Bayer AG’s finerenone demonstrated a relative risk reduction in both kidney disease progression and cardiovascular events compared to placebo in a large Phase III trial of type 2 diabetes patients with chronic kidney disease, but the mineralocorticoid receptor (MR) antagonist did not improve upon earlier members of its class for incidence of hyperkalemia and analysts do not think the benefits equal those offered by the SGLT-2 inhibitor class.
Bayer is planning to file for US Food and Drug Administration and European Medicines Agency approval for reduction in the risk of renal and cardiovascular events in type 2 diabetes patients with CKD on the basis of data from the FIDELIO-DKD study
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