Dapagliflozin is a sodium-glucose cotransporter 2 (SGLT2) inhibitor, and it was the first SLGT2 inhibitor to be approved. indicated for managing diabetes mellitus type 2. When combined with diet and exercise in adults, dapagliflozin helps to improve glycemic control by inhibiting glucose reabsorption in the proximal tubule of the nephron and causing glycosuria. Dapagliflozin has been investigated either as monotherapy or as an adjunct treatment with insulin or other oral hypoglycemic agents.
Dapagliflozin was originally approved by the FDA on Jan 08, 2014, to improve glycemic control in adults with type 2 diabetes in conjunction with diet and exercise. It was later approved to reduce the risk of kidney function decline, kidney failure, cardiovascular death, and hospitalization for heart failure in adults with chronic kidney disease in April 2021.
Dapagliflozin is indicated as an adjunct treatment to improve glycemic control in adult patients with type 2 diabetes mellitus along with diet and exercise.For patients with chronic kidney disease at risk of progression, dapagliflozin in used to reduce the risk of sustained eGFR decline, end-stage kidney disease, cardiovascular death, and
hospitalization for heart failure. Dapagliflozin is also indicated to either reduce the risk of cardiovascular death, hospitalization for heart failure, and urgent heart failure visit in adults with heart failure or reduce the risk of hospitalization for heart failure in adults with type 2 diabetes mellitus and either established cardiovascular disease or multiple cardiovascular risk factors. Combination products with dapagliflozin also exist, either as a dapagliflozin-saxagliptin or dapagliflozin-metformin hydrochloride formulation. Both are used as an adjunct treatment to diet and exercise to improve glycemic control in adults with type 2 diabetes.
Research Site, Baltimore, Maryland, United States
Diabetes Research Center, Tustin, California, United States
Endocrine Research Associates, Jackson, Mississippi, United States
Dallas Diabetes & Endocrine Center, Dallas, Texas, United States
Research Site, Zaporozhye, Ukraine
Research Site, Swansea, United Kingdom
Marin Endocrine Care & Research, Inc., Greenbrae, California, United States
Diabetes Medical Center Of California, Northridge, California, United States
Office Of Richard Cherlin, Md, Los Gatos, California, United States
Research Site, Trowbridge, United Kingdom
Southeastern Research Associates, Inc., Greenville, South Carolina, United States
Jackson Clinic, Rolling Fork, Mississippi, United States
Community Health Care, Inc., Canal Fulton, Ohio, United States
Local Institution, Vicente Lopez, Buenos Aires, Argentina
Prism Research, St. Paul, Minnesota, United States
Advanced Clinical Research Institute, Anaheim, California, United States
Elite Research Institute, Miami, Florida, United States
Bristol-Myers Squibb Clinical Pharmacology Unit, Hamilton, New Jersey, United States
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