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Recruiting Phase 4 NCT06472050

Romosozumab Versus Denosumab in GIOP: a 2-year Extension Study

Trial Parameters

Condition Osteoporosis
Sponsor Tuen Mun Hospital
Study Type INTERVENTIONAL
Phase Phase 4
Enrollment 63
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-08-20
Completion 2025-12
Interventions
RomosozumabDenosumab

Brief Summary

The investigators conducted an open-label randomized controlled trial (RCT) in chronic glucocorticoid (GC) users with moderate/high risk of fracture to compare the efficacy and tolerability of romosozumab (ROMO) for 12 months followed by denosumab (DEN) for 12 more months vs DEN for 24 months throughout. Superiority of ROMO/DEN to DEN/DEN in raising the spine bone mineral density (BMD) was demonstrated at month 12 and month 24. The present study was to report the further BMD changes at 48 months (2 year extension) for those participants who were maintained on DEN treatment.

Eligibility Criteria

Inclusion Criteria: 1. patients who are continued on 6-monthly subcutaneous injection of DEN in either the ROMO or DEN arms after month 24 in our original RCT 2. Those who are willing to have a repeat DXA assessment at the end of 4 years. Exclusion Criteria: 1. patients who refuse to be maintained on denosumab after month 24; 2. patients who are maintained on other anti-osteoporotic drugs after month 24; and 3. patients in whom prednisolone is planned to be tapered or discontinued after month 24.

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