Pharmacogenetic Study of CellCept (Mycophenolate Mofetil) in Kidney Transplant Patients.
Completed · Phase 4
Conditions studied: Kidney Transplantation
In brief
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.
Key facts
- Study ID
- NCT00337493
- Run by
- Hoffmann-La Roche
- People needed
- 155
- Starts
- 2005-12-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2012-09-17
Who can join
Age: 13 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- patients participating in study ML17225.
You may not qualify if…
- N/A.
Where it is running
- Study site — Birmingham, Alabama, United States
- Study site — Little Rock, Arkansas, United States
- Study site — Los Angeles, California, United States
- Study site — Denver, Colorado, United States
- Study site — Gainesville, Florida, United States
- Study site — Orlando, Florida, United States
- Study site — Augusta, Georgia, United States
- Study site — Chicago, Illinois, United States
- Study site — Indianapolis, Indiana, United States
- Study site — Lexington, Kentucky, United States
- Study site — Shreveport, Louisiana, United States
- Study site — Boston, Massachusetts, United States
- Study site — Hackensack, New Jersey, United States
- Study site — Livingston, New Jersey, United States
- Study site — Buffalo, New York, United States
- Study site — Chapel Hill, North Carolina, United States
- Study site — Fargo, North Dakota, United States
- Study site — Portland, Oregon, United States
- Study site — Philadelphia, Pennsylvania, United States
- Study site — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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