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临床试验/NCT07255209
NCT07255209招募中3 期

A Randomized, Double-blind, Placebo-controlled Phase 3 Clinical Trial to Assess the Efficacy and Safety of IBI362 in Chinese Adolescents With Obesity or Overweight(GLORY-YOUNG)

Innovent Biologics (Suzhou) Co. Ltd.1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2025年12月29日最近更新:
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
180
试验地点
1
主要终点
Percent Change from Baseline in BMI

研究概览

简要总结

The study is designed to assess the efficacy and safety of multiple doses of IBI362 in Chinese adolescent subjects with obesity or overweight. It plans to enroll 180 adolescents (aged ≥12 and <18 years) who have failed to achieve a 5 kg weight reduction after at least 12 weeks of dietary and exercise intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • Participants must meet all of the following inclusion criteria to be enrolled:
  • Key Inclusion Criteria:
  • Male or female participants aged ≥12 years and <18 years at the time of signing the informed consent/assent form.
  • BMI at screening meeting the obesity criteria defined by "WS/T 586-2018 Screening for Overweight and Obesity in School-Age Children and Adolescents" or meeting overweight criteria plus at least one weight-related comorbidity: prediabetes, type 2 diabetes, hypertension, dyslipidemia, fatty liver disease, or obstructive sleep apnea syndrome.
  • Weight change <5 kg after ≥12 weeks of diet and exercise alone before screening (per self/parental report).

排除标准

  • Prior diagnosis of type 1 diabetes.
  • Pre-pubertal participants (Tanner Stage I).
  • History of (or planned) bariatric surgery (except liposuction/abdominoplasty or acupuncture for weight loss performed >1 year before screening).

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

IBI362-dose2

Experimental

干预措施: IBI362 (Drug)

IBI362-dose1

Experimental

干预措施: IBI362 (Drug)

结局指标

主要结局

Percent Change from Baseline in BMI

时间窗: Week 32

次要结局

  • Percentage of Participants with ≥5% BMI Reduction(Week 32)
  • Percentage of Participants with ≥5% BMI Reduction(Week 52)
  • Percent Change from Baseline in BMI(Week 52)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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