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NCT00135421 · ClinicalTrials.gov registry record · Phase 1
Study of BMS-562086 in the Treatment of Outpatients With Major Depressive Disorder
A Phase 1 study, sponsored by Bristol-Myers Squibb.
- Completed
- Registry status
- Phase 1
- Development phase
- 271
- Enrollment target
NCT00135421 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 271 participants.
The verdict
NCT00135421, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 271 participants
- Enrollment target
Study Summary
The purpose of this clinical research study is to learn whether BMS-562086 is both safe and effective in treating outpatients with major depressive disorder.
Interventions
- DRUG Placebo
- DRUG Escitalopram
- DRUG Pexacerfont
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 271 participants |
| Start Date | 2005-11 |
| Est. Completion | 2007-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00135421
The ClinicalTrials.gov registry entry for NCT00135421 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 271 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT00135421 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00135421 about?
NCT00135421 is a clinical study titled "Study of BMS-562086 in the Treatment of Outpatients With Major Depressive Disorder". The purpose of this clinical research study is to learn whether BMS-562086 is both safe and effective in treating outpatients with major depressive disorder.
What is the current status of trial NCT00135421?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 271 participants. The study started on 2005-11. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00135421?
The interventions under investigation include: Placebo (DRUG), Escitalopram (DRUG), Pexacerfont (DRUG).
Who is sponsoring clinical trial NCT00135421?
This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.
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