drugset / Trial / NCT00043186

Determine the Efficacy, Safety and Tolerability of Denosumab (AMG 162) in the Treatment of Postmenopausal Women With Low Bone Mineral Density

NCT00043186

Phase 2 Completed 412 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To determine the effect of denosumab treatment compared with placebo over 12 months on bone mineral density (BMD) of the lumbar spine in postmenopausal women with low BMD. The clinical hypothesis is that denosumab subcutaneous injections administered every 3 or 6 months for 12 months will significantly increase lumbar spine bone mineral density and will be well tolerated.

Timeline

Start
2002-05
Primary completion
2007-04
Completion
2007-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Alendronic Acid Small molecule 70 mg Oral
Subject Denosumab Monoclonal antibody 6 mg Subcutaneous
Subject Denosumab Monoclonal antibody 14 mg Subcutaneous
Subject Denosumab Monoclonal antibody 30 mg Subcutaneous
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous
Subject Denosumab Monoclonal antibody 100 mg Subcutaneous
Subject Denosumab Monoclonal antibody 210 mg Subcutaneous

Indications