Effect of saxagliptin as add-on therapy in patients with poorly controlled type 2 diabetes on insulin alone or insulin combined with metformin

被引:158
作者
Barnett, Anthony H. [1 ,2 ]
Charbonnel, Bernard [3 ]
Donovan, Mark [4 ]
Fleming, Douglas [4 ]
Chen, Roland [4 ]
机构
[1] Univ Birmingham, Birmingham, W Midlands, England
[2] Heart England Natl Hlth Serv Fdn Trust, Biomed Res Ctr, Birmingham, W Midlands, England
[3] Ctr Hosp Univ Nantes, Nantes, France
[4] Bristol Myers Squibb Co, Investigators CV181 057, Princeton, NJ USA
关键词
Dipeptidyl peptidase-4 inhibitor; DPP-4; Hypoglycemia; Insulin; Saxagliptin; Type; 2; diabetes; IMPROVES GLYCEMIC CONTROL; RANDOMIZED CONTROLLED-TRIAL; BASAL INSULIN; MELLITUS; MANAGEMENT; EFFICACY; SAFETY; PIOGLITAZONE; HYPOGLYCEMIA; COMBINATION;
D O I
10.1185/03007995.2012.665046
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To evaluate efficacy and safety of saxagliptin as add-on therapy in patients with type 2 diabetes (T2D) with inadequate glycemic control on insulin alone or combined with metformin. Methods: Adults (n=455) with HbA(1c) 7.5-11% on stable insulin therapy (30-150 U/day +/- metformin) for at least 8 weeks were stratified by metformin use and randomly assigned 2: 1 to receive saxagliptin 5 mg or placebo once daily for 24 weeks. Patients were to maintain stable insulin doses but these could be decreased to reduce risk of hypoglycemia. Patients with hyperglycemia or substantially increased insulin use were rescued with a flexible insulin regimen and remained in the study. Metformin doses were kept stable. The primary efficacy endpoint was change in HbA(1c) from baseline to week 24 (or rescue). Results: Patients treated with saxagliptin versus placebo had significantly greater reductions in adjusted mean HbA(1c) (difference: -0.41%, p<0.0001), postprandial glucose (PPG) 180-minute area under the curve (-3829.8 mg.min/dL, p=0.0011), and 120-minute PPG (-23.0 mg/dL, p=0.0016) at 24 weeks. Treatment with saxagliptin resulted in similar reductions in HbA(1c) relative to placebo, irrespective of metformin treatment. At 24 weeks, difference in adjusted mean fasting plasma glucose for saxagliptin versus placebo was -4.02 mg/dL (p=0.3958); 17.3% and 6.7% of patients in the saxagliptin and placebo groups, respectively, achieved HbA(1c)<57%. Mean change from baseline in body weight at week 24 was 0.39 kg for saxagliptin and 0.18 kg for placebo. Hypoglycemia was reported in 18.4% and 19.9% of patients in the saxagliptin and placebo groups, respectively (confirmed hypoglycemia: 5.3%, 3.3%). Other adverse events reported in at least 5% of patients were urinary tract infection (saxagliptin, placebo: 5.9%, 6.0%), influenza (3.0%, 6.6%), and pain in extremity (1.6%, 6.0%). Conclusions: Saxagliptin 5-mg once-daily add-on therapy improves glycemic control in T2D patients on insulin alone or combined with metformin and is generally well-tolerated.
引用
收藏
页码:513 / 523
页数:11
相关论文
共 27 条
[1]  
[Anonymous], 2011, ONGL PROD INS
[2]  
[Anonymous], DIABETES
[3]   Discovery and preclinical profile of saxagliptin (BMS-477118): A highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes [J].
Augeri, DJ ;
Robl, JA ;
Betebenner, DA ;
Magnin, DR ;
Khanna, A ;
Robertson, JG ;
Wang, AY ;
Simpkins, LM ;
Taunk, P ;
Huang, Q ;
Han, SP ;
Abboa-Offei, B ;
Cap, M ;
Xin, L ;
Tao, L ;
Tozzo, E ;
Welzel, GE ;
Egan, DM ;
Marcinkeviciene, J ;
Chang, SY ;
Biller, SA ;
Kirby, MS ;
Parker, RA ;
Hamann, LG .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (15) :5025-5037
[4]   DPP-4 inhibitors and their potential role in the management of type 2 diabetes [J].
Barnett, A. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2006, 60 (11) :1454-1470
[5]   Key considerations around the risks and consequences of hypoglycaemia in people with type 2 diabetes [J].
Barnett, A. H. ;
Cradock, S. ;
Fisher, M. ;
Hall, G. ;
Hughes, E. ;
Middleton, A. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2010, 64 (08) :1121-1129
[6]   Use of Twice-Daily Exenatide in Basal Insulin-Treated Patients With Type 2 Diabetes A Randomized, Controlled Trial [J].
Buse, John B. ;
Bergenstal, Richard M. ;
Glass, Leonard C. ;
Heilmann, Cory R. ;
Lewis, Michelle S. ;
Kwan, Anita Y. M. ;
Hoogwerf, Byron J. ;
Rosenstock, Julio .
ANNALS OF INTERNAL MEDICINE, 2011, 154 (02) :103-+
[7]   Saxagliptin added to a submaximal dose of sulphonylurea improves glycaemic control compared with uptitration of sulphonylurea in patients with type 2 diabetes: a randomised controlled trial [J].
Chacra, A. R. ;
Tan, G. H. ;
Apanovitch, A. ;
Ravichandran, S. ;
List, J. ;
Chen, R. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2009, 63 (09) :1395-1406
[8]   Pharmacological management of type 2 diabetes: the potential of incretin-based therapies [J].
Charbonnel, B. ;
Cariou, B. .
DIABETES OBESITY & METABOLISM, 2011, 13 (02) :99-117
[9]   Pathogenesis of type 2 diabetes mellitus [J].
DeFronzo, RA .
MEDICAL CLINICS OF NORTH AMERICA, 2004, 88 (04) :787-+
[10]   The Efficacy and Safety of Saxagliptin When Added to Metformin Therapy in Patients With Inadequately Controlled Type 2 Diabetes With Metformin Alone [J].
DeFronzo, Ralph A. ;
Hissa, Miguel N. ;
Garber, Alan J. ;
Gross, Jorge Luiz ;
Duan, Raina Yuyan ;
Ravichandran, Shoba ;
Chen, Roland S. .
DIABETES CARE, 2009, 32 (09) :1649-1655