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Clinical Trials/NCT02686177
NCT02686177CompletedPhase 4

Effect of GLP-1 on Angiogenesis, Angiosafe Type 2 Diabetes Study 1

Assistance Publique - Hôpitaux de Paris1 site in 1 country50 target enrollmentStarted: May 18, 2016Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
Difference of ANGPTL4 concentration at 4 weeks of treatment from baseline in Liraglutide and control group

Study Overview

Brief Summary

GLP-1 receptor agonists are introduced in the treatment of type 2 Diabetes (T2D) and their efficacy is documented. However, safety aspects are also important to evaluate with respect to micro and macrovascular complications associated with T2D. Few studies have properly addressed the role of GLP-1-based therapies in regulating vascular integrity and angiogenesis. The study evaluate the impact of one-month treatment Liraglutide on both ANGPT2 and ANGLPT4 levels and endothelial circulating progenitor cells, angiogenesis biomarkers in type 2 diabetic patients.

Detailed Description

GLP-1 receptor agonists are introduced in the treatment of type 2 Diabetes (T2D) and their efficacy is documented. Beside their therapeutic benefits, direct cardiovascular effects have also been reported. However, safety aspects are also important to evaluate with respect to micro and macrovascular complications associated with T2D. T2D patients treated with GLP-1 analogs may suffer from microvascular complications such as macular oedema and proliferative retinopathy, characterized by excessive retinal angiogenesis. Few studies have properly addressed the role of GLP-1-based therapies in regulating vascular integrity and angiogenesis. The role of GLP-1 on endothelial cell (EC) growth, EC integrity and angiogenesis thus needs to be characterized. Our aim is to provide the proof of concept that agonists of GLP-1 regulate angiogenesis in humans and identify the underlying mechanisms. The present project is the translational part of the ANR Angiosafe-T2D, regarding clinical safety aspects of GLP-1 receptor agonists (namely Liraglutide) on angiogenesis.

The study evaluate the impact of one-month treatment Liraglutide on both ANGPT2 and ANGLPT4 levels and endothelial circulating progenitor cells, angiogenesis biomarkers in type 2 diabetic patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Type 2 diabetic patients (ADA criteria)
  • Age > 18 years
  • Obesity (BMI >= 25 kg/m2)
  • HbA1c > 6.5 %
  • Treatment with Metformin and/or secretagogues
  • Effective contraception (women)

Exclusion Criteria

  • Treatment with Exenatide, Liraglutide or other incretinergic regimen (<1 month before recruitment)
  • Type 1 diabetes
  • acute disease or infection
  • chronic renal failure (MDRD eGFR≤50 mL/min)
  • recent cardiovascular event or surgery (<3 months)
  • pancreatitis history
  • anti-VEGF treatment
  • untreated cancer
  • immunological disorders
  • pregnancy and lactation
  • Vulnerable people : deprivation of Liberty safeguards
  • hypersensitivity to the active substance or to any of the excipients of the investigational drug
  • diabetic ketoacidosis
  • heart failure stage 3 or 4 (NYHA III-IV)
  • Hepatic insufficiency
  • inflammatory bowel disease and gastroparesis
  • No affiliation to the social security

Arms & Interventions

1: Liraglutide

Experimental

Liraglutide 1,2 mg once daily subcutaneous injection for 1 month (4 weeks)

Intervention: Liraglutide (Drug)

2: Add on oral antidiabetic medication

Active Comparator

Metformin or sulfonylurea depending on monotherapy

Intervention: Metformin or sulfonylurea (Drug)

Outcomes

Primary Outcomes

Difference of ANGPTL4 concentration at 4 weeks of treatment from baseline in Liraglutide and control group

Time Frame: At 1 month

Secondary Outcomes

  • Difference of ANGPT2 concentration at 4 weeks of treatment from baseline in Liraglutide and control group(4 weeks)
  • Difference of endothelial circulating progenitor cells (CD34+KDR+) concentration at 4 weeks of treatment from baseline in Liraglutide and control group(4 weeks)
  • Difference of Circulating soluble adhesion molecules as endothelial activation markers: ICAM-1 and VCAM-1 concentration at 4 weeks of treatment from baseline (Liraglutide versus control group)(4 weeks)
  • Difference of AngiomiR-126 expression at 4 weeks of treatment from baseline in Liraglutide and control group(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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