Expired Study
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Minneapolis, Minnesota 55416


The purpose of this substudy is to obtain CGM data from individuals taking exenatide. The CGM measurements gathered before starting and during treatment with exenatide IR and/or exenatide LAR will help determine the characteristics of glucose control during treatment.


Inclusion Criteria: - participant in Amylin Protocol 2993LAR-105 - at least 16 years of age - type 2 diabetes being treated with stable regiment of metformin, SU, TZD, combination of metformin/SU, combination metformin/TZD, combination SU/TZD - A1c 7.1 - 11 - fasting glucose less than 280 at screening - BMI 25 - 45 - stable body weight 6 months prior to screening - not pregnant and willing to practice birth control - physical exam & ECG not clinically significant - lab values judged not to be clinically significant - able to understand & sign consent form Exclusion Criteria: - clinically significant medical condition as judged by investigator - drug or alcohol abuse - previous use of exenatide or any GLP-1 analog - has used any investigational drug in the past 30 days prior to screening - is currently using: alpha-glucosidase inhibitor, insulin, drugs that affect GI motility, use of systemic corticosteroids, use of medications with addictive potential, prescription or OTC weight-loss medications - has donated blood within 60 days of screening, or is planning to donate during the study - has had major surgery or blood transfusion within 2 months of screening - has had a surgical procedure that may impact gastric emptying - has any allergies or hypersensitivity to any component of study treatment - is an immediate family member of personnel affiliated with the study at the investigative site - is employed by Amylin, Lilly or Alkermes



Primary Contact:

Principal Investigator
Richard M Bergenstal, MD
Park Nicollet Institute dba International Diabetes Center

Backup Contact:


Location Contact:

Minneapolis, Minnesota 55416
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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