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KERENDIA (Bayer Australia Ltd)

Product name
KERENDIA
Date registered
Evaluation commenced
Decision date
Approval time
181 (255 working days)
Active ingredients
finerenone
Registration type
NCE/NBE
Indication

KERENDIA (film-coated tablet) is indicated to delay progressive decline of kidney function in adults with chronic kidney disease associated with Type 2 diabetes (with albuminuria), in addition to standard of care (see section 5.1 Pharmacodynamic properties, Clinical trials).