HomeTrialNCT06332014
🔬NCT06332014Phase 4ACTIVE NOT RECRUITING

Evaluation of Efficacy and Safety of Prolia in Subjects of Male Osteoporosis in Mainland China

Study Summary

The primary objective of this study is to evaluate the efficacy of Prolia on lumbar spine BMD at 12 months.

Conditions
Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment102 participants
Primary Completion
Lead SponsorAmgen
Data Retrieved2026-04-13 18:29:34.157435+00:00
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