The main purpose of this study is to determine the tolerability and safety of LY3461767 with any side effects that might be associated with it. Study drug will be provided in a continuous subcutaneous infusion lasting 24 hours to 96 hours, depending on the cohort. Blood tests will be performed to check concentrations of LY3461767 in the bloodstream and how long it takes the body to get rid of it in participants with chronic heart failure with reduced ejection fraction (HFrEF). The study will last up to 3 months and may include 5 visits.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
44
Henry Ford Hospital
Detroit, Michigan, United States
Washington University
St Louis, Missouri, United States
University of North Carolina, Division of Cardiology
Chapel Hill, North Carolina, United States
Tsuchiura Kyodo Hospital
Tsuchiura, Ibaraki, Japan
Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline through Day 90
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3461767
PK: AUC of LY3461767
Time frame: Predose up to 48 hours post end of infusion
PK: Maximum Concentration (Cmax) of LY3461767
PK: Cmax of LY3461767
Time frame: Predose up to 48 hours post end of infusion
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Kanagawa Prefectural Hospital Organization Kanagawa Cardiovascular and Respiratory Center
Kanazawa Ward,Yokohama, Kanagawa, Japan
National Cerebral and Cardiovascular Center
Suita-shi, Osaka, Japan
The University of Tokyo Hospital
Bunkyo-ku, Tokyo, Japan