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. 2019 Oct 15;191(41):E1128–E1135. doi: 10.1503/cmaj.190047

Table 1:

Summary of the major randomized controlled trials of sodium-glucose cotransporter-2 inhibitors

Study characteristics No. (%) of participants*
EMPA-REG OUTCOME8
n = 7020
CANVAS program9
n = 10 142
DECLARE-TIMI 5810
n = 17 160
CREDENCE11
n = 4401
Drug Empagliflozin Canagliflozin Dapagliflozin Canagliflozin
Dose, mg 10 or 25 100 or 300 10 100
Age, mean ± SD; yr 63.1 ± 8.7 63.3 ± 8.3 63.9 ± 6.8 63.0 ± 9.2
Sex, female 2004 (28.5) 3633 (35.8) 6422 (37.4) 1494 (33.9)
Follow-up time, median; yr 3.1 2.4 4.2 2.6
History of cardiovascular disease 7020 (100.0) 6656 (65.6) 6974 (40.6) 2220 (50.4)
History of heart failure 706 (10.1) 1461 (14.4) 1724 (10.0) 652 (14.8)
eGFR < 60 mL/min/1.73 m2 1819 (25.9) 2039 (20.1) 1265 (7.4) 2631 (59.8)
Micro- or macroalbuminuria 2782 (39.6) 3026 (29.8) 5199 (30.3) 4370 (99.3)
Primary outcome(s) MACE MACE MACE and admission to hospital for heart failure or CV death Doubling of serum creatinine level, ESKD, or CV or renal death

Note: CKD-EPI = chronic kidney disease epidemiology collaboration equation, CV = cardiovascular, eGFR = estimate glomerular filtration rate, ESKD = end-stage kidney disease, MACE = major adverse cardiovascular events (defined as nonfatal myocardial infarction, nonfatal stroke or CV death), MDRD = modification of diet in renal disease equation.

*

Unless specified otherwise.

eGFR based on the MDRD equation in the EMPA-REG OUTCOME trial8 and the CANVAS Program,9 and the CKD-EPI equation in DECLARE-TIMI 5810 and CREDENCE11 trials.