Efficacy and safety of alogliptin added to sulfonylurea in Japanese patients with type 2 diabetes: A randomized, double‐blind, placebo‐controlled trial with an open‐label, long‐term extension study

Abstract

Aims/Introduction

To evaluate the efficacy and safety of alogliptin added to treatment with glimepiride.

Materials and Methods

This multicenter, randomized, double‐blind, parallel‐group, 24‐week (12‐week observation and 12‐week treatment) study compared alogliptin 12.5 or 25 mg in combination with glimepiride (1–4 mg/day) vs placebo added to glimepiride monotherapy in Japanese patients with type 2 diabetes who had poor glycemic control despite treatment with diet and exercise plus a sulfonylurea. The primary end‐point was a change in glycated hemoglobin ( Hb A _1c) from baseline. A 40‐week open‐label extension study evaluated the long‐term safety and efficacy of the combination.

Results

Alogliptin 12.5 or 25 mg in combination with glimepiride significantly decreased Hb A _1c compared with glimepiride monotherapy after 12 weeks' treatment (−0.59, −0.65 and 0.35%, respectively; P < 0.0001 for both combination groups vs glimepiride monotherapy). Alogliptin 12.5 and 25 mg combination therapy was also associated with significantly higher responder rates ( Hb A _1c <6.9%: 9.6% and 7.7%, Hb A _1c <7.4%: 29.8% and 34.6%) compared with glimepiride monotherapy ( Hb A _1c <6.9%: 0%, Hb A _1c <7.4%: 3.9%). The incidence of adverse events was comparable between glimepiride monotherapy and alogliptin combination treatment, with most reported adverse events being mild in severity. In the extension study, the incidence of adverse events was comparable between the combination groups, with the majority of adverse events being mild.

Conclusions

Once‐daily alogliptin was effective and generally well tolerated when given as add‐on therapy to glimepiride in Japanese patients with type 2 diabetes who had inadequate glycemic control on sulfonylurea plus lifestyle measures. Clinical benefits were maintained for 52 weeks. This trial was registered with ClinicalTrials.gov (double‐blind study no. NCT01318083; long‐term study no. NCT01318135).