Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT00294723 LEAD-3 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin A1c (HbA1c) at Week 104 week 0, week 104 | Glimepiride | -0.28 percentage point of total HbA1c (±0.09 Standard Error) |
| Lira 1.2 | -0.59 percentage point of total HbA1c (±0.09 Standard Error) | |||
| Lira 1.8 | -0.88 percentage point of total HbA1c (±0.09 Standard Error) | |||
| NCT00294723 LEAD-3 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin A1c (HbA1c) at Week 156 week 0, week 156 | Glimepiride | -0.16 percentage point of total HbA1c (±0.08 Standard Error) |
| Lira 1.2 | -0.44 percentage point of total HbA1c (±0.09 Standard Error) | |||
| Lira 1.8 | -0.71 percentage point of total HbA1c (±0.09 Standard Error) | |||
| NCT00294723 LEAD-3 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin A1c (HbA1c) at Week 52 week 0, week 52 | Glimepiride | -0.51 percentage point of total HbA1c (±0.08 Standard Error) |
| Lira 1.2 | -0.84 percentage point of total HbA1c (±0.08 Standard Error) | |||
| Lira 1.8 | -1.14 percentage point of total HbA1c (±0.08 Standard Error) | |||
| NCT00318461 LEAD-2 | Diabetes Mellitus, Type 2 | Change in Glycosylated A1c (HbA1c) at Week 104 week 0, week 104 | Lira 0.6 + Met | -0.36 percentage of total haemoglobin (±0.08 Standard Error) |
| Lira 1.2 + Met | -0.56 percentage of total haemoglobin (±0.08 Standard Error) | |||
| Lira 1.8 + Met | -0.58 percentage of total haemoglobin (±0.08 Standard Error) | |||
| Met + Glim | -0.50 percentage of total haemoglobin (±0.08 Standard Error) | |||
| Met Mono | 0.25 percentage of total haemoglobin (±0.10 Standard Error) | |||
| NCT00318461 LEAD-2 | Diabetes Mellitus, Type 2 | Change in Glycosylated A1c (HbA1c) at Week 26 week 0, week 26 | Lira 0.6 + Met | -0.69 Percentage point of total HbA1c (±0.07 Standard Error) |
| Lira 1.2 + Met | -0.97 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| Lira 1.8 + Met | -1.00 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| Met + Glim | -0.98 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| Met Mono | 0.09 Percentage point of total HbA1c (±0.09 Standard Error) | |||
| NCT00393718 | Diabetes Mellitus, Type 2 | Glycosylated Haemoglobin A1c (HbA1c) After 24 Weeks of Treatment after 24 weeks of treatment | Glibenclamide | 7.50 percentage of total haemoglobin (±0.09 Standard Error) |
| Liraglutide | 6.99 percentage of total haemoglobin (±0.07 Standard Error) | |||
| NCT00395746 | Diabetes Mellitus, Type 2 | Glycosylated Haemoglobin A1c (HbA1c) After 24 Weeks of Treatment after 24 weeks of treatment | 0.6 mg + SU | 7.02 percentage of total haemoglobin (±0.10 Standard Error) |
| 0.9 mg + SU | 6.75 percentage of total haemoglobin (±0.11 Standard Error) | |||
| SU Mono | 8.02 percentage of total haemoglobin (±0.10 Standard Error) | |||
| NCT00518882 LEAD-6 | Diabetes Mellitus, Type 2 | Change in Glycosylated A1c (HbA1c) at Week 26 week 0, week 26 | Exenatide -> Liraglutide -> Liraglutide | -0.79 percentage point of total HbA1c (±0.08 Standard Error) |
| Liraglutide -> Liraglutide -> Liraglutide | -1.12 percentage point of total HbA1c (±0.08 Standard Error) | |||
| NCT00614120 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin A1c (HbA1c) week 0, week 16 | Glim + Met | -1.3 percentage point of total HbA1c (±0.98 Standard Deviation) |
| Lira 0.6 + Met | -1.0 percentage point of total HbA1c (±1.04 Standard Deviation) | |||
| Lira 1.2 + Met | -1.3 percentage point of total HbA1c (±1.09 Standard Deviation) | |||
| Lira 1.8 + Met | -1.4 percentage point of total HbA1c (±1.23 Standard Deviation) | |||
| NCT00620282 | Diabetes Mellitus, Type 2 | Change in Acetylcholine (ACh)-Mediated Forearm Blood Flow (FBF) week 0, week 12 | Glimepiride | 2.164 mL/100 mL/min (±2.568 Standard Error) |
| Lira 1.8 | 4.244 mL/100 mL/min (±2.551 Standard Error) | |||
| Placebo | -3.187 mL/100 mL/min (±2.758 Standard Error) | |||
| NCT00700817 | Diabetes Mellitus, Type 2 | Mean Change From Baseline in Glycosylated Haemoglobin A1c (HbA1c) at Week 26 Week 0, Week 26 | Lira 1.2 mg -> Lira 1.2 mg -> Lira 1.2 mg | -1.24 Percentage point of total HbA1c (±0.07 Standard Error) |
| Lira 1.8 mg -> Lira 1.8 mg -> Lira 1.8 mg | -1.5 Percentage point of total HbA1c (±0.06 Standard Error) | |||
| Sita -> Sita | -0.9 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| NCT00700817 | Diabetes Mellitus, Type 2 | Mean Change From Baseline in Glycosylated Haemoglobin A1c (HbA1c) at Week 52 Week 0, Week 52 | Lira 1.2 mg -> Lira 1.2 mg -> Lira 1.2 mg | -1.29 Percentage point of total HbA1c (±0.07 Standard Error) |
| Lira 1.8 mg -> Lira 1.8 mg -> Lira 1.8 mg | -1.51 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| Sita -> Sita | -0.88 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| NCT00700817 | Diabetes Mellitus, Type 2 | Mean Change From Baseline in Glycosylated Haemoglobin A1c (HbA1c) at Week 78 Week 0, Week 78 | Lira 1.2 mg -> Lira 1.2 mg -> Lira 1.2 mg | -0.94 Percentage point of total HbA1c (±0.08 Standard Error) |
| Lira 1.8 mg -> Lira 1.8 mg -> Lira 1.8 mg | -1.28 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| NCT00700817 | Diabetes Mellitus, Type 2 | Mean Change in Glycosylated Haemoglobin A1c (HbA1c) From Week 52 to Week 78 Week 52, Week 78 | Sita -> Sita -> Lira 1.2 mg | -0.24 Percentage point of total HbA1c (±0.7 Standard Deviation) |
| Sita -> Sita -> Lira 1.8 mg | -0.45 Percentage point of total HbA1c (±0.9 Standard Deviation) | |||
| NCT00781937 | Obesity | Mean Percentage Change in Fasting Body Weight From Baseline Week 0, week 56 | Lira 3.0 mg | -6.11 percentage (±0.66 Standard Error) |
| Placebo | -0.05 percentage (±0.63 Standard Error) | |||
| NCT00781937 | Obesity | Percentage of Subjects Who Lost More Than or Equal to 5% of Fasting Body Weight From Week 0 Week 0, week 56 | Lira 3.0 mg | 50.5 percentage of subjects |
| Placebo | 21.9 percentage of subjects | |||
| NCT00781937 | Obesity | Percentage of Subjects Who Maintained Their run-in Fasting Weight Loss From Week 0 Week 0, week 56 | Lira 3.0 mg | 80.8 percentage of subjects |
| Placebo | 47.9 percentage of subjects | |||
| NCT00856986 | Diabetes Mellitus, Type 2 | Mean Change From Randomisation in Glycosylated Haemoglobin A1c (HbA1c) at Week 26. Week 0 (Randomisation), week 26 | Insulin Detemir + Lira 1.8 | -0.51 Percentage point of total HbA1c (±0.07 Standard Error) |
| Lira 1.8 | 0.02 Percentage point of total HbA1c (±0.07 Standard Error) | |||
| NCT01029886 | Diabetes Mellitus, Type 2 | Change in HbA1c From Baseline to Week 26 Baseline, Week 26 | Exenatide Once Weekly | -1.28 percentage of total hemoglobin (±0.05 Standard Error) |
| Liraglutide Once Daily | -1.48 percentage of total hemoglobin (±0.05 Standard Error) | |||
| NCT01128894 | Diabetes Mellitus, Type 2 | Mean Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 32 Baseline and Week 32 | Albiglutide 50 mg | -0.78 Percentage of HbA1c in the blood (±0.047 Standard Error) |
| Liraglutide 1.8 mg | -0.99 Percentage of HbA1c in the blood (±0.046 Standard Error) | |||
| NCT01179048 LEADER® | Diabetes Mellitus, Type 2 | Time From Randomisation to First Occurrence of Cardiovascular Death, Non-fatal Myocardial Infarction, or Non-fatal Stroke (a Composite Cardiovascular Outcome) from randomisation (visit 3; month 0) to last contact (visit 16; up to month 60+30 days) | Liraglutide | 13.0 percentage of subjects |
| Placebo | 14.9 percentage of subjects | |||
| NCT01234649 | Diabetes Mellitus, Type 2 | Insulin Secretion-Sensitivity Index (IS-SI) 84 weeks of treatment | Metformin XR Plus Liraglutide | 418.4 index (±387 Standard Deviation) |
| Metformin XR Plus Placebo | 333 index (±206 Standard Deviation) | |||
| NCT01272219 | Obesity | Change From Baseline in Fasting Body Weight Week 0, Week 56 | Liraglutide 3.0 mg (56-Week) | -7.98 percent change (±6.67 Standard Deviation) |
| Liraglutide Placebo (56-Week) | -2.62 percent change (±5.74 Standard Deviation) | |||
| NCT01272219 | Obesity | Proportion of Subjects Losing at Least 5% of Baseline Fasting Body Weight. At Week 56 | Liraglutide 3.0 mg (56-Week) | 63.2 percentage of subjects |
| Liraglutide Placebo (56-Week) | 27.1 percentage of subjects | |||
| NCT01272219 | Obesity | Proportion of Subjects Losing More Than 10% of Baseline Fasting Body Weight At 56 weeks | Liraglutide 3.0 mg (56-Week) | 33.1 percentage of subjects |
| Liraglutide Placebo (56-Week) | 10.6 percentage of subjects | |||
| NCT01272219 | Obesity | Proportion of Subjects With Onset of Type 2 Diabetes At 160 weeks | Liraglutide 3.0 mg (160-Week) | 26 Subject |
| Liraglutide Placebo (160-Week) | 46 Subject | |||
| NCT01272232 | Obesity | Change (%) From Baseline in Body Weight (Fasting) Week 0, week 56 | Liraglutide 1.8 mg | -4.6 percent change (±5.5 Standard Deviation) |
| Liraglutide 1.8 mg | -3.6 percent change (±5.7 Standard Deviation) | |||
| Liraglutide 3.0 mg | -5.9 percent change (±5.5 Standard Deviation) | |||
| Liraglutide 3.0 mg | -4.7 percent change (±5.0 Standard Deviation) | |||
| Liraglutide Placebo | -2.0 percent change (±4.3 Standard Deviation) | |||
| Liraglutide Placebo | -2.7 percent change (±5.8 Standard Deviation) | |||
| NCT01272232 | Obesity | Proportion of Subjects Losing at Least 5% of Baseline Body Weight at 56 weeks | Liraglutide 1.8 mg | 35.6 percentage of subjects |
| Liraglutide 1.8 mg | 64.4 percentage of subjects | |||
| Liraglutide 3.0 mg | 50.1 percentage of subjects | |||
| Liraglutide 3.0 mg | 49.9 percentage of subjects | |||
| Liraglutide Placebo | 13.8 percentage of subjects | |||
| Liraglutide Placebo | 86.2 percentage of subjects | |||
| NCT01272232 | Obesity | Proportion of Subjects Losing More Than 10% of Baseline Body Weight at 56 weeks | Liraglutide 1.8 mg | 85.6 percentage of subjects |
| Liraglutide 1.8 mg | 14.4 percentage of subjects | |||
| Liraglutide 3.0 mg | 76.6 percentage of subjects | |||
| Liraglutide 3.0 mg | 23.4 percentage of subjects | |||
| Liraglutide Placebo | 4.3 percentage of subjects | |||
| Liraglutide Placebo | 95.7 percentage of subjects | |||
| NCT01296412 | Diabetes Mellitus, Type 2 | Change From Baseline in Hemoglobin A1c (A1C) Baseline and Week 26 | Liraglutide | -1.42 percent (±1.04 95% Confidence Interval) |
| Sitagliptin +/- Glimepiride | -1.32 percent (±1.06 95% Confidence Interval) | |||
| NCT01336023 DUAL™ I | Diabetes Mellitus, Type 2 | Mean Change From Baseline in HbA1c (Glycosylated Haemoglobin) at Week 26. Week 0, week 26 | IDeg | -1.44 Percentage of glycosylated haemoglobin (±1.03 Standard Deviation) |
| IDegLira | -1.91 Percentage of glycosylated haemoglobin (±1.07 Standard Deviation) | |||
| Liraglutide | -1.28 Percentage of glycosylated haemoglobin (±1.13 Standard Deviation) | |||
| NCT01388361 BEGIN™ | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c (%) (Glycosylated Haemoglobin) week 0, week 26 | IDeg | 0.10 percentage of glycosylated haemoglobin (±0.40 Standard Deviation) |
| IDeg + IAsp OD | -0.39 percentage of glycosylated haemoglobin (±0.72 Standard Deviation) | |||
| IDeg + Liraglutide | -0.74 percentage of glycosylated haemoglobin (±0.73 Standard Deviation) | |||
| NCT01392573 DUAL™ II | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c (Glycosylated Haemoglobin) Week 0, week 26 | IDeg | -0.89 percentage of glycosylated haemoglobin (±1.18 Standard Deviation) |
| IDegLira | -1.90 percentage of glycosylated haemoglobin (±1.09 Standard Deviation) | |||
| NCT01512108 | Diabetes Mellitus, Type 2 | Incidence of Treatment Emergent Adverse Events (AEs) Week 0 to Week 52 + 7 days | Additional OAD | 2 Events/100 years of patient exposure |
| Additional OAD | 9 Events/100 years of patient exposure | |||
| Additional OAD | 9 Events/100 years of patient exposure | |||
| Additional OAD | 321 Events/100 years of patient exposure | |||
| Additional OAD | 331 Events/100 years of patient exposure | |||
| Liraglutide 0.9 mg/Day | 345 Events/100 years of patient exposure | |||
| Liraglutide 0.9 mg/Day | 14 Events/100 years of patient exposure | |||
| Liraglutide 0.9 mg/Day | 361 Events/100 years of patient exposure | |||
| Liraglutide 0.9 mg/Day | 5 Events/100 years of patient exposure | |||
| Liraglutide 0.9 mg/Day | 2 Events/100 years of patient exposure | |||
| NCT01541215 Ellipse™ | Diabetes Mellitus, Type 2 | Change in HbA1c (Glycosylated Haemoglobin) Week 0, week 26 | Liraglutide 1.8 mg | -0.643 Percentage of HbA1c (±0.215 Standard Error) |
| Placebo | 0.415 Percentage of HbA1c (±0.216 Standard Error) | |||
| NCT01557166 | Obesity | Change From Baseline in Apnoea-hypopnoea Index (AHI) Week 0, Week 32 | Liraglutide 3.0 mg | -12.22 events/hour (±23.34 Standard Deviation) |
| Placebo | -6.08 events/hour (±25.90 Standard Deviation) | |||
| NCT01558271 | Diabetes Mellitus, Type 2 | Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks Baseline, 26 weeks | Liraglutide | -1.33 percentage of HbA1c (±0.07 Standard Error) |
| LY2189265 | -1.43 percentage of HbA1c (±0.05 Standard Error) | |||
| Placebo | 0.14 percentage of HbA1c (±0.10 Standard Error) | |||
| NCT01572740 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 16 Week 0, Week 16 | Lira + Insulin | -1.73 percentage of glycosylated haemoglobin (±0.06 Standard Error) |
| Placebo + Insulin | -0.43 percentage of glycosylated haemoglobin (±0.06 Standard Error) | |||
| NCT01617434 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) From Baseline to Week 26 Week 0 to Week 26 | Liraglutide | -1.30 percentage of glycosylated haemoglobin (±1.015 Standard Deviation) |
| Placebo | -0.11 percentage of glycosylated haemoglobin (±1.088 Standard Deviation) | |||
| NCT01618162 DUAL™IV | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) Week 0, Week 26 | IDegLira | -1.45 percentage of glycosylated haemoglobin (±0.84 Standard Deviation) |
| Placebo | -0.46 percentage of glycosylated haemoglobin (±0.83 Standard Deviation) | |||
| NCT01620489 | Diabetes Mellitus, Type 2 | Estimated Mean From the Statistical Model and Standard Deviation From Observed Data For Change From Baseline to Week 26 in HbA1c (%) (Glycosylated Haemoglobin) Week 0, Week 26 | Lira 1.8 mg | -1.05 percentage (%) (±0.8944 Standard Deviation) |
| Placebo | -0.38 percentage (%) (±0.8797 Standard Deviation) | |||
| NCT01624259 AWARD-6 | Diabetes Mellitus, Type 2 | Change From Baseline to 26 Weeks Endpoint in Glycosylated Hemoglobin (HbA1c) Baseline, 26 Weeks | 1.5 mg LY2189265 | -1.42 percentage of glycosylated hemoglobin (±0.05 Standard Error) |
| 1.8 mg Liraglutide | -1.36 percentage of glycosylated hemoglobin (±0.05 Standard Error) | |||
| NCT01664247 | Diabetes Mellitus, Type 2 | Change From Baseline in Glycosylated Haemoglobin (HbA1c) (%) Week 0, week 26 | IDeg | -0.99 percentage of glycosylated haemoglobin (±0.08 Standard Error) |
| Placebo | -0.07 percentage of glycosylated haemoglobin (±0.08 Standard Error) | |||
| NCT01676116 DUAL™ III | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) From Baseline (Randomisation, Visit 2) Week 0, week 26 | Insulin Degludec/Liraglutide + Oral Anti Diabetic Drugs (OADs) | -1.32 percentage of glycosylated haemoglobin (±0.05 Standard Error) |
| Liraglutide or Exenatide + OADs | -0.37 percentage of glycosylated haemoglobin (±0.07 Standard Error) | |||
| NCT01722240 1966 | Diabetes Mellitus, Type 1 | HbA1c (%) 52 Weeks | Liraglutide | 7.45 Percent of Hemoglobin (%) (±0.12 Standard Error) |
| Liraglutide | 7.92 Percent of Hemoglobin (%) (±0.15 Standard Error) | |||
| Placebo | 7.48 Percent of Hemoglobin (%) (±0.18 Standard Error) | |||
| Placebo | 7.58 Percent of Hemoglobin (%) (±0.14 Standard Error) | |||
| NCT01722266 | Diabetes Mellitus, Type 1 | Change in Mean Weekly Glucose Concentrations 12 Weeks | Liraglutide 0.6 mg | -0.3 mg/dl (±2 Standard Error) |
| Liraglutide 1.2mg | -10 mg/dl (±2 Standard Error) | |||
| Liraglutide 1.8mg | -10 mg/dl (±1 Standard Error) | |||
| Placebo | 1 mg/dl (±0 Standard Error) | |||
| NCT01733758 | Diabetes Mellitus, Type 2 | Mean HbA1c at Baseline, Week 24, and Change From Baseline at Week 24 Baseline and Week 24 | Albiglutide 30 mg Weekly | 8.06 Percentage of HbA1c in the blood (±0.783 Standard Deviation) |
| Albiglutide 30 mg Weekly | 6.98 Percentage of HbA1c in the blood (±0.735 Standard Deviation) | |||
| Albiglutide 30 mg Weekly | -1.08 Percentage of HbA1c in the blood (±0.619 Standard Deviation) | |||
| Albiglutide 50 mg Weekly | -1.32 Percentage of HbA1c in the blood (±0.702 Standard Deviation) | |||
| Albiglutide 50 mg Weekly | 8.15 Percentage of HbA1c in the blood (±0.825 Standard Deviation) | |||
| Albiglutide 50 mg Weekly | 6.83 Percentage of HbA1c in the blood (±0.659 Standard Deviation) | |||
| Open-Label Liraglutide 0.9 mg Daily | 6.87 Percentage of HbA1c in the blood (±0.642 Standard Deviation) | |||
| Open-Label Liraglutide 0.9 mg Daily | -1.19 Percentage of HbA1c in the blood (±0.636 Standard Deviation) | |||
| Open-Label Liraglutide 0.9 mg Daily | 8.07 Percentage of HbA1c in the blood (±0.787 Standard Deviation) | |||
| Placebo | 8.16 Percentage of HbA1c in the blood (±0.877 Standard Deviation) | |||
| Placebo | 8.39 Percentage of HbA1c in the blood (±1.066 Standard Deviation) | |||
| Placebo | 0.24 Percentage of HbA1c in the blood (±0.715 Standard Deviation) | |||
| NCT01733758 | Diabetes Mellitus, Type 2 | Model-adjusted Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 24 Baseline and Week 24 | Albiglutide 30 mg Weekly | -1.10 Percentage of HbA1c in the blood (±0.047 Standard Error) |
| Albiglutide 50 mg Weekly | -1.30 Percentage of HbA1c in the blood (±0.049 Standard Error) | |||
| Placebo | 0.25 Percentage of HbA1c in the blood (±0.068 Standard Error) | |||
| NCT01753362 | Diabetes Mellitus, Type 1 | HbA1c 26 weeks | Liraglutide | 7.94 percent (±1.05 Standard Deviation) |
| Liraglutide | 7.60 percent (±0.98 Standard Deviation) | |||
| Placebo | 7.64 percent (±0.84 Standard Deviation) | |||
| Placebo | 7.77 percent (±0.83 Standard Deviation) | |||
| NCT01779362 RISE Adult | Diabetes Mellitus, Type 2 | Insulin Sensitivity, M/I 3-months after a medication washout | Glargine Followed by Metformin | 3.38 x 10-5 mmol/kg/min per pmol/L |
| Liraglutide + Metformin | 3.49 x 10-5 mmol/kg/min per pmol/L | |||
| Metformin Alone | 3.53 x 10-5 mmol/kg/min per pmol/L | |||
| Placebo | 3.63 x 10-5 mmol/kg/min per pmol/L | |||
| NCT01779362 RISE Adult | Diabetes Mellitus, Type 2 | ß-cell Response Measured by Hyperglycemic Clamp 3-months after medication washout (Month 15) | Glargine Followed by Metformin | 3.58 nmol/L |
| Glargine Followed by Metformin | 4.32 nmol/L | |||
| Liraglutide + Metformin | 4.58 nmol/L | |||
| Liraglutide + Metformin | 3.73 nmol/L | |||
| Metformin Alone | 3.65 nmol/L | |||
| Metformin Alone | 4.61 nmol/L | |||
| Placebo | 4.45 nmol/L | |||
| Placebo | 3.60 nmol/L | |||
| NCT01784965 | Glucose Intolerance | Change in Weight Reported at 14 Weeks Baseline and 14 weeks | Liraglutide | -6.8 kg |
| Placebo | -3.3 kg | |||
| NCT01794143 GRADE | Diabetes Mellitus, Type 2 | HbA1c>=7%, While Receiving Metformin and the Randomly Assigned Glucose-lowering Study Medication Quarterly, 4-7 years | Glargine Insulin U-100 | 852 Participants |
| Glimepiride | 908 Participants | |||
| Liraglutide | 860 Participants | |||
| Sitagliptin | 981 Participants | |||
| NCT01794143 GRADE | Diabetes Mellitus, Type 2 | Time to HbA1c>=7%, While Receiving Metformin and the Randomly Assigned Glucose-lowering Study Medication Quarterly for 4 to 7 years | Glargine Insulin U-100 | 1.3 years |
| Glimepiride | 1.3 years | |||
| Liraglutide | 1.5 years | |||
| Sitagliptin | 0.8 years | |||
| NCT01836523 ADJUNCT ONE™ | Diabetes Mellitus | Change From Baseline in Body Weight Week 0, week 52 | Liraglutide 0.6 mg | -1.34 kg (±4.183 Standard Deviation) |
| Liraglutide 1.2 mg | -2.73 kg (±4.524 Standard Deviation) | |||
| Liraglutide 1.8 mg | -4.02 kg (±4.873 Standard Deviation) | |||
| Placebo | 0.94 kg (±3.828 Standard Deviation) | |||
| NCT01836523 ADJUNCT ONE™ | Diabetes Mellitus | Change From Baseline in HbA1c (Glycosylated Haemoglobin) Week 0, week 52 | Liraglutide 0.6 mg | -0.45 percentage of glycosylated haemoglobin (±0.741 Standard Deviation) |
| Liraglutide 1.2 mg | -0.50 percentage of glycosylated haemoglobin (±0.767 Standard Deviation) | |||
| Liraglutide 1.8 mg | -0.54 percentage of glycosylated haemoglobin (±0.729 Standard Deviation) | |||
| Placebo | -0.34 percentage of glycosylated haemoglobin (±0.707 Standard Deviation) | |||
| NCT01836523 ADJUNCT ONE™ | Diabetes Mellitus | Change From Baseline in Total Daily Insulin Dose Week 0, week 52 | Liraglutide 0.6 mg | 1.04 ratio (±23.75 Geometric Coefficient of Variation) |
| Liraglutide 1.2 mg | 0.98 ratio (±26.66 Geometric Coefficient of Variation) | |||
| Liraglutide 1.8 mg | 0.95 ratio (±24.21 Geometric Coefficient of Variation) | |||
| Placebo | 1.04 ratio (±26.69 Geometric Coefficient of Variation) | |||
| NCT01847313 | Diabetes Mellitus | MCP-1:Creatinine Ratio in Urine Up to 26 weeks | Control | 24.3 ng/mmol (±15.4 Standard Deviation) |
| Liraglutide | 27.9 ng/mmol (±14.3 Standard Deviation) | |||
| NCT01937598 | Diabetes Mellitus, Type 2 | Incremental Area Under the Plasma Glucose (BG) Concentration-time Profile (AUC) 0 to 300 min post mixed meal test | Placebo | 5557 [mg*min/dL] (±547 Standard Error) |
| Sitagliptin | 5678 [mg*min/dL] (±329 Standard Error) | |||
| NCT01952145 DUAL™ V | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c (Glycosylated Haemoglobin) Week 0, week 26 | Insulin Degludec/Liraglutide (IDegLira) | -1.81 Percentage (%) (±1.08 Standard Deviation) |
| Insulin Glargine (IGlar) | -1.13 Percentage (%) (±0.98 Standard Deviation) | |||
| NCT02098395 ADJUNCT TWO™ | Diabetes Mellitus | Change From Baseline in Glycosylated Haemoglobin (HbA1c) Week 0, Week 26 | Liraglutide 0.6 mg | -0.23 Percent (%) glycosylated haemoglobin (±0.744 Standard Deviation) |
| Liraglutide 1.2 mg | -0.23 Percent (%) glycosylated haemoglobin (±0.731 Standard Deviation) | |||
| Liraglutide 1.8 mg | -0.32 Percent (%) glycosylated haemoglobin (±0.73 Standard Deviation) | |||
| Liraglutide Placebo | 0.01 Percent (%) glycosylated haemoglobin (±0.674 Standard Deviation) | |||
| NCT02100475 DUAL™ | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c (Glycosylated Haemoglobin) Week 0, week 26 | IDegLira | -0.43 Percentage of glycosylated haemoglobin (±0.94 Standard Deviation) |
| IDegLira + IAsp | -0.14 Percentage of glycosylated haemoglobin (±1.09 Standard Deviation) | |||
| NCT02298192 DUAL™ VI | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c Week 0, week 32 | IDegLira | -2.02 percentage (±0.98 Standard Deviation) |
| IDegLira (1WT) | -2.01 percentage (±1.09 Standard Deviation) | |||
| NCT02420262 | Diabetes Mellitus, Type 2 | Change in HbA1c (Glycosylated Haemoglobin) Week 0, Week 26 | IDegLira | -1.48 Percentage of glycosylated haemoglobin (±0.05 Standard Error) |
| IGlar + IAsp | -1.46 Percentage of glycosylated haemoglobin (±0.05 Standard Error) | |||
| NCT02501161 DUAL™ VIII | Diabetes Mellitus, Type 2 | Time From Randomisation to Inadequate Glycaemic Control and Need for Treatment Intensification Weeks 0-104 + 7 days follow-up-1 + 30 days follow-up-2 | Insulin Degludec/Liraglutide | NA Weeks |
| Insulin Degludec/Liraglutide | 104.0 Weeks | |||
| Insulin Degludec/Liraglutide | NA Weeks | |||
| Insulin Degludec/Liraglutide | 106.7 Weeks | |||
| Insulin Glargine | 104.3 Weeks | |||
| Insulin Glargine | 26.6 Weeks | |||
| Insulin Glargine | 64.6 Weeks | |||
| Insulin Glargine | 90.3 Weeks | |||
| NCT02505334 | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) (Week 26) Week 0, Week 26 | Liraglutide 0.9 mg | 0.17 Percentage (%) of HbA1c (±0.06 Standard Error) |
| Liraglutide 1.8 mg | -0.23 Percentage (%) of HbA1c (±0.06 Standard Error) | |||
| NCT02516657 | Diabetes Mellitus, Type 1 | Mean Weekly Blood Glucose Visit 1 (Before Liraglutide) at baseline (Day 0) vs. Visit 2 (After Liraglutide) on Day 7; | Liraglutide 0.6 mg | 178 mg/dL (±42 Standard Deviation) |
| Liraglutide 0.6 mg | 187 mg/dL (±35 Standard Deviation) | |||
| NCT02518945 | Diabetes Mellitus, Type 1 | Absolute Change After 12 Weeks From Baseline in Mean HbA1c With Addition of Dapagliflozin Compared to Placebo. 12 weeks | Active Drugs | -0.66 % HbA1c (±0.1 Standard Error) |
| Placebo | 0 % HbA1c (±0.2 Standard Error) | |||
| NCT02527200 | Obesity | Change in Body Mass Index (BMI) Standard Deviation Score (SDS) From Baseline to 16 Weeks Week 0, Week 16 | Part A: Liraglutide | -0.18 SDS score (±0.21 Standard Deviation) |
| Part A: Placebo | -0.18 SDS score (±0.23 Standard Deviation) | |||
| Part A+B: Liraglutide | -0.33 SDS score (±0.49 Standard Deviation) | |||
| Part A+B: Placebo | -0.29 SDS score (±0.32 Standard Deviation) | |||
| Part B: Liraglutide | -0.50 SDS score (±0.65 Standard Deviation) | |||
| Part B: Placebo | -0.48 SDS score (±0.39 Standard Deviation) | |||
| NCT02527200 | Obesity | Change in Body Mass Index (BMI) Standard Deviation Score (SDS) From Baseline to 52 Weeks Week 0, Week 52 | Part A: Liraglutide | -0.27 SDS score (±0.37 Standard Deviation) |
| Part A: Placebo | -0.13 SDS score (±0.25 Standard Deviation) | |||
| Part A+B: Liraglutide | -0.50 SDS score (±0.88 Standard Deviation) | |||
| Part A+B: Placebo | -0.36 SDS score (±0.53 Standard Deviation) | |||
| Part B: Liraglutide | -0.79 SDS score (±1.21 Standard Deviation) | |||
| Part B: Placebo | -0.71 SDS score (±0.68 Standard Deviation) | |||
| NCT02607306 DUAL™ I Japan | Diabetes Mellitus, Type 2 | Change From Baseline in HbA1c (Glycosylated Haemoglobin) Tested for Non-inferiority of IDegLira vs IDeg and Superiority of IDegLira vs Lira Week 0, Week 52 | Insulin Degludec | -1.80 Percentage of HbA1c (±1.02 Standard Deviation) |
| Insulin Degludec/Liraglutide | -2.42 Percentage of HbA1c (±1.04 Standard Deviation) | |||
| Liraglutide | -1.80 Percentage of HbA1c (±0.92 Standard Deviation) | |||
| NCT02773368 DUALTM IX | Diabetes Mellitus, Type 2 | Change in HbA1c (Glycosylated Haemoglobin) Week 0, Week 26 | IDegLira | 8.20 Percentage of glycosylated haemoglobin (±0.93 Standard Deviation) |
| IDegLira | -1.94 Percentage of glycosylated haemoglobin (±0.95 Standard Deviation) | |||
| IGlar | 8.36 Percentage of glycosylated haemoglobin (±1.08 Standard Deviation) | |||
| IGlar | -1.68 Percentage of glycosylated haemoglobin (±1.05 Standard Deviation) | |||
| NCT02787551 LixiLan-G | Diabetes Mellitus, Type 2 | Change From Baseline in Glycated Hemoglobin (HbA1c) to Week 26: Core Period Baseline, Week 26 | GLP-1 Receptor Agonist | -0.38 percentage of HbA1c (±0.048 Standard Error) |
| Insulin Glargine/Lixisenatide Fixed Ratio Combination (FRC) | -1.02 percentage of HbA1c (±0.048 Standard Error) | |||
| NCT02787551 LixiLan-G | Diabetes Mellitus, Type 2 | Change From Baseline in Glycated Hemoglobin (HbA1c) to Week 52: Single Arm Extension Period Baseline, Week 52 | Insulin Glargine/Lixisenatide Fixed Ratio Combination (FRC) | -1.01 percentage of HbA1c (±0.063 Standard Error) |
| NCT02863419 PIONEER 4 | Diabetes Mellitus, Type 2 | Change in HbA1c (Week 26) Week 0, week 26 | Liraglutide 1.8 mg | -1.2 Percentage of HbA1c (±0.9 Standard Deviation) |
| Liraglutide 1.8 mg | -1.1 Percentage of HbA1c (±0.9 Standard Deviation) | |||
| Oral Semaglutide 14 mg | -1.2 Percentage of HbA1c (±0.9 Standard Deviation) | |||
| Oral Semaglutide 14 mg | -1.4 Percentage of HbA1c (±0.9 Standard Deviation) | |||
| Placebo | -0.1 Percentage of HbA1c (±0.7 Standard Deviation) | |||
| Placebo | -0.1 Percentage of HbA1c (±0.7 Standard Deviation) | |||
| NCT02889510 | Diabetes Mellitus, Type 2 | Changes From Baseline on Measurements of Respiratory Function Defined by Forced Expiratory Volume in 1 Second (FEV1) 7 weeks | Liraglutide | 4.1 % (FEV1) |
| Placebo | 4.3 % (FEV1) | |||
| NCT02911948 DUAL™ II Japan | Diabetes Mellitus, Type 2 | Change in Glycosylated Haemoglobin (HbA1c) week 0, week 26 | Insulin Degludec | -0.65 Percentage of HbA1c (±0.98 Standard Deviation) |
| Insulin Degludec/Liraglutide | -1.95 Percentage of HbA1c (±1.01 Standard Deviation) | |||
| NCT02918279 | Obesity | Change in BMI SDS (Week 0, Week 56) Week 0, week 56 | Liraglutide 3.0 mg | -0.25 SDS score (±0.51 Standard Deviation) |
| Placebo | -0.02 SDS score (±0.54 Standard Deviation) | |||
| NCT02963922 SCALE™ Insulin | Obesity | Change in Body Weight (%) Week 0, week 56 | Liraglutide 3.0 mg | -6.0 Percentage change (±6.0 Standard Deviation) |
| Liraglutide 3.0 mg | -6.5 Percentage change (±5.8 Standard Deviation) | |||
| Placebo | -1.7 Percentage change (±5.2 Standard Deviation) | |||
| Placebo | -1.5 Percentage change (±5.4 Standard Deviation) | |||
| NCT02963922 SCALE™ Insulin | Obesity | Participants Losing at Least 5% of Baseline Body Weight Week 56 | Liraglutide 3.0 mg | 56.92 Percentage of participants |
| Liraglutide 3.0 mg | 51.80 Percentage of participants | |||
| Placebo | 21.83 Percentage of participants | |||
| Placebo | 23.98 Percentage of participants | |||
| NCT02963935 SCALE™ IBT | Obesity | Change in Body Weight (%) Week 0, week 56 | Liraglutide 3.0 mg | -7.4 percent change (±7.9 Standard Deviation) |
| Liraglutide 3.0 mg | -9.1 percent change (±7.4 Standard Deviation) | |||
| Placebo | -4.8 percent change (±7.6 Standard Deviation) | |||
| Placebo | -4.0 percent change (±7.4 Standard Deviation) | |||
| NCT02963935 SCALE™ IBT | Obesity | Proportion of Subjects Losing at Least 5% of Baseline Body Weight at Week 56 Week 56 | Liraglutide 3.0 mg | 61.47 percentage of participants |
| Liraglutide 3.0 mg | 64.08 percentage of participants | |||
| Placebo | 38.57 percentage of participants | |||
| Placebo | 38.82 percentage of participants | |||
| NCT02964247 | Diabetes Mellitus, Type 2 | Change in HbA1c Week 0, Week 26 | Liraglutide | -1.00 Percentage of HbA1c (±0.86 Standard Deviation) |
| Liraglutide | -1.05 Percentage of HbA1c (±0.85 Standard Deviation) | |||
| Placebo | -0.35 Percentage of HbA1c (±0.80 Standard Deviation) | |||
| Placebo | -0.32 Percentage of HbA1c (±0.83 Standard Deviation) | |||
| NCT03018028 PIONEER 9 | Diabetes Mellitus, Type 2 | Change in HbA1c (Week 26) Week 0, week 26 | Liraglutide 0.9 mg | -1.4 Percentage point of HbA1c (±1.1 Standard Deviation) |
| Liraglutide 0.9 mg | -1.4 Percentage point of HbA1c (±1.1 Standard Deviation) | |||
| Oral Semaglutide 14 mg | -1.7 Percentage point of HbA1c (±0.9 Standard Deviation) | |||
| Oral Semaglutide 14 mg | -1.7 Percentage point of HbA1c (±0.8 Standard Deviation) | |||
| Oral Semaglutide 3 mg | -1.1 Percentage point of HbA1c (±0.8 Standard Deviation) | |||
| Oral Semaglutide 3 mg | -1.1 Percentage point of HbA1c (±0.8 Standard Deviation) | |||
| Oral Semaglutide 7 mg | -1.7 Percentage point of HbA1c (±0.8 Standard Deviation) | |||
| Oral Semaglutide 7 mg | -1.6 Percentage point of HbA1c (±0.8 Standard Deviation) | |||
| Placebo | -0.2 Percentage point of HbA1c (±0.7 Standard Deviation) | |||
| Placebo | -0.4 Percentage point of HbA1c (±1.0 Standard Deviation) | |||
| NCT03172494 DUAL™ I China | Diabetes Mellitus, Type 2 | Change in HbA1c Week 0, week 26 | Insulin Degludec | -1.20 Percentage points of HbA1c (±0.99 Standard Deviation) |
| Insulin Degludec/Liraglutide | -1.71 Percentage points of HbA1c (±0.88 Standard Deviation) | |||
| Liraglutide | -1.16 Percentage points of HbA1c (±0.89 Standard Deviation) | |||
| NCT03175120 DUAL™ II China | Diabetes Mellitus, Type 2 | Change in HbA1c Week 0, week 26 | Insulin Degludec | -1.06 Percentage point of HbA1c (±1.19 Standard Deviation) |
| Insulin Degludec/Liraglutide | -1.93 Percentage point of HbA1c (±1.14 Standard Deviation) | |||
| NCT03191396 SUSTAIN 10 | Diabetes Mellitus, Type 2 | Change in HbA1c Week 0, week 30 | Liraglutide 1.2 mg | -1.1 Percentage of glycosylated haemoglobin (±1.0 Standard Deviation) |
| Semaglutide 1.0 mg | -1.7 Percentage of glycosylated haemoglobin (±0.9 Standard Deviation) | |||
| NCT03279731 BELIEVE | Binge-Eating Disorder | Binge Episodes baseline and 17 weeks (or last observation carried forward) | Liraglutide | -3.97 objective binge episodes per week (±0.56 Standard Deviation) |
| Placebo | -2.50 objective binge episodes per week (±.053 Standard Deviation) | |||
| NCT03374956 | Obesity | Change in Total Body Weight baseline to 12 weeks | Control Group | -6.5 percent change |
| Intervention Group | -7.7 percent change | |||
| NCT03480022 SAXAPCOS | Weight Loss | Absolute Body Weight (BW) 32 weeks of treatment | Liraglutide Pen Injector (Saxenda) | 104.7 kilogram (±2.9 Standard Error) |
| Placebo Liraglutide Pen Injector | 117.9 kilogram (±5 Standard Error) | |||
| NCT03480022 SAXAPCOS | Weight Loss | Free Androgen Index (FAI) 32 weeks of treatment | Liraglutide Pen Injector (Saxenda) | 5.98 index score (±0.6 Standard Error) |
| Placebo Liraglutide Pen Injector | 6.4 index score (±.75 Standard Error) | |||
| NCT04074161 STEP 8 | Obesity | Change From Baseline (Week 0) to Week 68 in Body Weight (%) (Semaglutide 2.4 mg Versus Liraglutide 3.0 mg) Baseline (week 0), week 68 | Liraglutide 3.0 mg | -6.4 Percentage of body weight (±7.7 Standard Deviation) |
| Semaglutide 2.4 mg | -16.4 Percentage of body weight (±10.5 Standard Deviation) |