drugset / Trial / NCT00389077

Trial of Two Schedules of Perifosine for Patients With Solid Tumors or Lymphomas

NCT00389077

Phase 2 Completed 558 enrolled AEterna Zentaris
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a study of the drug perifosine for patients who have no standard treatment options. This study is designed to identify which cancer types respond to perifosine, and determine which regimen of perifosine is most effective in each one. Patients with either solid tumors or with lymphomas for whom this protocol represents reasonable or optimal treatment will be randomized to receive either perifosine 100 mg daily or 900 mg weekly until disease progression. Based on currently available data it is anticipated that these doses should be easily tolerated by most patients.

Timeline

Start
2005-01
Primary completion
2011-07
Completion
2011-09

Publications

  • Results 1) Journal of Clinical Oncology, 2009 ASCO Annual Meeting Proceedings (Post-Meeting Edition). Vol 27, No 15S (May 20 Supplement), 2009: e15505 / For HCC ( hepatic / sub-population) 2) Journal of Clinical Oncology, 2007 ASCO Annual Meeting Proceedings (Post-Meeting Edition). Vol 25, No 18S (June 20 Supplement), 2007: 15622 / For RCC (renal / sub-population)

Drugs

EvaluationDrugModalityDoseRoute
Subject Perifosine Small molecule 100 mg
Subject Perifosine Small molecule 900 mg

Indications