Trial record 4 of 43 for:
Open Studies | "Hypoglycemic Agents"
Anti-diabetic Effects of Liraglutide in Adolescents and Young Subjects With Type 1 Diabetes
This study is currently recruiting participants.
Verified November 2012 by Kaleida Health
American Diabetes Association
Information provided by (Responsible Party):
Paresh Dandona, MD, Kaleida Health
First received: November 2, 2012
Last updated: November 5, 2012
Last verified: November 2012
This is the first prospective randomized double-blind placebo-controlled study to investigate the effect of a GLP-1 analog, specifically liraglutide, on blood glucose levels and variability in subjects with type 1 diabetes treated with insulin. Liraglutide is the preferred GLP-1 analog for this study because the pharmacokinetics and pharmacodynamics of the drug are consistent with a sustained duration of action. The current gold standard for management of type 1 diabetes is based on insulin replacement with novel analogs with specified pharmacodynamic profiles or with unique insulin delivery systems (insulin pump therapy). No other adjuvant therapy has demonstrated sustained benefit in this population. This study will also investigate the effect of liraglutide on suppression of glucagon secretion during meal challenges. This is of particular importance since, in the absence of insulin secretion from the β-cell, there is no paracrine inhibition of glucagon secretion by the α-cell. Dysregulation of glucagon secretion may impact the glycemic control and overall pathogenesis in those with type 1 diabetes. The use of CGM technology in this study will allow us to determine the rapidity, consistency, and sustainability of any response to liraglutide.
Type 1 Diabetes
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
||Anti-diabetic Effects of Liraglutide in Adolescents and Young Subjects With Type 1 Diabetes
Primary Outcome Measures:
Secondary Outcome Measures:
- HbA1c [ Time Frame: 3 Months ] [ Designated as safety issue: No ]
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
| Estimated Primary Completion Date:
||November 2017 (Final data collection date for primary outcome measure)
Active Comparator: Liraglutide 0.6mg
Placebo Comparator: Placebo
|Ages Eligible for Study:
||15 Years to 30 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Females and males with Type 1 diabetes as ascertained by islet autoantibodies (GAD-65 and/or islet cell antibodies)
- Age 15-30 years - This age group is being chosen as most will have completed puberty with the accompanying physiologic phase of increased insulin resistance. In addition, this age group shows increased self-management capabilities. Extending the age up to 30 years will allow us to include young adults, since type 1 diabetes is frequently diagnosed in the late teen and early adult years. This study is not powered to detect differences in liraglutide efficacy in different age group but it may provide insight into the effectiveness in the teenage population, in whom optimal glycemic control is often a challenge.
- Type 1 diabetes duration greater than 1 year to ensure that a majority of subjects are beyond the partial remission period.
- Fasting C-peptide level ≤ 0.3 ng/ml.
- HbA1c level equal or less than 9%
- Insulin delivery by CSII - the choice is made to facilitate adherence to study drug and also to enable us have a homogeneous group to analyze without having to analyze the data for the covariants of CSII vs. multiple daily injection therapy.
- Subjects willing to wear a CGM sensor and perform home blood glucose monitoring four times daily and with symptoms of hypoglycemia.
- Subjects well-versed in carbohydrate counting.
- BMI < 95th% for age and gender.
- Previous exposure to liraglutide
- History of abdominal surgery
- History of gastroparesis or gastrointestinal reflux disease;
- History of acute or chronic pancreatitis
- Cirrhosis or hepatic disease defined as transaminases levels > 3 times normal
- Impaired renal function defined as serum creatinine >1.5.
- HIV or Hepatitis C positive status
- Pregnant/breastfeeding females
- Individuals with steroid-induced or cystic fibrosis related diabetes
- Diabetic Ketoacidosis within 6 months of the study
- History of severe hypoglycemia (seizure, loss of consciousness) within 6 months of the study
- History of medullary thyroid cancer or MEN2 syndrome
- Any other life-threatening cardiac or non-cardiac disease
- Participation in a concurrent clinical trial or participation in a trial within 30 days preceding the study period.
- Unable to give informed consent/assent.
Adolescents and adults who are considered underweight based on body mass index (BMI):
- For adolescents: BMI less than the 5th percentile
- For adults: BMI below 18.5
Please refer to this study by its ClinicalTrials.gov identifier: NCT01722227
|Contact: Sonja Williams
|Contact: Jeanne Hejna
|Diabetes-Endocrinology Center of WNY
|Williamsville, New York, United States, 14221 |
|Contact: Sonja Williams 716-626-7998 |
|Principal Investigator: Paresh Dandona, MBBS,PhD |
American Diabetes Association
No publications provided
||Paresh Dandona, MD, Distinguished Professor of Medicine, Kaleida Health
History of Changes
|Other Study ID Numbers:
||1964 Liraglutide ADA, 1-12-CT-20
|Study First Received:
||November 2, 2012
||November 5, 2012
||United States: Food and Drug Administration
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on April 16, 2014
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Endocrine System Diseases
Immune System Diseases
Glucagon-Like Peptide 1
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists