The Effect of Glucagon-like-peptide 1 (GLP-1) Receptor Agonism on Diabetic Kidney Disease
Information source: University College Dublin
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Diabetic Kidney Disease
Intervention: Liraglutide (Drug)
Phase: Phase 3
Status: Active, not recruiting
Sponsored by: Karl Neff Official(s) and/or principal investigator(s): Carel le Roux, MBBS PhD, Study Director, Affiliation: University College Dublin
Summary
Diabetic kidney disease (DKD) is a devastating complication of diabetes, that in it's worst
form, can lead to early cardiovascular death or kidney failure. A group of medicines used to
treat diabetes, glucagon-like-peptide-1 analogues (GLP-1), may be able to protect people
with diabetes from DKD by reducing inflammation in the kidney. This study aims to test this
theory by studying the effect of GLP-1 on kidney function in people with diabetes.
To understand how GLP-1 can affect inflammation, the investigators will give a GLP-1
treatment (Liraglutide) to people with DKD and monitor the effect on inflammation and kidney
function using blood and urine tests. The investigators will compare these results to
patients with DKD who do not receive GLP-1 treatment.
If GLP-1 proves to be effective in reducing inflammation and improving kidney function, then
it could be developed as a viable new treatment for people with DKD, and may significantly
reduce the disease burden, or the risk of DKD, in people with diabetes. This would be a
major advance in the treatment of DKD.
Clinical Details
Official title: Phase 3 Study of the Effect of Glucagon-like-peptide 1 (GLP-1) Receptor Agonism on Renal Outcomes in Humans With Diabetic Kidney Disease
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Urine albumin:creatinine ratio
Secondary outcome: MCP-1:creatinine ratio in urineAlbuminuria as measured by 24 hour albumin excretion rate and albumin:creatinine ratio Other biomarkers including sCD163 in serum
Detailed description:
A randomised controlled trial for patients with microalbuminuria and type 2 diabetes.
Treatment is 0. 6mg of liraglutide and is compared to standard care. Treatment duration is 6
months.
Eligibility
Minimum age: 30 Years.
Maximum age: 75 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Type 2 diabetes with a HbA1c of 42-75mmol/mol (6-9%DCCT)
- Male or female aged above 30 years
- Have a negative pregnancy test at screening (women of child bearing potential only)
- Body mass index (BMI) of 25kg/m2 or greater
- On a renin-angiotensin system antagonist, at a stable dose, for at least 8 weeks
before inclusion into the study
- Established microalbuminuria
- Estimated glomerular filtration rate (eGFR) 30ml/min/1. 73m2 or above by Modification
of Diet in Renal Disease (MDRD) formula
Exclusion Criteria:
- Patients with any cognitive impediment that preclude the patient from giving free and
informed consent
- Patients on dipeptidyl peptidase 4 inhibitors or thiazolidinedione treatment
- Patients with stage 4-5 renal disease, defined as an eGFR of 30ml/min/1. 73m2 or less
- Patients who have used a GLP-1 agent in the last 6 months
- Female patients of child bearing potential who are pregnant, breastfeeding, or
unwilling to practice an acceptable barrier and/or hormonal method of contraception
or abstinence during participation in the study
- Previous pancreatitis
- Hypersensitivity to GLP-1 analogues
- Proliferative diabetic retinopathy
- Any other contraindications, as per the SmPC for liraglutide
- Patients with any other clinical condition or prior therapy that, in the opinion of
the investigator, would make the patient unsuitable for the study or unable to comply
with the dosing requirements
- Concurrent treatment with an investigational drug or participation in another
clinical trial
- Use of an investigational drug within 4 weeks or 5 half-lives, whichever is longer,
preceding the first dose of investigational medicinal product
Locations and Contacts
St Vincent's Healthcare Group, Dublin Dublin 4, Ireland
Additional Information
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Starting date: April 2013
Last updated: June 5, 2015
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