Liraglutide in Children and Adolescents with Type 2 Diabetes
Abstract
This randomized, double blind, placebo controlled trial evaluated the efficacy and safety of liraglutide in children and adolescents (aged 10 17 years) with type 2 diabetes inadequately controlled by metformin (with or without basal insulin). Participants received subcutaneous liraglutide (up to 1.8 mg/day) or placebo for 26 weeks, followed by a 26-week open-label extension. The primary endpoint was the change in glycated hemoglobin (HbA1c) levels at 26 weeks. Results showed a significant reduction in HbA1c with liraglutide (0.64 percentage points) compared to an increase with placebo (+0.42 percentage points), yielding an estimated treatment difference of 1.06 percentage points (P<0.001). Liraglutide also improved fasting plasma glucose levels and increased the proportion of patients achieving HbA1c <7.0%. However, gastrointestinal adverse events were more frequent with liraglutide. The study concluded that liraglutide is effective for glycemic control in youth with type 2 diabetes but is associated with higher rates of gastrointestinal side effects.