Status:

COMPLETED

Regorafenib Post-marketing Surveillance

Lead Sponsor:

Bayer

Conditions:

Colorectal Neoplasms

Eligibility:

All Genders

Brief Summary

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 colorectal cancer. The objective o...

Eligibility Criteria

Inclusion

  • Patients
  • who are determined to start Regorafenib/ STIVARGA treatment

Exclusion

  • Patients who have previously received Regorafenib/ STIVARGA

Key Trial Info

Start Date :

April 22 2013

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 14 2016

Estimated Enrollment :

1301 Patients enrolled

Trial Details

Trial ID

NCT01843400

Start Date

April 22 2013

End Date

November 14 2016

Last Update

August 2 2018

Active Locations (1)

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1

Multiple Locations, Japan