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Effect of Linagliptin on Vascular Inflammation in Patients With Type 2 Diabetes Mellitus

Linagliptin as a Modulator of Vascular Inflammation in Patients With Type 2 Diabetes Mellitus

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02077309
Acronym
Lina-Plaque
Enrollment
4
Registered
2014-03-04
Start date
2014-08-31
Completion date
2015-11-30
Last updated
2017-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus Type 2 (T2DM), Plaque Morphology, Vascular Inflammation

Keywords

T2DM,, vascular inflammation,, 18-FDG-PET,, plaque morphology,, MRI,, DPP-4 Inhibition

Brief summary

Examination of the effect of Linagliptin versus placebo for 6 months on vascular inflammation of the carotic artery and on abdominal adipose tissue inflammation in patients with diabetes mellitus type 2. The effect will be assessed by FDG-PET scan. Furthermore the effect of Linagliptin on the vessel wall volume of the carotid artery will be assessed by MRI scan and biomarkers of vascular inflammation will be analyzed in blood samples.

Detailed description

As part of the screening a PET-CT scan is executed to examine baseline vascular inflammation of the carotid artery and to evaluate abdominal adipose tissues inflammation. Patients who are eligible to participate in the study according to the in- and exclusion criteria will be randomised in one of the two study arms. According to the randomisation the patients will receive 5 mg Linagliptin or placebo per day for a period of 6 months. To evaluate the effect of Linagliptin versus placebo the vessel wall volume of the artery will be assessed by MRI scan and the vascular inflammation of the carotid artery by FDG-PET, furthermore the vascular inflammation will be analyzed by biomarkers in blood samples and the abdominal adipose tissue inflammation will investigated by subcutaneous adipose tissue biopsies.

Interventions

DRUGLinagliptin
DRUGPlacebo

Sponsors

RWTH Aachen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Diabetes mellitus Type 2 2. HbA1c \> 7% 3. Age \> 50 years 4. Coronary artery disease or carotid artery disease 5. 18F-FDG uptake of the carotid arterial wall to background (blood) ratio \> 1.8 6. Written informed consent prior to study participation 7. Stable anti-diabetic and cholesterol lowering medication for the last 3 month 8. Stable anti-diabetic medication for the last 6 weeks which should include a maximal tolerated dose of metformin (unless contraindication or intolerance to metformin does exist); 9. Indication to increase anti-diabetic medication as judged by the investigator

Exclusion criteria

1. Diabetes mellitus type 1 2. Use of DPP-4 Inhibitor, GLP-1 agonists, Thiazolindinedione 3. Kidney disease CKD 4 and more (GFR \< 30 ml/min/1.73) 4. Liver disease (ALT or AST \> 3 times the upper limit of norm) or known liver cirrhosis 5. Any reason for not being able to sustain the imaging studies 6. Pacemaker/ICD/metallic clips in close relation to vessels in the brain 7. Uncontrolled thyroid disease 8. Active malignant disease 9. Chronic inflammatory disease 10. Chronic use of NSAR or cortison 11. HbA1c \> 8.5% 12. Recent (\<3 months) clinically significant coronary or cerebral vascular event 13. Pregnant females as determined by positive \[serum or urine\] HCG test at Screening or prior to dosing 14. Lactating females 15. The subject has a history of any other illness, which, in the opinion of the Investigator, might pose an unacceptable risk by administering study medication 16. The subject received an investigational drug within 30 days prior to inclusion into this study 17. The subject has any current or past medical condition and/or required medication to treat a condition that could affect the evaluation of the study 18. The subject is unwilling or unable to follow the procedures outlined in the protocol 19. The subject is mentally or legally incapacitated

Design outcomes

Primary

MeasureTime frameDescription
Effect of linagliptin on vascular inflammation of the carotic arteryup to 6 monthsExamination of the effect of 5 mg linagliptin qd versus placebo on vascular inflammation of the carotic artery by FDG-PET in patients with diabetes mellitus within 6 months.

Secondary

MeasureTime frameDescription
Effect of linagliptin on vessel wall volume of the carotid arterybaseline and 6 monthsExamination of the effect of 5mg linagliptin qd versus placebo on vessel wall volume of the carotid artery by MRI scan.
Effect of linagliptin on abdominal adipose tissue inflammationbaseline and 6 monthsEvaluation of the effect of 5mg linagliptin qd versus placebo on abdominal adipose tissue inflammation by FDG-PET in addition to adipose tissue biopsies.
Effect of linagliptin on biomarkers of vascular inflammationbaseline and 6 monthsBlood analysis to examine the effect of linagliptin on biomarkers of vascular inflammation.

Countries

Germany, Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026