A Study of LY2940680 in Healthy Participants
Completed · Phase 1
Conditions studied: Healthy Volunteers
In brief
This is a single dose study of radiolabelled LY2940680 taken by mouth in healthy participants to study how the body absorbs and removes LY2940680 from the blood. This study is for research purposes only and is not intended to treat any medical condition.
Key facts
- Study ID
- NCT01746745
- Run by
- Eli Lilly and Company
- People needed
- 6
- Starts
- 2013-01-01
- Expected to finish
- 2013-03-01
- Last updated by the study team
- 2019-07-22
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Generally healthy sterile males or surgically sterile females or postmenopausal females, as determined by medical history and laboratory assessments
- Have a body mass index (BMI) of 18.5 to 32.0 kilograms per square meter (kg/m\^2), inclusive
You may not qualify if…
- Regularly use known drugs of abuse and/or show positive findings on urinary drug screening
- Have consumed herbal supplements, grapefruit juice, grapefruits, grapefruit containing products, Seville orange juice, Seville oranges, star fruit, or star fruit juice within 7 days prior to dosing or intend to consume during the study
- Have donated blood of more than 500 milliliters (mL) within the last month
- Have participated in a [\^14C]-study within the last 6 months prior to admission for this study
- Exposure to significant radiation within 12 months prior to dose (for example, serial X-ray or computed tomography scans, barium meal, current employment in a job requiring radiation exposure monitoring)
- Have a pattern less than once per 2 days to expel feces from the bowel through the rectum or acute constipation within 3 weeks of the day prior to dose
Where it is running
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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