跳至主要内容
临床试验/jRCT2051250035
jRCT2051250035尚未招募不适用

A Master Protocol to Investigate the Efficacy and Safety of Orforglipron Tablet Once Daily Compared With Placebo in Participants With Obesity or Overweight With and Without Type 2 Diabetes J2A-MC-GZP2: Participants With Obesity or Overweight and Type 2 Diabetes (J2A-MC-GZP2 )

Eli Lilly Japan K.K.0 个研究点目标入组 600 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
600
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Double Blind

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • Have body mass index (BMI) >=25 kilograms per square meter (kg/m2) at screening
  • Have type 2 diabetes
  • Have hemoglobin A1c (HbA1c) >=7% and <=10% at screening
  • Have a history of at least one unsuccessful dietary effort to lose body weight

排除标准

  • Have type 1 diabetes
  • Have an unstable body weight within 90 days prior to screening
  • Have New York Heart Association functional classification IV congestive heart failure or an acute cardiovascular condition within 90 days prior to screening
  • Have acute or chronic hepatitis or pancreatitis
  • Are taking other medications or alternative remedies to manage weight loss

结局指标

主要结局

-

Change from Baseline in Hemoglobin A1c (HbA1c) [ Time Frame: Baseline, Week 40

次要结局

未报告次要终点

研究者

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