BI-10773,一种钠-葡萄糖共转运蛋白2抑制剂,用于2型糖尿病的潜在口服治疗。

Inês Aires, Joaquim Calado
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引用次数: 0

摘要

由勃林格殷格翰公司开发的BI-10773是一种钠-葡萄糖共转运蛋白(SGLT)2抑制剂,用于口服治疗2型糖尿病(T2DM)。临床前和临床研究表明,抑制肾糖重吸收的主要途径SGLT2可导致尿糖排泄增加,同时降低空腹和餐后血糖水平、糖化血红蛋白水平和体重。在T2DM患者的I期临床试验中,每日一次的BI-10773增加尿糖排泄,导致空腹血糖和平均每日血糖水平按剂量比例降低。BI-10773与显著的低血糖发作或其他临床重要不良事件无关。由于其作用机制,BI-10773可能与其他口服降糖药联合使用;事实上,小型试验的结果表明BI-10773和二甲双胍联合用药是安全且耐受性良好的。在动物研究中,BI-10773与尿量增加和体脂减少相关,但与水含量无关。这可能代表了BI-10773在控制T2DM方面的额外益处。在本文发表时,BI-10773的III期临床试验正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BI-10773, a sodium-glucose cotransporter 2 inhibitor for the potential oral treatment of type 2 diabetes mellitus.

BI-10773, being developed by Boehringer Ingelheim Corp, is a sodium-glucose cotransporter (SGLT)2 inhibitor for the oral treatment of type 2 diabetes mellitus (T2DM). Preclinical and clinical research has demonstrated that inhibition of SGLT2, the major pathway of renal glucose reabsorption, leads to increased urinary glucose excretion with concomitant reductions in fasting and postprandial plasma glucose levels, HbA1c levels and body mass. In phase I clinical trials in patients with T2DM, once-daily BI-10773 increased urinary glucose excretion resulting in dose-proportional reductions in fasting plasma glucose and mean daily glucose levels. BI-10773 was not associated with significant hypoglycemic episodes or other clinically important adverse events. Because of its mechanism of action, BI-10773 may be combined with other oral antidiabetic agents; indeed, the results of small trials suggested that coadministration of BI-10773 and metformin was safe and well tolerated. In animal studies, BI-10773 correlated with an increase in urinary volume and a reduction in body fat but not water content. This may represent an additional benefit of BI-10773 for the control of T2DM. At the time of publication, phase III clinical trials of BI-10773 were underway.

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