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Clinical Trial Summary

The main purpose of this study is to evaluate the safety and tolerability of LY3876602 after administering as single ascending doses and following a data review proceeding to multiple ascending doses in healthy participants. The blood tests will also be performed to check how much LY3876602 gets into the bloodstream and cerebrospinal fluid (CSF) and how long it takes the body to eliminate it. The study will last up to approximately 17 weeks. A subgroup of participants will be consented for CSF collections.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06007638
Study type Interventional
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email ClinicalTrials.gov@Lilly.com
Status Recruiting
Phase Phase 1
Start date August 23, 2023
Completion date June 2025

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