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Plasma Lipoprotein Response to Glucagon-like Peptide-2 (GLP-2 Plasma)

Primary Purpose

Hyperlipidemias

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Teduglutide
Placebo
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Hyperlipidemias focused on measuring Intestinal lipoprotein, Gut Peptide, Chylomicrons

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Men and women, aged 18 to 60 years.
  • Body mass index 20 to 27 kg/m2

Exclusion Criteria:

  • Patients with active inflammatory bowel disease
  • Patients with pre-existing Celiac disease, exocrine pancreatic insufficiency or small bowel malabsorption
  • Patients with active bowel malignancy
  • Patients with diabetes mellitus or known/ suspected motility disorders of the gut
  • Patients with decompensated liver disease
  • Patients on ezetimibe or bile acid sequestrants
  • Patients who are pregnant or breastfeeding.
  • Patients with renal disease.
  • Patients on benzodiazepine.
  • Unstable cardiac or respiratory disease
  • Any changes to medication in the preceding month

Sites / Locations

  • Toronto General Hopital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Teduglutide

Placebo

Arm Description

Teduglutide, up to 0.05mg/kg, subcutaneous, single dose

Placebo, subcutaneous, single dose

Outcomes

Primary Outcome Measures

Lipoprotein response to teduglutide
To quantify the plasma lipoprotein response to teduglutide (GLP-2 analogue) injection in healthy individuals

Secondary Outcome Measures

Full Information

First Posted
January 30, 2018
Last Updated
June 13, 2022
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT03422666
Brief Title
Plasma Lipoprotein Response to Glucagon-like Peptide-2
Acronym
GLP-2 Plasma
Official Title
Investigating the Plasma Lipoprotein Response to a Single Subcutaneous Dose of Analogue Glucagon-like Peptide-2 in Humans
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
September 21, 2018 (Actual)
Primary Completion Date
June 1, 2021 (Actual)
Study Completion Date
December 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Some of the fat (triglyceride) from the food humans eat gets stored in the bowel. This triglyceride can then be released into the blood when another meal is consumed or in response to hormones. How the gut hormone glucagon-like peptide-2 (GLP-2) releases the triglyceride from the gut is not known. The research team in this study is interested in finding out how teduglutide (a degradation resistant form of GLP-2) releases stored triglyceride from the gut by evaluating how blood lipoproteins respond to teduglutide in healthy individuals.
Detailed Description
The lipoprotein response will be performed in 15 healthy individuals recruited by newspaper advertisements. Each subject will be their own control, receiving both placebo and teduglutide, administered on separate occasions. A member of the study team will explain the study in detail on visit 1, and if the individual is interested in participating, informed consent will be obtained and preliminary screening will occur on visit 2. On visit 3 & 4 participants will receive a high fat liquid meal after an overnight fast. Hourly blood samples will be taken for 5 hours, followed by randomized assignment to receive either subcutaneous placebo or teduglutide at visit 3 and the opposite treatment at visit 4. Following the injection, blood samples will be taken every 15 minutes for the first hour and every 30 minutes for the subsequent 3 hours.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hyperlipidemias
Keywords
Intestinal lipoprotein, Gut Peptide, Chylomicrons

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Model Description
On visits 3 & 4, participants will receive either teduglutide or placebo, in random order, 5 hours after a high-fat drink
Masking
Participant
Masking Description
Single-blinded study with participant blinded to treatment
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Teduglutide
Arm Type
Experimental
Arm Description
Teduglutide, up to 0.05mg/kg, subcutaneous, single dose
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, subcutaneous, single dose
Intervention Type
Drug
Intervention Name(s)
Teduglutide
Intervention Description
Teduglutide
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Lipoprotein response to teduglutide
Description
To quantify the plasma lipoprotein response to teduglutide (GLP-2 analogue) injection in healthy individuals
Time Frame
8 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Men and women, aged 18 to 60 years. Body mass index 20 to 27 kg/m2 Exclusion Criteria: Patients with active inflammatory bowel disease Patients with pre-existing Celiac disease, exocrine pancreatic insufficiency or small bowel malabsorption Patients with active bowel malignancy Patients with diabetes mellitus or known/ suspected motility disorders of the gut Patients with decompensated liver disease Patients on ezetimibe or bile acid sequestrants Patients who are pregnant or breastfeeding. Patients with renal disease. Patients on benzodiazepine. Unstable cardiac or respiratory disease Any changes to medication in the preceding month
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary Lewis, MD
Organizational Affiliation
UHN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Toronto General Hopital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Plasma Lipoprotein Response to Glucagon-like Peptide-2

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