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NCT00150020 · ClinicalTrials.gov registry record · Phase 4
Safety and Tolerability of Enteric-Coated Mycophenolate Sodium (EC-MPS) in Renal Transplant Patients With GI Intolerance
A Phase 4 study, sponsored by Novartis.
- Completed
- Registry status
- Phase 4
- Development phase
- 728
- Enrollment target
NCT00150020: Completed Phase 4 study, sponsored by Novartis.
NCT00150020 is a Phase 4 study that has completed, run by Novartis. The registered enrollment target is 728 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (41% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00150020, a Phase 4 study, has completed, sponsored by Novartis.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 728 participants
- Enrollment target
Study Summary
The aim of this study is to evaluate the safety and tolerability of EC-MPS in maintenance renal transplant patients who experience gastrointestinal (GI) intolerance due to adverse events associated with mycophenolate mofetil (MMF) and were converted to EC-MPS.
Interventions
- DRUG Enteric-coated mycophenolate sodium (EC-MPS)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 728 participants |
| Start Date | 2004-10 |
| Phase | Phase 4 |
What the finished NCT00150020 record still lists
NCT00150020 is an interventional study that assigns participants to a tested intervention. The registered 728 participants enrollment target is mid-sized for trials with a published cap, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (41% higher).
The record links to 0 conditions, and to 1 intervention - of which Enteric-coated mycophenolate sodium (EC-MPS) is the first listed.
NCT00150020 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00150020 about?
NCT00150020 is a clinical study titled "Safety and Tolerability of Enteric-Coated Mycophenolate Sodium (EC-MPS) in Renal Transplant Patients With GI Intolerance". The aim of this study is to evaluate the safety and tolerability of EC-MPS in maintenance renal transplant patients who experience gastrointestinal (GI) intolerance due to adverse events associated with mycophenolate mofetil (MMF) and were converted to EC-MPS.
What is the current status of trial NCT00150020?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 728 participants. The study started on 2004-10.
What interventions are being tested in trial NCT00150020?
The interventions under investigation include: Enteric-coated mycophenolate sodium (EC-MPS) (DRUG).
Who is sponsoring clinical trial NCT00150020?
This trial is sponsored by Novartis, which has 265 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00150020's enrollment target sits among peer trials
728 114th of 2000 higher than 1,887 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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