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which Vortioxetine is the first listed.
NCT00707980 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00707980 about?
NCT00707980 is a clinical study titled "Safety and Tolerability of Vortioxetine (Lu AA21004) in Adults With Major Depressive Disorder". The purpose of this study is to determine the long-term efficacy and safety of vortioxetine, once daily (QD), in adults with major depressive disorder.
What is the current status of trial NCT00707980?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 836 participants. The study started on 2008-06. Estimated completion is 2010-08.
What interventions are being tested in trial NCT00707980?
The interventions under investigation include: Vortioxetine (DRUG).
Who is sponsoring clinical trial NCT00707980?
This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00707980's enrollment target sits among peer trials
836 396th of 2000 higher than 1,604 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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