Dual Add-on Therapy in Type 2 Diabetes Poorly Controlled With Metformin Monotherapy: A Randomized Double-Blind Trial of Saxagliptin Plus Dapagliflozin Addition Versus Single Addition of Saxagliptin or Dapagliflozin to Metformin

被引:257
作者
Rosenstock, Julio [1 ]
Hansen, Lars [2 ]
Zee, Pamela [2 ]
Li, Yan [3 ]
Cook, William [3 ]
Hirshberg, Boaz [3 ]
Iqbal, Nayyar [2 ]
机构
[1] Dallas Diabet & Endocrine Ctr, Dallas, TX 75230 USA
[2] Bristol Myers Squibb Co, Princeton, NJ USA
[3] AstraZeneca, Wilmington, DE USA
关键词
INADEQUATE GLYCEMIC CONTROL; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; PLACEBO-CONTROLLED TRIAL; CLINICAL-TRIALS; SGLT2; INHIBITOR; BODY-WEIGHT; EFFICACY; MELLITUS; SAFETY; SITAGLIPTIN;
D O I
10.2337/dc14-1142
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE This study compared the efficacy and safety of dual add-on of saxagliptin plus dapagliflozin versus saxagliptin and dapagliflozin added on alone in patients with type 2 diabetes poorly controlled with metformin. RESEARCH DESIGN AND METHODS This was a double-blind trial in adults with HbA(1c) >= 8.0% and <= 12.0% (64-108 mmol/mol), randomized to saxagliptin (SAXA) (5 mg/day) plus dapagliflozin (DAPA) (10 mg/day; n = 179), or SAXA (5 mg/day) and placebo (n = 176), or DAPA (10 mg/day) and placebo (n = 179) on background metformin extended release (MET) >= 1,500 mg/day. Primary objective compared changes from baseline in HbA1c with SAXA+DAPA+MET versus SAXA+MET and DAPA+MET. RESULTS Patients had a mean baseline HbA(1c) of 8.9% (74 mmol/mol), diabetes duration of 7.6 years, and a BMI of 32 kg/m(2). At week 24, the adjusted mean change from the baseline HbA(1c) was -1.5% (-16.1mmol/mol) with SAXA+DAPA+MET versus -0.9% (-9.6 mmol/mol) with SAXA+MET (difference -0.59% [-6.4 mmol/mol], P < 0.0001) and -1.2% (-13.1 mmol/mol) with DAPA+MET (difference -0.27% [3.0 mmol/mol], P < 0.02). The proportion of patients achieving HbA(1c) <7% (53 mmol/mol) was 41% with SAXA+DAPA+MET versus 18% with SAXA+MET and 22% with DAPA+MET. Urinary and genital infections occurred in <= 1% of patients receiving SAXA+DAPA+MET. Hypoglycemia was infrequent, with no episodes of major hypoglycemia. CONCLUSIONS In this first report of adding a well-tolerated combination of saxagliptin plus dapagliflozin to background metformin therapy in patients poorly controlled with metformin, greater improvements in glycemic control were obtained with triple therapy by the dual addition of saxagliptin and dapagliflozin than dual therapy with the addition of saxagliptin or dapagliflozin alone.
引用
收藏
页码:376 / 383
页数:8
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