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临床试验/NCT02198209
NCT02198209撤回4 期

Liraglutide Actions on the Liver: Effects on Glucose Phosphorylation

Cedars-Sinai Medical Center1 个研究点 分布在 1 个国家开始时间: 2019年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
撤回
试验地点
1
主要终点
Liver glucokinase activity (chronic effect)

研究概览

简要总结

Type 2 diabetes is a chronic disease that has reached epidemic proportions. In order to improve our strategies for preventing and treating type 2 diabetes the investigators need to better understand the mechanism of this disease, and the way in which current therapies, such as the drug liraglutide, work to control blood sugar. It is known that liraglutide acts via increasing the secretion of the hormone insulin from the pancreas, hormone that in turn controls blood sugar. However, it is not known whether liraglutide also has actions on the liver. Animal studies have suggested that liraglutide might act by controlling the liver enzyme glucokinase (GCK), an enzyme that increases blood sugar uptake by the liver. This could be a crucial mechanism in which liraglutide controls blood sugar independently of insulin, thus making it beneficial not only in type 2 but also in type 1 diabetes. The effect of liraglutide on GCK activity has not been yet measured in humans. The investigators propose to investigate the acute and chronic effect of liraglutide on GCK by using a simple, widely used procedure (an IntraVenous Glucose Tolerance Test-IVGTT) and a novel approach (mathematical modeling of data obtained from this procedure), to assess GCK activity in people with type 2 diabetes. The investigators will first compare data obtained form 2 IVGTTs (with and without liraglutide) performed 1 week apart (acute effect). The investigators will then give liraglutide to patients for 6 weeks and do another IVGTT to measure GCK activity (chronic effects). Data obtained from this study will be used to further understand the mechanism of liraglutide action and how to better employ our current therapeutic options and develop new strategies for preventing and treating diabetes.

详细描述

It is known that liraglutide impacts favorably glucose homeostasis in type 2 diabetic patients, but not the exact mechanism of this effect. In particular, liraglutide's acute and chronic effects on the liver are not well understood. The aim of our study is to determine whether liraglutide acutely and/or chronically changes hepatic GCK activity in vivo in type 2 diabetic patients, and to quantify this effect. We hypothesize that liraglutide increases GCK activity and that this results in increased hepatic glucose uptake, contributing to a lowering of glycemia.

Our specific aims are:

  1. to measure liraglutide's acute effect on GCK activity changes in vivo in type 2 diabetic patients;
  2. to assess whether chronic treatment with liraglutide determines a change in liver GCK activity in type 2 diabetic patients, as assessed during an IVGTT.

We expect that liraglutide acutely and/or chronically increases GCK activity, thus contributing to higher liver glucose uptake and lower glycemia.

Primary endpoints

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18- 65 years of age (inclusive)
  • Ability to provide informed consent before any trial-related activities
  • Ability to communicate effectively with research staff
  • Ability to return for follow up visit
  • Adequate IV access
  • If a female of childbearing potential, non-pregnant and taking reliable contraception
  • Documented T2DM (per most recent American Diabetes Association criteria);
  • Drug naïve or treated with metformin only;
  • Diabetes should be well controlled (as defined by HbA1 ≤ 7.5%, FPG <180 mg/dl).

排除标准

  • Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures
  • Presence of cancer or any clinically significant cardiac, respiratory, renal, hepatic, gastrointestinal, endocrinological, haematological, neurological, or psychiatric diseases or disorders (inclusion will be discussed with attending physician)
  • Liver disease; history of alcoholism.
  • Known or suspected allergy to liraglutide
  • Contraindications to liraglutide: patients with a personal or family history of medullary thyroid carcinoma or in patients with Multiple Endocrine Neoplasia syndrome type 2
  • Patients with a history of pancreatitits
  • Patients that have been treated with drugs that promote weight loss (e.g., Xenical® [orlistat], Meridia® [sibutramine], Acomplia® [rimonabant], Acutrim® [phenylpropanolamine], or similar over-the-counter medications) within 3 months of study start
  • Patients that have been treated with diabetes drugs: injectables, (e.g GLP-1R agonists (Byetta® [exenatide], Victoza® [liraglutide]) amylin analogues; insulin and insulin analogues) or oral agents other than metformin (e.g.DPP-IV- inhibitors (Januvia® [sitagliptin], Onglyza® [saxagliptin] or Janumet® [sitagliptin and metformin]),insulin sensitizers (thiazolidindiones: pioglitazone [Actos®]); or sulfonylureas) within 3 months of study start.
  • The receipt of any investigational drug within 3 months prior to study start.
  • Type 1 diabetes

研究组 & 干预措施

single arm

Other

Liraglutide (Victoza)

  1. acute study: one injection of 0.6 mg s.c. before IVGTT
  2. chronic study: 6 weeks of daily liraglutide administration (1 week at 0.6 mg, 1 week at 1.2 mg, 4 weeks at 1.8 mg, s.c).

干预措施: Liraglutide (Drug)

结局指标

主要结局

Liver glucokinase activity (chronic effect)

时间窗: 12 months

We will measure liver glucokinase (GCK) activity 'in vivo' during IVGTTs before and after 6 weeks of daily liraglutide administration

Liver glucokinase activity (acute effect)

时间窗: 12 months

We will measure liver glucokinase (GCK) activity 'in vivo' during IVGTTs with and without liraglutide administration

次要结局

  • insulin sensitivity(12 months)
  • Acute insulin response to glucose and the disposition index(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Marilyn Ader, PhD

Associate Director, Diabetes & Obesity Research Institute

Cedars-Sinai Medical Center

研究点 (1)

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