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Clinical Trial Summary

To evaluate the efficacy and safety of R484iv by intravenous intermittent administration to patients with primary osteoporosis in comparison with sodium risedronate hydrate (RIS) by oral administration every day. To evaluate also the dose response of R484iv.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00447915
Study type Interventional
Source Chugai Pharmaceutical
Contact
Status Completed
Phase Phase 3
Start date March 2007
Completion date December 2011

See also
  Status Clinical Trial Phase
Not yet recruiting NCT02142348 - Longitudinal Study of Primary Osteoporosis in Shanghai Postmenopausal Women N/A
Not yet recruiting NCT05370898 - The Study of Chinese Medicine for the Treatment of Primary Osteoporosis N/A
Recruiting NCT05606510 - The Effects of Mindful Exercise on Back Pain in Older Patients With Primary Osteoporosis N/A