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Trial · NCT00318474

Mycophenolate Mofetil (MMF) in Patients With IgA Nephropathy

NCT00318474, Phase 3, Terminated, St. Joseph's Hospital and Medical Center, Phoenix; results first posted 2014-10-01

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Mycophenolate Mofetil (MMF) in Patients With IgA Nephropathy. Trials, record NCT00318474. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00318474

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Mycophenolate Mofetil (MMF) in Patients With IgA Nephropathy
NCT number
NCT00318474
Status
Terminated
Phases
Phase 3
Enrollment
184 participants, actual
Lead sponsor
St. Joseph's Hospital and Medical Center, Phoenix
Conditions
IgA Nephropathy
Interventions
Mycophenolate Mofetil (MMF), MMF Placebo, ACEi, FOS
First posted
2006-04-26
Last updated
2016-03-07
Results first posted
2014-10-01

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Proteinuria - Uprotein/Creatinine RatioPlan was to measure uprotein/creatinine ratio for 12 months on MMF or placebo, and then 12 months post-treatment. Data given after 6 months MMF/placebo.Urine protein/creatinine ratio after 6 months treatment with MMF or placebo.
SecondaryChange in Estimated Glomerular Filtration Rate (GFR) to Less Than 60% of the Baseline Level12 months

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange in Proteinuria - Uprotein/Creatinine RatioPlan was to measure uprotein/creatinine ratio for 12 months on MMF or placebo, and then 12 months post-treatment. Data given after 6 months MMF/placebo.ratioMEAN
SECONDARYChange in Estimated Glomerular Filtration Rate (GFR) to Less Than 60% of the Baseline Level12 months

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change in Proteinuria - Uprotein/Creatinine RatioMycophenolate Mofetil (MMF)1.40Standard Deviation 0.72ratio
Change in Proteinuria - Uprotein/Creatinine RatioPlacebo1.58Standard Deviation 1.07ratio

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDMycophenolate Mofetil (MMF)25
Overall StudySTARTEDPlacebo27
Overall StudyCOMPLETEDMycophenolate Mofetil (MMF)7
Overall StudyCOMPLETEDPlacebo10
Overall StudyNOT COMPLETEDMycophenolate Mofetil (MMF)18
Overall StudyNOT COMPLETEDPlacebo17

Adverse events22

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherbackacheMusculoskeletal and connective tissue disordersMycophenolate Mofetil (MMF)625
otherbackacheMusculoskeletal and connective tissue disordersPlacebo627
othercommon coldRespiratory, thoracic and mediastinal disordersMycophenolate Mofetil (MMF)525
othercommon coldRespiratory, thoracic and mediastinal disordersPlacebo727
othercoughingRespiratory, thoracic and mediastinal disordersMycophenolate Mofetil (MMF)925
othercoughingRespiratory, thoracic and mediastinal disordersPlacebo927
otherdiarrheaGastrointestinal disordersMycophenolate Mofetil (MMF)425
otherdiarrheaGastrointestinal disordersPlacebo627
otheredemaGeneral disordersMycophenolate Mofetil (MMF)525
otheredemaGeneral disordersPlacebo327

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityMycophenolate Mofetil (MMF)
Total, all-cause mortalityPlacebo
Total, other adverse eventsMycophenolate Mofetil (MMF)2525
Total, other adverse eventsPlacebo2727
Total, serious adverse eventsMycophenolate Mofetil (MMF)125
Total, serious adverse eventsPlacebo127

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
38299639DERIVEDPubMed
38864363DERIVEDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Mycophenolate Mofetil (MMF) vs Placebo: serious adverse events

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00318474

GET https://conductscience.org/api/trials/v1/NCT00318474/events?page=2