drugset / Trial / NCT01477567

A First-in-Human Study of LY3009385 in Healthy Participants

NCT01477567 ↗

Phase 1 Completed 40 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study is to determine the safety of LY3009385 in healthy participants. The study drug is given as a single dose, by injections under the skin. Side effects will be documented. This study is approximately 28 days not including screening. Screening is required within 28 days prior to the start of the study.

Timeline

Start
2011-11
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Subject LY3009385 Unknown 0.3 mg Subcutaneous
Subject LY3009385 Unknown 1 mg Subcutaneous
Subject LY3009385 Unknown 3 mg Subcutaneous
Subject LY3009385 Unknown 9 mg Subcutaneous
Subject LY3009385 Unknown 22 mg Subcutaneous
Subject LY3009385 Unknown 54 mg Subcutaneous