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CompletedNCT06085482

A Phase I Study of LY3502970 in Healthy Participants

A Single-Group, Open-Label, Single-Period, Phase 1 Study to Determine the Absolute Bioavailability of LY3502970 in Healthy Participants

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
21 Years – 70 Years
Healthy volunteers
Accepted

Summary

The main purpose of this study is to evaluate how much of the study drug (LY3502970) and the radioactive substance 14C incorporated LY3502970 gets into the bloodstream, how its broken down, and how long it takes the body to get rid of it. The study will last up to approximately 9 weeks for each participant.

Conditions

Interventions

TypeNameDescription
DRUGLY3502970Administered orally
DRUG[14C]-LY3502970Administered IV

Timeline

Start date
2023-10-19
Primary completion
2024-01-05
Completion
2024-01-05
First posted
2023-10-17
Last updated
2024-03-25

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06085482. Inclusion in this directory is not an endorsement.

A Phase I Study of LY3502970 in Healthy Participants (NCT06085482) · Clinical Trials Directory