Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
54 participants
INTERVENTIONAL
2019-10-23
2020-02-12
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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LY3372689
LY3372689 administered orally
LY3372689
Administered orally
Placebo
Placebo administered orally
Placebo
Administered orally
Interventions
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LY3372689
Administered orally
Placebo
Administered orally
Eligibility Criteria
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Inclusion Criteria
* Have a body mass index (BMI) of 18.5 to ≤30 kilograms per square meter (kg/m²)
* Have normal blood pressure, pulse rate, electrocardiogram (ECG, heart tracing), blood and urine laboratory test results that are acceptable for the study
* Have veins suitable for ease of blood sampling
Exclusion Criteria
* Have previously participated or withdrawn from this study
* Smoke more than the equivalent of 10 cigarettes per day and are unwilling to stop smoking for study procedure
* Have or used to have health problems or laboratory test results or ECG readings that, in the opinion of the doctor, could make it unsafe to participate or could interfere with understanding the results of the study
18 Years
65 Years
ALL
Yes
Sponsors
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Eli Lilly and Company
INDUSTRY
Responsible Party
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Principal Investigators
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Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)
Role: STUDY_DIRECTOR
Eli Lilly and Company
Locations
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Covance
Dallas, Texas, United States
Countries
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Other Identifiers
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I9X-MC-MTAC
Identifier Type: OTHER
Identifier Source: secondary_id
17242
Identifier Type: -
Identifier Source: org_study_id
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