Overweight Clinical Trial
Official title:
Liraglutide in Type 1 Diabetes. A Randomised, Double-blind, Placebo Controlled Study of the Effect of Liraglutide as an Additional Treatment to Insulin on HbA1c, Body Weight and Hypoglycaemia in Poorly Regulated Type 1 Diabetes Patients
A randomised, double-blind, placebo controlled study of the effect of liraglutide as an
additional treatment to insulin on HbA1c, body weight and hypoglycaemia in poorly regulated
type 1 diabetes patients.
Background: Treatment with glucagon-like peptid 1 (GLP-1) agonists liraglutide and exanatide
leads to weight loss and decrease in haemoglobin A1c in oral anti diabetic treated type 2
diabetes patients.
It is estimated that 40-50 % of type 1 diabetes patients in the US suffers from overweight
or poor glycaemic control (HbA1c > 8 %).
Small studies, not placebo controlled, reports effects of adding liraglutide to a group of
well regulated (HbA1c < 7.5 %) normal to overweight insulin treated type 1 diabetes patients
for 24 weeks. A decrease in HbA1c, weight, insulin doses and glycaemic excursions measured
by continuous glucose monitoring was seen.
Primary objective:To investigate the effect of liraglutide 1.8 mg once daily compared to
placebo for 24 weeks on change in HbA1c in patients with type 1 diabetes as an add-on
therapy to insulin. Secondary objectives:To investigate the effect of liraglutide as an
add-on therapy to insulin compared to placebo on change in:Weight, insulin
dose,hypoglycaemic events, CGM, BMI, body composition, quality of life, treatment
satisfaction,food preferences, meal test, CIMT, PWV and 24 hour blood pressure.
A randomised, double-blind, placebo controlled study of the effect of liraglutide as an
additional treatment to insulin on HbA1c, body weight and hypoglycaemia in poorly regulated
type 1 diabetes patients.
Background Treatment with glucagon-like peptid 1 (GLP-1) agonists liraglutide and exenatide
leads to weight loss and decrease in haemoglobin A1c (HbA1c) in oral anti diabetic treated
type 2 diabetes patients. Smaller studies have shown similar effects in insulin treated type
2 diabetes patients, with no increased risk of hypoglycaemia.
It is estimated that 40-50 % of type 1 diabetes patients in the US suffers from overweight
or poor glycaemic control (HbA1c > 8 %). At present treatment of type 1 diabetes solely
consists of insulin injections.
A recent study reports effects of adding liraglutide to a group of well regulated (HbA1c <
7.5 %) normal to overweight insulin treated type 1 diabetes patients for 24 weeks. A
decrease in HbA1c, weight, insulin doses and glycaemic excursions measured by continuous
glucose monitoring was seen. The study was not placebo controlled.
The available literature suggests that GLP-1 agonists reduce insulin dose and weight in well
regulated type 1 diabetes patients, who are normal- to overweight. To our knowledge, no
study has addressed whether liraglutide will improve HbA1c and reduce bodyweight in
overweight and poorly regulated type 1 diabetes patients.
At present the most efficient way to reduce HbA1c is to use insulin pump therapy, and most
studies suggest that this will decreased HbA1c by approximately 0.5 %. Insulin pump therapy
is however only an option in very compliant patients. In most clinics treating type 1
diabetes 40-50 % of patients will have HbA1c > 8 % and many of these patients will, due to
insufficient compliance, not be candidates for an insulin pump.
At Steno Diabetes Center approximately 3000 well characterized type 1 diabetes patients is
followed in the outpatient clinic, and 40-50 % of these have HbA1c > 8.0 %. If liraglutide
given once daily results in a reduction of HbA1c of 0.5 % it will probably be a very
cost-effective additional therapy for type 1 diabetes patients in insufficient metabolic
control.
Several studies have shown that liraglutide lowers systolic blood pressure. Dysregulation
increases the risk of microvascular complications in type 1 diabetes of which
microalbuminuria results in a need for treatment with antihypertensive medication.
Overweight increases the risk of hypertension and arteriosclerosis and thereby
cardiovascular diseases. Carotis intima media thickness is a validated estimate for future
cardiovascular disease and pulse wave velocity is a measure of arterial stiffness. We
perform 24 hour blood pressure measurements to document possible effects of liraglutide on
blood pressure and CIMT and PWV to investigate the effect of liraglutide on cardiovascular
disease and arteriosclerosis.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment
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