Parameter | PIONEER 2 | NMA | ||
---|---|---|---|---|
Oral semaglutide 14Â mg | Empagliflozin 25Â mg | Oral semaglutide 14Â mg | Dulaglutide 1.5Â mg | |
Physiological parameters (applied in the first year of the analysis) | ||||
HbA1c (%) |  − 1.30 (0.05)* |  − 0.79 (0.05) |  − 1.50 (0.13) |  − 1.29 (0.11) |
Systolic blood pressure (mmHg) |  − 4.85 (0.65) |  − 4.34 (0.63) |  − 3.09 (1.13) |  − 3.57 (1.08) |
Total cholesterol (mg/dL) |  − 5.08 (1.62)* | 4.74 (1.57) | 0 (0)†| 0 (0)†|
HDL cholesterol (mg/dL) | 0.73 (0.35)* | 3.11 (0.34) | 0 (0)†| 0 (0)†|
BMI (kg/m2) |  − 1.73 (0.10)* |  − 1.37 (0.09) |  − 1.50 (0.18)* |  − 0.73 (0.17) |
Adverse event rates (applied while patients received initial therapies) | ||||
Non-severe hypoglycemia event rate (events per 100 patient years) | 2.25 | 1.90 | 0.00†| 0.00†|
Severe hypoglycemia event rate (events per 100 patient years) | 0.25 | 0.24 | 0.00†| 0.00†|
Proportion of nocturnal non-severe hypoglycemic events | 0.11 | 0.13 | 0.00†| 0.00†|
Proportion of nocturnal severe hypoglycemic events | 0.00 | 0.00 | 0.00†| 0.00†|