Dulaglutide in the treatment of adult type 2 diabetes: a perspective for primary care providers.
Postgrad Med · 2016
Last updated 2026-05-28In seven Phase 3 trials, dulaglutide taken once weekly at a 1.5 mg dose improved blood sugar control more than placebo, metformin, sitagliptin, exenatide twice daily, and insulin glargine in two trials. It also matched liraglutide in lowering HbA1c while avoiding hypoglycemia and weight gain better than metformin, sitagliptin, exenatide, or insulin glargine. Blood sugar benefits started quickly and lasted up to 104 weeks, and patients reported better experiences with dulaglutide.
AI summary of the abstract below.
| Journal | Postgrad Med, 2016 |
|---|---|
| Citations | 19 |
| Relative citation ratio | 0.70 |
| NIH percentile | 39 |
| Molecules | dulaglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
Approximately 90% of T2D patients in the US are diagnosed and treated in the primary care setting, and the majority of the burden of disease management falls to primary care providers. Here, we discuss the clinical data for once weekly dulaglutide, e.g. the results of seven completed Phase 3 trials, patient preference studies, patient reported outcomes (PRO), and clinical data surrounding the dulaglutide administration device. Dulaglutide 1.5 mg once weekly demonstrated superiority to placebo, metformin, sitagliptin, exenatide BID, and insulin glargine (in 2 trials), and non-inferiority to liraglutide in reduction of HbA1c from baseline, with an acceptable safety profile. Dulaglutide-treated patients achieved the composite endpoint of an HbA1c <7.0% with no hypoglycemia, no severe hypoglycemia, and no weight gain significantly more than metformin, sitagliptin, exenatide BID or insulin glargine treated patients. Dulaglutide consistently showed an early onset of glycemic control, lasting up to 104 weeks. Additionally, PRO and patient preference data support the benefit of once weekly dulaglutide for the treatment of T2D.
Verbatim abstract via PubMed 27488824 ↗
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