Regorafenib Post-marketing Surveillance in Japan

Status Completed

Clinical Trial Summary

The objective of this study is to assess safety and effectiveness of Regorafenib using in real clinical practice

Clinical Trial Description

This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Regorafenib for gastrointestinal stromal tumors progressed after cancer chemotherapy. A total of 135 patients are to be enrolled and assessed in 6 months standard observational period. At 12 months and 24 months after the first administration of Regorafenib for confirmation of efficacy information including treatment duration and survival status of the patient. ;

Study Design

Related Conditions & MeSH terms

Gastrointestinal Stromal Tumors

Clinical Trial Details

NCT number	NCT01933958
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase
Start date	September 4, 2013
Completion date	October 29, 2021

View Details

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