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Trial · Interventional

CompletedPhase 3Results postedRegistry data

A Study Comparing the Effects and Safety of Dulaglutide With Insulin Glargine in Type 2 Diabetes Mellitus

Short name AWARD-CHN2

NCTNCT01648582 (opens ClinicalTrials.gov in a new tab)Other id13439Other idH9X-CR-GBDK

Overview

Status
Completed
Phase
Phase 3
Enrollment
774 participants (actual)
Sponsor
Eli Lilly and Company · Industry
Design
Randomized · Open label (no masking)
Countries
4 countries

China, Mexico, Russia, South Korea

Start
Jul 2012
Primary completion
Aug 2014
Completion
Dec 2014
First posted
24 Jul 2012 (estimated)
Last update posted
18 Sept 2019
Conditions
Type 2 Diabetes Mellitus

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2012201320142015
  1. Ph 3

    AWARD-CHN2

    NCT01648582

    Jul 2012 to Dec 2014

Registry summary

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.

Interventions

  • DulaglutideDrug
  • Insulin glargineDrug
  • MetforminDrug
  • SulfonylureasDrug

Arms3

  • 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.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks

    Time frame · Baseline, 26 Weeks

    Registry description

    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.

Secondary outcomes(20)
  1. Change From Baseline in HbA1c at 52 Weeks

    Time frame · Baseline, 52 Weeks

    Registry description

    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.

  2. Percentage of Participants Attaining HbA1c of <7% or ≤6.5% at 26 Weeks and 52 Weeks

    Time frame · Up to 26 and 52 weeks

    Registry description

    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.

  3. Change From Baseline in Fasting Blood Glucose (FBG) at 26 Weeks and 52 Weeks

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    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.

  4. 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

    Registry description

    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.

  5. 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

    Registry description

    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.

  6. 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

    Registry description

    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.

  7. Rate of Hypoglycemic Events

    Time frame · Baseline through 26 weeks and 52 weeks

    Registry description

    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.

  8. Number of Self-reported Hypoglycemic Events

    Time frame · Baseline through 26 Weeks and 52 Weeks

    Registry description

    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.

  9. Change From Baseline to 26 Weeks and 52 Weeks on Blood Pressure (BP)

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    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.

  10. Change From Baseline at 26 Weeks and 52 Weeks on Pulse Rate

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    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.

  11. Change From Baseline in Electrocardiogram Parameters, Fridericia Corrected QT (QTcF) Interval and PR Interval

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    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.

  12. Change From Baseline in Electrocardiogram Parameters, Heart Rate (HR)

    Time frame · Baseline, 26 Weeks, 52 Weeks

  13. Change From Baseline in Pancreatic Enzymes

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    Amylase (total and pancreas-derived) and lipase concentrations were measured

  14. Change From Baseline in Serum Calcitonin

    Time frame · Baseline, 26 Weeks, 52 Weeks

  15. Number of Participants With Adjudicated Cardiovascular (CV) Events

    Time frame · Baseline through 52 weeks

    Registry description

    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.

  16. Number of Participants With Adjudicated Pancreatitis

    Time frame · Baseline through 52 Weeks

    Registry description

    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.

  17. Change From Baseline in Body Weight

    Time frame · Baseline, 26 Weeks, 52 Weeks

  18. Change in Body Mass Index

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    Body mass index is an estimate of body fat based on body weight divided by height squared.

  19. Percentages of Participants Developing Treatment-Emergent Dulaglutide Anti-drug Antibody (ADA)

    Time frame · Baseline through 52 Weeks

    Registry description

    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.

  20. EQ-5D Health State Score Responses

    Time frame · Baseline, 26 Weeks, 52 Weeks

    Registry description

    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.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeLeast squares mean· Baseline, 26 Weeks

Change From Baseline in Glycosylated Hemoglobin (HbA1c) at 26 Weeks

GroupValue (percentage of HbA1c)Spread
1.5 mg Dulaglutide-1.730.067
0.75 mg Dulaglutide-1.330.067
Insulin Glargine-1.160.067
Secondary and other outcome results(7)
Secondary outcomeLeast squares mean· Baseline, 52 Weeks

Change From Baseline in HbA1c at 52 Weeks

GroupValue (percentage of HbA1c)Spread
1.5 mg Dulaglutide-1.470.076
0.75 mg Dulaglutide-1.030.076
Insulin Glargine-0.890.075
Secondary outcomeNumber· Up to 26 and 52 weeks

Percentage of Participants Attaining HbA1c of <7% or ≤6.5% at 26 Weeks and 52 Weeks

GroupValue (percentage of participants)
1.5 mg Dulaglutide64.8
0.75 mg Dulaglutide52.8
Insulin Glargine40.0
Secondary outcomeLeast squares mean· Baseline, 26 Weeks, 52 Weeks

Change From Baseline in Fasting Blood Glucose (FBG) at 26 Weeks and 52 Weeks

GroupValue (millimoles per liter (mmol/L))Spread
1.5 mg Dulaglutide-2.350.162
0.75 mg Dulaglutide-1.710.161
Insulin Glargine-2.590.161
Secondary outcomeLeast squares mean· Baseline, 26 Weeks, 52 Weeks

Change From Baseline in 7-point Self-monitored Blood Glucose (SMBG) Profiles at 26 Weeks and 52 Weeks

GroupValue (mmol/L)Spread
1.5 mg Dulaglutide-2.180.104
0.75 mg Dulaglutide-1.890.103
Insulin Glargine-2.830.103
Secondary outcomeLeast squares mean· Baseline, 26 weeks, 52 weeks

Change From Baseline in Homeostasis Model Assessment 2 Steady-state Beta (β)- Cell Function (HOMA2-%B) at 26 Weeks and 52 Weeks

GroupValue (percentage of HOMA2-%B)Spread
1.5 mg Dulaglutide34.413.831
0.75 mg Dulaglutide31.173.761
Secondary outcomeLeast squares mean· Baseline, 26 Weeks, 52 Weeks

Change From Baseline in Homeostasis Model Assessment 2 Insulin Sensitivity - Cell Function (HOMA2-%S) at 26 Weeks and 52 Weeks

GroupValue (percentage of HOMA2-%S)Spread
1.5 mg Dulaglutide-6.863.649
0.75 mg Dulaglutide-10.033.591
Secondary outcomeMean· Baseline through 26 weeks and 52 weeks

Rate of Hypoglycemic Events

GroupValue (events per participant per year)Spread
1.5 mg Dulaglutide1.274.485
0.75 mg Dulaglutide0.984.202
Insulin Glargine2.136.724

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther 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 / 258184 / 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 / 257188 / 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 / 253157 / 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

Studies8

Studies that cite this trial.

Studies with results

8 studies on this page

PubMed tag: none · 2021

8 results

Efficacy and Safety of Once Weekly Dulaglutide in East Asian Patients with Type 2 Diabetes: Subgroup Analysis by Potential Influential Factors.

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

Free to read · publisher termsCC BY-NC8 results

PubMed tag: none · 2021

12 results

Pancreatic Safety of Once-Weekly Dulaglutide in Chinese Patients with Type 2 Diabetes Mellitus: Subgroup Analysis by Potential Influencing Factors.

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

Free to read · publisher termsCC BY-NC12 results

Indexing hint: Randomized controlled trial · 2021

3 results

Effects of GLP-1 Receptor Agonists on Bone Mineral Density in Patients with Type 2 Diabetes Mellitus: A 52-Week Clinical Study.

Cai et al. 2021BioMed research internationalcited by 64

PMID 34580638PMC8464416DOI 10.1155/2021/3361309PUB-34580638

CC BY3 results

PubMed tag: none · 2020

10 results

Efficacy and Safety of Dulaglutide by Baseline HbA1c in Chinese Patients with Type 2 Diabetes: A Post Hoc Analysis.

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

Free to read · publisher termsCC BY-NC10 results

PubMed tag: none · 2020

11 results

Evaluation of Characteristics of Gastrointestinal Adverse Events with Once-Weekly Dulaglutide Treatment in Chinese Patients with Type 2 Diabetes: A Post Hoc Pooled Analysis of Two Randomized Trials.

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

Free to read · publisher termsCC BY-NC11 results

PubMed tag: none · 2020

13 results

Efficacy and Safety of Once-Weekly Dulaglutide in Elderly Chinese Patients with Type 2 Diabetes: A Post Hoc Analysis of AWARD-CHN Studies.

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

Free to read · publisher termsCC BY-NC13 results

PubMed tag: none · 2019

7 results

Efficacy and Safety of Dulaglutide Versus Insulin Glargine in Chinese T2DM Patients: A Subgroup Analysis of a Randomized Trial (AWARD-CHN2).

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

Free to read · publisher termsCC BY-NC7 results

Indexing hint: Randomized controlled trial · 2019

19 results

The Effects of Once-Weekly Dulaglutide and Insulin Glargine on Glucose Fluctuation in Poorly Oral-Antidiabetic Controlled Patients with Type 2 Diabetes Mellitus.

Wang et al. 2019BioMed research internationalcited by 21

PMID 31950036PMC6943972DOI 10.1155/2019/2682657PUB-31950036

CC BY19 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Have type 2 diabetes mellitus for at least 6 months * Have been taking metformin and/or a sulfonylurea for at least 3 months before screening and have been on a stable therapeutic dose for at least 8 weeks * Glycosylated hemoglobin (HbA1c) value of ≥7.0% to ≤11.0% * Adult men or adult non-pregnant, non-breastfeeding women * Body Mass Index (BMI) of ≥19.0 to ≤35.0 kilograms/square meter (kg/m\^2) * Stable weight (±5%) ≥3 months prior to screening Exclusion Criteria: * Have type 1 diabetes mellitus * Have previous treatment with a glucagon-like peptide-1 (GLP-1) receptor agonist, GLP-1 analog, or any other incretin mimetic * Have treatment with dipeptidyl peptidase-IV (DPP-IV) inhibitor, an alpha-glucosidase inhibitor (AGI), thiazolidinedione (TZD), or glinide * Have gastric emptying abnormality * Have cardiac disorder defined as unstable angina, myocardial infarction, coronary artery bypass graft surgery, percutaneous coronary intervention, heart failure, arrhythmia, transient ischemic attack, or stroke * Have poorly controlled hypertension (systolic blood pressure above 160 millimeter of mercury\[mmHg\] or diastolic blood pressure above 95 mmHg) * Have impaired liver function * Have impaired kidney function * Have history of chronic pancreatitis or acute pancreatitis * Have a serum calcitonin ≥20 picograms per milliliter (pg/mL) * Have a personal or family history of medullary C-cell hyperplasia, focal hyperplasia, carcinoma, or multiple endocrine neoplasia type 2 (MEN 2)

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