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Clinical Trial Details

Trial ID: L0732
Source ID: NCT00446251
Associated Drug: Rituximab
Title: Effects of Rituximab and Mycophenolate Mofetil (MMF) on Highly Sensitized Patients Awaiting Renal Transplant
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT00446251/results
Conditions: Kidney Failure, Chronic|Diabetic Nephropathies|Glomerulonephritis, IGA|Hypertension, Renal
Interventions: DRUG: Rituximab|DRUG: Mycophenolate mofetil (MMF)
Outcome Measures: Primary: The Number of Subjects Who Experience a Decrease in Their Panel of Reactive Antibodies (PRA) at 6 Months Post Rituximab Infusion., the number of subjects who experience a decrease in their Panel of Reactive Antibodies (PRA) at 6 months and 12 months post Rituximab infusion, Month 6 from start of study | Secondary: The Number of Subjects Who Experience a Change From Baseline in Their Panel of Reactive Antibody (PRA) Titers at 12 Months Post Rituximab Infusion., Month 12 from start of study|The Number of Subjects With a Negative Crossmatch at the Time of Transplant., Month 12 from start of study
Sponsor/Collaborators: Sponsor: University of Washington | Collaborators: Genentech, Inc.
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 14
Study Type: INTERVENTIONAL
Study Designs: Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2006-12
Completion Date: 2008-12
Results First Posted: 2010-03-29
Last Update Posted: 2010-04-06
Locations:
URL: https://clinicaltrials.gov/show/NCT00446251