drugset / Trial / NCT00280007

Transarterial Chemoembolisation Plus Bevacizumab for Treatment of Hepatocellular Carcinoma

NCT00280007 ↗

Phase 2 Terminated 32 enrolled Medical University of Vienna
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Patients with liver cirrhosis and hepatocellular carcinoma will undergo transarterial chemoembolisation (TACE) as clinically indicated and will be randomized to receive bevacizumab or placebo every 2 weeks up to 1 year. Tumor response will be assessed using MR of the liver and PET-scanning. It will be tested whether the addition of bevacizumab as angiogenic inhibitor will slow down tumor progression, reduce the need for re-embolisation and will improve patient survival.

Timeline

Start
2006-01
Primary completion
2009-12
Completion
2010-12

Outcome

Outcome not reported

Stopped: “Safety concerns in the treatment arm”

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 5 mg/kg Intravenous