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Completed

NCT Number: NCT00667732

How Glargine Insulin, Oral Diabetes Medications and Exenatide May Improve Blood Sugar Control and Weight Gain in Type 2 Diabetics

This study is designed to look at how using glargine insulin with oral diabetes medications and exenatide may improve control of blood sugar levels and weight gain in type 2 diabetics.

The main study will last 32 weeks. However, all participants completing 32 weeks will be invited to continue for another 24 weeks taking the insulin and oral medication and exenatide treatment. This extension comparing insulin and oral medication with insulin and oral medication and exenatide will look at the long term weight loss/gain and blood sugar level control effects of this new drug regimen.

There is also a sub-study in the Clinical Research Center (CRC), which requires two 38-hour inpatient stays during the main study. This study offers the opportunity to study 24-hour blood sugar and metabolic patterns quantitatively.

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Key information

Age range

30 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Medstar Research Institute, Washington D.C., District of Columbia, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female patients with type 2 diabetes
  • Taking metformin at least 1000 mg daily plus a secretagogue, an alpha glucosidase inhibitor, a thiazolidinedione, or a single injection of any kind of insulin up to 0.4 units/kg daily for > 3 months
  • Age range 30 to 70 years
  • Body mass index 25-45 kg/m2
  • HbA1c 7.0 to 10.0% (or 7.0 to 8.5% if the second antihyperglycemic agent is insulin)
  • Less than 50% of randomized participants will have used insulin previously

Exclusion criteria

  • Use of more than two antihyperglycemic agents within the last 3 months
  • Use of more than one daily injection of any kind of insulin in the last 3 months
  • Positive anti-GAD antibody (test required in screening)
  • Fasting C-peptide <0.5 ng/mL (test required in screening)
  • Pregnancy (test required in screening if able to conceive) or lactation
  • Excessive use of alcohol or evidence of other form of drug dependency
  • Unwillingness or inability to grant informed consent
  • Unwillingness or inability to perform self-monitoring of blood glucose
  • Unwillingness or inability to inject insulin and/or inject exenatide
  • Serum creatinine >1.3 mg/dL in women or 1.4 in men
  • Retinopathy which has required photocoagulation for treatment
  • Major active systemic illness (e.g. neoplastic disorder, symptomatic ischemic heart disease, congestive heart failure) that might interfere with performing the study protocol
  • Clinically significant gastrointestinal disorder including prior gastric or intestinal surgery for weight-control
  • Ongoing use of any drug (e.g. narcotic analgesic, tricyclic antidepressant) that might alter gastric emptying
  • Use prednisone or other systemic glucocorticoid drug in the last 3 months
  • Use of any drug for weight-control (e.g. sibutramine, phentermine, orlistat) in the last 3 months
  • Use of any unproven investigational drug within the last 3 months

Treatment and study plan

exenatide

Drug

5mcg twice a day, increasing to 10mcg twice a day for 24 weeks

Other names: Byetta

Placebo

Drug

5mcg twice a day, increased to 10mcg twice a day for 24 weeks

Primary outcomes

  1. The Percentage of Intent to Treat Participants Randomized and Treated in Each Arm Who Had Lab-measured A1c <6.5% at 24 Weeks of Treatment

    Time frame: After 24 weeks of randomized treatment

Secondary outcomes

  1. The Percentage of Per Protocol Participants Randomized and Treated in Each Arm Who Had Lab-measured A1c <6.5% at 24 Weeks of Treatment

    Time frame: After 24 weeks of randomized treatment

    efficacy criteria, 50% of per protocol participants reached A1c target of <6.5%

Sponsors and collaborators

Lead sponsor

Oregon Health and Science University

Other

Collaborators

  • Amylin Pharmaceuticals, LLC.
  • Eli Lilly and Company

Registry information

Official study title

Metformin, Exenatide, and Glargine Insulin in Combination for Treatment of Patients With Type 2 Diabetes

Acronym: MEXELIN

Important dates

Study start
2007
Primary completion
2009
Study completion
2010
First posted
Apr 28, 2008
Registry last updated
Feb 6, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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