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临床试验/2025-523769-11-00
2025-523769-11-00招募中3 期

J3R-MC-YDAO - A Master Protocol for Phase 3 Randomized, Double-Blind, Placebo-Controlled Studies to Investigate the Efficacy and Safety of Once Weekly Eloralintide in Adult Participants With Moderate to Severe Obstructive Sleep Apnea, and Obesity or Overweight (ENLIGHTEN-3) Intervention-Specific Appendices (ISAs): J3R-MC-YSA1: Participants unable or unwilling to use positive airway pressure therapy J3R-MC-YSA2: Participants treated with positive airway pressure therapy

Eli Lilly & Co.17 个研究点 分布在 2 个国家目标入组 169 人开始时间: 2026年4月21日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
169
试验地点
17
主要终点
Percent Change from Baseline in Body Weight

研究概览

简要总结

To demonstrate that eloralintide is superior to placebo for change in body weight and apnea-hypopnea index.

入排标准

年龄范围
18 years 至 65+ years(65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • Have a confirmed history of moderate-to-severe obstructive sleep apnea (OSA)
  • Have a stable body weight (<5% body weight change) for 90 days prior to screening
  • Have an Apnea-Hypopnea Index (AHI) ≥ 15 on polysomnography (PSG) as part of the study at screening
  • For YSA1 participants: be unable or unwilling to use positive airway pressure (PAP) therapy
  • For YSA2 participants: have been on PAP therapy for at least three consecutive months prior to screening and plan to continue PAP therapy during the study

排除标准

  • Have had or are planning to have surgery, an endoscopic procedure, and/or devicebased therapy for weight loss (with exceptions)
  • Have had or are planning to have surgery for sleep apnea or major ear, nose, or throat surgery that still may affect breathing at the time of screening
  • Have type 1 diabetes, type 2 diabetes, or any other type of diabetes
  • Have had a serious heart condition within 90 days prior to screening
  • Have taken medications or alternative remedies intended for weight loss within 90 days prior to screening

研究组 & 干预措施

Placebo to match LY

Placebo

干预措施: Placebo to match LY (Drug)

Eloralintide, Eloralintide, Eloralintide, Eloralintide

Test

干预措施: Eloralintide (Drug)

结局指标

主要结局

Percent Change from Baseline in Body Weight

Percent Change from Baseline in Body Weight

次要结局

未报告次要终点

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Lilly Clinical Trials information desk

Scientific

Eli Lilly & Co.

研究点 (17)

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