Trial ID: | L0732 |
Source ID: | NCT00446251
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Associated Drug: |
Rituximab
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Title: |
Effects of Rituximab and Mycophenolate Mofetil (MMF) on Highly Sensitized Patients Awaiting Renal Transplant
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Acronym: |
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Status: |
COMPLETED
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Study Results: |
YES
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Results: |
https://ClinicalTrials.gov/show/NCT00446251/results
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Conditions: |
Kidney Failure, Chronic|Diabetic Nephropathies|Glomerulonephritis, IGA|Hypertension, Renal
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Interventions: |
DRUG: Rituximab|DRUG: Mycophenolate mofetil (MMF)
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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
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Sponsor/Collaborators: |
Sponsor: University of Washington | Collaborators: Genentech, Inc.
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE2
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Enrollment: |
14
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: NON_RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2006-12
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Completion Date: |
2008-12
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Results First Posted: |
2010-03-29
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Last Update Posted: |
2010-04-06
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Locations: |
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URL: |
https://clinicaltrials.gov/show/NCT00446251
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