Dutogliptin, a dipeptidyl peptidase-4 inhibitor for the treatment of type 2 diabetes mellitus

被引:0
|
作者
Johnson, Kathryn M. S. [1 ]
机构
[1] Beloit Coll, Dept Biol, Beloit, WI 53511 USA
关键词
GLUCAGON-LIKE PEPTIDE-1; GLYCEMIC CONTROL; POSTPRANDIAL GLUCOSE; EXENATIDE EXENDIN-4; ELIMINATION RATES; TREATED PATIENTS; DOUBLE-BLIND; CELL MASS; INCRETIN; GLP-1;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dutogliptin (PHX-1149T), being developed by Phenomix Corp, Forest Laboratories Inc and Chiesi Farmaceutici SpA, is a small-molecule dipeptidyl peptidase-4 (DPP-4) inhibitor for the potential oral treatment of type 2 diabetes mellitus (T2DM). DPP-4 quickly degrades the insulin secretory hormones, glucose-dependent insulinotropic peptide and glucagon-like peptide-1; thus inhibiting the degradation of these hormones is a viable treatment option for patients with T2DM. In preclinical studies, dutogliptin potently inhibited DPP-4 and, in a model of T2DM, treatment with dutogliptin improved glucose homeostasis. Pharmacokinetic analyses in animals, healthy individuals and patients with T2DM demonstrated that drug exposure increased in a dose-dependent manner. Results from phase II clinical trials indicated that once-daily dutogliptin, in combination with other oral diabetes therapies, reduces postprandial blood glucose and HbA1c levels, both indicators of successful diabetes management. In phase I and II trials, dutogliptin was safe, well tolerated and associated with extremely low rates of hypoglycemia. At the time of publication, phase III trials were underway and the results of these will be imperative to determine the efficacy of dutogliptin compared with other small molecule DPP-4 inhibitors, such as sitagliptin and vildagliptin.
引用
收藏
页码:455 / 463
页数:9
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