Rituximab in Renal Allograft Recipients Who Develop Early De Novo Anti-HLA Alloantibodies
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Study ID
- NCT00307125
- Phase
- PHASE2
- Status
- Completed
Conditions
- Graft Function/Survival
- Kidney Transplant
- Kidney Transplant Recipient
- de Novo HLA Antibodies Development
Eligibility Criteria
- Sex
- ALL
- Age
- 5 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Rituximab plus immunosuppression — DRUGGenetically engineered monoclonal antibody directed against the CD20 antigen on B cells and is known to deplete B cells when administered intravenously. Generally used in the treatment of non-Hodgkin's lymphoma Standard immunosuppression is site-specific.
- Placebo plus immunosuppression — DRUGPlacebo dosing: Adult Dosing (Subjects \>18 years): 1000 mg on days 0 and 14; Pediatric Dosing (Subject \<\\=18 years): 375 mg/m\^2/dose (maximum 500 mg/dose) in 4 doses, once per week (Days 0, 8, 15 and 22). Standard immunosuppression is site-specific.
Study Details
The purpose of this study is to determine whether treatment with rituximab (anti-CD20, Rituxan®, MabThera®) in individuals who develop new anti-HLA antibodies after renal (kidney) transplant will promote longer-term survival of the transplanted kidney.The pilot study compares the use of rituximab (Rituxan®) + site-specific standard immunosuppression to placebo + site-specific standard immunosuppression in the treatment of circulating anti-HLA antibodies in subjects who develop de novo anti-HLA antibodies between 3-36 months after transplant.
Key Dates
- Start date
- Mar 31, 2006
- Status verified
- Mar 2015
- Primary completion
- Dec 31, 2012
- Completion
- Dec 31, 2012
Study Design
- Enrollment
- 757 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Pilot Phase-Rituximab plus immunosuppressionEnrollment into a Stage 2 pilot treatment study will occur after Stage 1. Adult Rituximab Dosing (Subjects \> 18 years): 1000 mg on days 0 and 14; Pediatric Rituximab Dosing (Subjects \<\\=18 years): 375 mg/m\^2/dose (maximum 500 mg/dose) in 4 doses, once per week (Days 0, 8, 15 and 22). Standard immunosuppression is site-specific.
- Placebo Comparator: Pilot Phase-Placebo plus immunosuppressionAdult Placebo Dosing (Subjects \>18 years): 1000 mg on days 0 and 14; Pediatric Placebo Dosing (Subject \<\\=18 years): 375 mg/m\^2/dose (maximum 500 mg/dose) in 4 doses, once per week (Days 0, 8, 15 and 22). Standard immunosuppression is site-specific.
Primary Outcome Measure
During Screening Phase: Incidence of Alloantibody Development [ Time Frame: During screening window of 3-60 months post kidney transplant ]
Locations (17)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Alabama | Birmingham | Alabama | 35294 | - |
| University of Alabama, Pediatric Nephrology | Birmingham | Alabama | 35294 | - |
| University of California, San Francisco | San Francisco | California | 94143 | - |
| University of Florida | Gainesville | Florida | 32601 | - |
| Northwestern University | Chicago | Illinois | 60611 | - |
| University of Illinois | Chicago | Illinois | 60607 | - |
| University of Maryland | Baltimore | Maryland | 21201 | - |
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | - |
| Brigham and Women's Hospital | Boston | Massachusetts | 02115 | - |
| Children's Hospital Boston | Boston | Massachusetts | 02115 | - |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | - |
| Saint Barnabas Medical Center | Livingston | New Jersey | 07039 | - |
| Legacy Transplant Services | Portland | Oregon | 97210 | - |
| Oregon Health Science University | Portland | Oregon | 97219 | - |
| Children's Hospital of Philadelphia | Philadelphia | Pennsylvania | 19104 | - |
| The Methodist Hospital | Houston | Texas | 77030 | - |
| Children's Hospital and Regional Medical Center | Seattle | Washington | 98105 | - |
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