A Study of LY3885125 in Participants With Dyslipidemia or Non-Alcoholic Fatty Liver Disease (NAFLD)

第1相 早期終了 NCT06007651

概要

The main purpose of this study is to evaluate the safety and tolerability of LY3885125 after administration of single ascending doses in participants with dyslipidemia (part A) and multiple doses in participants with non-alcoholic fatty liver disease (part B). Blood tests will be performed to check how much LY3885125 gets into the bloodstream and how long it takes the body to eliminate it. The study will last up to approximately 49 weeks for part A and 62 weeks for part B, for a total of approximately 111 weeks.

Part A: Number of Participants With One or More Serious Adverse Event(s) Considered by the Investigator to be Related to Study Drug Administration

Baseline up to 36 weeks (Part A) · Participants

Part B: Number of Participants With One or More SAEs Considered by the Investigator to be Related to Study Drug Administration

Baseline up to 36 weeks (Part B)

BENITIONS で見る ClinicalTrials.gov の原文を見る

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