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Study identifier: NCT07056595 Synced from ClinicalTrials.gov · July 28, 2026
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Finerenone in Patients With IgA-nephropathy: Prospective Interventional Trial

Condition: IgA Nephropathy (IgAN)  ·  Sponsor: Botkin Hospital

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

: IgA-nephropathy is the most common glomerulonephritis with the unfavorable prognosis in patients with persistent albuminuria. Finerenone is a new nonsteroidal mineralocorticoid receptor antagonist that has demonstrated efficacy in reducing albuminuria in patients with CKD and type 2 diabetes in two major trials, FIGARO-DKD and FIDELIO. This finding supported the approval of finerenone by the U.S. Food and Drug Administration (FDA) for the treatment of chronic kidney disease (CKD). A subgroup analysis in the pooled FIDELITY trial demonstrated that in patients with CKD stages 1-4 and type 2 diabetes (T2D), the cardio- and nephroprotective effects of finerenone were independent of concomitant therapy with SGLT-2 inhibitors or GLP-1 receptor agonists. Thus, the role of finerenone in slowing CKD progression in T2D can be considered well-established. Given its albuminuria-reducing effects, finerenone is being investigated in multiple trials, including studies on non-diabetic kidney disease and IgA nephropathy, though no published results are available yet. In this trial finerenone will be used as a nephroprotective agent above standard treatment in terms of assessing adverse events and potential efficacy.

This description comes directly from the study's public registry record.

Talk to the study team

Evgeny Shytov, PhD  ·  +7 499 490 03 03  ·  shutov_e_v@mail.ru

Anastasiia Zykova, PhD  ·  ansezy@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Botkin HospitalMoscow, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07056595