GLP-1 Therapy for Weight Loss and Improved Glucose Tolerance in Obese Children

• ClinicalTrials.gov Identifier: NCT00886626
• Recruitment Status: Completed
• First Posted: April 23, 2009
• Results First Posted: August 17, 2012
• Last Update Posted: October 29, 2012
• Sponsor: University of Minnesota
• Information provided by (Responsible Party): University of Minnesota

Study Description

Brief Summary:

The prevalence of severely obese children is on the rise. Behavioral therapies for weight loss are successful in some, but others need more aggressive approaches such as drug therapy. In addition, up to 25% of severely obese children have impaired glucose tolerance (IGT), which places them at significantly elevated risk of developing type 2 diabetes mellitus and cardiovascular disease. Although various drug therapies for weight loss and IGT have been explored in adults, few have been evaluated in children.

Recently, a new drug class has emerged that targets deficiencies of GLP-1. One of the main glycemic mechanisms of action of the GLP-1 agonists such as exenatide is to enhance glucose disposal in the postprandial setting and improve glucose tolerance. In addition, exenatide can induce weight loss by decreasing appetite and slowing gastric motility.

Condition or disease	Intervention/treatment	Phase
Obesity, Morbid	Drug: Exenatide	Phase 2

Detailed Description:

This will be a randomized, open-label, controlled, crossover clinical trial in 12 patients. All patients will receive exenatide and undergo the control phase. Following baseline testing, participants will be randomly assigned to treatment order: therapy (exenatide) or control (lifestyle modification). Half (n = 6) will receive exenatide first (3-months) then cross over to control (no drug therapy for 3-months). Half (n = 6) will be assigned to control first (3-months) then cross over to exenatide (3-months). All efforts will be made to stratify randomization based on gender of the participants. Treatment and control conditions will be three months each. Because of the route of administration of exenatide (subcutaneous injection), placebo will not be utilized for the control phase of the study.

Participants in this study will engage in background intensive lifestyle modification offered by the University of Minnesota Pediatric Weight Management Clinic for the entire study, even during the active drug treatment phase. Intensive lifestyle modification will be purely clinical in nature in which children and their families receive continuing counseling from a team of trained professionals including physicians, dieticians, and psychologists to reduce weight by making healthier eating choices and increasing physical activity.

The screening visit will take place in the Pediatric Weight Management Clinic and will include a complete medical history and physical examination. Screening will include review of medical records for previous clinical and laboratory data (including clinically-ordered glucose tolerance test results). All research testing will take place in the University of Minnesota General Clinical Research Center (GCRC). Subjects will undergo testing at the following intervals: baseline, immediately after the first 3-month phase (whether exenatide or control), and immediately after the second 3- month phase (whether exenatide or control). The following measures will be collected after the subject has been fasting for at least twelve hours:

• Height, weight, body mass index, waist and hip circumference
• Fat and lean mass (dual energy x-ray absorptiometry: DXA)
• Tanner stage determination (performed during screening physical exam or may be obtained from medical chart)
• Fasting lipid profile (total-, LDL-, and HDL-cholesterol, triglycerides)
• Systolic and diastolic blood pressure
• Oral glucose tolerance test (glucose and insulin measured every 30 minutes for 2 hours)
• Endothelial function (digital reactive hyperemia: EndoPAT 2000, Itamar Medical) - in addition to the baseline measure, endothelial function testing will occur at hours one and two of the oral glucose tolerance test
• Frozen plasma for storage - in addition to the baseline blood draw, blood for endothelial biomarkers will be obtained at hours one and two of the oral glucose tolerance test
• Arterial stiffness (pulse wave velocity; augmentation index: Sphygmocor, AtCor Medical)
• Frozen plasma for pharmacokinetic determination of exenatide in children

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 12 participants
• Allocation: Randomized
• Intervention Model: Crossover Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: GLP-1 Therapy for Weight Loss and Improved Glucose Tolerance in Obese Children: A Randomized, Controlled, Pilot Study
• Study Start Date: May 2009
• Actual Primary Completion Date: February 2011
• Actual Study Completion Date: February 2011

Arms and Interventions

Arm	Intervention/treatment
Experimental: Exenatide; Exenatide	Drug: Exenatide; Exenatide, subcutaneous injection, 10 mcg, twice per day; Other Name: Byetta
No Intervention: Control; Control - no intervention

Outcome Measures

Primary Outcome Measures :

1. Change in Body Mass Index (BMI) [ Time Frame: 3-month ]
   Change in body mass index (BMI) over three months

Eligibility Criteria

• Ages Eligible for Study: 8 Years to 19 Years (Child, Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Age 8-19 years old
• Subject able to give assent, and parent/guardian capable of giving consent on behalf of the child
• Body mass index (BMI) ≥ 99th percentile (based on gender and age)

Exclusion Criteria:

• Type 1 or 2 diabetes mellitus
• Initiation of a new drug therapy within the past 30 days prior to the screening visit
• BMI ≥ 55
• History of weight loss surgery
• Obesity from a genetic cause (e.g., Prader-Willi)
• Central nervous system injury or severe neurological impairment
• Known systolic or diastolic dysfunction or heart failure
• Females who are currently pregnant or planning to become pregnant
• Liver enzymes > 2.5 times upper limit of normal
• Severe renal impairment (defined as creatinine clearance <30 mL/min)
• Gastrointestinal disease

Contacts and Locations

Locations

United States, Minnesota

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Sponsors and Collaborators

University of Minnesota

Investigators

• Principal Investigator: Aaron S. Kelly, Ph.D.; University of Minnesota

More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Kelly AS, Metzig AM, Rudser KD, Fitch AK, Fox CK, Nathan BM, Deering MM, Schwartz BL, Abuzzahab MJ, Gandrud LM, Moran A, Billington CJ, Schwarzenberg SJ. Exenatide as a weight-loss therapy in extreme pediatric obesity: a randomized, controlled pilot study. Obesity (Silver Spring). 2012 Feb;20(2):364-70. doi: 10.1038/oby.2011.337. Epub 2011 Nov 10.

• Responsible Party: University of Minnesota
• ClinicalTrials.gov Identifier: NCT00886626
• Other Study ID Numbers: 0902M59181
• First Posted: April 23, 2009
• Results First Posted: August 17, 2012
• Last Update Posted: October 29, 2012
• Last Verified: October 2012

Keywords provided by University of Minnesota:

Obesity; Impaired Glucose Tolerance; Children

Additional relevant MeSH terms:

Obesity, Morbid; Weight Loss; Obesity; Overnutrition; Nutrition Disorders; Overweight; Body Weight; Body Weight Changes; Exenatide; Hypoglycemic Agents; Physiological Effects of Drugs; Anti-Obesity Agents; Incretins; Hormones; Hormones, Hormone Substitutes, and Hormone Antagonists