drugset / Trial / NCT00377819

Study of Transitioning From Alendronate to Denosumab

NCT00377819 ↗

Phase 3 Completed 504 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study will evaluate the efficacy and safety of transitioning postmenopausal women on current alendronate therapy to denosumab. Endpoints studied will include bone mineral density, bone turnover markers and bone histology in a subset of subjects.

Timeline

Start
2006-09
Primary completion
2008-03
Completion
2008-07

Outcome

Met primary endpoint

paper total hip BMD increased by 1.90% at month 12 compared with a 1.05% increase in subjects continuing on alendronate (p < .0001). PMID 19594293 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alendronic Acid Small molecule 70 mg Oral
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous