drugset / Trial / NCT02576951

A Study of Galcanezumab in Healthy Participants

NCT02576951

Phase 1 Completed 178 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The purposes of this study are: * To evaluate tolerability of the Galcanezumab solution injectable formulation (Part A) * To measure how much of the Galcanezumab lyophilized (freeze dried) injectable formulation is absorbed into the blood stream and how long it takes the body to get rid of it compared to the Galcanezumab solution injectable formulation after a single injection under the skin (subcutaneous \[SC\]) (Part B). Information about any side effects that may occur will also be collected. Each part of the study will last about six months. Participants may only enroll in one part.

Timeline

Start
2015-10-19
Primary completion
2016-09-03
Completion
2018-01-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Galcanezumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.