| Literature DB >> 25643044 |
Maka S Hedrington1, Stephen N Davis.
Abstract
INTRODUCTION: Type 2 diabetes is the fastest growing non-communicable chronic disease worldwide. One of the newer treatment options is the class of sodium-glucose cotransporter 2 inhibitors that offer improved glycemia through increased urinary glucose excretion. The class has shown to be effective, safe and well-tolerated in newly diagnosed and long-standing diabetes. Additional benefits of the inhibitors include low risk of hypoglycemia and weight loss. AREAS COVERED: This perspective reviews ipragliflozin - a sodium-glucose cotransporter 2 inhibitor - that has gained approval for clinical use in Type 2 diabetes in Japan. The paper discusses pharmacokinetics (PK), pharmacodynamics, clinical efficacy, safety and tolerability of the drug. EXPERT OPINION: Due to its efficacy (hemoglobin A1c reduction of ≈1%), safety (low risk of hypoglycemia and very low rate of urinary tract infections), favorable PK interaction with other anti-diabetes medications and mechanism of action that is independent from β-cell function and insulin sensitivity, ipragliflozin can be used as a monotherapy or as an add-on to other agents in any stage of Type 2 diabetes.Entities:
Keywords: diabetes; glucose; ipragliflozin; sodium–glucose cotransporter 2 inhibitors
Mesh:
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Year: 2015 PMID: 25643044 DOI: 10.1517/17425255.2015.1009893
Source DB: PubMed Journal: Expert Opin Drug Metab Toxicol ISSN: 1742-5255 Impact factor: 4.481