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NCT00472927 · ClinicalTrials.gov registry record · Phase 1
Bioequivalence Study of 3 New Formulations of Premarin/MPA Compared With Premarin/MPA (Prempro)
A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 1
- Development phase
NCT00472927: Completed Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
NCT00472927 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00472927, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 1
- Development phase
Study Summary
To evaluate three new investigational tablet formulations of the Food and Drug Administration (FDA) approved medication Prempro™, Premarin combined with medroxyprogesterone acetate (MPA).
Interventions
- DRUG Premarin/MPA 0.45 mg/1.5 mg
Trial Details
| Field | Value |
|---|---|
| Start Date | 2007-05 |
| Est. Completion | 2007-08 |
| Phase | Phase 1 |
What the finished NCT00472927 record still lists
NCT00472927 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.
The record links to 0 conditions, and to 1 intervention - of which Premarin/MPA 0.45 mg/1.5 mg is the first listed.
NCT00472927 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00472927 about?
NCT00472927 is a clinical study titled "Bioequivalence Study of 3 New Formulations of Premarin/MPA Compared With Premarin/MPA (Prempro)". To evaluate three new investigational tablet formulations of the Food and Drug Administration (FDA) approved medication Prempro™, Premarin combined with medroxyprogesterone acetate (MPA).
What is the current status of trial NCT00472927?
This trial is currently completed. It is a Phase 1 study. The study started on 2007-05. Estimated completion is 2007-08.
What interventions are being tested in trial NCT00472927?
The interventions under investigation include: Premarin/MPA 0.45 mg/1.5 mg (DRUG).
Who is sponsoring clinical trial NCT00472927?
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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