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NCT00835393 · ClinicalTrials.gov registry record · Phase 1
Pantoprazole Sodium 40 mg DR Tablets Under Non-Fasting Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 50
- Enrollment target
NCT00835393: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00835393 is a Phase 1 study that has completed, run by Teva Pharmaceuticals USA. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00835393, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 50 participants
- Enrollment target
Study Summary
The Objective of this study is to compare the relative bioavailability of pantoprazole sodium 40 mg delayed-released tablets (manufactured by TEVA Pharmaceutical Industries,Ltd. and distributed by TEVA Pharmaceuticals USA)with that of PROTONIX® 40mg delayed-released tablets (Wyeth- Ayerst) in Healthy, adult, non-smoking subjects under non- fasting conditions.
Interventions
- DRUG Pantoprazole Sodium 40 mg delayed-release tablets
- DRUG PROTONIX® 40 mg delayed-release tablets.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2003-12 |
| Est. Completion | 2003-12 |
| Phase | Phase 1 |
What the finished NCT00835393 record still lists
NCT00835393 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).
The record links to 0 conditions, and to 2 interventions - of which Pantoprazole Sodium 40 mg delayed-release tablets is the first listed.
NCT00835393 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00835393 about?
NCT00835393 is a clinical study titled "Pantoprazole Sodium 40 mg DR Tablets Under Non-Fasting Conditions". The Objective of this study is to compare the relative bioavailability of pantoprazole sodium 40 mg delayed-released tablets (manufactured by TEVA Pharmaceutical Industries,Ltd. and distributed by TEVA Pharmaceuticals USA)with that of PROTONIX® 40mg delayed-released tablets (Wyeth- Ayerst) in Health...
What is the current status of trial NCT00835393?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2003-12. Estimated completion is 2003-12.
What interventions are being tested in trial NCT00835393?
The interventions under investigation include: Pantoprazole Sodium 40 mg delayed-release tablets (DRUG), PROTONIX® 40 mg delayed-release tablets. (DRUG).
Who is sponsoring clinical trial NCT00835393?
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 NCT00835393's enrollment target sits among peer trials
50 973rd of 2000 higher than 984 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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