Bazedoxifene Post Approval Safety Study (PASS) in the European Union (EU)

Status Completed

Clinical Trial Summary

This observational cohort study is being conducted to further characterize selected adverse events of interest among a patient population with osteoporosis who are prescribed bazedoxifene, raloxifene, or a bisphosphonate in usual clinical care outside of a randomized clinical trial setting. The study will compare the rates of the selected clinical events among the three treatment groups.

Clinical Trial Description

All women in the database meeting the inclusion criteria will be included in the study without any statistical sampling. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01416194
Study type	Observational
Source	Pfizer
Contact
Status	Completed
Phase
Start date	July 25, 2011
Completion date	April 30, 2019

View Details

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