Overview

A Study Comparing Two Formulations of Selpercatinib (LY3527723) in Healthy Participants

Status:
Not yet recruiting
Trial end date:
2022-06-19
Target enrollment:
Participant gender:
Summary
The main purpose of this study is to compare the amount of selpercatinib that gets into the blood stream and how long it takes the body to get rid of it, when given as different formulations. The information about any adverse effects experienced will be collected and the tolerability of selpercatinib will also be evaluated. The study may last up to 56 days including the 28 days of screening period.
Phase:
Phase 1
Details
Lead Sponsor:
Loxo Oncology, Inc.
Collaborator:
Eli Lilly and Company