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UnknownNCT05305183

A Phase III Clinical Study of Minodronate Tablets in Postmenopausal Women With Osteoporosis

A Randomized, Double-blinded, Active-controlled, Multicentered Phase III Trial to Assess the Efficacy and Safety of Minodronate Tablets in Postmenopausal Women With Osteoporosis

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
330 (estimated)
Sponsor
Shandong New Time Pharmaceutical Co., LTD · Industry
Sex
Female
Age
46 Years – 80 Years
Healthy volunteers
Not accepted

Summary

In the randomized, active-controlled, double-blinded, multicenter study, the efficacy and safety of monthly oral minodronate were examined and compared to that of weekly oral alendronate.

Conditions

Interventions

TypeNameDescription
DRUGMinodronate Tablets and Alendronate Sodium Tablets-matching placebo;Alendronate Sodium Tablets and Minodronate Tablets -matching placeboall subjects will receive Calcium Carbonate and Vitamin D3 Tablets as basic medication.

Timeline

Start date
2022-05-31
Primary completion
2023-05-31
Completion
2024-05-31
First posted
2022-03-31
Last updated
2022-03-31

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05305183. Inclusion in this directory is not an endorsement.

A Phase III Clinical Study of Minodronate Tablets in Postmenopausal Women With Osteoporosis (NCT05305183) · Clinical Trials Directory