Clinical Trials Directory

Trials / Completed

CompletedNCT04472676

A Study of LY3473329 in Healthy Participants

A Safety, Tolerability, and Pharmacokinetic Study of Single-and Multiple-Ascending Doses of LY3473329 in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
86 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years – 54 Years
Healthy volunteers
Accepted

Summary

The main purpose of this study in healthy participants is to learn more about the safety of LY3473329 and any side effects that might be associated with it. Blood tests will be performed to check how much LY3473329 gets into the bloodstream and how long the body takes to eliminate it. This is a two-part study. Participants may only enroll in one part. For each participant: * Part A will last up to about 19 weeks and may include 9 visits. * Part B will last up to about 28 weeks and may include 11 visits.

Conditions

Interventions

TypeNameDescription
DRUGLY3473329Administered orally.
DRUGPlaceboAdministered orally.

Timeline

Start date
2020-08-18
Primary completion
2021-11-09
Completion
2021-11-09
First posted
2020-07-15
Last updated
2021-12-14

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT04472676. Inclusion in this directory is not an endorsement.

A Study of LY3473329 in Healthy Participants (NCT04472676) · Clinical Trials Directory