drugset / Trial / NCT03396315

Bisphosphonates for Prevention of Post-Denosumab Bone Loss

NCT03396315

Phase 2 Completed 24 enrolled Columbia University Amgen · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary goal of the study is to assess the extent to which bisphosphonate therapy will prevent decreases in bone mass that may occur after cessation of denosumab in premenopausal women with idiopathic osteoporosis (IOP) enrolled in AAAN0161 (FD05114) "Denosumab for the prevention of post-teriparatide bone loss in premenopausal women with idiopathic osteoporosis". In addition, the investigator will observe participants for a second year off bisphosphonate therapy to assess duration of response. The hypothesis is that bisphosphonate therapy with alendronate or zoledronic acid, initiated after recovery of bone remodeling activity, will prevent significant bone loss after discontinuing denosumab.

Timeline

Start
2018-01-29
Primary completion
2023-06-09
Completion
2023-06-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alendronic Acid Small molecule 70 mg Oral
Comparator Zoledronic acid Other / unclassified 5 mg Intravenous

Indications