Status:

COMPLETED

Investigating Patient Characteristics of Intermediate Stage Hepatocellular Carcinoma Patients Treated With Nexavar and Their Distribution to Different Treatment Groups as Well as Determining Effectiveness and Safety

Lead Sponsor:

Bayer

Conditions:

Carcinoma, Hepatocellular

Eligibility:

All Genders

Brief Summary

The study aims to investigate patient characteristics of intermediate stage hepatocellular carcinoma patients treated with Nexavar and their distribution to different treatment groups as well as deter...

Eligibility Criteria

Inclusion

  • Patients with a diagnosis of unresectable intermediate stage hepatocellular carcinoma (BCLC-B) for whom the decision has been taken by the investigator to prescribe Nexavar (the BCLC intermediate stage (BCLC-B) consists of Child-Pugh A and B patients with large/multifocal HCC who do not have cancer related symptoms, macrovascular invasion or extrahepatic spread).

Exclusion

  • \- Prior targeted therapy for hepatocellular carcinoma.

Key Trial Info

Start Date :

August 1 2013

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 1 2015

Estimated Enrollment :

19 Patients enrolled

Trial Details

Trial ID

NCT01908322

Start Date

August 1 2013

End Date

September 1 2015

Last Update

November 11 2015

Active Locations (1)

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1

Many Locations, Germany