ELIQUIS (APIXABAN) Regulatory Post-Marketing Surveillance In Clinical

Clinical Trial Summary

The primary objectives of this study is to estimate the real-world safety profile of Eliquis in Japanese Venous Thromboembolism patients and to estimate the risk factors likely to affect the incidence of bleeding. Lastly, the secondary objective of this study is to estimate the real-world effectiveness profile of Eliquis in Japanese Venous Thromboembolism patients.

See also
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NCT number	NCT02836457
Study type	Observational
Source	Bristol-Myers Squibb
Contact
Status	Completed
Phase
Start date	July 1, 2016
Completion date	July 31, 2018

ELIQUIS (APIXABAN) Regulatory Post-Marketing Surveillance In Clinical Practice for Venous Thromboembolism (VTE) Treatment and Prevention Of Recurrent VTE

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms