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NCT00245973 · ClinicalTrials.gov registry record · Phase 3
Study Evaluating Bifeprunox in Bipolar Depression
A Phase 3 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 3
- Development phase
- 380
- Enrollment target
NCT00245973 is a Phase 3 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 380 participants.
The verdict
NCT00245973, a Phase 3 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 380 participants
- Enrollment target
Study Summary
The purpose of the study is to investigate whether eight weeks of treatment with flexible doses of Bifeprunox is superior to treatment with placebo in depressed patients with bipolar disorder.
Interventions
- DRUG Bifeprunox
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 380 participants |
| Start Date | 2005-06 |
| Est. Completion | 2007-10 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00245973
The ClinicalTrials.gov registry entry for NCT00245973 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 380 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Bifeprunox is the first listed.
NCT00245973 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00245973 about?
NCT00245973 is a clinical study titled "Study Evaluating Bifeprunox in Bipolar Depression". The purpose of the study is to investigate whether eight weeks of treatment with flexible doses of Bifeprunox is superior to treatment with placebo in depressed patients with bipolar disorder.
What is the current status of trial NCT00245973?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 380 participants. The study started on 2005-06. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00245973?
The interventions under investigation include: Bifeprunox (DRUG).
Who is sponsoring clinical trial NCT00245973?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.
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