A Phase II Randomized, Double-blind, Placebo-controlled Study of Sorafenib or Placebo in Combination With Transarterial Chemoembolization (TACE) Performed With DC Bead and Doxorubicin for Intermediate Stage Hepatocellular Carcinoma (HCC).

Completed · Phase 2 · Has a placebo group

Conditions studied: Carcinoma, Hepatocellular

In brief

This study will look at whether our drug (sorafenib) in combination with chemotherapy delivered directly into your tumor using beads (DC Bead) will slow the progression of the disease. The beads used with the chemotherapy will slowly release the chemotherapy reducing the adverse effects that normally occur with chemotherapy.

Key facts

Study ID

NCT00855218

Run by

Bayer

People needed

307

Starts

2009-03-01

Expected to finish

2013-02-01

Last updated by the study team

2017-08-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Unresectable, multinodular asymptomatic tumor without vascular invasion or extrahepatic spread
• Confirmed Diagnosis of HCC:
• Cirrhotic subjects: Clinical diagnosis by American Association for the Study of Liver Diseases (AASLD) criteria
• HCC can be defined in cirrhotic subjects by one imaging technique (Computed tomography [CT] scan, Magnetic resonance imaging [MRI], or second generation contrast ultrasound) showing a nodule larger than 2 cm with contrast uptake in the arterial phase and washout in venous or late phases or two imaging techniques showing this radiological behavior for nodules of 1-2 cm in diameter.
• Cytohistological confirmation is required for subjects who do not fulfill these eligibility criteria.
• Non-cirrhotic subjects:
• For subjects without cirrhosis, histological or cytological confirmation is mandatory
• Documentation of original biopsy for diagnosis is acceptable
• Child Pugh class A without ascites
• Adequate bone marrow, liver and renal function as assessed by central lab by means of the following laboratory requirements from samples within 7 days prior to randomization:

You may not qualify if…

• Patients on a liver transplantation list or with advanced liver disease as defined below:
• Child Pugh B and C
• Active gastrointestinal bleeding
• Encephalopathy
• Ascites
• Lesions having previously been treated with local therapy such as resection of HCC, radiofrequency ablation (RFA), percutaneous ethanol injection (PEI) or cryoablation can not be selected as the target lesions.

Where it is running

• Study site — Los Angeles, California, United States
• Study site — San Francisco, California, United States
• Study site — Gainesville, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Orlando, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Ann Arbor, Michigan, United States
• Study site — Detroit, Michigan, United States
• Abbott Northwestern Hospital — Minneapolis, Minnesota, United States
• Study site — St Louis, Missouri, United States
• Study site — New York, New York, United States
• Study site — Cleveland, Ohio, United States
• Study site — Columbus, Ohio, United States
• Study site — Portland, Oregon, United States
• Study site — Richmond, Virginia, United States
• Study site — Seattle, Washington, United States
• Study site — Seattle, Washington, United States
• Study site — Camperdown, New South Wales, Australia
• Study site — St Leonards, New South Wales, Australia
• Study site — Greenslopes, Queensland, Australia
• Study site — Clayton, Victoria, Australia
• Study site — Heidelberg, Victoria, Australia
• Study site — Melbourne, Victoria, Australia
• Study site — Nedlands, Western Australia, Australia
• Study site — La Jolla, California, United States

Full record on ClinicalTrials.gov

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