| NCT02918279Effect of Liraglutide for Weight Management in Pubertal Adolescent Subjects With Obesity | Liraglutide | Phase 3 | 251 | Change in BMI SDS (Week 0, Week 56) (SDS score), Week 0, week 56. Liraglutide 3.0 mg: -0.25; Placebo: -0.02. |
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| NCT04102189A Research Study on How Well Semaglutide Works in Adolescents With Overweight or Obesity | Semaglutide | Phase 3 | 201 | Change in Body Mass Index (BMI) (Percentage [%]) (Percentage change of BMI), Baseline (week 0), week 68. Semaglutide 2.4 mg: -16.2; Placebo: -0.1. |
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| AWARD-PEDSA Study of Dulaglutide (LY2189265) in Children and Adolescents With Type 2 Diabetes | Dulaglutide | Phase 3 | 154 | Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses) at Week 26 (percentage of HbA1C), Baseline, Week 26. Placebo: 0.5; Pooled Dulaglutide: -0.7. |
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| Ellipse™Efficacy and Safety of Liraglutide in Combination With Metformin Compared to Metformin Alone, in Children and Adolescents With Type 2 Diabetes | Liraglutide | Phase 3 | 135 | Change in HbA1c (Glycosylated Haemoglobin) (Percentage of HbA1c), Week 0, week 26. Liraglutide 1.8 mg: -0.643; Placebo: 0.415. |
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| PIONEER TEENSA Research Study to Compare a New Medicine Oral Semaglutide to a Dummy Medicine in Children and Teenagers With Type 2 Diabetes | Semaglutide | Phase 3 | 132 | Change From Baseline (Week 0) to Week 26 in Glycosylated Haemoglobin (HbA1c)- Percentage Point (Percentage point), Baseline (Week 0), Week 26. Oral Semaglutide: -1.0; Placebo: -0.3. |
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| NCT00658021Safety and Efficacy of Exenatide as Monotherapy and Adjunctive Therapy to Oral Antidiabetic Agents in Adolescents With Type 2 Diabetes | Exenatide | Phase 3 | 122 | Adjusted Change From Baseline in Glycated Hemoglobin A1c (HbA1c) at Week 28 (percentage (%HbA1c)), Baseline (Day 1) and Week 28. Total Exenatide Twice Daily (EBID): 0.11; Placebo: 0.38. |
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| SURPASS-PEDSA Study to Evaluate Tirzepatide (LY3298176) in Pediatric and Adolescent Participants With Type 2 Diabetes Mellitus Inadequately Controlled With Metformin or Basal Insulin or Both | Tirzepatide | Phase 3 | 99 | Change From Baseline in Hemoglobin A1c (HbA1c) (Pooled Doses of Tirzepatide 5 mg and 10 mg) (percentage of HbA1c), Baseline, Week 30. Pooled Doses of Tirzepatide (5 mg, 10 mg): -2.03; Placebo: -0.23. |
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| APPLELiver and Fat Regulation in Overweight Adolescent Girls | Exenatide | Phase 2/3 | 92 | Hepatic Glucose Release (mg/kg/min), Measured up to 4 months from enrollment. Control: 1.85; PCOS Medication Naive: 1.46; PCOS, Medication Naive + Byetta: 1.54; PCOS on COCPs: 1.88; PCOS on Metformin: 1.57. |
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| NCT01554618Safety and Efficacy Study of Exenatide Once Weekly in Adolescents With Type 2 Diabetes | Exenatide | Phase 3 | 84 | Change From Baseline in Glycosylated Hemoglobin A1c (HbA1c) to Week 24 (Controlled Assessment Period) (percentage (% HbA1c)), Baseline (Week 0) and Week 24. Controlled Assessment Period - Exenatide: -0.36; Controlled Assessment Period - Placebo: 0.49. |
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| TEALTreating PCOS With Semaglutide vs Active Lifestyle Intervention | Semaglutide | Phase 2/3 | 60 | Change in Hepatic Fat Fraction (Change in percentage of liver fat), Baseline and 12 weeks. Diet Intervention: -1.41; GLP-1 Intervention: -1.84. |
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| NCT02527200Effect of Liraglutide for Weight Management in Paediatric Subjects With Prader-Willi Syndrome | Liraglutide | Phase 3 | 56 | Change in Body Mass Index (BMI) Standard Deviation Score (SDS) From Baseline to 16 Weeks (SDS score), Week 0, Week 16. Part A: Liraglutide: -0.18; Part A: Placebo: -0.18; Part B: Liraglutide: -0.50; Part B: Placebo: -0.48; Part A+B: Liraglutide: -0.33; Part A+B: Placebo: -0.29. |
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| NCT02516657Liraglutide in Adolescents With Type 1 Diabetes | Liraglutide | Phase 3 | 5 | On ClinicalTrials.gov |
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| NCT02496611Enhancing Weight Loss Maintenance With GLP-1RA (BYDUREON™) in Adolescents With Severe Obesity | Exenatide | Phase 2 | 100 | Body Mass Index (percentage (body mass index)), 52 weeks. Weight Loss Maintenance Without Pharmacotherapy: 10.1; Weight Loss Maintenance With Pharmacotherapy: 4.6. |
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| NCT04883346Liraglutide (Saxenda(R)) in Adolescents With Obesity After Sleeve Gastrectomy | Liraglutide | Phase 2 | 34 | On ClinicalTrials.gov |
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| NCT01237197Exenatide in Extreme Pediatric Obesity | Exenatide | Phase 2 | 26 | Percent Change From Baseline in Body Mass Index at 3-months (percentage of change in BMI), Baseline and 3-months. Exenatide: -2.9; Placebo Injection: -0.15. |
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| NCT02960659Title: Therapeutic Targets in African-American Youth With Type 2 Diabetes | Liraglutide | Phase 1/2 | 24 | Change in Absolute Gluconeogenesis From Baseline to 12 Weeks (mg/kg LBM/min), Baseline to 12 weeks. Metformin: 0.018; Metformin and Liraglutide: -0.050. |
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| NCT00886626GLP-1 Therapy for Weight Loss and Improved Glucose Tolerance in Obese Children | Exenatide | Phase 2 | 12 | Change in Body Mass Index (BMI) (change in kg/m^2), 3-month. Exenatide: -0.9; Control: 0.84. |
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| NCT05696847A Study of Tirzepatide (LY3298176) in Pediatric Participants With Obesity | Tirzepatide | Phase 1 | 28 | Percentage of Participants With One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) (Percentage of participants), Baseline through Week 14, TEAE. Cohort 1: Placebo (BW >=50 kg): 0.0; Cohort 1: 2.5-5 mg Tirzepatide (BW >=50 kg): 83.3; Cohort 2: Placebo (BW <50 kg): 0.0; Cohort 2: 1.25-2.5 mg Tirzepatide (BW <50 kg): 85.7; Cohort 3: Placebo (BW 40 to 60 kg): 33.3; Cohort 3: 2.5-5 mg Tirzepatide (BW 40 to 60 kg): 100.0. |
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| NCT01444898Effects of Exenatide on Overweight Adolescents With Prader-Willi Syndrome | Exenatide | Not phased | 10 | On ClinicalTrials.gov |
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