Overview

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

Status:
Not yet recruiting
Trial end date:
2022-06-19
Target enrollment:
0
Participant gender:
All
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
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Loxo Oncology, Inc.
Collaborator:
Eli Lilly and Company
Criteria
Inclusion Criteria:

- Participants who are overtly healthy as determined by medical evaluation including
medical history, physical examination, and vital signs.

- Participants who have clinical laboratory test results within the normal reference
range for the population or investigative site, or results with acceptable deviations
that are judged to be not clinically significant by the investigator.

Exclusion Criteria:

- Have a history of allergic reactions to medications or food products

- Have a clinically significant abnormality of blood pressure and/or pulse rate as
determined by the investigator

- Clinically significant abnormalities on ECG as determined by the investigator or
prolongation of the QTcB or QTcF >450 msec at screening

- Have clinically significant active cardiovascular disease or history of myocardial
infarction within 6 months prior to the planned start of selpercatinib

- Have a history or presence of cardiovascular, respiratory, renal, gastrointestinal,
endocrine, hematological, or neurological disorders capable of significantly altering
the absorption, metabolism, or elimination of drugs; of constituting a risk when
taking the investigational product; or of interfering with the interpretation of data.
Appendectomy, splenectomy, and cholecystectomy are considered as acceptable

- Use of H2 blockers, proton pump inhibitors, and other drugs that affect selpercatinib
exposure within 7 days of screening

- Are intending to use over-the-counter or prescription medication, including dietary
supplements, within 14 days prior to dosing and until study discharge (apart from
occasional acetaminophen (≤2 g/24 hours), hormonal contraception, or hormone
replacement therapy)