130
Participants
Start Date
January 1, 2026
Primary Completion Date
January 1, 2028
Study Completion Date
January 1, 2030
Denosumab (Prolia)
60mg subcutaneous Denosumab (1mL solution) every 6 months and intravenous placebo (100mL normal saline) once yearly
Zoledronic acide (Aclasta)
5mg intravenous Zoledronic Acid (100mL solution) once yearly and subcutaneous placebo (1mL normal saline) every 6 months
The Chinese University of Hong Kong, Hong Kong
Prince of Wales Hospital, Shatin, Hong Kong
OTHER