4.7 Article

Better Glycemic Control and Weight Loss With the Novel Long-Acting Basal Insulin LY2605541 Compared With Insulin Glargine in Type 1 Diabetes A randomized, crossover study

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DIABETES CARE
卷 36, 期 3, 页码 522-528

出版社

AMER DIABETES ASSOC
DOI: 10.2337/dc12-0067

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资金

  1. Eli Lilly and Company
  2. Pfizer, Inc.
  3. sanofi-aventis
  4. Novo Nordisk
  5. Roche Pharmaceuticals
  6. Bristol-Myers Squibb Company
  7. Forest Laboratories, Inc.
  8. GlaxoSmithKline
  9. Takeda Pharmaceutical Company, Ltd.
  10. Novartis Pharmaceuticals Corporation
  11. AstraZeneca LP
  12. Amylin Pharmaceuticals, Inc.
  13. Johnson Johnson
  14. Daiichi-Sankyo
  15. MannKind Corporation
  16. Lexicon Pharmaceuticals, Inc.
  17. Boehringer Ingelheim Pharmaceuticals, Inc.
  18. Abbott Diabetes Care
  19. Bayer Health Care
  20. Becton
  21. Dickinson and Company
  22. Calibra Medical, Inc.
  23. Dexcom, Inc.
  24. Halozyme Therapeutics
  25. Helmsley Trust
  26. Hygieia, Inc.
  27. Intarcia Therapeutics, Inc.
  28. Medtronic
  29. National Institutes of Health
  30. ResMed
  31. Novartis
  32. Amylin
  33. Halozyme

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OBJECTIVE-To compare effects of LY2605541 versus insulin glargine on daily mean blood glucose as part of a basal-bolus regimen for type 1 diabetes. RESEARCH DESIGN AND METHODS-In this randomized, Phase 2, open-label, 232 crossover study, 137 patients received once-daily basal insulin (LY2605541 or glargine) plus mealtime insulin for 8 weeks, followed by crossover treatment for 8 weeks. Daily mean blood glucose was obtained from 8-point self-monitored blood glucose profiles. The noninferiority margin was 10.8 mg/dL. RESULTS-LY2605541 met noninferiority and superiority criteria compared with insulin glargine in daily mean blood glucose (144.2 vs. 151.7 mg/dL, least squares mean difference = -9.9 mg/dL [90% CI -14.6 to -5.2], P < 0.001). Fasting blood glucose variability and A1C were reduced with LY2605541 compared with insulin glargine (both P < 0.001). Mealtime insulin dose decreased with LY2605541 and increased with insulin glargine. Mean weight decreased 1.2 kg with LY2605541 and increased 0.7 kg with insulin glargine (P, 0.001). The total hypoglycemia rate was higher for LY2605541 (P = 0.04) and the nocturnal hypoglycemia rate was lower (P = 0.01), compared with insulin glargine. Adverse events (including severe hypoglycemia) were similar, although more gastrointestinal-related events occurred with LY2605541 (15% vs. 4%, P < 0.001). Mean changes (all within normal range) were higher for alanine aminotransferase, aspartate aminotransferase, triglycerides, and LDL-cholesterol and lower for HDL-cholesterol with LY2605541 compared with insulin glargine (all P < 0.02). CONCLUSIONS-In type 1 diabetes, compared with insulin glargine, LY2605541, a novel, long-acting basal insulin, demonstrated greater improvements in glycemic control, increased total hypoglycemia, and reduced nocturnal hypoglycemia, as well as reduced weight and lowered mealtime insulin doses. Diabetes Care 36:522-528, 2013

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