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NCT07654972RecruitingPhase 1

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

Source: ClinicalTrials.gov · Last updated 15 Oct 2026

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
116 (estimated)
First submitted
12 Jun 2026
Start date
24 Jun 2026
Primary completion date
Apr 2029
Lead sponsor
Eli Lilly and Company
Diseases
Obesity
NCT number
NCT07654972

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 116
  • From 24 Jun 2026 to the primary completion date, Apr 2029
  • 3 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Other

  • Is an individual of childbearing potential (IOCBP)

Who the study is looking for

  • 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

Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Lilly Centre for Clinical Pharmacology
Coordinator of this site? Confirm its status
SingaporeSingaporeNot yet recruiting
ICON Early Phase Services, LLC
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesNot yet recruiting
ICON Early Phase Services, LLC
Coordinator of this site? Confirm its status
San AntonioUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.