A Study of Merestinib (LY2801653) in Healthy Participants



Status:Not yet recruiting
Conditions:Healthy Studies
Therapuetic Areas:Other
Healthy:No
Age Range:18 - 65
Updated:5/21/2016
Start Date:May 2016
End Date:August 2016
Contact:This is a single site clinical trial. 1-877-CTLILLY (1-877-285-4559) or
Phone:1-317-615-4559

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The Effect of Food on the Bioavailability of Merestinib in Healthy Subjects

The purpose of this study is to evaluate the effect of food on merestinib (standard meal and
high-fat meal) compared to the fasted state. The study will also measure how much of the
study drug gets into the blood stream and how long it takes the body to get rid of it. In
addition, the tolerability of the study drug will be evaluated. Information about any side
effects that may occur will also be collected. The study will last approximately 28 days.
Screening is required within 28 days prior to the start of the study.


Inclusion Criteria:

- Generally healthy sterile male and female participants

- Body mass index (BMI) of 18.0 to 32.0 kilograms per square meter (kg/m²), inclusive

- Are willing and able to eat the protocol specified high-fat breakfast

Exclusion Criteria:

- Have consumed grapefruits or grapefruit-containing products, Seville oranges or
Seville orange juice, star fruit, star fruit juice, or star fruit-containing
products, or commercial apple or orange juice within 14 days prior to first dosing

- Regularly use known drugs of abuse and/or show positive findings on urinary drug
screening

- Have donated blood of more than 500 milliliters (mL) within the last month

- Cannot stop taking over-the-counter (OTC) or prescription medications that alter
gastric pH, at least 14 days prior to first dosing

- Have previously completed or withdrawn from this study or any other study
investigating merestinib, and have previously received the investigational product
We found this trial at
1
site
Daytona Beach, Florida 32117
Principal Investigator: Hugh A Coleman
Phone: 386-366-6446
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mi
from
Daytona Beach, FL
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