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Summary
January 2008, Vol. 17, No. 1, Pages 105-113
, DOI 10.1517/13543784.17.1.105
Update: vildagliptin for the treatment of Type 2 diabetesAlan J Garber1Professor of Medicine, Biochemistry & Molecular Biology, and Molecular & Cellular Biology, Baylor College of Medicine, Division of Diabetes, Endocrinology & Metabolism, 1709 Dryden, Suite 1000, Houston, TX 77030, USA +1 713 798 0230; +1 713 798 2750; agarber@bcm.edu 2Assistant Professor of Medicine, Baylor College of Medicine, Division of Diabetes, Endocrinology & Metabolism, 1709 Dryden, Suite 1000, Houston, TX 77030, USA Vildagliptin is a selective inhibitor of dipeptidyl peptidase-4, and prevents the rapid degradation of the incretin hormones glucagon-like peptide-1 and glucose-dependent insulinotropic polypeptide. Vildagliptin has been evaluated in > 4800 patients in nine Phase III studies in the range of 24 – 52 weeks in duration: four placebo- or active-controlled monotherapy trials that enrolled drug-naive patients; four add-on studies in which vildagliptin was added to a stable regimen of either metformin, a sulfonylurea, a thiazolidinedione or insulin; and a study in which an initial combination of vildagliptin plus pioglitazone in drug-naive patients was evaluated. Across studies, vildagliptin was effective in reducing HbA1c, had a low risk of hypoglycemia and was weight-neutral and well tolerated. Forward Links to Citing ArticlesE. Ferrannini, V. Fonseca, B. Zinman, D. Matthews, B. Ahrén, S. Byiers, Q. Shao, S. Dejager. (2009) Fifty-two-week efficacy and safety of vildagliptin vs. glimepiride in patients with type 2 diabetes mellitus inadequately controlled on metformin monotherapy. Diabetes, Obesity and Metabolism 11:2, 157-166 Online publication date: 1-Mar-2009. CrossRef Jamie D Croxtall, Susan J Keam. (2008) Vildagliptin. Drugs 68:16, 2387-2409 Online publication date: 1-Feb-2008. CrossRef Users who read this article also read:
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