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A Relative Bioavailability Study of Peresolimab (LY3462817) Formulations in Healthy Participants

Healthy Clinical Trial

Official title:
A Phase 1, Single-Dose Study to Assess the Relative Bioavailability and Tolerability of Subcutaneous Peresolimab Test Formulations in Healthy Participants

Clinical Trial Summary

The main purpose of this study is to look at the amount of the study drug, peresolimab, that gets into the blood stream and how long it takes the body to get rid of it when given under the skin using test formulations versus reference formulation in healthy participants. The study will also evaluate the safety and tolerability of peresolimab and information about any side effects experienced will be collected. For each participant, the total duration of the study will be approximately up to 17 weeks, including screening.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05959109
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date July 21, 2023
Completion date January 11, 2024
View Details
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