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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of ONO-5920 in patients with involutional osteoporosis.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00212628
Study type Interventional
Source Ono Pharmaceutical Co. Ltd
Contact
Status Completed
Phase Phase 3
Start date June 2004

See also
  Status Clinical Trial Phase
Completed NCT00212719 - Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan Phase 3
Active, not recruiting NCT02063854 - A Phase II/III, Double-blind, Parallel Group Comparative Study of Oral Administration of NE-58095 Tablets Phase 2/Phase 3
Completed NCT02066376 - A Phase II/III, Double-blind, Parallel Group Comparative Study of Oral Administration of NE-58095 Tablets Phase 2/Phase 3
Completed NCT00212667 - Controlled Study of ONO-5920 in Patients With Involutional Osteoporosis in Japan Phase 3