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NCT07357415Active, not recruitingPhase 3

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

A Phase 3b Study to Investigate the Efficacy and Safety of Different Retatrutide Dose Escalation Schemes in Participants Without Type 2 Diabetes Who Have Obesity or Overweight: A Randomized, Controlled, Double-Blind Trial

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
600 (estimated)
First submitted
16 Jan 2026
Start date
24 Jan 2026
Primary completion date
Oct 2028
Lead sponsor
Eli Lilly and Company
NCT number
NCT07357415

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 600
  • From 24 Jan 2026 to the primary completion date, Oct 2028
  • 35 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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 had within the past 90 days before screening:
    • heart attack
    • stroke
    • hospitalization for unstable angina or heart failure
  • Have taken weight loss drugs, including over-the counter medications within 90 days prior to screening

Other illness

  • 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 New York Heart Association Functional Classification Class IV congestive heart failure
  • Have a history of chronic or acute pancreatitis

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (35)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cicemo Srl
Coordinator of this site? Confirm its status
Buenos AiresArgentinaUnknown status
Stat Research S.A.
Coordinator of this site? Confirm its status
Buenos AiresArgentinaUnknown status
Centro de Investigaciones Metabólicas (CINME)
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Buenos AiresArgentinaUnknown status
CARDIAMET Investigaciones Médicas
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Buenos AiresArgentinaUnknown status
Centro Médico Viamonte
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Buenos AiresArgentinaUnknown status
Aggarwal and Associates Limited
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BramptonCanadaUnknown status
Med Trust Research
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CourticeCanadaUnknown status
Winterberry Research Inc.
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HamiltonCanadaUnknown status
Diex Recherche Inc. Division Joliette
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JolietteCanadaUnknown status
Milestone Research Inc.
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LondonCanadaUnknown status
Diex Recherche Inc. Division Quebec
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QuébecCanadaUnknown status
Diex Recherche Inc. Division Sherbrooke
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SherbrookeCanadaUnknown status
Canadian Phase Onward
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TorontoCanadaUnknown status
Dr. Anil K. Gupta Medicine Professional Corporation
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TorontoCanadaUnknown status
C.I.C. Mauricie inc.
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Trois-RivièresCanadaUnknown status
Great Lakes Research Group, Inc.
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Bay CityUnited StatesUnknown status
Brigham and Women's Hospital Diabetes Program
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BostonUnited StatesUnknown status
CAMC Institute for Academic Medicine
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CharlestonUnited StatesUnknown status
Cedar Health Research
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DallasUnited StatesUnknown status
Velocity Clinical Research, Dallas
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DallasUnited StatesUnknown status
Cedar Health Research - Texas Native Health
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DallasUnited StatesUnknown status
Cedar Health Research - Fort Worth
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Fort WorthUnited StatesUnknown status
Pacific Diabetes & Endocrine Center
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HonoluluUnited StatesUnknown status
Care Access - Huntington Beach
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Huntington BeachUnited StatesUnknown status
New Phase Research And Development
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KnoxvilleUnited StatesUnknown status
NYC Research Inc.
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Long Island CityUnited StatesUnknown status
Los Angeles Institute for Metabolic Research
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Los AngelesUnited StatesUnknown status
Monroe Biomedical Research - Louisville
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LouisvilleUnited StatesUnknown status
New Horizon Research Center
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MiamiUnited StatesUnknown status
Weill Cornell Medical College
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New YorkUnited StatesUnknown status
Advanced Research Institute
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OgdenUnited StatesUnknown status
Arizona Research Center
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PhoenixUnited StatesUnknown status
Care Access - Raleigh
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RaleighUnited StatesUnknown status
Dominion Medical Associates, Inc.
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RichmondUnited StatesUnknown status
Encore Medical Research - Weston
Coordinator of this site? Confirm its status
WestonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.