Phase 3 · Liraglutide

DUAL I China trial results

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.

Participants
720
Status
completed
Completed
2019-07-13
Sponsor
Novo Nordisk A/S

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.

Primary outcome

What DUAL I China measured first

Change in HbA1cPercentage points of HbA1c · Week 0, week 26 · mean
Insulin Degludec/Liraglutiden=341Insulin Degludecn=167Liraglutiden=151
-1.71(0.88)-1.20(0.99)-1.16(0.89)
Side effects by arm

Side effects in DUAL I China

Percent of participants affected, Weeks 0-30. The most common events the registry lists.

EventInsulin Degludec/LiraglutideInsulin DegludecLiraglutide
Any serious event3.9%4%7.8%
Upper respiratory tract infection18.4%17.7%10%
Decreased appetite3.6%1.1%14.4%
Diarrhoea6.4%1.7%14.4%
Lipase increased7.5%2.9%12.2%
Nausea3.9%0.6%11.7%
Diabetic retinopathy7.8%3.4%5.6%
Gastrointestinal disorder0.3%0%5.6%
Hyperlipidaemia4.5%3.4%5.6%
Nasopharyngitis4.5%5.1%2.8%
Abdominal discomfort0.3%0%5%
Secondary outcomes

What else it measured

Change in Body WeightKilogram (Kg) · Week 0, week 26 · mean
Insulin Degludec/Liraglutiden=341Insulin Degludecn=167Liraglutiden=151
0.2(2.7)1.3(2.7)-2.5(2.7)
Number of Treatment Emergent Severe or BG Confirmed Hypoglycaemic Episodes(Number of episodes/PYE)*100 · Weeks 0-26 · number
Insulin Degludec/Liraglutiden=29Insulin Degludecn=14Liraglutiden=3
23.9417.013.60
Insulin DoseUnits of insulin (U) · Week 26 · mean
Insulin Degludec/Liraglutiden=340Insulin Degludecn=167
24.8(11.9)30.1(14.4)
Participants Who Achieved HbA1c < 7.0%, American Diabetes Association (ADA) Target (Yes/no)Participants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=341Insulin Degludecn=167Liraglutiden=151
Yes2728380
No698471
Participants Who Achieved HbA1c ≤ 6.5%, International Diabetes Federation (IDF) Target (Yes/no)Participants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=341Insulin Degludecn=167Liraglutiden=151
Yes2014841
No140119110
Participants Who Achieved HbA1c <7.0% and Change in Body Weight From Baseline Below or Equal to ZeroParticipants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes1473474
No214145106
Participants Who Achieved HbA1c ≤ 6.5% and Change From Baseline in Body Weight Below or Equal to ZeroParticipants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes1112137
No250158143
Participants Who Achieved HbA1c < 7.0% Without Severe or Blood Glucose (BG) Confirmed Hypoglycaemic EpisodesParticipants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes2658084
No969996
Participants Who Achieved HbA1c ≤ 6.5% Without Severe or BG Confirmed Hypoglycaemic EpisodesParticipants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes1954643
No166133137
Participants Who Achieved HbA1c < 7.0% Without Severe or BG Confirmed Episodes, and Change From Baseline in Body Weight Below or Equal to Zero.Participants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes1363372
No225146108
Participants Who Achieved HbA1c ≤ 6.5% Without Severe or BG Confirmed Episodes and Change From Baseline in Body Weight Below or Equal to Zero.Participants · Week 26 · count of participants
MeasureInsulin Degludec/Liraglutiden=361Insulin Degludecn=179Liraglutiden=180
Yes1032136
No258158144
Change in Fasting Plasma Glucose (FPG)mmol/L · Week 0, week 26 · mean
Insulin Degludec/Liraglutiden=341Insulin Degludecn=167Liraglutiden=150
-3.64(2.27)-3.45(2.34)-1.86(2.11)
The trial

How DUAL I China was run

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

  • Insulin degludec/liraglutide
  • Insulin degludec
  • Liraglutide
Who could join the trial

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),...

Published papers

Papers from DUAL I China

Trial averages do not predict what one person will experience. Results are shown as the registry posts them, without interpretation.

GLPcompare is an informational data platform, not a medical provider or pharmacy. Nothing here is medical advice, a diagnosis, or a recommendation to start, stop, or change any treatment. Data is aggregated from public sources and can be incomplete or out of date. Always confirm with a licensed clinician and the current FDA label.