drugset / Trial / NCT05215977

Efficacy and Safety of MW031 in PMO Subjects

NCT05215977

Phase 3 Completed 448 enrolled Mabwell (Shanghai) Bioscience Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is a multicenter, randomized, double-blinded, placebo-controlled Phase III clinical study to evaluate the clinical efficacy and safety of MW031 in Chinese postmenopausal osteoporotic subjects with increased bone fracture risk .

Timeline

Start
2019-12-27
Primary completion
2021-09-27
Completion
2021-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous