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Completed Phase 3 Interventional Results available

Obstructive Sleep Apnea Master Protocol GPIF: A Study of Tirzepatide (LY3298176) in Participants With Obstructive Sleep Apnea

ClinicalTrials.gov ID: NCT05412004

Public ClinicalTrials.gov record NCT05412004. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 1, 2026, 8:26 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Master Protocol to Investigate the Efficacy and Safety of Tirzepatide Once Weekly in Participants Who Have Obstructive Sleep Apnea and Obesity: A Randomized, Double-Blind, Placebo-Controlled Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the effect and safety of tirzepatide in participants with moderate to severe obstructive sleep apnea and obesity who are both unwilling or unable to use Positive Airway Pressure (PAP) therapy in GPI1 and those who are and plan to stay on PAP therapy in GPI2.

Study identification

NCT ID
NCT05412004
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
469 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 21, 2022 (Actual)
Primary completion
Mar 12, 2024 (Actual)
Completion
Mar 29, 2024 (Actual)
Last update posted
Apr 30, 2025

2022 – 2024

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
Artemis Institute for Clinical Research Riverside California 92503 —
Teradan Clinical Trials, LLC Brandon Florida 33511 —
Renstar Medical Research Ocala Florida 34470 —
Palm Beach Research Center West Palm Beach Florida 33409 —
NeuroTrials Research Inc Atlanta Georgia 30328 —
Rocky Mountain Clinical Research Idaho Falls Idaho 83404 —
Brengle Family Medicine Indianapolis Indiana 46260 —
Lillestol Research Fargo North Dakota 58104 —
NeuroScience Research Center Canton Ohio 44718 —
CTI-CRC Cincinnati Ohio 45212 —
Office 18 Pittsburgh Pennsylvania 15236 —
Preferred Primary Care Physicians Uniontown Pennsylvania 15401 —
FutureSearch Trials of Neurology Austin Texas 78731 —
Gadolin Research Beaumont Texas 77702 —
Advanced Neuro Research Center - ANRC El Paso Texas 79912 —
Epic Medical Research Red Oak Texas 75154 —
Sleep Therapy Research Center San Antonio Texas 78229 —
Rainier Clinical Research Center Renton Washington 98057 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05412004, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 30, 2025 · Synced Nov 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05412004 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →