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Clinical Trial ● Currently Recruiting Phase III NCT07232719

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

A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight — Recruiting • Phase III • Oncology • NCT07232719.

📅 25 Mar 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07232719
Sponsor
Eli Lilly and Company
Start
2025-11-17
ClinicaliQ Trial Snapshot
  • A Study of Retatrutide (LY3437943) in Participants With Obesity or Overweight — Recruiting • Phase III • Oncology • NCT07232719.
  • The purpose of this study is to evaluate the efficacy and safety of retatrutide compared with placebo for body weight reduction. Participation in the study will last about 65 weeks and may include about 18 visits. Lead.
  • Sponsor: Eli Lilly and Company.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

The purpose of this study is to evaluate the efficacy and safety of retatrutide compared with placebo for body weight reduction. Participation in the study will last about 65 weeks and may include about 18 visits. Lead Sponsor: Eli Lilly and Company Start Date: 2025-11-17 Primary Completion: 2027-07

Eligibility Snapshot
  • : * Have a body mass index (BMI) of: * ≥30 kilogram per square meter (kg/m2) OR * ≥27 kg/m2 with at least one of the following weight-related conditions: high blood pressure, abnormal levels of lipid, obstructive sleep apnea, heart disease * Have at least one unsuccessful attempt to lose weight by dieting

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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