Abstract

Saxagliptin is a potent, selective DPP4 inhibitor. Highlights from abstracts presented at the 2010 meetings of the European Association for the Study of Diabetes and the American Diabetes Association include studies and analyses that shed light on the promising role for saxagliptin within the management of type 2 diabetes mellitus. Data show that saxagliptin combination therapy improves HbA1c levels compared with placebo, particularly in patients with high HbA1c at baseline, long duration of disease, low baseline creatinine clearance, and low homeostasis model assessment 2 β-cell function at baseline. These efficacy benefits are achieved without any increase in hypoglycemia or other adverse events. The study results also show that the saxagliptin plus metformin combination is a good candidate for initial therapy in drug-naïve patients treated for as long as 72 weeks. Survey data presented confirm that hypoglycemia (and fear of hypoglycemia) is a barrier to patients' acceptance of diabetes treatment, limiting its efficacy. Therefore, therapies such as saxagliptin that have a low risk of hypoglycemia may be more acceptable to patients in helping them to achieve glycemic control and to optimize their quality of life. In patients with renal impairment, for whom metformin is contraindicated, saxagliptin monotherapy is a promising option for antidiabetic management as, when given at a reduced dose, it is well-tolerated with a safety profile similar to that of placebo.

Highlights

  • The dipeptidyl peptidase-4 (DPP4) inhibitors are a novel class of antidiabetic drugs with a good safety profile and which are being considered in some algorithms for the treatment of type 2 diabetes mellitus (T2DM)

  • We present here some of the key data on saxagliptin (SAXA) - a potent, selective DPP4 inhibitor - derived from abstracts presented at the 2010 meetings of the American Diabetes

  • Monotherapy in patients with renal impairment To explore the clinical use of SAXA in patients with renal impairment, a multicenter, randomized, doubleblind, parallel-group, placebo-controlled 12-week study conducted to the assess the efficacy and safety of SAXA 2.5 mg/day in adult patients with T2DM, HbA1c 7%-11%, and moderate to severe renal impairment, including end-stage renal disease (ESRD) with hemodialysis [6]

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Summary

Introduction

The dipeptidyl peptidase-4 (DPP4) inhibitors are a novel class of antidiabetic drugs with a good safety profile and which are being considered in some algorithms for the treatment of type 2 diabetes mellitus (T2DM). Göke et al at tested this hypothesis in a 52-week multicenter, randomized, double-blind, noninferiority, Phase IIIb trial comparing the efficacy and safety of adding SAXA 5 mg/d or glipizide (GPZ) to MET in T2DM patients inadequately controlled on MET with an HbA1c > 6.5%-10% and on a stable MET dose ≥1500 mg/day.

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Conclusion
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