drugset / Trial / NCT05630768

Efficacy and Safety of Actonel® After Denosumab Discontinuation in Postmenopausal Osteoporosis Women

NCT05630768

Phase 4 Completed 149 enrolled Dong-A ST Co., Ltd.
NaSingle-groupOpen-labelPrevention

Summary

To evaluate the effect of 1 year of risedronate treatment on the prevention of bone loss after denosumab discontinuation in denosumab-treated post-menopausal osteoporosis for a year

Timeline

Start
2023-01-03
Primary completion
2025-07-23
Completion
2025-07-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Risedronate Small molecule 35 mg Oral
Background Calcium carbonate Other / unclassified Oral
Background Vitamin D Other / unclassified Oral