Dapagliflozin met criteria for noninferiority and was associated with reduced risk for heart failure hospitalization.
Dapagliflozin, a sodium–glucose cotransporter 2 (SGLT2) inhibitor, blocks glucose resorption in the kidney's proximal tubule and reduces not only glucose levels but also risk for heart failure. The DECLARE–TIMI 58 trial (NCT01730534) tested the effect of dapagliflozin in people with diabetes who had, or were at high risk for, cardiovascular disease. The primary outcome was the combination of cardiovascular death, myocardial infarction, or ischemic stroke.
A total of 17,160 people were randomized to receive dapagliflozin (10 mg/day) or placebo. Median follow-up was 4.2 years; mean HbA1c was 8.3%. In a safety analysis, dapagliflozin met the prespecified criterion for noninferiority. An efficacy analysis found no significant difference in risk …
Reviewing Author
DisclosuresConsultant/Advisory BoardUnited Healthcare; Element Science; Eyedentifeye, F-Prime
EquityHugo Health; Refactor Health; Element Science
Grant/Research SupportPfizer; Agency for Healthcare Research and Quality; Janssen Research and Development, National Institute of Biomedical Imaging and Engineering; National Heart, Lung, and Blood Institute; Centers for Disease Control and Prevention; National Cancer Institute; American Heart Association
DisclosuresConsultant/Advisory BoardUnited Healthcare; Element Science; Eyedentifeye, F-Prime
EquityHugo Health; Refactor Health; Element Science
Grant/Research SupportPfizer; Agency for Healthcare Research and Quality; Janssen Research and Development, National Institute of Biomedical Imaging and Engineering; National Heart, Lung, and Blood Institute; Centers for Disease Control and Prevention; National Cancer Institute; American Heart Association