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Clinical trialNCT00451867TerminatedPhase 3Interventional

A Randomized Multicenter Double-Blind CT to Evaluate the Efficacy and Safety of Mycophenolate Mofetil . . .

SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Enrollment210Interstitial CystitisPainful Bladder Syndrome
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to investigate the safety and effectiveness of a medication called CellCept in treating refractory (has not responded to other treatments) interstitial cystitis. CellCept belongs to a class of medications called immuno-suppressants. Immuno-suppressants work in the body by reducing the immune system's ability to produce certain reactions that can cause inflammation. In some people, the inflammation produced by their immune system can damage healthy tissues and cause symptoms of pain and discomfort. CellCept is approved by the U.S. Food and Drug Administration (FDA) for use in patients who have had an organ transplant. When used in combination with other drugs, CellCept helps to prevent the rejection of the transplanted organ and is used widely in patients who have received kidney, liver and heart transplants. CellCept is also frequently used but not FDA approved for the treatment of severe rheumatoid arthritis which is a disease caused when the body's immune system acts against healthy tissues in the joints. Due to its special activity, CellCept may be useful in treating certain inflammatory diseases or conditions like interstitial cystitis.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Canada
  • Queen'S University

    Kingston, Ontario, Canada

United States
  • Univeristy of California San Diego

    San Diego, California, United States

  • Stanford University Medical Center

    Stanford, California, United States

  • Loyola University Medical Center

    Maywood, Illinois, United States

  • University of Iowa

    Iowa City, Iowa, United States

  • University of Maryland

    Baltimore, Maryland, United States

  • Henry Ford Hospital

    Detroit, Michigan, United States

  • William Beaumont Hospital

    Royal Oak, Michigan, United States

  • University of Rochester

    Rochester, New York, United States

  • University of Pennsylvania Health System

    Philadelphia, Pennsylvania, United States

  • University of Washington

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Mycofenolate MofetilMycophenolate mofetilPlacebo
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Mar 2007
Primary completion
29 Feb 2008
Completion
30 Apr 2008
Last update posted
14 Jan 2010
Registered enrollment
210
Registry id
NCT00451867

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.