BI 187004(一种11β -羟基类固醇脱氢酶-1抑制剂)在超重或肥胖健康男性志愿者中的安全性、耐受性、药代动力学和药效学

Susanna Bianzano, Tim Heise, Arvid Jungnik, Cornelia Schepers, Corinna Schölch, Ulrike Gräfe-Mody
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引用次数: 9

摘要

背景:本研究在超重或肥胖的健康男性中研究了单次增加剂量的11β -羟基类固醇脱氢酶-1 (11β - hsd1)抑制剂BI 187004的安全性、耐受性、药代动力学和药效学特征。方法:这是一项随机、双盲、平行组、安慰剂对照研究,在72名超重或肥胖的健康男性志愿者中,每天给药2.5-360 mg BI 187004或安慰剂一次。评估包括肝脏(通过尿四氢皮质醇/四氢可的松比值间接评估)和体外皮下脂肪组织中的11β - hsd1抑制以及下丘脑-垂体-肾上腺轴激素的测定。结果:BI 187004在各剂量组均具有良好的耐受性和安全性。所有9个BI 187004剂量组的药物相关不良事件发生率为16.7% (n = 9),安慰剂组为5.9% (n = 1)。所有治疗组不良事件的种类和强度相似。临床实验室或心电图参数均无临床相关偏差。BI 187004的暴露在整个测试剂量范围内呈非比例增加。几何平均表观末端半衰期从33.5 h (5 mg)下降到14.5 h (160 mg),保持稳定到360 mg。BI 187004的肾排泄较低(3-5%)。尿四氢皮质醇/四氢可的松比值下降,表明肝脏11 β - hsd1抑制。单次给药对皮下脂肪组织活检11β - hsd1的中位抑制作用在10小时后从86.8% (10 mg)到99.5% (360 mg)不等,24小时后从59.4% (10 mg)到98.6% (360 mg)不等。结论:单次给药BI 187004安全且耐受性良好,适合每日一次给药。肝脏和脂肪组织中存在显著的、持续的11 β - hsd1抑制。试验注册:ClinicalTrials.gov,编号NCT01587417,注册日期为2012年4月26日。
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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Safety, tolerability, pharmacokinetics and pharmacodynamics of single oral doses of BI 187004, an inhibitor of 11beta-hydroxysteroid dehydrogenase-1, in healthy male volunteers with overweight or obesity.

Background: The study characterizes safety, tolerability, pharmacokinetic and pharmacodynamic profiles of single rising doses of the 11beta-hydroxysteroid dehydrogenase-1 (11beta-HSD1) inhibitor BI 187004 in healthy men with overweight or obesity.

Methods: This was a randomized, double-blind, parallel group, placebo-controlled study with administration of 2.5-360 mg BI 187004 or placebo once daily as single dose in 72 healthy male volunteers with overweight or obesity. Assessments included 11beta-HSD1 inhibition in the liver (assessed indirectly by urinary tetrahydrocortisol/tetrahydrocortisone ratio) and in subcutaneous adipose tissue ex vivo and determination of hypothalamus-pituitary-adrenal axis hormones.

Results: BI 187004 was well tolerated and safe in all tested dose groups. The incidence of drug-related adverse events was 16.7% (n = 9) for all 9 BI 187004 dose groups and 5.9% (n = 1) for placebo. All treatment groups were similar concerning kind and intensity of adverse events. No clinically relevant deviations in clinical laboratory or ECG parameters were reported. Exposure of BI 187004 increased non-proportionally over the entire dose range tested. The geometric mean apparent terminal half-life decreased from 33.5 h (5 mg) to 14.5 h (160 mg) remaining stable up to 360 mg. Renal excretion of BI 187004 was low (3-5%). Urinary tetrahydrocortisol/tetrahydrocortisone ratio decreased, indicating liver 11beta-HSD1 inhibition. Median inhibition of 11beta-HSD1 in subcutaneous adipose tissue biopsies following single dosing ranged from 86.8% (10 mg) to 99.5% (360 mg) after 10 h and from 59.4% (10 mg) to 98.6% (360 mg) after 24 h.

Conclusions: BI 187004 as single dose was safe and well tolerated and is suitable for once daily dosing. There was significant, sustained 11beta-HSD1 inhibition in liver and adipose tissue.

Trial registration: ClinicalTrials.gov, NCT01587417 , registered on 26-Apr-2012.

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来源期刊
自引率
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发文量
7
审稿时长
8 weeks
期刊介绍: Clinical Diabetes and Endocrinology is an open access journal publishing within the field of diabetes and endocrine disease. The journal aims to provide a widely available resource for people working within the field of diabetes and endocrinology, in order to improve the care of people affected by these conditions. The audience includes, but is not limited to, physicians, researchers, nurses, nutritionists, pharmacists, podiatrists, psychologists, epidemiologists, exercise physiologists and health care researchers. Research articles include patient-based research (clinical trials, clinical studies, and others), translational research (translation of basic science to clinical practice, translation of clinical practice to policy and others), as well as epidemiology and health care research. Clinical articles include case reports, case seminars, consensus statements, clinical practice guidelines and evidence-based medicine. Only articles considered to contribute new knowledge to the field will be considered for publication.
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