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NCT00834795 · ClinicalTrials.gov registry record · Phase 1
Carvedilol 25 mg in 36 Fasted, Healthy, Adult Subjects
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 36
- Enrollment target
NCT00834795: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00834795 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 36 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00834795, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 36 participants
- Enrollment target
Study Summary
The objective of this randomized, single-dose, two-way crossover evaluation is to compare the relative bioequivalence of a test carvedilol formulation (TEVA Pharmaceuticals USA) to and equivalent oral dose of the commercially available carvedilol (COREG®, SmithKline Beecham Pharmaceuticals) in a test population of 36 adult individuals under fasting conditions.
Primary Outcome
Bioequivalence based on Cmax
Interventions
- DRUG Carvedilol 25 mg tablets
- DRUG COREG® 25 mg tablets
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2001-12 |
| Est. Completion | 2001-12 |
| Phase | Phase 1 |
What the finished NCT00834795 record still lists
NCT00834795 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower).
The record links to 0 conditions, and to 2 interventions - of which Carvedilol 25 mg tablets is the first listed.
NCT00834795 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00834795 about?
NCT00834795 is a clinical study titled "Carvedilol 25 mg in 36 Fasted, Healthy, Adult Subjects". The objective of this randomized, single-dose, two-way crossover evaluation is to compare the relative bioequivalence of a test carvedilol formulation (TEVA Pharmaceuticals USA) to and equivalent oral dose of the commercially available carvedilol (COREG®, SmithKline Beecham Pharmaceuticals) in a tes...
What is the current status of trial NCT00834795?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2001-12. Estimated completion is 2001-12.
What interventions are being tested in trial NCT00834795?
The interventions under investigation include: Carvedilol 25 mg tablets (DRUG), COREG® 25 mg tablets (DRUG).
Who is sponsoring clinical trial NCT00834795?
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 NCT00834795's enrollment target sits among peer trials
36 1210th of 2000 higher than 743 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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