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NCT00910663 · ClinicalTrials.gov registry record · Phase 1
Mycophenolate Mofetil 250 mg Capsules Under Fed Conditions
A Phase 1 study, sponsored by Teva Pharmaceuticals USA.
- Completed
- Registry status
- Phase 1
- Development phase
- 60
- Enrollment target
NCT00910663: Completed Phase 1 study, sponsored by Teva Pharmaceuticals USA.
NCT00910663 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
NCT00910663, a Phase 1 study, has completed, sponsored by Teva Pharmaceuticals USA.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 60 participants
- Enrollment target
Study Summary
The objective of this study was to compare the oral availability of a test product of Mycophenolate Mofetil 250 mg capsule to an equivalent oral dose of the commercially available reference product, CellCept® 250 mg capsule administered to healthy subjects under fed conditions.
Primary Outcome
Bioequivalence based on Cmax - Maximum Drug Concentration
Interventions
- DRUG Mycophenolate Mofetil
- DRUG CellCept®
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2006-10 |
| Est. Completion | 2006-11 |
| Phase | Phase 1 |
What the finished NCT00910663 record still lists
NCT00910663 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 Mycophenolate Mofetil is the first listed.
NCT00910663 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00910663 about?
NCT00910663 is a clinical study titled "Mycophenolate Mofetil 250 mg Capsules Under Fed Conditions". The objective of this study was to compare the oral availability of a test product of Mycophenolate Mofetil 250 mg capsule to an equivalent oral dose of the commercially available reference product, CellCept® 250 mg capsule administered to healthy subjects under fed conditions.
What is the current status of trial NCT00910663?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2006-10. Estimated completion is 2006-11.
What interventions are being tested in trial NCT00910663?
The interventions under investigation include: Mycophenolate Mofetil (DRUG), CellCept® (DRUG).
Who is sponsoring clinical trial NCT00910663?
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 NCT00910663'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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