Literature DB >> 25643044

Ipragliflozin , a sodium-glucose cotransporter 2 inhibitor, in the treatment of type 2 diabetes.

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:

Substances:

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


  5 in total

1.  Moieties in antidiabetic drugs as a target of insulin receptors in association with common neurological disorders.

Authors:  David Calderón Guzmán; Hugo Juárez Olguín; Ernestina Hernández García; Maribel Ortiz Herrera; Norma Osnaya Brizuela
Journal:  Biomed Rep       Date:  2016-02-26

Review 2.  The role of empagliflozin in the management of type 2 diabetes by patient profile.

Authors:  Maka S Hedrington; Stephen N Davis
Journal:  Ther Clin Risk Manag       Date:  2015-05-05       Impact factor: 2.423

3.  Distinct Glucose-Lowering Mechanisms of Ipragliflozin Depending on Body Weight Changes.

Authors:  Eiji Kutoh; Teruma Murayama; Asuka Wada; Mitsuru Hirate
Journal:  Drugs R D       Date:  2016-12

4.  A concise and practical stereoselective synthesis of ipragliflozin L-proline.

Authors:  Shuai Ma; Zhenren Liu; Jing Pan; Shunli Zhang; Weicheng Zhou
Journal:  Beilstein J Org Chem       Date:  2017-06-01       Impact factor: 2.883

5.  Addition of Ipragliflozin to Metformin Treatment in Korean Patients with Type 2 Diabetes Mellitus: Subgroup Analysis of a Phase 3 Trial.

Authors:  Kyung Wan Min; Bon Jeong Ku; Ji Hyun Lee; Min Seon Kim; Kyu Jeung Ahn; Moon Kyu Lee; Satoshi Kokubo; Satoshi Yoshida; Hyun Ji Cho; Bong Soo Cha
Journal:  Diabetes Metab J       Date:  2017-04       Impact factor: 5.376

  5 in total

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