drugset / Trial / NCT00980174

Study to Compare the Efficacy and Safety of DenosumAb Versus Placebo in Males With Osteoporosis

NCT00980174

Phase 3 Completed 242 enrolled Amgen
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to assess how effective and safe denosumab is in a population of males with low bone mass at risk of fracture. The primary clinical hypothesis is that in men with low bone mineral density, the mean percent change in lumbar spine bone mineral density at 12 months in subjects receiving denosumab will be greater than in subjects receiving placebo. Denosumab is a fully human monoclonal antibody with a high affinity for Receptor Activator of Nuclear Factor (RANK) Ligand that can bind and neutralize the activity of human RANK Ligand similar to the action of endogenous osteoprotegerin.

Timeline

Start
2009-10-01
Primary completion
2011-06-21
Completion
2012-05-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous

Indications