A Research Study Looking at Similarity Between LY3437943 Versions for Different Injection Devices

Completed · Phase 1

Conditions studied: Healthy

In brief

The main purpose of this study is to look at the amount of the study drug, LY3437943, that gets into the blood stream and how long it takes the body to get rid of it when given using two different devices. The study will also evaluate the safety and tolerability of LY3437943 and information about any side effects experienced will be collected. For each participant, the total duration of the study will be approximately 16 weeks, including screening.

Key facts

Study ID

NCT06003465

Run by

Eli Lilly and Company

People needed

57

Starts

2023-08-29

Expected to finish

2024-02-08

Last updated by the study team

2024-03-29

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Healthy males or non-pregnant females as determined by medical history, physical examination, and other screening procedures
• Body mass index (BMI) between 18.5 and 32.0 kilograms per meter squared (kg/m²), inclusive
• Have clinical laboratory test results, blood pressure and pulse rate that are acceptable for the study
• Are agreeable to receiving study treatment by injections under the skin
• Males who agree to use highly effective/effective methods of contraception and women not of childbearing potential (postmenopausal or oophorectomized)

You may not qualify if…

• Have or used to have health problems that, in the opinion of the doctor, could make it unsafe to participate, or could interfere with understanding the results of the study
• Smoke more than the equivalent of 10 cigarettes per day
• Is a known user of drugs of abuse
• Have known allergies to LY3437943 or related compounds

Where it is running

• Qps-Mra, Llc — Miami, Florida, United States
• ICON Early Phase Services — San Antonio, Texas, United States
• ICON — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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