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Farxiga DAPA-CKD Phase III trial reduced worsening of kidney function, risk of cardiovascular or renal death in patients with chronic kidney disease, irrespective of underlying cause.- AstraZeneca
A new subgroup analysis from the ground-breaking DAPA-CKD Phase III trial showed that AstraZeneca’s Farxiga (dapagliflozin), on top of standard of care, reduced the composite of worsening of kidney function or risk of cardiovascular (CV) or renal death in patients with chronic kidney disease (CKD), irrespective of the underlying cause of the disease.
In the subgroup analysis, compared to placebo Farxiga showed a relative risk reduction (RRR) of 37% for patients whose CKD was primarily driven by diabetic kidney disease (absolute risk reduction [ARR] = 5.8%); 25% for high blood pressure (ARR = 2.2%); 57% for glomerulonephritis (ARR = 7.5%); and 42% for CKD of other or unknown causes (ARR = 5.0%) (p?interaction for RRR 0.53).1 Similarly, Farxiga showed a reduction in all-cause mortality, a secondary outcome, compared to placebo regardless of underlying CKD cause (p-interaction 0.55). The safety and tolerability of Farxiga was consistent with the well-established safety profile of the medicine. The data were presented at the American Society of Nephrology (ASN) Kidney Week Reimagined 2020.
Condition: Diabetes Type 2 and Kidney Disease
Type: drug