← Back to Search

GLP-1 Receptor Agonist

Retatrutide for Type 2 Diabetes and Obesity (TRIUMPH-2 Trial)

Verified Trial
Phase 3
Recruiting
Research Sponsored by Eli Lilly and Company
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Have a body mass index (BMI) greater than or equal to 27.0 kilogram/square meter (kg/m ²)
Have Type 2 Diabetes (T2D)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 80
Awards & highlights
Pivotal Trial

Summary

This trial is testing retatrutide, a medication for people with type 2 diabetes who are overweight or obese, including some with sleep apnea. The medication aims to help control blood sugar levels and may also aid in weight loss.

Who is the study for?
This trial is for adults with Type 2 Diabetes and a BMI of at least 27, who have tried to lose weight unsuccessfully. Participants may also have moderate-to-severe obstructive sleep apnea (OSA) but should not be on certain OSA treatments or recent weight loss drugs. They mustn't have had significant weight changes recently or any history of specific thyroid cancers.
What is being tested?
The study tests the effectiveness and safety of Retatrutide in people with Type 2 Diabetes who are overweight or obese, including some with OSA. It's an approximately 89-week study involving up to 24 visits, comparing Retatrutide against a placebo.
What are the potential side effects?
While the side effects for Retatrutide aren't specified here, common side effects for diabetes medications can include nausea, vomiting, digestive issues, potential low blood sugar events, and sometimes injection site reactions.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
You have a body mass index (BMI) of 27.0 or higher.
Select...
I have Type 2 Diabetes.
Select...
I have been on a stable treatment for type 2 diabetes for at least 3 months.
Select...
I have been diagnosed with obstructive sleep apnea.
Select...
You have a score of 15 or higher on a sleep test, which means you have moderate-to-severe obstructive sleep apnea.
Select...
I have used PAP therapy for 3 months and can stop it for 7 days before sleep studies.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 80
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 80 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change from Baseline in Apnea-Hypopnea Index (AHI) for GSA2 Subset
Percent Change from Baseline in Body Weight
Secondary study objectives
A Hierarchical Combination of Functional Outcomes of Sleep Questionnaire (FOSQ) 10 score, FOSQ Vigilance Domain Score, and FOSQ Activity Level Domain Score for GSA2 Subset
Change from Baseline in Body Mass Index (BMI)
Change from Baseline in Diastolic Blood Pressure (DBP)
+11 more

Awards & Highlights

Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.

Trial Design

4Treatment groups
Experimental Treatment
Placebo Group
Group I: Retatrutide Dose 3Experimental Treatment1 Intervention
Participants will receive retatrutide SC.
Group II: Retatrutide Dose 2Experimental Treatment1 Intervention
Participants will receive retatrutide SC.
Group III: Retatrutide Dose 1Experimental Treatment1 Intervention
Participants will receive retatrutide subcutaneously (SC).
Group IV: PlaceboPlacebo Group1 Intervention
Participants will receive placebo.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
GLP-1 receptor agonists, such as Retatrutide, are effective in treating obesity by enhancing insulin secretion, inhibiting glucagon release, and slowing gastric emptying, which together help regulate blood sugar levels and promote weight loss. Other treatments include orlistat, which reduces fat absorption in the intestines, and bariatric surgery, which restricts food intake and alters gut hormone levels. These mechanisms are important for obesity patients as they help customize treatment plans to individual metabolic profiles, thereby increasing the chances of successful weight management.

Find a Location

Who is running the clinical trial?

Eli Lilly and CompanyLead Sponsor
2,670 Previous Clinical Trials
3,227,769 Total Patients Enrolled
69 Trials studying Obesity
54,372 Patients Enrolled for Obesity
Study DirectorEli Lilly and Company
1,385 Previous Clinical Trials
425,391 Total Patients Enrolled
51 Trials studying Obesity
33,914 Patients Enrolled for Obesity

Media Library

Retatrutide (GLP-1 Receptor Agonist) Clinical Trial Eligibility Overview. Trial Name: NCT05929079 — Phase 3
Obesity Research Study Groups: Retatrutide Dose 1, Retatrutide Dose 2, Retatrutide Dose 3, Placebo
Obesity Clinical Trial 2023: Retatrutide Highlights & Side Effects. Trial Name: NCT05929079 — Phase 3
Retatrutide (GLP-1 Receptor Agonist) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05929079 — Phase 3
Obesity Patient Testimony for trial: Trial Name: NCT05929079 — Phase 3
~515 spots leftby May 2026