Viewing Study NCT05841277



Ignite Creation Date: 2024-05-06 @ 6:57 PM
Last Modification Date: 2024-10-26 @ 2:57 PM
Study NCT ID: NCT05841277
Status: COMPLETED
Last Update Posted: 2024-03-29
First Post: 2023-04-24

Brief Title: A Study of LY3819469 in Participants With Impaired and Normal Renal Function
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: Pharmacokinetics of LY3819469 Following Subcutaneous Dose in Participants With Renal Impairment Compared With Participants With Normal Renal Function
Status: COMPLETED
Status Verified Date: 2024-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main purpose of this study is to assess the amount of study drug LY3819469 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 LY3819469 will also be evaluated in these participants The study will last up to 17 weeks including screening period
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
J3L-MC-EZED OTHER Eli Lilly and Company None