Study to Evaluate AMG 162 in the Prevention of Postmenopausal Osteoporosis

Status Completed

Clinical Trial Summary

This study will determine whether treatment with AMG 162 can prevent lumbar spine bone loss in both early and late postmenopausal women with osteopenia, and to further test the safety and tolerability of AMG 162 in this population.

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: Prevention

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00091793
Study type	Interventional
Source	Amgen
Contact
Status	Completed
Phase	Phase 3
Start date	August 2004
Completion date	March 2009

View Details

See also
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