drugset / Trial / NCT00401388

A Trial of Perifosine in Patients With Chemo-Insensitive Sarcomas

NCT00401388

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a phase II study of perifosine in patients with chondrosarcomas, alveolar soft part sarcomas and extra-skeletal myxoid chondrosarcomas. Patients will receive perifosine 100 mg orally qhs with food until disease progression. The goals of this study include: * In this study a daily dose of perifosine previously determined to be relatively non-toxic will be evaluated in patients with chondrosarcomas, alveolar soft part sarcomas and extra-skeletal myxoid chondrosarcomas. * Response to therapy will be based on regression of measurable disease according to Choi criteria. Time to progression and duration of stable disease will be measured as secondary endpoints of the study.

Timeline

Start
2006-11
Primary completion
2011-01
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Perifosine Small molecule 100 mg Oral