Effect of Rimonabant on Glycemic Control in Insulin-Treated Type 2 Diabetes: The ARPEGGIO Trial

OBJECTIVE - To examine the efficacy and safety of rimonabant, a selective cannabinoid receptor type-1 antagonist, in patients with type 2 diabetes receiving insulin monotherapy. RESEARCH DESIGN AND METHODS - Patients (n = 368; A1C >= 7%) were randomized to 20 mg/day rimonabant or placebo in this 48-week, double-blind, placebo-controlled I multicenter trial. Change in baseline A1C to week 48 (primary outcome) and changes in body weight, waist circumference, and lipid levels (secondary outcomes) were assessed. RESULTS - Rimonabant significantly reduced baseline A1C versus placebo (-0.89 vs. -0.24% P < 0.0001), and significantly greater improvements were observed in cardiometabolic risk factors. More rimonabant. Patients achieved >10% reduction in mean total daily insulin dose versus placebo (P = 0.0012), and fewer required rescue medication (P < 0.0001). Hypoglycemia, nausea, dizziness, anxiety, and depression were more frequent with rimonabant. CONCLUSIONS - Rimonabant improved glycerine control and cardiometabolic risk factors in patients with type 2 diabetes receiving insulin.