Liraglutide Actions on the Liver: Effects on Glucose Phosphorylation

Withdrawn before enrolling · Phase 4

Conditions studied: Type 2 Diabetes

In brief

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.

Key facts

Study ID: NCT02198209
Run by: Cedars-Sinai Medical Center
People needed: 0
Starts: 2019-12-01
Expected to finish: 2020-12-01
Last updated by the study team: 2019-09-30

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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).

You may not qualify if…

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

Where it is running

Cedars Sinai Medical Center — Los Angeles, California, United States

Full record on ClinicalTrials.gov

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