drugset / Trial / NCT00422877

Taxoprexin® Treatment for Advanced Primary Cancers of the Liver, Gallbladder or Biliary Tract

NCT00422877

Phase 2 Terminated 13 enrolled American Regent, Inc.
NaSingle-groupOpen-labelTreatment

Summary

To evaluate objective response rate and duration of response to weekly Taxoprexin®. To evaluate the safety profile of weekly Taxoprexin® in this patient population. To evaluate overall survival in the same patient population. To evaluate time to disease progression, and the time to treatment failure in patients with primary liver cancer being treated with weekly Taxoprexin® Injection. To explore the trough and peak blood levels of Taxoprexin® and paclitaxel in these patients.

Timeline

Start
2007-01
Primary completion
2008-03
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Subject PACLITAXEL DOCOSAHEXAENOIC ACID Small molecule 400 mg/m2 Intravenous
Subject PACLITAXEL DOCOSAHEXAENOIC ACID Small molecule 500 mg/m2 Intravenous

Indications