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Terminated Phase 4 Interventional Results available

A Study Designed to Compare the Tolerability of an Increased Dose of Enteric-coated Mycophenolate Acid (MPA) in Renal Transplant Patients Whose Dose of Mycophenolate Mofetil (MMF) Was Reduced Due to Gastrointestinal Symptoms

ClinicalTrials.gov ID: NCT00658333

Public ClinicalTrials.gov record NCT00658333. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 1:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double Blind, Double Dummy Controlled Study to Assess the Tolerability of an Increased Dose of Enteric Coated MPA After Conversion From MMF in Renal Transplant Recipients Who Required MMF Dose Reductions Due to Gastrointestinal Symptoms

Study identification

NCT ID
NCT00658333
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
30 participants

Conditions and interventions

Interventions

  • Enteric-coated Mycophenolate Acid (EC-MPA) Drug
  • Mycophenolate Mofetil (MMF) Drug
  • Placebo MMF Drug
  • Placebo EC-MPA Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 29, 2008
Primary completion
Feb 28, 2009
Completion
Feb 28, 2009
Last update posted
Aug 6, 2012

2008 – 2009

United States locations

U.S. sites
37
U.S. states
22
U.S. cities
31
Facility City State ZIP Site status
Novartis Phoenix Arizona 85012
Novartis Los Angeles California 90033
Novartis Los Angeles California 90057
Novartis Los Angeles California 90095
Novartis Orange California 92868
Novartis San Diego California 92123
Novartis San Francisco California 94143
Novartis Aurora Colorado 80010
Novartis Washington D.C. District of Columbia 20007
Novartis Orlando Florida 32804
Novartis New Orleans Louisiana 70121
Novartis Portland Maine 04102
Novartis Baltimore Maryland 21201
Novartis Boston Massachusetts 02114
Novartis Boston Massachusetts 02215
Novartis Springfield Massachusetts 01107
Novarits Detroit Michigan 48236
Novartis New York New York 10029
Novartis New York New York 10032
Novartis New York New York 10065
Novartis Charlotte North Carolina 28207
Novartis Durham North Carolina 27710
Novartis Greenville North Carolina 27834
Novartis Winston-Salem North Carolina 27103
Novarits Fargo North Dakota 58123
Novartis Cleveland Ohio 44106
Novartis Portland Oregon 97210
Novartis Portland Oregon 97239
Novartis Philadelphia Pennsylvania 19140
Novartis Providence Rhode Island 02903
Novartis Nashville Tennessee 37232
Novartis Dallas Texas 75230
Novartis Houston Texas 77054
Novartis Temple Texas 76508
Novartis Murray Utah 84107
Novartis Burlington Vermont 05401
Novartis Charlottesville Virginia 22908

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00658333, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 6, 2012 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00658333 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →