Initial Combination of Empagliflozin and Linagliptin in Subjects With Type 2 Diabetes

被引:179
作者
Lewin, Andrew [1 ]
DeFronzo, Ralph A. [2 ]
Patel, Sanjay [3 ]
Liu, Dacheng [4 ]
Kaste, Renee [4 ]
Woerle, Hans J. [5 ]
Broedl, Uli C. [5 ]
机构
[1] Natl Res Inst, Los Angeles, CA USA
[2] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA
[3] Boehringer Ingelheim Ltd, Bracknell, Berks, England
[4] Boehringer Ingelheim Pharmaceut Inc, Ridgefield, CT 06877 USA
[5] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
关键词
COTRANSPORTER; 2; INHIBITORS; METFORMIN THERAPY; MELLITUS; MONOTHERAPY; SAFETY; CONTRAINDICATIONS; METAANALYSIS; TRIAL;
D O I
10.2337/dc14-2365
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE To evaluate the efficacy and safety of empagliflozin/linagliptin in subjects with type 2 diabetes. RESEARCH DESIGN AND METHODS Subjects not receiving antidiabetes therapy for >= 12 weeks were randomized to empagliflozin 25 mg/linagliptin 5 mg (n = 137), empagliflozin 10 mg/linagliptin 5 mg (n = 136), empagliflozin 25 mg (n = 135), empagliflozin 10 mg (n = 134), or linagliptin 5 mg (n = 135) for 52 weeks. The primary end point was change from baseline in HbA(1c) at week 24. RESULTS Mean HbA1c at baseline was 7.99-8.05% (64 mmol/mol). At week 24, adjusted mean (SE) changes from baseline in HbA(1c) with empagliflozin 25 mg/linagliptin 5 mg, empagliflozin 10 mg/linagliptin 5 mg, empagliflozin 25 mg, empagliflozin 10 mg, and linagliptin 5 mg were -1.08 (0.06)% (-11.8 [0.7] mmol/mol), -1.24 (0.06)% (-13.6 [0.7] mmol/mol), -0.95 (0.06)% (-10.4 [0.7] mmol/mol), -0.83 (0.06)% (-9.1 [0.7] mmol/mol), and -0.67 (0.06)% (-7.3 [0.7] mmol/mol), respectively. Reductions in HbA(1c) were significantly greater for empagliflozin 25 mg/linagliptin 5 mg compared with linagliptin 5 mg (P < 0.001) but not compared with empagliflozin 25 mg and were significantly greater for empagliflozin 10 mg/linagliptin 5 mg compared with the individual components (P < 0.001 for both). At week 24, 55.4%, 62.3%, 41.5%, 38.8%, and 32.3% of subjects with baseline HbA(1c) >= 7% (>= 53 mmol/mol) reached HbA(1c) <7% with empagliflozin 25 mg/linagliptin 5 mg, empagliflozin 10 mg/linagliptin 5 mg, empagliflozin 25 mg, empagliflozin 10 mg, and linagliptin 5 mg, respectively. Efficacy was maintained at week 52. The proportion of subjects with adverse events (AEs) over 52 weeks was similar across groups (68.9-81.5%), with no confirmed hypoglycemic AEs. CONCLUSIONS Reductions from baseline in HbA(1c) with empagliflozin/linagliptin were significantly different versus linagliptin and empagliflozin 10 mg but not versus empagliflozin 25 mg. Empagliflozin/linagliptin was well tolerated.
引用
收藏
页码:394 / 402
页数:9
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