Author: Kosiborod, Mikhail; Berwanger, Otavio; Koch, Gary G.; Martinez, Felipe; Mukhtar, Omar; Verma, Subodh; Chopra, Vijay; Javaheri, Ali; Ambery, Philip; Gasparyan, Samvel B.; Buenconsejo, Joan; Sjöström, C. David; Langkilde, Anna Maria; Oscarsson, Jan; Esterline, Russell
Title: Effects of dapagliflozin on prevention of major clinical events and recovery in patients with respiratory failure because of COVIDâ€19: Design and rationale for the DAREâ€19 study Cord-id: ljkvmttz Document date: 2021_1_19
ID: ljkvmttz
Snippet: AIMS: Coronavirus disease 2019 (COVIDâ€19) is caused by a novel severe acute respiratory syndrome coronavirus 2. It can lead to multiorgan failure, including respiratory and cardiovascular decompensation, and kidney injury, with significant associated morbidity and mortality, particularly in patients with underlying metabolic, cardiovascular, respiratory or kidney disease. Dapagliflozin, a sodiumâ€glucose cotransporterâ€2 inhibitor, has shown significant cardio†and renoprotective benefits
Document: AIMS: Coronavirus disease 2019 (COVIDâ€19) is caused by a novel severe acute respiratory syndrome coronavirus 2. It can lead to multiorgan failure, including respiratory and cardiovascular decompensation, and kidney injury, with significant associated morbidity and mortality, particularly in patients with underlying metabolic, cardiovascular, respiratory or kidney disease. Dapagliflozin, a sodiumâ€glucose cotransporterâ€2 inhibitor, has shown significant cardio†and renoprotective benefits in patients with type 2 diabetes (with and without atherosclerotic cardiovascular disease), heart failure and chronic kidney disease, and may provide similar organ protection in highâ€risk patients with COVIDâ€19. MATERIALS AND METHODS: DAREâ€19 (NCT04350593) is an investigatorâ€initiated, collaborative, international, multicentre, randomized, doubleâ€blind, placeboâ€controlled study testing the dual hypotheses that dapagliflozin can reduce the incidence of cardiovascular, kidney and/or respiratory complications or allâ€cause mortality, or improve clinical recovery, in adult patients hospitalized with COVIDâ€19 but not critically ill on admission. Eligible patients will have ≥1 cardiometabolic risk factor for COVIDâ€19 complications. Patients will be randomized 1:1 to dapagliflozin 10 mg or placebo. Primary efficacy endpoints are time to development of new or worsened organ dysfunction during index hospitalization, or allâ€cause mortality, and the hierarchical composite endpoint of change in clinical status through day 30 of treatment. Safety of dapagliflozin in individuals with COVIDâ€19 will be assessed. CONCLUSIONS: DAREâ€19 will evaluate whether dapagliflozin can prevent COVIDâ€19â€related complications and allâ€cause mortality, or improve clinical recovery, and assess the safety profile of dapagliflozin in this patient population. Currently, DAREâ€19 is the first large randomized controlled trial investigating use of sodiumâ€glucose cotransporter 2 inhibitors in patients with COVIDâ€19.
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