LIR-CG
UnknownPhase NAEffect of Liraglutide on Clock Genes
Advantages of Liraglutide Mediated Through Its Effect on Clock Gene mRNA Expression
Lead sponsor
Asset
Liraglutide
Subcutaneous · GLP-1 agonist
Listed sites
1
Recruiting sites
-
Estimated enrollment
14
Study population
Type 2 diabetes
Eligibility highlights
•BMI 26-32•HbA1c 7-10%
Primary endpoint
•Clock Gene expression
Registered trial locations
Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Who this study enrolls
Who can enroll
Inclusion criteria
1. Patients with T2D diagnosed that were diagnosed < 20 years.
2. HbA1c: 7 to 10 % at screening and at qualification
3. BMI: 26-32 kg/m2.
4. Men and women
5. Between the ages of 30 and 75 years.
6. Patients treated with diet alone or diet plus metformin and SGLT2 inhibitors, at a stable dose for at least 3 months.
7. Concomitant medication i.e. antihypertensive, anti-lipidemic, anti-thrombotic drugs will be allowed.
8. Patients that usually wake up between 06:00 and 07:00 and go to sleep between 22:00 and 24:00.
9. Subjects should not have shift work within 6 month of the study and should not have crossed time zones within 1 month of the study.
10. For woman of child bearing potential, negative pregnancy test and willingness to use birth control during the study :
Exclusion criteria
1. Type 1 diabetes or secondary forms of diabetes.
2. Use of glucose-lowering therapy apart from metformin and SGLT2 inhibitors.
3. Treatment with GLP-1 receptor agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors within the last 3 months.
4. Major illness with life expectancy < 5 years.
5. Serum creatinine level >2mg/d or renal dysfunction: (estimated glomerular filtration rate <45 mL/min/1.73 m2).
6. Hepatic dysfunction: liver disease or transaminase levels >3-fold above normal.
7. History of acute or chronic pancreatitis or high risk for pancreatitis i.e. triglycerides over 400 mg/dl or alcoholism.
8. Family or personal history of Multiple Endocrine Neoplasia type 2 (MEN-2) or familial medullary thyroid carcinoma.
9. Familial or personal history of multiple endocrine neoplasia type 2 (MEN2), familial or non-familial medullary thyroid carcinoma (MTC)
10. Malignant neoplasm requiring chemotherapy, surgery, radiation or palliative therapy within the previous 5 years (with the exception of basal cell skin cancer).
11. Those taking psychotropic, anorectic medication, steroid treatment or with illicit drug abuse or alcoholism within one year prior to study onset.
12. Congestive heart failure and all cardiac arrhythmias i.e. atrial fibrillation.
13. Pregnancy or lactation.
14. Eating disorders and subjects after bariatric surgery or affected by gastroparesis.
15. Night or rotating shift workers or those who crossed more than 2 time zones during the 2-week period prior to study onset.
16. No change in medication or nutrition supplements or physical activity will be made during the study period.
17. Known proliferative retinopathy or maculopathy
Endpoints (5)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Glycemic / diabetes
2 endpointsBeta-cell function
Time frame:Up to 92 days
descriptive
Overall glycemia
Time frame:Up to 95 days
descriptive, improvement
Other (unclassified)
3 endpointsClock Gene expression
Time frame:Up to 95 days
descriptive
AMPK mRNA expression
Time frame:Up to 95 days
descriptive
SIRT1 mRNA expression
Time frame:Up to 95 days
descriptive
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 6, 2026 snapshot.