Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses) at Week 26
| Group | Value (percentage of HbA1C) | Spread |
|---|---|---|
| Placebo | 0.5 | 0.24 |
| Pooled Dulaglutide | -0.7 | 0.16 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataShort name AWARD-PEDS
United States, Brazil, France, Germany, Hungary, India, Mexico, Puerto Rico, Saudi Arabia, Turkey (Türkiye), United Kingdom
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 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.
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.
Outcomes the sponsor listed as primary.
Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses) at Week 26
Time frame · Baseline, Week 26
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).
Change From Baseline in HbA1c (Individual Doses) at Week 26
Time frame · Baseline, Week 26
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).
Change From Baseline in Fasting Blood Glucose (FBG) at Week 26
Time frame · Baseline, Week 26
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%).
Percentage of Participants With HbA1c ≤7.0%
Time frame · Week 26
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 Body Mass Index (BMI) at Week 26
Time frame · Baseline, Week 26
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%).
Percentage of Participants With Self-Reported Events of Hypoglycemia
Time frame · Week 26
Summary and analysis of Incidence of all hypoglycemia with Plasma Glucose \<54mg/dL.
Percentage of Participants Requiring Rescue for Severe, Persistent Hyperglycemia
Time frame · Week 26
Percentage of Participants Requiring Rescue for Severe, Persistent Hyperglycemia was summarized.
Number of Participants With Adjudicated Pancreatitis
Time frame · Week 26
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.
Change From Baseline in Pancreatic Enzymes at Week 26
Time frame · Baseline, Week 26
Serum Amylase (total and pancreas-derived) and lipase concentrations were measured.
Number of Participants With Thyroid Treatment-Emergent Adverse Events
Time frame · Week 26
Number of Participants with Thyroid Treatment-Emergent Adverse Events were summarized.
Change From Baseline in Serum Calcitonin at Week 26
Time frame · Baseline, Week 26
Change from Baseline in Serum Calcitonin was evaluated.
Percentage of Participants With Allergic, Hypersensitivity Reactions
Time frame · Week 26
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.
Percentage of Participants With Injection Site Reactions
Time frame · Week 26
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.
Number of Participants With Anti-Dulaglutide Antibodies
Time frame · Baseline through Week 56
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.
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
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.
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
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.
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 |
|---|---|---|
| Placebo | 0.5 | 0.24 |
| Pooled Dulaglutide | -0.7 | 0.16 |
| Group | Value (percentage of HbA1c) | Spread |
|---|---|---|
| Placebo | 0.5 | 0.24 |
| 0.75 mg Dulaglutide | -0.5 | 0.22 |
| 1.5 mg Dulaglutide | -1.0 | 0.22 |
| Group | Value (millimoles per liter (mmol/L)) | Spread |
|---|---|---|
| Placebo | 0.96 | 0.45 |
| 0.75 mg Dulaglutide | -0.47 | 0.41 |
| 1.5 mg Dulaglutide | -1.54 | 0.41 |
| Pooled Dulaglutide | -1.03 | 0.29 |
| Group | Value (percentage of participants) |
|---|---|
| Placebo | 18.42 |
| 0.75 mg Dulaglutide | 60.00 |
| 1.5 mg Dulaglutide | 53.19 |
| Pooled Dulaglutide | 56.52 |
| Group | Value (kilograms/square meter (kg/m^2)) | Spread |
|---|---|---|
| Placebo | -0.0 | 0.21 |
| 0.75 mg Dulaglutide | -0.2 | 0.20 |
| 1.5 mg Dulaglutide | -0.1 | 0.19 |
| Pooled Dulaglutide | -0.1 | 0.14 |
| Group | Value (percentage of participants) |
|---|---|
| Placebo | 1.96 |
| 0.75 mg Dulaglutide | 3.92 |
| 1.5 mg Dulaglutide | 3.85 |
| Group | Value (percentage of participants) |
|---|---|
| Placebo | 17.6 |
| 0.75 mg Dulaglutide | 3.9 |
| 1.5 mg Dulaglutide | 1.9 |
| Pooled Dulaglutide | 2.9 |
| Group | Value (participants) |
|---|---|
| Placebo | 0 |
| 0.75 mg Dulaglutide | 0 |
| 1.5 mg Dulaglutide | 0 |
| Pooled Dulaglutide | 0 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| Placebo: Double-Blind PeriodParticipants received placebo administered SC for 26 weeks. | 0 / 51 | 3 / 51 | 26 / 51 |
| 0.75 mg Dulaglutide: Double-Blind PeriodParticipants received 0.75 mg/week dulaglutide administered SC for 26 weeks. | 0 / 51 | 1 / 51 | 25 / 51 |
| 1.5 mg Dulaglutide: Double-Blind PeriodParticipants received 1.5 mg/week dulaglutide administered SC for 26 weeks. | 0 / 52 | 1 / 52 | 28 / 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 / 47 | 0 / 47 | 18 / 47 |
| 0.75 mg Dulaglutide: OLEParticipants received 0.75 mg/week dulaglutide administered SC for additional 26 weeks after the double-blind period. | 0 / 49 | 1 / 49 | 16 / 49 |
| 1.5 mg Dulaglutide: OLEParticipants received 1.5 mg/week dulaglutide administered SC for additional 26 weeks after the double-blind period. | 0 / 50 | 2 / 50 | 20 / 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
Studies that cite this trial.
2 studies on this page
Indexing hint: Meta-analysis (pooled) · 2025
Natale et al. 2025The Cochrane database of systematic reviewscited by 8
PMID 39963952PMC11834151DOI 10.1002/14651858.cd015849.pub2PUB-39963952
Indexing hint: Randomized controlled trial · 2022
Arslanian et al. 2022The New England journal of medicinecited by 120
PMID 35658022DOI 10.1056/nejmoa2204601PUB-35658022
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