drugset / Trial / NCT00422877
Taxoprexin® Treatment for Advanced Primary Cancers of the Liver, Gallbladder or Biliary Tract
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PACLITAXEL DOCOSAHEXAENOIC ACID | Small molecule | 400 mg/m2 | Intravenous |
| Subject | PACLITAXEL DOCOSAHEXAENOIC ACID | Small molecule | 500 mg/m2 | Intravenous |