Safety and efficacy of IDegLira titrated once weekly versus twice weekly in patients with type 2 diabetes uncontrolled on oral antidiabetic drugs: DUAL VI randomized clinical trial
Autor: | Serge Jabbour, Natalie Halladin, Keval Chandarana, Stewart B. Harris, Rudolf Prager, Győző Kocsis, Terry Ridge |
---|---|
Rok vydání: | 2016 |
Předmět: |
Insulin degludec
Blood Glucose Male randomized clinical trials Endocrinology Diabetes and Metabolism efficacy Once weekly Type 2 diabetes 030204 cardiovascular system & hematology Gastroenterology law.invention 0302 clinical medicine Endocrinology Randomized controlled trial law Medicine Middle Aged Metformin Insulin Long-Acting Drug Combinations Treatment Outcome Drug Therapy Combination Female Original Article type 2 diabetes Algorithms medicine.drug safety medicine.medical_specialty 030209 endocrinology & metabolism Equivalence Trials as Topic Drug Administration Schedule 03 medical and health sciences Internal medicine Internal Medicine Humans Hypoglycemic Agents In patient Adverse effect Aged Glycated Hemoglobin Pioglitazone business.industry Liraglutide Weight change Original Articles medicine.disease Surgery Diabetes Mellitus Type 2 insulin therapy Thiazolidinediones business |
Zdroj: | Diabetes, Obesity & Metabolism |
ISSN: | 1463-1326 |
Popis: | Aims To compare the safety and efficacy of a simpler titration algorithm for insulin degludec/liraglutide (IDegLira) with that used in previous DUAL trials in insulin-naive patients with type 2 diabetes. Research design and methods This 32-week, open-label, non-inferiority trial randomized adults with type 2 diabetes uncontrolled on metformin ± pioglitazone to receive IDegLira, titrated either once weekly, based on the mean of 2 pre-breakfast plasma glucose (PG) readings (n = 210), or twice weekly, based on the mean of 3 pre-breakfast PG readings (n = 210). Results Mean HbA1c decreased from 8.2% (65 mmol/mol) to 6.1% (43 mmol/mol) with once-weekly titration and from 8.1% (65 mmol/mol) to 6.0% (42 mmol/mol) with twice-weekly titration; non-inferiority was confirmed (estimated treatment difference: 0.12% [−0.04; 0.28]95% CI , 1.30 mmol/mol [−0.41; 3.01]95% CI ). Approximately 90% of patients achieved HbA1c |
Databáze: | OpenAIRE |
Externí odkaz: |