Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -1.73 | 0.067 |
| 0.75 mg Dulaglutide | -1.33 | 0.067 |
| Insulin Glargine | -1.16 | 0.067 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataShort name AWARD-CHN2
China, Mexico, Russia, South Korea
1 trial · 1 completed · 1 with posted results
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
The purpose of this study is to examine if once-weekly dulaglutide is efficient and safe compared to once-daily insulin glargine in participants with type 2 diabetes mellitus who have inadequate glycemic control with 1 or 2 oral antihyperglycemic medications (OAM) (metformin and/or a sulfonylurea), in addition to any healthy lifestyle changes recommended by their healthcare providers.
Experimental
1.5 mg Dulaglutide
1.5 milligrams (mg) dulaglutide administered as one subcutaneous (SC) injection once-weekly added to participant's pre-study prescribed dose of metformin and/or a sulfonylurea for up to 52 weeks. Participants are blinded to the dulaglutide dose.
Experimental
0.75 mg Dulaglutide
0.75 mg Dulaglutide administered as one SC injection once-weekly added to participant's pre-study prescribed dose of metformin and/or a sulfonylurea for up to 52 weeks. Participants are blinded to the dulaglutide dose.
Active comparator
Insulin Glargine
Insulin glargine administered based on fasting blood glucose concentrations per the dosing titration schedule as once daily SC injection at bedtime added to participant's pre-study prescribed dose of metformin and /or a sulfonylurea for up to 52 weeks.
Outcomes the sponsor listed as primary.
Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks
Time frame · Baseline, 26 Weeks
HbA1c is a form of hemoglobin that is measured primarily to identify the average plasma glucose concentration over prolonged periods of time. Least square (LS) means of change from baseline in HbA1c were calculated using a mixed-effects model for repeated measures (MMRM) with the change in HbA1c as the dependent variable and treatment, baseline HbA1c, country, oral antihyperglycemic medication (OAM) , visit, and treatment-by-visit interaction as fixed effects, and participant was the random effect.
Change From Baseline in HbA1c at 52 Weeks
Time frame · Baseline, 52 Weeks
HbA1c is a form of hemoglobin that is measured primarily to identify the average plasma glucose concentration over prolonged periods of time. LS means of change from baseline in HbA1c were calculated using a MMRM with the change in HbA1c as the dependent variable and treatment, baseline HbA1c, country, OAM, visit, and treatment-by-visit interaction as fixed effects, and participant was as the random effect.
Percentage of Participants Attaining HbA1c of <7% or ≤6.5% at 26 Weeks and 52 Weeks
Time frame · Up to 26 and 52 weeks
The percentage of participants was calculated by dividing the number of participants reaching target HbA1c by the total number of participants analyzed, multiplied by 100.
Change From Baseline in Fasting Blood Glucose (FBG) at 26 Weeks and 52 Weeks
Time frame · Baseline, 26 Weeks, 52 Weeks
LS means of change from baseline were calculated using MMRM with the change in FBG as the dependent variable and treatment, baseline value, country, OAM, visit, and treatment-by-visit interaction as fixed effects, and participant was the random effect.
Change From Baseline in 7-point Self-monitored Blood Glucose (SMBG) Profiles at 26 Weeks and 52 Weeks
Time frame · Baseline, 26 Weeks, 52 Weeks
Participants were required to perform 7-point SMBG profiles on 2 separate, nonconsecutive days during the 2 weeks before randomization and Weeks 8, 14, 20, 26, 39, and 52 (or the Early Discontinuation Visit). SMBG measurements were taken using a plasma-equivalent blood glucose (BG) meter at 7 time points: morning pre-meal, morning 2 hours post-meal, mid-day pre-meal, mid-day 2 hours post-meal, evening pre-meal, evening 2 hours post-meal, and at bedtime. Mean and Week 26 and Week 52 was assessed in all treatment groups. LS means of change from baseline were calculated using MMRM with the change in 7-point SMBG as the dependent variable and treatment, baseline value, country, OAM, visit, and treatment-by-visit interaction as fixed effects, and participant was the random effect.
Change From Baseline in Homeostasis Model Assessment 2 Steady-state Beta (β)- Cell Function (HOMA2-%B) at 26 Weeks and 52 Weeks
Time frame · Baseline, 26 weeks, 52 weeks
The updated Homeostasis Model Assessment (HOMA2) was used to quantify steady state beta-cell function (%B). HOMA2-%B is a computer model that uses fasting plasma insulin and glucose concentrations to estimate %B as a percentage of a normal reference population. LS means were calculated using a homeostasis model assessment with change from baseline in HOMA-%B as a covariate and country, baseline measurement, OAM, and treatment as fixed effects.
Change From Baseline in Homeostasis Model Assessment 2 Insulin Sensitivity - Cell Function (HOMA2-%S) at 26 Weeks and 52 Weeks
Time frame · Baseline, 26 Weeks, 52 Weeks
The HOMA2 was used to estimate the steady-state insulin sensitivity (%S). HOMA2-S is a computer model that uses fasting plasma insulin and glucose concentrations to estimate insulin sensitivity (%S) as a percentage of the normal reference population. LS means were calculated using an homeostasis model assessment with change from baseline in HOMA-%S as a covariate and country, baseline measurement, OAM, and treatment as fixed effects.
Rate of Hypoglycemic Events
Time frame · Baseline through 26 weeks and 52 weeks
Hypoglycemic events (HE) were classified as documented symptomatic hypoglycemia, asymptomatic hypoglycemia, severe hypoglycemia, and probable symptomatic hypoglycemia. The 1-year adjusted rate of HEs was summarized cumulatively at 26 weeks and 52 weeks. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.
Number of Self-reported Hypoglycemic Events
Time frame · Baseline through 26 Weeks and 52 Weeks
Hypoglycemic events (HE) were classified as severe (defined as episodes requiring the assistance of another person to actively administer resuscitative actions), documented symptomatic (defined as any time a participant felt that he/she was experiencing symptoms and/or signs associated with hypoglycemia, and had a plasma glucose level of less than or equal to 3.9 millimoles/liter \[mmol/L\]), asymptomatic (defined as events not accompanied by typical symptoms of hypoglycemia but with a measured plasma glucose of less than or equal to 3.9 mmol/L), nocturnal (defined as any hypoglycemic event that occurred between bedtime and waking), or probable symptomatic (defined as events during which symptoms of hypoglycemia were not accompanied by a plasma glucose determination). The number of self-reported hypoglycemic events was summarized cumulatively at 52 weeks. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.
Change From Baseline to 26 Weeks and 52 Weeks on Blood Pressure (BP)
Time frame · Baseline, 26 Weeks, 52 Weeks
Seated systolic blood pressure (SBP) and seated diastolic blood pressure (DBP) were measured. LS means of change from baseline were calculated using a MMRM with treatment, country, visit, and treatment-by-visit interaction as fixed effects and baseline as a covariate.
Change From Baseline at 26 Weeks and 52 Weeks on Pulse Rate
Time frame · Baseline, 26 Weeks, 52 Weeks
Seated pulse rate was measured. LS means of change from baseline were calculated using a MMRM with treatment, country, visit, and treatment-by-visit interaction as fixed effects and baseline as a covariate.
Change From Baseline in Electrocardiogram Parameters, Fridericia Corrected QT (QTcF) Interval and PR Interval
Time frame · Baseline, 26 Weeks, 52 Weeks
The QT interval is a measure of the time between the start of the Q wave and the end of the T wave and was calculated from electrocardiogram (ECG) data using Fridericia's formula: QTc = QT/RR\^0.33. Corrected QT (QTc) is the QT interval corrected for heart rate and RR, which is the interval between two R waves. PR is the interval between the P wave and the QRS complex.
Change From Baseline in Electrocardiogram Parameters, Heart Rate (HR)
Time frame · Baseline, 26 Weeks, 52 Weeks
Change From Baseline in Pancreatic Enzymes
Time frame · Baseline, 26 Weeks, 52 Weeks
Amylase (total and pancreas-derived) and lipase concentrations were measured
Change From Baseline in Serum Calcitonin
Time frame · Baseline, 26 Weeks, 52 Weeks
Number of Participants With Adjudicated Cardiovascular (CV) Events
Time frame · Baseline through 52 weeks
Deaths and nonfatal cardiovascular adverse events were adjudicated by a committee of physicians with cardiology expertise external to the Sponsor. The nonfatal cardiovascular events subjected to adjudication included myocardial infarction, hospitalization for unstable angina, hospitalization for heart failure, coronary interventions (such as coronary artery bypass graft or percutaneous coronary intervention), and cerebrovascular events including cerebrovascular accident (stroke) and transient ischemic attack. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.
Number of Participants With Adjudicated Pancreatitis
Time frame · Baseline through 52 Weeks
The number of participants with pancreatitis confirmed by adjudication is summarized. Events of pancreatitis (including suspected pancreatitis and severe or serious abdominal pain) were adjudicated by a committee of expert physicians external to the Sponsor. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.
Change From Baseline in Body Weight
Time frame · Baseline, 26 Weeks, 52 Weeks
Change in Body Mass Index
Time frame · Baseline, 26 Weeks, 52 Weeks
Body mass index is an estimate of body fat based on body weight divided by height squared.
Percentages of Participants Developing Treatment-Emergent Dulaglutide Anti-drug Antibody (ADA)
Time frame · Baseline through 52 Weeks
Number of participants with treatment emergent (TE) dulaglutide anti-drug antibodies from postbaseline to follow up were summarized. A participant was considered to have TE dulaglutide ADA if the participant had at least one titer that was treatment-emergent relative to baseline, defined as a 4-fold or greater increase in titer from baseline measurement.
EQ-5D Health State Score Responses
Time frame · Baseline, 26 Weeks, 52 Weeks
The EQ-5D questionnaire is a widely used, generic questionnaire that assesses health-related quality of life. It consists of 2 parts. The first part assesses 5 dimensions associated with quality of life (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression). Each dimension has 3 possible levels of response: no problem, some problem, and extreme problem. Additional categories of response include ambiguous and missing. The number of participants per each of the 3 response categories is summarized for each of the 5 dimensions.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -1.73 | 0.067 |
| 0.75 mg Dulaglutide | -1.33 | 0.067 |
| Insulin Glargine | -1.16 | 0.067 |
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -1.47 | 0.076 |
| 0.75 mg Dulaglutide | -1.03 | 0.076 |
| Insulin Glargine | -0.89 | 0.075 |
| Group | Value (percentage of participants) |
|---|---|
| 1.5 mg Dulaglutide | 64.8 |
| 0.75 mg Dulaglutide | 52.8 |
| Insulin Glargine | 40.0 |
| Group | Value (millimoles per liter (mmol/L)) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -2.35 | 0.162 |
| 0.75 mg Dulaglutide | -1.71 | 0.161 |
| Insulin Glargine | -2.59 | 0.161 |
| Group | Value (mmol/L) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -2.18 | 0.104 |
| 0.75 mg Dulaglutide | -1.89 | 0.103 |
| Insulin Glargine | -2.83 | 0.103 |
| Group | Value (percentage of HOMA2-%B) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | 34.41 | 3.831 |
| 0.75 mg Dulaglutide | 31.17 | 3.761 |
| Group | Value (percentage of HOMA2-%S) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | -6.86 | 3.649 |
| 0.75 mg Dulaglutide | -10.03 | 3.591 |
| Group | Value (events per participant per year) | Spread |
|---|---|---|
| 1.5 mg Dulaglutide | 1.27 | 4.485 |
| 0.75 mg Dulaglutide | 0.98 | 4.202 |
| Insulin Glargine | 2.13 | 6.724 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| 1.5 mg Dulaglutide1.5 mg dulaglutide administered as 1 SC injection once-weekly added to participant's pre-study prescribed dose of metformin and/or a sulfonylurea. | – | 24 / 258 | 184 / 258 |
| 0.75 mg Dulaglutide0.75 mg dulaglutide administered as 1 SC injection once-weekly added to participant's pre-study prescribed dose of metformin and/or a sulfonylurea. | – | 15 / 257 | 188 / 257 |
| Insulin GlargineInsulin glargine administered per dosing titration schedule as once daily SC injection at bedtime added to participant's pre-study prescribed dose of metformin and /or a sulfonylurea. | – | 9 / 253 | 157 / 253 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
8 studies on this page
PubMed tag: none · 2021
Ma et al. 2021Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 2
PMID 33161492PMC7843818DOI 10.1007/s13300-020-00955-2PUB-33161492
PubMed tag: none · 2021
Zhou et al. 2021Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 2
PMID 34453682PMC8479006DOI 10.1007/s13300-021-01139-2PUB-34453682
Indexing hint: Randomized controlled trial · 2021
Cai et al. 2021BioMed research internationalcited by 64
PMID 34580638PMC8464416DOI 10.1155/2021/3361309PUB-34580638
PubMed tag: none · 2020
Yu et al. 2020Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 11
PMID 32277401PMC7192976DOI 10.1007/s13300-020-00804-2PUB-32277401
PubMed tag: none · 2020
Guo et al. 2020Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 5
PMID 32621083PMC7376772DOI 10.1007/s13300-020-00869-zPUB-32621083
PubMed tag: none · 2020
Kuang et al. 2020Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 4
PMID 32857293PMC7509013DOI 10.1007/s13300-020-00910-1PUB-32857293
PubMed tag: none · 2019
Li et al. 2019Diabetes therapy : research, treatment and education of diabetes and related disorderscited by 14
PMID 31228090PMC6612357DOI 10.1007/s13300-019-0646-yPUB-31228090
Indexing hint: Randomized controlled trial · 2019
Wang et al. 2019BioMed research internationalcited by 21
PMID 31950036PMC6943972DOI 10.1155/2019/2682657PUB-31950036
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