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Clinical Trial Summary

The main purpose of this study is to evaluate the safety and tolerability of LY3372993 in healthy participants and participants with AD. The study will also investigate how much LY3372993 gets into the bloodstream and test the effects of LY3372993 in participants with AD.

The study has two parts:

- Part A - Healthy participants will receive LY3372993 or placebo. Part A will last up to 17 weeks;

- Part B - Participants with AD will receive LY3372993 or placebo. Part B will last about 317 days.


Clinical Trial Description

In April, 2019, Eli Lilly and Company made a business decision to terminate Part B. No participants were enrolled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03720548
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date November 5, 2018
Completion date May 14, 2019

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