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NCT00745173 · ClinicalTrials.gov registry record · Phase 1
Study Evaluating Premarin and Bazedoxifene Potential Interaction
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
- 30
- Enrollment target
NCT00745173 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 30 participants.
The verdict
NCT00745173, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 30 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the pharmacokinetics (absorption, distribution, breakdown and elimination in the body) of a single dose of bazedoxifene (BZA) 20 mg tablet when administered together with multiple doses of Premarin (conjugated estrogens or CE) to healthy postmenopausal women. Information will also be obtained regarding the safety and tolerability of this combination in healthy, postmenopausal women.
Interventions
- DRUG Premarin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2008-09 |
| Est. Completion | 2008-10 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00745173
The ClinicalTrials.gov registry entry for NCT00745173 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 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 Premarin is the first listed.
NCT00745173 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00745173 about?
NCT00745173 is a clinical study titled "Study Evaluating Premarin and Bazedoxifene Potential Interaction". The purpose of this study is to evaluate the pharmacokinetics (absorption, distribution, breakdown and elimination in the body) of a single dose of bazedoxifene (BZA) 20 mg tablet when administered together with multiple doses of Premarin (conjugated estrogens or CE) to healthy postmenopausal women....
What is the current status of trial NCT00745173?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2008-09. Estimated completion is 2008-10.
What interventions are being tested in trial NCT00745173?
The interventions under investigation include: Premarin (DRUG).
Who is sponsoring clinical trial NCT00745173?
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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