| Literature DB >> 26305874 |
Norm Rosenthal1, Gary Meininger1, Kirk Ways1, David Polidori2, Mehul Desai1, Rong Qiu1, Maria Alba1, Frank Vercruysse1, Dainius Balis1, Wayne Shaw1, Robert Edwards1, Scott Bull3, Nicholas Di Prospero1, Sue Sha1, Paul Rothenberg1, William Canovatchel1, Keith Demarest1.
Abstract
The sodium glucose co-transporter 2 (SGLT2) inhibitor canagliflozin is a novel treatment option for adults with type 2 diabetes mellitus (T2DM). In patients with hyperglycemia, SGLT2 inhibition lowers plasma glucose levels by reducing the renal threshold for glucose (RTG ) and increasing urinary glucose excretion (UGE). Increased UGE is also associated with a mild osmotic diuresis and net caloric loss, which can lead to reductions in body weight and blood pressure (BP). After promising results from preclinical and phase I/II studies, the efficacy and safety of canagliflozin was evaluated in a comprehensive phase III development program in over 10,000 patients with T2DM on various background therapies. Canagliflozin improved glycemic control and provided reductions in body weight and BP versus placebo and active comparators in studies of up to 2 years' duration. Canagliflozin was generally well tolerated, with higher incidences of adverse events (AEs) related to the mechanism of action, including genital mycotic infections and AEs related to osmotic diuresis. Results from the preclinical and clinical studies led canagliflozin to be the first-in-class SGLT2 inhibitor approved in the United States, and support canagliflozin as a safe and effective therapeutic option across a broad range of patients with T2DM.Entities:
Keywords: SGLT2 inhibitor; antihyperglycemic agent; canagliflozin; type 2 diabetes
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Year: 2015 PMID: 26305874 DOI: 10.1111/nyas.12852
Source DB: PubMed Journal: Ann N Y Acad Sci ISSN: 0077-8923 Impact factor: 5.691