drugset / Trial / NCT00926380

Denosumab, Teriparatide or Both for the Treatment of Postmenopausal Osteoporosis

NCT00926380

Phase 2 Completed 94 enrolled Massachusetts General Hospital Amgen · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The aim of this study is to determine whether denosumab (an FDA-approved osteoporosis therapy), in combination with teriparatide (an FDA-approved osteoporosis therapy), will increase bone mineral density more than either one alone in postmenopausal osteoporotic women.

Timeline

Start
2009-06
Primary completion
2016-12
Completion
2016-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous
Subject Teriparatide Protein / enzyme biologic 20 ug Subcutaneous