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A Study of Eloralintide (LY3841136) in Participants With Obstructive Sleep Apnea and Obesity or Overweight

RecruitingPhase 3

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

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Confirmed history of moderate-to-severe OSA
* Have an AHI ≥ 15 on polysomnography (PSG) as part of the study at screening
* Have a BMI ≥27 kg/m2 at screening
* Have a stable body weight (\<5% body weight change) for 90 days prior to screening
* Have a history of at least one self-reported unsuccessful dietary effort to reduce body weight

For YSA1 Participants:

* Are unable or unwilling to use 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

Exclusion Criteria:

* Have a prior or planned surgical treatment for obesity (liposuction, cryolipolysis, or abdominoplasty allowed if performed \>1 year before screening)
* Have a prior or planned endoscopic procedure and/or device-based therapy for obesity (prior device-based therapy acceptable if device removal was more than 6 months prior to screening)
* Any previous or planned surgery for sleep apnea or major ear, nose or throat surgery that still may affect breathing at time of screening
* Have type 1 diabetes, type 2 diabetes, or any other type of diabetes
* Have had within 90 days prior to screening:

  * acute myocardial infarction
  * cerebrovascular accident (stroke)
  * coronary artery revascularization
  * unstable angina, or
  * hospitalization due to congestive heart failure
* Have a history or diagnosis of New York Heart Association Functional Classification Class IV congestive heart failure
* Have taken medications or alternative remedies intended for weight loss within 90 days of screening

About the study

The purpose of the studies is to evaluate the efficacy and safety of eloralintide in participants with moderate-to-severe obstructive sleep apnea and obesity or overweight. YDAO is a master protocol designed to support two independent studies: YSA1 and YSA2. Study YSA1 will include participants who are unable or unwilling to use Positive Airway Pressure (PAP) therapy and study YSA2 will include participants who are on PAP therapy for at least 3 months at time of screening and plan to continue PAP therapy during the study.

Participants will be assigned to the Intervention-Specific Appendix (ISA) that reflects their current PAP usage. Participation in the study will last about 76 weeks.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 800 · Started: Feb 10, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07369011

Locations in the U.S.

AlabamaCullman Clinical Trials, Cullman
CaliforniaArk Clinical Research, Long Beach
Collaborative Neuroscience Research, LLC, Los Alamitos
Artemis Institute for Clinical Research, Riverside
ColoradoCare Access - Aurora, Aurora
FloridaFlourish Research - Miami, LLC, Miami
PharmaDev Clinical Research Institute, LLC, Miami
Emerald Coast Neurology - Airport Boulevard, Pensacola
GeorgiaTeak Research Consults, Lawrenceville
EBGS Clinical Research Center, Snellville
LouisianaCare Access - Shreveport 2, Shreveport
MarylandFlourish Research - Bowie, Bowie
MichiganRevive Research Institute, Inc., Southfield
MinnesotaHeadlands Research-Twin Cities, Maplewood
MissouriClayton Sleep Institute - St. Louis - Tesson Ferry Road, St Louis
NevadaPalm Research Center Tenaya, Las Vegas
New MexicoThe Sleep Spot - Maimonides, Albuquerque
New YorkRochester Clinical Research - Buffalo, Buffalo
OhioCTI Clinical Research Center, Cincinnati
South CarolinaBogan Sleep Consultants, Columbia
TexasFutureSearch Trials of Neurology, Austin
Sleep Therapy Research Center, San Antonio
Consano Clinical Research, LLC, Shavano Park

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.