Long-Term Efficacy and Safety of Linagliptin in Patients With Type 2 Diabetes and Severe Renal Impairment: A 1-year, randomized, double-blind, placebo-controlled study

This placebo-controlled study assessed long-term efficacy and safety of the dipeptidyl peptidase-4 inhibitor linagliptin in patients with type 2 diabetes and severe renal impairment (RI). In this 1-year, double-blind study, 133 patients with type 2 diabetes (HbA^sub 1c^ 7.0-10.0%) and severe RI (est...

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Bibliographic Details
Published in:Diabetes care Vol. 36; no. 2; pp. 237 - 244
Main Authors: McGill, Janet B, Sloan, Lance, Newman, Jennifer, Patel, Sanjay, Sauce, Christophe, von Eynatten, Maximilian, Woerle, Hans-Juergen
Format: Journal Article
Language:English
Published: Alexandria American Diabetes Association 01-02-2013
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Summary:This placebo-controlled study assessed long-term efficacy and safety of the dipeptidyl peptidase-4 inhibitor linagliptin in patients with type 2 diabetes and severe renal impairment (RI). In this 1-year, double-blind study, 133 patients with type 2 diabetes (HbA^sub 1c^ 7.0-10.0%) and severe RI (estimated glomerular filtration rate [eGFR] <30 mL/min/1.73 m^sup 2^) at screening were randomized to linagliptin 5 mg (n = 68) or placebo (n = 65) once daily, added to existing background therapy. The primary efficacy end point was HbA^sub 1c^ change from baseline to week 12. Efficacy and safety end points were assessed after 1 year. At week 12, adjusted mean HbA^sub 1c^ decreased by -0.76% with linagliptin and -0.15% with placebo (treatment difference, -0.60%; 95% CI -0.89 to -0.31; P < 0.0001). HbA^sub 1c^ improvements were sustained with linagliptin (-0.71%) over placebo (0.01%) at 1 year (treatment difference -0.72%, -1.03 to -0.41; P < 0.0001). Mean insulin doses decreased by - 6.2 units with linagliptin and -0.3 units with placebo. Overall adverse event incidence was similar over 1 year (94.1 vs. 92.3%). Incidence of severe hypoglycemia with linagliptin and placebo was comparably low (three patients per group). Linagliptin and placebo had little effect on renal function (median change in eGFR, -0.8 vs. -2.2 mL/min/1.73 m^sup 2^), and no drug-related renal failure occurred. In patients with type 2 diabetes and severe RI, linagliptin provided clinically meaningful improvements in glycemic control with very low risk of severe hypoglycemia, stable body weight, and no cases of drug-related renal failure. The potential for linagliptin to spare insulin and provide long-term renal safety warrants further investigations. [PUBLICATION ABSTRACT]
ISSN:0149-5992
1935-5548
DOI:10.2337/dc12-0706