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Recruiting Phase 1 NCT06809400

A Study of LY4006896 in Healthy Participants and Participants With Parkinson's Disease

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Plain-language summary for patients

Trial Parameters

Condition Parkinson Disease
Sponsor Eli Lilly and Company
Study Type INTERVENTIONAL
Phase Phase 1
Enrollment 127
Sex ALL
Min Age 30 Years
Max Age 85 Years
Start Date 2025-02-18
Completion 2028-01
Interventions
LY4006896Placebo

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Brief Summary

The purpose of this study is to generate evidence of the safety, tolerability, and pharmacokinetics/pharmacodynamics of IV LY4006896 compared with placebo in healthy participants and participants with Parkinson's disease.

Eligibility Criteria

Inclusion Criteria: Part A Single Ascending Dose (SAD) and B Multiple Ascending Dose (MAD) * Have a body mass index within the range of 18 to 34 kilogram/square meter (kg/m²) (inclusive). * For Japanese participants: To qualify as a participant of first-generation Japanese origin, the participant, the participant's biological parents, and all of the participant's biological grandparents must be of exclusive Japanese descent and born in Japan. * Have venous access sufficient to allow for blood sampling or administration of study intervention for IV administration, or both. Part A (SAD) Only * Participant must be 30 to 85 years of age (inclusive), at the time of signing the informed consent * Are overtly healthy * For Chinese participants: To qualify as Chinese for this study, all 4 of the participant's biological grandparents must be exclusive Chinese descent and born in China. Part B (MAD) Only * Participant must be 40 to 85 years of age (inclusive), at the time of signing the informed

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