Actively Recruiting
Obinutuzumab in Treatment of Fibrillary Glomerulonephritis
Led by Mayo Clinic · Updated on 2026-04-13
20
Participants Needed
1
Research Sites
127 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to learn if Obinutuzumab is effective and safe in treating patients with fibrillary glomerulonephritis (FGN).
CONDITIONS
Official Title
Obinutuzumab in Treatment of Fibrillary Glomerulonephritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Biopsy-confirmed fibrillary glomerulonephritis
- Proteinuria greater than 1.0 g/24 hours before starting immunosuppressive therapy
- Estimated glomerular filtration rate (eGFR) of at least 20 ml/min/BSA
You will not qualify if you...
- Secondary fibrillary glomerulonephritis caused by monoclonal gammopathy, autoimmune disease, or cancer
- Presence of other kidney diseases on biopsy, such as diabetic nephropathy
- Positive test for hepatitis B, hepatitis C, or HIV
- Pregnant or breastfeeding
- Active infection at the time of screening
- History of kidney transplant
- Anemia with hemoglobin less than 8.0 g/dL
- Low platelet count below 100,000
- Any other condition or abnormal test that increases risk or affects study results
- Use of cyclophosphamide within the past 6 months
- Use of ACTH or mycophenolate mofetil within the past 30 days
- Use of prednisone above 10 mg/day in the past 15 days
- Previous rituximab treatment with CD20 count below 5 cells/microliter at enrollment
- For women who are not postmenopausal or surgically sterile: agreement to use two effective contraception methods during treatment and for 18 months after
- For men: agreement to use two effective contraception methods during treatment and for 6 months after
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
N
Nicholas Geroux
CONTACT
C
Corbyn Bendtsen
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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