Iptacopan for idiopathic IC-MPGN with heavy protein in urine
Treatments studied
Part of Kidney & urinary, Women’s health & pregnancy clinical trials.
This trial tests iptacopan (an add-on medicine) in people with idiopathic immune-complex membranoproliferative glomerulonephritis (IC-MPGN), a kidney disease causing significant protein loss in urine. It aims to improve kidney outcomes and safety when added to standard treatments.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You have idiopathic IC-MPGN, confirmed by a kidney biopsy done recently (within 12 months for adults; within 3 years for adolescents).
- You’ve been on the best tolerated “blood pressure kidney protection” medicines (ACE inhibitor or ARB) for at least 90 days before starting.
- Your urine protein level is high: first-morning urine test shows UPCR at least 1.0 g/g at two study timepoints.
- Your kidney filtration is not too low (eGFR or measured GFR is at least 30 at screening and at the next check).
- Before treatment, you must be up to date on vaccines against meningococcal and pneumococcal infections (and possibly Hib).
- You should not have recent serious infections or fever, and you should not be using certain immune/complement-blocking medicines.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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This Phase 3 trial looks at how well and how safely iptacopan works over the long term for people with C3G or IC-MPGN. You may be able to join if you already finished a specific earlier study and you’re currently healthy enough for long-term treatment.
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