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NCT00755872 · ClinicalTrials.gov registry record · Phase 1
Assess the Influence of a High-fat Meal on the Relative Bioavailability Of Two Formulations of Risedronate
A Phase 1 study, sponsored by Warner Chilcott.
- Completed
- Registry status
- Phase 1
- Development phase
- 76
- Enrollment target
NCT00755872: Completed Phase 1 study, sponsored by Warner Chilcott.
NCT00755872 is a Phase 1 study that has completed, run by Warner Chilcott. 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
NCT00755872, a Phase 1 study, has completed, sponsored by Warner Chilcott.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 76 participants
- Enrollment target
Study Summary
This is a randomized, open-label, multi-center, 4-treatment, 4-period crossover study. Approximately 72 healthy, surgically sterile or postmenopausal subjects will be enrolled and have urine collected over 72 hours following administration of risedronate for all 4 treatment periods).
Interventions
- DRUG Risedronate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 76 participants |
| Start Date | 2007-11 |
| Est. Completion | 2008-02 |
| Phase | Phase 1 |
What the finished NCT00755872 record still lists
NCT00755872 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 1 intervention - of which Risedronate is the first listed.
NCT00755872 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00755872 about?
NCT00755872 is a clinical study titled "Assess the Influence of a High-fat Meal on the Relative Bioavailability Of Two Formulations of Risedronate". This is a randomized, open-label, multi-center, 4-treatment, 4-period crossover study. Approximately 72 healthy, surgically sterile or postmenopausal subjects will be enrolled and have urine collected over 72 hours following administration of risedronate for all 4 treatment periods).
What is the current status of trial NCT00755872?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2007-11. Estimated completion is 2008-02.
What interventions are being tested in trial NCT00755872?
The interventions under investigation include: Risedronate (DRUG).
Who is sponsoring clinical trial NCT00755872?
This trial is sponsored by Warner Chilcott, which has 53 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00755872'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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