drugset / Trial / NCT01742091

A Multiple Dose Study of LY2541546 in Healthy Postmenopausal Women

NCT01742091 ↗

Phase 1 Completed 59 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The purpose of this study is to assess the safety and side effects of multiple doses of LY2541546 in postmenopausal women when given subcutaneously (injection just under the skin) and intravenously (directly into a vein). The study will also test how long it takes the study drug to get into the body, how long it takes the body to get rid of it, the overall effect of the study drug on the body, and whether antibodies to the study drug are formed.

Timeline

Start
2009-09
Primary completion
2010-03
Completion
2010-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Blosozumab Monoclonal antibody 180 mg Subcutaneous
Subject Blosozumab Monoclonal antibody 270 mg Subcutaneous
Subject Blosozumab Monoclonal antibody 540 mg Subcutaneous
Subject Blosozumab Monoclonal antibody 750 mg Subcutaneous

Indications

No indication recorded.