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Completed Phase 4 Interventional

Pharmacogenetic Study of CellCept (Mycophenolate Mofetil) in Kidney Transplant Patients.

ClinicalTrials.gov ID: NCT00337493

Public ClinicalTrials.gov record NCT00337493. 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 Oct 7, 2026, 10:44 AM 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 Study to Investigate the Impact of Pharmacogenetics on CellCept Use, in Patients Participating in a Study in Renal Transplantation

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will determine which, if any, allelic variants of mycophenolic acid (MPA) metabolizing enzymes, drug transporters and drug targets are associated with the observed variation in pharmacokinetic and pharmacodynamic outcomes observed with CellCept usage. Patients participating in study ML17225 will be eligible for this pharmacogenetic investigation, and will have one additional blood sample taken during the study. The anticipated time on study treatment in study ML17225 is 1-2 years, and the target sample size is 500+ individuals.

Study identification

NCT ID
NCT00337493
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
155 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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
Dec 2005 (Type not available)
Primary completion
Jan 2008 (Actual)
Completion
Jan 2008 (Actual)
Last update posted
Sep 17, 2012

2005 – 2008

United States locations

U.S. sites
20
U.S. states
18
U.S. cities
20
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294 —
Not listed Little Rock Arkansas 72205-7199 —
Not listed Los Angeles California 90057 —
Not listed Denver Colorado 80262 —
Not listed Gainesville Florida 32610-0224 —
Not listed Orlando Florida 32804 —
Not listed Augusta Georgia 30912 —
Not listed Chicago Illinois 60637 —
Not listed Indianapolis Indiana 46202-5167 —
Not listed Lexington Kentucky 40536-0293 —
Not listed Shreveport Louisiana 71130 —
Not listed Boston Massachusetts 02111 —
Not listed Hackensack New Jersey 07601 —
Not listed Livingston New Jersey 07039 —
Not listed Buffalo New York 14203 —
Not listed Chapel Hill North Carolina 27599 —
Not listed Fargo North Dakota 58122 —
Not listed Portland Oregon 97210 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Madison Wisconsin 53792 —

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 NCT00337493, 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 Sep 17, 2012 · Synced Oct 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00337493 live on ClinicalTrials.gov.

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