drugset / Trial / NCT05067335

A Study to Test the Efficacy, Safety and Tolerability of Romosozumab Treatment in Postmenopausal Chinese Women With Osteoporosis

NCT05067335

Phase 3 Completed 327 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the effect of treatment with romosozumab for 6 months compared with placebo on the percent changes in bone mineral density (BMD) at the lumbar spine, at the total hip and femoral neck in postmenopausal Chinese women with osteoporosis.

Timeline

Start
2021-10-21
Primary completion
2023-11-09
Completion
2023-11-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 210 mg

Indications