Nexavar Post-marketing Surveillance for Renal Cell Carcinoma in Japan

Status Completed

Clinical Trial Summary

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have been administered with Nexavar for unresectable or advanced renal cell carcinoma (RCC). The objective of this study is to assess safety and effectiveness of Nexavar under real-life practice conditions. This study is an all case investigation of which the enrollment period is 15 months, and all patients who received Nexavar will be recruited and followed one year since starting Nexavar administration.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01411423
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase
Start date	April 18, 2008
Completion date	February 28, 2016

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