Bayer's new CKD treatment Kerendia approved in EU
Following a December positive opinion from the European Medicines Agency’s advisory committee, the European Commission has granted marketing authorization in the European Union (EU) for Kerendia (finerenone).
Developed by German pharma major Bayer (BAYN: DE), Kerendia (10mg or 20mg), a non-steroidal, selective mineralocorticoid receptor antagonist, is indicated for the treatment of chronic kidney disease (CKD) (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults.
Finerenone is different to existing CKD in T2D treatments. It acts by blocking mineralocorticoid receptor (MR) overactivation, which is thought to contribute to CKD progression and cardiovascular damage.
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