Patrick Nachman, MD | University of Minnesota
Ignacio Sanz, MD | Emory University
University of Alabama at Birmingham | Birmingham, AL
Stanford University | Stanford, CA
The Lundquist Institute | Torrance, CA
Mayo Clinic Jacksonville | Jacksonville, FL
National Institutes of Health Clinical Center | Bethesda, MD
University of Minnesota | Minneapolis, MN
Columbia University | New York, NY
University of North Carolina | Chapel Hill, NC
Ohio State University | Columbus, OH
University of Pennsylvania | Philadelphia, PA
Providence Medical Research Center | Spokane, WA
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Primary membranous nephropathy (Primary MN) is a disease that causes damage to the parts of the kidney that filter the blood, called the glomeruli. Damage to these filters can lead to high levels of protein in the urine, as well as reduced kidney function. If untreated, about half of patients with nephrotic syndrome will eventually develop kidney failure, also known as end stage renal disease.
In REBOOT, researchers are testing whether a combination of two different drugs, belimumab and rituximab, is safe and if this combination is more effective at blocking the immune attack on the kidney compared to rituximab alone.
Rituximab is a medication that works by blocking B cells (an immune cell that is known to have a role in autoimmune diseases like Primary MN). Rituximab is approved by the FDA for use in rheumatoid arthritis, vasculitis, and certain types of cancers. A few studies have shown that rituximab can be effective in treating some people with Primary MN, but is not FDA approved for Primary MN.
Belimumab is a medication that blocks different types of B cells than rituximab. Belimumab is approved by the FDA for systemic lupus erythematosus (SLE).
REBOOT is a two-part clinical study:
People with Primary MN lose more protein in their urine because the filters in their kidneys may be damaged. It is possible that some belimumab may also be lost in the urine because of this. To make up for this loss, people with higher levels of protein in their urine may need a higher dose of belimumab than the FDA approved dose. One purpose of Part A is to measure belimumab in the blood to determine if people with more protein in their urine should receive a higher dose of belimumab.
All Part A participants will receive belimumab injections under the skin (subcutaneously) once a week for 1 year. They will also receive an infusion of rituximab at the 4th and 6th week of the study. Participants will then be followed for an additional 2 years to determine if Primary MN gets better or worse after stopping study treatment.
Part B participants will be randomly assigned to 1 of 2 treatment groups. You cannot choose your group. A computer will randomly pick which group you will be in.
One group will receive weekly belimumab for 1 year. The other group will receive weekly placebo for 1 year. All participants will receive intravenous (IV) rituximab at weeks 4 and 6. Participants will be followed for an additional 2 years to determine if Primary MN gets better or worse after stopping study treatment and to determine if treatment with belimumab and rituximab results in a more durable remission than rituximab alone.
You may be eligible to participate in REBOOT if you:
