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NCT00758004 · ClinicalTrials.gov registry record · Phase 1
Bioequivalence Study Of Pediatric Appropriate Formulation
A Phase 1 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- Completed
- Registry status
- Phase 1
- Development phase
- 76
- Enrollment target
NCT00758004: Completed Phase 1 study, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
NCT00758004 is a Phase 1 study that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 76 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00758004, a Phase 1 study, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 76 participants
- Enrollment target
Study Summary
To determine bioequivalence of pediatric appropriate 80 mg atorvastatin formulation comparing to the 80 mg commercial atorvastatin calcium tablet formulation.
Interventions
- DRUG Atorvastatin
- DRUG Atorvastatin pediatric appropriate formulation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2008-10 |
| Est. Completion | 2009-03 |
| Phase | Phase 1 |
What the finished NCT00758004 record still lists
NCT00758004 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher).
The record links to 0 conditions, and to 2 interventions - of which Atorvastatin is the first listed.
NCT00758004 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00758004 about?
NCT00758004 is a clinical study titled "Bioequivalence Study Of Pediatric Appropriate Formulation". To determine bioequivalence of pediatric appropriate 80 mg atorvastatin formulation comparing to the 80 mg commercial atorvastatin calcium tablet formulation.
What is the current status of trial NCT00758004?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2008-10. Estimated completion is 2009-03.
What interventions are being tested in trial NCT00758004?
The interventions under investigation include: Atorvastatin (DRUG), Atorvastatin pediatric appropriate formulation (DRUG).
Who is sponsoring clinical trial NCT00758004?
This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00758004's enrollment target sits among peer trials
76 705th of 2000 higher than 1,290 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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