Skip to content

Trial · Interventional

CompletedPhase 3Results postedRegistry data

A Study of Dulaglutide (LY2189265) in Children and Adolescents With Type 2 Diabetes

Short name AWARD-PEDS

NCTNCT02963766 (opens ClinicalTrials.gov in a new tab)Other id14171Other idH9X-MC-GBGCOther id2016-000361-22Other id2016

Overview

Status
Completed
Phase
Phase 3
Enrollment
154 participants (actual)
Sponsor
Eli Lilly and Company · Industry
Design
Randomized · Double masking
Countries
11 countries

United States, Brazil, France, Germany, Hungary, India, Mexico, Puerto Rico, Saudi Arabia, Turkey (Türkiye), United Kingdom

Start
29 Dec 2016
Primary completion
12 Jun 2021
Completion
12 Jan 2022
First posted
15 Nov 2016 (estimated)
Last update posted
1 Jul 2022
Conditions
Type 2 Diabetes

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2016201820202022
  1. Ph 3

    AWARD-PEDS

    NCT02963766

    29 Dec 2016 to 12 Jan 2022

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The purpose of this study is to evaluate the safety, efficacy, pharmacokinetics and pharmacodynamics of the study drug dulaglutide compared to placebo in pediatric participants with type 2 diabetes. The study duration is approximately 60 weeks.

Interventions

  • DulaglutideDrug
  • PlaceboDrug

Arms3

  • Experimental

    Placebo/0.75 milligram (mg) Dulaglutide

    Participants received placebo administered subcutaneously (SC) for 26 weeks during the double-blind period and open-label 0.75 mg/week dulaglutide for 26 weeks during the Open Label Extension (OLE).

  • Experimental

    0.75 mg Dulaglutide

    Participants received 0.75 mg/week dulaglutide administered SC for 26 weeks during the double-blind period and open-label 0.75 mg/week for 26 weeks during the OLE.

  • Experimental

    1.5 mg Dulaglutide

    Participants received 1.5 mg/week dulaglutide administered SC for 26 weeks during the double-blind period and open-label 1.5 mg/week for 26 weeks during the OLE.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses) at Week 26

    Time frame · Baseline, Week 26

    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) mean in HbA1c was calculated using a restricted maximum likelihood (REML) based mixed-effects model for repeated measures (MMRM) and adjusted by, baseline + insulin Use + metformin Use + treatment + time + treatment\*time (Type III sum of squares). Variance-covariance structure = unstructured (for actual value) / unstructured (for change from baseline).

Secondary outcomes(15)
  1. Change From Baseline in HbA1c (Individual Doses) at Week 26

    Time frame · Baseline, Week 26

    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 mean in HbA1c was calculated using a REML based MMRM and adjusted by, baseline + insulin use + metformin use + treatment + time + treatment\*time (Type III sum of squares). Variance-covariance structure = unstructured (for actual value) / unstructured (for change from baseline).

  2. Change From Baseline in Fasting Blood Glucose (FBG) at Week 26

    Time frame · Baseline, Week 26

    Registry description

    Fasting blood glucose is a test to determine how much glucose (sugar) is in a blood sample after an overnight fast. Least squares (LS) means were calculated using a mixed-effects model for repeated measures (MMRM) analysis and adjusted by baseline, strata, treatment, time, treatment\*time, (Type III sum of squares). Variance-Covariance structure = Unstructured (for actual value) / Unstructured (for change from baseline). Strata refer to: insulin use + metformin use + baseline HbA1c group \[ less than (\<) 8%, greater than or equal to (\>=) 8%).

  3. Percentage of Participants With HbA1c ≤7.0%

    Time frame · Week 26

    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.

  4. Change From Baseline in Body Mass Index (BMI) at Week 26

    Time frame · Baseline, Week 26

    Registry description

    BMI is an estimate of body fat based on body weight divided by height squared. LS mean were calculated using a MMRM analysis and adjusted by baseline, strata, treatment, time, treatment\*time, (Type III sum of squares). Variance-Covariance structure = Unstructured (for actual value) / Unstructured (for change from baseline). Strata refer to: insulin use + metformin use + baseline HbA1c group (\< 8%, \>= 8%).

  5. Percentage of Participants With Self-Reported Events of Hypoglycemia

    Time frame · Week 26

    Registry description

    Summary and analysis of Incidence of all hypoglycemia with Plasma Glucose \<54mg/dL.

  6. Percentage of Participants Requiring Rescue for Severe, Persistent Hyperglycemia

    Time frame · Week 26

    Registry description

    Percentage of Participants Requiring Rescue for Severe, Persistent Hyperglycemia was summarized.

  7. Number of Participants With Adjudicated Pancreatitis

    Time frame · Week 26

    Registry description

    The number of participants with pancreatitis confirmed by adjudication is summarized cumulatively at 26 weeks. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.

  8. Change From Baseline in Pancreatic Enzymes at Week 26

    Time frame · Baseline, Week 26

    Registry description

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

  9. Number of Participants With Thyroid Treatment-Emergent Adverse Events

    Time frame · Week 26

    Registry description

    Number of Participants with Thyroid Treatment-Emergent Adverse Events were summarized.

  10. Change From Baseline in Serum Calcitonin at Week 26

    Time frame · Baseline, Week 26

    Registry description

    Change from Baseline in Serum Calcitonin was evaluated.

  11. Percentage of Participants With Allergic, Hypersensitivity Reactions

    Time frame · Week 26

    Registry description

    The percentage of Participants with Allergic and hypersensitivity reactions that were considered possibly related to study drug by the investigator are presented. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.

  12. Percentage of Participants With Injection Site Reactions

    Time frame · Week 26

    Registry description

    The percentage of participants with at least one treatment-emergent injection site reaction is presented. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.

  13. Number of Participants With Anti-Dulaglutide Antibodies

    Time frame · Baseline through Week 56

    Registry description

    Dulaglutide anti-drug antibodies (ADA) were assessed at baseline, Weeks 26 and 56. A participant was considered to have treatment-emergent (TE) dulaglutide ADAs if the participant had at least 1 titer that was TE relative to baseline, defined as a 4-fold or greater increase in titer from baseline measurement.

  14. Pharmacokinetics (PK): Maximum Concentration of Dulaglutide at Steady-state (Cmax,ss)

    Time frame · Week 9: pre-dose,1 to 12 hours post dose and 24 to 96 hours post dose; Week 13: predose and 1 to 12 hours post dose; Week 26: predose; Week 39: up to 2 days postdose; Week 52 and Week 56: PK sample can be taken at any time during the visit

    Registry description

    PK: Maximum Concentration of Dulaglutide at steady-state (Cmax,ss) was derived by a population pharmacokinetics approach. As part of addendum, additional PK samples were taken at week 9.

  15. PK: Area Under the Concentration Time Curve Over a 1-week Interval of Dulaglutide at Steady-State [AUC(0-168)ss]

    Time frame · Week 9: pre-dose,1 to 12 hours post dose and 24 to 96 hours post dose; Week 13: predose and 1 to 12 hours post dose; Week 26: predose; Week 39: up to 2 days postdose; Week 52 and Week 56: PK sample can be taken at any time during the visit

    Registry description

    PK: Area Under the Concentration Time Curve over a 1-week interval of Dulaglutide at Steady-State \[AUC(0-168)ss\] was derived by a population pharmacokinetics approach. As part of addendum, additional PK samples were taken at week 9.

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, Week 26

Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses) at Week 26

GroupValue (percentage of HbA1C)Spread
Placebo0.50.24
Pooled Dulaglutide-0.70.16
Secondary and other outcome results(7)
Secondary outcomeLeast squares mean· Baseline, Week 26

Change From Baseline in HbA1c (Individual Doses) at Week 26

GroupValue (percentage of HbA1c)Spread
Placebo0.50.24
0.75 mg Dulaglutide-0.50.22
1.5 mg Dulaglutide-1.00.22
Secondary outcomeLeast squares mean· Baseline, Week 26

Change From Baseline in Fasting Blood Glucose (FBG) at Week 26

GroupValue (millimoles per liter (mmol/L))Spread
Placebo0.960.45
0.75 mg Dulaglutide-0.470.41
1.5 mg Dulaglutide-1.540.41
Pooled Dulaglutide-1.030.29
Secondary outcomeNumber· Week 26

Percentage of Participants With HbA1c ≤7.0%

GroupValue (percentage of participants)
Placebo18.42
0.75 mg Dulaglutide60.00
1.5 mg Dulaglutide53.19
Pooled Dulaglutide56.52
Secondary outcomeLeast squares mean· Baseline, Week 26

Change From Baseline in Body Mass Index (BMI) at Week 26

GroupValue (kilograms/square meter (kg/m^2))Spread
Placebo-0.00.21
0.75 mg Dulaglutide-0.20.20
1.5 mg Dulaglutide-0.10.19
Pooled Dulaglutide-0.10.14
Secondary outcomeNumber· Week 26

Percentage of Participants With Self-Reported Events of Hypoglycemia

GroupValue (percentage of participants)
Placebo1.96
0.75 mg Dulaglutide3.92
1.5 mg Dulaglutide3.85
Secondary outcomeNumber· Week 26

Percentage of Participants Requiring Rescue for Severe, Persistent Hyperglycemia

GroupValue (percentage of participants)
Placebo17.6
0.75 mg Dulaglutide3.9
1.5 mg Dulaglutide1.9
Pooled Dulaglutide2.9
Secondary outcomeNumber· Week 26

Number of Participants With Adjudicated Pancreatitis

GroupValue (participants)
Placebo0
0.75 mg Dulaglutide0
1.5 mg Dulaglutide0
Pooled Dulaglutide0

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Placebo: Double-Blind PeriodParticipants received placebo administered SC for 26 weeks.0 / 513 / 5126 / 51
0.75 mg Dulaglutide: Double-Blind PeriodParticipants received 0.75 mg/week dulaglutide administered SC for 26 weeks.0 / 511 / 5125 / 51
1.5 mg Dulaglutide: Double-Blind PeriodParticipants received 1.5 mg/week dulaglutide administered SC for 26 weeks.0 / 521 / 5228 / 52
Placebo/0.75 mg Dulaglutide: Open Label Extension (OLE)Participants who had received placebo during the double-blind period were given 0.75 mg/week dulaglutide administered SC for additional 26 weeks after the double-blind period.0 / 470 / 4718 / 47
0.75 mg Dulaglutide: OLEParticipants received 0.75 mg/week dulaglutide administered SC for additional 26 weeks after the double-blind period.0 / 491 / 4916 / 49
1.5 mg Dulaglutide: OLEParticipants received 1.5 mg/week dulaglutide administered SC for additional 26 weeks after the double-blind period.0 / 502 / 5020 / 50

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

Studies2

Studies that cite this trial.

Studies with results

2 studies on this page

Indexing hint: Meta-analysis (pooled) · 2025

15 results

Glucagon-like peptide 1 (GLP-1) receptor agonists for people with chronic kidney disease and diabetes.

Natale et al. 2025The Cochrane database of systematic reviewscited by 8

PMID 39963952PMC11834151DOI 10.1002/14651858.cd015849.pub2PUB-39963952

Rights unknown15 results

Indexing hint: Randomized controlled trial · 2022

7 results

Once-Weekly Dulaglutide for the Treatment of Youths with Type 2 Diabetes.

Arslanian et al. 2022The New England journal of medicinecited by 120

PMID 35658022DOI 10.1056/nejmoa2204601PUB-35658022

Full text at the publisher7 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 10 Years up to 17 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Have type 2 diabetes, treated with diet and exercise, with or without metformin and/or basal insulin. Metformin and/or basal insulin dose must be stable for at least 8 weeks prior to study screening. * Have HbA1c \>6.5% to ≤11% at screening visit. If newly diagnosed and not on medicine for diabetes, HbA1c must be between \>6.5 % to ≤9%. * Have a BMI (body mass index) \>85 percentile for age, gender and body weight ≥50 kilograms (110 pounds). Exclusion Criteria: * Known type 1 diabetes, or positive GAD65 or IA2 antibodies, or history of diabetic ketoacidosis or hyperglycemic hyperosmolar syndrome. * A history of, or at risk for pancreatitis. * Self or family history of Multiple Endocrine Neoplasia (MEN) type 2A or B, thyroid C-cell hyperplasia or medullary thyroid cancer, or a blood calcitonin result ≥20 picograms per milliliter (pg/ml) at screening. * A systolic blood pressure of ≥160 millimeters of mercury (mmHg) or diastolic ≥100 mmHg. * Active or treated cancer. * A blood disorder where an accurate HbA1c may not be obtainable. * A female of childbearing age, sexually active and not on birth control. * Pregnant or plan to be pregnant during the study, or breastfeeding. * Taking any diabetic medication other than metformin or basal insulin and have not stopped it 3 months prior to the screening visit (6 weeks for bolus or mealtime insulin). * Have taken oral steroids within the last 60 days or more than 20 days use within the past year or 1000 micrograms fluticasone propionate per day. * Using prescription weight loss medications in the last 30 days, or plan to use. * Taking psychiatric medications for depression or illness or attention deficit hyperactivity disorder (ADHD) if, the doses has changed within the last 3 months.

PepBank is a research reference. Talk to a doctor before you use any peptide.