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EMA Product

Kerendia

Product approved by European Medicines Agency (EU)

Basic Information

Kerendia

Regulatory Information

EMEA/H/C/005200

Authorised

February 16, 2022

December 16, 2021

2

September 17, 2024

Company Information

Germany

51368 Leverkusen

BAYER AG

Drug Classification

Additional Monitoring

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Kerendia is indicated for the treatment of chronic kidney disease (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults.

Overview Summary

Kerendia is a medicine used to treat chronic kidney disease in adults with type 2 diabetes. It is used for patients with moderate or severe kidney damage who pass albumin (a type of protein) in their urine. Kerendia contains the active substance finerenone.

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