What DUAL I China measured first
| Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=151 |
|---|---|---|
| -1.71(0.88) | -1.20(0.99) | -1.16(0.89) |
A Trial Comparing the Efficacy and Safety of Insulin Degludec/Liraglutide, Insulin Degludec, and Liraglutide in Chinese Subjects With Type 2 Diabetes Inadequately Controlled on Oral Antidiabetic Drugs (OADs)
Change in HbA1c (Percentage points of HbA1c), Week 0, week 26. Insulin Degludec/Liraglutide: -1.71; Insulin Degludec: -1.20; Liraglutide: -1.16.
As posted on ClinicalTrials.gov (NCT03172494), updated at source Dec 14, 2022. Read again whenever the registry updates it. Registry figures can differ from a published paper, which may use another analysis.
| Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=151 |
|---|---|---|
| -1.71(0.88) | -1.20(0.99) | -1.16(0.89) |
Percent of participants affected, Weeks 0-30. The most common events the registry lists.
| Event | Insulin Degludec/Liraglutide | Insulin Degludec | Liraglutide |
|---|---|---|---|
| Any serious event | 3.9% | 4% | 7.8% |
| Upper respiratory tract infection | 18.4% | 17.7% | 10% |
| Decreased appetite | 3.6% | 1.1% | 14.4% |
| Diarrhoea | 6.4% | 1.7% | 14.4% |
| Lipase increased | 7.5% | 2.9% | 12.2% |
| Nausea | 3.9% | 0.6% | 11.7% |
| Diabetic retinopathy | 7.8% | 3.4% | 5.6% |
| Gastrointestinal disorder | 0.3% | 0% | 5.6% |
| Hyperlipidaemia | 4.5% | 3.4% | 5.6% |
| Nasopharyngitis | 4.5% | 5.1% | 2.8% |
| Abdominal discomfort | 0.3% | 0% | 5% |
| Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=151 |
|---|---|---|
| 0.2(2.7) | 1.3(2.7) | -2.5(2.7) |
| Insulin Degludec/Liraglutiden=29 | Insulin Degludecn=14 | Liraglutiden=3 |
|---|---|---|
| 23.94 | 17.01 | 3.60 |
| Insulin Degludec/Liraglutiden=340 | Insulin Degludecn=167 |
|---|---|
| 24.8(11.9) | 30.1(14.4) |
| Measure | Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=151 |
|---|---|---|---|
| Yes | 272 | 83 | 80 |
| No | 69 | 84 | 71 |
| Measure | Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=151 |
|---|---|---|---|
| Yes | 201 | 48 | 41 |
| No | 140 | 119 | 110 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 147 | 34 | 74 |
| No | 214 | 145 | 106 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 111 | 21 | 37 |
| No | 250 | 158 | 143 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 265 | 80 | 84 |
| No | 96 | 99 | 96 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 195 | 46 | 43 |
| No | 166 | 133 | 137 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 136 | 33 | 72 |
| No | 225 | 146 | 108 |
| Measure | Insulin Degludec/Liraglutiden=361 | Insulin Degludecn=179 | Liraglutiden=180 |
|---|---|---|---|
| Yes | 103 | 21 | 36 |
| No | 258 | 158 | 144 |
| Insulin Degludec/Liraglutiden=341 | Insulin Degludecn=167 | Liraglutiden=150 |
|---|---|---|
| -3.64(2.27) | -3.45(2.34) | -1.86(2.11) |
This trial is conducted in Asia. The aim of this trial is to confirm the efficacy of insulin degludec/liraglutide in controlling glycaemia in Chinese subjects with type 2 diabetes mellitus inadequately controlled on oral antidiabetic agents
Inclusion Criteria: * Informed consent obtained before any trial-related activities. Trial-related activities are any procedures that are carried out as part of the trial, including activities to determine suitability for the trial * Type 2 diabetes mellitus (clinically diagnosed) * Male or female, age at least 18 years at the time of signing informed consent * HbA1c 7.0-10.0 % (both inclusive) by central laboratory analysis, with the aim of a median of8.3%. When approximately 50% of the randomised subjects have an HbA1c above 8.3%, the remaining subjects randomised must have an HbA1c below or equal to 8.3%; or when approximately 50% of the randomised subjects have an HbA1c below or equal to 8.3%, the remaining subjects randomised must have an HbA1c above 8.3% * Current treatment for at least 90 calendar days prior to screening with metformin plus/minus one other OAD: α-glucosidase inhibitors, sulphonylureas, glinides or thiazolidinediones. For above or equal to 60 calendar days prior to screening subjects should be on a stable dose of: * Metformin (above or equal to 1500 mg or max tolerated dose) or * Metformin (above or equal to 1500 mg or max tolerated dose) and sulphonylureas (above or equal to half of the max approved dose according to local label) or * Metformin (above or equal to 1500 mg or max tolerated dose) and glinides (above or equal to half of the max approved dose according to local label) or * Metformin (above or equal to 1500 mg or max tolerated dose) and α-glucosidase inhibitors (above or equal to half of the max approved dose according to local label) or * Metformin (above or equal to 1500 mg or max tolerated dose) and thiazolidinediones (above or equal to half of the max approved dose according to local label) Exclusion Criteria: * Treatment with insulin (except for short-term treatment at the discretion of the investigator) * Treatment with glucagon-like-peptide-1 receptor agonists or dipeptidyl-peptidase-4 inhibitors within 90 days prior to screening * Impaired liver function, defined as alanine aminotransferase above or equal to 2.5 times upper normal range * Impaired renal function defined as serum-creatinine above or equal to 133 μmol/L for males and above or equal to 125 μmol/L for females, or as defined according to local contraindications for metformin * Screening calcitonin above or equal to 50 ng/L * Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia type 2 (MEN2) * Cardiac disorder defined as: congestive heart failure (NYHA class III-IV), diagnosis of unstable angina pectoris, cerebral stroke and/or myocardial infarction within the last 12 months prior to screening and/or planned coronary, carotid or peripheral artery revascularisation procedures * Severe uncontrolled treated or untreated hypertension (systolic blood pressure above or equal to 180 mmHg or diastolic blood pressure above or equal to 100 mmHg * Proliferative retinopathy or maculopathy (macular oedema),...
Trial averages do not predict what one person will experience. Results are shown as the registry posts them, without interpretation.