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NCT00366327 · ClinicalTrials.gov registry record · Phase 3
Study Evaluating Bifeprunox in Patients With Schizophrenia.
A Phase 3 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Terminated
- Registry status
- Phase 3
- Development phase
- 400
- Enrollment target
NCT00366327 is a Phase 3 study that was terminated before completion, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 400 participants.
The verdict
NCT00366327, a Phase 3 study, was terminated before completion, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 400 participants
- Enrollment target
Study Summary
An open-label extension study using a variable dose (20 to 30 mg daily) of bifeprunox to evaluate long-term safety.
Interventions
- DRUG Bifeprunox
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2007-01 |
| Est. Completion | 2008-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00366327
The ClinicalTrials.gov registry entry for NCT00366327 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 400 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.
NCT00366327 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00366327 about?
NCT00366327 is a clinical study titled "Study Evaluating Bifeprunox in Patients With Schizophrenia.". An open-label extension study using a variable dose (20 to 30 mg daily) of bifeprunox to evaluate long-term safety.
What is the current status of trial NCT00366327?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 400 participants. The study started on 2007-01. Estimated completion is 2008-03.
What interventions are being tested in trial NCT00366327?
The interventions under investigation include: Bifeprunox (DRUG).
Who is sponsoring clinical trial NCT00366327?
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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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.