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NCT00649155 · ClinicalTrials.gov registry record · Phase 1
Fasting Study of Ciprofloxacin Extended-Release Tablets 500 mg and Cipro® XR Tablets 500 mg
A Phase 1 study, sponsored by Mylan Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 36
- Enrollment target
NCT00649155 is a Phase 1 study that has completed, run by Mylan Pharmaceuticals. The registered enrollment target is 36 participants.
The verdict
NCT00649155, a Phase 1 study, has completed, sponsored by Mylan Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 36 participants
- Enrollment target
Study Summary
The objective of this study was to investigate the bioequivalence of Mylan's ciprofloxacin extended-release 500 mg tablets to Bayer's Cipro® XR 500 mg tablets following a single, oral 500 mg (1 x 500 mg) dose administered under fasting conditions.
Interventions
- DRUG Ciprofloxacin Extended-Release Tablets 500 mg
- DRUG Cipro® XR Tablets (500 mg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2005-11 |
| Est. Completion | 2005-11 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00649155
The ClinicalTrials.gov registry entry for NCT00649155 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mylan Pharmaceuticals, which has 146 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ciprofloxacin Extended-Release Tablets 500 mg is the first listed.
NCT00649155 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00649155 about?
NCT00649155 is a clinical study titled "Fasting Study of Ciprofloxacin Extended-Release Tablets 500 mg and Cipro® XR Tablets 500 mg". The objective of this study was to investigate the bioequivalence of Mylan's ciprofloxacin extended-release 500 mg tablets to Bayer's Cipro® XR 500 mg tablets following a single, oral 500 mg (1 x 500 mg) dose administered under fasting conditions.
What is the current status of trial NCT00649155?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2005-11. Estimated completion is 2005-11.
What interventions are being tested in trial NCT00649155?
The interventions under investigation include: Ciprofloxacin Extended-Release Tablets 500 mg (DRUG), Cipro® XR Tablets (500 mg (DRUG).
Who is sponsoring clinical trial NCT00649155?
This trial is sponsored by Mylan Pharmaceuticals, which has 146 total clinical trials registered on ClinicalTrials.gov.
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