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
Phase 2
Completed
34 enrolled
Memorial Sloan Kettering Cancer Center
Wake Forest University · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Floxuridine | Unknown | 0.16 mg/kg | — |