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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02518932
Other study ID # VTC-G15
Secondary ID
Status Recruiting
Phase Phase 1
First received June 25, 2015
Last updated August 7, 2015
Start date March 2015
Est. completion date March 2016

Study information

Verified date August 2015
Source Elahi, Dariush, PhD
Contact Dariush E;ahi, PhD
Phone 210-283-4520
Email dariush.elahi@iconplc.com
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

To asses the modulating properties of the cleaved pentapeptide product of GLP-1 amide.


Description:

The investigators have previously demonstrated that infusion of the pentapeptide during hyperglycemic clamps in dogs significantly increases the glucose infusion rate necessary to maintain stable hyperglycemia without any significant differences in insulin or glucagon secretion. The present study's aim is to examine whether this also occurs in humans. It may be necessary to examine a dose response curve. Specifically, in twenty healthy volunteers glucose infusion rate during the peptide infusion will be compared to the glucose infusion rate during saline administration during a 4 hour hyperglycemic clamp, in a cross over design(mg/kg/min).


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- BMI 18.5-25;

- 33-38

Exclusion Criteria:

- T2D

- T1D

- Hypoglycemic agents

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
Last 5 amino acids of GLP-1
To examine insulinomimetic properties of LVKGR
placebo saline


Locations

Country Name City State
United States ICON PLC San Antonio Texas

Sponsors (4)

Lead Sponsor Collaborator
Elahi, Dariush, PhD ICON plc, Massachusetts General Hospital, National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The effect of VTC-G15 on whole body glucose metabolism in man will be assessed by comparison of amont of glucose infusion during the peptide infusion compared to amount of infusion during placebo infusion (saline) mg/kg/min. one year No
Secondary THe effect of VTC-G15(A pentapeptide cleavage product of GLP-1) on whole body glucose metabolism in man. changes in insulin or glucagon release. one year No
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