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NCT00574743 · ClinicalTrials.gov registry record · Phase 4

Efficacy and Safety of Enteric-coated Mycophenolate Sodium (EC-MPS) in Comparison to Mycophenolate Mofetil (MMF) in de Nove Heart Patients

A Phase 4 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
162
Enrollment target

NCT00574743: Completed Phase 4 study, sponsored by Novartis Pharmaceuticals.

NCT00574743 is a Phase 4 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 162 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00574743, a Phase 4 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
162 participants
Enrollment target

Study Summary

This study will evaluate the safety and efficacy of EC-MPS (ERL080) in comparison to MMF in de novo heart recipients.

Interventions

  • DRUG Enteric-coated Mycophenolate Sodium

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2002-01
Phase Phase 4
Novartis Pharmaceuticals

1,375 total trials

What the finished NCT00574743 record still lists

NCT00574743 is an interventional study that assigns participants to a tested intervention. The registered 162 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (69% lower).

The record links to 0 conditions, and to 1 intervention - of which Enteric-coated Mycophenolate Sodium is the first listed.

NCT00574743 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00574743 about?

NCT00574743 is a clinical study titled "Efficacy and Safety of Enteric-coated Mycophenolate Sodium (EC-MPS) in Comparison to Mycophenolate Mofetil (MMF) in de Nove Heart Patients". This study will evaluate the safety and efficacy of EC-MPS (ERL080) in comparison to MMF in de novo heart recipients.

What is the current status of trial NCT00574743?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 162 participants. The study started on 2002-01.

What interventions are being tested in trial NCT00574743?

The interventions under investigation include: Enteric-coated Mycophenolate Sodium (DRUG).

Who is sponsoring clinical trial NCT00574743?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00574743's enrollment target sits among peer trials

162 503rd of 2000 higher than 1,495 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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Source: ClinicalTrials.gov NCT00574743, the US trial registry maintained by the National Library of Medicine. NCT00574743 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.