Summary
2008, Vol. 24, No. 2, Pages 489-496

Sitagliptin, a DPP-4 inhibitor for the treatment of patients with type 2 diabetes: a review of recent clinical trials

Avraham Karasika, Pablo Aschnerb, Harvey Katzeffc, Michael J. Daviesc and Peter P. Steinc
Address for correspondence:Peter P. Stein, MD, Merck Research Laboratories, 126 East Lincoln Avenue, Mail Code: RY34-A220, Rahway, NJ 07065-0900, USA.



ABSTRACT

Background: Dipeptidyl peptidase-4 (DPP-4) inhibitors are a new class of oral antihyperglycemic agents that enhance the body's ability to regulate blood glucose by increasing the active levels of incretins, glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic peptide (GIP). There are numerous DPP-4 inhibitors in develop­ment with sitagliptin as the first approved agent for the treatment of patients with type 2 diabetes.

Objective: The purpose of this review is to provide an overview of the clinical trial results with sitagliptin.

Methods: Clinical trials published between January 2005 (first sitagliptin publication) and November 2007 were included in this review. Medline was searched using the search terms: MK-0431 or sitagliptin.

Findings: Sitagliptin, an oral, once-daily, and highly selective DPP-4 inhibitor, has been evaluated in clinical trials as monotherapy, as add-on therapy, or as initial combination therapy with metformin. Sitagliptin provided effective fasting and postprandial glycemic control in a wide range of patients with type 2 diabetes. Markers of β-cell function (HOMA-β and proinsulin/insulin ratio) were improved with sitagliptin treatment. In these clinical trials, sitagliptin was generally well tolerated with an overall incidence of adverse experiences comparable to placebo, a low risk of hypoglycemia or gastrointestinal adverse experiences, and a neutral effect on body weight. The findings presented in this review are limited to the specific patient population enrolled in each clinical trial and for durations for up to 1 year. Future clinical studies should evaluate whether this class of agents has the potential to delay progression and/or prevent type 2 diabetes.

Conclusions: Sitagliptin has been shown to be effective and well-tolerated in various treatment regimens and may be considered for both initial therapy and as add-on therapy for patients with type 2 diabetes.

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Forward Links to Citing Articles

Bo Ahrén. (2008) Emerging dipeptidyl peptidase-4 inhibitors for the treatment of diabetes. Expert Opinion on Emerging Drugs 13:4, 593-607
Online publication date: 1-Dec-2008.
Summary | Full Text | PDF (326 KB) | PDF Plus (377 KB) 
Joan K Bardsley, Robert E Ratner. (2008) Sitagliptin: an oral agent for glucose control. Expert Review of Endocrinology & Metabolism 3:6, 691-697
Online publication date: 1-Dec-2008.
CrossRef
J. C. N. Chan, R. Scott, J. C. Arjona Ferreira, D. Sheng, E. Gonzalez, M. J. Davies, P. P. Stein, K. D. Kaufman, J. M. Amatruda, D. Williams-Herman. (2008) Safety and efficacy of sitagliptin in patients with type 2 diabetes and chronic renal insufficiency. Diabetes, Obesity and Metabolism 10:7, 545-555
Online publication date: 1-Aug-2008.
CrossRef


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Authors:
Avraham Karasik
Pablo Aschner
Harvey Katzeff
Michael J. Davies
Peter P. Stein
Keywords:
DPP-IV
Glycemic control
Incretins
MK-0431
Type 2 diabetes