A Study of LY4086940 in Healthy Participants and Participants With Overweight or Obesity, With or Without Type 2 Diabetes

This is a registry record, not a result. A trial being listed, recruiting or completed says nothing by itself about whether the compound works or is safe.

Registry numberNCT06945419
StatusCompleted
PhasePhase 1
SponsorEli Lilly and Company
Enrollment219 participants
DesignInterventional, Randomized, Parallel, Masking: Double
ConditionsHealthy; Overweight; Obesity; Type 2 Diabetes
InterventionsLY4086940; Placebo; LY4086940
StartApr 23, 2025
Primary completionAug 5, 2026
Study completionAug 5, 2026
Results postedNot yet
Registry last updatedAug 19, 2026

Compounds on this site that cite this trial

What the registry says the trial is about

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.

Primary outcomes

These are what the trial was designed to measure first. They are registered in advance, which is what makes a later result checkable.

Outcome measureTime frame
Number of Participants with One or More Serious Adverse Events (SAE) Considered by the Investigator to be Related to Study Drug AdministrationBaseline up to Week 9

2 secondary outcomes also registered. See the registry record for the full list.

Source: ClinicalTrials.gov (U.S. National Library of Medicine). Last checked against the registry on Oct 30, 2026. See the trial changes feed for what has changed recently.