Effect of Liraglutide on Clock Genes
NCT02783196 · Unknown status
Last updated 2026-05-28This clinical trial tests whether the medication liraglutide affects the activity of genes related to the body's internal clock in adults with type 2 diabetes.
What this study is testing ClinicalTrials.gov NCT02783196 ↗
Description as written by the study sponsor.
This study is undertaken to search whether glucagon-like peptide-1 (GLP-1) analogue, Liraglutide, by enhancing clock gene and AMPK-SIRT-1 mRNA expression, may reverse the metabolic abnormalities of type 2 diabetes, improving overall glycemic excursion, inflammatory cytokines and β-cell function in type 2 diabetes individuals. The investigators aim is to compare the effect of 40 days treatment with Liraglutide (LIR) vs. 40 days with placebo (PLA) in T2D participants on the following end points: Primary end-points: * Change in the oscillation of CG (i.e. CLOCK, BMAL1, Per1, Per2, Cry1, Cry2, Rev-erb-alpha Ror-alpha), AMPK, SIRT1 and inflammatory cytokines mRNA expression in white blood cells (WBCs). Secondary end-points: * Overall daily glycemic variation assessed with continuous glucose monitoring system (CBMS) * Serum levels of inflammatory cytokines (TNF-α, IL-1β, IL-6) * β-Cell function derived from glucose and insulin response to OGTT
Treatments tested
- Liraglutide also known as LIR Drug
In the LIR arm, the participants will be provided with instructions in using pre-filled single-use plastic syringes ready for once daily subcutaneous injection of LIR. From day 1 to day 10, with LIR daily dose of 0.6 mg (0.1 ml), followed by other 10 day courses (from day 11 to day 20) with LIR 1.2 mg (0.2 ml), then will be up-titrated to high dose 1.8 mg (0.3 ml) of LIR (from day 21 to day 40). At crossover-day 40, the participants will undergo a 14 days wash-out period, day 41 to day 55.
- Placebo also known as PLA Drug
In the PLA arm, the participants will be provided with instructions in using pre-filled single-use plastic syringes ready for once daily subcutaneous injection of PLA. Will start with PLA with matched volume saline injections of 0.1 ml PLA during the first 10 days, followed by 10 days, with 0.2 ml PLA, thereafter PLA will be up-titrated to highest volume 0.3 ml placebo for the rest of the PLA treatment period . At crossover-day 40, the participants will undergo a 14 days wash-out period, day 41 to day 55.
| Main thing measured | Clock Gene expression |
|---|---|
| Sponsor | Tel Aviv University |
| Conditions studied | Type 2 Diabetes |
| GLP-1 drugs | liraglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT02783196 ↗