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NCT00864734 · ClinicalTrials.gov registry record · Phase 1
A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets Under Non-fasting Conditions
A Phase 1 study, sponsored by Actavis.
- Completed
- Registry status
- Phase 1
- Development phase
- 24
- Enrollment target
NCT00864734: Completed Phase 1 study, sponsored by Actavis.
NCT00864734 is a Phase 1 study that has completed, run by Actavis. The registered enrollment target is 24 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00864734, a Phase 1 study, has completed, sponsored by Actavis.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 24 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the relative bioavailability of 5 mg Glyburide/500 mg Metformin Hydrochloride Tablets by Purepac Pharmaceutical Co. with that of 5 mg/500 mg CLUCOVANCE® Tablets by Bristol-Myers Squibb Company following a single oral dose (1 x 5 mg/500 mg tablet) in healthy adult volunteers under non-fasting conditions.
Interventions
- DRUG Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg
- DRUG CLUCOVANCE® 5 mg/500 mg Tablets, single dose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2002-11 |
| Est. Completion | 2002-11 |
| Phase | Phase 1 |
What the finished NCT00864734 record still lists
NCT00864734 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (60% lower).
The record links to 0 conditions, and to 2 interventions - of which Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg is the first listed.
NCT00864734 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00864734 about?
NCT00864734 is a clinical study titled "A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets Under Non-fasting Conditions". The purpose of this study is to compare the relative bioavailability of 5 mg Glyburide/500 mg Metformin Hydrochloride Tablets by Purepac Pharmaceutical Co. with that of 5 mg/500 mg CLUCOVANCE® Tablets by Bristol-Myers Squibb Company following a single oral dose (1 x 5 mg/500 mg tablet) in healthy ad...
What is the current status of trial NCT00864734?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2002-11. Estimated completion is 2002-11.
What interventions are being tested in trial NCT00864734?
The interventions under investigation include: Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg (DRUG), CLUCOVANCE® 5 mg/500 mg Tablets, single dose (DRUG).
Who is sponsoring clinical trial NCT00864734?
This trial is sponsored by Actavis, which has 79 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00864734's enrollment target sits among peer trials
24 1520th of 2000 higher than 405 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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