NCT02109042

A Study of Blosozumab (LY2541546) in Postmenopausal Female Participants

A Multiple Dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Blosozumab Proposed Phase 3 Formulation in Postmenopausal Women

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 15 (actual)
• Sponsor: Eli Lilly and Company · Industry
• Sex: Female
• Age: 60 Years
• Healthy volunteers: Accepted

Summary

The purpose(s) of this study is to measure how much of the study drug gets into the blood stream and how long it takes the body to get rid of it when given in multiple doses, subcutaneously (SC) (by inserting a needle just under the surface of the skin in the lower abdominal area), to postmenopausal (PMP) female participants. Information about any side effects that may occur will also be collected. This study will also be looking for special markers called "biomarkers" that can be used to study osteoporosis and/or the effects of the study drug. There will be 2 parts to this study. The first part will last approximately 6 weeks and the second part will last approximately 7 weeks.

Conditions

• Osteoporosis, Postmenopausal

Interventions

Type	Name	Description
DRUG	Blosozumab	Administered subcutaneously

Timeline

• Start date: 2014-04-01
• Primary completion: 2014-07-01
• Completion: 2014-07-01
• First posted: 2014-04-09
• Last updated: 2018-07-16
• Results posted: 2018-07-16

Locations

2 sites across 1 country: United States