Viviant 20mg Special Investigation (Regulatory Post Marketing Commitment

Status Completed

Clinical Trial Summary

In this survey, to collect the safety and efficacy information of Bazedoxifene in daily medical practice will be examined. In addition, the necessity of special Investigation and post-marketing clinical studies will be examined, while investigating unexpected adverse drug reactions during the survey period and understanding of the status of frequency of adverse drug reactions in daily medical practice.

Clinical Trial Description

All the subjects whom an investigator prescribes the first Bazedoxifene (Viviant) Tablets should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into the investigation at random. ;

Study Design

Related Conditions & MeSH terms

Osteoporosis

Clinical Trial Details

NCT number	NCT01470326
Study type	Observational
Source	Pfizer
Contact
Status	Completed
Phase
Start date	November 2011
Completion date	June 2016

View Details

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Viviant 20mg Special Investigation (Regulatory Post Marketing Commitment Plan) — VIOLINE

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms