Colesevelam Pediatric Type 2 Diabetes Mellitus Study
Status: | Recruiting |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 10 - 17 |
Updated: | 12/29/2017 |
Start Date: | November 2010 |
End Date: | June 2019 |
Contact: | Tina Roberts, PhD |
Email: | T.Roberts@Medpace.com |
Phone: | 800-730-5779 |
Colesevelam Oral Suspension as Monotherapy or Add-on to Metformin Therapy in Pediatric Subjects With Type 2 Diabetes Mellitus
Colesevelam oral suspension will be studied as treatment of type 2 diabetes mellitus (T2DM)
to evaluate clinical safety and efficacy in patients aged 10-17 years. The patients may have
been treated with Metformin or have had no antidiabetic drug treatment in the previous three
months.
Study Hypothesis: Colesevelam oral suspension for pediatric subjects with T2DM is safe, well
tolerated, and shows improved blood sugar control (as evidenced by a significant change from
baseline in hemoglobin A1C [HbA1c]).
to evaluate clinical safety and efficacy in patients aged 10-17 years. The patients may have
been treated with Metformin or have had no antidiabetic drug treatment in the previous three
months.
Study Hypothesis: Colesevelam oral suspension for pediatric subjects with T2DM is safe, well
tolerated, and shows improved blood sugar control (as evidenced by a significant change from
baseline in hemoglobin A1C [HbA1c]).
Inclusion Criteria:
- Diagnosis of type 2 diabetes mellitus, as defined by the American Diabetes
Association;
- Understand study procedures and agree to participate by giving written assent and
obtaining written consent from a parent or legal guardian at screening;
- Males and females aged 10 to 17 years, inclusive, at randomization (randomization must
occur before 18th birthday);
- HbA1c at screening between 7.0% and 10.0%, inclusive;
- Fasting C-peptide >0.6 ng/mL; and
- Anti-diabetic treatment at screening:
- Treatment-naïve or untreated; OR
- On metformin monotherapy: Metformin monotherapy has been initiated prior to
screening.
Exclusion Criteria:
- Fasting plasma glucose >270 mg/dL;
- Diagnosis of type 1 diabetes;
- History of more than one episode of ketoacidosis after the initial diagnosis of type 2
diabetes mellitus;
- Positive autoimmune markers;
- Creatinine clearance <70 mL/min;
- Alanine transaminase or aspartate aminotransferase elevation >2.5 X upper limit of
normal;
- Participation in another interventional research study protocol in the past 60 days;
- Female subjects who are lactating, pregnant, or plan to become pregnant within 1 year
of screening;
- Female subjects who are sexually active and unwilling to use appropriate contraception
for the duration of the study;
- History of bowel obstruction;
- Other significant organ system illness or condition (including psychiatric or
developmental disorder) that, in the opinion of the Investigator, would prevent full
participation;
- Triglycerides >500 mg/dL.
We found this trial at
24
sites
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