Viewing Study NCT05916560


Ignite Creation Date: 2025-12-25 @ 2:13 AM
Ignite Modification Date: 2026-01-09 @ 12:42 AM
Study NCT ID: NCT05916560
Status: COMPLETED
Last Update Posted: 2025-04-18
First Post: 2023-06-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study of LY3437943 in Participants With Impaired and Normal Liver Function
Sponsor: Eli Lilly and Company
Organization:

Study Overview

Official Title: A Parallel-Group, Single-Dose, Phase 1, Open-Label Study to Investigate the Pharmacokinetics of LY3437943 in Participants With Hepatic Impairment Compared With Healthy Participants
Status: COMPLETED
Status Verified Date: 2025-04
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 measure how much of LY3437943 gets into the bloodstream and how long it takes the body to eliminate it in participants with mild, moderate and severe impaired liver function compared to healthy participants with normal liver function. The safety and tolerability of LY3437943 will also be evaluated. The study may last up to 9 weeks for each participant including the screening period.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
J1I-MC-GZBT OTHER Eli Lilly and Company View