Observational Study of Denosumab (Prolia®) in Postmenopausal Women With Osteoporosis

NCT01668589 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1501

Last updated 2018-01-30

Study results available
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Summary

The main objective of this observational study was to describe medication-taking behavior of patients treated with denosumab for postmenopausal osteoporosis (PMO) at 12 and 24 months.

Conditions

  • Postmenopausal Osteoporosis

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-11-28
Primary Completion
2015-08-31
Completion
2015-08-31

Countries

  • Austria
  • Belgium
  • Germany
  • Greece

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01668589 on ClinicalTrials.gov