drugset / Trial / NCT00523341

Extension Study to Evaluate the Long Term Safety and Efficacy of Denosumab in the Treatment of Osteoporosis

NCT00523341

Phase 3 Completed 4550 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

The primary objective was to describe the safety and tolerability of up to 10 years or 7 years denosumab administration as measured by adverse event monitoring, immunogenicity and safety laboratory parameters in participants who previously received denosumab or placebo, respectively.

Timeline

Start
2007-08-07
Primary completion
2015-07-19
Completion
2015-07-19

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous

Indications