Comparison of the administration of teneligliptin every day versus every other day in Japanese patients with type 2 diabetes: a randomized non-inferior test.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Journal of clinical pharmacology Pub Date : 2015-02-01 Epub Date: 2014-09-07 DOI:10.1002/jcph.385
Kazunari Kamiko, Kazutaka Aoki, Hiroshi Kamiyama, Masataka Taguri, Eriko Shibata, Yumiko Ashiya, Fuyuki Minagawa, Kazuaki Shinoda, Shigeru Nakajima, Yasuo Terauchi
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引用次数: 5

Abstract

The half life (t1/2 ) of teneligliptin is 24.2 hours. Accordingly, we hypothesized that the administration of teneligliptin every other day might improve glycemic control. In this study, we evaluated the effectiveness of the administration of teneligliptin every other day in Japanese patients with type 2 diabetes. Fifty-one patients were randomly assigned to receive treatment with 20 mg of teneligliptin every day (Group A) or 20 mg of teneligliptin every other day (Group B) for 12 weeks. HbA1c, glycoalbumin (GA), 1,5-anhydroglucitol (1,5-AG), lipid, blood pressure, body weight, urine albumin-to-creatinine ratio, overall treatment satisfaction level, adverse events and drug adherence were all measured. Forty-seven patients completed this study, and the HbA1c, GA, and 1,5-AG levels in group B were found to be decreased to the same extent as those in group A. No distinct differences in the overall treatment satisfaction level, adverse events, or drug adherence were seen between the two groups at 12 weeks. The administration of teneligliptin every other day had a similar efficacy, patient satisfaction level, and safety compared with its administration every day. This information will be useful for reducing the economic load without changing the patients' satisfaction and glycemic control.

日本2型糖尿病患者每日与隔日给药替尼格列汀的比较:一项随机非劣效试验
替尼格列汀的半衰期(t1/2)为24.2小时。因此,我们假设每隔一天服用替尼格列汀可能会改善血糖控制。在这项研究中,我们评估了日本2型糖尿病患者每隔一天服用替尼格列汀的有效性。51名患者被随机分配接受每天20mg替尼格列汀(A组)或每隔一天20mg替尼格列汀(B组)的治疗,为期12周。检测糖化血红蛋白(HbA1c)、糖蛋白(GA)、1,5-无氢葡萄糖醇(1,5- ag)、血脂、血压、体重、尿白蛋白/肌酐比、总体治疗满意度、不良事件及药物依从性。47名患者完成了这项研究,发现B组的HbA1c、GA和1,5- ag水平下降的程度与a组相同。12周时,两组在总体治疗满意度、不良事件或药物依从性方面没有明显差异。与每天给药相比,隔天给药的疗效、患者满意度和安全性相似。这些信息将有助于在不改变患者满意度和血糖控制的情况下减少经济负荷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
176
审稿时长
2 months
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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