Efficacy and safety of sitagliptin when added to ongoing metformin therapy in patients with type 2 diabetes

To assess the addition of sitagliptin to ongoing metformin therapy in patients with type 2 diabetes who were inadequately controlled [haemoglobin A₁c (HbA₁c) 7-11%] on metformin monotherapy. Patients (n = 273) on metformin (>=1500 mg/day) were randomized to receive the addition of once-daily plac...

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Veröffentlicht in:Diabetes, obesity & metabolism obesity & metabolism, 2008-10, Vol.10 (10), p.959-969
Hauptverfasser: Scott, R, Loeys, T, Davies, M.J, Engel, S.S
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Sprache:eng
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Zusammenfassung:To assess the addition of sitagliptin to ongoing metformin therapy in patients with type 2 diabetes who were inadequately controlled [haemoglobin A₁c (HbA₁c) 7-11%] on metformin monotherapy. Patients (n = 273) on metformin (>=1500 mg/day) were randomized to receive the addition of once-daily placebo, sitagliptin 100 mg or rosiglitazone 8 mg in a 1 : 1 : 1 ratio for 18 weeks. The efficacy analysis was based on the all-patients-treated population using an analysis of co-variance with change in HbA₁c from baseline as the primary endpoint. The mean baseline HbA₁c was 7.7% for the entire cohort. After 18 weeks, both active add-on therapies led to greater improvements in HbA₁c from baseline: -0.73% for sitagliptin (p < 0.001 vs. placebo) and -0.79% for rosiglitazone compared with -0.22% for placebo. No difference was observed between the sitagliptin and rosiglitazone treatments (0.06% [95% confidence interval (CI): -0.14 to 0.25]). The proportion of patients achieving an HbA₁c < 7% was greater with sitagliptin (55%) and rosiglitazone (63%) compared with placebo (38%). Body weight increased from baseline with rosiglitazone (1.5 kg) compared with body weight reduction with sitagliptin (-0.4 kg) and placebo (-0.8 kg). The difference in body weight between the sitagliptin and rosiglitazone groups was 1.9 kg (95% CI: 1.3-2.5). In a prespecified analysis, the proportion of patients experiencing a greater than 3-kg increase in body weight was 21% in the rosiglitazone group compared with 2% in both the sitagliptin and placebo groups. Both active treatments were generally well tolerated, with no increased risk of hypoglycaemia or gastrointestinal adverse events compared with placebo. In this 18-week study, the addition of sitagliptin was effective and well tolerated in patients with type 2 diabetes inadequately controlled with metformin monotherapy. Treatment with sitagliptin produced similar reductions in HbA₁c compared with the addition of rosiglitazone.
ISSN:1462-8902
1463-1326
DOI:10.1111/j.1463-1326.2007.00839.x