Safety and Efficacy of Exenatide Once Weekly Plus Dapagliflozin Once Daily Versus Exenatide or Dapagliflozin Alone in Patients With Type 2 Diabetes Inadequately Controlled With Metformin Monotherapy: 52-Week Results of the DURATION-8 Randomized Controlled Trial.
Diabetes Care · 2018
Last updated 2026-05-28In a 52-week study of 695 adults with type 2 diabetes not well-controlled by metformin alone, combining exenatide (a weekly injection) and dapagliflozin (a daily pill) led to greater improvements in blood sugar control (average hemoglobin A1c dropped by 1.75%), weight loss (3.31 kg), and lower blood pressure (4.5 mmHg) compared to either drug alone. The combination was generally safe, though more people on exenatide alone reported stomach or injection-related side effects, and no cases of severe low blood sugar were reported.
AI summary of the abstract below.
| Journal | Diabetes Care, 2018 |
|---|---|
| Citations | 81 |
| Relative citation ratio | 3.34 |
| NIH percentile | 86 |
| Molecules | exenatide |
| Conditions studied | Type 2 Diabetes |
Abstract
OBJECTIVE: Among patients with type 2 diabetes uncontrolled with metformin, exenatide once weekly (QW) plus dapagliflozin combination produced greater reductions in glycemia, weight, and systolic blood pressure (SBP) at 28 weeks than exenatide QW or dapagliflozin alone (DURATION-8). Here, we investigated the safety and maintenance of efficacy at 52 weeks, after a 24-week extension.
RESEARCH DESIGN AND METHODS: This phase 3, multicenter, double-blind study randomized adults with type 2 diabetes (with glycated hemoglobin [HbA] 8.0-12.0% [64-108 mmol/mol] and on metformin ≥1,500 mg/day) to exenatide QW (2-mg subcutaneous injection) plus once-daily dapagliflozin (10-mg oral tablet), exenatide QW plus oral placebo, or dapagliflozin plus injected placebo. Extension-period values were nominal.
RESULTS: Of 1,375 patients screened, 695 were randomized (mean baseline HbA 9.3% [78 mmol/mol]); 81.2% completed the study, and 75.3% completed treatment. At 52 weeks, HbA reductions were greater with exenatide QW plus dapagliflozin (least squares mean change -1.75% [-19.1 mmol/mol]) versus exenatide QW (-1.38% [-15.1 mmol/mol]; 0.006) or dapagliflozin (-1.23% [-13.4 mmol/mol]; 0.001); mean HbA values were 6.9% (52 mmol/mol), 7.2% (55 mmol/mol), and 7.4% (57 mmol/mol), respectively. Weight and SBP reductions were greater with exenatide QW plus dapagliflozin (-3.31 kg and -4.5 mmHg) versus exenatide QW (-1.51 kg and -0.7 mmHg; both 0.001) but similar to those with dapagliflozin (-2.28 kg and -2.7 mmHg; 0.057 and = 0.100, respectively). The exenatide QW plus dapagliflozin regimen was well tolerated with no unexpected safety findings; more patients treated with exenatide QW experienced gastrointestinal and injection site-related adverse events. No major hypoglycemia occurred.
CONCLUSIONS: Among patients with type 2 diabetes uncontrolled with metformin, exenatide QW plus dapagliflozin provided sustained improvements in glycemia, weight, and SBP over 52 weeks, with no unexpected safety findings.
Verbatim abstract via PubMed 30082326 ↗
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