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A Study of [14C]-LOXO-783 in Healthy Adult Participants

Healthy Clinical Trial

Official title:
A Phase 1, Open-label Two-part Study of the Absorption, Metabolism, Excretion, and the Absolute Bioavailability of [14C]-LOXO-783 in Healthy Adult Subjects

Clinical Trial Summary

The main purpose of this study is to evaluate how much of the study drug, the radioactive substance 14C incorporated LOXO-783 ([¹⁴C]-LOXO-783) passes from blood into urine, feces and expired air in healthy adult participants when administered as a single dose. The study will also measure how much of the LOXO-783 and [¹⁴C]-LOXO-783 gets into the bloodstream, how its broken down, and how long it takes the body to get rid of it. The study is conducted in two parts and will last up to approximately 72 and 61 days for part 1 and 2, respectively.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06102512
Study type Interventional
Source Eli Lilly and Company
Contact Patient Advocacy
Phone 8555696305
Email clinicaltrials@loxooncology.com
Status Not yet recruiting
Phase Phase 1
Start date October 23, 2023
Completion date January 11, 2024
View Details
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