A Study of LY3475766 in Healthy Participants

Completed · Phase 1 · Has a placebo group

Conditions studied: Dyslipidemias

In brief

This study will evaluate the safety and tolerability of LY3475766 when given to participants with high levels of blood fat called triglycerides. It will also investigate how the body processes the study drug and the effect of the study drug on the body. Information about any side effects will be documented. This study will last up to 16 weeks for each participant.

Key facts

Study ID: NCT04052594
Run by: Eli Lilly and Company
People needed: 48
Starts: 2019-09-03
Expected to finish: 2021-03-31
Last updated by the study team: 2021-04-28

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

Are overtly healthy males or females, apart from dyslipidemia
Male participants must agree to adhere to contraception restrictions
Female participants must be of nonchildbearing potential and include those who are infertile due to surgical sterilization or those who are postmenopausal
Have a body mass index (BMI) >18.5 and <40 kilograms per meter squared (kg/m²)
Have clinical laboratory test results within normal reference range, or acceptable deviations per investigator discretion
Have a fasting triglyceride (TG) level that is 135 to 499 milligrams per deciliter (mg/dL), inclusive, at both screening and Day -1
Have a fasting low density lipoprotein cholesterol (LDL-C) level greater than or equal to (≥) 70 mg/dL, inclusive, at screening and Day -1
Have had a stable body weight for the 3 months prior to randomization (<5% body weight change)
Have not modified diet or adopted any nutritional lifestyle modification within 3 months prior to randomization

You may not qualify if…

Are taking or have started taking Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors within 3 months prior to randomization; or statins, fibrates, or niacin ≤1000 mg/day within 8 weeks prior to randomization; or niacin >1000 milligrams per day (mg/day) within 16 weeks prior to randomization; or any other lipid-lowering agents within 1 month prior to randomization
Are taking or have started taking a beta-blocker, antiarrhythmic, non-dihydropyridine calcium channel blocker, ivabradine, or any other heart rate lowering agent within 1 month or 5 half-lives prior to randomization, whichever is longer
Have a diagnosis of diabetes mellitus (type 1 diabetes mellitus or type 2 diabetes mellitus) or have 1 of the following at screening: fasting plasma glucose concentration ≥126 mg/dL (7.0 millimoles per liter [mmol/L]) OR a glycated hemoglobin level ≥6.5% (48 millimoles per mole [mmol/mol])
Have previously completed or withdrawn from this study or any other study investigating LY3475766, and have previously received the investigational product
Have known allergies to LY3475766, related compounds, or any components of the formulation, or history of significant atopy
Have a seated heart rate ≤50 beats per minute
Have clinically significant abnormal electrocardiogram (ECG) results constituting a risk while taking the investigational product, as determined by the investigator
Have an abnormal blood pressure (BP) as determined by the investigator

Where it is running

WCCT Global — Cypress, California, United States
Covance Clinical Research Inc — Daytona Beach, Florida, United States
Covance Dallas — Dallas, Texas, United States
Covance Clinical Research Inc — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.