drugset / Trial / NCT01525069

Hepatic Arterial Infusion in Treating Patients With Locally Advanced, Non-Metastatic Cholangiocarcinoma

NCT01525069

Phase 1 Terminated 27 enrolled Washington University School of Medicine
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This pilot clinical trial studies the safety and effectiveness of continuous hepatic arterial infusion (HAI) of floxuridine (FUDR) alone or in combination with other chemotherapeutic drugs in treating patients with locally advanced cholangiocarcinoma that cannot be removed by surgery. HAI is a method to deliver higher concentrations of FUDR more directly to liver tumors and reduces side effects. HAI alone or in combination with oxaliplatin and/or gemcitabine may significantly improve clinical outcomes of patients with locally advanced cholangiocarcinoma.

Timeline

Start
2012-04-03
Primary completion
2018-08-08
Completion
2022-08-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Floxuridine Unknown Other
Subject Gemcitabine Small molecule Intravenous
Subject Oxaliplatin Small molecule Intravenous
Background Dexamethasone Small molecule Other

Indications