A Study of LY4086940 in Healthy Participants and Participants With Overweight or Obesity, With or Without Type 2 Diabetes
Running, not enrolling · Phase 1 · Has a placebo group
Conditions studied: Healthy, Overweight, Obesity, Type 2 Diabetes
In brief
The main purpose of this study is to evaluate the safety, tolerability of LY4086940 and how it is processed in the body. Participation in Part A of the study will last about 10 weeks and may include up to 6 visits. Participation in Parts B, C, D will last approximately 15 weeks and may include up to 10 visits. Participation in Part E will last approximately 7 weeks and may include up to 12 visits.
Key facts
- Study ID
- NCT06945419
- Run by
- Eli Lilly and Company
- People needed
- 216
- Starts
- 2025-04-23
- Expected to finish
- 2026-08-01
- Last updated by the study team
- 2026-06-16
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Have no significant body weight change for the 3 months prior to screening
- Part A and Part E:
- Are considered healthy
- Have a body mass index (BMI) of 22 to 35 kilograms per square meter (kg/m2) at screening
- Part B:
- Have a BMI of 27 to 45 kg/m2 at screening
- Part C:
- Have a BMI of 25 to 45 kg/m2 at screening
- Part D:
- Have type 2 diabetes
- Have hemoglobin A1C (HbA1c) ≥6.5% and ≤10.5% at screening
- Have a BMI of 27 to 45 kg/m2 at screening
You may not qualify if…
- Have had an acute cardiovascular condition within the past 6 months prior to screening
- Have liver disease or pancreatitis
- Have used medications for weight loss within the 3 months prior to screening
- Parts A, B, C, E:
- Have any form of diabetes
- Part D:
- Have type 1 diabetes
Where it is running
- Fortrea Clinical Research Unit — Daytona Beach, Florida, United States
- Clinical Pharmacology of Miami — Miami, Florida, United States
- Fortrea Clinical Research Unit — Dallas, Texas, United States
- Endeavor Clinical Trials — San Antonio, Texas, United States
- Lilly Centre for Clinical Pharmacology — Singapore, Singapore
Full record on ClinicalTrials.gov
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