Overview

A Study of LY3473329 in Participants With Impaired and Normal Renal Function

Status:
Not yet recruiting
Trial end date:
2023-12-04
Target enrollment:
0
Participant gender:
All
Summary
The main purpose of this study is to assess the amount of study drug (LY3473329) that reaches the bloodstream and the time it takes for the body to get rid of it when given to participants with renal (kidney) impairment compared to participants with normal renal function. The safety and tolerability of LY3473329 will also be evaluated in these participants. The study will last up to 8 weeks including screening period.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Eli Lilly and Company
Criteria
Inclusion Criteria:

- Have a body mass index within the range 19.0 to 42.0 kilograms per meter squared
(kg/m²)

- Men who agree to use highly effective or effective methods of contraception, women of
childbearing potential (WOCP) who agree to use highly effective or effective methods
of contraception, and women not of childbearing potential (WNOCBP) may participate in
this trial

- Have clinical laboratory test results within the normal reference range for the
population

Exclusion Criteria:

- Have a history or presence of an underlying disease, or surgical, physical, medical,
or psychiatric condition that, in the opinion of the investigator, would potentially
affect participant safety within the study

- Have any abnormality in the 12-lead electrocardiogram (ECG), blood pressure and/or
pulse rate that, in the opinion of the investigator, increases the risks associated
with participating in the study

- Hemoglobin less than 8 grams/deciliter (g/dL) and/or clinically significant anemia
symptoms

- Have an average weekly alcohol intake that exceeds 21 units per week for males and 14
units per week for females or males older than 65 years of age

- Smoke more than 10 cigarettes per day or the equivalent

- Have donated blood of more than 500 milliliter (mL) within 3 months prior to screening