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 Our Mission

Improve evidence-based

treatment options and optimize

health outcomes for

patients with proteinuric

kidney disease

KRN engages patients, medical teams, researchers, regulatory experts, industry , patient advocates, and other partners to accelerate research in the rare diseases associated with nephrotic syndrome. Our teams collaborate to improve clinical trials and bring evidence to support patient-provider decision making. Through quality initiatives, KRN strives to facilitate the best care for every patient.

Registry Hosting

Nephrology Research

Analytics to support research questions

FSGS

Clinical Trials

Support for the KRN is provided by the University of Michigan and Atrium Health Foundation with additional

support from each contributing registry site. 
 

Kidney Research Network 2024

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