drugset / Trial / NCT01575834

Efficacy and Safety of Romosozumab Treatment in Postmenopausal Women With Osteoporosis

NCT01575834 ↗

Phase 3 Completed 7180 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if treatment with romosozumab is effective in preventing fractures in women with postmenopausal osteoporosis

Timeline

Start
2012-03-15
Primary completion
2015-12-14
Completion
2016-12-28

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Romosozumab; p < 0.001; Odds Ratio (OR) 0.27 (95% CI 0.15 to 0.47); NCT01575834 ↗

registry analysis (superiority test); Placebo/Denosumab vs Romosozumab/Denosumab; p < 0.001; Odds Ratio (OR) 0.24 (95% CI 0.15 to 0.39); NCT01575834 ↗

release “In the placebo-controlled FRAME study, treatment with EVENITY resulted in a significant reduction of new vertebral (spine) fracture at 12 months compared to placebo.” amgen.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 210 mg Subcutaneous
Background Denosumab Monoclonal antibody 60 mg Subcutaneous