A Study of LY4174794 in Participants With Obesity or Overweight Who Are Otherwise Healthy
A Phase 1, Randomized, Placebo-Controlled, Single- and Multiple-Ascending Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY4174794 in Participants With Obesity or Overweight Who Are Otherwise Healthy
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years to 65 Years
- Sex
- All sexes
- Healthy volunteers
- Accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: Blood draws
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Blood tests will be performed to check how much LY4174794 gets into the bloodstream and how long it takes the body to eliminate it."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests how safe LY4174794 is and how well people with overweight or obesity who are otherwise healthy can tolerate it. Blood tests will measure how much of the drug enters the blood and how long the body takes to clear it. The study lasts about 7 to 10 months.
The main purpose of this study is to understand how safe and well-tolerated LY4174794 is in participants with obesity or overweight who are otherwise healthy. Blood tests will be performed to check how much LY4174794 gets into the bloodstream and how long it takes the body to eliminate it. Participation in this study will last about 30 to 39 weeks (7 to 10 months).
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Are otherwise healthy, with no weight-related health problems, such as type 2 diabetes or unstable heart or blood vessel disease.
- Have a BMI of 27 or higher. BMI is a measure based on height and weight.
- Report that your weight has stayed stable for 3 months before screening.
Who can't join
- Have or have had a heart, lung, liver, kidney, digestive, hormone, blood, or nervous system disorder that could affect how your body handles drugs, make the study drug unsafe, or affect how study results are understood.
- Are able to become pregnant.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Are overtly healthy with no comorbidities related to body mass index (BMI), such as type 2 diabetes mellitus or unstable cardiovascular disease * Are overweight with a BMI of ≥27 kilogram per meter square (kg/m²), or have obesity with a BMI of ≥30 kg/ m² * Have had a self-reported stable weight for 3 months prior to screening Exclusion Criteria: * Have a history or presence of cardiovascular, respiratory, hepatic, renal, GI, endocrine, hematological, or neurological disorders capable of significantly altering the absorption, metabolism, or elimination of drugs, or of constituting a risk when taking the study intervention, or of interfering with the interpretation of data * Is an individual of childbearing potential (IOCBP)
Study sites (2)
TX
- ICON Early Phase Services, LLC · San Antonio, TX 78232 · Study contact · (210) 225-5437Cassandra Key · Principal investigatorMore trials in San Antonio
UT
- ICON Early Phase Services, LLC · Salt Lake City, UT 84124 · Study contact · 801-261-3341Ahad Sabet · Principal investigatorMore trials in Salt Lake City