drugset / Trial / NCT01796301

An Open-label Study to Evaluate the Effect of Treatment With Romosozumab or Teriparatide in Postmenopausal Women

NCT01796301

Phase 3 Completed 436 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of the study was to evaluate the effect of 12 months of treatment with romosozumab compared with teriparatide on total hip bone mineral density (BMD) in postmenopausal women with osteoporosis who were previously treated with bisphosphonate therapy.

Timeline

Start
2013-01-31
Primary completion
2015-05-14
Completion
2015-05-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 210 mg Subcutaneous
Comparator Teriparatide Protein / enzyme biologic 20 ug Subcutaneous