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Study identifier: NCT06728462 Synced from ClinicalTrials.gov · July 29, 2026
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A Study of Amorphous Calcium Carbonate in Postmenopausal Women

Condition: Calcium · Osteoporosis · Bone Mineral Density  ·  Sponsor: Universal Integrated Corp.

PhaseNA
Planned participants205
Who can joinFemale, 60 Years to 90 Years
Healthy volunteersNo

About this study

Using the FREEDOM substudy as a benchmark, evaluate the effects of amorphous calcium carbonate (ACC) on bone mineral density (BMD) in postmenopausal women, both with and without the combination of Denosumab treatment.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (1)

Kaohsiung Chang Gung Memorial HospitalKaohsiung City, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT06728462