Clinical Trials Directory

Trials / Completed

CompletedNCT00532337

Controlled Study of ONO-5334 in Postmenopausal Women With Osteopenia or Osteoporosis

A Multi-centre, Randomized, Double Blind, Parallel Group Study to Investigate Efficacy and Safety of ONO-5334 in Postmenopausal Women With Osteopenia or Osteoporosis

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
285 (actual)
Sponsor
Ono Pharma USA Inc · Industry
Sex
Female
Age
55 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy and safety of ONO-5334 in postmenopausal women with osteopenia or osteoporosis.

Conditions

Interventions

TypeNameDescription
DRUGONO-5334Placebo - 24/mos.
DRUGONO-5334100mg QD /24 months
DRUGONO-533450mg BID /24 mos.
DRUGONO-5334300mg QD /24 mos.
DRUGONO-5334Alendronate 70mg once weekly / 24 mos

Timeline

Start date
2007-10-01
Primary completion
2010-07-01
First posted
2007-09-20
Last updated
2012-06-13

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00532337. Inclusion in this directory is not an endorsement.