drugset / Trial / NCT02791516

A Safety and Efficacy Study to Evaluate Romosozumab (AMG 785) in South Korean Women With Osteoporosis

NCT02791516

Phase 3 Completed 67 enrolled Amgen
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective is to evaluate the effect of treatment with romosozumab for 6 months compared with placebo on percent changes in bone mineral density (BMD) at the lumbar spine as assessed by dual-energy X-ray absorptiometry (DXA) in postmenopausal women with osteoporosis.

Timeline

Start
2017-01-16
Primary completion
2018-02-12
Completion
2018-12-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 210 mg Subcutaneous