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NCT06728462

A Study of Amorphous Calcium Carbonate in Postmenopausal Women

Recruiting now NA Last updated 7 March 2025
What this trial tests

NA trial testing Amorphous calcium carbonate in Calcium in 205 participants. Currently enrolling.

Timeline
4 March 2025
Primary endpoint
14 December 2025
1 March 2027

Quick facts

Lead sponsorUniversal Integrated Corp.
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment205
Start date4 March 2025
Primary completion14 December 2025
Estimated completion1 March 2027
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Universal Integrated Corp. — full company profile →

Who can join

Adults 60 to 90, female only, with Calcium or Osteoporosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Universal Integrated Corp. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06728462.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing