drugset / Trial / NCT00587067

A Phase II Study of Continuous Hepatic Arterial Infusion With Floxuridine (FUDR) and Dexamethasone (DEX) in Patients With Unresectable Primary Hepatic Malignancy

NCT00587067

NaSingle-groupOpen-labelTreatment

Summary

This phase II study aims to evaluate regional chemotherapy in patients with unresectable primary hepatic malignancy. Specifically, eligible patients with hepatocellular carcinoma and peripheral cholangiocarcinoma, considered unresectable after review by the Hepatobiliary Surgery service, will undergo hepatic artery pump placement and continuous infusion of FUDR. The protocol includes radiological and biological correlative studies.

Timeline

Start
2003-06
Primary completion
2016-05-19
Completion
2016-05-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Floxuridine Unknown 0.16 mg/kg

Indications