drugset / Trial / NCT00249262

Taxoprexin Treatment for Advanced Skin Melanoma

NCT00249262

Phase 2 Completed 30 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 metastatic malignant melanoma being treated with weekly Taxoprexin® Injection.

Timeline

Start
2005-10
Primary completion
2007-04
Completion
2007-04

Drugs

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

Indications