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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, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. 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.
Primary Outcome
Bioequivalence based on Cmax
Interventions
- DRUG Clarithromycin
- DRUG Biaxin®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2002-09 |
| Est. Completion | 2002-09 |
| Phase | Phase 1 |
What the finished NCT00835692 record still lists
NCT00835692 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Clarithromycin is the first listed.
NCT00835692 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00835692's enrollment target sits among peer trials
60 831st of 2000 higher than 1,106 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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