Center For Pediatric And Adolescent Medicine Of The Johannes Gutenberg University Mainz
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Mainz, Germany
Rare diseases
Investigational molecules
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A plain-language summary of the goals, design and what participants do
This clinical trial is focused on studying two kidney diseases: C3 Glomerulopathy and Idiopathic Immune-Complex Membranoproliferative Glomerulonephritis. These are conditions where the immune system affects the kidneys, leading to inflammation and potential damage. The treatment being tested in this study is a medication called Iptacopan, which is taken orally in the form of hard gelatin capsules. The purpose of the study is to evaluate the long-term effectiveness, safety, and tolerability of Iptacopan in individuals with these kidney diseases.
Participants in the study will receive Iptacopan over a period of time, with the maximum treatment period being 66 weeks. The study will monitor how well the medication works in managing the kidney conditions and will also keep track of any side effects or issues that may arise during the treatment. The study aims to provide valuable information on how Iptacopan can help in treating these specific kidney diseases.
Throughout the study, participants will have regular check-ups to assess their kidney function and overall health. This will include monitoring important health indicators and any changes in the condition of the kidneys. The study is designed to ensure that participants are closely observed to gather comprehensive data on the long-term use of Iptacopan for these kidney diseases.
The trial runs in 7 steps – from screening to follow-up. Each step says what happens and what the team monitors.
4 criteria
5 criteria
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Mainz, Germany
Leiden, The Netherlands
Nijmegen, The Netherlands
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This is a rare kidney disease characterized by the abnormal accumulation of C3 protein in the glomeruli, which are tiny filters in the kidneys. The disease can lead to inflammation and damage to these filters, affecting their ability to properly filter waste from the blood. Over time, this can result in proteinuria, where excess protein is found in the urine, and a decline in kidney function. The progression of the disease can vary, with some individuals experiencing a slow decline in kidney function, while others may have a more rapid progression. The exact cause of C3 glomerulopathy is not fully understood, but it is believed to involve genetic and immune system factors. Regular monitoring of kidney function and protein levels in urine is important for managing the condition.
This is a kidney disorder characterized by the buildup of immune complexes in the glomeruli, leading to inflammation and thickening of the glomerular basement membrane. The condition can cause the kidneys to become less effective at filtering waste from the blood, resulting in symptoms such as blood in the urine, proteinuria, and swelling in various parts of the body. The progression of the disease can vary, with some individuals experiencing a gradual decline in kidney function, while others may have a more rapid progression. The exact cause of the disease is unknown, but it is thought to involve an abnormal immune response. Regular monitoring of kidney function and urine protein levels is crucial for managing the condition.
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