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临床试验/NCT07215559
NCT07215559招募中2 期

A Phase 2, Parallel-Group, Double-Blind, Placebo-Controlled Study to Investigate Weight Reduction With Macupatide and Eloralintide, Alone or in Combination, in Adult Participants With Obesity or Overweight and With Type 2 Diabetes

Eli Lilly and Company74 个研究点 分布在 4 个国家目标入组 200 人开始时间: 2025年10月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
200
试验地点
74
主要终点
Percent Change from Baseline in Body Weight

研究概览

简要总结

The purpose of this study is to investigate weight reduction with macupatide and eloralintide, alone or in combination, in adult participants with obesity or overweight and with type 2 diabetes. Participation in the study will last about 48 weeks.

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
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have type 2 diabetes
  • Have an HbA1c ≥7.5% to ≤10.5% at screening
  • Have been treated with any of the following, alone or in combination, for at least 3 months prior to screening
  • Diet and exercise
  • Stable dose of metformin
  • Sodium-glucose cotransporter-2 (SGLT2) inhibitor
  • Have had a stable body weight (<5% body weight gain and/or loss) for the 3 months prior to screening
  • Have a BMI of 27 or greater at screening

排除标准

  • Have any form of diabetes other than type 2 diabetes
  • Have a prior or planned surgical treatment for obesity, except prior liposuction or abdominoplasty, if performed >1 year prior to screening
  • Have any of the following cardiovascular conditions within 3 months prior to screening:
  • acute myocardial infarction
  • cerebrovascular accident (stroke)
  • unstable angina, or
  • hospitalization due to congestive heart failure
  • Have a history of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years, exceptions include
  • basal or squamous cell skin cancer
  • in situ carcinomas of the cervix, or
  • in situ prostate cancer
  • Have been prescribed any of the following receptor agonists (RA) or their combination for any indication within the last 6 months:
  • amylin RA
  • dual amylin and calcitonin RA
  • glucagon-like peptide-1 receptor (GLP-1) RA
  • glucose-dependent insulinotropic peptide (GIP)/GLP-1 RA
  • GLP-1/glucagon (GCG) RAs, or
  • GIP/GLP-1/GCG RAs
  • Have used excluded antihyperglycemic medications within 3 months prior to screening (including, but not limited to, sulfonylureas, dipeptidyl peptidase-4 inhibitors, alpha-glucosidase inhibitors, thiazolidinediones, and meglitinides
  • Have used insulin for diabetic control within the prior year (short term use in certain situations allowed

研究组 & 干预措施

Placebo (Macupatide Placebo + Elorlintide Placebo)

Placebo Comparator

Participants will be administered eloralintide placebo SC and macupatide placebo SC

干预措施: Macupatide Placebo (Drug)

Placebo (Macupatide Placebo + Elorlintide Placebo)

Placebo Comparator

Participants will be administered eloralintide placebo SC and macupatide placebo SC

干预措施: Eloralintide Placebo (Drug)

Macupatide + Eloralintide

Experimental

Participants will be administered eloralintide SC and macupatide SC

干预措施: Eloralintide (Drug)

Macupatide + Eloralintide

Experimental

Participants will be administered eloralintide SC and macupatide SC

干预措施: Macupatide (Drug)

Eloralintide (Elorlintide + Macupatide Placebo)

Experimental

Participants will be administered eloralintide SC and macupatide placebo SC

干预措施: Eloralintide (Drug)

Macupatide (Macupatide + Eloralintide Placebo)

Experimental

Participants will be administered macupatide subcutaneously (SC) and eloralintide placebo SC

干预措施: Eloralintide Placebo (Drug)

Eloralintide (Elorlintide + Macupatide Placebo)

Experimental

Participants will be administered eloralintide SC and macupatide placebo SC

干预措施: Macupatide Placebo (Drug)

Macupatide (Macupatide + Eloralintide Placebo)

Experimental

Participants will be administered macupatide subcutaneously (SC) and eloralintide placebo SC

干预措施: Macupatide (Drug)

结局指标

主要结局

Percent Change from Baseline in Body Weight

时间窗: Baseline, Week 32

次要结局

  • Change from Baseline in Hemoglobin A1c (HbA1c)(Baseline, Week 32)
  • Change from Baseline in Body Mass Index (BMI)(Baseline, Week 32)
  • Change from Baseline in Fasting Glucose(Baseline, Week 32)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (74)

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