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NCT00835692 · ClinicalTrials.gov registry record · Phase 1
Clarithromycin 500 mg Tablets Under Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
NCT00835692: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00835692 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 60 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00835692, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
Study Summary
This study will compare the relative bioavailability (rate and extent of absorption) of 500 mg Clarithromycin Tablets with that of 500 mg BIAXIN® Tablets following a single oral dose (1 x 500 mg tablet) in healthy adult subjects under fasting conditions.
Interventions
- DRUG Clarithromycin
- DRUG Biaxin®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2002-09 |
| Est. Completion | 2002-09 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00835692
The ClinicalTrials.gov registry entry for NCT00835692 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Pharmaceuticals USA, which has 83 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Clarithromycin is the first listed.
NCT00835692 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00835692 about?
NCT00835692 is a clinical study titled "Clarithromycin 500 mg Tablets Under Fasting Conditions". This study will compare the relative bioavailability (rate and extent of absorption) of 500 mg Clarithromycin Tablets with that of 500 mg BIAXIN® Tablets following a single oral dose (1 x 500 mg tablet) in healthy adult subjects under fasting conditions.
What is the current status of trial NCT00835692?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2002-09. Estimated completion is 2002-09.
What interventions are being tested in trial NCT00835692?
The interventions under investigation include: Clarithromycin (DRUG), Biaxin® (DRUG).
Who is sponsoring clinical trial NCT00835692?
This trial is sponsored by Teva Pharmaceuticals USA, which has 83 total clinical trials registered on ClinicalTrials.gov.
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