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NCT00577850 · ClinicalTrials.gov registry record · Phase 1
Pharmacokinetics of a Single 14C-labeled Dose of Risedronate or Alendronate Followed by Once-a-week Unlabeled Oral Dose
A Phase 1 study of Osteoporosis and Osteopenia, sponsored by Warner Chilcott.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
- 2
- Study locations
NCT00577850 is a Phase 1 study of Osteoporosis and Osteopenia that has completed, run by Warner Chilcott. The registered enrollment target is 32 participants, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT00577850, a Phase 1 study of Osteoporosis and Osteopenia, has completed, sponsored by Warner Chilcott.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
- 2
- Study locations
Study Summary
The primary objective of this study is to compare the urinary excretion of 14C-labeled risedronate and alendronate over 28 days.
Conditions Studied
Interventions
- DRUG alendronate
- DRUG risedronate
Study Locations (2)
Florida
- Research Facility - Gainesville
Louisiana
- Research Site - New Orleans
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2002-11 |
| Est. Completion | 2004-02 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00577850
The ClinicalTrials.gov registry entry for NCT00577850 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (98% lower). The listed sponsor is Warner Chilcott, which has 53 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Osteoporosis appearing as the primary indexed condition, and to 2 interventions - of which alendronate is the first listed.
NCT00577850 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, Louisiana.
Frequently Asked Questions
What is clinical trial NCT00577850 about?
NCT00577850 is a clinical study titled "Pharmacokinetics of a Single 14C-labeled Dose of Risedronate or Alendronate Followed by Once-a-week Unlabeled Oral Dose". The primary objective of this study is to compare the urinary excretion of 14C-labeled risedronate and alendronate over 28 days.
What is the current status of trial NCT00577850?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2002-11. Estimated completion is 2004-02.
What conditions does trial NCT00577850 study?
This clinical trial studies the following conditions: Osteoporosis, Osteopenia.
What interventions are being tested in trial NCT00577850?
The interventions under investigation include: alendronate (DRUG), risedronate (DRUG).
Who is sponsoring clinical trial NCT00577850?
This trial is sponsored by Warner Chilcott, which has 53 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00577850 being conducted?
This trial has 2 study locations across Florida, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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