drugset / Trial / NCT01588509

Transition From Alendronate to Romosozumab (AMG 785)

NCT01588509

Phase 1 Completed 60 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to estimate the percent change from baseline in lumbar spine bone mineral density (BMD) following multiple-dose administrations of romosozumab in postmenopausal women with low BMD previously treated with alendronate.

Timeline

Start
2012-03-30
Primary completion
2012-11-21
Completion
2012-11-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 140 mg Subcutaneous
Subject Romosozumab Monoclonal antibody 210 mg Subcutaneous

Indications