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Study Title: Sorafenib vs Placebo for Hepatocellular Carcinoma
Category: Cancer, General

Currently accepting participants?
Yes - please read the description below and contact the study coordinator if you are interested.

Principal Investigator: Thomas Malpass
Study Coordinator: Andrea Jacks
Phone: 206-625-7373 Ext.63979
Email: andrea.jacks@vmmc.org

What is the Sorafenib vs Placebo for Hepatocellular Carcinoma study?

Regimen: Subjects will take 2 tablets of sorafenib (200 mg tablets) or placebo orally twice daily.

Who can participate?

Patients diagnosed for the first time with hepatocellular carcinoma.
Patients who have recently had surgical resection or ablation with curative intent.
Patients who have a low-risk of recurrence are not eligible to participate.
Patients who are already taking anti-cancer therapy are not eligible.

What do I have to do as a study participant?

Study Summary:

The study will include subjects diagnosed for the first time with HCC. After surgery or ablation, subjects will be randomized to sorafenib or placebo.

Detailed Study Description:

(No information)

Study Design: Interventional, Blinded
Phase of Study: Phase III
Study Type: Interventional
Condition or Study Focus: Hepatocellular Carcinoma (Liver Cancer)
Intervention Type: Drug
Intervention Name: Sorafenib Tablets
Gender: Male and Female
Age group: Interventional
Sponsor: Bayer


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