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Active, not recruiting Phase 3 Interventional

A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight

ClinicalTrials.gov ID: NCT07232719

Public ClinicalTrials.gov record NCT07232719. 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 Jun 25, 2026, 9:39 PM EDT

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

Official title

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

Study identification

NCT ID
NCT07232719
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
250 participants

Conditions and interventions

Interventions

  • Retatrutide Drug
  • Placebo Drug

Drug

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
Nov 16, 2025
Primary completion
Jun 30, 2027
Completion
Jun 30, 2027
Last update posted
Apr 16, 2026

2025 – 2027

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Artemis Institute for Clinical Research Riverside California 92503
JEM Research Institute Atlantis Florida 33462
Headlands Research Orlando Orlando Florida 32806
Care Access - Tamarac Tamarac Florida 33321
Care Access - Arlington Heights Arlington Heights Illinois 60005
L-MARC Research Center Louisville Kentucky 40213
IMA Clinical Research Monroe - Armand Monroe Louisiana 71201
Pharmasite Research, Inc. Baltimore Maryland 21208
Clinical Research Professionals Chesterfield Missouri 63005
Clinvest Headlands Llc Springfield Missouri 65807
IMA Clinical Research Warren Warren Township New Jersey 07059
IMA Clinical Research Manhattan New York New York 10036
Trial Management Associates - Wilmington - Floral Parkway Wilmington North Carolina 28403
Cedar Health Research Dallas Texas 75251
Headlands Research-El Paso El Paso Texas 79902
Cedar Health Research - Euless Euless Texas 76040
Cedar Health Research - Fort Worth Fort Worth Texas 76132
Care Access - Houston Houston Texas 77054
IMA Clinical Research San Antonio San Antonio Texas 78229

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07232719, 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 16, 2026 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07232719 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →