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临床试验/NCT06260722
NCT06260722进行中(未招募)3 期

A Phase 3, Randomized, Multicenter, Open-label Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly Compared With Semaglutide Once Weekly in Adult Participants With Type 2 Diabetes and Inadequate Glycemic Control With Metformin With or Without SGLT2 Inhibitor (TRANSCEND-T2D-2)

Eli Lilly and Company148 个研究点 分布在 2 个国家目标入组 1,250 人开始时间: 2024年2月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
1,250
试验地点
148
主要终点
Change from Baseline in Hemoglobin A1c (HbA1c) (%)

研究概览

简要总结

The purpose of this study is to investigate the efficacy and safety of retatrutide compared with semaglutide in participants with Type 2 Diabetes and inadequate glycemic control with metformin with or without sodium-glucose cotransporter-2 inhibitor (SGLT2i). The study will last about 26 months and may include up to 24 visits.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have Type 2 Diabetes (T2D)
  • Have HbA1c ≥ 7.0% (53 millimoles per mole (mmol/mol)) to ≤ 10.5% (91 mmol/mol)
  • Have been on a stable diabetes treatment consisting of metformin ≥ 1500 milligrams per day (mg/day) with or without SGLT2i during 90 days prior to screening
  • Are of stable weight for at least 90 days prior to screening
  • Have a Body Mass Index (BMI) ≥ 25.0 kilograms per meter squared (kg/m^2)

排除标准

  • Have Type 1 Diabetes (T1D)
  • Have a history of ketoacidosis or hyperosmolar state or coma within the last 6 months prior to screening
  • Have a history of severe hypoglycemia or hypoglycemia unawareness within the last 6 months prior to screening
  • Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema
  • Have an estimated glomerular filtration rate (eGFR) <45 milliliters/minute/1.73 meter squared (mL/min/1.73 m^2) or lower than the country-specific threshold for discontinuing metformin therapy per local label as determined by the central laboratory
  • Have a prior or planned surgical treatment for obesity
  • Have New York Heart Association Functional Classification IV congestive heart failure
  • Have had an acute myocardial infarction, stroke, or were hospitalized for congestive heart failure within 90 days prior to screening
  • Have a known clinically significant gastric emptying abnormality
  • Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years
  • Have any lifetime history of a suicide attempt
  • Had chronic or acute pancreatitis
  • Have a family or personal history of medullary thyroid carcinoma or multiple endocrine neoplasia (MEN) syndrome Type 2
  • Have taken prescribed or over-the-counter medication, or alternative remedies, intended to promote body weight reduction within 90 days prior to screening.

研究组 & 干预措施

Retatrutide Dose Level 2

Experimental

Participants will receive retatrutide administered SC.

干预措施: Retatrutide (Drug)

Retatrutide Dose Level 1

Experimental

Participants will receive retatrutide administered subcutaneously (SC).

干预措施: Retatrutide (Drug)

Semaglutide

Active Comparator

Participants will receive semaglutide administered SC.

干预措施: Semaglutide (Drug)

结局指标

主要结局

Change from Baseline in Hemoglobin A1c (HbA1c) (%)

时间窗: Baseline, Week 80

次要结局

  • Percentage of Participants Who Achieve HbA1c < 5.7%(Week 80)
  • Percent Change from Baseline in Body Weight(Week 80)
  • Change from Baseline in Body Weight(Baseline, Week 80)
  • Percentage of Participants Who Achieve Weight Reduction of ≥ 5%(Week 80)
  • Percentage of Participants Who Achieve Weight Reduction of ≥ 10%(Week 80)
  • Percentage of Participants Who Achieve Weight Reduction of ≥ 15%(Week 80)
  • Change from Baseline in HbA1c (%)(Baseline, Week 80)
  • Percentage of Participants Who Achieve HbA1c ≤ 6.5%(Week 80)
  • Percentage of Participants Who Achieve HbA1c ≤ 6.5% and ≥ 10% Weight Reduction(Week 80)
  • Percent Change from Baseline in Triglycerides(Week 80)
  • Percent Change from Baseline in Non- high-density lipoprotein (HDL) Cholesterol(Week 80)
  • Change from Baseline in Systolic Blood Pressure (SBP)(Baseline, Week 80)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (148)

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