Effects of Adding Linagliptin to Basal Insulin Regimen for Inadequately Controlled Type 2 Diabetes: A ≥52-week randomized, double-blind study

• Published in: Diabetes care Vol. 36; no. 12; pp. 3875 - 3881
• Main Authors: YKI-JÄRVINEN, Hannele, ROSENSTOCK, Julio, DURAN-GARCIA, Santiago, PINNETTI, Sabine, BHATTACHARYA, Sudipta, THIEMANN, Sandra, PATEL, Sanjay, WOERLE, Hans-Juergen
• Format: Journal Article
• Language: English
• Published: Alexandria, VA American Diabetes Association 01.12.2013
• Subjects: Adult; Aged; Analysis; Biological and medical sciences; Blood Glucose - metabolism; Diabetes Mellitus, Type 2 - blood; Diabetes Mellitus, Type 2 - drug therapy; Diabetes therapy; Diabetes. Impaired glucose tolerance; Dose-Response Relationship, Drug; Double-Blind Method; Drug Therapy, Combination; Endocrine pancreas. Apud cells (diseases); Endocrinopathies; Etiopathogenesis. Screening. Investigations. Target tissue resistance; Female; Follow-Up Studies; Glycated Hemoglobin A - metabolism; Humans; Hypoglycemic Agents - administration & dosage; Insulin; Insulin - administration & dosage; Linagliptin; Male; Medical sciences; Metabolic diseases; Metformin - administration & dosage; Middle Aged; Original Research; Pharmaceutical industry; Purines - administration & dosage; Quinazolines - administration & dosage; Retrospective Studies; Thiazolidinediones - administration & dosage; Treatment Outcome; Type 2 diabetes; France; Endocrinopathy; Type 2 diabetes; Human; Pancreatic hormone; Nutrition; Controlled diabetes; Metabolic diseases; Insulin; Randomization; Treatment; Double blind study; Therapeutic protocol; Endocrinology
• ISSN: 0149-5992; 1935-5548
• DOI: 10.2337/dc12-2718

To evaluate the efficacy and long-term safety of linagliptin added to basal insulins in type 2 diabetes inadequately controlled on basal insulin with or without oral agents. A total of 1,261 patients (HbA1c ≥7.0% [53 mmol/mol] to ≤10.0% [86 mmol/mol]) on basal insulin alone or combined with metformin and/or pioglitazone were randomized (1:1) to double-blind treatment with linagliptin 5 mg once daily or placebo for ≥52 weeks. The basal insulin dose was kept unchanged for 24 weeks but could thereafter be titrated according to fasting plasma glucose levels at the investigators' discretion. The primary end point was the mean change in HbA1c from baseline to week 24. The safety analysis incorporated data up to a maximum of 110 weeks. At week 24, HbA1c changed from a baseline of 8.3% (67 mmol/mol) by -0.6% (-6.6 mmol/mol) and by 0.1% (1.1 mmol/mol) with linagliptin and placebo, respectively (treatment difference -0.65% [95% CI -0.74 to -0.55] [-7.1 mmol/mol]; P < 0.0001). Despite the option to uptitrate basal insulin, it was adjusted only slightly upward (week 52, linagliptin 2.6 IU/day, placebo 4.2 IU/day; P < 0.003), resulting in no further HbA1c improvements. Frequencies of hypoglycemia (week 24, linagliptin 22.0%, placebo 23.2%; treatment end, linagliptin 31.4%, placebo 32.9%) and adverse events (linagliptin 78.4%, placebo 81.4%) were similar between groups. Mean body weight remained unchanged (week 52, linagliptin -0.30 kg, placebo -0.04 kg). Linagliptin added to basal insulin therapy significantly improved glycemic control relative to placebo without increasing hypoglycemia or body weight.