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Efficacy and Safety of Mycophenolate Mofetil in Refractory IgA Nephropathy
Sponsor: Shaheed Suhrawardy Medical College and Hospital
Summary
This study is testing whether a medicine called mycophenolate mofetil (MMF) works better than the usual treatment for people whose kidney disease, called IgA nephropathy, has not improved with standard care. IgA nephropathy is a kidney disease that can cause protein to leak into the urine and, over time, can damage the kidneys. Some people with this disease do not get better even after standard treatment. Doctors call this "refractory" disease. Right now, there is no proven best treatment for these patients in Bangladesh. This study will include 116 adults with kidney disease that has been confirmed by a kidney tissue sample and has not improved with standard treatment. Participants will be split into two equal groups by chance, like a coin flip. One group will take MMF by mouth for 6 months, along with the usual supportive care. The other group will take a steroid medicine called prednisolone, along with the usual supportive care. Both groups will also continue treatments like blood pressure medicines that are already part of standard care for this condition. Researchers want to find out how many people in each group get better, meaning their urine protein drops to a low level and their kidney function stays stable. They will also look at changes in kidney function and any side effects from the medicines. The study will take place at the National Institute of Kidney Diseases and Urology Hospital in Dhaka, Bangladesh, over about one year. Each participant will be followed for 6 months, with check-up visits and blood and urine tests at the start, at 3 months, and at 6 months.
Official title: Efficacy and Safety of Mycophenolate Mofetil in Patients With Refractory IgA Nephropathy in Bangladesh: A Phase II Randomized Controlled Trial
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
104
Start Date
2026-09-01
Completion Date
2027-08-31
Last Updated
2026-08-25
Healthy Volunteers
No
Conditions
Interventions
Mycophenolate Mofetil (MMF)
dministered orally at a total daily dose of 1.5 g in divided doses for a duration of 6 months. Dose adjustment permitted at the discretion of the treating physician in the event of adverse effects.
Prednisolon
Administered orally at 0.8 mg/kg/day, followed by a tapering regimen after the study period according to clinical response and tolerability.
Locations (3)
Dhaka Medical College, Dhaka
Dhaka, Bangladesh
National Institute of Kidney Diseases and Urology
Dhaka, Bangladesh
Shaheed Suhrawardi Medical College Hospital
Dhaka, Bangladesh