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NCT01153009 · ClinicalTrials.gov registry record · Phase 3
Safety and Efficacy of Vortioxetine (Lu AA21004) in Adults With Major Depressive Disorder
A Phase 3 study, sponsored by Takeda.
- Completed
- Registry status
- Phase 3
- Development phase
- 614
- Enrollment target
NCT01153009 is a Phase 3 study that has completed, run by Takeda. The registered enrollment target is 614 participants.
The verdict
NCT01153009, a Phase 3 study, has completed, sponsored by Takeda.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 614 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the efficacy, safety and tolerability of vortioxetine, once daily (QD), compared with placebo in adults with major depressive disorder.
Interventions
- DRUG Placebo
- DRUG Duloxetine
- DRUG Vortioxetine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 614 participants |
| Start Date | 2010-06 |
| Est. Completion | 2012-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01153009
The ClinicalTrials.gov registry entry for NCT01153009 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 614 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Takeda, which has 408 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT01153009 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01153009 about?
NCT01153009 is a clinical study titled "Safety and Efficacy of Vortioxetine (Lu AA21004) in Adults With Major Depressive Disorder". The purpose of this study is to evaluate the efficacy, safety and tolerability of vortioxetine, once daily (QD), compared with placebo in adults with major depressive disorder.
What is the current status of trial NCT01153009?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 614 participants. The study started on 2010-06. Estimated completion is 2012-03.
What interventions are being tested in trial NCT01153009?
The interventions under investigation include: Placebo (DRUG), Duloxetine (DRUG), Vortioxetine (DRUG).
Who is sponsoring clinical trial NCT01153009?
This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.
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