4.7 Article

Efficacy and Safety of Once-Weekly Dulaglutide Versus Insulin Glargine in Patients With Type 2 Diabetes on Metformin and Glimepiride (AWARD-2)

Journal

DIABETES CARE
Volume 38, Issue 12, Pages 2241-2249

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc14-1625

Keywords

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Funding

  1. Eli Lilly and Company
  2. AstraZeneca Pharmaceuticals LP
  3. Bristol-Myers Squibb Company
  4. LifeScan Animas
  5. Sanofi
  6. Novo Nordisk, Inc.
  7. Boehringer Ingelheim Pharmaceuticals, Inc.
  8. Novartis Pharmaceuticals Corporation
  9. Lotus Pharmaceutical Co., Ltd
  10. Astellas Pharma Taiwan, Inc.
  11. AstraZeneca Taiwan Tld.

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OBJECTIVEThis study compared the efficacy and safety of once-weekly dulaglutide, a glucagon-like peptide-1 receptor agonist, with daily insulin glargine, both combined with maximally tolerated doses of metformin and glimepiride in patients with type 2 diabetes. The primary objective was noninferiority of dulaglutide 1.5 mg to glargine in the HbA(1c) change from baseline at 52 weeks.RESEARCH DESIGN AND METHODSIn this 78-week, open-label study, 810 patients were randomized to dulaglutide 1.5 mg, dulaglutide 0.75 mg, or glargine.RESULTSThe baseline mean SD HbA(1c) was 8.1 +/- 1.0% (65.5 +/- 10.8 mmol/mol). The least squares mean +/- SE HbA(1c) change from baseline to the primary end point was -1.08 +/- 0.06% (-11.8 +/- 0.7 mmol/mol) for dulaglutide 1.5 mg, -0.76 +/- 0.06% (-8.3 +/- 0.7 mmol/mol) for dulaglutide 0.75 mg, and -0.63 +/- 0.06% (-6.9 +/- 0.7 mmol/mol) for glargine, with an end point mean +/- SD dose of 29 +/- 26 units (0.33 +/- 0.24 units/kg), and a fasting plasma glucose (mean +/- SD) of 118 +/- 23 mg/dL from self-monitored plasma glucose. Statistical criteria for superiority were met with dulaglutide 1.5 mg and for noninferiority with dulaglutide 0.75 mg. More patients on dulaglutide 1.5 mg achieved HbA(1c) targets <7.0% (53 mmol/mol) versus glargine (P < 0.001). Body weight decreased with dulaglutide and increased with glargine. Total hypoglycemia rates were lower with dulaglutide; severe hypoglycemia was minimal. Increases in pancreatic enzymes were observed for dulaglutide. Incidence of nausea (15.4, 7.7, and 1.5%) and diarrhea (10.6, 9.2, and 5.7%) were more common with dulaglutide 1.5 mg and 0.75 mg than with glargine.CONCLUSIONSOnce-weekly dulaglutide 1.5 mg, compared with daily insulin glargine without forced titration, demonstrated greater HbA(1c) reduction and weight loss, with a higher incidence of gastrointestinal adverse events and a lower risk of hypoglycemia.

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