Current partner codePEPTIDESDE
NCT07357415·Phase 3·INTERVENTIONAL

A Study of Retatrutide (LY3437943) in Participants Without Type 2 Diabetes Who Have Obesity or Overweight

Status

Active, not recruiting

Phase

Phase 3

Enrollment

600

Locations

35

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The purpose of this study is to investigate the efficacy and safety of different retatrutide dose escalation schemes in participants without type 2 diabetes who have obesity or overweight. Participation in the study will last about 113 weeks.

Interventions

Treatment arms and agents.

DRUG

Retatrutide

Administered SC

Timeline

From registration to results.

  1. First posted

    Jan 22, 2026

  2. Study start

    Jan 24, 2026

  3. Primary completion

    Oct 2028

  4. Study completion

    Nov 2028

  5. Results posted

    Not reported

  6. Registry updated

    Jun 9, 2026

Outcomes

What the study measures.

Primary outcomes

Percent Change from Baseline in Body Weight

Time frame · Baseline, Week 104

Secondary outcomes

Change from Baseline in Waist Circumference

Time frame · Baseline, Week 104

Percent Change from Baseline in Triglycerides

Time frame · Baseline, Week 104

Change from Baseline in Systolic Blood Pressure

Time frame · Baseline, Week 104

Percent Change from Baseline in High Sensitivity C-Reactive Protein

Time frame · Baseline, Week 104

Change from Baseline in Impact of Weight on Quality of Life-Lite-Clinical Trials (IWQOL-Lite-CT) Total Score

Time frame · Baseline, Week 104

Overall Treatment Satisfaction with Medication for Obesity (TS-MO) Scores

Time frame · Week 104

Pharmacokinetics (PK): Steady state Average Trough PK Concentration

Time frame · Baseline through Week 104

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Have a Body Mass Index (BMI) at screening * ≥ 30 kilogram per square meter (kg/m2) OR * ≥ 27 kg/m2 with presence of at least one of the following weight-related conditions at screening: high blood pressure, abnormal levels of lipid, obstructive sleep apnea, heart disease * Have at least one unsuccessful attempt to lose weight by dieting Exclusion Criteria: * Have a self-reported change in body weight \>5 kilograms (kg) (11 pounds) within 90 days before screening * Have a prior or planned surgical treatment for obesity * Have type 1 diabetes or type 2 diabetes * Have a family or personal history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN-2) * Have had within the past 90 days before screening: * heart attack * stroke * hospitalization for unstable angina or heart failure * Have New York Heart Association Functional Classification Class IV congestive heart failure * Have a history of chronic or acute pancreatitis * Have taken weight loss drugs, including over-the counter medications within 90 days prior to screening

Study locations

35 registered sites.

Argentina · Canada · United States. Showing up to 24 locations stored in the fast local snapshot.

Arizona Research Center

Phoenix, Arizona, United States

Care Access - Huntington Beach

Huntington Beach, California, United States

Los Angeles Institute for Metabolic Research

Los Angeles, California, United States

New Horizon Research Center

Miami, Florida, United States

Encore Medical Research - Weston

Weston, Florida, United States

Pacific Diabetes & Endocrine Center

Honolulu, Hawaii, United States

Monroe Biomedical Research - Louisville

Louisville, Kentucky, United States

Brigham and Women's Hospital Diabetes Program

Boston, Massachusetts, United States

Great Lakes Research Group, Inc.

Bay City, Michigan, United States

NYC Research INC

Long Island City, New York, United States

Weill Cornell Medical College

New York, New York, United States

Care Access - Raleigh

Raleigh, North Carolina, United States

New Phase Research and Development

Knoxville, Tennessee, United States

Velocity Clinical Research, Dallas

Dallas, Texas, United States

Cedar Health Research - Texas Native Health

Dallas, Texas, United States

Cedar Health Research

Dallas, Texas, United States

Cedar Health Research - Fort Worth

Fort Worth, Texas, United States

Advanced Research Institute

Ogden, Utah, United States

Dominion Medical Associates, Inc.

Richmond, Virginia, United States

CAMC Institute for Academic Medicine

Charleston, West Virginia, United States

Cicemo Srl

Buenos Aires, Argentina

CARDIAMET Investigaciones Médicas

Buenos Aires, Argentina

Stat Research S.A.

Buenos Aires, Argentina

Centro de Investigaciones Metabólicas (CINME)

Buenos Aires, Argentina

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Retatrutide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.