Bayer begins phase II CONFIDENCE study of initial combo therapy of finerenone with empagliflozin in patients with CKD & type 2 diabetes

Bayer begins phase II CONFIDENCE study of initial combo therapy of finerenone with empagliflozin in patients with CKD & type 2 diabetes

Bayer announced the initiation of the CONFIDENCE study, a phase II, three-arm study that will investigate simultaneous initial combination therapy with finerenone and the SGLT2 inhibitor empagliflozin, compared with finerenone alone and empagliflozin alone respectively in patients with chronic kidney disease (CKD) and type 2 diabetes (T2D). The primary objective of the study is to demonstrate that the simultaneous initiation and combined use of finerenone and empagliflozin is superior to either empagliflozin alone, or finerenone alone, in reducing urine albumin-to-creatinine ratio (UACR). The primary outcome is the relative change from baseline in UACR at 180 days in the combination therapy group vs the monotherapy groups.

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