Expired Study
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Salt Lake City, Utah 84106


Purpose:

This study involves single doses of LY3154207 and will evaluate the effects of LY3154207 on the body. There will be 3 parts to this study. Part A will test single increasing doses of LY3154207 and will last approximately 7 weeks for each participant. Each participant will receive two doses of LY3154207, if part A is completed. Part B will test a single dose of LY3154207 and will last approximately 5 weeks for each participant. Part B includes collecting fluid from the spinal column to measure levels of LY3154207. Part C will include a single dose of LY3154207 given alone and then a second dose given along with itraconazole to look for change in LY3154207 levels. Part C will last about 3 weeks for each participant. Participants may only enroll in 1 of the 3 parts of the study.


Criteria:

Inclusion Criteria: - Overtly healthy males or females, as determined by medical history and physical examination - Female participants not of child-bearing potential - Are reliable and willing to make themselves available for the duration of the study and are willing to follow study procedures - Have given written informed consent - Have a body mass index (BMI) of 18 to 35 kilograms per square meter (kg/m^2) Exclusion Criteria: - Part B only: Have medical or surgical conditions in which lumbar puncture is contraindicated - Part C only: Have known allergy or contraindications to itraconazole


NCT ID:

NCT02365571


Primary Contact:

Study Director
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)
Eli Lilly and Company


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah 84106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 22, 2017

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