A Study of LY2484595 on the Electrical Activity of the Heart
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers
In brief
The purpose of this study is to evaluate the effect on the electrical activity of the heart as measured by an electrocardiogram (ECG) after dosing with 10 days of LY2484595 compared to 10 days of placebo in relation to a single dose of moxifloxacin. Information about any side effects that occur will also be collected.
Key facts
- Study ID
- NCT01537887
- Run by
- Eli Lilly and Company
- People needed
- 72
- Starts
- 2012-02-01
- Expected to finish
- 2012-06-01
- Last updated by the study team
- 2019-03-07
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy males and females
- Body mass index (BMI) of 18.5 to 29 kilograms per square meter (kg/m²)
- Reliable and willing to be available for the duration of the study and are willing to follow study procedures
- Provided written informed consent
You may not qualify if…
- Known allergies to LY2484595 or moxifloxacin
- Personal or family history of long QT syndrome, heart failure, or low blood potassium (hypokalemia) a family history of sudden death, or unexplained syncope within the last year
- Positive findings on urinary drug screening
- Cigarette smokers
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. — Daytona Beach, Florida, United States
- 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. — Evansville, Indiana, United States
Full record on ClinicalTrials.gov
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